Key result
Modified Warden procedure with mechanical MVR resolves severe heart failure and cuts sPAP by ~27 mmHg.
Why the study?
Partial anomalous pulmonary venous return is very rare, with an incidence of 0.4% to 0.7% in autopsy series, and isolated cases account for less than 10% of all cases.
Case Report (n=1)
No
Answers are grounded in this paper and cite their sources.
Demonstrates that the rare coexistence of isolated supracardiac PAPVR without ASD and severe rheumatic mitral stenosis can be safely and effectively treated via a combined modified Warden procedure and mechanical mitral valve replacement.
Background: Partial anomalous pulmonary venous return (PAPVR) is a very rare condition, with an incidence ranging from 0.4% to 0.7% in autopsy series. Isolated PAPVR without autism spectrum disorder is extremely rare, accounting for less than 10% of all PAPVR. Case presentation: ; a Wilkins score of 9/16). She underwent a modified Warden procedure and mechanical mitral valve replacement using a 27 mm bileaflet valve. The postoperative course was uneventful. After 12 months, she improved to NYHA Class I, with a prosthetic mean gradient of 4 mmHg, a normal right ventricular size, and a low systolic pulmonary artery pressure (38 mmHg). No arrhythmias, SVC obstruction, or prosthetic dysfunction were noted. Conclusion: This is an example of the complicated hemodynamic relationship between PAPVR and severe rheumatic mitral stenosis. The two conditions can be repaired together successfully with careful multimodality imaging assessment and an individualized surgical plan.
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Rizvi et al. (2026) conducted a case report in Isolated partial anomalous pulmonary venous return (PAPVR) without ASD and severe recurrent rheumatic mitral stenosis (n=1). Modified Warden procedure and mechanical mitral valve replacement (27 mm bileaflet valve) was evaluated on Clinical functional status (NYHA class), echocardiographic hemodynamics, and prosthetic function at 12 months. Combined modified Warden procedure and mechanical mitral valve replacement improved functional status from functional class IV to I and reduced systolic pulmonary artery pressure from 65 to 38 mmHg at 12 months.
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