Cardiovascular Disease· Topic 2.5 Congenital heart disease in adults· 2.5.1

Atrial septal defect

Atrial septal defect is a communication in the interatrial septum causing a left-to-right shunt, often silent until adulthood. It classically produces a fixed split second heart sound and, over time, right heart volume overload, atrial arrhythmias, and pulmonary hypertension; hemodynamically significant defects are closed by device or surgery.

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What this article covers

  • Overview

    Definition: atrial septal defect (ASD) is a persistent communication in the interatrial septum allowing a shunt, usually left-to-right, between the atria.

  • Epidemiology

    A common congenital defect, frequently diagnosed in adulthood.

  • Risk factors

    Congenital malformation (often isolated).

  • Pathophysiology

    Left-to-right atrial shunt: the more compliant right heart receives shunted blood, causing right atrial and ventricular volume overload and pulmonary overcirculation.

  • Clinical features

    Often asymptomatic until adulthood. A fixed split second heart sound and a pulmonary flow (systolic ejection) murmur.

  • Differential diagnosis

    Patent foramen ovale: a flap-valve communication with no true septal tissue deficiency and usually no significant shunt, so right heart enlargement is absent, unlike ASD (Patent foramen ovale).

  • Diagnosis

    Establish and characterize with echocardiography and a bubble study, quantifying the shunt and right heart effect: the diagnostic basis is echocardiography (often transesophageal, with an…

  • Management

    First-line, close a hemodynamically significant defect: device closure (for suitable ostium secundum defects) or surgical repair is indicated for a significant shunt or right heart enlargement, before irreversible pulmonary hypertension.

  • Complications

    Right heart volume overload and failure. Atrial fibrillation and flutter.

  • Prognosis

    Excellent after timely closure, with reduced arrhythmia and improved function.

  • Prevention

    Timely closure of hemodynamically significant defects (pulmonary-to-systemic flow ratio, Qp:Qs, of 1.5:1 or more, or right heart enlargement) to prevent right heart and pulmonary complications.

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