5-Minute Clinical Consult

Ventricular Septal Defect

Ventricular Septal Defect is a topic covered in the 5-Minute Clinical Consult.

To view the entire topic, please or purchase a subscription.

Medicine Central™ is a quick-consult mobile and web resource that includes diagnosis, treatment, medications, and follow-up information on over 700 diseases and disorders, providing fast answers—anytime, anywhere. Explore these free sample topics:

Medicine Central

-- The first section of this topic is shown below --

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, it is the most common congenital heart malformation reported in infants and children. It also occurs as a complication of acute myocardial infarction (MI).
  • Severity of the defect is correlated with its size, with large defects being the most severe.
  • Blood flow across the defect typically is left to right, depending on defect size and pulmonary vascular resistance (PVR).
  • Prolonged left to right shunting of blood can lead to pulmonary hypertension (HTN). Eventually, there will be reversal of flow across the defect and cyanosis (Eisenmenger complex).

Geriatric Considerations
Almost entirely associated with MI

Pediatric Considerations
Congenital defect
ALERT
  • Pregnancy may exacerbate symptoms and signs of a ventricular septal defect (VSD).
  • Can be tolerated during pregnancy if VSD is small
  • May be associated with an increased risk of preeclampsia in women with an unrepaired VSD

Epidemiology

Incidence
  • Congenital defect: no gender predilection, occurs in ~2/1,000 live births
  • Post-MI: males are affected more than females

Prevalence

In the US:

  • Congenital defect: lowered prevalence in adults due to spontaneous closure
  • Post-MI: estimated to complicate 1–3%

Etiology and Pathophysiology

  • Congenital
  • In adults, complication of MI

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

Risk Factors

  • Congenital:
    • Risk of sibling being affected: 4.2%
    • Risk of offspring being affected: 4%
    • Prematurity
  • Complication of MI:
    • First MI
    • HTN
    • Most frequently within 1st week after MI
    • Occurs in 1–3% of MIs, most commonly after anterior MI

General Prevention

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

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

-- To view the remaining sections of this topic, please or purchase a subscription --