Step3 30 Flashcards

1
Q

Vaccines that contain egg

Wich ones
Recommendation

A

Influenza
Yellow fever

Personal or family history of egg allergy is not a contraindication

If an anaphylactic reaction to egg.. administer the vaccine in the hospital setting

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2
Q

If the patient has minor cold symptoms, can you administer immunizations?

A

YES

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3
Q

First step in HIV in post-exposure prophylaxis if the patient refuses to get tested, results are pending or HIV status is unknown

A

Start treatment

Stop after the result is negative or continue for 4 weeks if tolerated

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4
Q

Necrotizing fasciitis presentation and classification

A

Hx of minor skin trauma
Pain out of proportion, swelling, erythema,
Systemic symptoms: fever, hypotension

Type 1: Usually seen in patients with underlying diabetes and PAD
S. aureus
Bacteroides: crepitus
E. coli
S. pyogenes
Clostridium: crepitus
Pseudomonas: immunocompromised

Type II: occur in individuals with no current medical illness.
S. pyogenes is the most common organism

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5
Q

Management of necrotizing fasciitis

A

Hemodynamic support

Antibiotics
Piperacillin/Tazobactam: S. pyogenes and anaerobes
Vanco: S. aureus including MRSA
Clynda: added to inhibit toxin formation

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6
Q

Erythrasma vs. intertrigo

A
Erythrasma:
Corynebacterium minutisimun
Well defined borders or thing plaques with fine wrinkling
Fusidic acid cream
Clindamycin solution
Benzoyl peroxide

Intertrigo
Candida
Erythematous plaques, satellite papules, and significant inflammation
Topical antifungals: miconazole, nystatin, terbinafien

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7
Q

Approach to sicca symptoms

What’s the gold standard?

A

Dry eyes, dry mouth

Confirm secretory deficiency: eg. Shirmer test (slit lamp to assess tear break up time)

Anti Jo/Anti La
ANA
Rheumatoid factor

The gold standard is salivary gland biopsy. Reserve for young patients with severe symptoms

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8
Q

Treatment of xerostomia alone

A

Initial treatment is with salivary stimulation

Mechanical or topical

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9
Q

Diagnosis of Autosomal Dominant Polycystic Disease

A

Renal ultrasound

Family hx but unknown genotype:
18-39: >3 cyst uni or bilateral
40-59: >2 in each kidney
>60: >4 in each kidney

Unknown family history:
Multiple (>10 cysts) in each kidney regardless of age

Genetic testing: usually saved for patients where US does not yield a diagnosis

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10
Q

Management of Autosomal dominant polycystic kidney disease

A

Aggressive control of risk factors CV and CKD
ACEI preferred for hypertension
Statins

Renal transplant or hemodialysis if end-stage renal disease

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11
Q

Extra external features of Autosomal dominant polycystic kidney disease (6)

A

Cerebral aneurysms

Liver and pancreatic cyst

Colonic diverticula

Ventral and hinguinal hernias

Aortic regurge

Mitral prolapse

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12
Q

Laboratory findings of polymyalgia rheumatica

A

ESR >40 (sometimes >1000)

Elevated CRP

+/- Anemia

20% normal

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13
Q

Clinical presentation of polymyalgia rheumatica

A

Age >50

Bilateral pain and morning stiffness >1 month

>2 of the following
Neck or torso
Shoulder or proximal arms
Proximal thigh or hips
Constitutional: fever, malaise, weight loss
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14
Q

Treatment of polymyalgia rheumatica

A

Steroids
Low dose for pain
High dose for giant cell artheritis

(absence of response indicates another diagnosis is possible)

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