Chiavarelli M, Puga F J, Julsrud P R
Circulation. 1987 Sep;76(3 Pt 2):III34-8.
Establishment of right ventricular-pulmonary arterial continuity without the use of cardiopulmonary bypass was undertaken in 36 patients with different anomalies associated with pulmonary atresia or severe stenosis. Hospital mortality was 11% with no late death. Fourteen of the 27 individuals with pulmonary atresia, ventricular septal defect, and hypoplastic confluent pulmonary arteries had adequate angiographic follow-up, which demonstrated significant pulmonary artery enlargement. Five patients underwent total correction, two after unifocalization operations to establish lobar pulmonary arterial continuity. Symmetric growth of the left and right pulmonary artery was not achieved. However, the enlargement was adequate for potential final repair in all the patients with an unrestricted outflow tract.
36例合并肺动脉闭锁或严重狭窄等不同畸形的患者在未使用体外循环的情况下建立了右心室-肺动脉连续性。住院死亡率为11%,无晚期死亡病例。27例肺动脉闭锁、室间隔缺损及肺总动脉发育不良的患者中有14例获得了充分的血管造影随访,结果显示肺动脉有显著增粗。5例患者接受了根治性手术,其中2例在进行单灶化手术以建立叶肺动脉连续性后接受了根治性手术。左右肺动脉未实现对称生长。然而,对于所有流出道无梗阻的患者,肺动脉增粗程度足以进行最终修复。