Exam 3 Peds Flashcards

1
Q

VSD: ventricular septal defect (most common form of CHD): Pathophysiology

A

Abnormal opening between the right and left ventricles; causing increased blood volume to the lungs

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2
Q

VSD: ventricular septal defect (most common form of CHD): Manifestations

A

Heart failure, loud hollosystolic (during systole) murmur (LSB), increased risk for pulmonary vascular obstructive disease

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3
Q

VSD: ventricular septal defect (most common form of CHD): Management

A

surgical interventions
- small complete repair: closed with a suture
- large complete repair: Dacron patch
VSD Prognosis depends on location, number, and other associated defects

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4
Q

Patent Ductus Arteriosus (PDA): Pathophysiology

A

Failure of the fetal ductus arteriosus to close; blood flows from the high-pressure aorta to the low-pressure pulmonary artery

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5
Q

Patent Ductus Arteriosus (PDA): Manifestations

A

Heart failure, machine like murmur, widened pulse pressure, bounding pulses

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6
Q

Patent Ductus Arteriosus (PDA): Management

A
  • Medical: indomethacin (does not have great side effects)
    • Surgical: ligation of patent vessel
    • Nonsurgical: coils used to occlude PDA
      Prognosis: low risk; increased in preterm infants
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7
Q

Role of Prostaglandin E:

A

Keeps the ductus arteriosus open; indomethacin (medication) blocks prostaglandin E and is used to help close the ductus arteriosus

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8
Q

Coarctation of the Aorta (COA): Pathophysiology

A

Localized narrowing near insertion of ductus arteriosus; increased pressure proximal to the defect (head/upper extremities); decreased pressure distal to the obstruction (lower extremities)

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9
Q

Coarctation of the Aorta (COA): Manifestations

A
  • HTN and bounding pulses in the upper extremities
  • Low BP and weak/absent pulses in the lower extremities
  • dizziness, headaches, fainting spells, epistaxis (bloody nose) – HTN; All ages are at an increased risk for: HTN, ruptured aorta, aortic aneurysm, stroke
  • something that is often diagnosed in infancy, sometimes it can be missed
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10
Q

Coarctation of the Aorta (COA): Management

A
  • surgical: treatment of choice for infants < 6 months
    • nonsurgical: balloon angioplasty
    • postoperative: hypertension
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11
Q

Tetralogy of Fallot: Pathophysiology

A

MAJOR DEFECTS:

1. pulmonary stenosis
2. right ventricular hypertrophy 
3. overriding aorta 
4. ventricular septal defect
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12
Q

Tetralogy of Fallot: Manifestations

A

Mild to severe cyanosis; systolic murmur

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13
Q

Tetralogy of Fallot: Management

A
  • palliative shunt: modified blalock-taussig shunt
    • complete repair: usually in the first year of life
    • indications for repair: increasing cyanosis, increase in hypercyanotic spells
    • close VSD, resect infundibular stenosis with placement patch to enlarge RVOT
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