Department of Cardiovascular Surgery, Children's Hospital Boston, Boston, Mass., USA.
J Thorac Cardiovasc Surg. 2012 Feb;143(2):338-43. doi: 10.1016/j.jtcvs.2011.05.031. Epub 2011 Sep 8.
Long-term outcomes of repair of tetralogy of Fallot associated with complete atrioventricular septal defect are seldom reported. We report our survival and reintervention outcomes over a 29-year time period.
Between March 1979 and April 2008, 61 patients with the combined cardiac defect of atrioventricular septal defect and tetralogy of Fallot were surgically managed. Trisomy 21 was present in 49 (80%) patients. Primary repair was performed in 36 patients at a median age of 9 months (range, 1 month to 16 years), whereas 25 patients had initial palliation by systemic-pulmonary shunt at a median age of 21 months (range, 0 days to 36 years). Thirty-one (51%) patients had a transannular patch. Fifty-three patients required right ventriculotomy for relief of the right ventricular outflow tract obstruction. Four patients had a right ventricle-pulmonary artery conduit with a homograft. Relationships between patient characteristics and outcome variables were examined using Kaplan-Meier survival curves; comparisons were performed using the log-rank test.
Median follow-up was 4.7 years. A total of 12 patients died during the course of follow-up: 4 (7%)deaths within 30 days of surgery and 8 late deaths (range, 4 months to 9.9 years after repair). Since 2000, there have been no early deaths and 1 late death, 5 months after the operation. The estimated survival at 5 years after definitive repair was 82% (95% confidence interval, 69%, 90%). Time to death was not associated with any patient or surgical variables examined. Overall, 30% of the survivors required a reoperation. The type of reoperations was on the mitral valve (4 repairs, 4 replacements) and 7 pulmonary valve replacements. We did not find an effect of era on mortality (P = .23 for comparison of 1979-1989, 1990-1999, and 2000-2008). The percentage of patients with primary repair did not change during the different quartiles. The estimated freedom from reoperation at 5 years was 80% (65%, 90%). Time to reoperation was shorter for patients with a conduit (P = .01).
Excellent long-term survival was achieved after repair of tetralogy of Fallot associated with complete atrioventricular septal defect. Palliation and primary repair resulted in comparable outcomes; as such, primary repair is favored. The choice of right ventricular outflow tract reconstruction affects the need for reoperation.
法洛四联症合并完全性房室间隔缺损的长期治疗效果鲜有报道。本文报告了我们在 29 年的时间内的生存和再干预结果。
1979 年 3 月至 2008 年 4 月,共有 61 例同时合并房室间隔缺损和法洛四联症的患者接受了手术治疗。21 例(80%)患者存在 21 三体综合征。其中,36 例患者在中位年龄 9 个月(1 个月至 16 岁)时接受了一期根治术,25 例患者在中位年龄 21 个月(0 天至 36 岁)时接受了体肺分流术。31 例患者接受了跨环补片。53 例患者因右心室流出道梗阻接受了右心室切开术。4 例患者接受了同种带瓣肺动脉。采用 Kaplan-Meier 生存曲线分析患者特征与预后变量之间的关系,采用对数秩检验进行比较。
中位随访时间为 4.7 年。随访期间共有 12 例患者死亡:4 例(7%)死亡发生在术后 30 天内,8 例(4 个月至 9.9 年)为晚期死亡。自 2000 年以来,无早期死亡,仅有 1 例晚期死亡,发生在术后 5 个月。根治术后 5 年生存率为 82%(95%置信区间,69%,90%)。死亡时间与任何患者或手术变量均无关。总的来说,30%的幸存者需要再次手术。再手术的类型为二尖瓣(4 例修复,4 例置换)和 7 例肺动脉瓣置换。我们没有发现不同时期死亡率的差异有统计学意义(1979-1989、1990-1999 和 2000-2008 年的比较,P =.23)。不同四分位期间一期根治术的比例没有变化。根治术后 5 年免于再次手术的比例为 80%(65%,90%)。带管患者的再手术时间更短(P =.01)。
法洛四联症合并完全性房室间隔缺损的患者,经根治术后获得了良好的长期生存。姑息治疗和一期根治术的效果相当,因此更倾向于选择一期根治术。右心室流出道重建的选择影响再次手术的需求。