Q#1 Flashcards

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1
Q

Describe Lead-time bias.

A

When we mistakenly think that the survival for a disease increased even though it’s not true. We just got better at screening and identifying the disease earlier.

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2
Q

Describe selection bias.

A

When a study sample cannot be used to make generalizations about a population. This happens because the sample does not match the demographics of the population or when the sample participants were not assigned to groups randomly.

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3
Q
  • Describe procedure bias. *
A

This will probably never be the answer.

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4
Q

Describe recall bias.

A

This occurs when patients are asked to remember things about their past that are only really salient after they were exposed to a negative outcome.

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5
Q

What non-pharmacological intervention has the most mortality benefit in patients with COPD?

A

Continuous oxygen therapy.

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6
Q

What good does lung transplantation do for patients with COPD?

A

Lung transplants only help with improving the quality of life in patients with COPD. They do now, however, reduce mortality or prolong life of patients with COPD.

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7
Q

What are the indications of continuous oxygen therapy in patients with COPD?

What does it depend on?

A

*Give continuous O2 to pts with COPD if they:
-Have an O2 sat. (SpO2)of under 88%.
-Have an arterial oxygen partial pressure (PaO2) of under 55 mm Hg.

or

Any signs of right-sided heart failure.
-SpO2 of under 89%.
-PaO2 of under 59 mm Hg.

*It depends on if the patient has signs of right-sided heart failure, such as liver swelling or abdominal swelling, edema, Hct of over 55, etc.

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8
Q

What is the point of putting COPD patients on long-term antibiotic therapy?

A

Antibiotics such as azithromycin can reduce their recurrence of COPD exacerbations by reducing inflammation chronically, as well as preventing infections.

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9
Q

Describe the anatomy of HOCM?

A

In HOCM, there is this unequal thickening of the cardiac ventricular septum on the left ventricle side. There is also this lengthening of the mitral valve leaflets. As a result, the mitral valve leaflet and the thickened ventricular septum are super close together and they clash whenever the ventricle contracts, impeding outflow of blood from the heart.

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10
Q

What factors make HOCM worse, in terms of impeding cardiac outflow?

What medications should we avoid giving to patients with HOCM.

A

-Decreased preload/ventricular volume or increased contractility.

-Avoid giving diuretics, which decrease the preload. Also avoid giving inotropes that increased contractility.

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11
Q

What will make a murmur louder in patients with HOCM?

A

Decreasing the preload, whereas in all others, this will reduce the sound of a murmur.

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12
Q

How do patients with HOCM present?

A

Patients with HOCM are typically young (in their 20s and under) who are athletes who have histories of passing out while doing some physical activity. There is usually no warning when they faint.

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13
Q

What are the categories that we monitor for pediatric milestones?

A

-Gross motor
-Fine motor
-Language
-Cognition
-Social

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14
Q

What is true of premature babies, in terms of pediatric milestones?

A

We have to adjust their age to determine their milestones until they are two years of age. Then, they are judged just like everyone else.

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15
Q

How do we adjust for age in premature infants?

A

Their actual age (time after birth) - # of weeks born early.

Premature baby is 9 months. He we was born at 32 weeks. Since he was born 5 weeks early, he is 36 weeks - 5 = 31 weeks.

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16
Q

What are some mnemonics for milestones?

A

-The # of blocks stacked = age in years X 3.

-Kids can pee at three.

-Kids can speak 2-word sentences at 2-years old.

-Kids can ride a tricycle at three.

-Kids can “hop” on a four square plaything at four.

-Kids can draw a circle at 3 (round-looking number).

-Kids can draw a + at 4 (number has a cross in it).

-Kids can draw a square at 5 years old. (ITDK).

-Kids can draw a triangle at 6 (IDK, the number has 3 in it twice).

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17
Q

What is VaIN?

What occurs in VaIN?

What are risk factors for developing VaIN?

A

-VaIN stands for Vaginal Intraepithelial Neoplasia.

-In VaIN, the squamous cells become atypical and just build up within the epithelial layer of the tissue.

-Risk factors for VaIN include having HPV (associated with sex) strains 16 and 18 and smoking.

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18
Q

Describe the staging of VaIN.

A

-VaIN 1 is when the squamous cells that become atypical are from the lower layers of the epithelium.

-VaIN 2 is when the atypical squamous cells are located in the bottom 2/3s of the epithelium.

-VAIN 3 is when the atypical squamous cells fill more than 2/3 of the epithelium and include CARCINOMA INSITU.

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19
Q

How do lesions with VaIN look like? Describe it.

Is there usually invasion with VaIN?

What are signs that invasion might be occurring with VaIN?

A

-They are typically whitish lesions in the vagina that have raised boarders.

-VaIN does not usually have invasion underneath the epithelium.

-If the borders are irregular or if the lesion is ulcerative.

20
Q

What is the treatment for patients with patients with high-grade (3) VaIN?

If we suspect invasion of VaIN, what treatment options are contraindicated?

A

-Wide local excision.

-If suspicion of invasion or actual invasion is present, avoid 5-FU or any lasers to treat VaIN.

21
Q

When should we use vaginal estrogen cream?

A

Use vaginal estrogen cream when the pt is postmenopausal and has vaginal atrophy or if a patient has low-grade VaIN without evidence or suspicion of invasion.

22
Q

If there are multiple high-grade VaIN lesions, how do we treat them?

A

Ablative therapy.

23
Q

What is true regarding parent decision-making for their children?

*especially with vaccines.

A

Parents can make total and final decisions for their children, even if it is not in their best interest - as long as there is no immediate and significant threat to the child’s health.

*So, parents can say no to vaccines because the vaccine rates in our communities are pretty high, so herd immunity will keep the kid fine.

24
Q

What is fifth disease?

A

Fifth disease is aka erythema infectiosum. It is a viral infection caused by the single-stranded DNA virus called Parvovirus B19.

25
Q

How does Fifth disease present?

A

Patients with Fifth disease present with low-grade fevers, headaches, myalgias, and upper respiratory symptoms (URI) that resolve within a few days. After flu-like symptoms resolve, there is this characteristic red (erythematous) rash that appears on both cheeks. Their mouth also becomes pale. The rash can also spread to their trunks.

26
Q

When should children and pregnant ladies stay away from someone infected with Parvovirus B 19?

A

When said person is febrile or has URI symptoms. Once those sysmptoms resolve, and the rash comes along, pregnant women and other children are safe and won’t get the infection - b/c the patient is no longer infectious.

26
Q

How do we treat Fifth disease?

A

-Supportive care if they are immunocompetent.

-Immunoglobulin therapy if the patient is immunocompromised.

27
Q

How is Parvovirus B19 spread?

A

Via the large respiratory droplets, so they are not airborne for long or over long distances - mostly maintain 6 ft from them and wear a surgical mask and not a respiratory such as N95.

28
Q

What is a special consideration for sickle cells patients infected with parvovirus B19?

A

These sickle cell patients can develop aplastic anemic crisis as a result of a Parvovirus B19 infection. As a result, we must treat them with blood transfusions to prevent this.

29
Q

Pts with DM on long term NSAIDs are at risk of what and why?

A

Pts with DM likely have some form of kidney issues, so they are at increased risk of renal insufficiency when taking NSAIDs.

30
Q

What antidiabetic drugs end in …ride, ….zide, etc?

What is the risk of taking these medications?

A

-Sulfonylureas.

-Hypoglycemia and liver toxicity.

31
Q

What is true about metformin and renal toxicity?

A

Metformin does not cause renal toxicity. However, patients with renal insufficiency are at increased risk of developing lactic acidosis.

32
Q

When do we try to control blood pressure in patients having a stroke who are not treated with thrombectomy or thrombolysis?

A

When the blood pressure is over 220 systolic or 120 diastolic.

33
Q

When a patient with an ischemic stroke presents at 2 hours after onset of symptoms, what intervention can be given?

What about if they are 6 hours after the onset of symptoms?

A

We can give them thrombolysis with alteplase as long as they are within 4.5 hours of symptoms onset.

Give them aspirin only if they are past the 4.5 hour window till 48 hours after the onset of symptoms.

34
Q

What are the different type of transplant rejection reactions?

A

-Hyperacute
-Acute
-Chronic
-Graft vs Host

35
Q

Describe histological findings in Hyperacute transplant rejection.

A

In hyperacute transplant rejection, there is capillary thrombosis which prevents blood perfusion of the transplanted organ.

36
Q

What is the underlying cause of hyperacute transplant rejection reactions?

A

In hyperacute transplant rejection, there are pre-existing antibodies in the donor organ that do not mix with those antibodies of the new host.

37
Q

What is the timeline of hyperacute transplant rejection reactions?

A

Within minutes.

38
Q

Describe the underlying cause of acute transplant rejection reactions.

Timeline.

A

-There is CD4 and CD8 cells that react to the MHC complexes on the donor organ tissue.

-Within weeks to months.

39
Q

What are the histological findings for acute transplant rejection reactions?

A

For acute transplant rejection reactions, we see lymphocytes infiltrating the interstitial space and tissue.

40
Q

How do we treat transplant rejection reactions?

A

With immunosuppressants.

41
Q

What is the underlying cause of chronic transplant rejection reactions?

A

The CD4 cells of the new host react against the antigen presenting cells of the donor organ.

42
Q

What are histological findings in chronic transplant rejection reactions?

A

In chronic transplant rejection reactions, we tend to see smooth muscle proliferation and fibrosis.

43
Q

What is the timeline of chronic transplant rejection reactions?

A

Months to years.

44
Q

How do we diagnose transplant rejection reactions?

A

Get a biopsy of the organ.

45
Q

How does graft vs host disease present?

What is the underlying cause of graft vs host disease?

A

The pt will have a transplant but then systemic symptoms such as diarrhea, rash, fever - as opposed to just end organ damage to the donated organ.

The underlying cause of graft vs host disease is the lymphocytes of the donor organ tissue reacting against the new recipient cells.

46
Q
A