AKT 4 Flashcards

1
Q

What is the initial empirical therapy for meningitis in patients aged < 3 months?

A

IV cefotaxime + amoxicillin (or ampicillin)

This treatment covers common pathogens in young infants.

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2
Q

What is the recommended initial empirical therapy for meningitis in patients aged 3 months to 59 years?

A

IV ceftriaxone

Ceftriaxone is effective against many pathogens causing meningitis in this age group.

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3
Q

What is the initial empirical therapy for meningitis in patients aged ≥ 60 years?

A

IV ceftriaxone + amoxicillin (or ampicillin)

This combination targets a broader range of pathogens due to increased risk in older adults.

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4
Q

What is the treatment for meningococcal meningitis?

A

IV benzylpenicillin or IV ceftriaxone

Both antibiotics are effective against Neisseria meningitidis.

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5
Q

What is the recommended treatment for pneumococcal meningitis?

A

IV ceftriaxone

Ceftriaxone is a preferred agent for Streptococcus pneumoniae infections.

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6
Q

What is the treatment for meningitis caused by Haemophilus influenzae?

A

IV ceftriaxone

This antibiotic effectively targets Haemophilus influenzae.

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7
Q

What is the treatment for meningitis caused by Listeria?

A

IV amoxicillin (or ampicillin) + gentamicin

This combination is used to effectively treat Listeria monocytogenes infections.

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8
Q

When do most neurologists start antiepileptics?

A

Following a second epileptic seizure

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9
Q

What does NICE guidelines suggest regarding starting antiepileptics after the first seizure?

A

Start if any of the following are present:
* Neurological deficit
* Structural abnormality on brain imaging
* Unequivocal epileptic activity on EEG
* Patient or family considers risk of further seizure unacceptable

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10
Q

What is the first-line drug treatment for males with generalised tonic-clonic seizures?

A

Sodium valproate

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11
Q

What is the first-line drug treatment for females with generalised tonic-clonic seizures?

A

Lamotrigine or levetiracetam

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12
Q

What is the first-line treatment for girls under 10 years with generalised tonic-clonic seizures?

A

Sodium valproate may be offered first-line

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13
Q

What is the first-line treatment for focal seizures?

A

Lamotrigine or levetiracetam

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14
Q

What are the second-line treatments for focal seizures?

A

Carbamazepine, oxcarbazepine or zonisamide

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15
Q

What is the first-line treatment for absence seizures (Petit mal)?

A

Ethosuximide

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16
Q

What is the second-line treatment for male patients with absence seizures?

A

Sodium valproate

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17
Q

What is the second-line treatment for female patients with absence seizures?

A

Lamotrigine or levetiracetam

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18
Q

What drug may exacerbate absence seizures?

A

Carbamazepine

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19
Q

What is the first-line treatment for males with myoclonic seizures?

A

Sodium valproate

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20
Q

What is the first-line treatment for females with myoclonic seizures?

A

Levetiracetam

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21
Q

What is the first-line treatment for males with tonic or atonic seizures?

A

Sodium valproate

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22
Q

What is the first-line treatment for females with tonic or atonic seizures?

A

Lamotrigine

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23
Q

What substances may worsen seizure control in patients with epilepsy?

A

Alcohol, cocaine, amphetamines, ciprofloxacin, levofloxacin, aminophylline, theophylline, bupropion, methylphenidate, mefenamic acid

These substances can negatively impact seizure management.

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24
Q

Which medications may provoke seizures during withdrawal?

A

Benzodiazepines, baclofen, hydroxyzine

Withdrawal from these medications can lead to increased seizure activity.

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25
Q

True or False: Alcohol can improve seizure control in patients with epilepsy.

A

False

Alcohol is known to worsen seizure control.

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26
Q

Fill in the blank: _______ is a medication that may worsen seizure control in patients with epilepsy.

A

Bupropion

Bupropion is listed among drugs that can worsen seizures.

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27
Q

Name one fluoroquinolone that may worsen seizure control.

A

Ciprofloxacin or levofloxacin

Both ciprofloxacin and levofloxacin are known to negatively affect seizure control.

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28
Q

What class of drugs does methylphenidate belong to?

A

Stimulants

Methylphenidate is commonly used in the treatment of ADHD.

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29
Q

What is Infantile spasms also known as?

A

West’s syndrome

Characterized by brief spasms beginning in the first few months of life.

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30
Q

What are the key features of Infantile spasms?

A
  • Flexion of head, trunk, limbs
  • Extension of arms (Salaam attack)
  • Last 1-2 seconds
  • Repeat up to 50 times
  • Progressive mental handicap
  • EEG: hypsarrhythmia

These features indicate the severity and nature of the spasms.

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31
Q

What are potential causes of Infantile spasms?

A
  • Serious neurological abnormality (e.g. tuberous sclerosis)
  • Encephalitis
  • Birth asphyxia
  • Idiopathic

These conditions may lead to the development of Infantile spasms.

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32
Q

What are possible treatments for Infantile spasms?

A
  • Vigabatrin
  • Steroids

These treatments are used to manage the condition, but the prognosis remains poor.

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33
Q

What is the prognosis for Infantile spasms?

A

Poor prognosis

Indicates that many affected children may face severe long-term challenges.

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34
Q

Typical absence seizures are also known as what?

A

Petit mal seizures

These seizures typically occur in children.

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35
Q

What is the typical age of onset for typical absence seizures?

A

4-8 years

This is the age range when these seizures commonly begin.

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36
Q

What is the duration of typical absence seizures?

A

Few-30 seconds

These seizures have a very short duration.

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37
Q

What is the EEG finding for typical absence seizures?

A

3Hz generalized, symmetrical

This characteristic EEG pattern helps in diagnosis.

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38
Q

What is the prognosis for children with typical absence seizures?

A

90-95% become seizure free in adolescence

Indicates a favorable outcome for most children.

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39
Q

What is Lennox-Gastaut syndrome often an extension of?

A

Infantile spasms

This syndrome may evolve from earlier seizure types.

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40
Q

What is the typical age of onset for Lennox-Gastaut syndrome?

A

1-5 years

Early childhood is when this syndrome typically manifests.

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41
Q

What are the key features of Lennox-Gastaut syndrome?

A
  • Atypical absences
  • Falls
  • Jerks
  • 90% moderate-severe mental handicap
  • EEG: slow spike

These features highlight the complexity of the syndrome.

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42
Q

What treatment may help in Lennox-Gastaut syndrome?

A

Ketogenic diet

This dietary approach can be beneficial for some patients.

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43
Q

What is the most common childhood epilepsy?

A

Benign rolandic epilepsy

This type of epilepsy is particularly prevalent in children.

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44
Q

What are the features of benign rolandic epilepsy?

A
  • Paraesthesia (e.g. unilateral face)
  • Usually on waking up

These symptoms are characteristic of this type of epilepsy.

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45
Q

What is juvenile myoclonic epilepsy also known as?

A

Janz syndrome

Named after the physician who first described it.

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46
Q

What is the typical age of onset for juvenile myoclonic epilepsy?

A

Teenage years

This condition typically begins during adolescence.

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47
Q

What are the features of juvenile myoclonic epilepsy?

A
  • Infrequent generalized seizures
  • Daytime absences
  • Sudden, shock-like myoclonic seizure

These features are crucial for diagnosis and management.

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48
Q

What is the treatment response for juvenile myoclonic epilepsy?

A

Usually good response to sodium valproate

This medication is effective for many patients with this condition.

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49
Q

What are focal seizures previously termed?

A

Partial seizures

Focal seizures start in a specific area on one side of the brain.

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50
Q

What are the classifications of awareness in focal seizures?

A
  • Focal aware (previously ‘simple partial’)
  • Focal impaired awareness (previously ‘complex partial’)
  • Awareness unknown

The level of awareness can vary in focal seizures.

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51
Q

What types of features can focal seizures have?

A
  • Motor (e.g. Jacksonian march)
  • Non-motor (e.g. déjà vu, jamais vu)
  • Aura

Focal seizures can be classified based on their features.

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52
Q

What characterizes generalized seizures?

A

Engage networks on both sides of the brain at the onset

Consciousness is lost immediately during generalized seizures.

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53
Q

What is not needed in the classification of generalized seizures?

A

Level of awareness

All patients lose consciousness during generalized seizures.

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54
Q

What are the subdivisions of generalized seizures?

A
  • Motor (e.g. tonic-clonic)
  • Non-motor (e.g. absence)

Generalized seizures can be further classified into these categories.

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55
Q

What are the specific types of generalized seizures?

A
  • Tonic-clonic (grand mal)
  • Tonic
  • Clonic
  • Typical absence (petit mal)
  • Atonic

These are specific examples of generalized seizures.

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56
Q

What does ‘unknown onset’ refer to in seizure classification?

A

When the origin of the seizure is unknown

This classification is reserved for seizures without a defined starting point.

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57
Q

What are focal to bilateral seizures previously termed?

A

Secondary generalized seizures

These seizures start on one side of the brain in a specific area before spreading to both lobes.

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58
Q

What is the referral guideline for lung cancer according to the 2015 NICE guidelines?

A

Refer people using a suspected cancer pathway referral for lung cancer if they have chest x-ray findings suggesting lung cancer or are aged 40 and over with unexplained haemoptysis.

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59
Q

What is the age threshold for urgent chest x-ray referral to assess lung cancer symptoms?

A

40 years and over.

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60
Q

What symptoms warrant an urgent chest x-ray in people aged 40 and over?

A

If they have 2 or more of the following unexplained symptoms or if they have ever smoked and have 1 or more of the following symptoms:
* cough
* fatigue
* shortness of breath
* chest pain
* weight loss
* appetite loss.

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61
Q

List the symptoms that indicate a need for urgent chest x-ray in smokers aged 40 and over.

A

At least 1 of the following unexplained symptoms:
* cough
* fatigue
* shortness of breath
* chest pain
* weight loss
* appetite loss.

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62
Q

What additional factors should be considered for urgent chest x-ray in people aged 40 and over?

A

Consider an urgent chest x-ray for:
* persistent or recurrent chest infection
* finger clubbing
* supraclavicular lymphadenopathy or persistent cervical lymphadenopathy
* chest signs consistent with lung cancer
* thrombocytosis.

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63
Q

True or False: A person aged 40 and over with unexplained haemoptysis should be referred for lung cancer assessment.

A

True.

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64
Q

Fill in the blank: An urgent chest x-ray should be performed within _______ to assess for lung cancer.

A

2 weeks.

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65
Q

What does the acronym NICE stand for in the context of cancer referral guidelines?

A

National Institute for Health and Care Excellence.

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66
Q

What are the referral guidelines for suspected breast cancer published by NICE in 2015?

A

Refer people using a suspected cancer pathway referral for breast cancer if they are:
* aged 30 and over with an unexplained breast lump with or without pain
* aged 50 and over with nipple discharge, retraction, or other changes of concern

The guidelines emphasize the urgency based on age and symptoms.

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67
Q

What age and symptom criteria warrant an urgent referral for breast cancer?

A

People aged 30 and over with an unexplained breast lump or aged 50 and over with nipple changes.

Symptoms include discharge, retraction, or other concerning changes.

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68
Q

What additional criteria should be considered for a suspected cancer pathway referral?

A

Consider referral for:
* Skin changes that suggest breast cancer
* People aged 30 and over with an unexplained lump in the axilla

This allows for early detection of potential breast cancer.

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69
Q

What is the recommendation for non-urgent referral in individuals under 30?

A

Non-urgent referral for people under 30 with an unexplained breast lump with or without pain.

This reflects a lower risk profile in younger individuals.

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70
Q

True or False: All individuals with unexplained breast lumps should be referred urgently.

A

False

The urgency of referral depends on age and the presence of specific symptoms.

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71
Q

What is dyspepsia?

A

A condition characterized by discomfort or pain in the upper abdomen.

Dyspepsia can include symptoms like bloating, nausea, and indigestion.

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72
Q

According to the 2015 NICE guidelines, who needs urgent referral for an endoscopy?

A

Patients with:
* dysphagia
* upper abdominal mass consistent with stomach cancer
* aged >= 55 years with weight loss and any of:
* upper abdominal pain
* reflux
* dyspepsia

These guidelines aim to identify potential cases of cancer quickly.

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73
Q

What symptoms indicate non-urgent referral for endoscopy?

A

Patients with:
* haematemesis
* aged >= 55 years with:
* treatment-resistant dyspepsia
* upper abdominal pain with low haemoglobin levels
* raised platelet count with any of:
* nausea
* vomiting
* weight loss
* reflux
* dyspepsia
* upper abdominal pain
* nausea or vomiting with any of:
* weight loss
* reflux
* dyspepsia
* upper abdominal pain

Non-urgent cases still require evaluation but are not as time-sensitive.

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74
Q

What is the significance of weight loss in patients aged >= 55 years?

A

It is a critical factor in determining the need for urgent referral for endoscopy when combined with upper abdominal pain, reflux, or dyspepsia.

Weight loss can indicate serious underlying conditions, including cancer.

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75
Q

True or False: All patients with dyspepsia require urgent referral for endoscopy.

A

False

Only specific cases of dyspepsia, particularly in older patients with additional concerning symptoms, require urgent referral.

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76
Q

Fill in the blank: Patients with _______ and weight loss are considered for urgent endoscopy referral.

A

upper abdominal pain

This combination raises concerns for serious underlying conditions.

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77
Q

What is the recommended age to consider PSA testing in men?

A

Men older than 50 years of age who request a PSA test

PSA testing should also be considered in men with suspected prostate cancer.

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78
Q

What should be done if a patient’s PSA level is above the threshold for their age?

A

Refer on the suspected cancer pathway referral for an appointment within 2 weeks

This applies to patients with possible symptoms of prostate cancer.

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79
Q

What is the PSA threshold for men aged 50-59?

A

> 3.5 ng/ml

This threshold indicates a higher likelihood of prostate cancer for this age group.

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80
Q

What are the PSA level thresholds for men aged 60-69?

A

> 4.5 ng/ml

Patients above this threshold should be referred if symptomatic.

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81
Q

What factors can raise PSA levels?

A
  • Benign prostatic hyperplasia (BPH)
  • Prostatitis and urinary tract infection (postpone test for 6 weeks after treatment)
  • Ejaculation (ideally not in the previous 48 hours)
  • Vigorous exercise (ideally not in the previous 48 hours)
  • Urinary retention
  • Instrumentation of the urinary tract

These factors can affect the accuracy of PSA testing.

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82
Q

True or False: Around 33% of men with a PSA of 4-10 ng/ml will be found to have prostate cancer.

A

True

This statistic highlights the poor specificity of PSA testing.

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83
Q

What percentage of men with a PSA of 10-20 ng/ml will likely have prostate cancer?

A

60%

This indicates an increased risk with higher PSA levels.

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84
Q

What percentage of men with prostate cancer have a normal PSA?

A

Around 15%

This underscores the limitations of PSA testing in diagnosing prostate cancer.

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85
Q

What should be used for men under 40 when considering PSA testing?

A

Clinical judgement

There is no specific threshold for this age group.

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86
Q

What is bladder cancer?

A

The second most common urological cancer.

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87
Q

What age group is most commonly affected by bladder cancer?

A

Males aged between 50 and 80 years.

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88
Q

What is the increased risk factor for bladder cancer in smokers?

A

2-5 fold increased risk.

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89
Q

What substance exposure increases the risk of bladder cancer?

A

Hydrocarbons such as 2-Naphthylamine.

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90
Q

What is a rare cause of chronic bladder inflammation that can lead to squamous cell carcinomas?

A

Schistosomiasis infection.

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91
Q

What are two examples of benign tumours of the bladder?

A
  • Inverted urothelial papilloma
  • Nephrogenic adenoma
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92
Q

What type of carcinoma accounts for over 90% of bladder malignancies?

A

Urothelial (transitional cell) carcinoma.

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93
Q

What percentage of bladder malignancies are squamous cell carcinomas?

A

1-7%.

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94
Q

What percentage of bladder malignancies are adenocarcinomas?

A

2%.

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95
Q

What is ‘field change’ in relation to urothelial carcinomas?

A

The effect that allows tumours to arise as multifocal lesions.

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96
Q

What is the growth pattern of up to 70% of transitional cell carcinomas?

A

Papillary growth pattern.

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97
Q

What is the prognosis for superficial urothelial tumours?

A

Better prognosis.

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98
Q

What is the risk of regional or distant lymph node metastasis for those with T3 disease or worse?

A

30% (or higher) risk.

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99
Q

What does T0 indicate in TNM staging?

A

No evidence of tumour.

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100
Q

What does Ta indicate in TNM staging?

A

Non invasive papillary carcinoma.

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101
Q

What does T1 indicate in TNM staging?

A

Tumour invades sub epithelial connective tissue.

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102
Q

What does T2a indicate in TNM staging?

A

Tumour invades superficial muscularis propria (inner half).

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103
Q

What does T2b indicate in TNM staging?

A

Tumour invades deep muscularis propria (outer half).

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104
Q

What does T3 indicate in TNM staging?

A

Tumour extends to perivesical fat.

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105
Q

What does T4 indicate in TNM staging?

A

Tumour invades prostatic stroma, seminal vesicles, uterus, vagina.

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106
Q

What does T4a indicate in TNM staging?

A

Invasion of uterus, prostate or bowel.

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107
Q

What does T4b indicate in TNM staging?

A

Invasion of pelvic sidewall or abdominal wall.

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108
Q

What does N0 indicate in TNM staging?

A

No nodal disease.

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109
Q

What does N1 indicate in TNM staging?

A

Single regional lymph node metastasis in the true pelvis.

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110
Q

What does N2 indicate in TNM staging?

A

Multiple regional lymph node metastasis in the true pelvis.

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111
Q

What does N3 indicate in TNM staging?

A

Lymph node metastasis to the common iliac lymph nodes.

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112
Q

What does M0 indicate in TNM staging?

A

No distant metastasis.

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113
Q

What does M1 indicate in TNM staging?

A

Distant disease.

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114
Q

When should men be referred for a suspected prostate cancer pathway?

A

If their prostate feels malignant on digital rectal examination

Referral should be for an appointment within 2 weeks.

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115
Q

What tests should be considered to assess for prostate cancer?

A

Prostate-specific antigen (PSA) test and digital rectal examination

These tests are recommended for men with specific symptoms.

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116
Q

What symptoms warrant consideration of a PSA test and digital rectal examination?

A
  • Any lower urinary tract symptoms (nocturia, urinary frequency, hesitancy, urgency, retention)
  • Erectile dysfunction
  • Visible haematuria

These symptoms may indicate the need for further investigation.

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117
Q

What PSA levels indicate a need for referral for prostate cancer?

A

If PSA levels are above the age-specific reference range

This is a critical factor for referral.

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118
Q

What is a suspected cancer pathway referral for penile cancer?

A

An appointment within 2 weeks for suspected penile cancer.

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119
Q

What conditions warrant a referral for suspected penile cancer?

A

Either a penile mass or ulcerated lesion with excluded sexually transmitted infection, or a persistent penile lesion post-STI treatment.

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120
Q

What should be excluded as a cause for a penile mass before referral?

A

A sexually transmitted infection.

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121
Q

What symptoms may indicate a need for referral for penile cancer?

A

Unexplained or persistent symptoms affecting the foreskin or glans.

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122
Q

What is the time frame for a suspected cancer pathway referral for penile cancer?

A

Within 2 weeks.

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123
Q

Fill in the blank: A persistent penile lesion after treatment for a sexually transmitted infection may require a _______.

A

[suspected cancer pathway referral]

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124
Q

What is the age threshold for referral using a suspected cancer pathway for bladder cancer?

A

45 years and over

This age threshold is crucial for identifying individuals at risk for bladder cancer.

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125
Q

What is a key symptom for referral for bladder cancer in individuals aged 45 years and over?

A

Unexplained visible haematuria without urinary tract infection

Visible haematuria is a significant indicator of potential bladder cancer.

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126
Q

What condition must be present for individuals aged 60 years and over to be referred for bladder cancer?

A

Unexplained non-visible haematuria and either dysuria or a raised white cell count on a blood test

These symptoms warrant urgent investigation for bladder cancer.

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127
Q

What is the recommendation for non-urgent referral for bladder cancer in people aged 60 years and over?

A

Recurrent or persistent unexplained urinary tract infection

This indicates a need for further evaluation for bladder cancer.

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128
Q

What is the age threshold for referral using a suspected cancer pathway for renal cancer?

A

45 years and over

Similar to bladder cancer, this age threshold is critical for renal cancer referrals.

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129
Q

What is a key symptom for referral for renal cancer in individuals aged 45 years and over?

A

Unexplained visible haematuria without urinary tract infection

This symptom is a significant red flag for renal cancer.

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130
Q

What additional condition must be met for referral for renal cancer if visible haematuria is present?

A

Visible haematuria that persists or recurs after successful treatment of urinary tract infection

This persistence indicates the need for further investigation.

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131
Q

Fill in the blank: Referral for bladder cancer should be made if a patient has unexplained visible haematuria without _______.

A

urinary tract infection

This condition is a key indicator for bladder cancer.

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132
Q

True or False: Individuals aged 60 years and over with unexplained non-visible haematuria should be referred for renal cancer.

A

False

The referral criteria for renal cancer focus on visible haematuria.

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133
Q

What is the primary development pathway for most colorectal cancers?

A

Most cancers develop from adenomatous polyps.

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134
Q

By what percentage has screening for colorectal cancer been shown to reduce mortality?

A

16%

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135
Q

What type of screening does the NHS offer to older adults for colorectal cancer?

A

Home-based, Faecal Immunochemical Test (FIT) screening.

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136
Q

What age group is targeted by the NHS national screening programme FIT in England?

A

Men and women aged 60 to 74 years.

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137
Q

What is the age range for colorectal cancer screening in Scotland?

A

50 to 74 years.

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138
Q

What can patients aged over 74 years do regarding colorectal cancer screening?

A

They may request screening.

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139
Q

How are eligible patients notified about the Faecal Immunochemical Test (FIT)?

A

They are sent FIT tests through the post.

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140
Q

What does the Faecal Immunochemical Test (FIT) specifically detect?

A

Human haemoglobin (Hb).

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141
Q

What is the main advantage of FIT over conventional faecal occult blood (FOB) tests?

A

It only detects human haemoglobin, not animal haemoglobin from diet.

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142
Q

How many faecal samples are needed for the FIT compared to conventional FOB tests?

A

Only one sample is needed for FIT, compared to 2-3 for conventional FOB tests.

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143
Q

What information is provided to the patient regarding the numerical value generated by FIT?

A

It is not reported to the patient or GP.

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144
Q

What happens to patients with abnormal FIT results?

A

They are offered a colonoscopy.

145
Q

At colonoscopy, what percentage of patients typically have a normal exam?

A

5 out of 10 patients.

146
Q

What percentage of patients at colonoscopy may be found to have polyps?

A

4 out of 10 patients.

147
Q

What is the potential risk associated with the polyps found during colonoscopy?

A

They may have premalignant potential.

148
Q

What percentage of patients at colonoscopy will be found to have cancer?

A

1 out of 10 patients.

150
Q

When should I refer a person with suspected colorectal cancer?

A

Refer if they have:
* An abdominal mass
* A change in bowel habit
* Iron-deficiency anaemia
* Aged 60 years and over with anaemia (even without iron deficiency)
* Aged 40 years and over with unexplained weight loss and abdominal pain
* Aged under 50 years with rectal bleeding and unexplained abdominal pain or weight loss
* Aged 50 years and over with unexplained rectal bleeding, abdominal pain, or weight loss

These criteria help guide timely referrals for suspected cases.

151
Q

What quantitative testing should be offered to guide referral for suspected colorectal cancer?

A

Offer quantitative faecal immunochemical testing (FIT) using HM-JACKarc or OC-Sensor

FIT is used to detect hidden blood in the stool, which can indicate colorectal cancer.

152
Q

What should be considered if people need help returning their faecal sample?

A

Consider if people need additional help, information, or support

Ensuring that individuals can return their samples is crucial for accurate testing.

153
Q

Should FIT be offered even if a person has had a negative result from the NHS bowel screening programme?

A

Yes, offer FIT even if the person has previously had a negative FIT result

This ensures that potential cases are not overlooked.

154
Q

What FIT result indicates a referral for colorectal cancer using a suspected cancer pathway?

A

A FIT result of at least 10 micrograms of haemoglobin per gram of faeces

This threshold helps identify individuals at higher risk of colorectal cancer.

155
Q

What should be done if a person has not returned a faecal sample or has a FIT result below 10 micrograms?

A

Ensure safety netting processes are in place

This is important to monitor symptoms and ensure timely intervention.

156
Q

What action should be taken if there is a strong clinical concern of cancer due to ongoing unexplained symptoms?

A

Do not delay referral to an appropriate secondary care pathway

Timeliness is crucial in managing potential cancer cases.

157
Q

What is a sign that might indicate an CONSIDERATION of urgent referral is necessary?

A

Evidence of rectal mass

A rectal mass is a significant clinical finding that requires prompt action.

159
Q

What is the most common cause of cancer in the UK?

A

Breast

Other common causes include lung, colorectal, prostate, bladder, non-Hodgkin’s lymphoma, melanoma, stomach, oesophagus, and pancreas.

160
Q

What is the leading cause of death from cancer in the UK?

A

Lung

Other leading causes include colorectal, breast, prostate, pancreas, oesophagus, stomach, bladder, non-Hodgkin’s lymphoma, and ovarian.

161
Q

Fill in the blank: The most common cause of cancer in women in the UK is _______.

162
Q

Which cancer has the highest incidence in men in the UK?

A

PROSTATE

Other common cancers in men include lung and bowel.

163
Q

List the common causes of cancer in the UK.

A
  • Breast
  • Lung
  • Colorectal
  • Prostate
  • Bladder
  • Non-Hodgkin’s lymphoma
  • Melanoma
  • Stomach
  • Oesophagus
  • Pancreas
164
Q

List the most common causes of death from cancer in the UK.

A
  • Lung
  • Colorectal
  • Breast
  • Prostate
  • Pancreas
  • Oesophagus
  • Stomach
  • Bladder
  • Non-Hodgkin’s lymphoma
  • Ovarian
165
Q

Fill in the blank: The second most common cause of cancer in the UK is _______.

166
Q

What is the third most common cause of cancer in the UK?

A

Colorectal

167
Q

What is the fourth most common cause of cancer in the UK?

168
Q

Fill in the blank: The fifth most common cause of cancer in the UK is _______.

169
Q

What type of cancer is the most common in women after breast cancer?

A

Lung

Bowel cancer also has significant incidence among women.

170
Q

What is a common site of cancer incidence in women aside from breast and lung?

171
Q

ORDER of cancer incidence in women

A

Incidence of cancer in women:
1.BREAST
2.lung
3.Bowel
4.OTTHER SITES
5. UTERUS

172
Q

Order of cancer incidence in men

A

Incidence of cancer in men:
1. PROSTATE

2.lung
3.Bowel

174
Q

What are the two main categories of treatment for ulcerative colitis?

A

Inducing and maintaining remission

175
Q

What is the classification of ulcerative colitis severity?

A

Mild, moderate, severe

176
Q

Define mild ulcerative colitis.

A

< 4 stools/day, only a small amount of blood

177
Q

Define moderate ulcerative colitis.

A

4-6 stools/day, varying amounts of blood, no systemic upset

178
Q

Define severe ulcerative colitis.

A

> 6 bloody stools/day + features of systemic upset (pyrexia, tachycardia, anaemia, raised inflammatory markers)

179
Q

What is the first-line treatment for mild-to-moderate proctitis?

A

Topical (rectal) aminosalicylate

180
Q

If remission is not achieved within 4 weeks for proctitis, what should be added?

A

Oral aminosalicylate

181
Q

What should be done if remission is still not achieved after adding oral aminosalicylate for proctitis?

A

Add topical or oral corticosteroid

182
Q

What is the first-line treatment for proctosigmoiditis and left-sided ulcerative colitis?

A

Topical (rectal) aminosalicylate

183
Q

After 4 weeks of treatment for proctosigmoiditis and left-sided ulcerative colitis, if remission is not achieved, what options are available?

A
  • High-dose oral aminosalicylate
  • Switch to high-dose oral aminosalicylate and topical corticosteroid
184
Q

What is the treatment approach for extensive disease in ulcerative colitis?

A

Topical (rectal) aminosalicylate and a high-dose oral aminosalicylate

185
Q

What is the treatment protocol for severe colitis?

A

Should be treated in hospital with IV steroids first-line

186
Q

What should be considered if there is no improvement after 72 hours of treating severe colitis?

A
  • Add IV ciclosporin to IV corticosteroids
  • Consider surgery
187
Q

What is the maintenance treatment following a mild-to-moderate ulcerative colitis flare for proctitis and proctosigmoiditis?

A
  • Topical (rectal) aminosalicylate alone
  • Oral aminosalicylate plus topical (rectal) aminosalicylate
  • Oral aminosalicylate by itself
188
Q

What maintenance treatment is recommended for left-sided and extensive ulcerative colitis?

A

Low maintenance dose of an oral aminosalicylate

189
Q

What is the recommended treatment following a severe relapse or >=2 exacerbations in the past year?

A

Oral azathioprine or oral mercaptopurine

190
Q

Is methotrexate recommended for the management of ulcerative colitis?

A

No, it is not recommended

191
Q

What evidence exists regarding probiotics in ulcerative colitis management?

A

Probiotics may prevent relapse in patients with mild to moderate disease

192
Q

What is the surgical option when ulcerative colitis is unresponsive to optimal medical therapy?

A

Consider surgery

193
Q

What does subtotal colectomy involve?

A

Removal of part of the colon, usually with a temporary loop ileostomy

194
Q

What is the preferred surgical approach for ulcerative colitis?

A

Restorative proctocolectomy (IPAA)

195
Q

What does complete panproctocolectomy entail?

A

Removal of the entire colon and rectum, resulting in a permanent ileostomy

196
Q

What is Crohn’s disease?

A

A form of inflammatory bowel disease that commonly affects the terminal ileum and colon but may occur anywhere from the mouth to anus.

197
Q

When did NICE publish guidelines on the management of Crohn’s disease?

198
Q

What lifestyle change should patients with Crohn’s disease be strongly advised to make?

A

Stop smoking.

199
Q

What medications are generally used to induce remission in Crohn’s disease?

A

Glucocorticoids (oral, topical, or intravenous).

200
Q

What is an alternative medication to glucocorticoids for inducing remission in some patients?

A

Budesonide.

201
Q

What dietary approach may be used to induce remission in Crohn’s disease?

A

Enteral feeding with an elemental diet.

202
Q

What second-line drugs are used after glucocorticoids to induce remission?

A

5-ASA drugs (e.g., mesalazine).

203
Q

Which medications may be used as an add-on to induce remission but not as monotherapy?

A

Azathioprine or mercaptopurine.

204
Q

What is the role of infliximab in Crohn’s disease?

A

Useful in refractory disease and fistulating Crohn’s.

205
Q

What is the first-line medication to maintain remission in Crohn’s disease?

A

Azathioprine or mercaptopurine.

206
Q

What should be assessed before starting azathioprine or mercaptopurine?

A

TPMT activity.

207
Q

What is the second-line medication used to maintain remission?

A

Methotrexate.

208
Q

What percentage of patients with Crohn’s disease will eventually require surgery?

A

Around 80%.

209
Q

What surgical procedure is indicated for stricturing terminal ileal disease?

A

Ileocaecal resection.

210
Q

What is a perianal fistula?

A

An inflammatory tract or connection between the anal canal and the perianal skin.

211
Q

What is the investigation of choice for suspected perianal fistulae?

212
Q

What is the typical treatment for symptomatic perianal fistulae?

A

Oral metronidazole.

213
Q

What may be effective in closing and maintaining closure of perianal fistulas?

A

Anti-TNF agents such as infliximab.

214
Q

What is a draining seton used for?

A

Complex fistulae.

215
Q

What is required for a perianal abscess?

A

Incision and drainage combined with antibiotic therapy.

216
Q

What are the standard incidence ratios for small bowel cancer and colorectal cancer in Crohn’s disease?

A

Small bowel cancer = 40; colorectal cancer = 2.

217
Q

What additional health risk is associated with Crohn’s disease?

A

Osteoporosis.

218
Q

What is Von Willebrand’s disease?

A

The most common inherited bleeding disorder

219
Q

How is Von Willebrand’s disease primarily inherited?

A

In an autosomal dominant fashion

220
Q

What are common symptoms of Von Willebrand’s disease?

A
  • Epistaxis
  • Menorrhagia
221
Q

What symptoms are rare in Von Willebrand’s disease?

A
  • Haemoarthroses
  • Muscle haematomas
222
Q

What is the role of von Willebrand factor?

A
  • Promotes platelet adhesion to damaged endothelium
  • Carrier molecule for factor VIII
223
Q

What is the size of von Willebrand factor multimers?

A

Up to 1,000,000 Da

224
Q

What are the types of Von Willebrand’s disease?

A
  • Type 1: partial reduction in vWF
  • Type 2: abnormal form of vWF
  • Type 3: total lack of vWF
225
Q

Which type of Von Willebrand’s disease is the most common?

226
Q

What is a characteristic finding in the investigation of Von Willebrand’s disease?

A

Prolonged bleeding time

227
Q

What might be a prolonged test in Von Willebrand’s disease?

A

APTT may be prolonged

228
Q

What happens to factor VIII levels in Von Willebrand’s disease?

A

They may be moderately reduced

229
Q

What is a specific test finding in Von Willebrand’s disease?

A

Defective platelet aggregation with ristocetin

230
Q

What is a treatment option for mild bleeding in Von Willebrand’s disease?

A

Tranexamic acid

231
Q

What is desmopressin (DDAVP) used for in Von Willebrand’s disease?

A

Raises levels of vWF by inducing release from Weibel-Palade bodies

232
Q

What is another treatment option for Von Willebrand’s disease?

A

Factor VIII concentrate

233
Q

What is thrombophilia?

A

A condition that increases the risk of thrombosis.

234
Q

What is the most common inherited cause of thrombophilia?

A

Factor V Leiden (activated protein C resistance).

235
Q

What is the second most common inherited cause of thrombophilia?

A

Prothrombin gene mutation.

236
Q

What are the deficiencies of naturally occurring anticoagulants associated with thrombophilia?

A
  • Antithrombin III deficiency
  • Protein C deficiency
  • Protein S deficiency
237
Q

Which deficiency has the highest relative risk of venous thromboembolism (VTE)?

A

Antithrombin III deficiency.

238
Q

What is an acquired cause of thrombophilia?

A

Antiphospholipid syndrome.

239
Q

What drug is associated with an increased risk of thrombophilia?

A

The combined oral contraceptive pill.

240
Q

Fill in the blank: The most common cause of thrombophilia is _______.

A

factor V Leiden (activated protein C resistance).

241
Q

True or False: Protein S deficiency is one of the deficiencies of naturally occurring anticoagulants.

242
Q

List three inherited causes of thrombophilia.

A
  • Factor V Leiden (activated protein C resistance)
  • Prothrombin gene mutation
  • Deficiencies of naturally occurring anticoagulants
243
Q

What is thrombocytosis?

A

An abnormally high platelet count, usually > 400 * 10^9/l.

244
Q

What are the causes of reactive thrombocytosis?

A
  • Severe infection
  • Surgery
  • Iron deficiency anaemia
245
Q

Name two malignancies associated with thrombocytosis.

A
  • Chronic myeloid leukaemia
  • Polycythaemia rubra vera
246
Q

What is essential thrombocytosis?

A

A myeloproliferative disorder characterized by megakaryocyte proliferation and overproduction of platelets.

247
Q

What is the platelet count indicative of essential thrombocytosis?

A

> 600 * 10^9/l

248
Q

What are two complications associated with essential thrombocytosis?

A
  • Thrombosis (venous or arterial)
  • Haemorrhage
249
Q

What is a characteristic symptom of essential thrombocytosis?

A

A burning sensation in the hands

250
Q

What mutation is found in around 50% of patients with essential thrombocytosis?

A

JAK2 mutation

251
Q

What medication is widely used to manage essential thrombocytosis?

A

Hydroxyurea (hydroxycarbamide)

252
Q

Which treatment may be used for younger patients with essential thrombocytosis?

A

Interferon-α

253
Q

True or False: Low-dose aspirin may be used in essential thrombocytosis to reduce thrombotic risk.

254
Q

Fill in the blank: Thrombocytosis can occur as a result of _______.

A

hyposplenism

255
Q

What age range should be considered for suspected haematological malignancy management?

A

0-24 years

256
Q

What is the urgency for a full blood count if features of leukaemia are present?

A

Very urgent, within 48 hours

257
Q

Name a symptom that should prompt a full blood count in young people suspected of leukaemia.

258
Q

What symptom indicates a need for immediate investigation in young people for leukaemia related to energy levels?

A

Persistent fatigue

259
Q

What unexplained symptom could suggest leukaemia in a young person?

A

Unexplained fever

260
Q

What type of persistent infections should raise suspicion for leukaemia in young individuals?

A

Unexplained persistent infections

261
Q

What physical finding, characterized by swelling of lymph nodes, should prompt a full blood count?

A

Generalised lymphadenopathy

262
Q

What symptom related to bone health may indicate leukaemia in young people?

A

Persistent or unexplained bone pain

263
Q

What unexplained symptom involving skin discoloration may suggest leukaemia?

A

Unexplained bruising

264
Q

What type of abnormality involving bleeding could indicate leukaemia in young individuals?

A

Unexplained bleeding

265
Q

What is immune thrombocytopenia (ITP)?

A

An immune-mediated reduction in the platelet count

Antibodies are directed against the glycoprotein IIb/IIIa or Ib-V-IX complex.

266
Q

How does ITP commonly present in children?

A

Usually has an acute thrombocytopenia that may follow infection or vaccination.

267
Q

How does ITP commonly present in adults?

A

Tends to have a more chronic condition.

268
Q

What demographic is more commonly affected by ITP?

A

Older females.

269
Q

How may ITP be detected in adults?

A

Incidentally following routine blood tests.

270
Q

What are common symptoms of ITP in adults?

A
  • Petechiae
  • Purpura
  • Bleeding (e.g. epistaxis)
271
Q

Is catastrophic bleeding (e.g. intracranial) a common presentation of ITP?

A

No, it is not a common presentation.

272
Q

What is the typical finding in a full blood count for ITP?

A

Isolated thrombocytopenia.

273
Q

What investigations are used for ITP?

A
  • Full blood count
  • Blood film
274
Q

Is a bone marrow examination routinely used in the investigation of ITP?

A

No, it is no longer used routinely.

275
Q

What is the sensitivity of antiplatelet antibody testing in ITP?

A

Poor sensitivity.

276
Q

What is the first-line treatment for ITP?

A

Oral prednisolone.

277
Q

What is the role of pooled normal human immunoglobulin (IVIG) in ITP management?

A

Raises the platelet count quicker than steroids; may be used if active bleeding or an urgent invasive procedure is required.

278
Q

Is splenectomy commonly used in the management of ITP?

A

No, it is now less commonly used.

279
Q

What is Evan’s syndrome?

A

ITP in association with autoimmune haemolytic anaemia (AIHA).

280
Q

What is Haemophilia?

A

An X-linked recessive disorder of coagulation

281
Q

What percentage of patients with Haemophilia have no family history of the condition?

282
Q

What causes Haemophilia A?

A

A deficiency of factor VIII

283
Q

What is Haemophilia B also known as?

A

Christmas disease

284
Q

What causes Haemophilia B?

A

A lack of factor IX

285
Q

List three features of Haemophilia.

A
  • haemoarthroses
  • haematomas
  • prolonged bleeding after surgery or trauma
286
Q

What blood test result is prolonged in Haemophilia?

287
Q

What are the normal blood test results in Haemophilia?

A
  • bleeding time
  • thrombin time
  • prothrombin time
288
Q

What percentage of patients with Haemophilia A develop antibodies to factor VIII treatment?

A

Up to 10-15%

289
Q

What are the inducers of the P450 system?

A

Inducers include:
* phenytoin
* carbamazepine
* phenobarbitone
* rifampicin
* St John’s Wort
* chronic alcohol intake
* griseofulvin
* smoking

Smoking affects CYP1A2, which is why smokers require more aminophylline.

290
Q

What mnemonic can help remember the inducers of the P450 system?

A

PCBRASS + griseofulvin

291
Q

Name two antiepileptic drugs that are inducers of the P450 system.

A

phenytoin and carbamazepine

292
Q

Which barbiturate is an inducer of the P450 system?

A

phenobarbitone

293
Q

What is the effect of chronic alcohol intake on the P450 system?

A

It induces the P450 system.

294
Q

What are the inhibitors of the P450 system?

A

Inhibitors include:
* ciprofloxacin
* erythromycin
* isoniazid
* cimetidine
* omeprazole
* amiodarone
* allopurinol
* ketoconazole
* fluconazole
* fluoxetine
* sertraline
* ritonavir
* sodium valproate
* acute alcohol intake
* quinupristin

These inhibitors reduce the effect of the desired drug.

295
Q

True or False: Rifampicin is an inhibitor of the P450 system.

296
Q

Which two antibiotics are known inhibitors of the P450 system?

A

ciprofloxacin and erythromycin

297
Q

Fill in the blank: _______ is an imidazole that inhibits the P450 system.

A

ketoconazole

298
Q

What is the effect of acute alcohol intake on the P450 system?

A

It inhibits the P450 system.

299
Q

Name one SSRI that inhibits the P450 system.

A

fluoxetine or sertraline

300
Q

What is the chemical name for Vitamin A?

301
Q

What is the deficiency state associated with Vitamin A?

A

Night-blindness (nyctalopia)

302
Q

What is the chemical name for Vitamin B1?

303
Q

What are the deficiency states associated with Vitamin B1?

A
  • Beriberi
  • Polyneuropathy
  • Wernicke-Korsakoff syndrome
  • Heart failure
304
Q

What is the chemical name for Vitamin B3?

305
Q

What are the deficiency states associated with Vitamin B3?

A
  • Pellagra
  • Dermatitis
  • Diarrhoea
  • Dementia
306
Q

What is the chemical name for Vitamin B6?

A

Pyridoxine

307
Q

What are the deficiency states associated with Vitamin B6?

A
  • Anaemia
  • Irritability
  • Seizures
308
Q

What is the chemical name for Vitamin B7?

309
Q

What are the deficiency states associated with Vitamin B7?

A
  • Dermatitis
  • Seborrhoea
310
Q

What is the chemical name for Vitamin B9?

A

Folic acid

311
Q

What are the deficiency states associated with Vitamin B9?

A
  • Megaloblastic anaemia
  • Neural tube defects during pregnancy
312
Q

What is the chemical name for Vitamin B12?

A

Cyanocobalamin

313
Q

What are the deficiency states associated with Vitamin B12?

A
  • Megaloblastic anaemia
  • Peripheral neuropathy
314
Q

What is the chemical name for Vitamin C?

A

Ascorbic acid

315
Q

What are the deficiency states associated with Vitamin C?

A
  • Scurvy
  • Gingivitis
  • Bleeding
316
Q

What is the chemical name for Vitamin D?

A

Ergocalciferol, cholecalciferol

317
Q

What are the deficiency states associated with Vitamin D?

A
  • Rickets
  • Osteomalacia
318
Q

What is the chemical name for Vitamin E?

A

Tocopherol

319
Q

What are the deficiency states associated with Vitamin E?

A
  • Mild haemolytic anaemia in newborn infants
  • Ataxia
  • Peripheral neuropathy
320
Q

What is the chemical name for Vitamin K?

A

Naphthoquinone

321
Q

What are the deficiency states associated with Vitamin K?

A
  • Haemorrhagic disease of the newborn
  • Bleeding diathesis
322
Q

What protozoa is primarily responsible for the majority of malaria cases?

A

Plasmodium falciparum

Around 75% of malaria cases are caused by this protozoa.

323
Q

What percentage of patients who develop malaria did not take prophylaxis?

A

The majority

This indicates a significant gap in preventative measures.

324
Q

What happens to UK citizens from malaria endemic areas regarding immunity?

A

They quickly lose their innate immunity.

325
Q

What should be consulted prior to prescribing malaria prophylaxis?

A

Up-to-date charts with recommended regimes for malarial zones.

326
Q

What is the time to begin Atovaquone + proguanil (Malarone) before travel?

A

1 - 2 days.

327
Q

What are the side effects of Atovaquone + proguanil (Malarone)?

328
Q

How long after travel should Atovaquone + proguanil (Malarone) be continued?

329
Q

How often is Chloroquine taken for malaria prophylaxis?

330
Q

What side effects are associated with Chloroquine?

A

Headache, contraindicated in epilepsy.

331
Q

What is the time to begin Chloroquine before travel?

332
Q

How long after travel should Chloroquine be continued?

333
Q

What are the side effects of Doxycycline?

A

Photosensitivity, Oesophagitis.

334
Q

What is the time to begin Doxycycline before travel?

A

1 - 2 days.

335
Q

How long after travel should Doxycycline be continued?

336
Q

What is the time to begin Mefloquine (Lariam) before travel?

A

2 - 3 weeks.

337
Q

What are the side effects of Mefloquine (Lariam)?

A

Dizziness, Neuropsychiatric disturbance, contraindicated in epilepsy.

338
Q

How often is Mefloquine taken for malaria prophylaxis?

339
Q

What is the time to begin Proguanil (Paludrine) before travel?

340
Q

How long after travel should Proguanil (Paludrine) be continued?

341
Q

What should pregnant women be advised regarding travel to malaria endemic regions?

A

To avoid travelling.

342
Q

What is a challenge in diagnosing malaria in pregnant women?

A

Parasites may not be detectable in the blood film due to placental sequestration.

343
Q

What is advised for folate supplementation in pregnant women taking Proguanil?

344
Q

What is the recommendation for children travelling to malaria endemic regions?

A

They should take malarial prophylaxis.

345
Q

What percentage of DEET has been shown to repel mosquitoes effectively?

346
Q

What is the licensing age for Doxycycline in the UK for children?

A

Over 12 years.

347
Q

True or False: Doxycycline is contraindicated for pregnant women.

348
Q

What are the major congenital infections encountered in examinations?

A

Rubella, toxoplasmosis, cytomegalovirus

349
Q

Which congenital infection is the most common in the UK?

A

Cytomegalovirus

350
Q

Is maternal infection of cytomegalovirus usually symptomatic or asymptomatic?

A

Asymptomatic

351
Q

What are the characteristic features of rubella?

A
  • Sensorineural deafness
  • Congenital cataracts
  • Congenital heart disease (e.g. patent ductus arteriosus)
  • Glaucoma
352
Q

What are additional features of rubella?

A
  • Growth retardation
  • Hepatosplenomegaly
  • Purpuric skin lesions
  • ‘Salt and pepper’ chorioretinitis
  • Microphthalmia
  • Cerebral palsy
353
Q

What are the characteristic features of toxoplasmosis?

A
  • Cerebral calcification
  • Chorioretinitis
  • Hydrocephalus
  • Low birth weight
354
Q

What are other features of toxoplasmosis?

A
  • Anaemia
  • Hepatosplenomegaly
  • Cerebral palsy
355
Q

What are the characteristic features of cytomegalovirus?

A
  • Purpuric skin lesions
  • Sensorineural deafness
  • Microcephaly
356
Q

What are other features of cytomegalovirus?

A
  • Visual impairment
  • Learning disability
  • Encephalitis/seizures
  • Pneumonitis
  • Hepatosplenomegaly
  • Anaemia
  • Jaundice
  • Cerebral palsy
357
Q

Fill in the blank: The characteristic feature of rubella that involves heart defect is _______.

A

Congenital heart disease (e.g. patent ductus arteriosus)

358
Q

True or False: Hydrocephalus is a characteristic feature of toxoplasmosis.

359
Q

Fill in the blank: One of the other features of cytomegalovirus is _______.

A

Visual impairment