Pediatrics Flashcards

1
Q

What is the ddx for the constantly crying infant? (8)

A
"TIM'S CRIES" / IT CRIES
T - Trauma (acc/NAI), bites + Tumous
I - infxn (AOM, herpes stomatitis, UTI, meningitis, OM, etc)
M - mat/pat stress, anx, depression
S - strangulation (hair tourniquet)

C - Cardiac dx
R - Reflux, Rxn to formula/meds, Rectal fissures
I - Immunizations, Intolerance (cow’s milk,etc.), ICP
E - Eyes (occ FB, abrasion, glaucoma, hemorrhage)
S - Surgical (volv, intussusception, inguinal hernia, testicular torsion)

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2
Q

What are criteria for simple febrile seizure?

A

Brief <15 min
Single within 24 hours
Nonfocal

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3
Q

What is the recurrence rate of febrile seizures? Any features make higher or lower risk?

A

33%, 3/4 within first year
50% recur if <1 year
Less like recur if with temp > vs < 40 (13 vs 35%)

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4
Q

What are typical features of JIA? Systemic onset JIA?

A

Insidious onset
- Morning stiffness or gelling phenomenon (ie, stiffness
after long periods of sitting or inactivity)
- Arthralgias during the day (often symm polyarthraliga)
- May complain of pain; disuse of limbs may be more common than pain complaints
- In young kids may have morning limp that improves with time, or not standing in crib anymore after naps
- May have hx of school absences / inability to participate in sports

SYSTEMIC
High fevers/chills - often intermittent spikes up to 39C for 2+ weeks, often 1-2 times per day at same time (very specific pattern)
Polyarticular symm arthritis
Effervescent rash

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5
Q

What is life-threatening complication associated with systemic onset JIA? What are features/findings (#)?

A
MAS = macrophage activating syndrome
Macrocyte and T-cell proliferation with multi-systemic organ failure
- High fever
- Purpura
- Spont mucosal bleeding / DIC
- Altered LOC
- Hepatosplenomegaly
- may see pancytopenia, abn liver function tests
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6
Q

What is the definition of colic (there’s a “Rule)?

A

Colic = excessive crying for >3h/d, for >3d/week for at least 3 weeks (rule of 3s)

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7
Q

What are the diagnostic criteria of Kawasaki’s disease?

A
  • Fever >= 5 days AND
  • 4+ of the following:
    • bilat nonexudative conjunctival injection (scleral inj’n w/ perilimbic sparing)
    • oropharyngeal MM changes (pharyngeal erythema, red/cracked lips, strawberry tongue)
    • cervical LN (1+ node > 1.5 cm diameter)
    • peripheral extremity changes (acute = diffuse palmar/hand, feet erythema + swelling)
    • polymorphic generalized rash (no specific pathognomonic rash)

– may have other sx: arthritis, keratitis/uveitis, diarrhea/vomiting, gb disease, coryza, cough

– note can also have atypical / incomplete kawasaki’s

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8
Q

What are important ddx for Kawasaki disease?

A
Viral exanthems (not measles -- should be different specific rash)
Streptococcal disease (SF, TSS)
Staphylococcal disease (SSS, TSS)
Bilateral cervical lymphadenitis
Leptospirosis
Rikettsial disease
SJS/TENS
Drug rxn (e.g. mercury hypersensitivty rxn)
Juvenile chronic arthritis
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9
Q

What is the MOST important investigative test in KD and when should it be done? What complication are you looking for?

A

Echocardiography – repeat @4-6 weeks if first normal
Carditis during febrile phase (myocarditis with ST changes, pericardial eff, others), with coronary vessel abn (aneurysm formation) peaking at 2-4 weeks if untreated

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10
Q

What is the treatment for KD?

A

IVIG (2g/kg IV over 10h, best if started within first 10d – 2nd dose if persistent fever)

ASA – 3-5mg/kg PO daily for 6-8 weeks (some argue give higher dose until afebrile 2-3d but may not offer additional benefit)

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11
Q

What is Reye’s syndrome?

A

Acute metabolic encephalopathy associated with hepatic dysfunction.

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12
Q

What are clinical and historical features of Reye’s syndrome?

A
  • Recent viral illness or vaccination (esp influenza, varicella)
  • Recent salicylate (aspirin) use (80 of carse reports have aspirin within 3 weeks)
  • vomiting, esp abrupt onset w/n few days viral illness
  • neurologic symptoms: lethargy, irritability, restlessness, delirium, seizures, loss brainstem refelxes, decorticate/decerebrate coma, flaccid paralysis
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13
Q

What is the management of Reye’s syndrome?

A

SUpportive management:
ABCs, hypoglycemia tx, seizure tx, vomiting tx, fluid resuscitaiton, correct hyperammonemia (?sodium phenylacetate, sodium benzoate), prevent/tx raised ICP, tx severe metabolicacidosis, corect coagulopathy

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