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房室间隔缺损与法洛四联症:15年经验

Atrioventricular septal defect and tetralogy of Fallot: a 15-year experience.

作者信息

Delius R E, Kumar R V, Elliott M J, Stark J, de Leval M R

机构信息

Cardiothoracic Unit, Great Ormond Street Hospital for Children, NHS Trust, London, UK.

出版信息

Eur J Cardiothorac Surg. 1997 Aug;12(2):171-6. doi: 10.1016/s1010-7940(97)00165-6.

Abstract

AIM

Atrioventricular septal defect and tetralogy of Fallot is a relatively uncommon lesion in which there is a risk of right ventricular dysfunction related to inlet and outlet valve problems. For this reason, conservative management involving an initial palliative procedure is often chosen. The aim of this report is to retrospectively review our experience with this lesion.

PATIENT POPULATION

35 patients with atrioventricular septal defect and tetralogy of Fallot have been surgically managed at this institution between January 1980 and June 1995. Twenty-one (60%) of these patients underwent 28 initial palliative shunt procedures. Fourteen (40%) patients underwent primary definitive repair. The criteria for choosing one management strategy over another was based on a number of factors, including age at presentation, anatomy of the lesion, and severity of symptoms. Of the 21 patients who underwent an initial shunt procedure, 15 have undergone definitive operation. Of the 6 patients who did not undergo definitive operation, three died (two directly related to complications of the shunt procedure), two are awaiting operation, and one was lost to follow-up.

RESULTS

The primary indication for operation in all patients was cyanosis. Freedom from reoperation at 5 years after definitive operation was 65.1% for all patients; most reoperations were related to left atrioventricular valve regurgitation or residual leaks across the ventricular septal defect patch. The operative mortality at definitive operation was 10.3% (70% CL 4.5-20%) for all patients. The actuarial estimate of survival 7 years following definitive repair was 77.3% (70% CL 68.7-85.9%) for all patients. The actuarial estimate of survival at 7 years was 84.4% (70% CL 73.8-95%) in the patients undergoing primary repair and 65% (70% CL 52.4-77.6%) in patients initially palliated if the mortality of the palliative shunt procedure is included (P = 0.35).

CONCLUSION

Patients with atrioventricular septal defect and tetralogy of Fallot can be successfully managed with a variety of surgical strategies. Primary repair may be a reasonable option in carefully selected patients, as this eliminates the morbidity and mortality of an initial shunt procedure and the subsequent interval between initial palliation and definitive repair.

摘要

目的

房室间隔缺损合并法洛四联症是一种相对罕见的病变,存在与流入道和流出道瓣膜问题相关的右心室功能障碍风险。因此,通常选择包括初始姑息手术在内的保守治疗方法。本报告的目的是回顾性分析我们在处理这种病变方面的经验。

患者群体

1980年1月至1995年6月期间,本机构对35例房室间隔缺损合并法洛四联症患者进行了手术治疗。其中21例(60%)患者接受了28次初始姑息分流手术。14例(40%)患者接受了一期根治性修复。选择一种治疗策略而非另一种的标准基于多种因素,包括就诊时的年龄、病变解剖结构和症状严重程度。在接受初始分流手术的21例患者中,15例接受了根治性手术。在未接受根治性手术的6例患者中,3例死亡(2例与分流手术并发症直接相关),2例等待手术,1例失访。

结果

所有患者手术的主要指征均为发绀。所有患者根治性手术后5年免于再次手术的比例为65.1%;大多数再次手术与左房室瓣反流或室间隔缺损补片残余漏有关。所有患者根治性手术的手术死亡率为10.3%(70%可信区间4.5 - 20%)。根治性修复后7年的精算生存率估计值为所有患者77.3%(70%可信区间68.7 - 85.9%)。如果将姑息分流手术的死亡率包括在内,一期修复患者7年的精算生存率估计值为84.4%(70%可信区间73.8 - 95%),初始接受姑息治疗患者为65%(70%可信区间52.4 - 77.6%)(P = 0.35)。

结论

房室间隔缺损合并法洛四联症患者可通过多种手术策略成功治疗。对于精心挑选的患者,一期修复可能是一个合理的选择,因为这消除了初始分流手术的发病率和死亡率以及初始姑息治疗与根治性修复之间的后续间隔。

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