Pediatric Cardiology II - Nazeri Flashcards

1
Q

Kawasaki Disease aka infantile polyarteritis nodosa*

A
  • most common heart disease in children
  • arteritis* –> mainly coronary arteries*
  • <5 y/o (more common in boys)
  • higher in Asians*
  • high fever lasting 1-2 weeks*
  • ECHO most used due to lack of tapering of arteries
  • can form aneurysms (measured with Z score)
  • z score >/= 10 –> giant aneurysm and need anticoagulation
  • no live vaccines if on aspirin to avoid Reye syndrome (encephalopathy)

hallmarks***

  • bilateral non-exudative conjuctivitis
  • strawberry tongue
  • edema/erythema of hands/feet
  • various rashes
  • non-suppurative cervical lymphadenopathy (unilateral)
  • maybe desquamation
  • low mortality, usually return to normal

labs

  • high platelet count is giveaway***
  • high ESR/CRP
  • CSF pleocytosis*
  • normal WBCs

treat

  • IVIG and high dose aspirin (anti-inflammatory) –> reduces risk of CAA
  • start anticoagulation aspirin later
  • give 2nd dose of IVIG if fever persists for 36 hr. after 1st IVIG infusion (IVIG resistant KD)
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2
Q

KD clinical phases

A
  1. acute - fever and other symptoms for 1-2 weeks
  2. subacute - desquamation, thrombocytosis, CAA* develop
  3. convalescent - clinical signs disappear, high ESR/CRP persist
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3
Q

management of KD aneurysms

A
  • small, single aneurysm –> remain on aspirin
  • multiple, large aneurysms –> need anticoagulants
  • may need surgery –> recannulate coronary arteries or bypass graft
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4
Q

rheumatic fever

A
  • acute migratory arthritis from GAS pharyngitis**
  • decreased incidence due to antibiotic use
  • most common acquired heart disease in all age groups*

hallmarks** JONES**

  • polyarthritis (migratory)
  • carditis
  • subcu nodules (erythema nodosum)
  • erythema marginatum
  • chorea

primary prevention
-10 day course of oral penicillin to treat GAS (erythro/azithro/clindamycin if allergic)

secondary prevention

  • no carditis in 1st attack –> antibiotics until 21 or 5 years after 1st attack bc of high recurrence
  • if carditis in 1st attack –> antibiotics until adult or rest of life
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5
Q

how to look for prior GAS

A
  • throat culture
  • rapid strep antigen test
  • elevated ASO titer
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6
Q

migratory arthritis in ARF

A
  • most common
  • large joints (swollen, tender)
  • multiple joint involvement
  • severity of arthritis is INVERSELY related to cardiac issues*** (ex. severe arthritis –> mild carditis and vice versa)
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7
Q

carditis in ARF

A
  • 2nd most common
  • usually has tachycardia and systolic murmur
  • pancarditis, but MUST have endocarditis (valvulitis) for RF***
  • usually viral if endocarditis is not present
  • mitral valve most common** followed by aortic
  • acute phase –> mitral insufficiency –> holosystolic murmur
  • severe cases –> mitral stenosis –> mid-diastolic murmur
  • aortic insufficiency –> decrescendo diastolic
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8
Q

sydenham chorea

A
  • movement disorder, disappears with sleep
  • milkmaid’s grip, darting movement of tongue
  • chance of developing RHD in 20 years if not given secondary prevention
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9
Q

mitral insufficency

A

-can lead to Afib, cardiac failure, infective endocarditis

treat

  • after load reducing agents (ACEI, ARB)
  • valve replacement

-if prosthetic mitral valve present, prophylaxis against bacterial endocarditis with dental procedures*

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10
Q

mitral stenosis

A

-build up pressure in LA –> LA hypertrophy –> redistribute pulmonary blood flow** –> pulmonary HTN and right side heart failure

treat
-valvotomy, balloon catheter, valve replacement

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11
Q

aortic insufficiency

A
  • volume overload –> dilation of LV –> can lead to mitral insufficiency
  • does not regress***, just like mitral stenosis cannot regress (mitral insufficiency can)
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12
Q

aortic stenosis

A
  • treat with afterload reducing agents or valve replacement

- ST-T wave changes on EKG show decreasing LV ejection fraction

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13
Q

myocarditis

A
  • inflammation of cardiac muscle
  • usually due to viral infection*** (hepC in Asia)
  • bacterial infection less common (diphtheritic myocarditis)
  • could also be due to connective tissue disorder
  • bad if progresses to chronic myocarditis

symptoms
-tachycardia, gallop rhythm*, hypotension

  • more severe in infants –> death
  • more mild in older children/adolescents –> may need heart transplant if present with other cardiomyopathy or if symptoms worsen

cardiac MRI is standard for diagnosing**

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14
Q

pericarditis

A
  • fluid accumulation in outer sac
  • small fluid –> well tolerated
  • moderate fluid –> sharp chest pain (worse with inspiration), cough, dyspnea, fever
  • mostly viral*

-can lead to cardiac tamponade***

non-infectious pericarditis
-postpericardiotomy syndrome after cardiac surgery –> fever, lethargy, anorexia, pleural effusion

constrictive pericarditis
- fibrous thickening and calcification –> impairs distensibility and venous return

diagnosis**

  • low QRS amplitude on EKG***
  • water bottle appearance on chest Xray*

treat
-non steroidals, pericardiocentesis for tamponade, pericardiectomy for constrictive

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15
Q

cardiac tamponade

A
  • too much fluid in pericardial sac compresses RA and RV reducing venous return and BP
  • impair filling –> shock and sudden death*
  • pulsus paradoxus –> fall of BP >10mmHg on deep inspiration
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16
Q

infective endocarditis

A

-alpha hemolytic strep and staph aureus most common**

  • tender osler nodes**
  • janeway lesions (painless) in palms/soles
  • splinter hemorrhages beneath nails

diagnosed by blood cultures or TTE/TEE

treat

  • antibiotics immediately* (vancomycin/gentamycin)
  • fungal treated with amphotericin B and 5-fluorocytosine
  • prophylaxis not recommeded, but improving dental hygiene is more important
  • do use prophylaxis before dental procedures if have CHD, RHD, respiratory tract procedures, cardiac transplant patients