Congenital Heart Defects Flashcards

1
Q

Etiology

A
  • Genetic component
  • Associated with other conditions (Downs, Turner, Williams, Marfan, DiGeorge, Costello, VACTERL)
  • Maternal medical problems (diabetes, obesity)
  • Environmental conditions
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2
Q

Defects- Acyanotic

A
  • Atrial septal defects (ASD)
  • Ventricular septal defects (VSD)
  • Atrioventricular septal defects (AVSD)
  • Patent ductus arteriosus (PDA)
  • Coarctation of the aorta
  • Aortic valve stenosis
  • Pulmonary valve stenosis

  • Child is pink with normal oxygen saturation
  • Blood shunts from left side of heart to right
  • Oxygenated blood goes to lungs and body
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3
Q

Defects- Cyanotic

A
  • Tetralogy of Fallot (TOF)
  • Double-outlet right ventricle
  • Transposition of the great arteries
  • Tricuspid atresia
  • Pulmonary atresia
  • Truncus arteriosus
  • Hypoplastic left heart
  • Arterial oxygen saturation 15-30% below normal
  • Blood shunts from the right side of heart to the left
  • Unoxygenated blood is returned to body
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4
Q

ASD

A

–Failure of septal tissue between atria to form (not PFO)

–Oxygen rich blood flows into chamber with oxygen poor

–Small defects spontaneously close

–Larger defects corrected surgically 2-5 yo

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5
Q

VSD

A

–Most common CHD

–Often close spontaneously by preschool

–Surgical repair at 1yo for large VSD not closing

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6
Q

AVSD

A

–Seen commonly in kids with Down syndrome

–Extra blood flows to lungs; causes pulmonary hypertension

–Heart overworked

and enlarges

–Surgery in early infancy

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7
Q

PDA

A

–Seen in preemies or maternal rubella

–Communication between pulmonary artery and descending aorta

–Closes soon after birth except in response to hypoxia

–Treated with prostaglandins to encourage patency

–Treated with prostaglandin inhibitors to encourage closure (indomethacin)

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8
Q

Coarctation of Aorta

A

–Narrowing of aorta

–Must keep PDA open with meds

–Requires surgical correction

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9
Q

Pulmonary Stenosis:

A
  • narrowing of the right ventricular outflow tract
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10
Q

Aortic Stenosis:

A

•narrowing of the left ventricular outflow tract

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11
Q

TOF

A

Most common complex cardiac defect

–VSD

–Pulmonary stenosis

–Overriding aorta (sits over VSD, not left ventricle)

–Hypertrophy of right ventricle

Must be surgically repaired – often in stages

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12
Q

Transposition of Great Arteries

A
  • Pulmonary artery arises from left ventricle
  • Aorta arises from right ventricle

Systemic blood returns to body unoxygenated and…

Pulmonary blood returns to lungs fully oxygenated

—–Death unless ductus arteriosus remains open

—–Surgery (arterial switch in first month of life)

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13
Q

Double-Outlet Right Ventricle

A

–Aorta and pulmonary artery come off of right ventricle

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14
Q

Hypoplastic Left Heart Syndrome

A

–Small or absent left ventricle and hypoplasia of ascending aorta

–Meds used to keep PDA

–Surgical correction or heart transplant

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15
Q

Cyanotic Episodes-what can we do?

A

•Squat or bring knees to chest

—–Increases systemic vascular resistance to help increase pulmonary blood flow

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16
Q

Surgical Repair Required

A
  • Tricuspid atresia: lack of communication between right atrium and right ventricle
    • Typically ASD and/or VSD exist to allow pulmonary blood flow
  • Pulmonary atresia: obstruction of blood flow from right side of hear to lungs
    • Blood flow maintained by PDA
    • ASD and/or VSD may also be present to shunt blood RàL
  • Truncus Arteriosus: aorta and pulmonary artery fail to separate leading to a common trunk arising from both ventricles
17
Q

Cardiac Transplant

A
  • Due to heart failure, cardiac defects, cardiomyopathy, pulmonary hypertension —Most common due to CHD or cardiomyopathy
  • Graft vs host disease (GVHD)
  • Results in denervated heart so cannot assess exercise intensity via heart rate – must use Rate of Perceived Exertion Scale (RPE) such as the Borg (11-13 desired) or modified Borg (5 desired)

18
Q

PT Implications

A
  • Fatigue
  • Poor feeding/nutrition/growth – takes too much effort/calories to sustain eat/life – dx failure to thrive (FTT) and gross motor delay
  • Low oxygen sats
  • Medications

–Anticoagulants

–Immunosuppressants (transplant)

19
Q

Children at highest risk for Neurodevelopmental Impairments

A
  • Neonate of infant requiring open heart sx
  • Child with other cyanotic hear lesion not requiring surgery
  • Congenital heart disease in combo with..

–Prematurity

–DD

–Suspected genetic abnormality or syndrome associated with DD

–H/O mechanical support

–Heart transplant

–CPR

–Hospital stay >2 weeks post surgery

–Perioperative seizures

–Abnormal finds on brain imaging or small head circumference