Hisamochi K, Ishino K, Kawada M, Ohshima Y, Aoki A, Arai S, Sano S
Department of Cardiovascular Surgery, Okayama University Medical School, Okayama, Japan.
Kyobu Geka. 2001 Jul;54(8 Suppl):671-5.
We have preferably utilized monocusp valved outflow patch (MVOP) for right ventricular outflow tract (RVOT) reconstruction in pulmonary atresia with ventricular septal defect (PA + VSD). The purpose of this study was to evaluate the influence of the presence of major aorto-pulmonary collateral arteries (MAPCAs) on probability of MVOP reconstruction and development of RVOT restenosis in midterm. 49 patients underwent complete repair (either MVOP reconstruction or Rastelli procedure) of PA + VSD in our service. These patients were divided into 2 groups: group 1; 21 patients with MAPCAs, group 2; 28 patients without MAPCAs. There was one operative death (group 1). The probably of MVOP reconstruction was similar between group 1 and group 2 (71 vs 79%, p = 0.57, chi 2 test). Follow-up was completed for 48 survivors with the period ranged 3-108 months (mean 47 months). In group 1, one patient died suddenly at home 10 months after surgery. For 47 long-term patients, the ratio of freedom from RVOT restenosis was 72% (95% CI: 52-92%, Kaplan-Meier method) at 5 year. There was no difference between 2 groups (group 1; 73%, 95% CI: 45-100%, group 2; 74%, 95% CI: 48-99%, respectively, p = 0.85 by Log-Rank test). The presence of MAPCAs in PA + VSD was not a risk factor for either the probably of MVOP reconstruction or development of RVOT restenosis in midterm.
在肺动脉闭锁合并室间隔缺损(PA + VSD)的手术中,我们优先使用单瓣带瓣流出道补片(MVOP)来重建右心室流出道(RVOT)。本研究的目的是评估中期主要体肺侧支动脉(MAPCAs)的存在对MVOP重建概率及RVOT再狭窄发生情况的影响。我们科室有49例患者接受了PA + VSD的完全修复(MVOP重建或Rastelli手术)。这些患者被分为两组:第1组,21例有MAPCAs的患者;第2组,28例无MAPCAs的患者。有1例手术死亡(第1组)。第1组和第2组MVOP重建的概率相似(分别为71%和79%,p = 0.57,卡方检验)。48例幸存者完成了随访,随访时间为3 - 108个月(平均47个月)。在第1组中,1例患者术后10个月在家中突然死亡。对于47例长期随访患者,5年时无RVOT再狭窄的比例为72%(95%可信区间:52 - 92%,Kaplan - Meier法)。两组之间无差异(第1组为73%,95%可信区间:45 - 100%;第2组为74%,95%可信区间:48 - 99%,Log - Rank检验p = 0.85)。PA + VSD中MAPCAs的存在既不是MVOP重建概率的危险因素,也不是中期RVOT再狭窄发生的危险因素。