Sandbox: Pulmonary Valve regurgitation

Causes

Congenital Causes	Acquired Causes	Chronic PR	Acute PR
Quadricuspid or Bicuspid valves Hypoplasia of the valves Prolapse of the pulmonary valve	Infective endocarditis Post repair of tetralogy of Fallot Post repair of pulmonary valve stenosis Rheumatic heart disease Carinoid Syndrome Myxomatous Degeneration of the pulmonary valve.	Following repair of tetralogy of Fallot Following balloon or surgical valvulotomy or valvuloplasty for pulmonary stenosis Absent pulmonary valve syndrome Isolated congenital PR Peripheral pulmonary artery stenosis Pulmonary hypertension Right ventricular outlet aneurysm	Neonatal Ebstein’s anomaly Following balloon dilation of critical pulmonary stenosis Perforation of valvar pulmonary atresia

Diagnosis

History and Symptoms

Clinical presentation of pulmonary regurgitation varies on the severity of the regurgitation and the right ventricular function.

• Isolated pulmonary regurgitation is usually asymptomatic and is an incidental finding on 2D echo even when the regurgitation is severe.
• Patients with chronic PR develop right heart failure and present with the following symptoms:
  • Intitial symptom of chronic PR is functional limitation
  • Ankle edema or swelling of the feet and legs
  • Dyspnea on exertion
  • Fatigue
  • Hemoptysis or frothy sputum
  • Nocturnal cough
  • Palpitations or extra heart beats

Physical Examination

The physical examination findings in significant pulmonary regurgitation include:

• Soft diastolic, decrescendo murmur best heard in the left upper sternal region which increases in intensity with inspiration.
• It can accompanied by a systolic ejection murmur.
• Right ventricular heave is present when the right ventricle is enlarged.

EKG

• EKG findings in chronic PR are non specific.
• In patients with tetralogy of Fallot increased QRS duration with widened QRS complex reflect the severity of PR and consequent right ventricular dilation.

Chest X-Ray

Chest X-Ray in chronic PR the following findings can be demonstrated:

• Cardiomegaly in chronic PR involving the right sided chambers.
• Pulmonary artery dilation