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经导管闭合右心室发育不良儿童的房间隔缺损

Transcatheter closure of atrial septal defects in children with a hypoplastic right ventricle.

作者信息

Atiq Mehnaz, Lai Lillian, Lee Kyong-Jin, Benson Lee N

机构信息

Department of Pediatrics, Division of Cardiology, Hospital for Sick Children, University of Toronto School of Medicine, Toronto, Ontario, Canada.

出版信息

Catheter Cardiovasc Interv. 2005 Jan;64(1):112-6. doi: 10.1002/ccd.20245.

Abstract

The efficacy and safety of device closure of atrial defects in children with complex congenital heart disease and a hypoplastic right ventricle have not been detailed. The objective of this study was to determine the clinical impact and outcomes of a staged surgical catheter-based management strategy. A retrospective analysis of 17 children with a hypoplastic right ventricle who had undergone cardiac catheterization and attempted device occlusion of an atrial defect was undertaken. Clinical data, anatomical diagnoses, previous surgeries, and interventions were noted. The clinical course and echocardiographic findings were compared before and after defect closure (6 +/- 4 months of follow-up). Nine children had pulmonary atresia with an intact ventricular septum, six had Ebstein's anomaly of the tricuspid valve, and two had isolated right ventricular hypoplasia. The mean age at defect closure was 6.6 +/- 3.4 years. Under general anesthesia, closure of the atrial defect was undertaken after initial temporary test occlusion. The Qp:Qs ratio before closure was 1.1 +/- 0.4. Oxygen saturation improved in all children from 91% +/- 1% to 98% +/- 1% (P < 0.0005). Mean right atrial pressure increased from 9 +/- 3 to 11 +/- 4 mm Hg after closure, but the difference was not statistically significant (P = 0.2). Follow-up revealed an increased right ventricular length (P = 0.009) and Z-score (P = 0.02), although no significant increase in the diameter of the tricuspid valve annulus was observed in children with pulmonary atresia. Right ventricular systolic pressures or systolic function did not change significantly during follow-up (P = 0.5 and 0.29, respectively). Exercise tolerance improved in all children and clinical evidence of right ventricular decompensation was absent. Catheter closure of atrial defects in children with a hypoplastic right ventricle is well tolerated, safe, and effective as a treatment strategy in the staged management.

摘要

复杂先天性心脏病合并右心室发育不良患儿经导管封堵房间隔缺损的疗效和安全性尚未详细报道。本研究的目的是确定基于分期手术导管治疗策略的临床影响和结果。对17例右心室发育不良且接受过心导管检查并尝试封堵房间隔缺损的患儿进行了回顾性分析。记录了临床资料、解剖诊断、既往手术及干预情况。比较了缺损封堵前后(随访6±4个月)的临床过程和超声心动图结果。9例患儿为室间隔完整的肺动脉闭锁,6例为三尖瓣埃布斯坦畸形,2例为孤立性右心室发育不良。缺损封堵时的平均年龄为6.6±3.4岁。在全身麻醉下,初始临时试验封堵后进行房间隔缺损封堵。封堵前的Qp:Qs比值为1.1±0.4。所有患儿的血氧饱和度从91%±1%提高到98%±1%(P<0.0005)。封堵后平均右心房压力从9±3mmHg升高至11±4mmHg,但差异无统计学意义(P = 0.2)。随访显示右心室长度增加(P = 0.009)和Z值增加(P = 0.02),尽管肺动脉闭锁患儿的三尖瓣环直径未观察到显著增加。随访期间右心室收缩压或收缩功能无显著变化(分别为P = 0.5和0.29)。所有患儿的运动耐量均有改善且无右心室失代偿的临床证据。右心室发育不良患儿经导管封堵房间隔缺损作为分期治疗策略耐受性良好、安全且有效。

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