Kreutzer C, Mayorquim R C, Kreutzer G O, Conejeros W, Roman M I, Vazquez H, Schlichter A J, Kreutzer E A
Divisions of Cardiovascular Surgery and Cardiology, Ricardo Gutierrez Children's Hospital, Cardiovascular Surgery, Bazterrica Clinic, Buenos Aires, Argentina.
J Thorac Cardiovasc Surg. 1999 Apr;117(4):662-8. doi: 10.1016/S0022-5223(99)70285-0.
This article presents a 10-year experience with one and a half ventricle repair for right ventricular hypoplasia or dysfunction.
From November 1986 to December 1996, 30 patients (mean age 6.7 +/- 8.5 years, range 4 months-40 years) with functionally abnormal right ventricles underwent a bidirectional Glenn shunt as part of the repair. Diagnoses included pulmonary atresia with intact ventricular septum (n = 15), Ebstein anomaly (n = 5), levotransposition of the great arteries (n = 3), pulmonary stenosis with right ventricular hypoplasia (n = 2), tetralogy of Fallot (n = 3), dextrotransposition of the great arteries (n = l), and Uhl anomaly (n = l). Concomitantly performed cardiac procedures included atrial septal defect closure (n = 27), fenestration of the atrial septum (n = 2), right ventricular cavity augmentation (n = 8), right ventricular outflow tract enlargement (n = 6), transannular patch (n = 13), modified Blalock-Taussig shunt closure (n = 16), tricuspid replacement (n = 3), tricuspid repair (n = 2), Rastelli procedure (n = 3), tricuspid commissurotomy (n = 2), and double switch (n = l).
There were 2 early deaths (6.6%) and 1 late death. Mean early postoperative superior vena caval pressure was 14. 12 +/- 3.55 mm Hg and mean right atrial pressure was 10.3 +/- 5.16 mm Hg. Early oxygen saturation in the operating room with an inspired oxygen fraction of 1 was 97.2 +/- 2.5; oxygen saturation was 92.3 +/- 4.8 on room air at discharge. Mean oxygen saturations were 93.6% +/- 3.6% at 1 year of follow-up (P =.10) and 93.5% +/- 4. 1% at 5 years (P =.12). Overall survival was 90% at 5 years, and 21 patients (77%) were in New York Heart Association class I, 5 (18%) were in class II, and 1 (2.7%) was in class III.
This procedure provides a valid alternative for correction of right ventricle hypoplasia or dysfunction. Early and intermediate follow-up results compare favorably with those of the Fontan procedure, but long-term follow-up is needed.
本文介绍了对右心室发育不全或功能障碍进行单心室与半心室修复的10年经验。
1986年11月至1996年12月,30例右心室功能异常患者(平均年龄6.7±8.5岁,范围4个月至40岁)接受双向格林分流术作为修复手术的一部分。诊断包括室间隔完整的肺动脉闭锁(n = 15)、埃布斯坦畸形(n = 5)、大动脉左旋位(n = 3)、肺动脉狭窄合并右心室发育不全(n = 2)、法洛四联症(n = 3)、大动脉右旋位(n = 1)和乌尔畸形(n = 1)。同期进行的心脏手术包括房间隔缺损修补(n = 27)、房间隔开窗(n = 2)、右心室腔扩大(n = 8)、右心室流出道扩大(n = 6)、跨环补片(n = 13)、改良布莱洛克-陶西格分流术关闭(n = 16)、三尖瓣置换(n = 3)、三尖瓣修复(n = 2)、拉斯泰利手术(n = 3)、三尖瓣交界切开术(n = 2)和双调转术(n = 1)。
有2例早期死亡(6.6%)和1例晚期死亡。术后早期平均上腔静脉压力为14.12±3.55 mmHg,平均右心房压力为10.3±5.16 mmHg。手术室中吸入氧分数为1时的早期血氧饱和度为97.2±2.5;出院时室内空气中的血氧饱和度为92.3±4.8。随访1年时平均血氧饱和度为93.6%±3.6%(P = 0.10),5年时为93.5%±4.1%(P = 0.12)。5年时总体生存率为90%,21例患者(77%)为纽约心脏协会I级,5例(18%)为II级,1例(2.7%)为III级。
该手术为纠正右心室发育不全或功能障碍提供了一种有效的替代方法。早期和中期随访结果与方坦手术的结果相比具有优势,但需要长期随访。