Cardiac 3 Flashcards

1
Q

what is important to remember when administering digoxin

A

-count apical pulse for full min and hold dose if <90-110 in infants or <70-85 in children

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2
Q

what should you observe for if administering digoxin

A
  • observe for toxicity (arrhythmias are a sign)

- obtain serum dig level at least 6 hrs after daily dose

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3
Q

how is digoxin given

A

IV or by mouth

must maintain a therapeutic level**

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4
Q

describe rheumatic fever

A

aka scarlet fever
occurs 1-3 wks after untreated strep (secondary to strep)
**important to culture for strep to treat and prevent this
systemic inflammatory disease involving heart (vulvular damage), joints and CNS

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5
Q

what is the acute phase of rheumatic fever

A

2-3 wks (lasts < 3 months)

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6
Q

meds for strep

A

amoxicillin (in high doses)
azithromycin
*important to take all meds

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7
Q

major criteria for rheumatic fever

A
  • joint inflammation
  • carditis (new murmur, tachy)
  • chorea (involuntary limb movement, slurred)
  • ***erythema marginatum (rash on trunk and proximal limbs)
  • subcutaneous nontender nodules
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8
Q

what is erythema marginatum

A

scarlet rash

rash is rough like sandpaper

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9
Q

minor criteria for rheumatic fever

A
  • fever is spiked
  • arthralgia
  • elevated erythrocyte sedimentation rate
  • prolonged PR interval
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10
Q

how to determine if fits critera

A

-2 major or 1 mjor and 2 minor to diagnose

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11
Q

nursing diagnoses for rheumatic fever

A
  • high risk for injury (carditis)
  • pain
  • high risk for diversional activity deficit
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12
Q

treatment for rheumatic fever

A
  • bedrest until normal ESR (sed rate)
  • antiinflammatory (corticosteroids to decrease inflammation and ASPIRIN to reduce pain/fever)
  • penicillin or erythromycin to reduce risk of reccurrance
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13
Q

what analgesic is used for rheumatic fever

A

aspirin is only used in this instance (usually not used for any kids)
ibuprofen typcially given if >6 mos

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14
Q

describe steptoccal prophylaxis with rheumatic

A
  • damaged valves can sustain more damage with repeated infections
  • strep prophylaxis continues for 5 yrs through adolescence
  • *IM penicillin administered monthly
  • alternative is oral penicillin 2x daily or sulfadiazine 1x daily
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15
Q

describe kawasaki’s

A
  • cause is unkown
  • children <2
  • multisystem vasculitis (inflammation in multiple systems)
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16
Q

how do you treat kawasaki’s

A
  • ASPIRIN (start on high dose then decrease dose: 80-100 mg/kg/day in four divided doses to start)
  • IV immunoglobulin (IVIG) 2kg/kg given in single infusion to prevent cardiovascular events from happening (give quickly)
17
Q

acute phase of kawasaki’s

A

(1-2 wks)

  • high fever >5 days
  • conjunctivitis
  • red throat
  • swollen hands and feet
  • rash
  • lymphadenopathy
18
Q

subacute phase of kawasaki’s

A

(2-4 wks)

  • crackling lips/fissures
  • desquamation of skin
  • joint pain
  • cardiac disease
  • thrombocytosis
19
Q

covalescent phase of kawasaki’s

A

(6-8 wks)

  • child appears normal
  • lingering signs of inflammation
20
Q

nursing care for kawasaki’s

A
  • administer aspirin and IVIG
  • monitor for side effects (ie/ bleeding and GI upset)
  • IVIG is a blood product*** (reaction??)
  • keep skin clean and dry
  • lubricate lips
  • passive range of motion exercises to facilitate joint movement
21
Q

diagnostic criteria of kawasaki’s

A
  • need 5/6
  • fever >5 days
  • bilateral conjunctivitis w/out exudate
  • strawberry tongue, red oropharynx, dryness, erythema, fissuring of lips
  • peripheral edema, erethyma of palms or soles, peeling of feet
  • polymorphous rash
  • cervical lyphadenopathy
22
Q

20% of children with kawasaki’s develop this

A

cardiac sequele

23
Q

what is the most serious complication of kawasaki’s

A

-myocardial infarction d/t thrombotic occlusion of a coronary aneurysm

24
Q

s/s of MI in children

A
  • abdominal pain
  • V
  • restlessness
  • inconsolable
  • crying
  • pallor
  • shock
25
describe dyslipidemia
one or more lipids with abnormal level in blood | total cholesterol, low density lipoproteins, triglycerides, high density lipoproteins
26
describe hyperlipidemia
excessive fat and fat like substance in blood
27
describe hypercholesterolemia
excessive cholesterol in the blood
28
hyperlipidemia and hypercholesterolemia play a role in what
producing atherosclerosis which leads to CAD | *predispose to cardiovascular disease early
29
what can help prevent CAD
exercise and proper diet
30
presymptomatic phase of athersclerosis begins when
in childhood
31
what is the goal of dyslipidemia
identify children at risk and intervene EARLY - screening and managing lipid levels in childhood - screen anyone who appears to be overweight at 4 y/r visit and has a family hx of it
32
treatment of dyslipidemia
dietary modifications and exercise | in severe cases drug therapy (do not start with giving drugs d/t potential SE)
33
describe HTN
- BP persistently between 90-95% on 3 occasions - primary (has no identifiable cause) - secondary (attributable to structural abnormality or to an underlying disease)
34
factors contributing to HTN
diet, contraceptive use, family hx, obesity, lack of adequate exercise
35
treatment of HTN
* focus on diet and exercise (rare to use drugs) - diet modification: decrease sodium and saturated fat intake, 3-5 servings fruit/day, adequate calcium and dietary fiber) - nonpharmalogical: decrease wt, increase exercise (30-60 min a day)
36
what is important in young athletes
prevent cardiac death EKG for sports physical family hx of heart disease *important for thorough exam for sports physicals
37
describe sudden cardiac death
- blunt nonpenatratory force to heart wall will cause trauma - abrupt ventricular fib: acquired or underlying congenital disease - cardiac arrest
38
what are some s/s to watch for during exercise in children
- chest pain - SOB - syncope - palpitations * *if any of these document and follow up with cardio eval