General Practice/Public Health Flashcards

1
Q

On a routine health exam, a 40-year-old woman is found to have hypercholesterolemia. She mentions that her older sister has hypertension. Which one of the following suggests a familial cause for her hypercholesterolemia?

A. Tendon xanthomas.
B. Xanthelasma of the eye.
C. The family history of hypertension.
D. Age of the patient.
E. The presence of corneal arcus.

A

A. Tendon xanthomas

Familial hypercholesterolemia (FH) is an autosomal-dominant inherited condition characterized by a genetic defect in one of several genes affecting receptor-mediated uptake of low-density lipoprotein (LDL). Affected individuals present with characteristic metabolic and clinical features including high cholesterol levels and increased risk of premature cardiovascular disease.

Clinical features of FH are:
-Premature cardiovascular disease (CVD) 
-Aortic stenosis
-Tendon xanthomas (11%)
-Corneal arcus (27%)
-Xanthelasmas (12%)

There are many other potential causes of premature CVD and aortic stenosis. Likewise, corneal arcus and xanthelasma are non-specific signs, but tendon xanthomas, which may gradually develop in Achilles’ tendons and extensor tendons of the dorsum of the hand, are pathognomonic for FH. However, they are rarely identifiable before adulthood.

Corneal arcus in a young adult is suggestive of FH, but not pathognomonic.

  • See picture of achilles tendon xanthoma, xanthelasma, corneal arcus below -
  • RACGP - AJGP- Familial hypercholesterolaemia: A guide for general practice
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2
Q

A 52-year-old man presents to your clinic, seeking advice on screening for colon cancer. Although he has no gastrointestinal symptoms, he is concerned because his younger brother has been recently diagnosed with colon cancer at the age of 50 years. There is no other family history of colorectal cancer. Which one of the following is the most appropriate advice regarding current and future management?

A. He should have a fecal occult blood test (FOBT) now.
B. No screening procedure is required now.
C. Colonoscopy should be performed now, and if normal, no further testing is required.
D. Colonoscopy should be performed now and yearly thereafter.
E. Colonoscopy should be performed now and 5-yearly thereafter.

A

E. Colonoscopy should be performed now and 5-yearly thereafter.

Colorectal cancer (CRC) screening methods and intervals depend on the individual’s risk category. Based on the risk of developing CRC, the population is classified in four categories:
- See table below

This patient is asymptomatic, but has a brother (first-degree relative) diagnosed with CRC at the age of 50 years (< 55 years).

Therefore, he should be placed in category 2. People in category 2 should be offered iFOBT every two years fron the age of 40 to 50 years and colonoscopy everu five years from 50 to 74 years of age. Since he is 52 years now, colonoscopy now and then every five years afterwards is the most appropriate option.

Latest guideline from RACGP
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3
Q

Sarah, whose husband has a plasma cholesterol of 6.4 mmol/L (normal < 5.5mmol/l), wants to know which cooking oil she should use when she cooks. Which one of the following would you advise?

A. There is not much difference between cooking oils.
B. Any margarine is suitable.
C. An oil rich in saturated fat rather than those rich in unsaturated fats.
D. She should use either canola or sunflower oil.
E. None of the above.

A

D. She should use either canola or sunflower oil.

Epidemiological studies have shown reduced mortality from cardiovascular causes if diets containing increased levels of mono- and polyunsaturated fatty acids are used. Canola oil and olive oil have a high concentration of monounsaturated fatty acids, while sunflower oil is rich in polyunsaturated fatty acids. Both canola and sunflower oil are appropriate dietary oils for Sarah’s husband.

For lowering the plasma cholesterol levels, the National Heart Foundation of Australia recommends that saturated fat (option C) in the diet be replaced with a combination of mono- and polyUNsaturated fats.

Cholesterol content of foods does increases LDL cholesterol. LDL cholesterol is directly related to the amount of saturated and trans fat contents of dietary intake.

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4
Q

A 42-year-old olive-skinned man comes to your GP practice because he is concerned about contacting melanoma after he watched a TV program about it. He has no family history of melanoma or other skin cancers. On examination, there is no abnormal finding. You reassure him but he says that he will come back to you if he finds anything unusual. Which one of the following will you recommend instead for follow-up?

A. Follow-up every six months.
B. Follow-up every two years.
C. Follow-up every five years.
D. Start him on regular medication.
E. Follow-up every 12 months.

A

C. Follow-up every five years.

Australia has the highest incidence of skin cancer in the world. Current clinical guidelines DO NOT recommend systemic skin cancer screening, but in clinical practice many general practitioners do provide skin checks for their patients.

A ‘skin-check’ can be defined as a comprehensive assessment of any asymptomatic patient for any evidence of skin cancer. Current Australian guidelines advise against general population screening for skin cancer, based on lack of evidence that justifies organized screening as an effective method to reduce mortality. Patient self examination with opportunistic screening is the current standard.

One’s risk of contracting skin cancer is classified as ‘high-risk’, ‘intermediate risk’, or ‘low risk’ according to the following table: - See table below -

Recommendations for skin check are as follows:

* High-risk: 3-monthly self examination and 12 monthly skin check with doctor
* Medium-risk: 3- to 6-monthly self examination and 2- to 5-yearly skin check with doctor
* Low-risk: 12-monthly self examination and check with doctor for assessment of risk and advice regarding skin care

With olive-colored skin, this man has a skin type of IV to V. Considering the additional fact that he has no family history of skin cancer, he is low-risk for developing skin cancer. The recommendations for this patient are annual self examination and one-shot check with doctor. However, he has not been fully reassured despite your efforts. For this reason and for putting his mind at ease 5-yearly check – up can be offered.

TOPIC REVIEW
The Fitzpatrick Skin Type is a skin classification system that classifies skin types based on a scoring system

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5
Q

A 37-year-old computer software engineer man comes to you because he is concerned about developing malignant melanoma. His concerned arose when his father was diagnoses with melanoma eight months ago. He does not drink alcohol nor does he smoke. On examination, only multiple benign nevi are noted. Which one of the following would be the most appropriate management of this patient?

A. Excision of his benign nevi.
B. Refer him to a dermatologist.
C. Review him in 12 months.
D. Reassure him.
E. Review him in 2-5 years.

A

C. Review him in 12 months.

Australia has the highest incidence of skin cancer in the world. Current clinical guidelines do not recommend systemic skin cancer screening, but, in clinical practice many general practitioners do provide skin checks for their patients.

A ‘skin-check’ can be defined as a comprehensive assessment of any asymptomatic patient for any evidence of skin cancer. Current Australian guidelines advise against general population screening for skin cancer, based on lack of evidence to justy organized screening as an effective method to reduce mortality. Patient self-examination with opportunistic screening is the current standard.

One’s risk of contracting skin cancer is classified as ‘high-risk’, ‘intermediate risk’, or ‘low risk’ according to the following table: - See table below -

Recommendations for skin check are as follows:

* High-risk: 3-monthly self examination and 12 monthly skin check with doctor
* Medium-risk: 3- to 6-monthly self examination and 2- to 5-yearly skin check with doctor
* Low-risk: 12-monthly self examination and check with doctor for assessment of risk and advice regarding skin care

With the father being diagnosed with melanoma, this man is categorised as ‘high-risk’ for skin cancers. It is recommended that high-risk people have 3-6 monthly self examination and check up with doctor every 12 months.

(Option A) Removing simple nevi to prevent melanoma is not recommended, because melanoma often arise de novo from other sites other than the nevi.

(Option B) Referring the patient to a dermatologist is not necessary at this stage because the patient is asymptomatic now.

(Option D) Reassuring the patient is not appropriate because he is high risk for melanoma.

(Option E) Check up with doctor every 2-5 years would be the option if this man was categorised as medium risk.

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6
Q

You are giving a lecture in a primary school regarding skin cancer awareness. Which one of the following is the most appropriate advice you should emphasize on?

A. Using sunscreens in the morning.
B. Avoiding or lessening sun-exposure between 10am and 4pm.
C. Annual skin checks and screening.
D. Excision of moles.
E. Avoiding sun-exposure.

A

B. Avoiding or lessening sun-exposure between 10am and 4pm.

Australia has the highest rate of skin cancers in the world. Protective measures help reduce development of skin cancers. Of all known risk factors for skin cancer, sun-exposure is the most important MODIFIABLE one (not the most important one in general).

All people (especially children aged ≤ 10 years) should be advised to use protective measures when UV levels are 3 and above. UV level throughout the day depends on the season, but generally UV levels are highest between 10am and 4pm, the time during which protection against sun-exposure should be advised.

These measures include:
**Broad-brimmed, bucket or legionnaire-style hats
**Protective clothing
**Sunglasses
**Sunscreens with at least a sun protection factor (SPF) of (needs reapplication every 2 hours)

(Option A) Using sunscreens only in the morning is not because sunscreens are required to be reapplied every 2 hours. UV level in the early hours of the morning is not expected to be that high compared to later hours such as noon and afternoon.

(Option C) Annual skin checks is advisable for those who are high risk for skin cancers, and is not recommended for general population.

(Option D) Excision of moles has not shown to be associated with decreased risk of skin cancers. Furthermore, melanomas have shown to often arise de novo (from areas of the skin with no pre-existing moles).

(Option E) Complete avoidance from sun-exposure results in vitamin D insufficiency and its complications, and is not recommended.

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7
Q

In a randomized controlled trial (RCT) conducted to study the effect of aspirin on prevention of coronary artery events among diabetic smokers, the results in the two arms of the study are as follows: - See table below -

Which one of the following is the relative risk of not using ASA?
A. 1%.
B. 2%.
C. 100%.
D. 200%.
E. 50%.

A

D. 200%.

D. 200%.

  1. Relative Risk (RR):
    • Measures the risk of an event occurring in an exposed group versus a non-exposed group.
  2. Incidence Calculation:
    • Exposed Group (Aspirin): 1 event out of 100 = 1%.
    • Non-Exposed Group (Placebo): 2 events out of 100 = 2%.
  3. Relative Risk Calculation:
    • RR = Incidence in Exposed Group / Incidence in Non-Exposed Group
    • RR = 1% / 2% = 0.5
  4. Interpreting RR:
    • RR of 0.5: Indicates that taking aspirin halves the risk of a coronary event.
    • Risk Reduction: 50% less risk for those on aspirin.
    • Increased Risk for Non-Exposed: Those not taking aspirin are twice as likely to have a coronary event compared to those taking it.
  5. 200% Increase:
    • Explanation: If not taking aspirin, the risk is doubled (or 200% increased).

The concept of a 200% increase comes from understanding the relative risk (RR) and translating it into a percentage increase.

  1. Relative Risk (RR):
    • The RR calculated is 0.5. This means that the risk of developing a coronary event for those taking aspirin is half (50%) of the risk for those not taking aspirin.
  2. Interpreting the RR:
    • If RR = 0.5, it indicates that the risk is reduced by 50% for those taking aspirin compared to those not taking aspirin.
  3. Inverse of the RR:
    • To find out the increase in risk for those not taking aspirin, we take the inverse of 0.5:
      [
      \text{Inverse RR} = \frac{1}{0.5} = 2
      ]
    • This means that those not taking aspirin have twice the risk (or 2 times the risk) of having a coronary event compared to those taking aspirin.
  4. Translating to Percentage:
    • Saying that the risk is twice as high can be expressed as a 100% increase. However, since it’s twice (2 times), it’s actually a 200% increase.
    • Mathematically:
      [
      \text{Percentage Increase} = (2 - 1) \times 100\% = 100\% \times 2 = 200\%
      ]
  • 200% increase means that the risk of a coronary event for those not taking aspirin is three times (300%) the risk for those taking aspirin, but specifically, it’s a 200% increase relative to the baseline risk (100%).

Not taking aspirin leads to a 200% increased risk of a coronary event compared to taking aspirin.

In statistics and epidemiology, relative risk or risk ratio (RR is the ratio of the probability of an event occurring in an exposed group to the probability of the event occurring in a non-exposed, comparison group.

Of 100 diabetic smokers who are on aspirin, 1 person has developed a coronary event. So the incidence of coronary event in this group is 1% [1/(1+99)x100], while the incidence of coronary events in the group taking placebo instead of aspirin is 2% [2/(2+98)x100].

In this scenario the exposure is taking aspirin. Exposed group has a 1% chance of developing a coronary event versus 2% in those who do not take aspirin.
The RR is then calculated by dividing the odds of the condition in the exposed group (1%) by that of the non-exposed group:

RR= P(exposed) / P(non-exposed) : RR=1% / 2%=0.5

Here, the RR indicates that the odds of developing a coronary event in those diabetic smokers who are on aspirin is half compared to those on placebo. In other words, those who are on aspirin has a 50% risk reduction. Inversely, those who are not taking aspirin are twice as likely to develop a coronary event compared to those who are taking it. So the RR. This means that not taking aspirin is associated with a 200% increase in incidence of coronary events.

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8
Q

A 67-year-old woman presents for receiving her annual influenza vaccination. She also mentions that her daughter is going to have a baby in 2 months and asks if she should receive other vaccines that may help. Which one of the following vaccines will you advise?

A. Pneumococcal vaccine.
B. Varicella vaccine.
C. Hepatitis B vaccine.
D. DPT vaccine.
E. Hemophilus influenza vaccine.

A

D. DPT vaccine.

According to vaccination national program every child should be vaccinated against pertussis (whooping cough infection at ages 6 weeks, 4 months and 6 months.
The mother, the father and other adults in close contact with young babies can be the source of whooping cough infection in children who are still too young to be vaccinated. For this reason, they should seek advice from their GPs about the benefits of getting an adult pertussis-containing vaccine.

Vaccination against whooping cough (pertussis) is strongly recommended for adults in contact with children too young to be vaccinated. These people should be vaccinated before or as early as possible after the birth of the baby if they have not had a pertussis vaccine in the past 10 years.

Pneumococcal was indicated for this woman for her own sake, and not the baby’s, if she was older than 65.

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9
Q

You are going to give a lecture about obesity and body mass index (BMI). Which one of the following is the most appropriate advice?

A. BMI alone is the best way to estimate obesity.
B. BMI gives false estimates in elderly people because of a fatty abdomen.
C. Waist circumference is the best way to estimate obesity.
D. BMI in conjunction with waist circumference is the best way to estimate obesity.
E. BMI alone is the best predictor of cardiovascular risk.

A

D. BMI in conjunction with waist circumference is the best way to estimate obesity.

An adult’s BMI can be compared to thresholds to define whether a person is underweight, of healthy weight, overweight or obese based on the WHO classifications.
BMI is calculated by dividing weight in kilograms by the square of height in meters.

WHO classification is shown in the following table: -See table below-

Individuals with the same BMI may have different ratios of body fat to lean mass. People with high muscle mass (e.g. athletes) may have a lower proportion of body fat than less muscular people, so a higher BMI threshold must be considered.

Women have more body fat than men with equal BMIs. People lose lean tissue with age, so an older person will have more body fat than a younger one at the same BMI.
This fact necessitates waist circumference as an additional factor. Waist circumference is a good indicator of total body fat and is also a useful predictor of visceral fat. Compared to BMI, waist circumference is a better predictor of cardiovascular risk and type 2 diabetes (in women, but not in men).

The best method for estimation of obesity in adults is a combination of BMI and waist circumference. The latter takes into account fat distribution, and in combination with BMI, gives a more accurate benchmark for obesity. Alhtough this combination is useful for determining the cardiovacular risk due to obesity, the most accurate measure for prediction of cardiovascular risk and ischmeic heart disease is ‘waist to hip ratio’ (not an option here).

(Option A) BMI alone is never the best predictor of cardiovascular risk in adults.

(Option B) BMI gives false negative results in older people due to decreased total lean mass, not only the abdomen. Even in an elderly with a flat abdomen, BMI may not be accurate due to the fact the most of their weight is comprised of fat rather than lean mass.

(Option C) Waist circumference alone is not accurate and should not be interpreted as an indicator of cardiovascular risk.

(Option E) BMI is not a predictor of cardiovascular risk an as mentioned earlier, may not be an accurate tool for estimation of obesity in certain groups such as muscular athletes, the elderly, etc

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10
Q

A 49-year-old male, commercial truck driver by profession, presents with left-sided chest pain radiating to his left arm and jaw. Electrocardiography shows ST segment elevation myocardial infarction (STEMI). Thrombolysis is done with tenecteplase, which resulted in resolution of symptoms. Which one of the following would be the best advice regarding driving?

A. He can drive a private car after four weeks.
B. He can drive his commercial truck after four weeks.
C. There is no driving restriction.
D. He can never drive his truck.
E. He should drive carefully and avoid driving on main highways.

A

B. He can drive his commercial truck after four weeks.

Following an acute myocardial infarction, the patient cannot drive private vehicles for two weeks and commercial vehicles for four weeks.

TOPIC REVIEW
There are several conditions or procedures which lead to reduced ability to drive. Under these circumstances, the treating physician should give appropriate advice regarding driving. It is the patients’ duty (not the treating physician) to inform the Road Safety Department about their condition. Failing to do so will lead to prosecution. The most commonly encountered medical problems/procedures that may be faced and the consequent driving limitations, including non-driving periods, are listed in the following table.

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11
Q

A 65-year-old man presented to the emergency department with complaint of chest pain that turned out to be of cardiac origin. Electrocardiographic changes were consistent with inferior ST elevation myocardial infarction (STEMI). He underwent coronary artery bypass graft the next day. He is a commercial driver and on discharge wants to know if he can continue driving. Which one of the following would be the most appropriate advice?

A. He can drive private and commercial vehicles as long as he feels fine.
B. He should write a letter to road safety department.
C. No commercial driving for four weeks.
D. No commercial driving for three months
E. He can never drive commercial vehicles, but he can drive private vehicles after three months

A

D. No commercial driving for three months

After coronary artery bypass grafting, one should not drive private vehicles for at least four weeks and commercial vehicles for three months.
(Longer wait compared to acute MI without CABG)

TOPIC REVIEW
There are several conditions or procedures which lead to reduced ability to drive. Under these circumstances, the treating physician should give appropriate advice regarding driving. It is the patients’ duty (not the treating physician) to inform the Road Safety Department about their condition. Failing to do so will lead to prosecution. The most commonly encountered medical problems/procedures that may be faced and the consequent driving limitations, including non-driving periods, are listed in the following table:

ST’s Summary: CABG, vascular repairs (aneurysm, valvular repair), syncope, stroke > can’t drive private car for 1 month, commercial cars for 3 months!

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12
Q

A 65-year-old was found to have an abdominal aortic aneurysm. The aneurysm was repaired by a vascular surgeon, and the patient was transferred to the Intensive Care Unit (ICU) where he stayed for 24 hours. The recovery period was uneventful. The patient is now ready to be discharged, and wants to know whether he can drive his private car. Which one of the following is the most appropriate advice regarding driving?

A. He is unfit to drive for six months post-repair.
B. He is unfit to drive for six months as he has been in intensive care unit.
C. He can drive after he spends a week at home without any symptoms.
D. After his general practitioner considers him fit to drive.
E. He is unfit to drive for four weeks.

A

E. He is unfit to drive for four weeks.

After repair of an aortic aneurysm or cardiac valvular repair, one is unfit to drive their private motor vehicles for at least four weeks. This extends to three months for commercial vehicles. They can then have their unconditional driving license again.

ICU admission for 24 hours is a normal routine after some surgeries and does not pose any restriction on driving by itself.

Referral to general practitioner is not the correct answer as the patient should be informed of the restrictions upon discharge. The patient may plan to visit his general practitioner in a week and without knowing about his driving limitations.

ST’s Summary: CABG, vascular repairs (aneurysm, valvular repair), syncope, stroke > can’t drive private car for 1 month, commercial cars for 3 months!

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13
Q

You are counselling a patient who is concerned about the cholesterol content of foods. Which one of the following foods contains the most cholesterol content?

A. Yoghurt.
B. Avocado.
C. Coconut oil.
D. Peanut butter.
E. Canola.

A

A. Yoghurt.

Cholesterol is only found in animal products such as meat, poultry, fish, dairy products and egg. Although vegetable products have different levels of fat, they do not contain cholesterol. Of the given options, only yoghurt (a dairy product) contains cholesterol.

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14
Q

A 45-year-old man presents to the emergency department with a self-limiting episode of seizure. He is known to have epilepsy which has been well-controlled with carbamazepine for the last 12 months. Full investigations including blood tests and CT scan of the head reveals no apparent cause for the seizure. The patient is keen to know about the driving restriction. Which one of the following is the appropriate advice regarding driving?

A. He cannot drive for 4 weeks.
B. He cannot drive for 3 months.
C. He cannot drive for 6 months.
D. He cannot drive for 12 months.
E. He cannot drive for 3 years.

A

B. He cannot drive for 3 months.

If one develops an episode of seizure after at least 12 months of being well-controlled by antiepileptic drugs, they cannot drive for 4 weeks if a provocative factor (sleep deprivation, alcohol, electrolyte abnormality, CNS lesion, etc) can be identified, and for 3 months if no cause is found.

The patient then may be eligible to hold a conditional driving license provided that the patient does not experience another attack during the mentioned periods.

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15
Q

A 65-year-old commercial driver sustained stroke and presented with left hemiparesis and left homonyms hemianopia. He is now making a good recovery. Which of the following is most appropriate step regarding driving?

A. Permanent restriction of driving.
B. Driving assessment supervised by an occupational therapist.
C. He should not drive for two weeks.
D. Refer him to a neurologist to decide about fitness to drive.
E. He can continue driving.

A

B. Driving assessment supervised by an occupational therapist.

Cerebrovascular events (e.g. stroke, TIA) make the patient unfit to drive non-commercial vehicles for at least four weeks. Once there is no residual deficit and the risk of recurrence is minimized by appropriate measures such as prophylactic anticoagulation, the patient should be assessed by an occupational therapist (or any other relevant consultants such as ophthalmologist, neurologist, etc. depending on the residual defects) for evaluation of fitness to drive.

There are a wide range of practical assessments available, including off-road, on-road and driving simulator assessments, each with strengths and limitations. Assessments may be conducted by occupational therapists trained in driver assessment
or by others approved by the particular driver licensing authority. Processes for initiating and conducting driver assessments vary between the states and territories and choice of assessment depends on resource availability, logistics, cost and individual requirements. The assessments may also be initiated by the examining health professional, other referrers (e.g. police, self, family) or by the driver licensing authority.

In this case, improvement should be assessed by an occupational therapist and ophthalmologist. Any further process regarding driving private or commercial depends on expert opinions from these disciplines.

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16
Q

A 39-year-old woman presents with second episode of seizure within one week. An EEG confirms the diagnosis of epilepsy. She is started on carbamazepine. She asks you when she can drive again. Which one of the following would be the correct answer?

A. Six months.
B. Four weeks.
C. She cannot drive as long as she is on carbamazepine.
D. She can drive as long as she is on carbamazepine.
E. She cannot drive for five years.

A

A. Six months.

If a patient is diagnosed with epilepsy for the first time, a conditional license may be considered by the driver licensing authority subject to at least annual review, taking into account information provided by the treating doctor as to whether the following criteria are met:

  • The patient has been treated for at least six months
  • There have been no seizures in the preceding six months
  • If any seizures occurred after the start of treatment, they happened only in the first six months after starting treatment and not in the last six months
  • The person follows medical advice, including adherence to medication

For this patient, who has been diagnosed with epilepsy for the first time, a limitation of six months and she cannot drive non-commercial vehicles during this period.

When treatment with an anti-epileptic drug is started in a previously untreated person, sufficient time should pass to establish that the drug is effective before driving is recommenced. However, effectiveness cannot be established until the person reaches an appropriate dose.

For example, if a drug is being gradually introduced over three weeks and a seizure occurs in the second week, it would be premature to consider the drug ineffective. The standard allows seizures to occur within the first six months after starting treatment without lengthening the required period of seizure freedom. However, if seizures occur more than six months after starting therapy, a longer seizure-free period is required. For commercial drivers, the default standard applies.

Example: if a patient has a seizure three months after starting therapy, they may be fit to drive six months after the most recent seizure (nine months after starting therapy). However, if a person experiences a seizure 8 months after starting therapy, the default standard applies and they may not be fit to drive until 12 months after the most recent seizure.

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17
Q

A 37-year-old epileptic man seeks advice regarding driving. He was diagnosed with epilepsy five years ago and was started on carbamazepine; however, he experienced intermittent seizures despite treatment. Three months ago, carbamazepine was switched to phenytoin. He has not had any seizures since then. Which one of the following would be the most appropriate advice regarding driving a non-commercial vehicle?

A. He cannot drive for three months.
B. He cannot drive for six months.
C. He cannot drive for one year.
D. He cannot drive for two years.
E. He can never drive.

A

C. He cannot drive for one year.

All patients with seizures and epilepsy should avoid driving non-commercial vehicles for 12 months and commercial vehicles for 10 years as default standards.

NOTE - There are circumstances under which these periods may be subject to reduction. Some of these circumstances are listed in the following table

This patient does not fulfill any of the above criteria to be subject to an exception to the general rules; therefore, he should not drive a non-commercial vehicle for at least 12 months after his last seizure, provided that no seizures occurred during the preceding 12 months.

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18
Q

A 23-year-old woman presents for advice regarding driving after a first-time generalised seizure. She had episodes of sudden spasms and twitching of muscles in the past few years. Which one of the following would be the most appropriate advice regarding driving a non-commercial vehicle?

A. No driving for six months.
B. No driving for three months.
C. No driving for one month.
D. She cannot drive anymore.
E. No driving for 12 months

A

A. No driving for six months.

All patients with seizures and epilepsy should avoid driving non-commercial vehicles for 12 months and commercial vehicles for 10 years as per default standards for patients with seziure. However, there are circumstances under which theseperiods may be subject to reduction.

These circumstances are listet in the following table: -see table below

Those who experience first-time seizure are exceptions to the general rule. They should not drive non- commercial vehicles for six months and commercial vehicles for five years. Thereafter, a conditional driving license for non-commercial vehicles may be considered by driving authority subject to at least annual review, if there has been no seizures (with or without treatment for at least six months).

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19
Q

A 42-year-old epileptic man, who had intermittent seizures despite being on treatment with sodium valproate, was switched to carbamazepine one month ago. Since starting the medication, there has been no seizure. Which one of the following would be the most appropriate advice regarding driving a non-commercial vehicles for him?

A. He can never drive.
B. He can drive after six months of seizure-free period.
C. He can only drive after 12 months of seizure-free period.
D. He can drive after 10 years of seizure-free period.
E. He can drive now.

A

C. He can only drive after 12 months of seizure-free period.

The scenario describes a case of chronic seizure. Generally, patients with seizures and epilepsy should not drive non-commercial vehicles for 12 months and commercial vehicles for 10 years as default standards after the last episode of their seizures, unless their condition is one of the exceptions for them different limitations is applied. These conditions are listed in the following table:

(Picture on page 1677)

This patient fulfills none of the above-mentioned condition; therefore, general rule applies for him: he should not drive non-commercial vehicles for 12 months.

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20
Q

An 85-year-old man presents to your clinic for annual check to renew his driver’s license. He has long-standing history of hypertension which is well-controlled on antihypertensive medications. Which one of the following is the investigation you should conduct before you issue a certificate?

A. Visual acuity.
B. Mini-mental status exam.
C. Blood sugar.
D. Cholesterol.
E. Liver function tests

A

A. Visual acuity.

Individuals, who have blood pressure consistently greater than 200 systolic or greater than 110 diastolic (treated or untreated), are not fit to hold an unconditional driving license for non-commercial vehicles. The threshold for commercial vehicles is 170 mmHg and 100 mmHg for systolic and diastolic blood pressure, respectively.

A conditional license may be considered by the driver licensing authority subject to periodic review, taking into account the nature of the driving task and information provided by the treating doctor as to whether the following criteria are met:

  • Blood pressure is well controlled; AND
  • There are no side effects from the medication that will impair safe driving; AND
  • There is no evidence of damage to target organs relevant to driving.

As far as driving is concerned, eyes are the most important end-organ potentially affected by chronic hypertension. Those with hypertension are at risk of hypertensive retinopathy and impaired vision. For that reason, examining the visual acuity will be the most crucial investigation before a certificate is issued for driving license renewal in this patient.

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21
Q

Which one of the following is the best predictor of obesity and its associated risks?

A. Body mass index (BMI).
B. Waist circumference.
C. Mid arm circumference.
D. Waist-to-hip ratio.
E. BMI and waist circumference together.

A

D. Waist-to-hip ratio.

BMI is advocated by World Health Organization (WHO) as the epidemiological measure of obesity; nevertheless, BMI is a crude index that does not take into account the distribution of body fat, resulting in variability in different individuals and populations. For example, individuals with the same BMI may have different ratios of body fat to lean mass. A muscular athlete may have the same BMI of a less muscular person. Women have more body fat than men at equal BMIs and people lose lean tissue with age so an older person will have more body fat than a younger one with same BMI.

Waist circumference has been recommended as a simple and practical measure for indentifying overweight and obese patients, but it does not take into account body size and height.

Waist-to-hip ratio (WHR) has been suggested as the preferred measure of obesity for predicting cardiovascular disease, with more universal application in individuals and population groups of different body builds. This parameter reflects abdominal (central) fat which is strongly associated with ischemic heart disease, hypertension and type II diabetes mellitus. In terms of predicting obesity-related mortality, WHR is more reliable than BMI and waist circumference together. Waist circumference alone comes next and BMI alone last.

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22
Q

You are asked to give advice regarding breast cancer to a 37-year-old woman who has come to your clinic with concerns about the disease. Her mother was diagnosed with breast cancer at the age of 60 years. She is asymptomatic and her clinical examination is normal. Which one of the following is the next best step in management?

A. She should start mammography now and every two years until the age of 74 years.
B. She should start ultrasonography now and every two years until the age of 74 years.
C. She should perform six-monthly self-breast examination.
D. She should start mammography now and then yearly until the age of 74 years.
E. Reassure her.

A

E. Reassure her.

Woman with family history of breast cancer in one first-degree relative older than 50 years are considered to be at slightly elevated risk above the normal population for breast cancer. For these women, two-yearly screening mammography starting from the age of 50 is the currently recommended screening; therefore, reassurance for now would be the most appropriate action. This woman however, should be advised that she should start mammography from the age of 50 years.

In general population, breast cancer screening is aimed at asymptomatic women aged 50-69 years; however, all women between 40 and 74 are eligible to enter the program if they wish.

Mammography is not recommended for women younger than 40 years due to dense breast tissue. Other modalities such as ultrasound or MRI can be used as alternatives if indicated.

Risk Level:
- Slightly elevated risk: Family history of breast cancer in one first-degree relative older than 50 years.

Screening Recommendations:
- Age 50-69: Biennial (every two years) mammography screening is recommended.
- Age 40-74: Women can opt for screening if desired.

Younger Women:
- <40 years: Mammography is not recommended due to dense breast tissue. Ultrasound or MRI may be considered if indicated.

A 45-year-old woman with a family history of breast cancer in one first-degree relative older than 50 years.

  1. What is the recommended action?
    • A) Start annual mammography now
    • B) Reassure and start biennial mammography at age 50
    • C) Start annual MRI screening now
    • D) Immediate ultrasound screening
    • E) Genetic testing for BRCA mutation
    Answer: B) Reassure and start biennial mammography at age 50Explanation: For women with a slightly elevated risk, biennial mammography starting at age 50 is recommended.
    • Why not A): Annual mammography is not necessary.
    • Why not C): MRI is not routinely recommended without higher risk.
    • Why not D): Ultrasound is not standard for screening.
    • Why not E): Genetic testing is not indicated for slightly elevated risk.

A 42-year-old woman without any family history of breast cancer wants to know if she is eligible for screening.

  1. What should you advise?
    • A) She should wait until age 50
    • B) She can opt for biennial mammography screening now
    • C) She should start annual MRI screenings
    • D) She needs immediate mammography screening
    • E) She should get genetic testing for breast cancer
    Answer: B) She can opt for biennial mammography screening nowExplanation: Women aged 40-74 are eligible for screening if they wish.
    • Why not A): She is eligible to start now if she wishes.
    • Why not C): MRI is not routine for the general population.
    • Why not D): Immediate screening is not necessary without symptoms or high risk.
    • Why not E): Genetic testing is not needed without a family history.

A 35-year-old woman with concerns about breast cancer.

  1. What is the best screening modality for her?
    • A) Mammography
    • B) Ultrasound
    • C) MRI
    • D) No screening until 40
    • E) Annual physical exam only
    Answer: B) UltrasoundExplanation: For women under 40 with dense breast tissue, ultrasound or MRI can be considered.
    • Why not A): Mammography is not effective in women under 40 due to dense breast tissue.
    • Why not C): MRI can be considered but is not the first-line screening tool.
    • Why not D): She may need screening based on individual risk.
    • Why not E): Additional imaging may be necessary beyond physical exams.

A 50-year-old woman with a family history of breast cancer in her mother diagnosed at 55.

  1. What is the recommended screening frequency?
    • A) Annual mammography
    • B) Biennial mammography
    • C) Annual MRI and mammography
    • D) No screening needed
    • E) Genetic testing only
    Answer: B) Biennial mammographyExplanation: Women with a slightly elevated risk due to family history should have biennial mammography starting at age 50.
    • Why not A): Annual mammography is not necessary for slightly elevated risk.
    • Why not C): MRI is not routinely indicated.
    • Why not D): Screening is needed.
    • Why not E): Genetic testing is not the primary recommendation.

A 35-year-old woman with a strong family history of breast cancer (mother and sister diagnosed before 50).

  1. What is the appropriate screening recommendation?
    • A) Annual mammography starting now
    • B) Biennial mammography starting at age 50
    • C) Annual MRI starting now
    • D) Genetic counseling and possible testing
    • E) No screening needed until symptoms appear
    Answer: D) Genetic counseling and possible testingExplanation: Given the strong family history, genetic counseling and testing for BRCA mutation may be appropriate.
    • Why not A): While annual screening may be needed, genetic counseling is the first step.
    • Why not B): She is at higher risk and may need earlier screening.
    • Why not C): MRI may be considered, but after genetic counseling.
    • Why not E): Screening is necessary due to high risk.

A 45-year-old woman presents with a palpable breast lump and no prior history of breast cancer screening.

  1. What is the most appropriate next step?
    • A) Reassure and start biennial screening at 50
    • B) Immediate mammography and ultrasound
    • C) Wait 6 months and re-evaluate
    • D) Annual MRI screening
    • E) Genetic testing for BRCA mutation
    Answer: B) Immediate mammography and ultrasoundExplanation: Any woman presenting with a palpable breast lump requires immediate imaging and further evaluation, regardless of age or screening history.
    • Why not A): Immediate action is needed due to symptoms.
    • Why not C): Delaying evaluation is inappropriate.
    • Why not D): MRI is not the first step for symptomatic evaluation.
    • Why not E): Genetic testing is not the first step; imaging is required.

A 50-year-old woman with a BRCA1 mutation.

  1. What is the recommended screening protocol for her?
    • A) Biennial mammography only
    • B) Annual mammography and MRI
    • C) No screening needed until symptoms appear
    • D) Monthly self-breast exams only
    • E) Annual ultrasound only
    Answer: B) Annual mammography and MRIExplanation: Women with a BRCA1 mutation are at high risk and require more intensive screening, including both mammography and MRI annually.
    • Why not A): Biennial screening is not sufficient for high-risk individuals.
    • Why not C): Regular screening is crucial for early detection.
    • Why not D): Self-breast exams are not enough.
    • Why not E): MRI and mammography are preferred for high-risk screening.

A 52-year-old woman with no family history of breast cancer and normal previous mammograms wants to know if she can extend the interval between screenings.

  1. What should you advise?
    • A) Annual mammography
    • B) Biennial mammography
    • C) Extend screening interval to every 3 years
    • D) No further screening needed
    • E) Switch to MRI screening
    Answer: B) Biennial mammographyExplanation: Biennial mammography is appropriate for average-risk women aged 50-69.
    • Why not A): Annual screening is not necessary for average risk.
    • Why not C): Extending to every 3 years is not recommended.
    • Why not D): Screening is still needed.
    • Why not E): MRI is not indicated for average-risk screening.
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23
Q

Julian, 35 years old, presents to your office for breast cancer screening after she found out that one of her maternal aunts was diagnosed with breast and ovarian cancer at the age of 40 years. Which one of the following would be the most appropriate advice for her?

A. Two-yearly mammography.
B. Two-yearly ultrasound.
C. Genetic risk screening.
D. Referral for BRCA gene screening.
E. Six-monthly self-breast examination.

A

C. Genetic risk screening.

Here’s a simplified explanation of the information:

Who is at increased risk of breast and/or ovarian cancer due to a gene mutation (mostly BRCA1 and BRCA2)?
- People with many relatives who have had breast (male or female) or ovarian cancer.
- Relatives who were diagnosed with cancer at a young age.
- Relatives who have had both breast and ovarian cancer.
- Relatives who have had breast cancer in both breasts.
- People of Ashkenazi Jewish ancestry.

How common are inherited genetic mutations in breast cancer?
- 5-10% of all breast cancers are caused by inherited genetic mutations.
- BRCA1 and BRCA2 mutations are the most significant ones for hereditary breast and ovarian cancer.

What should primary care providers do?
- They should use screening tools to identify women with a family history that might suggest an increased risk of harmful mutations in breast cancer genes (BRCA1, BRCA2).
- These tools are questionnaires that help estimate a person’s likelihood of developing breast or ovarian cancer or having a faulty gene mutation.

What is FRA-BOC?
- FRA-BOC is a widely used screening tool in Australia for assessing breast and ovarian cancer risk.
- It’s available from Cancer Australia: FRA-BOC Tool.

What happens if a woman has a positive screening result?
- She should receive genetic counseling.
- If advised during counseling, she should undergo BRCA testing.

For Julian, using a screening tool like FRA-BOC is the best next step. If she is found to be at high risk, she should be referred for genetic counseling and testing.

The following groups are at increased risk of breast and/or ovarian cancer due to a gene mutation (mostly BRCA1 and BRCA2):
**Multiple relatives affected by breast (male or female) or ovarian cancer
**Young age at cancer diagnosis in relatives
**Relatives affected by both breast and ovarian cancer
**Relatives affected with bilateral breast cancer
**Ashkenazi Jewish ancestry

Of all breast cancers, 5-10% are caused by inherited genetic mutation. BRCA1 and BRCA2 mutation are the most important causes for hereditarily increased risk of breast/ovarian cancer. It is recommended that primary care provider screen high-risk woman with screening tools designed to identify a family history that may be associated with an increased risk for potentially harmful mutations in breast cancer susceptibility genes (BRCA1, BRCA2). These screening tools are questionnaires used
by the health provider to take into account the family history of the person, and estimating the likelihood of developing breast and/or ovarian cancer in future, or whether they are high risk for having a faulty gene mutation.

FRA-BOC is one of the most commonly used screening tools in Australia for this purpose. FRA-BOC is available from: https://canceraustralia.gov.au/clinical-best-practice/gynaecological-cancers/fra-boc/evaluate

Women with positive screening results should receive genetic counselling and, if indicated after counselling, BRCA testing. For Julian, genetic risk assessment using screening tools such as FRA-BOC is the most appropriate next step. Referral for pretest counselling and genetic testing is an appropriate option once she is found to be at high risk.

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24
Q

You are working in a rural area. A 4-year-old Somali boy is presented to you by his mother for polio vaccine. He has received 3 doses of oral polio vaccine (OPV) at 2, 4 and 6 months of age back at his country with the last dose being given approximately 3 years ago. You only have injectable polio vaccine available in your office. Which one of the following would be the best appropriate management?

A. Check his immune status.
B. No further vaccination is needed.
C. Refer him to another clinic.
D. Give the injectable polio vaccine.
E. Try to find oral polio vaccine for him.

A

D. Give the injectable polio vaccine.

Injectable Inactivated polio vaccine (IPV) is the polio vaccine currently in use in Australia, and is given intramuscularly. Oral polio vaccine (OPV) is no longer in use in Australia. OPV nd IPV are interchangeable. Children, who have been started on OPV should complete their polio vaccination schedule using IPV (IPOL®) or IPV-containing vaccines.

IPV (IPOL) or IPV-containing vaccines are recommended for infants at 2, 4 and 6 months of age. The 1st dose of an IPV-containing vaccine can be given as early as 6 weeks of age.

If the 1st dose is given at 6 weeks of age, the next scheduled doses should still be given at 4 months and 6 months of age. A booster dose of IPV (IPOL®) or IPV-containing vaccine is recommended at 4 years of age. This is commonly provided as DTPa-IPV, which can be given as early as 3.5 years, but if DTPa-IVP is not available, IPV alone is used.

The only absolute contraindications to IPV (IPOL®) or IPV-containing vaccines are:
**Anaphylaxis following a previous dose of any IPV-containing vaccine
**Anaphylaxis following any vaccine component

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25
Q

A 30-year-old woman is concerned about breast cancer because her mother was diagnosed with breast cancer at the age of 48 years. Clinical examination of the breast is normal. Which one of the following would be the most appropriate advice for her?

A. Mammography yealy from the age of 40 years.
B. Mammography every 2 years from 50 to 74 years.
C. Refer to a surgeon.
D. Refer for genetic studies.
E. Reassure her that she is not at increased risk of breast cancer

A

A. Mammography yealy from the age of 40 years.

With a first-degree relative affected by breast cancer diagnosed before the age of 50, this woman is considered as having moderate risk for breast cancer. For such patients yearly screening mammography starting from the age of 40 is the best advice to give.

(Option B) Mammography every 2 years is the most appropriate recommendation for general population and those with just slightly increased risk above average for breast cancer.

(Option C) Referral to a surgeon would have been indicated if a diagnosis of breast cancer was established.

(Option D) Referral for genetic testing is an acceptable step for those women who are likely to have a predisposition for familial forms of breast/ovarian cancer. Referral for genetic testing should be considered once screening tools raise suspicion against strong risks of such cancers.

(Option E) Although this woman is not in high-risk category and is categorized as having moderate risk, reassuring is not appropriate because she needs a more extensive surveillance program for breast cancer than general population

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26
Q

A 67-year-old woman presents to your clinic for advice regarding reducing the risk of shingles infection after her husband was diagnosed with ophthalmic shingles 3 days ago. He had a vesicular rash on his face involving the eye, for which he was referred to an ophthalmologist for consultation. She wants to know if she should be vaccinated. She clearly remembers that she had chicken pox at the age of 12 years. Which one of the following is the most appropriate advice for her regarding herpes zoster prophylaxis?

A. Vaccination at this age will not benefit her.
B. Vaccination is indicated if she develops clinical shingles.
C. Vaccination will reduce her risk of infection regardless of her previous exposure.
D. A varicella serology testing is required for further decision making.
E. With the childhood history of chicken pox, she will not benefit from vaccination.

A

C. Vaccination will reduce her risk of infection regardless of her previous exposure.

  • VZV is a DNA virus and part of the herpes virus family.
  • Primary Infection: Known as varicella or ‘chickenpox’.
  • Reactivation: Known as herpes zoster (HZ) or ‘shingles’. This happens when dormant VZV reactivates in nerve cells.
  • 5th Cranial Nerve (CN V): Causes herpes ophthalmicus.
  • 7th Cranial Nerve (CN VII): Causes Ramsay-Hunt syndrome.
  • Unilateral Vesicular Rash: Appears in a specific nerve distribution (dermatome).
  • Prodromal Phase: Occurs 48 to 72 hours before the rash, with symptoms like headache, photophobia, malaise, itching, tingling, or severe pain.
  • Rash Duration: 10 to 15 days.
  • Common Complication: Post-herpetic neuralgia (PHN), which is pain persisting for more than 3 months after the rash.
  • Other Complications: Include eye problems, neurological issues, skin infections, scarring, and pneumonia. Disseminated HZ can affect the whole body, especially in immunocompromised individuals.
  • Type: Live attenuated vaccine.
  • Purpose: Prevents HZ in people over 50 years old.
  • Effectiveness: Contains a higher viral titer to boost immunity in adults.
  • Not for Treatment: Does not treat established HZ or PHN, only for prevention.
  • Recommendation: A single dose for adults 60 years or older, regardless of childhood vaccination status or previous chickenpox infection.
  • Routine Use: Not recommended for people under 50 years old, and routine use in people aged 50–59 is not generally recommended.
  • VZV causes chickenpox initially and shingles upon reactivation.
  • Shingles manifests as a painful rash and can have severe complications.
  • Zostavax® is used to prevent shingles in older adults but does not treat it once it occurs.
  • Vaccination is recommended for those 60 years and older.

This summary makes it easier to understand the connection between VZV, its reactivation, and the role of the Zostavax® vaccine in prevention.

Varicella-zoster virus (VZV) is a DNA virus and a member of the herpes virus family. Primary infection with VZV is known as varicella or ‘chickenpox’. Herpes zoster (HZ), or ‘shingles’, is caused by reactivation of latent VZV, which typically resides dormant in the dorsal root or trigeminal nerve ganglia following primary infection. Cranial nerves most commonly involved are 5th cranial nerve (CN V) and 7th cranial nerve (CN VII) resulting in herpes ophthalmicus and Ramsay-Hunt syndrome, respectively.

Reactivation of VZV causing HZ is thought to be particularly due to a decline in cellular immunity to the virus, and presents clinically as a unilateral vesicular rash in a dermatomal distribution in most cases. A prodromal phase occurs 48 to 72 hours prior to the appearance of the lesions in 80% of patients. Prodromal symptoms may include headache, photophobia, malaise, and an itching, tingling or severe pain in the affected dermatome. In most patients, HZ is an acute and self-limiting disease,
with the rash lasting 10 to 15 days. However, complications can occur, especially in older adults.

Post-herpetic neuralgia (PHN), the most frequently faced and debilitating complication of HZ, is a neuropathic pain syndrome that persists or develops after the dermatomal rash has resolved. By definition, PHN is established when pain persists for longer than 3 months after the onset of the rash.

Other complications may occur, depending on the site of reactivation. These include ophthalmic disease (such as keratitis and chorioretinitis), neurological complications (e.g. meningoencephalitis and myelitis), secondary bacterial skin infection, scarring and pneumonia. Rarely, disseminated HZ may develop, with widespread vesicular rash, and visceral, central nervous system and pulmonary involvement. Disseminated disease is more common in people who are immunocompromised.

Dermatomal pain without the appearance of rash is also documented (zoster siné herpéte).

Zostavax® is a live attenuated vaccine formulated from the same VZV vaccine strain (Oka/Merck) as the registered varicella (chickenpox) vaccine Varivax®, but is much more potent (on average, at least 14 times). This higher potency is owed to higher viral titer in Zostavax, and is required to elicit a boost in immune response of adults who usually remain seropositive to VZV following primary infection, but have declining cellular immunity with increasing age.

Zostavax® is used for the prevention of HZ in people>50 years of age. It is important to note that the registered varicella vaccines are not indicated for use in preventing HZ in older people and Zostavax is not indicated for use in younger people who have not been previously immunized or infected with VZV. Zostavax® is used solely for prophylaxis in a potentially-exposed asymptomatic patient. It has no therapeutic effect on established HZ infection or PHN; therefore, not indicated once infection develops. However, if given prophylactically, it can reduces the risk of HZ and PHN.

(Option A) A single dose of Zostavax® is recommended for adults ≥60 years of age who have not previously received a dose of it regardless of their childhood VZ vaccination status. Routine serological testing prior to vaccination is not indicated.

(Option D) Zostavax® is given regardless of a history of previous varicella (chickenpox) infection; therefore, inquiring about previous chicken pox infection is not required.

Routine population-based use of zoster vaccine in persons aged 50–59 years is not recommended. Although the incidence of HZ in persons 50–59 years of age is higher than in younger age groups, and zoster vaccine seems effective in those 50–59 years of age, the likelihood of developing PHN and other complications of HZ is lower in this age group than in those ≥60 years of age. People aged 50–59 years who wish to protect themselves against HZ can be vaccinated; however, the duration of efficacy, and need for a booster dose at a later age, is not yet determined. The routine use of vaccine is not recommended for those younger than 50 years.

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27
Q

A 29-year-old woman presents to your clinic at 14 weeks pregnancy for consultation regarding smoking cessation. She tried to give up smoking when she found out she is pregnant but she failed. She is worried about her baby’s wellbeing and wants to quit smoking. Which one of the following is the most appropriate management option for her?

A. Nicotine replacement therapy.
B. Non-nicotinic chewing gums.
C. Bupropion.
D. Varenicline.
E. Advise that she smoke less cigarettes.

A

A. Nicotine replacement therapy.

Smoking in pregnancy is the most important preventable cause of a wide range of adverse pregnancy outcomes. Smoking causes obstetric and fetal complications. Furthermore, there is growing evidence that harms can extend into childhood and even adulthood. Unfortunately, most smokers who become pregnant continue to smoke, and most of those who quite relapse after delivery.

Pregnancy is a window of opportunity for health professionals to help smokers quit. Women are motivated to protect their baby’s health, and quitting smoking during pregnancy reduces the risk of complications.

Interventions during pregnancy are modestly effective and assist 6 in every 100 smokers to quit. Many light smokers quit without assistance when they find out they are pregnant. The remaining smokers may need more intensive treatment.

The Australian Smoking Cessation guidelines recommend that pregnant smokers first try to quit with behavioral counselling and support as the first-line treatment. Smoking should be addressed at every GP visit during pregnancy in view of its serious health impact. Counselling in pregnancy produces a 4%-6% increase in the quit rate, compared with no counselling.

Nicotine Replacement Therapy (NRT) should then be considered if the patient is unable to succeed without it. NRT should be used under the supervision of a qualified health professional.

Intermittent, short-acting forms of NRT such as the lozenge or mouth spray are recommended to deliver a lower total daily nicotine dose. However, this may result in under-dosing and reduced effectiveness. The guidelines also advise that if patches are used they should be removed at bedtime.

Although guidelines recommend the smallest effective dose of nicotine, larger doses or even combination therapy may be required. Adequate doses to relieve cravings and withdrawal symptoms, and a full course of at least 8 weeks treatment are supported. The risks and benefits of NRT during pregnancy should be explained without making the patient unduly concerned.

There is no evidence of increased rates of miscarriage, stillbirth, admission to neonatal intensive care unit (NICU) or neonatal death between NRT and control groups. There is currently insufficient evidence to determine whether NRT is safe in pregnancy, but available data and expert opinion suggest it is less harmful than continuing to smoke.

This patient should be started on counselling and support (not an option). NRT should be considered if the patient requires it.

Australian Smoking Cessation Guidelines recommend against the two prescription medicines for smoking cessation, varenicline and bupropion during pregnancy and breastfeeding.

NOTE - Quitting smoking before conception or in the first trimester results in similar rates of adverse pregnancy outcomes compared with non-smokers; however, quitting at any time during produces health benefits. Quitting before pregnancy also allows the use of full range of pharmacotherapies

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28
Q

A 72-year-man presents to your practice for assessment. He does not smoke and has no history of diabetes mellitus or cardiovascular disease. On examination, he has a blood pressure of 172/100 mmHg, confirmed with a second reading. On blood tests, he has a total cholesterol level of 6.2 and HDL of 1mmol/L. According to the following chart which one of the following is his absolute cardiovascular risk?

A. 10-15%.
B. 16-19%.
C. 20-24%.
D. 25-29%.
E. ≥30%

A

D. 25-29%.

Assessment of cardiovascular disease (CVD) risk on the basis of the combined effect of multiple risk factors (absolute CVD risk) is more accurate than the use of individual risk factors because the cumulative effects of multiple risk factors may be additive or synergistic. In Australia, 64% of the adult population have 3 or more modifiable risk factors. Since CVD is largely preventable, an approach focusing on comprehensive risk assessment will enable effective management of identified modifiable risk factors through lifestyle changes and, where needed, pharmacological therapy.

Absolute risk is the numerical probability of a CVD event occurring within 5 years expressed as a percentage. For example, if one patient’s risk is 15%, he/she could be told he/she has a 15% chance of having a CVD event within the next 5 years.

In Australia, the following charts are used for calculation of absolute CVD risk in any given patient. The risk percentages are extracted from Framingham Risk Equation (FRE). It takes into account the following variables for calculation of absolute CVD risk:

  • Age
  • Gender
  • Smoking
  • Systolic blood pressure
  • Total cholesterol to HDL ratio

NOTE - Different rules apply to diabetic versus nondiabetic individuals and Aboriginal and Torres Strait Islanders.

These charts are used as follows:
Identify the chart relating to the person’s sex, diabetes status, smoking history and age. The charts should be used for all adults aged 45 years or over (and all Aboriginal and Torres Strait Islander adults aged 35 - 74 years) without known history of CVD, and not already known to be at clinically determined high risk. On the chart, choose the cell nearest to the person’s age, systolic blood pressure (SBP) and total cholesterol (TC):HDL ratio. The color of the cell that can be the person falls into
provides their 5 year absolute cardiovascular risk level. People who fall exactly on a threshold between cells are placed in the cell indicating higher risk. For those older than 74 years, calculate as if they are 74.

This patient is male, non-smoker and 72 years. The part of the chart that should be used for risk calculation is shown in the following picture:

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29
Q

Hypertension is the most important preventable risk factor for which one of the following conditions?

A. Coronary artery disease.
B. Peripheral arterial disease.
C. Renal arterial disease.
D. Ischemic stroke.
E. Atrial fibrillation.

A

D. Ischemic stroke.

Although hypertension is a risk factor for all of the given to some extent, it remains the most important modifiable risk factor for stroke and intracerebral hemorrhage (ICH). The risk of stroke increases progressively with increasing blood pressure, independent of other factors.

Hypertension is the cause of stroke in >50% cases worldwide. Most estimates for hypertension indicate a relative risk of approximately 4 when hypertension is defined as systolic blood pressure ≥160mmHg and/or
diastolic blood pressure ≥95mmHg.

Hypertension and hypertensive heart disease results in development of left ventricular hypertrophy and diastolic dysfunction that are important risk factors for atrial fibrillation accounting for 20% of cases.

Hypertension is also a major risk factor for coronary artery disease (CAD), and treatment of hypertension reduces the risk of a coronary artery disease by one-third; however, the most important reversible risk factor for CAD is hypercholesterolemia and cigarette smoking. Cessation of cigarette smoking is the single most important preventive measure for coronary artery disease. Moreover, smoking has the highest association with peripheral arterial disease.

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30
Q

Which one of the following risk factors is most signficant for ischemic stroke?

A. Hypercholesterolemia.
B. Smoking.
C. Obesity.
D. Type 2 diabetes mellitus.
E. Hypertension.

A

E. Hypertension.

All of the given options can be potential risk factors for ischemic stroke; however, hypertension is associated with the highest risk. Hypertension is the cause of stroke in >50% cases worldwide. Most estimates for hypertension indicate a relative risk of approximately 4 when hypertension is defined as systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥95mmHg. The following table compares the relative risk of different preventable risk factors for stroke: - See table below.

NOTE - Age is the single most important risk factor for stroke. For each successive 10 years after age 55, the stroke rate more than doubles in both men and women. Stroke incidence rates are 1.25 times greater in men, but because women tend to live longer than men, more women than men die of stroke each year. Obesity is associated with elevated vascular risk in population studies. Furthermore, it has been associated with glucose intolerance, insulin resistance, hypertension, physical inactivity and dyslipidaemia.

(Option A) Hypercholesterolemia seems to act in a complex fashion and does not directly act as a risk factor; however, it is an important modifiable risk factor for coronary artery disease.

(Options B and C) Smoking and obesity are associated with relative risks of 1.5 and 1.5-2.0 respectively.

(Option D) Diabetes mellitus is associated with a relative risk of 1.8-3.0.

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31
Q

A 46-year-old man presents to your clinic for a routine check-up. He runs a butchery, and is an smoker. Sometimes, he also uses cocaine and cannabis at parties. On examination, he has a blood pressure of 135/95 mmHg. His BMI is 29. Which one of the following is the most significant risk factor for developing coronary artery disease in this patient?

A. Obesity.
B. Cannabis.
C. Age.
D. Cocaine.
E. Cigarette smoking

A

E. Cigarette smoking

Major traditional risk factors for cardiovascular diseases are:
**Hypercholesterolemia (high LDL)
**Smoking
**Hypertension
**Diabetes mellitus

Other traditional risk factors include:
**Family history of premature coronary artery disease in a first-degree relative (female<65 years; male<55 years)
**Low physical activity
**Obesity

Of the options, smoking is a major risk factor for coronary artery disease (CAD). People who smoke more than 20 cigarettes a day have a 2- to 3-fold increase in total incidence of heart disease. Continued smoking is a major risk factor for recurrent heart attack. Cessation of cigarette smoking is the single most important preventive measure for CAD.

Although family history of premature heart disease (male< 55 years and female< 65 years), low level of physical activity, and obesity are considered risk factors for CAD, these factors work through major risk factors to a large extent.

Age, by itself, is not a risk factor unless other major risk factors are present. The incidence of CAD increases after the age of 45 years in men and 55 in women.

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32
Q

A 60 year-old man presents to your clinic for a routine medical check-up. He smokes 45 cigarettes a day, and drinks 10 standard drinks daily. He has a body mass index (BMI) of 32 kg/m2. He wears seat-belt almost 60% of the times when he drives.

He is motivated to follow lifestyle modification advice. Which one of the following is the most significant advice for prevention of cardiovascular disease and premature death in this patient?

A. Smoking cessation.
B. Reduction of alcohol intake.
C. Wearing seatbelt all the time when he drives.
D. Weight reduction.
E. Regular exercise.

A

A. Smoking cessation.

By far, the most common cause of coronary artery disease (CAD) is atherosclerotic changes of coronary arteries. The most common underlying cause is hypercholestrolemia (high LDL). Smoking is also strongly associated with increased risk of cardiovascular diseases, and its cessation is considered the most effective lifestyle modification to prevent cardiovascular events (more than lipid modification). In a patient with coronary artery disease, quitting smoking is associated with a 36%
reduction in mortality.

Although family history of premature heart disease (male < 65 and female < 55), low level of physical activity and obesity are considered risk factors for coronary artery disease, these factors exert their effects in the presence of major risk factors.

(Option B) This patient should also be advised to reduce alcohol consumption to a maximum of 2 standard drinks (one for women) with 2 alcohol-free days every week. This measure is beneficial for general health but does not have a specific effect on cardiovascular status as does smoking cessation.

(Option C) Wearing a properly-adjusted seatbelt reduces the risk of mortality by 50%; however this reduction is related to trauma and severe injuries, not to cardiovascular diseases.

(Option D) Blood pressure and body weight are directly related. For every 1kg reduction in weight, the systolic blood pressure will drop by 1mmHg. Weight reduction is particularly beneficial if the patient has insulin resistance and/or hyperlipidemia. Weight reduction, however, is not as effective as smoking cessation in improving cardiovascular risk.

(Option E) Regular exercise increases high-density lipoprotein cholesterol and reduces body weight, and contribute to improved cardiovascular status, but not as smoking cessation does.

TOPIC REVIEW
Major traditional risk factors for coronary artery disease (CAD) are as follow:
**Hypercholesterolemia (high LDL)
**Smoking (especially smoking cigarettes)
**Hypertension
**Diabetes mellitus

Other traditional risk factors include:
**Family history of heart disease (premature)
**Low level of physical activity
**Obesity

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33
Q

A 62-year-old man presents for ‘absolute cardiovascular risk’ assessment. His past medical history includes type 2 diabetes mellitus for which he is on metformin 500 mg 12-hourly and gliclizide 60 mg daily. Laboratory studies show an albumin/creatinine ratio of 5mg/mmol. Which one of the following options is correct regarding this scenario?

A. Inform him that he is already in high risk group for cardiovascular disease and do not need risk calculation.
B. Perform absolute risk calculation for him now and 2-yearly.
C. Reassure him.
D. Start him on insulin.
E. Increase the dose of his medications.

A

A. Inform him that he is already in high risk group for cardiovascular disease and do not need risk calculation.

Assessment of cardiovascular disease risk on the basis of the combined effect of multiple risk factors (absolute CVD risk) is more accurate than the use of individual risk factors, because the cumulative effects of multiple risk factors may be additive or synergistic. In Australia, 64% of the adult population have 3 or more modifiable risk factors. As CVD is largely preventable, an approach focusing on comprehensive risk assessment will enable effective management of identified modifiable risk factors through lifestyle changes and, where needed, pharmacological therapy.

Absolute cardiovascular risk assessment should be conducted at least every 2 years in all adults aged 45 years or older who are not known to have CVD or to be at clinically-determined high risk. Calculation of the absolute risk requires information on the patient’s age, sex, smoking status, total and HDL cholesterol, systolic blood pressure and if the patient is known to have diabetes or left ventricular hypertrophy.

Absolute risk calculation is not indicated if:
The patient has current or history of cardiovascular disease e.g. stroke, transient ischemic attack (TIA), ischemic heart disease (IHD), or peripheral arterial disease (PAD).

The patient is already clinically-determined high risk:

  • Diabetes and age >60 years
  • Diabetes with microalbuminuria (>20 µg/min or urine albumin:creatinine ratio (UACR) >2.5 mg/mmol for males, >3.5 mg/mmol for females)
  • Moderate or severe CKD (persistent proteinuria or estimated glomerular filtration rate (eGFR< 45mL/min/1.73 m2)
  • Previous diagnosis of familial hypercholesterolaemia (FH)
  • SBP ≥180 mmHg or diastolic blood pressure (DBP) ≥110 mmHg
  • Serum total cholesterol >7.5 mmol/L
  • Aboriginal or Torres Strait Islander peoples aged over 74 years

With diabetes and age of 62 (>60) on one hand and an albumin/creatinine ratio of 5mg/mmol (>2.5mg/mmol), this patient has 2 conditions that categorizes him as clinically-determined high risk; therefore, risk calculation is not required.

(Option B) He does not need absolute cardiovascular risk assessment now or any other time because he is already clinically-determined high risk.

(Option C) Reassurance of a patient who high-risk for CVD is not wise.

(Options D and E) There are no pointers in the scenario towards inadequacy of diabetes treatment; hence, increasing the dose of the current medications or commencement of insulin appears irrelevant.

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34
Q

A 47-year-old man presents for cholesterol check. He smokes 20 cigarettes a day. On examination, he has a blood pressure of 140/90 mmHg. Among the blood tests performed, a cholesterol level of 5.5 mmol/L is remarkable. Which one of the following would be the most appropriate advice for him at this stage?

A. He should start statins.
B. He should start antihypertensive medications.
C. He should be involved in a smoking cessation program.
D. His cholesterol level should be checked in 3 months.
E. He should start regular exercise and diet.

A

C. He should be involved in a smoking cessation program.

By far,** smoking is the single most modifiable risk factor for coronary artery diseases (CAD)**. Smoking is associated with a 2- to 3-fold increase in CAD. Smoking cessation alone reduces the risk of CAD by 32%; therefore, advice against smoking and encouraging the patient to actively participate in a smoking cessation program will be the most appropriate step.

Adopting a healthy lifestyle including regular exercise and diet is also important for reduction in CAD risk but smoking remains the most important factor. The patient’s blood pressure is at the cut-off point for hypertension. Presently, antihypertensive medications are not indicated.

The target cholesterol level is < 4mmol/L. With a cholesterol level of 5.5 mmol/L, this patient should initially be advised to start regular exercise and a healthy diet. Statins as first-line medications for hypercholesterolaemia are indicated if diet and exercise fail to lower the cholesterol levels in 3-6 months.

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35
Q

Which one of the following measures is of most importance in reducing the prevalence of trachoma infection in a susceptible community such as indigenous Australians?

A. Childhood vaccination.
B. Prophylactic use of tetracycline.
C. Avoidance of community bathing.
D. Regular hand and face washing.
E. Eradication of mosquitoes.

A

D. Regular hand and face washing.

To reduce the prevalence of trachoma infection, the strategy defined and implemented by the World Health Organization (WHO) should be followed. This strategy is called SAFE that stands for surgery, antibiotics, facial hygiene (cleanliness) and environmental factors.

  • Surgery is used to correct the entropion before it leads to permanent damage to the cornea.
  • Azithromycin is the antibiotic of choice in this strategy and is given, in oral form, to family members with active trachoma.
  • Facial hygiene is achieved through regular hand and face washing.
  • Environmental factors should be addressed by improving water supply, better community hygiene and dust and fly control.

Among the following measures surgery and antibiotics are used for treatment not prevention; hence they have no effect on prevalence. The most important measure, which with proper education will significantly reduce the prevalence of the disease, is regular hand and face washing.

(Option A) There is no effective vaccine against Chlamydia trachomatis.

(Optipn B) Tetracycline is not used for prophylaxis or treatment of Chlamydia. Azithromycin is the drug of choice for such purposes.

(Option C) Chlamydia trachomatis is spread via direct contact e.g. from mother to the child. Avoidance of community bathing does not seem to have a significant impact on the prevalence.

(Option E) Trachoma is transmitted by flies not mosquitoes; therefore, eradication of mosquitoes would not be an effective measure

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36
Q

A 37-year-old man is about to travel to Central Africa and has presented for advice regarding prevention of yellow fever. Which one of the following options is the most appropriate advice for him?

A. He should avoid swimming or wading in fresh water.
B. He should use bottled or boiled water.
C. He should be careful with fecal-oral hygiene.
D. He should use yellow fever vaccine.
E. He should receive prophylactic doxycycline.

A

D. He should use yellow fever vaccine.

Yellow fever is caused by a flavivirus. The virus is transmitted to humans from the bite of insect mosquito vectors such as Aedes Egypti. The reservoir for the virus is the monkey population of tropical rainforests of South and Central America and West and South Africa. Travellers to these areas are prone to the disease. Yellow fever presents with rigors and fever, jaundice, petechiae, hematemesis and circulatory failure. Treatment is almost supportive and symptomatic.

Stamaril ® is the live, attenuated yellow fever virus (17D-204 strain) freeze-dried vaccine available in Australia. It is given as a single intramuscular or subcutaneous injection of 0.5mL of reconstituted vaccine. Stamaril ® is almost 100% effective against yellow fever and should be advised as the most important preventive means for those travelling to endemic areas. Protective immunity occurs within 1–2 weeks in 90–95% of people, and a single dose lasts at least 10 years.

Under international health regulations, revaccination is required every 10 years.

NOTE - Stamaril ® is contraindicated in patients with history of egg allergy or previous anaphylaxis to the vaccine. It is also contraindicated in pregnancy. Pregnant woman should be advised against travelling to endemic areas; however, if the travel is inevitable, the benefits of vaccination outweigh the risks.

Other protective measures include staying indoors or under mosquito nets to avoid contributing to the transmission cycle. Advice should be given regarding avoidance of epidemics and minimization of high risk behavior (e.g. jungle visits). Personal protective measures are an important part of any travel medicine consultation where the traveller is heading to any region of mosquito-borne disease. Mosquito avoidance includes the use of treated mosquito nets and screening of living and work
areas

37
Q

A previously healthy 2-year-old child is brought to your practice with signs and symptoms of meningitis. She has been fully immunized with pneumococcal conjugated vaccine. You refer the child to the hospital, where she is found to have pneumococcal meningitis. Which one of the following is the most likely cause of the infection despite immunization?

A. An underlying primary immune deficiency.
B. A pneumococcal serotype that the vaccine did not protect against.
C. Failure of the vaccine to elicit a protective immune response against a pneumococcal serotype contained in the vaccine.
D. A cardiac defect with right-to-left shunt.
E. Contamination of the specimens used for testing in the hospital.

A

B. A pneumococcal serotype that the vaccine did not protect against.

Streptococcus pneumoniae (Pneumococcus) is a Gram-positive coccus. Capsule polysaccharide is the most important virulence factor of pneumococci. Over 90 capsular antigen types (serotypes) have been recognized, each of which elicits type-specific immunity in the host. The natural reservoir of pneumococci is the mucosal surface of the upper respiratory tract of humans. Different pneumococcal serotypes vary in their propensity to cause nasopharyngeal colonization or the disease.

Worldwide, only a limited number of serotypes are responsible for most cases of invasive pneumococcal disease (IPD), but the predominant serotypes vary by age group and geographic area.

The introduction of 7-valent pneumococcal conjugate vaccine (7vPCV) in Australia has led to a dramatic reduction in the overall incident of IPD. However, since the implementation of the universal 7vPCV program, increased rates of IPD caused by serotypes not contained in 7vPCV (replacement disease) have been observed in Australia and several other countries. This is particularly so common among non-Indigenous children aged < 2 years, and is the most likely cause to IPD in immunized children.

This child has been diagnosed with meningitis as an IPD despite a full course of vaccination against pneumococci; therefore, the most likely explanation is infection with a specific serotype which has not been covered by 7vPCV.

(Option A) An underlying immune deficiency is also a possible explanation; however, this is unlikely in a previously healthy child.

(Option C) Failure of the vaccine to elicit an immune response in a healthy patient with intact immune system is a very remote possibility.

(Option D) A cardiac defect with right-to-left shunt does not explain the event.

(Option E) Sample contimantion would have caused growth of different types of organisms on culture. With growth of streptococcus in isolation, such an event is not likely

38
Q

A mother brings her 15-month-old son to your office for vaccination. The child has not received any vaccines since birth because the mother had been strongly against vaccination until last week when she was convinced that immunization is in best interest of her child. Now the mother is asking you how she should catch up. Which one of the following would be the most appropriate action now?

A. A full course of vaccination should be started now.
B. Vaccination should be started now with the vaccines scheduled for this age.
C. The vaccination should be postponed as there is no need for vaccination at this stage.
D. The family should be reported to Child Protection Service.
E. The child should receive both initial and catch-up doses at once right now

A

A. A full course of vaccination should be started now.

A physician should take every opportunity to review one’s vaccination history and administer the appropriate vaccine(s). For those, who do not have a documented receipt of vaccines scheduled in the National Immunisation Program (NIP) appropriate for their age, a catch-up schedule should be planned, documented and discussed with the person or their caretakers/parents. The number of doses to give and the intervals may differ according to the age at which the catch-up is planned. The objective of catch-up vaccination is to complete a course of vaccination and provide optimal protection as quickly as possible. The assessment of vaccination status should be based on the schedule for the state or territory where the person to be vaccinated is residing.

(Option B) Commencement of vaccination with vaccines appropriate for the child’s current age while previous doses have been missed will not be appropriate because adequate protection may not be achieved.

(Option C) Postponing vaccination is not appropriate because this child should receive his vaccines right now.

(Option D) The decision regarding vaccination of children completely lies within parents hands. They can refuse vaccination of their chidlren as their legal right, and reporting the family to child protection services not appropriate.

(Option E) Receiving both initial and catch-up doses at the same time is not appropriate. This child shoud receive initial doses at this visit followed by catch-up doses according to the vaccination guidelines

39
Q

In which one of the following infections, administration of immunoglobulin as prophylaxis is not useful?

A. Hepatitis B.
B. Hepatitis A.
C. Mumps.
D. Varicella.
E. Rubella

A

C. Mumps.

Hepatitis B Immunoglobulin (HBIG)
- Use: For neonates born to mothers with Hepatitis B, and non-immune persons exposed to infected individuals.
- Funding: Typically covered by Medicare.

Hepatitis A Vaccine vs. NHIG
- Vaccine: Preferred for persons ≥12 months who are immunocompetent.
- NHIG: Used for infants <12 months or immunocompromised individuals.

Zoster Immunoglobulin (ZIG)
- Use: Prevents varicella in high-risk individuals after exposure.
- Timing: Administer within 96 hours, effective up to 10 days post-exposure.

NHIG for Rubella
- Not recommended for prevention, but may reduce symptoms and fetal risk in rare situations within 72 hours of exposure.

Types of Immunoglobulin
1. Normal Human Immunoglobulin (NHIG): Derived from pooled plasma, contains antibodies prevalent in the population.
2. Specific Immunoglobulins: Derived from donors with high antibody levels, used for specific infections like Hepatitis B, varicella, rabies, etc.

A neonate born to a mother with chronic hepatitis B infection.

  1. What is the most appropriate post-exposure prophylaxis?
    • A) Hepatitis A vaccine
    • B) Hepatitis B specific immunoglobulin (HBIG)
    • C) NHIG
    • D) Zoster immunoglobulin
    • E) No prophylaxis needed
    Answer: B) Hepatitis B specific immunoglobulin (HBIG)Explanation: HBIG provides immediate protection for neonates at risk of hepatitis B transmission from the mother.
    • Why not A): Hepatitis A vaccine is irrelevant here.
    • Why not C): NHIG is not specific for hepatitis B.
    • Why not D): Zoster immunoglobulin is for varicella prevention.
    • Why not E): Prophylaxis is needed due to the high risk of transmission.

A 14-month-old immunocompetent child exposed to hepatitis A.

  1. What is the recommended post-exposure prophylaxis?
    • A) NHIG
    • B) Hepatitis A vaccine
    • C) No prophylaxis needed
    • D) Hepatitis B vaccine
    • E) Zoster immunoglobulin
    Answer: B) Hepatitis A vaccineExplanation: Hepatitis A vaccine is preferred for post-exposure prophylaxis in immunocompetent individuals ≥12 months of age.
    • Why not A): NHIG is used when the vaccine is contraindicated.
    • Why not C): Prophylaxis is needed.
    • Why not D): Hepatitis B vaccine is irrelevant.
    • Why not E): Zoster immunoglobulin is for varicella.

A 3-year-old child on immunosuppressive therapy exposed to varicella.

  1. What is the appropriate prophylaxis?
    • A) Varicella vaccine
    • B) Zoster immunoglobulin (ZIG)
    • C) NHIG
    • D) No prophylaxis needed
    • E) Hepatitis B immunoglobulin
    Answer: B) Zoster immunoglobulin (ZIG)Explanation: ZIG is used to prevent varicella in high-risk individuals exposed to the virus.
    • Why not A): Varicella vaccine is not used in immunocompromised individuals for immediate prophylaxis.
    • Why not C): NHIG is not specific for varicella.
    • Why not D): Prophylaxis is needed.
    • Why not E): Hepatitis B immunoglobulin is irrelevant.

A 9-month-old infant exposed to hepatitis A.

  1. What is the most appropriate post-exposure prophylaxis?
    • A) Hepatitis A vaccine
    • B) NHIG
    • C) No prophylaxis needed
    • D) Hepatitis B immunoglobulin
    • E) Zoster immunoglobulin
    Answer: B) NHIGExplanation: NHIG is used for hepatitis A prophylaxis in infants <12 months of age as they are too young for the vaccine.
    • Why not A): The vaccine is contraindicated in infants <12 months.
    • Why not C): Prophylaxis is needed.
    • Why not D): Hepatitis B immunoglobulin is irrelevant.
    • Why not E): Zoster immunoglobulin is irrelevant.

Hepatitis B specific immunoglobulin (HBIG) is used for neonates born to mothers with hepatitis B infection and non-immune persons who are exposed through occupational exposure to the blood of unidentified persons, or to persons who are chronically infected with hepatitis B or whose hepatitis status cannot be established in time.

Hepatitis A vaccination is recommended in preference to NHIG for post-exposure hepatitis A prophylaxis in persons ≥12 months of age who are immunocompetent. NHIG can be used when hepatitis A vaccine administration is contraindicated such as in infants < 12 months of age, or in persons who are immunocompromised and who might not mount a sufficient response following vaccination. NHIG contains sufficiently high levels of antibody against hepatitis A to prevent or ameliorate infection in susceptible persons, if administered within 2 weeks of exposure.

Specific zoster immunoglobulin (ZIG) is highly efficacious. Normal high-titer zoster immunoglobulin is available from the Australian Red Cross Blood Service on a restricted basis for the prevention of varicella in high-risk subjects who report a significant exposure to varicella or herpes zoster. ZIG has no proven use in the treatment of established varicella or zoster infection. ZIG must be given early in the incubation period (within 96 hours of exposure), but may have some efficacy if administered as late as 10 days post exposure. ZIG is able to prevent or ameliorate varicella in infants < 1 month of age, in children who are being treated with immunosuppressive therapy, and in pregnant women.

Administration of NHIG for rubella infection is not recommended and does not prevent infection in non-immune contacts; however it may prolong incubation period and marginally reduce fetal risk and maternal clinical symptoms. Its use may be considered in rare situations (within 72 hours of exposure), or in outbreaks as a pre-exposure prophylactic for non-immune pregnant women in high risk occupations. Serological follow-up is required for up to 2 months.

NIHG has not proven effective in prevention or treatment of mumps.

TOPIC REVIEW
Immunoglobulin preparations are used to provide passive immunization, that is, the direct administration of antibodies to a non-immune person to provide immediate protection against infection or disease.
There are two types of immunoglobulin:

  1. Normal human immunoglobulin (NHIG) - NHIG is derived from the pooled plasma of blood donors. It contains antibody to microbial agents that are prevalent in the general population.
  2. Specific immunoglobulins - Specific immunoglobulin preparations are obtained from pooled blood donations from patients convalescing from the relevant infection, donors recently vaccinated with the relevant vaccine, or those who, on screening, have been found to have sufficiently high antibody concentrations. These blood-derived specific immunoglobulins contain concentrations of antibody to an individual organism or toxin at a higher titer than would be present in NHIG.

Specific immunoglobulins available in Australia include:

  • Hepatitis B specific immunoglobulin
  • Rabies specific immunoglobulin
  • Varicella zoster specific immunoglobulin
  • Botulism antitoxin
  • Tetanus immunoglobulin
  • Respiratory syncytial virus monoclonal antibodies
  • Cytomegalovirus immunoglobulin

For infections or disease other than above, NHIG is used if indicated and there is proven efficacy. NHIG use for passive prophylaxis has proven effective for measles and hepatitis A if vaccination is contraindicated; however, in selected cases, NHIG is used for poliomyelitis and rubella as well with less efficacy.

40
Q

One of the nurses of the ward you are working in sustains a needle stick injury while she is setting up a new intravenous line for a patient. The patient is HBsAg negative. History reveals that the patient is unlikely to be within the window period. The nurse is unsure of her hepatitis B immunization status. Which one of the following is the most appropriate next step in management?

A. No further follow up is required.
B. Give hepatitis B immunoglobulin and full course of hepatitis B vaccination.
C. Organize a full course of hepatitis B immunization.
D. Report the incidence to the infectious disease specialist.
E. Perform a blood test to check the HBsAg status in 3 months.

A

C. Organize a full course of hepatitis B immunization.

Hepatitis B
- If the source is HBsAg-negative and unlikely in the window period, no prophylaxis is needed. The healthcare worker should start a full HBV vaccination course ideally within 24 hours if not already immunized.
- HBIG should be given as soon as possible if indicated, preferably within 24 hours.

Hepatitis C
- If the source is HCV antibody-negative and unlikely in the window period, no follow-up is needed. Otherwise, follow-up testing at 4-6 weeks (HCV RNA) and 4-6 months (HCV antibody, ALT).

HIV
- If the source is HIV antibody-negative and unlikely in the window period, no follow-up is needed. Otherwise, follow-up testing at 6 weeks, 3 months, and up to 6 months. PEP should be started as soon as possible if indicated, ideally within 24-36 hours.

A nurse is exposed to a needle stick injury from a patient whose HBsAg status is negative and unlikely to be in the window period. The nurse has an uncertain immunization status.

  1. What is the most appropriate next step?
    • A) No follow-up required.
    • B) Start a full course of hepatitis B vaccine.
    • C) Administer HBIG.
    • D) Check the nurse’s HBsAg status.
    • E) Immediate referral to an infectious disease specialist.
    Answer: B) Start a full course of hepatitis B vaccine.Explanation: The nurse should start a full course of hepatitis B vaccine as soon as possible due to uncertain immunization status.
    • Why not A): Immunization is needed due to uncertain status.
    • Why not C): HBIG is not needed as the source is HBsAg negative.
    • Why not D): Checking the nurse’s HBsAg status is unnecessary in this context.
    • Why not E): Referral to an infectious disease specialist is not required.

A healthcare worker is exposed to blood from a patient who is HCV antibody-negative and unlikely to be in the window period.

  1. What is the appropriate follow-up for the healthcare worker?
    • A) Immediate HCV RNA testing.
    • B) No further follow-up required.
    • C) Start antiviral therapy.
    • D) HCV antibody testing at 6 months.
    • E) Immediate referral to a hepatologist.
    Answer: B) No further follow-up required.Explanation: No further follow-up is needed if the source is HCV antibody-negative and unlikely to be in the window period.
    • Why not A): Testing is unnecessary if the source is negative.
    • Why not C): Antiviral therapy is not needed without evidence of infection.
    • Why not D): Follow-up testing is unnecessary.
    • Why not E): Referral is not required.

A healthcare worker has a needle stick injury from a patient whose HIV status is unknown.

  1. What is the appropriate initial management?
    • A) Immediate HIV antibody testing for the healthcare worker.
    • B) Start PEP immediately.
    • C) No action required until the patient’s HIV status is confirmed.
    • D) HCV RNA testing for the healthcare worker.
    • E) Hepatitis B vaccination.
    Answer: B) Start PEP immediately.Explanation: PEP should be started as soon as possible after exposure if the patient’s HIV status is unknown.
    • Why not A): Immediate testing of the healthcare worker does not affect PEP.
    • Why not C): Delay can reduce the effectiveness of PEP.
    • Why not D): HCV testing is unrelated to HIV PEP.
    • Why not E): Hepatitis B vaccination is irrelevant in this context.

A healthcare worker is exposed to blood from a patient who is HBsAg positive.

  1. What is the recommended prophylaxis?
    • A) No follow-up required.
    • B) HBIG and start hepatitis B vaccine.
    • C) Immediate hepatitis B antibody testing.
    • D) Start antiviral therapy.
    • E) Refer to an infectious disease specialist.
    Answer: B) HBIG and start hepatitis B vaccine.Explanation: HBIG and starting the hepatitis B vaccine series are recommended for post-exposure prophylaxis when exposed to an HBsAg-positive source.
    • Why not A): Prophylaxis is required.
    • Why not C): Immediate testing is not the first step.
    • Why not D): Antiviral therapy is not used for prophylaxis.
    • Why not E): Referral is not immediately necessary.

If the index case is HBsAg negative and unlikely to be within the window period, no post-exposure prophylaxis for the nurse was required if she had been immunized. There is no risk for the nurse to contract hepatatis B from this exposure; however, she should receive a full course of hepatitis B vaccine. This ideally should be started within 24 hours.

Another appropriate approach (not an option) is to check for HBV antibody titer of the nurse. If the titre was equal or greater than 10mIU/ml, no vaccination is required either.

(Option A) Although the nurse is not likely to become infected from this exposure, she should have follow-up for immunization due to uncertain immunization status.

(Option B) Since the index case is HBsAg negative and unlikely to be in window period, post-exposure prophylaxis is not required.

(Option D) It is important that the incident is reported to a team manager or supervisor, but reporting to an infectious disease specialist in not necessary.

(Option E) Checking for the nurse’s HBsAg status was indicated if the index case was HBsAg positive.

TOPIC REVIEW
Recommendations regarding post-occupational exposure prophylaxis:

Hepatitis B

  • If the source is HBsAg-negative, and unlikely to be in the window period, no further follow-up testing is required for source or healthcare worker. The healthcare worker should have full HBV immunization if it has not been already performed. It should be commenced as soon as possible, and preferably within 24 hours of exposure.
  • If hepatitis B immunoglobulin (HBIG) is indicated, it should be given as soon as possible and preferably within 24 hours exposure. Efficacy of HBIG beyond 7 days of exposure is unknown.

Hepatitis C

  • If the source is HCV antibody negative, and unlikely to be in the window period, no further follow-up testing is required for the source or healthcare worker.
  • Follow-up testing of the healthcare worker should be done in all other circumstances, and should include HCV RNA testing at 4 to 6 weeks, and HCV antibody and ALT at 4 to 6 months.
  • There is no effective or active immunoprophylaxis. Early therapy if seroconversion occurs should be considered.

HIV

  • If the source is HIV antibody negative, and unlikely to be in the window period, no further follow-up testing is required for the source or healthcare worker.
  • In all other circumstances, the healthcare worker should have follow-up antibody testing at 6 weeks and 3 months, and up to 6 months, along with tests for other blood-borne viruses as above.
  • If post-occupational exposure prophylaxis (PEP) for HIV is indicated, it should be commenced as soon as possible after exposure. It is substantially less effective in animal studies when started more than 24-36 hours after exposure, but the interval after which no benefit is gained is unknown.
  • Recommendation for PEP include a basic regimen of 2 nucleoside/nucleotide reverse transcriptase inhibitors for most HIV exposures, and an expanded regimen with the addition of a third drug when the exposure poses an increased risk for transmission.
  • Expert advice from an HIV physician or adherence to local agreed guideline is essential before PEP for HIV infection is initiated.
41
Q

Mother of an 11-month-old boy brings him to your practice for vaccination. Three weeks ago, the boy had a fever and rash suggestive of rubella infection. Which one of the following will be the most appropriate step in management?

A. Vaccinate him with MMR vaccine now.
B. Order a serum anti-rubella antibody to guide further decision.
C. Do not give rubella vaccine as he is already immune.
D. Tell her she should wait until the boy turns 12 months before MMR vaccination.
E. Vaccinate him at 15 months of age.

A

A. Vaccinate him with MMR vaccine now.

MMR Vaccine Administration:
- Routine Schedule: First dose at 12 months, second dose at 18 months.
- Early Administration: Can be given as early as 9 months in high-risk situations (e.g., travel to endemic areas).
- Rubella Immunity: Infection provides lifelong immunity, but vaccination is still needed for measles and mumps.
- Convenience: First dose can be administered at 11 months.
- Catch-Up: Second dose can be given early if at risk of exposure.

A 11-month-old infant with no known immunization status is brought to your clinic.

  1. What is the most appropriate action regarding MMR vaccination?
    • A) Defer vaccination until 12 months
    • B) Administer the first dose of MMR vaccine now
    • C) Check anti-rubella serology before vaccination
    • D) Administer only the measles vaccine
    • E) Defer vaccination until 15 months
    Answer: B) Administer the first dose of MMR vaccine nowExplanation: MMR can be administered at 11 months for convenience, especially if the child is already at the clinic.
    • Why not A): Vaccination does not need to be deferred if the child is at the clinic.
    • Why not C): Anti-rubella serology is not needed to proceed with MMR.
    • Why not D): MMR vaccine includes measles, mumps, and rubella.
    • Why not E): Deferring to 15 months is not appropriate; 12 months is standard.

A 9-month-old infant is exposed to a confirmed case of measles.

  1. What is the most appropriate management?
    • A) Wait until 12 months for MMR vaccine
    • B) Administer MMR vaccine immediately
    • C) Administer NHIG
    • D) No action required
    • E) Administer a measles-only vaccine
    Answer: B) Administer MMR vaccine immediatelyExplanation: MMR vaccine can be given as early as 9 months in high-risk situations such as exposure to measles.
    • Why not A): Immediate action is needed due to exposure.
    • Why not C): NHIG is not the preferred option for measles exposure in this case.
    • Why not D): Action is required due to exposure risk.
    • Why not E): MMR vaccine is preferred even in infants as young as 9 months in high-risk scenarios.

A 12-month-old child has received one dose of MMR vaccine and is going to an area with a measles outbreak.

  1. What is the most appropriate action?
    • A) No further action needed
    • B) Administer the second dose of MMR vaccine early
    • C) Administer NHIG
    • D) Administer a booster dose of rubella vaccine
    • E) Check anti-measles antibody titer
    Answer: B) Administer the second dose of MMR vaccine earlyExplanation: The second dose of MMR can be given early if the child is at risk of exposure to measles.
    • Why not A): Further action is needed due to the outbreak.
    • Why not C): NHIG is not needed for this situation.
    • Why not D): A rubella-only booster is not necessary; MMR covers all.
    • Why not E): Immediate vaccination is more appropriate than antibody titer testing.

A 11-month-old child has recovered from rubella infection.

  1. What is the appropriate vaccination plan?
    • A) Defer MMR vaccination
    • B) Administer the first dose of MMR vaccine
    • C) Administer a rubella-only vaccine
    • D) Administer the second dose of MMR vaccine
    • E) Check for immunity to rubella
    Answer: B) Administer the first dose of MMR vaccineExplanation: Despite rubella infection providing immunity, MMR vaccine is still needed for measles and mumps protection.
    • Why not A): Vaccination should not be deferred.
    • Why not C): A rubella-only vaccine is not available.
    • Why not D): The child needs the first dose, not the second.
    • Why not E): Checking for immunity to rubella is unnecessary for vaccination decision.

MMR-containing vaccines are not routinely recommended for infants younger than 12 months of age because maternal antibodies to measles (if the mother has immunity) are known to persist in many infants until approximately 11 months of age
and may interfere with active immunization if performed before 12 months of age. However, there is some evidence that the first dose if given at ≥11 months (but prior to 12 months) is sufficiently immunologic.
Rubella infection provides life-long immunity in an immunocompetent person, but not against measles and mumps. This child is still in risk of catching measles and mumps, and MMR vaccine is still indicated regardless of immune status for rubella.

He is 11 months of age; therefore, the first dose of MMR vaccine can be administrated now.

(Options B) The results of anti-rubella serology will not affect further plans regarding MMR vaccination; therefore, serologic studies for rubella is inappropriate.

(Option C) Although the child will be immune against rubella after the infection, he is still in need for MMR for measles and mumps. A monovalent vaccine for rubella does not exist.

(Option D) Although the recommended time for first dose of MMR is at 12 months of age, for the sake of convenience, this child can receive his first dose of MMR vaccine in this visit and at the age of 11 months. MMR vaccine can also be administered as early as 9 months of age if the infant is high risk for measles, mumps, or rubella, e.g. travel to endemic area, outbreaks, etc.

(Option E) The first dose of MMR vaccine should be given at 12 months of age (≥11 months). Deferring the first dose untill 15 months is not appropriate

TOPIC REVIEW
Update on MMR vaccination

Two doses of measles-containing vaccine are recommended for all children. The first dose should be given at 12 months of age as MMR vaccine. MMRV (measles, mumps, rubella, varicella) vaccines are NOT recommended for use as the 1st dose of MMR-containing vaccine in children < 4 years of age, due to a small but increased risk of fever and febrile seizures when given as the 1st MMR-containing vaccine dose in this age group.

The second dose of measles-containing vaccine is recommended to be given routinely at 18 months of age as MMRV vaccine. The recommended age for administration of the second dose of measles-containing vaccine has been moved down from 4 years of age, to provide earlier 2-dose protection against measles, mumps and rubella, and to improve vaccine uptake.

Catch-up vaccination of children who did not receive the second dose of MMR-containing vaccine at 18 months of age can occur at the 4-year-old schedule point. Use of MMRV vaccine at the 4-year-old schedule point is preferred when varicella vaccination is also indicated.

Children >12 months of age who have received 1 dose of MMR vaccine can be offered their second dose of MMR-containing vaccine early (if at least 4 weeks after the 1st dose has elapsed) if they are considered at risk of coming in contact with measles.

If MMRV vaccine is inadvertently administered as dose 1 of MMR-containing vaccine, the dose does not need to be repeated (providing it was given at ≥12 months of age). However, parents/carers should be advised regarding the small but increased risk of fever and febrile seizures (compared with the expected risk following MMR vaccine)

42
Q

A 31-year-old woman presents to your GP clinic quite concerned about contracting measles. Three days ago she met one of her old friends from school in a shopping mall. After having a coffee, her friend drove her back home. Last night, she called her friend to invite her for lunch, but her friend was down with measles confirmed by her GP after she developed a rash yesterday morning. She does not remember if she has been vaccinated in childhood, nor is she sure if she had measles before.
She asks about what she should do. Which one of the following is the most appropriate advice for her?

A. Perform measles serology.
B. She should receive MMR vaccine now.
C. She should receive natural human immunoglobulin (NHIG).
D. She is not at risk of the infection as she is immune.
E. She should come back if symptoms develop.

A

B. She should receive MMR vaccine now.

Transmission: Measles spreads via respiratory droplets and rarely through contaminated objects. Infectious from 2 days before to 4 days after rash onset.

Immunity: Those with a history of measles, 2 doses of MMR vaccine (≥12 months), or positive measles antibody test are considered immune.

Post-Exposure Prophylaxis:
- Non-pregnant, immunocompetent individuals: MMR vaccine within 72 hours.
- Pregnant or immunocompromised individuals: NHIG within 6 days if exposure is confirmed.

Symptoms:
- Initial: Fever, malaise, cough, coryza, conjunctivitis, Koplik’s spots.
- Rash: Starts on face/neck, spreads to body.

Complications:
- Otitis media, bronchopneumonia, encephalitis.

A woman has been in contact with a friend who developed a measles rash. She does not recall her immunization status or having measles.

  1. What is the most appropriate next step?
    • A) Measles serology
    • B) Administer MMR vaccine
    • C) Administer NHIG
    • D) No further action needed
    • E) Wait until she develops symptoms
    Answer: B) Administer MMR vaccineExplanation: In the case of uncertain immunity, the recommendation is to administer the MMR vaccine within 72 hours of exposure.
    • Why not A): Serology is only recommended for pregnant or immunocompromised individuals.
    • Why not C): NHIG is used if the MMR vaccine is contraindicated.
    • Why not D): Action is needed due to potential exposure.
    • Why not E): Waiting for symptoms is not appropriate; preventive measures are needed.

A 9-month-old infant exposed to measles and is at high risk for complications.

  1. What is the most appropriate post-exposure prophylaxis?
    • A) MMR vaccine immediately
    • B) NHIG
    • C) No action needed
    • D) Vitamin A supplementation
    • E) Delay any action until 12 months
    Answer: A) MMR vaccine immediatelyExplanation: Infants 9-11 months can receive the MMR vaccine within 72 hours of exposure.
    • Why not B): NHIG is for infants <9 months or if the exposure is between 73-144 hours.
    • Why not C): Action is required due to high risk.
    • Why not D): Vitamin A supplementation is supportive but not primary prophylaxis.
    • Why not E): Immediate action is required.

An immunocompromised adult has been exposed to measles.

  1. What is the most appropriate management?
    • A) MMR vaccine
    • B) NHIG within 6 days
    • C) No action needed
    • D) Antiviral therapy
    • E) Routine blood tests
    Answer: B) NHIG within 6 daysExplanation: Immunocompromised individuals should receive NHIG as early as possible, within 6 days of exposure.
    • Why not A): Live vaccines are contraindicated in immunocompromised patients.
    • Why not C): Prophylaxis is needed.
    • Why not D): Antiviral therapy is not indicated.
    • Why not E): Prophylaxis is the priority.

A pregnant woman has been exposed to measles.

  1. What is the recommended prophylaxis?
    • A) MMR vaccine
    • B) NHIG within 6 days
    • C) Wait for symptoms
    • D) Start antiviral therapy
    • E) Immediate isolation
    Answer: B) NHIG within 6 daysExplanation: Pregnant women exposed to measles should receive NHIG within 6 days due to the risk of complications.
    • Why not A): MMR vaccine is contraindicated in pregnancy.
    • Why not C): Waiting for symptoms is not appropriate.
    • Why not D): Antiviral therapy is not the primary prophylaxis.
    • Why not E): Isolation may be necessary, but NHIG is the priority.

Measles is highly infectious. The main route of transmission is by respiratory airborne droplets; however, it can rarely be passed on to others by means of particles soiled with respiratory droplets.

The infectivity of a person with measles begins 2 days before the onset of the symptoms until 4 days after eruption of the rash. This woman has been in contact with her friend 2 days before the rash; therefore, within the infectivity period, and is at risk of contracting measles if not already immune.

Any non-immunocompromised individual with a definite positive history of measles disease, documented evidence of having received 2 doses of a measles-containing vaccine (MMR) administered at least 4 weeks apart and with both doses administered ≥ 12 months of age, or positive measles antibody test is considered to be immune.

This woman does not remember if she has been immunized or contracted measles. In such situations, where the immunity status is unknown, it is recommended that all immunocompetent, non-pregnant patient receive MMR of vaccine within 72
hours of exposure
. A second dose should then follow at least 4 weeks later.

(Option A) Measles serology was the correct answer if the woman was pregnant or immunocompromised and considered for prophylaxis with natural human immunoglobulin (NHIG). In such cases, if time allows, serology testing is recommended, as a positive IgG against measles will indicate immunity and no need for prophylaxis.

(Option C) NHIG is used if the patient is in need for prophylaxis but there is a contraindication to MMR vaccination such as pregnancy or immunodeficiency.

(Option D) This woman is uncertain about her immune status. She does not remember contracting measles or if she had been vaccinated. She cannot be considered immune and post-exposure prophylaxis should be considered.

(Option E) While post-exposure is indicated in this patient in an attempt to decrease the risk of measles infection, telling the patient to wait until she develops active infection is not appropriate.

TOPIC REVIEW
Measles (rubeola) virus is a single-stranded RNA virus of the family Paramyxoviridae. Humans and monkeys are the only known hosts. There are no carrier states. Measles has an incubation period of 10-14 days. Initially, the illness presents with the following:

  • Fever
  • Malaise
  • Cough
  • Coryza (inflammation of the mucous membranes of the nose)
  • Conjunctivitis
  • Koplik’s spots (white spots, each surrounded by a red ring, found on the buccal mucosa)

Two to 4 days after the initial symptoms, a maculopapular rash develops. The rash typically starts from face and upper neck and later spreads to involve the whole body. The infectivity periods starts 2 days before the onset of rash untill 4 days after the rash develops.

Measles is often a severe disease. Complication may occur, and include otitis media in 7% and bronchopneumonia in 6% of immunocompetent patients. Acute encephalitis is a rare complication occurring in between 2 and 10 per 10,000 reported cases with measles in the general population, with an associated mortality rate of 10 -15 %. Around 15 - 40 % of survivors of measles encephalitis will have permanent brain damage.

Measles can be more sever in the following groups:

  • Immunocompromised people, especially those with T-cell deficiencies such as certain leukemias, lymphomas and acquired immunodeficiency syndrome (AIDS), in whom measles can be severe, atypical (e.g. without rash) and prolonged, with virus shedding for several weeks after the acute illness
  • Malnourished children, particularly those with vitamin A deficiency
  • Children younger than 5 years and adults 20 years of age and older, in whom complications of measles are more common
  • Pregnant women in whom infection is associated with increased risk of premature labor, spontaneous abortion, and low birth weight. Birth defects have not conclusively been associated with measles virus infection.

Management of contacts

Neonates or infants less than 12 months of age

  • This group is at high risk of developing complications from measles infection if they have not acquired maternal antibodies from a measles-immune mother; therefore, NHIG should be administered to infants of non-immune mothers as early as possible, and at the latest within 6 days (144 hours) of potential exposure.
  • NHIG should be administered to pre-term neonates (< 37 weeks) or immune-suppressed infants regardless of maternal history or antibody status.
  • Infants 6-8 months of age exposed within 144 hours should receive NHIG (irrespective of mother’s immune status)
  • If exposure has occured within 72 hours, immune competent infants 9-11 months should receive MMR now then second dose at 12 months or 4 weeks later (whichever is later).
  • If exposure within 73-144 hours, give NHIG

Non-immunosuppressed non-vaccinated people over 1 year of age

  • Consider MMR vaccination within 72 hours of exposure for all non-immune contacts.

Individuals in whom protection is desirable, but live vaccination is contraindicated

  • Pregnant women and immunocompromised children (or adults) should not be given live vaccine. NHIG should be administered as early as possible and up to 6 days (144 hours) of exposure
43
Q

A 6-month-old male infant is brought to your clinic by his mother for receiving his third dose of DTPa vaccine. He has received his previous doses at 6 weeks and 4 months of age. The child sneezes, has a runny nose and a fever of 38.2°. Exam findings are consistent with upper respiratory tract infection (URTI). According to the mother, last time he received his DTPa vaccine, he developed a huge swelling at the injection site. Which one of the following is the most appropriate management regarding vaccination with DTPa in this situation?

A. Vaccinate him now.
B. Vaccinate after his URTI settles.
C. Do not give the pertussis component.
D. Use dTpa instead.
E. Vaccinate him after 2 months.

A

A. Vaccinate him now.

Vaccine Formulations:
- DTPa: Child formulations (higher doses of diphtheria and pertussis).
- dTpa: Adolescent/adult formulations (lower doses of diphtheria and pertussis).

Schedule:
- Primary doses: 2, 4, and 6 months (can start at 6 weeks).
- Adverse reactions: Extensive limb swelling is benign and self-limiting.

Contraindications:
- Anaphylaxis to previous dose or any component.

Conditions Safe for Vaccination:
- Mild illness and fever <38.5°C, mild diarrhea, or URTI.

A 2-month-old infant with mild URTI and a fever of 38°C is due for the first DTPa dose.

  1. What is the appropriate action?
    • A) Defer vaccination until fever subsides
    • B) Administer DTPa vaccine now
    • C) Administer only diphtheria and tetanus vaccines
    • D) Check for contraindications
    • E) Give NHIG instead
    Answer: B) Administer DTPa vaccine nowExplanation: Mild illness and fever <38.5°C are not contraindications to DTPa vaccination.
    • Why not A): Deferment is unnecessary for mild illness.
    • Why not C): DTPa should be given in combination.
    • Why not D): No contraindications present.
    • Why not E): NHIG is not relevant here.

A child experienced extensive limb swelling after the previous DTPa dose.

  1. What should be done for the next scheduled dose?
    • A) Administer the next DTPa dose
    • B) Skip the pertussis component
    • C) Defer all future vaccinations
    • D) Administer NHIG instead
    • E) Refer to an allergist
    Answer: A) Administer the next DTPa doseExplanation: Extensive limb swelling is not a contraindication and resolves without sequelae.
    • Why not B): Pertussis vaccination is still recommended.
    • Why not C): Vaccinations should not be deferred.
    • Why not D): NHIG is not indicated here.
    • Why not E): Referral to an allergist is not necessary.

A 6-week-old infant is at high risk for pertussis exposure.

  1. What is the best course of action?
    • A) Wait until 2 months for the first dose
    • B) Administer the first dose of DTPa now
    • C) Give NHIG until vaccination
    • D) Isolate the infant until vaccination
    • E) Administer a single pertussis vaccine
    Answer: B) Administer the first dose of DTPa nowExplanation: The first dose can be given as early as 6 weeks to reduce the risk of pertussis.
    • Why not A): Early vaccination is beneficial.
    • Why not C): NHIG is not indicated for pertussis prevention.
    • Why not D): Isolation is impractical and unnecessary.
    • Why not E): Pertussis vaccine is given in combination (DTPa).

A child had a febrile convulsion after the last DTPa dose.

  1. What is the appropriate action for future doses?
    • A) Discontinue all pertussis vaccinations
    • B) Administer future doses with fever prevention measures
    • C) Give only diphtheria and tetanus vaccines
    • D) Defer vaccination indefinitely
    • E) Administer NHIG for future protection
    Answer: B) Administer future doses with fever prevention measuresExplanation: Febrile convulsions can be managed with measures to prevent fever, and vaccination should continue.
    • Why not A): Vaccination should not be discontinued.
    • Why not C): Pertussis vaccination is still important.
    • Why not D): Indefinite deferment is not appropriate.
    • Why not E): NHIG is not used for this purpose.

A parent is concerned about the risk of extensive limb swelling with the DTPa vaccine.

  1. What is the most appropriate advice?
    • A) Extensive limb swelling is a common and serious reaction
    • B) Extensive limb swelling is rare, self-limiting, and not a contraindication
    • C) Defer the vaccine to avoid any risk
    • D) Administer only the pertussis component
    • E) Replace with NHIG
    Answer: B) Extensive limb swelling is rare, self-limiting, and not a contraindicationExplanation: Extensive limb swelling, though rare, resolves without sequelae and is not a contraindication to further vaccination.
    • Why not A): It is rare and not serious.
    • Why not C): Deferment is not necessary.
    • Why not D): Pertussis vaccine is given in combination.
    • Why not E): NHIG is not a substitute for the vaccine.

Pertussis vaccine is available in Australia only in combination with diphtheria, tetanus and other antigens.
The acronym DTPa, using capital letters, signifies child formulations of diphtheria, tetanus and acellular pertussis-containing vaccines. The acronym dTpa is used for formulations that contain substantially lesser amounts of diphtheria toxoid and pertussis antigens than child (DTPa-containing) formulations; dTpa vaccines are usually used in adolescents and adults.

Pertussis-containing vaccine is recommended in a 3-dose primary schedule for infants at 2, 4 and 6 months of age. Due to the high morbidity and occasional mortality associated with pertussis in the first few months of life, the first dose can be given as early as 6 weeks of age. Giving a first dose at 6 weeks of age rather than 2 months of age is estimated to prevent an additional 8% of infant pertussis cases. The next scheduled doses should still be given at 4 months and 6 months of age.

Extensive limb swelling, defined as swelling and/or redness involving at least half the circumference of the limb and the joints both above and below the injection site is a recognized adverse event that occurs rarely following booster doses of DTPa.

Such reaction begins within 48 hours of vaccination, last for 1 to 7 days and resolve completely without sequelae. History of such event is not a contraindication to the vaccine use. No change in the formulation is required or recommended either.

NOTE – The only absolute contraindications to pertussis containing vaccines are:

  • Anaphylaxis following a previous dose of any acellular pertussis-containing vaccine
  • Anaphylaxis following any vaccine component

Children with mild disease and fever < 38.5°C can be safely vaccinated. However, if the fever is ≥38.5°C, or the child has serious systemic illness, vaccination should be deferred until the child improves. The rationale behind such recommendations is to avoid adverse events in an already unwell child, or to avoid attributing symptoms to vaccination. Conditions such as mild diarrhea or URTI without systemic symptoms are safe for vaccination.

This child had an adverse reaction to the DTPa vaccine that is known to be benign and self-limiting, and is not a contraindication to vaccination with pertussis containing vaccines. Although febrile, his fever is less than 38.5°C associate with a mild disease; therefore, he can be safely vaccinated with DTPa now.

Other facts about pertussis-containing vaccines

  • Febrile convulsions are very infrequently reported following DTPa-containing vaccines within 48 hours of vaccination. The risk is even lower in infants who complete their primary course at 6 months of age, as febrile convulsions are uncommon in children < 6 months of age. Children who experience a febrile convulsion after a dose of DTPa-containing vaccine have a slightly greater risk of a further febrile convulsion following a subsequent dose of a DTPa containing vaccine. This risk can be minimized by appropriate measures to prevent fever, so vaccination still recommended.
  • Pertussis-containing vaccines do not cause infantile spasms or epilepsy. Infants and children known to have active or progressive neurological disease can be safely vaccinated with DTPa-containing vaccines.
  • Sudden infant death syndrome (SIDS) is not associated with either DTPa or any pertussis-containing vaccine. Some studies suggest a decreased risk of SIDS in children who have been vaccinated.
  • Brachial neuritis (inflammation of a nerve in the arm, causing weakness or numbness) has been described following the administration of tetanus toxoid-containing vaccines, with an estimated excess risk of approximately 0.5–1 in 100,000 doses in adults.
44
Q

A mother had brought her 18-month-old female child for MMR vaccination. The baby has flu-like symptoms of runny nose, cough and sneezes. She looks slightly ill. On examination, she has a fever of 38.7°C. Which one of the following is the most appropriate management?

A. Give MMR vaccine without the rubella portion.
B. Give MMR vaccine without the rubella portion and give the rubella portion after she recovers from her illness.
C. Give MMR vaccine now.
D. Postpone the vaccination untill after recovery from her current illness.
E. She should receive the second dose at 4 years of age

A

D. Postpone the vaccination untill after recovery from her current illness.

Children with mild disease and fever < 38.5°C can be safely vaccinated. However, if the fever is ≥38.5°C, or the child has serious systemic illness, vaccination should be deferred until the child improves. The rationale behind such recommendations is to avoid adverse events in an already unwell child, and to avoid attributing symptoms to vaccination. Conditions such as mild diarrhea or URTI without systemic symptoms and fever < 38.5°C are safe for vaccination.

This child has a fever of 38.7°C; therefore, vaccination is recommended to be deferred until she is out of the disease and the fever subsides.

The only vaccines available in Australia is MMR (measles, mumps, rubella) and MMRV (measles, mumps, rubella, varicella). Separate monovalent vaccines against rubella, measles or mumps do not exist.

Current guidelines recommend two doses of MMR vaccine at 12 months and 18 months of age. Postponing MMR vaccine until the age of 4 years is against recommendations and not appropriate.

45
Q

A 62-year-old man presents to your GP clinic for a routine health check after he sustained a myocardial infarction (MI) few months ago. After the event, he stopped smoking and has been following a healthy diet. He also does regular exercise. On examination, he has a blood pressure of 137/85 mmHg. His cholesterol level is 4.0 mmol/L. Which one of the following would be the most appropriate advice for him?

A. Maintaining the diet and regular exercise.
B. He should have his cholesterol checked in 3 months.
C. He should be started on lipid lowering agents.
D. He should be started on antihypertensive medications.
E. He should have cholesterol level checked annually

A

C. He should be started on lipid lowering agents.

Key Points:
- High Risk: Patients with a previous MI are already at high risk (>15%) for cardiovascular events.
- Lifestyle Modifications: Quitting smoking, regular exercise, and a healthy diet are crucial.
- Statin Therapy: Recommended for all patients with coronary heart disease (CHD) regardless of current lipid profile. Check lipid profile every 3-6 months.
- Lipid Targets:
- LDL-C < 1.8 mmol/L
- HDL-C > 1.0 mmol/L
- Triglycerides < 2.0 mmol/L
- Non-HDL-C < 2.5 mmol/L
- Blood Pressure: Target ≤130/85 mmHg. A BP of 137/85 mmHg is not of significant concern compared to starting lipid-lowering agents.

A 60-year-old man with a history of MI is following strict lifestyle modifications but has not started any medication yet.

  1. What is the most appropriate next step?
    • A) Continue lifestyle modifications only
    • B) Start statin therapy
    • C) Wait for lipid profile results before deciding
    • D) Start antihypertensive therapy
    • E) Perform absolute cardiovascular risk calculation
    Answer: B) Start statin therapyExplanation: Statins should be started in all patients with CHD regardless of their current lipid profile as it is associated with decreased mortality.
    • Why not A): Lifestyle modifications alone are insufficient.
    • Why not C): Statin therapy should not be delayed.
    • Why not D): Lipid-lowering is prioritized over current BP.
    • Why not E): Risk calculation is unnecessary for high-risk patients.

A patient with CHD started on statin therapy asks about the frequency of lipid profile monitoring.

  1. How often should the lipid profile be checked?
    • A) Annually
    • B) Every 3-6 months
    • C) Only if symptoms worsen
    • D) Every 2 years
    • E) Monthly
    Answer: B) Every 3-6 monthsExplanation: Regular monitoring of the lipid profile every 3-6 months is recommended to ensure targets are met.
    • Why not A): Annual monitoring is not frequent enough.
    • Why not C): Regular monitoring is required regardless of symptoms.
    • Why not D): Biannual monitoring is insufficient.
    • Why not E): Monthly checks are unnecessary.

A patient with CHD has a blood pressure of 137/85 mmHg.

  1. What should be the focus of management?
    • A) Intensify antihypertensive therapy immediately
    • B) Focus on starting and optimizing statin therapy
    • C) Perform an absolute cardiovascular risk calculation
    • D) Refer to a cardiologist immediately
    • E) Ignore blood pressure management
    Answer: B) Focus on starting and optimizing statin therapyExplanation: The primary focus should be on lipid-lowering agents. Blood pressure of 137/85 mmHg is not a significant concern compared to the importance of statins.
    • Why not A): BP management is secondary here.
    • Why not C): Risk calculation is not needed for already high-risk patients.
    • Why not D): Immediate referral is not necessary.
    • Why not E): BP should be managed but is not the primary concern.

A 55-year-old woman with CHD on statin therapy presents for follow-up.

  1. What are the target lipid levels for this patient?
    • A) LDL-C < 2.5 mmol/L, HDL-C > 1.0 mmol/L, TG < 2.5 mmol/L
    • B) LDL-C < 1.8 mmol/L, HDL-C > 1.0 mmol/L, TG < 2.0 mmol/L
    • C) LDL-C < 1.5 mmol/L, HDL-C > 1.2 mmol/L, TG < 1.5 mmol/L
    • D) LDL-C < 2.0 mmol/L, HDL-C > 1.5 mmol/L, TG < 2.0 mmol/L
    • E) LDL-C < 1.8 mmol/L, HDL-C > 1.5 mmol/L, TG < 1.5 mmol/L
    Answer: B) LDL-C < 1.8 mmol/L, HDL-C > 1.0 mmol/L, TG < 2.0 mmol/LExplanation: These are the recommended target lipid levels for patients with CHD.
    • Why not A): LDL-C target is too high.
    • Why not C): HDL-C and TG targets are not standard.
    • Why not D): HDL-C target is too high.
    • Why not E): TG target is too low and HDL-C too high.

A 58-year-old man with CHD has a blood pressure reading of 135/80 mmHg.

  1. What is the target blood pressure for this patient?
    • A) ≤120/80 mmHg
    • B) ≤130/85 mmHg
    • C) ≤140/90 mmHg
    • D) ≤125/75 mmHg
    • E) ≤135/85 mmHg
    Answer: B) ≤130/85 mmHgExplanation: The target blood pressure for patients with CHD is ≤130/85 mmHg.
    • Why not A): This is too stringent.
    • Why not C): This is not strict enough for CHD.
    • Why not D): This is too stringent.
    • Why not E): This is close but the precise target is ≤130/85 mmHg.

A patient with CHD asks about the most impactful lifestyle modification.

  1. What is the single most modifiable risk factor for cardiovascular disease?
    • A) Diet
    • B) Exercise
    • C) Smoking cessation
    • D) Stress management
    • E) Alcohol consumption
    Answer: C) Smoking cessationExplanation: Quitting smoking is the single most impactful modifiable risk factor for reducing cardiovascular disease risk.
    • Why not A): While important, it is not the most impactful alone.
    • Why not B): Exercise is crucial but smoking cessation has a greater immediate impact.
    • Why not D): Important, but not the single most impactful.
    • Why not E): Reducing alcohol helps but smoking cessation is more impactful.

A patient with CHD on statin therapy shows an LDL-C of 1.9 mmol/L after 3 months.

  1. What should be the next step?
    • A) Increase statin dose
    • B) Add another lipid-lowering agent
    • C) Recheck lipid profile in 3-6 months
    • D) Discontinue statin therapy
    • E) No further action needed
    Answer: C) Recheck lipid profile in 3-6 monthsExplanation: Regular monitoring every 3-6 months is appropriate to ensure lipid targets are maintained.
    • Why not A): An LDL-C of 1.9 mmol/L is close to target.
    • Why not B): Not necessary if levels are close to target.
    • Why not D): Statin therapy should not be discontinued.
    • Why not E): Monitoring is still needed.

With a previous MI, this man is already high risk (absolute risk >15%), and absolute cardiovascular risk calculation should not be performed for him. This patient is following strict lifestyle modification. He quit smoking which is the single most modifiable risk factor for cardiovascular diseases. He takes exercise on a regular basis, and follows a healthy diet.

Statins should be started in all patients with coronary heart disease (CHD) regardless of they current lipid profile status as it is associated with decreased mortality. His lipid profile then should be checked evey 3-6 months.

Target values for patients with CHD are:

  • Low-density lipoprotein cholesterol (LDL-C) < 1.8 mmol/L
  • High-density lipoprotein cholesterol (HDL-C) > 1.0 mmol/L
  • Triglyceride (TG) < 2.0 mmol/L
  • Non–high-density lipoprotein cholesterol (NHDL-C) < 2.5 mmol/L

Although the target blood pressure in patients with CHD is ≤130/85mmHg, his blood pressure of 137/85mmHg is not of significant concern compared to importance of commencement of lipid-lowering agents. He should also be advised to keep on diet and regular exercise.

46
Q

Which one of the following conditions requires major attention for prevention of blindness in Aboriginal Australians?

A. Trichiasis.
B. Diabetes mellitus.
C. Bacterial conjunctivitis.
D. Herpetic keratitis.
E. Chronic simple glaucoma.

A

A. Trichiasis.

Blindness from Chlamydia trachomatis is a major cause of blindness where the socioeconomic status is poor and people disadvantaged. Many Aboriginal Australian communities exemplify such situation.

Recurrent infections with Chlamydia trachomatis cause chronic keratoconjunctivitis. This is then followed by scarring of the tarsal conjunctiva. A the condition progresses, tarsal plates become distorted eyelids and eyelashes turn inwards (entropion) as do eyelashes. Inwardly-turned eyelashes will irritate the cornea (trichiasis). Chronic irritation leads to abrasions, corneal opacification and eventually blindness.

Although all other options can potentially lead to blindness, infection with Chlamydia trachomatis remains the major risk and concern in Aboriginal communities

47
Q

Which one of the following is the study of choice for determining the state of vitamin D deficiency in Australia?

A. Cohort study.
B. Case control study.
C. Randomized controlled trial (RCT).
D. Cross sectional study.
E. Case series.

A

D. Cross sectional study.

Objective: Determine the prevalence of vitamin D deficiency in Australia.

Best Method: Cross-sectional studies

  • Purpose: Assess a population at a single point in time.
  • Measures: Prevalence, odds ratio, absolute risk, and relative risk.
  • Usage: Identify the presence or absence of a condition in the study population.
  • Characteristics:
    • Investigate both diseased and non-diseased individuals.
    • Describe the entire population, not just specific characteristics.
  • Cohort Studies:
    • Type: Prospective.
    • Purpose: Follow a group over time to compare those exposed and not exposed to a risk factor.
    • Measures: Incidence and causal relationships.
  • Case-Control Studies:
    • Type: Retrospective.
    • Purpose: Compare subjects with a condition (cases) to those without (controls).
    • Measures: Frequency of risk factor exposure.
  • Randomized Controlled Trials (RCTs):
    • Type: Interventional.
    • Purpose: Assess effectiveness and safety of interventions.
  • Case Series:
    • Purpose: Report clinical characteristics or outcomes in a group of patients.
    • Usage: Typically descriptive and not used to determine prevalence.

Conclusion: Cross-sectional studies are the method of choice for determining the prevalence of conditions in a population.

A research team wants to determine the prevalence of vitamin D deficiency in a specific population.

  1. Which study design should they choose?
    • A) Cohort study
    • B) Case-control study
    • C) Cross-sectional study
    • D) Randomized controlled trial
    • E) Case series
    Answer: C) Cross-sectional studyExplanation: Cross-sectional studies are ideal for determining prevalence at a single point in time.
    • Why not A): Cohort studies are for determining incidence and causal relationships over time.
    • Why not B): Case-control studies compare past exposures between cases and controls.
    • Why not D): RCTs assess the effectiveness of interventions.
    • Why not E): Case series describe clinical characteristics, not prevalence.

A researcher is conducting a study to measure the prevalence of hypertension in adults.

  1. Which type of study provides the best data for this measurement?
    • A) Cohort study
    • B) Case-control study
    • C) Cross-sectional study
    • D) Randomized controlled trial
    • E) Case series
    Answer: C) Cross-sectional studyExplanation: Cross-sectional studies measure the prevalence of a condition at a specific point in time.
    • Why not A): Cohort studies are more suited for incidence and causal analysis.
    • Why not B): Case-control studies are retrospective.
    • Why not D): RCTs are for testing interventions.
    • Why not E): Case series do not provide prevalence data.

A study aims to compare the prevalence of smoking among adults with and without lung cancer.

  1. What type of study design is this?
    • A) Cohort study
    • B) Case-control study
    • C) Cross-sectional study
    • D) Randomized controlled trial
    • E) Case series
    Answer: B) Case-control studyExplanation: Case-control studies compare exposures between those with the condition (cases) and those without (controls).
    • Why not A): Cohort studies follow subjects over time based on exposure.
    • Why not C): Cross-sectional studies measure prevalence, not past exposures.
    • Why not D): RCTs test interventions.
    • Why not E): Case series describe clinical characteristics.

A study follows a group of people over 10 years to see who develops diabetes based on their diet.

  1. Which study design is used?
    • A) Cohort study
    • B) Case-control study
    • C) Cross-sectional study
    • D) Randomized controlled trial
    • E) Case series
    Answer: A) Cohort studyExplanation: Cohort studies follow a group over time to study the development of outcomes based on exposures.
    • Why not B): Case-control studies are retrospective.
    • Why not C): Cross-sectional studies are at a single point in time.
    • Why not D): RCTs are for testing interventions.
    • Why not E): Case series describe clinical characteristics.

A study tests the effectiveness of a new drug on lowering blood pressure.

  1. What type of study design is this?
    • A) Cohort study
    • B) Case-control study
    • C) Cross-sectional study
    • D) Randomized controlled trial
    • E) Case series
    Answer: D) Randomized controlled trialExplanation: RCTs assess the effectiveness and safety of interventions by randomly assigning subjects to treatment or control groups.
    • Why not A): Cohort studies follow subjects based on exposure, not intervention.
    • Why not B): Case-control studies are retrospective.
    • Why not C): Cross-sectional studies do not test interventions.
    • Why not E): Case series describe clinical outcomes, not interventions.

The objective of the study is determining the prevalence of vitamin D deficiency in Australia. When prevalence of a specific condition in a population is the aim, cross sectional studies are used as the most appropriate method.

Cross sectional studies are also called prevalence studies, because one of the main measures available is the ‘population prevalence’. These studies consist of assessing a population, as represented by the study sample, at a single point in time.

Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study. Cross sectional studies can also describe the odd ratio, absolute risk and relative risk. These parameters cannot be elicited from case-control studies. Cross-sectional are also able to support (not establish) the interference of cause and effect.

Cross-sectional studies are different from case-control studies in that they aim to provide data on the entire population under study, whereas case-control studies typically include only individuals with a specific characteristic.

(Option A) In cohort studies, the population group is identified. Subjects who have been exposed to a certain risk factor are followed over time and compared with a group not exposed to the risk factor. Cohort studies are prospective (forward-looking), and subjects are tracked forward in time. It can determine incidence and causal relationship; however, the population must be followed long enough for the incidence to appear.

(Option B) Case-control studies are observational studies that compare subjects who have a disease or outcome (cases) with subjects who do not have the disease or outcome (controls), and look back retrospectively to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease.

(Option C) Randomized controlled trials (RCTs) are interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

(Option E) Case series is objective report of a clinical characteristic or outcome from a group of clinical subjects (n>1). For example, patient at a local hospital with hospital acquired pneumonia.

NOTE - Cross sectional studies are the method of choice for determining prevalence in a population.

48
Q

To study the prevalence of cancer in a city, which one of the following studies is most appropriate?

A. Double blind clinical trial.
B. Cross sectional study.
C. Cohort.
D. Case control.
E. Randomized controlled trial (RCT).

A

B. Cross sectional study.

For determining the prevalence of a disease or a condition in a population, cross sectional studies are used as the method of choice.

Cross sectional studies are also called prevalence studies because one of the main purposes and measures available is determining the ‘prevalence’ of a condition (e.g. disease). These studies consist of assessing a population, as represented by the study sample, at a single point in time. Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study.

(Option A) Double blind studies are gold-standard for interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

(Option C) The main objective in cohort studies is to see if there is an established link between one variable and the disease. In cohort studies, the population group is identified. Subjects who have been exposed to a certain risk factor are followed over time and compared with a group not exposed to the risk factor. The outcome is the disease incidence in each group, as well as the linkage between the cause (risk factor) and the effect (disease). Cohort studies are prospective (forward-looking), and subjects are tracked forward in time. A cohort study can determine incidence and causal relationship (such as hypercholesterolemia and myocardial infarction); however, the population must be followed long enough for the incidence to appear.

(Option D) Case-control studies (also known as retrospective studies and case-referent studies) are observational studies that compares subjects who have a disease or outcome (cases) with subjects who do not have the disease or outcome (controls), and looks back retrospectively to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease.

NOTE – The main differences between cohort study and case control study are:

In case control study the subjects in the study population have the disease, while in cohort subjects are not diseased.

Cohort study is prospective (forward-looking), while case control study is retrospective (back-looking)

(Option E) Similar to randomized double blind studies, RCTs are also interventional studies.

49
Q

Which one of the following studies should be used to investigate the relationship between the number of nevi and melanoma?

A. Cross sectional study.
B. Cohort study.
C. Case-control study.
D. Comparative analysis.
E. Case series report

A

B. Cohort study.

Cohort studies are the option of choice when a causal relationship between a variable (e.g. a risk factor) and a disease or condition is the objective of the study. In fact they are best for identification of risk factors, as well as the incidence.

Cohort studies are usually prospective (forward-looking). They are planned in advance and carried out over a future period of time.

In a prospective cohort study, a research question is raised first, forming a hypothesis about potential causes of a disease. The researcher then observe a group of people (the cohort) over a period of time (often several years), collecting data that may be relevant to the disease. This allows the researchers to detect any changes in health in relation to the potential risk factors they have indentified.

To establish a relationship between the number of nevi (risk factor) and melanoma (the disease), cohort study is the study of choice.

(Option A) Cross sectional studies are the studies of choice whenever determination of the prevalence of particular condition of disease is desired.

(Option C) Case-control studies (also known as retrospective studies and case-referent studies) are observational studies that compares subjects who have a disease or outcome (cases) with subjects who do not have the disease or outcome (controls), and looks back retrospectively to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease.

(Option D) Comparative analysis is the item-by-item comparison of two or more comparable alternatives, processes, products, qualifications, set of data, etc. It can be used, for example, for comparing two treatments for one condition, but generally it is not a distinct research entity, nor can it establish or exclude a relationship between a risk factor and a condition.

(Option E) Case report (study) is an article describing and interpreting an individual case, often written in the form of a detailed story. Case reports are considered the lowest level of evidence, but they are also the first line of evidence, because they are where new issues and ideas emerge. Case series report (study) is similar to case report (study) with the only difference being the number of cases compared to case report (n=1 versus n>1)

50
Q

You want to find the causality between hypertension and myocardial infarction. Which one of the following studies should you use?

A. Cohort study.
B. Cross-sectional study.
C. Case-control study.
D. Randomization.
E. Double-blind clinical trial (RCT

A

A. Cohort study.

To see if there is a relationship between hypertension as a risk factor and myocardial infarction as the outcome, cohort studies are the most appropriate option.
Cohort studies are the option of choice when a casual relationship between a variable (e.g. a risk factor) and a disease or condition is investigated. They are best for identification of risk factors, as well as the incidence. Cohort studies are usually prospective (forward-looking). They are planned in advance and carried out over a future period of time.

In a prospective cohort study, a research question is raised first, forming a hypothesis about potential causes of a disease. The researcher then observe a group of people (the cohort) over a period of time (often several years), collecting data that may be relevant to the disease. This allows the researchers to detect any changes in health in relation to the potential risk factors they have indentified.

(Option B) Cross sectional studies are also called prevalence studies because one of the main purposes and measures available is population prevalence. These studies consist of assessing a population, as represented by the study sample, at a single point in time. Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study.

(Option C) Case-control studies (also known as retrospective studies and case-referent studies) are observational studies that compare subjects who have a disease or outcome (cases) with subjects who do not have the disease or outcome (controls), and look back retrospectively to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease.

(Option D) Randomization is a sampling method used for unbiased sample definition and selection for research studies which is a necessary element for a study to be valid and trustable. It is not a study.

(Option E) Double blinded studies are gold-standard for interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

51
Q

Which one of the following is the study of choice to assess the efficacy of a vaccine on a group of people?

A. Randomized controlled trial.
B. Cohort study.
C. Case control study.
D. Cross-sectional study.
E. Case series report

A

A. Randomized controlled trial.

Randomized controlled trials (RCTs) are the gold-standard study for assessment of safety and effectiveness of an intervention such as a vaccine, drug, or method of treatment.

Cohort study, cross-sectional study, case-control study and case series report are all observational, and not interventional studies. Observational studies are used for assessment and examining the etiology and potential risk factors of a disease

52
Q

A young scientist has decided to study the cause of neonatal jaundice. He selects 150 babies with and 150 babies without jaundice, and investigates their histories including the maternal obstetric history for factors that could have caused jaundice in them. Which one of the following is the type of study she is using?

A. Cohort study.
B. Case report.
C. Case control study.
D. Prospective study.
E. Randomized controlled trial (RCT)

A

C. Case control study.

When evaluation of a causal relationship between a variable such as a risk factor and a disease or condition is desired, either a case control or a cohort study should be considered and designed. The decision as to whether which one should be used depends on several factors.
Cohort study is a study designed when one or more samples (called cohorts) are followed prospectively (forward-looking) to see if there is a linkage between a variable, such as a risk factor, and an outcome of interest. Cohort studies are used to investigate the cause of disease, and establishing links between risk factors and health outcomes. Cohort studies are usually prospective (forward-looking). They are planned in advance and carried out over a future period of time.

Case control studies compare patients who have a disease or outcome of interest (cases) with patients who do not have the disease or outcomes (controls), and looks back (retrospective) to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease. Case control studies are observational because no intervention is attempted and no attempt is made to alter the course of the disease. The goal is to retrospectively determine the exposure to the risk factor of interest from each of the two groups of individuals: cases and controls. These studies are designed to estimate odds. Case control studies are also known as “retrospective studies” and “case-referent studies”.

This scientist wants to compare a group of neonates with jaundice (disease present) with a group of neonates without jaundice, by looking back at the history to see how exposure to hypothesized parameters could have resulted in jaundice. Therefore, he should use a case control study as the most appropriate method.

(Option A) Cohort study is a forward-looking study for assessment of the relationship between a variable (risk factor) and a condition e.g. the relationship between hypertension and ischemic heart disease. The relation can also be determined by case-control studies; however, cohort study has many advantages over the latter, making it the preferred study.

(Option B) Case report (study) is an article describing and interpreting an individual case, often written in the form of a detailed story.

(Option D) Prospective study is the term sometimes used for a cohort study.

(Option E) RCTs are interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

53
Q

You want to design a study about the asthmatic children to find out if there is a relationship between asthma and exposure to smoking and its severity. Which one of the following studies is the most appropriate study for this purpose?

A. Case control study.
B. Cross-sectional study.
C. Cohort study.
D. Observational study.
E. Randomized controlled trial (RCT)

A

A. Case control study.

This study is intended to assess if there is a causal linkage between a risk factor (exposure to smoke and the severity) and an outcome of interest (asthma) in a group, who already have the condition (asthmatic patients). For such an approach, case control study should be conducted.

Case control studies compare patients who have a disease or outcome of interest (cases) with patients who do not have the disease or the outcomes (controls), and looks back (retrospective) to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease. Case control studies are observational because no intervention is attempted and no attempt is made to alter the course of the disease. The goal is to
retrospectively determine the exposure to the risk factor of interest from each of the two groups of individuals: cases and controls. These studies are designed to estimate odds.

(Option B) Cross sectional studies are also called prevalence studies because one of the main purposes and measures available is population prevalence. These studies consist of assessing a population, as represented by the study sample, at a single point in time. Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study.

(Option C) Cohort study is another method to see if a relationship between cause and effect exist, in a retrospective (forward-looking) manner. It consists of observing the development of the condition of interest (e.g. asthma) in case who do not have asthma at the beginning of the study and seeing whether the case develops the condition in the future, and if so, how relevant it can be to the cause (smoke in this question). Unlike case control study, cohort is usually prospective, and the population studied has not the condition in the outset.

(Option D) Observational study is a term used for studies in which no intervention is attempted during the study. Cohort, case control, cross sectional, case report, and case series report are all observational studies.

(Option E) RCTs are interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

54
Q

A medical doctor wants to investigate the causal relationship between alcohol intake and dementia. He designs a study and starts to collect cases with dementia and the history of alcohol use. Which one of the following is the type of study he intends to use?

A. Case series.
B. Cohort study.
C. Case control study.
D. Cross sectional study.
E. Randomized control trial (RCT).

A

C. Case control study.

The objective of this study is to see if there in a causal relationship between a risk factor (alcohol) and a condition of interest (dementia). When establishment of such association or linkage is the purpose, two studies can be used:

Case control studies - Compare patients who have a disease or outcome of interest (cases) with patients who do not have the disease or outcomes (controls), and looks back to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease. These studies are designed to estimate odds.

Cohort studies - Cohort study is another method to investigate a relationship between cause and effect, but it is prospective (forward-looking), and observes the development of the condition of the interest (e.g. dementia) in cases who do not have the disease at the beginning of the study and sees if they develop the condition in the future, and if so how relevant it can be to the cause (amalgam in this question). Unlike case control study, cohort is usually prospective and the population studied has not the condition in the beginning of the study.

This doctor is using a sample of people who already have dementia and wants to look back at their history of alcohol intake to see if he can find a relationship. These features are characteristics of a case control study.

(Option A) Case report (study) is an article describing and interpreting an individual case, often written in the form of a detailed story. Case series report (study) is similar to case repot (study) with the only difference being the number of cases compared to case report (n=1 versus n>1).

(Option B) In cohort study, the target group has not the disease yet. In the study conducted by this doctor, dementia (the disease) has already established in the study group.

(Option D) Cross sectional studies consist of assessing a population, as represented by the study sample, at a single point in time. Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study. They are used mostly to see how prevalent a condition is in a population.

(Option E) RCTs are interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

55
Q

You are a doctor in a hospital who has decided to conduct a research about the outcomes of babies born to diabetic mothers compared to those born to non-diabetics mothers. Which one of the following studies should you select?

A. Cross sectional study.
B. Cohort study.
C. Case control study.
D. Randomized controlled trial (RCT).
E. Case report study.

A

B. Cohort study.

When evaluation of a causal relationship between a variable such as a risk factor and a disease of condition is desired, either a case-control or a cohort study should be considered and designed. The decision as to whether which one should be used depends on several factors.

Cohort studies are used to investigate the cause of disease, and establishing links between risk factors and health outcomes. Cohort studies are usually prospective (forward-looking). They are planned in advance and carried out over a future period of time.

In a prospective cohort study, a research question is raised first, forming a hypothesis about potential causes of a disease. The researcher then observe a group of people (the cohort), over a period of time (often several years), collecting data that may be relevant to the disease. This allows the researchers to detect any changes in health in relation to the potential risk factors they have indentified. For example, scientists may ask participants to record specific lifestyle details over the course of a study, before going on to analyze any possible correlations between lifestyle factors and disease.

In contrast, case control studies are retrospective, looking back at data that already exist and, through this, try to indentify risk factors for particular conditions. The drawback to this study is the fact that the researchers are limited in their interpretations because they cannot retrospectively retrieve missing data.

Here, being born to a diabetic mother has been considered a risk factor, and the intended future outcomes related to this risk factor is the objective of this study. For this purpose, a cohort study serves best.

(Option A) Cross sectional studies consist of assessing a population, as represented by the study sample, at a single point in time. Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study group. They are used mostly to see how prevalent a condition is in a population.

(Option C) Case control study was the choice if the aim of the study was to find out how a current problem in the babies could be related to the maternal obesity (retrospective approach).

(Option D) RCTs are interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

(Option E) Case report (study) is an article describing and interpreting an individual case, often written in the form of a detailed story.

56
Q

You are a dentist and you want to find the relationship between mercury amalgam and the risk of development of dementia. You select 2 groups of patients, one with dementia and the other with mercury amalgam. Which one of the following studies is the study you are using?

A. Cross sectional study.
B. Randomized controlled trial (RCT).
C. Case control study.
D. Cohort study.
E. Case series

A

C. Case control study.

The objective of this study is to see if there in a causal relationship between a risk factor (amalgam) and dementia. When investigating such association or linkage is the purpose, two studies can be used:

Case control studies - Compare patients who have a disease or outcome of interest (cases) with patients who do not have the disease or outcomes (controls), and looks back to compare how frequently the exposure to a risk factor is present in each group to determine the relationship between the risk factor and the disease. These studies are designed to estimate odds.

Cohort studies - Cohort study is another method to investigate a relationship between cause and effect, but it is prospective (forward-looking), and observes the development of the condition of the interest (e.g. dementia) in cases who do not have the disease at the beginning of the study and sees if they develop the condition in the future, and if so how relevant it can be to the cause (amalgam in this question). Unlike case control study, cohort is usually prospective and the population studied has not the condition in the beginning of the study.

Of the two of your samples, one consists of the cases who already have dementia, and you want to look back at their history of dental fillings with amalgam to see if there is a meaningful linkage between amalgam as a risk factor and dementia as an outcome. These features are characteristics of a case control study.

(Option A) Cross sectional study has different structure and is mostly used for prevalence studies.

(Option B) RCTs are interventional studies conducted for the assessment of effectiveness and safety of a drug, procedure or any other intervention.

(Option D) In cohort study, the target group has not the disease yet. In this study, dementia (the disease) has already established in the study group.

(Option E) Case report is an article describing and interpreting an individual case, often written in the form of a detailed story. Case series report (study) is similar to case repot with the only difference being the number of cases compared to case report (n=1 versus n>1).

57
Q

A junior doctor in the hospital had a needle stick injury while setting up a line for intravenous fluids. The patient status for hepatitis B is unknown. The doctor has no history of previous hepatitis B vaccination. A blood sample of the doctor is sent to laboratory for hepatitis B serology which came back positive for HBsAg. Which one of the following is the next best step in management?

A. Give immunoglobulin.
B. Give hepatitis B vaccine and immunoglobulin.
C. Counselling and follow-up.
D. Lamivudine.
E. Give hepatitis B vaccine.

A

C. Counselling and follow-up.

This health care worker had a needle stick injury and blood test came back positive for hepatitis B surface antigen meaning that he has hepatitis B infection. This healthcare worker should be counseled about the result and should have follow-up testing at 3 months and 6 months. If the blood tests remain positive for hepatitis surface antigen beyond 6 months, the patient should be referred to specialist.

58
Q

Which one of the following is the study of choice to investigate the effect of vitamin C in treatment of influenza?

A. Cohort study.
B. Case control study.
C. Case series.
D. Randomized controlled trial (RCT).
E. Randomization.

A

D. Randomized controlled trial (RCT).

When it comes to assessment of the efficacy or safety of a drug, procedure, or any other interventional treatment of any kind, RCTs or randomized double blind trials are the option of choice.

RTCs in humans are used to test the safety and potential benefit of a treatment. While the harms of a treatment sometimes prove to outweigh the benefits, this form of testing is acceptable to the participants because the investigators are aiming to develop a new treatment and usually have a reasonable expectation of safety at least, if not a positive effect of treatment.

RCTs, especially if double blind, are the gold-standard study for medical interventions. They have become the standard for assessment of efficacy and safety of an experimental drug or method of treatment.

(Options A and B) Cohort and case control are observational studies and not used for assessment of an intervention.

(Option C) Case report (study) is an article describing and interpreting an individual case, often written in the form of a detailed story. Case series report (study) is similar to case repot (study) with the only difference being the number of cases compared to case report (n=1 versus n>1). Case reports, as the name implies, just report a condition and are not able to define a cause.

(Option E) Randomization is a sampling method used for unbiased sample definition and selection for research studies which is a necessary element for a study to be valid and trustable. It is not a study.

59
Q

Which one of the following studies should be used to assess the effect of vitamin C on the efficacy of iron tablets in treatment of iron deficiency anemia?

A. Cohort.
B. Case control study.
C. Case series study.
D. Double blind clinical trial.
E. Randomization.

A

D. Double blind clinical trial.

Logically, when the effect of vitamin C on the efficacy of iron tablets is intended as the objective of this study, an interventional study should be conducted. Two groups are selected randomly from persons who are taking iron tablet in a similar controlled way. The intervention will be the addition of vitamin C to one group only, and to see how effective vitamin can be in treatment outcomes compared to the control group. This is called randomized controlled trial (RCT).

A double blind clinical trial is an RTC, in which neither the group populations, nor the researchers are aware of who is being intervened during the trial. No one in trial groups knows if he/she is taking vitamin C, nor does the researcher. This method is the gold standard study in clinical trials, and should be used as first-line study (if possible) for assessment of the efficacy or safety of a drug or therapy.

(Options A, B and C) Cohort, case control and case series are all observational studies. Observational are not interventional and inappropriate and irrelevant when efficacy of an intervention is the objective of the study.

(Option E) Randomization is a sampling method used for unbiased sample definition and selection for research studies which is a necessary element for a study to be valid and trustable. It is not a study.

60
Q

There was an outbreak of salmonella infection in your area 3 weeks ago. As a GP you are asked to perform a study to find out the cause. Which one of the following is the most appropriate study for this purpose?

A. Case control.
B. Case series.
C. Cross sectional study.
D. Randomization.
E. Cohort study.

A

A. Case control.

Case control studies are the most appropriate option to find the possible cause(s) of the disease in outbreaks. Case-control studies are useful when epidemiologists investigate an outbreak of a disease, because the study design is powerful enough to identify the cause of the outbreak especially when the sample size is small. Attributable risks may also be calculated.

(Option B) Case report (study) is an article describing and interpreting an individual case, often written in the form of a detailed story. Case series report (study) is similar to case repot (study) with the only difference being the number of cases compared to case report (n=1 versus n>1). Case report, as the name implies, just reports a condition, and is not able to define a cause.

(Option C) Cross sectional studies consist of assessing a population, as represented by the study sample, at a single point in time. Cross-sectional study investigates the presence or absence of any disease or other condition in each member of the study. They are used mostly to see how prevalent a condition is in a population.

(Option D) Randomization is a sampling method used for unbiased sample definition and selection for research studies which is a necessary element for a study to be valid and trustable. It is not a study.

(Option E) Cohort studies are used to establish linkage between a cause (e.g. risk factor) and the effect (disease) in a prospective approach. They are also excellent for determining incidence.

61
Q

A 17-year-old high school student boy presents to your clinic with a fever and diarrhea for the past 24 hours. Evaluation, including a stool exam and culture, establishes the diagnosis of salmonella infection. You have been already informed that there is an outbreak of salmonella in your area. Which one of the following is the most important question to ask the patient?

A. Where do you go to school?
B. What is your part time job?
C. Have you been engaged in school excursion recently?
D. Are you using public transport?
E. Where do you live?

A

B. What is your part time job?

Salmonella gastroenteritis is febrile diarrheal disease presenting with fever, vomiting, bloody diarrhea and abdominal pain. The disease is food-borne, and the main rout of spread is food handling. Therefore, of the questions, the most important question to ask is if the patients job has the potentials to spread the infection to others. The risk of disease spread is particularly high in those who handle or prepare food and dishes. If this patient has a job related to food or food handling, or other jobs that might pose risk to others, it is very important that he is excluded from work until 48 hours after the diarrhea stops. Exclusion from school until 24 hours after resolution of the diarrhea is also important.

Salmonella infection transmission occurs through oral-fecal route. Public transport is NOT a significant route of transmission if general hygienic measures, such as frequent hand washing, are considered.

Other questions are not as important as the question asking whether he has a part time job that includes food handling.

62
Q

Which one of the following is the least reliable study to consider for studying patients with acute ascending cholangitis?

A. Randomized controlled trial.
B. Cohort study.
C. Case control study.
D. Case report.
E. Systematic review.

A

D. Case report.

To answer this question, one should be familiar with the hierarchy of studies used for medical research. Each study provides some evidence. The more qualified evidence a specific type of study provides, the higher it is in the order of hierarchy. The research studies used in medical research, in order of their ability to reliably provide evidence are as follows:

  1. Meta-analysis
  2. Systematic review
  3. Practice guideline
  4. Randomized controlled trial
  5. Cohort study
  6. Case control study
  7. Cross sectional study
  8. Case report
  9. Individual opinion papers

Of the given options case report is weakest in providing evidence. Meta-analysis provides the strongest evidence

63
Q

Tim is 6 years old and is brought to your GP clinic by his mother, who is concerned about him getting chickenpox after he was in contact with a child with the disease 2 days ago. He is asymptomatic now. Which one of the following is the most appropriate step in management?

A. Varicella zoster immunoglobulin (VZIG).
B. Acyclovir.
C. Chickenpox vaccine.
D. Observe for a few days.
E. Exclude him from school.

A

C. Chickenpox vaccine.

If varicella-containing vaccines are not contraindicated, vaccination can be offered to non-immune, age-eligible children and adults, who have a significant exposure to varicella or herpes zoster, and wish to protect against primary infection with varicella zoster virus (VZV).

Post-exposure vaccination is generally successful when given within 3 days (72 hours) and up to 5 days after exposure; the earlier, the better.

Live attenuated varicella vaccine (VV) is currently available in Australia as a monovalent vaccine. Two quadrivalent combination vaccines containing live attenuated measles, mumps, rubella and varicella viruses (MMRV) are also registered in Australia. MMRV vaccine can be given to children in this setting, particularly if MMR vaccination is also indicated.

(Option A) VZIG is indicated for patients in whom prophylaxis is indicated, but vaccination is contraindicated.

(Option B) Acyclovir is the treatment of choice and indicated once the child has the clinical symptoms of varicella zoster.

(Option D) While post-exposure prophylaxis can reduce the risk of infection, just observation to see if symptoms develop is not an appropriate option.

(Option E) Exclusion from school until the blisters are dried out (usually 5 days) is indicated if the child develops chickenpox. The child is not affected yet.

64
Q

A 24-year-old woman presents concerning about the risk of breast cancer after her mother was recently diagnosed with breast cancer and was found to have BRCA1 gene mutation. She is keen to know if she should undergo genetic testing for BRCA1 and the expenses. Which one of the following is correct in this regard?

A. She can be screened at her own expense.
B. She can be screened at her employer’s expense.
C. Screening for her is funded by the government.
D. She does not require screening.
E. She can be screened at the expense of Medicare.

A

C. Screening for her is funded by the government.

Despite the fact that a family history of breast and/or ovarian cancer is common in women with breast or ovarian cancer, only less than 10% of all breast cancers and less than 15% of ovarian cancers are associated with inherited genetic mutations.

Mutations in BRAC1 and BRCA2 account for the majority of hereditary breast/ovarian cancers. Less common mutations are TP53 (Li-Fraumeni syndrome) and PTEN (Cowden syndrome).

Hereditary syndromes associated with BRCA1 and BRCA2 are inherited in an autosomal dominant fashion, meaning that 50% of offspring of a person with such mutations will have the faulty gene.

There are national guidelines to use when offering publically funded BRCA gene testing in Australia. It is generally accepted that when offering BRCA testing in a family for the first time, the person who is offered testing must be either affected by a relevant cancer (usually breast or ovarian cancer) and have a more than 10% likelihood of a gene mutation, or if unaffected and have more than a 20% chance of a gene mutation.

This woman is unaffected; however, with a mother with proven BRCA1 mutation, she has a 50% of chance of having a BRCA1 gene mutation; therefore, she is eligible for BRCA gene testing at the expense of government.

BRCA1 and BRCA2 testing is not subsidized by Medicare. These tests are done through the public hospital system, funded by state health department.

The following patients are eligibe for BRCA gene testing funded by public health system:

  • Breast cancer < 30 years; triple negative breast cancer < 40 years**, ovarian cancer (high grade serous, endometrioid or clear cell) < 70 years
  • Males with breast cancer < 60 year would usually be eligible for testing while older men require additional family history

Other (usually eligible):

  • Ashkenazi Jewish heritage and either a personal or family history of breast or ovarian cancer
  • An affected woman with a family history of breast and ovarian cancer
  • Three first- or second-degree relatives with breast cancer, especially if < 50 years
  • Bilateral breast cancer with the first cancer occurring in the 30’s or 40’s
  • Affected patients whose family history scores >16 on the Manchester risk score

TOPIC REVIEW
The following screening strategy is recommended by expert groups for women with hereditary breast/ovarian cancer (HBOC) syndrome, who have not undergone risk-reducing surgery (i.e., bilateral mastectomy, oophorectomy):

  • Monthly breast self-examination beginning at age 18
  • Clinical breast examination 2 to 4 times annually beginning at age 25
  • Annual mammography and breast magnetic resonance imaging (MRI) screening (commonly alternated every 6 months) beginning at age 25 or individualized based on the earliest age of onset in the family
  • Twice yearly ovarian cancer screening with transvaginal ultrasound and serum CA-125 levels (preferably drawn on day 1 to 10 of menstrual cycle for premenopausal women) beginning at age 35, or 5 to 10 years earlier than the earliest age of first diagnosis of ovarian cancer in the family

NOTE - The lack of efficacy of ovarian cancer screening has prompted many clinicians to recommend risk-reducing bilateral salpingo-oophorectomy at the completion of childbearing rather than intensified screening for ovarian cancer.

**Any breast cancer than does not express the genes for estrogen receptor, progesterone receptor (PR) or Her2/neu

65
Q

While establishing an intravenous line, a 26-year-old nurse sustains a needle stick injury from a patient who is known to be HBsAg positive. She is 15 weeks pregnant. Serologic tests of nurse shows both HBsAg and HBsAb are negative. Which one of the following is the most appropriate management for her?

A. Reassure her as she is HBsAg negative.
B. A full course of hepatitis B vaccine.
C. Hepatitis B immunoglobulin (HBIG).
D. A full course of hepatitis B vaccine and HBIG.
E. Repeat HBsAg and HBsAb in 3 months.

A

D. A full course of hepatitis B vaccine and HBIG.

Post-exposure prophylaxis for hepatitis B during pregnancy is the same for non-pregnant persons and follows the same general guidelines.

After exposure to hepatitis B, serology testing for the person who has had the exposure should be performed urgently. A negative HBsAg and a HBsAb titer of >10IU/mL indicates sufficient immunity against hepatitis B, and no further action is required.

With HBsAb titers < 10 (and HBsAg negative), the person has not enough immunity, and should receive both hepatitis B vaccine and HBIG within 72 hours of exposure, ideally within 24 hours. Vaccine should also be given at 1 and 6 months after the first dose (0, 1 and 6 months). Serology testing should be repeated in 3 months. If the mother is found to be HBsAg positive despite prophylaxis, the baby should receive vaccine and HBIG within 12 hours of birth.

66
Q

A pharmaceutical company receives approval from the ethical committee to start trial of a new antihypertensive drug. The ethical committee sets a target P-value of ≤0.02. At the end of the trial, the company claims that the efficacy of their new drug is superior to other available drugs in the market. The computed P-value of the trial is 0.04. What does the P value of 0.04 indicate in this trial?

A. The new drug is safer than other available drugs.
B. The new drug is as useful as other available drugs but has fewer side effects.
C. The new drug is superior to other available drugs.
D. The new drug is not superior to other available drugs.
E. The new drug is inferior to other available drugs.

A

D. The new drug is not superior to other available drugs.

A P-value is used to interpret output from a statistical test (a clinical trial here). P-value is used to control if the new results are statistically different from previous trials. A standard P-value is set in the beginning of the trial. After the study is concluded, the P-value of the study is computed and compared with the standard P-value:
If the computed P-value from the study is ≤ standard P-value then the results has statistical significance.

If the computed P-value from the study is > standard P-value then the results has not reached statistical significance.

For this study, a standard P-value of ≤0.02 has been set by the ethical committee, meaning that if the computed P-value from the study is ≤0.02 the new drug has statistical significance and can be claimed to be superior to other available drugs. With a computed P-value of >2, this new drug cannot be told to be superior to other available drugs.

At the end of the trial, this new drug has a computed P-value of 0.04 that is > 0.02. This means that the new drug has no superiority over the available drugs.

(Options A and B) P-value does not indicate adverse effects. It can only determine if a new drug has superiority over others or not.

(Option C) With a P-value> standard P-value, this drug cannot be claimed to be superior to other available drugs.

(Option E) P-value predicts if a drug can be superior or not superior to other drugs. Inferiority cannot be predicted by P-value.

67
Q

Which one the following test is a mass population screening test which has been demonstrated to reduce cancer mortality significantly?

A. Annual fecal occult blood testing in people over the age of 50 years.
B. Annual colposcopy in sexually active women.
C. Annual plasma CA125 in post menopausal women.
D. Annual colonoscopy in siblings of patients with colon cancer.
E. 2-yearly mammography in women aged 35-45 years.

A

A. Annual fecal occult blood testing in people over the age of 50 years.

There have been at least three randomized control trials conducted which show that 1- to 2-yearly fecal occult blood testing (FOBT) in the population over the age of 50 years reduces the mortality from colorectal cancer by approximately 20%.

(Option B) Colposcopy is a diagnostic, not a screening test. The appropriate screening test for cancer of the cervix in sexually active women is the Papanicolaou (Pap) smear.

(Option C) Plasma CA125 levels may be raised in asymptomatic women with ovarian cancer but there is not any current evidence to support it as a mass screening test.

(Option D) Colonoscopy for siblings of patients with colorectal cancer may reduce their mortality, but this is a ‘selective’ screening targeting a high-risk group. It is not a mass screening.

(Option E) While mammography in the 50-70 age group has been shown to reduce mortality from breast cancer by up to 30%, the benefit for women between 40-50 years is small. This benefit is even smaller in younger women

NOTE – Regular pap smear has been shown to reduce the incidence and mortality of cervical cancer by up to 80% and would be the correct answer if it was an option.

68
Q

A young female intern accidentally pricked herself with the needle while taking blood sample from an HIV positive patient. Which one of the following is the most appropriate action?

A. Give antiretroviral drugs for 4 weeks.
B. Test both the patient and doctor for HIV viral load now.
C. Do not allow the doctor to draw blood for 3 months.
D. Give her intravenous immunoglobulin.
E. Tell her that the risk of disease transmission is very low.

A

A. Give antiretroviral drugs for 4 weeks.

In the event of needle stick injury and exposure to an HIV positive person, post-exposure HIV prophylaxis is recommended. Provision of post exposure prophylaxis should not be delayed while establishing the HIV status of the source. Early initiation of post-exposure prophylaxis (PEP), as soon as possible after exposure, is strongly recommended. PEP should not be delayed more than 72 hours post-exposure. A 28-day (4-week) course of PEP is recommended.

This health care worker should have follow-up HIV antibody testing at baseline, 6 weeks, 3 months, and 6 months, along with tests for other blood-borne viruses.

Recommendations for occupational post-exposure prophylaxis include a basic regimen of two nucleoside/nucleotide reverse transcriptase inhibitors for most HIV exposures, and an expanded regimen with the addition of a third drug when the exposure poses an increased risk for transmission.

69
Q

In a randomized controlled trial (RCT) conducted to study the effect of aspirin on prevention of coronary artery events among diabetic smokers, the results in the two arms of the study are as follows: - See table below.

Which one of the following is the relative risk of not using ASA?
A. 1%.
B. 2%.
C. 100%.
D. 200%.
E. 50%

A

D. 200%.

In statistics and epidemiology, relative risk or risk ratio (RR is the ratio of the probability of an event occurring in an exposed group to the probability of the event occurring in a non-exposed, comparison group.

Of 100 diabetic smokers who are on aspirin, 1 person has developed a coronary event. So the incidence of coronary event in this group is 1% [1/(1+99)x100], while the incidence of coronary events in the group taking placebo instead of aspirin is 2% [2/(2+98)x100].

In this scenario the exposure is taking aspirin. Exposed group has a 1% chance of developing a coronary event versus 2% in those who do not take aspirin.

The RR is then calculated by dividing the odds of the condition in the exposed group (1%) by that of the non-exposed group:
RR= P(exposed) / P(non-exposed) : RR=1% / 2%=0.5

Here, the RR indicates that the odds of developing a coronary event in those diabetic smokers who are on aspirin is half compared to those on placebo. In other words, those who are on aspirin has a 50% risk reduction. Inversely, those who are not taking aspirin are twice as likely to develop a coronary event compared to those who are taking it. So the RR. This means that not taking aspirin is associated with a 200% increase in incidence of coronary events.

70
Q

Marian, 55 years old, is in your office for consultation. She is obese and has a BMI of 33, waist circumference of 125 and hip circumference of 110cm. Laboratory studies you ordered before show an LDL of 3mmol/L (normal <0.2 mmol/L) and HDL of 0.7 (normal:0.9-1.93 mmol/L). Which one of her physical or biochemical markers is the most important predictor of her health risk?

A. BMI.
B. Waist-to-hip ratio.
C. Waist circumference.
D. High LDL.
E. Low HDL.

A

B. Waist-to-hip ratio.

Waist-to-hip ratio (WHR) has been suggested as the preferred measure of obesity for predicting cardiovascular disease, with more universal application in individuals and population groups of different body builds. This parameter reflects abdominal
(central) fat which is strongly associated with ischemic heart disease, hypertension and type II diabetes mellitus. In terms of predicting obesity-related mortality, WHR is more reliable than BMI and waist circumference together. Waist circumference alone comes next and BMI alone last.

(Option A) BMI is advocated by World Health Organization (WHO) as the epidemiological measure of obesity; nevertheless, BMI is a crude index that does not take into account the distribution of body fat, resulting in variability in different individuals and populations. For example, individuals with the same BMI may have different ratios of body fat to lean mass. A muscular athlete may have the same BMI of a less muscular person. Women have more body fat than men at equal BMIs and people lose lean tissue with age so an older person will have more body fat than a younger one with same BMI.

(Option C) Waist circumference has been recommended as a simple and practical measure for identifying overweight and obese patients, but it does not take into account body size and height.

High LDL (option D) and low HDL (option E) are associated with increased cardiovascular disease risk, but these two are not strong predictors per se. For example they are not strong predictors for development of hypertension or insulin resistance.

NOTE – for each 1 cm increase in waist circumference, there is an increase of 2% in the relative risk (RR) for a cardiovascular event. For a 0.01 unit increase in waist-to-hip ratio, this relative risk is 5%

71
Q

A 36-year-old man presents to a general practice for advice about vaccination before he goes on a business trip to Cambodia. His past medical history is significant for splenectomy two years ago after he sustained a car accident and had his spleen severely injured. To which one of the following infections would he be most susceptible during this trip?

A. Dengue fever.
B. Hepatitis B.
C. Hepatitis A.
D. Malaria.
E. Traveler’s diarrhea.

A

D. Malaria.

Patients who are asplenic (no spleen) or hyposplenic (for example, decreased function of spleen due to ongoing microinfarcts caused by sickle cell disease) are at increased risk of severe septicemia with Streptococcus pneumoniae (S.pneumoniae), Hemophilus influenza type b (Hib), Neisseria meningitidis, and Capnocytophaga canimorsus (acquired by dog or cat bites). Infection with these organisms in asplenic (or hyposplenic) individuals is called overwhelming post-splenectomy infection (OPSI). Risk of OPSI is highest in the first two years of splenectomy.

S. pneumoniae accounts for approximately 50% of patients. Therefore, it is recommended that all patients receive pneumococcal 23 valent polysaccharide vaccine PPV23 (Pneumovax 23). It is recommended that the vaccine be given at least 2 weeks before elective splenectomy or, in case of emergency splenectomy, after 7 days but not later than 14 days post-splenectomy (or at discharge). A booster dose is required at 5 years. It is also recommended that such patients receive prophylactic antibiotic (e.g. amoxicillin 250mg/day) until two years after splenectomy.

Other recommended vaccines are Neisseria meningitidis, Hib, and annual influenza vaccine. The reason for recommending influenza vaccine even though it is not among OPSI, is that influenza infection can result in S. pneumoniae being superimposed.

Another important issue to consider for such patients is travel advice and prophylaxis. Although all the given options can pose a risk to the patient’s health during his visit to Cambodia, malaria is the most serious condition to take care of. People with asplenia or hyposplenia are at increased risk of severe malaria when traveling to endemic areas. He should be advised for prevention when travelling to a malaria endemic region such as Cambodia. This advice includes vector avoidance (using protective measures such as wearing long sleeved clothing, sleeping in closed and protected areas, and insect repellent), antimalarial medications, and seeking immediate medical advice if there is any symptom.

Dengue fever (option A) is endemic in Cambodia and the patient should be advised regarding it; however, health risks caused by this viral infection is almost the same as patients with intact spleen. This is true about hepatitis A (option C), hepatitis B (option B) and traveler’s diarrhea (option E).

72
Q

Daniel, 52 years old, is in your office with complaint of excessive daytime sleepiness for the past six months. He says he has never felt his night sleeps refreshing enough, and he takes every opportunity to take a nap during the day. On further questioning, he admits to snoring and that some nights his wife leaves the bedroom to sleep on the couch in the living room because his snoring does not let her sleep, and in fact, she has made him to see you for this problem. He denies smoking or any other significant medical condition. On examination, his blood pressure is 150/88 mmHg, pulse rate of 80 bpm and respiratory rate of 17 breaths per minute. He has a BMI of 37 and waist circumference of 135 cm. The rest of the examination is inconclusive. You suspect sleep apnea as the diagnosis, and arrange for him to see a sleep specialist. You advise him not to drive until a full assessment is undertaken by the specialist, including sleep studies. He becomes upset and says he cannot
stop driving as this is his job. Which one of the following would be the most appropriate next step to take in this situation?

A. Explain to him about the serious risks he could pose to himself and others if he keeps driving while he is untreated.
B. Ask him to report his condition to the relevant driver licensing authority.
C. Inform the driver licensing authority (DLA).
D. Ask him to submit his driver’s license to you now.
E. Advise weight reduction to alleviate the condition and decrease the risk of accidents.

A

A. Explain to him about the serious risks he could pose to himself and others if he keeps driving while he is untreated.

Assessment of fitness to drive is one of the most challenging situations in medical practice. On one side is the patient’s important issues such as independence, and in this case financial problems Daniel will face if he is prevented from driving as a commercial driver, and on the other side, lies health and safety of the public. A medical practitioner should be able to balance between their duty to the patient and the duty to act in public’s interest.

In case a patient is likely to pose risk to health and wellbeing of others, the following measures should be taken:

STEP 1 - most importantly, it should become clear to the patient that driving under their medical condition is dangerous both for him/her and the public. Many patients are likely to choose not to drive when the condition is explained to them in an empathetic and reasonable manner.

STEP 2 - the patient should become aware of his/her civil responsibility to self-report the medical condition to the driver licensing authorities. This discussion and the given advice should be documented in the patient’s notes.

STEP 3 - reporting to the licensing authorities if the patient:

  • is unable to understand the impact of their condition; OR
  • is unable to take notice of the health professional’s recommendations due to cognitive impairment; OR
  • continues driving despite appropriate advice and is likely to endanger the public

Daniel has the provisional diagnosis of sleep apnea (or other sleep disorders) that has resulted in daytime sleepiness. Driving while drowsy or sleepy poses a significant risk to his or others’ health. This should be explained to him as the first step in management. He should also be asked to self-report to driving licensing authorities (option B).

If you find out that Daniel keeps driving despite the advice, you can breach the confidentiality and personally inform the authorities (option C).

(Option D) asking a patient to surrender his/her driver’s license is not a task of doctors. Doctors are not in a position, legally or morally, to make such a request.

(Option E) Weight reduction will benefit Daniel not only for the sleep apnea but also in terms of general health and should be advises; however, it is a long-term management with future results and not likely to resolve his daytime sleepiness in short term.

73
Q

Peter, 33 years of age, is concerned about colon cancer because his father had it at the age of 49 and his elder brother at the age of 46 years. He denies any symptoms such as rectal bleeding, altered bowel habits or those related to anemia. Which one of the following would be the most appropriate advice for him regarding colon cancer screening?

A. Screening with FOBT 2-yearly from the age of 50 years.
B. Screening with FOBT 2-yearly from the age 40 years.
C. Screening with yearly FOBT starting from now.
D. Screening with colonoscopy 5-yearly from the age of 50 years.
E. Screening with colonoscopy 5-yearly starting from now.

A

B. Screening with FOBT 2-yearly from the age 40 years.

Recommendations for colorectal cancer screening is based on individual risk. The risk categories, criteria, and recommended screening program for colorectal cancer currently in use in Australia (recently updated) is outlined in the following table: - See table below.

Peter has two first-degree relatives diagnosed with colorectal cancer. With this in history, he falls in category 2, and requires FOBT testing 2-yearly from the age of 45 years until 49, and colonoscopy every 5 year from the age of 50 years.

74
Q

Ted, 63 years old, is a regular smoker patient of your clinic. Last year, he was diagnosed with chronic obstructive pulmonary disease (COPD) and was advised to give up smoking. On every visit, you have briefly advised him about smoking cessation as the best step thing he can do for his COPD and his health in general, but he did not seem interested. Today he says he has decided to quit and asks for help. He confides in you that he has tried three times before but to no avail because every time he tried to quit, he had severe craving and agitation, so he had to smoke again. He is frustrated and believes there is no way for him to get rid of it. After consulting him regarding his good decision and that there are ways you can help him, you decide to start him on nicotine replacement therapy. Which one of the following is the most important factor in the history supporting such decision?

A. His failed previous attempts.
B. Withdrawal symptoms.
C. His COPD.
D. His frustration with his failed attempts.
E. Nicotine replacement therapy is recommended for all patients attempting to quit smoking.

A

B. Withdrawal symptoms.

The five important steps in consulting every patient with drug, alcohol or smoking problems are known as the 5 ‘A’s (ask, assess, advice, assist and arrange).

One important part is assessing the degree of dependence to that drug. For smokers trying to quit, assessment of dependence is a key step in management because it determines whether pharmacotherapy (nicotine, bupropion, or varenicline [Champix®]) or a combination of these is required assist the patient in quitting smoking.

While patients who are not nicotine dependent are managed non-pharmacologically by counselling, cognitive and behavioral coping strategies, written information (e.g. Quit Pack), those with dependence need pharmacotherapy to increase the chances of successful quit attempt.

In assessment of dependence, the following questions should be asked:

  • How many minutes after waking do you smoke your first cigarette?
  • How many cigarettes do you smoke a day?
  • Have you had cravings or withdrawal symptoms in previous quit attempts?

The following strongly indicate nicotine dependence and the need for pharmacotherapy:

  • Smoking within 30 minutes of waking.
  • Smoking more than 10 cigarettes a day.
  • Craving or withdrawal symptoms in previous attempt.

Based on the above, Ted requires pharmacotherapy because he has had craving and agitation (a symptom of nicotine withdrawal) in previous attempts, indicating nicotine dependence. Other options are bupropion or varenicline that could be added to nicotine based on his condition and preferences.

(Option A) failed previous attempts alone do not justify use of pharmacotherapy for Ted. Such failure may have been caused by social and psychological factors, and not necessarily nicotine dependence. Unless there is nicotine dependence, one can still make another attempt to quit without pharmacotherapy.

A medical condition (COPD) (option C) does not justify the use of pharmacological therapy for a patient if there is no nicotine dependence, neither does frustration with previous failed attempts (option D) unless withdrawal symptoms have caused such failure.

(Option E) Nicotine replacement therapy is only indicated for patients with nicotine dependence. Not all smokers are nicotine dependent.

75
Q

Patricia is a 28-year-old sex worker, working in a licensed brothel. She is in your office for sexual health assessment and receiving a sexual health certificate. In consulting her, which one of the following is the correct advice?

A. She needs to perform vaginal and anal swabs every 12 months.
B. She should be screened for chlamydia and gonorrhea using a mid-stream urine every 3 months.
C. She should be screened for hepatitis C infection every 12 months.
D. She should be screened for chlamydia and gonorrhea using high vaginal swabs every 3 months.
E. She should be screened for syphilis every 12 months.

A

D. She should be screened for chlamydia and gonorrhea using high vaginal swabs every 3 months.

This question asks about requirements by law in order to renew a license for sex work practice. Requirements for such issue is different from current guidelines by the RACGP and STI guidelines in Australia. Based on clinical guidelines, it is recommended that high risk individuals for STIs (such as sex workers) undergo screening every 12 months; however, these guidelines advise that state legislations should be followed regarding the intervals of such tests for legal matters such as issuance or renewal of a sexual health certificate for sex workers. Based on current legislations in Australia, sex workers require to be screened for STIs quarterly (every 3 months) to have their licenses renewed.

Legislations for STI screening are in accordance with the Public Health and Wellbeing Act 2008. Based on this act, sex workers are required to undergo the following tests and measures every 3 months:
Blood tests:

  • Syphilis Antibody
  • HIV Antigen/Antibody
  • Hepatitis B core antibody and surface antibody (HBcAb and HBsAb)
  • Hepatitis A antibody (where appropriate)

Swabs (Women):

  • Chlamydia (High Vaginal Swab)
  • Gonorrhea (High Vaginal Swab)
  • Trichomoniasis (High Vaginal Swab) (only at first presentation or if the woman is a contact of infection)
  • Cervical Screening when required as per policy
  • Gonorrhea (pharyngeal)
  • Chlamydia (pharyngeal)

Genital Examination (Women):

  • Vulval examination is performed at each visit to exclude visible lesions of genital wart or genital herpes
  • A speculum examination is not routinely performed on asymptomatic women unless they require a cervical screening
  • A speculum examination should be considered if the woman is symptomatic, has experienced a condom break/slip, or they have a retained sponge/tampon/condom.

Gonorrhea and chlamydia testing for Male Sex Workers:

  • As per the policy - Screening of Asymptomatic Men for Sexually Transmitted Infections by Sexual Health Nurses.
  • Men must also undergo a genital examination to exclude visible lesions of genital warts and genital herpes.

Provision of vaccinations:
vaccinations should be advised, when appropriate against:

  • Hepatitis B
  • Hepatitis A

Based on current legislation, the only correct option would be high vaginal swabs for chlamydia and gonorrhea testing using Nucleic acid amplification test (NAAT) every 3 months.

(Option A) Vaginal swabs should be performed every 3 months for renewal of sex work certificate. Anal swabs are required only if there has been anal sex.

(Option B) If instead of high vaginal swabs, a urine sample is considered, the specimen used should be a first catch urine, not midstream urine.

(Option C) Screening for hepatitis C is not routinely required unless there is a high risk for such infection, e.g., injection drug users.

(Option E) Although testing for syphilis is required in sex workers, the interval proposed by law is 3 months, not 12 months.

TOPIC REVIEW

76
Q

John is 72 years old and a regular patient of yours in your GP clinic. He has depression and has been treated for that a few times. He also smokes 15-20 cigarettes a day and drinks alcohol in moderation. He is in the clinic today and wants to quit smoking. Which one of the following would be the most important option to consider for him to assist his quitting?

A. Cognitive behavioral therapy (CBT).
B. Nicotine replacement therapy (NRT).
C. Varenicline (Champix®).
D. Bupropion.
E. Coping skills and lifestyle counselling.

A

B. Nicotine replacement therapy (NRT).

There is a strong association between smoking and depression. Patients with current or past history of depression are approximately twice as likely to be current smokers and smoke more cigarettes per day than those who are not depressed.

Quitting is a health priority for smokers with depression because they are at higher risks of smoking related diseases than the general population of smokers.

Compared to the general population of smokers, the chances for successful quitting are lower and relapse rates are higher in depressed smokers. Depressed smokers are more nicotine dependent and usually experience more severe withdrawal symptoms.

First-line pharmacological treatments for quitting smoking are NRT, bupropion, and varenicline. All these treatments can be used for depressed smokers as well with about the same efficacy. Varenicline (option C) is more effective than bupropion (option D) for quitting, but the additional antidepressant action of bupropion may be beneficial in some cases. However, NRT would be the mainstay of treatment for John because of its safety profile and the fact that depressed smokers are more nicotine dependent. On the other hand, nicotine has some antidepressant effects as well. Varenicline or bupropion, if given along with NRT can provide additional benefits. The combination of a nicotine patch with a quick acting form of nicotine such as gum or lozenge and precessation use of nicotine patches are likely to increase success rates further.

CBT (option A) is a good option to address the depression and has been shown to be of a small positive effect on quitting. The effect is greater for patients with recurrent episode of depression. CBT can be considered along with NRT for John but is not the most important arm of treatment for him.

Coping skills and lifestyle counselling (e.g. exercise, diet, sleep, pleasurable activities) (option E) as well as other psychological strategies such as problem solving, stress management, mindfulness, distraction have been applied and tested for their efficacy but with mixed results and uncertain efficacy. Such measures can be recommended for their overall benefits but not for a definite result for smoking cessation.

77
Q

A 25-year-old woman presents with a history of greenish-yellow vaginal discharge. Testing for sexually transmissible infections (STIs) is positive for chlamydia infection. The woman has had multiple sex partners in the past six months. Which one of the following would be the most appropriate advice for her in terms of priority?

A. Trace all her sexual contacts in the past six months and treat them.
B. Ask her to bring her most recent sexual contacts for testing and treatment.
C. Ask her to practice safe sex.
D. Advise that she should not use intrauterine contraception devices until there is no infection.
E. Tell that she should report her infection to the relevant health authorities.

A

A. Trace all her sexual contacts in the past six months and treat them.

Chlamydia infection is a communicable disease and contact tracing is mandatory. For Chlamydia infection, it is recommended that sexual contacts of the index case in the past six months be traced and treated if infected.

Initiation of contact tracing is the responsibility of the diagnosing physician. Contact tracing starts with a conversation with the patient about informing their partners. The patient can decide to inform their own contacts (patient referral) or organize for someone else to inform them (provider referral). Patient referral is the most common type of contact tracing used in general practice. For this type of contact tracing to be successful, it is important that the diagnosing doctor informs the patient about who needs to be informed and what information needs to be given. If the patient decides to use provider referral, the diagnosing doctor can collect the contacts’ details and either notify the contacts directly or pass the details to a practice nurse or a sexual health clinic who can undertake this.

NOTE - Currently in Victoria, reporting Chlamydia infection is the responsibilty of the testing laboratories, not the doctor.

(Option B) This patient’s sexual contacts in the past six months must be traced. Only testing and treating her most recent contacts is inadequate and inappropriate.

(Option C) Asking the patient to practice safe sex is an essential part of consultation but not the most appropriate option here. This woman should avoid sex until the infection is treated. Her current partner(s) should also be treated to reduce the risk
of re-infection.

(Option D) Intrauterine devices are contraindicated in the presence of pelvic infection. This patient should be advised not to use intrauterine devices while she has the infection but contact tracing should take precedence in priority.

(Option E) Chlamydia infection is a notifiable disease, and notifying such diseases is the diagnosing physician’s responsibility not that of the patient.

78
Q

A 31-year-old woman, sex worker by profession, presents to your practice for a regular check up. Testing for sexually transmissible infections (STIs) shows she has gonorrhea infection. In addition to treating her for gonorrhea, which one of the following would be the next best action?

A. Trace her sexual contacts in the past 12 months and treat them.
B. Trace her sexual contacts in the past 6 months and treat them.
C. Ask her to avoid sex.
D. Inform the Health Department.
E. Tell that she should tell her clients to use male condoms.

A

D. Inform the Health Department.

Gonorrhea infection is a notifiable disease and confirmed cases should be reported to the relevant health authorities (health department). A confirmed case requires laboratory definitive evidence only. Confirmation may be through isolation of Neisseria gonorrhea, or detection of Neisseria gonorrhoeae by nucleic acid testing, or detection of typical Gram-negative intracellular diplococci in a smear from a genital tract specimen.

This woman has confirmed gonorrhea infection and informing the health department is the most appropriate of the options.

(Options A and B) Contact tracing of this woman’s sexual contacts in the past two months is another important step. The patient can decide to inform their own contacts (patient referral) or organize for someone else to inform them (provider referral). Often, a sex worker is reluctant to disclose the name of his/her clients and provider referral is the method of choice to consider. However, tracing her contacts for the past 6 or 12 months is unnecessary and inappropriate.

(Option C) Sex workers should not practice sex until their current STI is adequately treated. In case of HIV infection, they cannot work as a sex worker anymore. Gonorrhea is a curable disease. She should avoid sex as long as she is infected and undergoing treatment but asking to avoid sex forever is not appropriate.

(Option E) Advising male condoms is important but not a priority because protected sex is almost practiced universally in sex industry. Re-emphasizing is a good idea; however, as long as this woman is under treatment for her current infection and within exclusion period, no sex of any kind must be practiced because although male condoms reduce the risk of infection transmission to or re-infection from male partners, it does not eliminate the risk.

79
Q

A nurse at your clinic sustains a needle stick injury at workplace. She was previously vaccinated for hepatitis B. Her anti HBs antibody is measured and is below 10 mIU/ml. The patient is known to be HBsAg positive. Which one of the following is the most appropriate next step?

A. Hepatitis B vaccine.
B. Hepatitis B vaccine and immunoglobulin.
C. Hepatitis B serology.
D. Reassure and follow up.
E. No prophylaxis is needed.

A

B. Hepatitis B vaccine and immunoglobulin.

Post-exposure prophylaxis for hepatitis B (hepatitis B vaccine and immunoglobulin) is recommended in the following situations:

  • The exposed person has been vaccinated in the past and post-vaccination anti-HBs level is below 10mIU/ml
  • Unvaccinated exposed individuals
  • Unknown vaccination status of the exposed person

In previously vaccinated individuals, who have been exposed to either an HBsAg-positive source or a source whose hepatitis B status cannot be determined, post-exposure prophylaxis is not necessary if there is a documented protective response (anti-HBs level ≥10 mIU/mL) at any time after vaccination.

80
Q

Steven is a 67-year-old patient of yours, who has presented a year and a half ago for a health review before renewal of his driver’s license. Your examination revealed 6/24 vision for his both eyes; therefore, you advised that he should not drive anymore and encouraged him to self-report to licensing authorities and is referred for assessment by an ophthalmologist. Today, he has presented again and asks if you could change your mind and give him a letter than he can drive. You examine him again and realize he still has poor eye sight and is unfit to drive. When you tell him so, he becomes irritated and says that last year he saw another doctor who give him a letter and he has been driving since then, and why you cannot just go on and give him a similar letter as well. Which one of the following is the most appropriate action now that you are aware of him driving despite his unfitness to drive?

A. Call the police.
B. Call the doctor who issued the letter and ask him why he has done so.
C. Report the patient to the relevant Road and Traffic department.
D. Ask him to drive only if there is someone else in the car to supervise him.
E. It is not your duty to report him to anyone. Just tell him again that he is unfit to drive and has to submit his license to authorities.

A

E. It is not your duty to report him to anyone. Just tell him again that he is unfit to drive and has to submit his license to authorities.

According to Australian Road Safety (Austroads), a person is not fit to hold a driver licence if:

  • The corrected visual acuity (with glasses or contact lenses) is less than 6/12 for the better eye for private vehicle drivers.
  • The corrected visual acuity is less than 6/18 for the worse eye and less than 6/9 for the better eye.

This patient has a visual acuity of 6/24 both eyes which is less than the minimum standard; so, he is not fit to drive for now and should be referred to ophthalmologist or optometrist for clinical assessment with regards to the driving task.

Assessment of fitness to drive is one of the most challenging situations in medical practice. On one side is the patient’s important issues such as independence, and probably financial issues especially for commercial vehicles drivers, and on the other side is the health and safety of the public. A medical practitioner should be able to balance between their duty to the patient and the duty to act in public’s interest.

When a patient is likely to pose risk to health and wellbeing of others, it should become clear to the patient that driving under their medical condition is dangerous both for him/her and the public.

Many patients are likely to choose not to drive when the condition is explained to them in an empathetic and reasonable manner. The patient should also become aware of his/her civil responsibility to self-report the medical condition to the driver licensing authorities. This discussion and the given advice should be documented in the patient’s notes.

However, it is important to note that the relationship between a patient and the treating doctor is confidential; therefore, doctors will not normally communicate directly with the Driver Licensing Authority and will provide the patient with advice about the ability to drive safely as well as a letter or report to take to the authority. It is NOT the doctor’s duty to report the patient to the police (option A) or driving licensing authority (option C) directly. What they must do though is refusing to sign the ‘fitness to drive’ form and encourage the patient to self-report himself.

In terms of the duty to the public, if a doctor believes that patient is not heeding advice to cease driving, he/she may report directly to the Driver Licensing Authority; however, except in South Australia (SA) and Northern Territory (NT) this reporting is not mandatory.

In this case, Steven should be clearly made aware of all the risks involved, his responsibility to self-report and not driving. If you form a belief that he will not follow the instructions and is likely to place the public at risk, you may choose to report or must report to authorities depending on the state you are practicing in.

(Option C) It is not a doctor’s responsibility to investigate other doctors as to their decision and actions. Calling the doctor who allegedly has given the patient a certificate of fitness to drive is beyond a doctor’s limits of practice.

(Option D) The presence of a supervisor does not make an unfit person fit to drive

81
Q

Which one of the following is correct regarding chronic use of marijuana?

A. It is associated with decreased incidence of COPD.
B. It masks psychosis.
C. It reduces anxiety.
D. It impairs the ability to drive.
E. It is associated with improved job performance.

A

D. It impairs the ability to drive.

Marijuana is the second most commonly smoked substance worldwide after tobacco. The constituents of marijuana smoke are qualitatively and, to a large extent, quantitatively similar to those of tobacco smoke, with the exceptions of 9-tetrahydrocannabinol (THC), found only in marijuana, and nicotine, found only in tobacco.

Given these similarities, there is concern that the health risks of regular marijuana smoking may be similar to those of habitual tobacco smoking. Chronic obstructive pulmonary disease (COPD), which is associated with high morbidity and mortality, is among those risks. Firm conclusions cannot be drawn about the association between use of marijuana and COPD based on the limited and inconsistent data available. The conducted studies are limited by their small numbers of participants and by the uncertain accuracy of self-reported use of marijuana, particularly in view of its illegality and the difficulty of accurately recalling amounts previously used. Some of these studies are also limited by their cross-sectional design, and most are limited by the young age (40 years or younger) of participants.

Nevertheless, the consistency of some aspects of the available data allows us to more firmly conclude that smoking marijuana by itself can lead to respiratory symptoms because of injurious effects of the smoke on larger airways. Given the consistently reported absence of an association between use of marijuana and abnormal diffusing capacity, and signs of macroscopic emphysema, it can be close to concluding that smoking marijuana by itself does not lead to COPD.

Cannabis use is likely to increase the risk of developing schizophrenia and other psychoses; the higher the use, the greater the risk.

Cannabis use does not mask the psychosis (option B); rather results in it or worsens it. However, in individuals with schizophrenia and other psychoses, a history of cannabis use may be linked to better performance on learning and memory tasks.

Cannabis use does not appear to increase the likelihood of developing depression, anxiety, and posttraumatic stress disorder in general; however, evidence suggest that regular cannabis use is likely to increase the risk for developing social anxiety disorder.

In patients diagnosed with bipolar disorders, near daily cannabis use may be linked to greater symptoms of bipolar disorder than for nonusers. Moreover, heavy cannabis users are more likely to report thoughts of suicide than are nonusers.

Although there has been no strong link between regular cannabis use and increased incidence of anxiety disorders in general, it has not shown to reduce anxiety (option C) either.

Because cannabis use acutely impairs cognitive processes, there is a concern that chronic cannabis use may cause chronic cognitive impairment. Such a chronic effect is not necessarily permanent but it can persist even after the elimination of cannabinoids from the body, and therefore would be the result of secondary changes induced by cumulative exposure to cannabinoids. Such chronic effects could produce relatively enduring behavioural deficits which presumably reflect changes in
brain function. Given these, cannabis is could potentially decrease the work performance and is not associated with increased work performance (option E).

Marijuana significantly impairs judgment, motor coordination, and reaction time, and studies have found a direct relationship between blood THC concentration and impaired driving ability.

82
Q

As a general practitioner, you are trying to follow the current Australian guidelines to reduce the incidence of HIV infection in your community by administration of Pre-exposure prophylaxis (PrEP) to those who are at risk. Which one of the following is in need for PrEP?

A. Commercial sex workers.
B. Intravenous drug users.
C. Men who have sex with men.
D. Female partner of an HIV-positive man with undetectable viral load.
E. HIV-positive male partner of a female.

A

C. Men who have sex with men.

PrEP is used to significantly reduce the risk of HIV transmission in the community using antiretroviral drugs, usually tenofovir/ emtricitabine, in people who are HIV negative but at a significantly increased risk of HIV infection.

One important point to consider is that PrEP is used in those who are currently HIV negative as means of prophylaxis; therefore, those who are already HIV positive do not require PrEP and should be referred for HIV prescription.

The following groups are considered to be at “high risk” if they had these risks in the previous 3 months, or if they foresee these risks in the upcoming 3 months. For such patients, PrEP is recommended: - See table below.

Of the options, only men who have sex with men (MSM) are high-risk for HIV Infection and require PrEP.

(Option A) Commercial sex worker are usually on routine STI follow-up programs and do not require PrEP merely for their carrier. However, once they have any of the high-risk conditions as outlined in the above table, they will require PrEP.

(Option B) Unless the intravenous drug user is not sharing needles with an HIV-positive individual or with MSM of unknown HIV status, PrEP is not indicated.

(Option D) As long as a man has undetectable viral load and take precautionary measures such as use of male condoms, PrEP for his female partner is not indicated as the risk of transmission is extremely low.

(Option E) Prophylaxis aims to prevent the infection. Once a person is HIV infected, prophylaxis has no point, and treatment with antiretroviral regimens should be started

83
Q

A 47-year-old man presents for cholesterol check. On examination, he has a blood pressure of 140/90 mmHg. His laboratory studies show a cholesterol level of 6 mmol/L and fasting blood sugar of 5.4 mmol/L. He smokes 20 cigarettes per day and drinks alcohol on weekends and social occasions. Which one of the following would be the most appropriate management of this patient?

A. Advise that he should start smoking cessation program.
B. Order an oral glucose tolerance test (OGTT).
C. Start him on antihypertensive medications.
D. Start him on statins.
E. Start him on aspirin.

A

A. Advise that he should start smoking cessation program.

The remarkable findings in this scenario are an upper limit normal for blood pressure both systolic and diastolic (SBP>140mmHg, DBP>90 mmHg), smoking history, and a cholesterol level of 6 mmol/L (normal < 5.5 mmol/L) are significant risk factors for cardiovascular diseases.

Of the given options, advice that she should start smoking cessation program is the most appropriate one. Smoking is associated with significantly increased risk of cardiovascular disease such as myocardial infarction, stroke, and limb ischemia, as well as other harms to health such as increased risk of various malignancies just to name one. Every smoker should be briefly consulted about benefits of quitting at each visit.

This patient has a normal blood glucose and does not any specific interventions for now except; however, based on current Australian guidelines, he should have his blood glucose monitored every 3 years using fasting blood sugar (FBS) or HbA1C.

OGTT (option B) is not required now or used as test to monitor this patient for diabetes in the future. He also has slightly elevated cholesterol level for which regular exercise and a healthy diet for 6 months should be advised before decision as to commencement of anti-lipid therapy using statins is made. Therefore, starting him in statins (option D) is not appropriate for now.

This patient has systolic and diastolic blood pressures right at the upper limit of normal blood pressure. He can be consider pre-hypertensive and advised for life style modification such as regular exercise, healthy diet (including low salt intake), weight reduction (if overweight or obese), and smoking cessation. At this stage he does not need to be started on hypertensive medications (option C). Generally, pharmacotherapy for hypertension is not considered as long as the blood pressure is
less than 160 mmHg (systolic) or 10 mmHg (diastolic).

In general, aspirin (option E) is not recommended for primary prevention of cardiovascular diseases in patients with low and moderate cardiovascular risk based on absolute CVD risk assessment (see the topic review).

TOPIC REVIEW
Absolute CVD risk assessment

In non-aboriginal patients over the age of 45 without cardiovascular disease and aboriginal and Torres Strait Islander patients over the age of 35 without cardiovascular absolute cardiovascular disease (CVD) assessment should be performed.

Absolute CVD risk assessment combines risk factors to calculate the probability of development of cardiovascular event or vascular event within a specified time frame (usually 5 years). Based on calculations, patients fall into either low-risk, medium risk, or high-risk for CVD.

Absolute CVD risk assessment should be conducted at least every two years. This calculation requires information on the patient’s age, sex, smoking status, total and high-density lipoprotein-cholesterol (HDL–C), systolic blood pressure (SBP), and whether the patient is known to have diabetes or left ventricular hypertrophy (LVH). In adults at low absolute CVD risk, blood test results within 5 years may be used for review of absolute CVD risk unless there are reasons to the contrary.

Adults >74 years of age may have their absolute CVD risk assessed with age entered as 74 years. This is likely to underestimate five-year risk but will give an estimate of minimum risk. Patients with a family history of premature CVD (in a first-degree relative – men aged < 55 years, women aged < 65 years) or obesity (body mass index [BMI] above 30 kg/m2 or more) may be at greater risk. Similarly, patients with depression and atrial fibrillation (AF) may also be at increased risk.

Adults with any of the following DO NOT require absolute CVD risk assessment using the absolute risk calculator, because they are already known to be at clinically determined high risk of CVD:

  • Diabetes and >60 years of age
  • Diabetes with microalbuminuria (>20 μg/min or urine albumin-to-creatinine ratio (UACR) >2.5 mg/mmol for males, >3.5 mg/mmol for females)
  • Moderate or severe chronic kidney disease (CKD; persistent proteinuria or estimated glomerular filtration rate [eGFR] < 45 mL/min/1.73 m2)
  • Previous diagnosis of familial hypercholesterolemia (FH)
  • Systolic blood pressure (SBP) ≥180 mmHg or diastolic blood pressure (DBP) ≥110 mmHg
  • Serum total cholesterol >7.5 mmol/L
  • Aboriginal or Torres Strait Islander peoples aged >74 years (Practice Point)

According to the RACGP guideline, aspirin is not recommended for low-risk and moderate-risk patients. Also blood pressure lowering and/or lipid-lowering agents should be considered in addition to lifestyle advice if 3-6 months of lifestyle intervention does not reduce the risk or:

  • Blood pressure is persistently ≥160/100 mmHg
  • There is a family history of premature CVD
  • Specific population where the absolute CVD risk assessment underestimates the risk such as in Aboriginal and Torres Strait Islander, South Asian, Maori, Pacific Islander and Middle Eastern peoples

Lifestyle modification includes:

  • Smoking cessation (if smoker)
  • Following a diet rich in vegetables and fruit, low in salt and saturated and trans fats
  • At least 30 minutes of physical activity on most or preferably every day of the week
  • Limit alcohol intake
84
Q

A mother has brought her 7-year-old son for evaluation because her husband has been recently diagnosed with familial hypercholesterolemia and low-density lipoprotein receptor (LDLR) gene mutation after evaluation for established diagnosis of acute coronary syndrome. She insists that her son undergo genetic testing for the condition. Which one of the following will be the most appropriate next step in management?

A. Refer the son for LDLR gene mutation testing.
B. Pre-test counselling.
C. Send the whole family for LDLR gene mutation testing.
D. Refer the son to a specialist dietitian.
E. Refer the mother for LDLR gene mutation testing.

A

B. Pre-test counselling.

Familial hypercholesterolaemia (FH) is a dominantly inherited condition due to a genetic defect in one of several genes that affect receptor-mediated uptake of low-density lipoprotein (LDL). Affected individuals have metabolic and clinical features
including impaired uptake of plasma LDL cholesterol, resulting in high cholesterol levels and increased risk of premature cardiovascular disease. Untreated, men have a 50% chance of coronary heart disease (CHD) before the age of 50 years and women a 30% risk by the age of 60 years. Atherosclerosis caused by FH starts in childhood and adolescence, highlighting the need to identify cases early and commencement of preventive measures.

Offspring of FH patients will inherit either the normal gene or the defective gene; therefore, they have a 50% chance of being affected. This leads to quite a high prevalence in the general population. Estimates range between 1:200 and 1:500, but some groups exhibit a “founder gene effect” that enriches the prevalence of the disorder. It is more common in Mediterranean countries, Christian Lebanese, French Canadians and Afrikaaner South Africans. In these populations the prevalence may exceed 1:100. The prevalence of homozygous FH is around 1:1 million in the general population.

Index cases of FH present with one or more of the following features:

  • Severe hypercholesterolaemia that is not explained by secondary causes - relative hypercholesterolaemia is present from birth, but levels rise with age
  • A strong personal or family history of premature atherosclerotic cardiovascular disease
  • Tendon Xanthomas

Although the clinical picture of FH will be clear-cut in many cases, the diagnostic criteria suggest that genetic testing can provide certainty of diagnosis in some cases where confounding factors such as borderline cholesterol levels, inconclusive family histories or tendon injuries have resulted in a diagnostic dilemma. The major value in making a molecular diagnosis is its use in predictive testing of other family members for FH. This is useful in early detection of cases that need intervention
to prevent CVD and in re-assuring family members who may not have the condition. Individuals in whom predictive genetic tests are required should be offered pre-test genetic counselling prior to consenting to sample collection for genetic analysis
because the genetic testing is expensive and time consuming
, and sometimes no mutation can be detected with current methods. These facts should be shared with the patients in full details and informed consent is obtained before proceeding to genetic testing.

Since the father is an established case of, there is a 50% chance that the son has the condition as well. The best option after pre-test counselling and informed consent would be referring the son for genetic testing.

85
Q

You, as a GP, are assigned to give a lecture in a girls’ high school. At school, you are told that girls you will be talking to today are 13 years old, and that sex education topic has already been covered by another doctor. Which one of the following topics is the most important one you would consider to cover at this session?

A. Sunscreening.
B. Regular cancer screening.
C. Bullying.
D. Cervical screening.
E. Alcohol

A

A. Sunscreening.

According to the RACGP guidelines for age-related health checks in children and young people, promotion of sunscreen use to prevent screen damage and skin cancers in future is the only option that should be covered for this age group.

The following are the assessment and preventive measures recommended by the RACGP for children aged 6-13 years
Assessment:

  • Measure growth and BMI routinely
  • Promote oral health
  • Promote healthy eating and drinking
  • ‘Lift the lip’ dental check. Encourage regular dental reviews
  • Promote healthy physical exercise and reduction of sedentary behaviour
  • Enquire about progress at school as an index of wellbeing
  • When behaviour is a concern, explore possible contributing factors within the family and the wider social environment

Preventive counselling and advice:

  • Injury prevention
  • Promote social and emotional wellbeing
  • Promote sun protection

(Options B and D) Regular cancer screening programs currently in place in Australia are colorectal cancer screening starting at 50 years, breast cancer screening at starting at 50 years, and cervical cancer screening starting at 25 years. No cancer screening topic is recommended to be covered for children 6-19 years.

(Option C) Assessment of progress at school as part of wellbeing is part of preventive programme for children aged 6-19 years; however, bullying by itself is not one of the quoted factors that has to be questioned and covered.

(Option E) Alcohol is covered for children aged 14-19 years under the topic ‘healthy eating and drinking’ as is asking about smoking and provision of a strong anti-smoking message.

86
Q

Tom, 18 months of age is brought to your general practice for vaccination. Today, he has a runny nose and fever of 38.1°C but otherwise is doing well and healthy. He had an episode of febrile seizure 7 months ago when he had an upper respiratory tract infection. Which one of the following vaccine is best to not be given to him today?

A. Pneumococcal vaccine.
B. Polio vaccine.
C. DTPa vaccine.
D. MMR vaccine.
E. Influenza vaccine.

A

D. MMR vaccine.

Infants and young children are most at risk for febrile seizures. Up to 5% of young children will have a febrile seizure at some time in their life. Febrile seizures happen in children between the ages of 6 months and 5 years, with a peak prevalence between 14 and 18 months of age. About one third of children with one episode of febrile seizure will have at least one more later during childhood.

Fevers can be caused by common childhood illnesses like colds, ear infection, roseola, or any other febrile conditions. Although most vaccines can cause a mild fever as an adverse effect, febrile seizures are uncommon after vaccination. However, caution should be exercised about MMR (measles, mumps, and rubella) and MMRV (measles, mumps, rubella, and varicella) vaccines because studies suggest a small increased risk of febrile seizures during the 5 to 12 days after the vaccine.

Studies have not shown an increased risk for febrile seizures after the separate varicella (chickenpox) vaccine.

For this child with a current mild fever (38.1°C) and history of febrile seizures, it is best to postpone the MMR vaccine to a later date when he is out of his current illness and there is least chance of febrile seizure following vaccination.

NOTE – while children with mild illnesses and fever less than 38.5°C can be safely vaccinated, it is still best to avoid the MMR vaccine as precautionary measure in this child. Children with fevers of 38.5°C or higher should receive their vaccines when they have improved.

One specific formulation of trivalent influenza vaccine (TIV) had a link with febrile seizures in the past, especially if co-administered with pneumococcal vaccine, but current TIV formulations (option E) do not cause febrile seizures, nor does the pneumococcal vaccine (option A).

Currently, there is no evidence to link Polio vaccine (option B) or DTPa vaccine (option C) to febrile seizures.

NOTE - febrile convulsion following vaccination is not a contraindication to vaccination.

87
Q

A 35-year-old Caucasian lady comes to your GP practice for a follow-up. She initially had a BMI of 32 kg/m2 and was referred to a dietician for nutritional advice. She otherwise has no comorbid but has a strong family history of type 2 diabetes mellitus. She has come to you 6 months later feeling discontented with her weight loss of 1.5kg. She tells you that she is motivated to continue her weight loss but would like further advice for better results. What is the most appropriate next step in
management?

A. Semaglutide.
B. Orlistat.
C. Bariatric surgery.
D. Psychotherapy.
E. Reduce meals to 2x a day with no snacks in between.

A

E. Reduce meals to 2x a day with no snacks in between.

Supervised lifestyle interventions are the essential component of all weight loss strategies and are the first line of management for individuals with a BMI of 30-40kg/m2. Options for initial weight loss strategies include a reduced energy diet (RED) or low energy diet (LED). When these options have failed, a very low-energy diet (VLED) is recommended as the next step. (E is correct)

VLEDs are often recommended for 12 weeks. However, VLEDs can be continued for 6-12 months under careful supervision. Individuals may follow a partial or a complete VLED regimen. The partial regimen is the most common program recommended and is based on 2-meal replacements per day (typically breakfast and lunch) and 1 serving of lean protein, usually for dinner, with vegetables. Milk (other than small quantities in tea or coffee) should be avoided. The complete VLED
regimen is based on 3 meal replacements per day, plus vegetables. The choice of the program (partial vs. complete) depends on the target weight and the individual’s ability to tolerate the VLED. Baseline blood tests should be taken and reviewed every 4 to 6 weeks.

Contraindications to VLED:

  • Pregnancy or lactation
  • Severe psychological disturbance (e.g., unstable anxiety disorders, major depression), alcoholism or drug dependence
  • Recent myocardial infarction, cerebrovascular event, or unstable angina
  • Porphyria
  • Age >65 years (VLED in this age group should be advised with caution)

Caution in the following groups:

  1. Diabetes on insulin or sulphonylureas
  • The dose of sulphonylureas or insulin should be reduced by 50% on the commencement of the VLED. It should be stressed that if hypoglycemia occurs, it takes precedence over the diet and must be treated with
    appropriate carbohydrate ingestion.
  1. Chronic kidney disease
  • Individuals with an estimated glomerular filtration rate (eGFR)< 60 mL/min/1.73m2 need closer supervision and should have electrolytes assessed more frequently.
  1. Taking Warfarin
  • The diet increases vegetable intake and may alter the international normalized ratio (INR). Individuals on Warfarin should be instructed to test INR one week after commencing the VLED to adjust the warfarin dose.

Individuals are considered to be responding to the VLED if they lose on average 1.0 to 1.5 kg per week. Once the target weight is reached, individuals are weaned off the VLED, and food is progressively re-introduced over a period of 8 weeks.

If no weight is lost or less than 1.0 kg is lost per week over 4 weeks, review the person’s adherence to the VLED or other factors that may be affecting weight loss. Otherwise, pharmacotherapy is the next step.

Semaglutide (option A), a glucagon-like peptide-1 (GLP-1) receptor agonist, was recently approved for the treatment of obesity and type 2 diabetes mellitus. It is given as a weekly subcutaneous injection. However, VLED would still be the most appropriate next step.

Orlistat (option B) inhibits pancreatic and gastric lipase, and in the long-term results in the deficiency of the fat-soluble vitamins A, D, E, and K, and the development of oxalate kidney stones. It is not recommended as a first-line option for weight loss.

Other approved medications for weight loss are phentermine (centrally acting adrenergic agonist) and liraglutide (GLP-1 receptor agonist). Off-label medication includes topiramate.

Although considered the most efficacious means of weight reduction, bariatric surgery (option C) which is an invasive procedure is reserved for those who are unresponsive to more conservative means; therefore, not the best initial option.

NOTE - Indications for bariatric surgery:

  • BMI >40 kg/m2
  • BMI >35 kg/m2 and comorbidities that may improve with weight loss
  • BMI >30 kg/m2 who have poorly controlled type 2 diabetes and are at increased cardiovascular risk

Psychotherapy (option D) would be pertinent to review the underlying factors as to why this patient failed her initial diet plan but not as a weight loss management option per se.

88
Q

A medical student sustained needle stick injury while providing an intravenous access for a patient. He is not immunized for hepatitis B. The patient’s hepatitis B status is unknown. Which one of the following is the most appropriate next step in management?

A. Immunoglobulin.
B. Immunoglobulin and hepatitis B vaccine.
C. Hepatitis B vaccine.
D. Request serology and wait for the result before commencing the vaccine.
E. Reassure and counseling regarding safe occupational practice.

A

B. Immunoglobulin and hepatitis B vaccine.

Since the exposed person is not immune to hepatitis B, he should be given a single dose of hepatitis B immunoglobulin (preferably within the first 24 hours post-exposure) and 3 doses of hepatitis B vaccine over 6 months.

The status of the source and exposed person should be followed up by requesting full hepatitis B serology. However, if the exposed person has previously been vaccinated for hepatitis B, and has a blood test documenting an adequate response to the vaccine (HBsAB≥10mIU/ml), no prophylaxis is necessary.