5-Minute Clinical Consult

Ventricular Septal Defect

Ventricular Septal Defect was found in 5-Minute Clinical Consult which helps you diagnose, treat, and follow up on over 900 medical conditions seen in everyday practice.

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Basics

Description

  • Congenital or acquired defect of the interventricular septum that allows communication of blood between the left and the right ventricles
  • Other than bicuspid aortic valve, this is the most common congenital heart malformation reported in infants and children. It also occurs as a complication of acute myocardial infarction (MI).
  • Blood flow across the defect typically is left to right and depends on the size of the defect and the pulmonary vascular resistance (PVR).
  • Prolonged shunting of blood can lead to pulmonary hypertension (HTN) and eventual reversal of flow across the defect, as well as to cyanosis (Eisenmenger complex).
  • System(s) affected: Cardiovascular

Geriatric Considerations
In this population, almost entirely associated with MI

Pediatric Considerations
Congenital

  • Pregnancy may exacerbate symptoms and signs of a ventricular septal defect (VSD).
  • Tolerated during pregnancy if the septal defect is small
  • May be associated with an increased risk of preeclampsia in women with an unrepaired VSD (1)

Epidemiology


Incidence
  • Predominant sex: No gender predilection
  • Males are affected more than females if associated with MI.
  • Occurs in ∼2/1,000 live births (2)
Prevalence
In the US:
  • Acute MI: Estimated to complicate 1–3%
  • Lowered prevalence in adults due to spontaneous closure of defects

Risk Factors

  • Congenital:
    • Risk of sibling being affected: 4.2%
    • Risk of offspring being affected: 4%
  • Postacute MI:
    • First MI
    • Limited coronary artery disease
    • HTN
    • Most frequent within 1st week after MI
    • Occurs in 1–3% of MIs, most commonly after anterior MI

Genetics
Multifactorial etiology; autosomal-dominant and -recessive transmissions have been reported.

General Prevention

For adults, avoid risk factors for MI and obtain evaluation before pregnancy.

Etiology

  • Congenital
  • In adults, secondary to MI

Commonly Associated Conditions

  • Congenital:
    • Tetralogy of Fallot
    • Aortic valvular deformities, especially aortic insufficiency and bicuspid aortic valve
    • Down syndrome (trisomy 21), endocardial cushion defect
    • Transposition of great arteries
    • Coarctation of aorta
    • Tricuspid atresia
    • Truncus arteriosus
    • Patent ductus arteriosus
    • Atrial septal defect
    • Pulmonic stenosis
    • Subaortic stenosis
  • Adult: Coronary artery disease

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