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唐氏综合征患儿的完全性房室间隔缺损:越来越小年龄手术矫治的良好效果

[Complete atrioventricular septal defect in children with Down's syndrome: good results of surgical correction at younger and younger ages].

作者信息

Kortenhorst M S Q, Hazekamp M G, Rammeloo L A J, Schoof P H, Ottenkamp J

机构信息

Centrum Aangeboren Hartafwijkingen Amsterdam/Leiden, Leids Universitair Medisch Centrum, Willem-Alexander Kinder- & Jeugd-centrum, Postbus 9600, 2300 RC, Leiden.

出版信息

Ned Tijdschr Geneeskd. 2005 Mar 12;149(11):589-93.

Abstract

OBJECTIVE

To evaluate the results of cardiosurgical treatment of children with Down's syndrome and a complete atrioventricular septal defect (cAVSD).

DESIGN

Retrospective.

METHOD

Data were collected from the records of all patients with Down's syndrome who had been subjected to primary corrective surgery for cAVSD in the period 1980-2003 in Leiden, The Netherlands. Exclusion criteria were: concomitant tetralogy of Fallot or interruption of the aortic arch and palliative banding of the pulmonary artery. Children with an abnormal shape of the ventricle making it impossible to correct biventricularly were not considered in the study. Data on mortality >30 days after the operation and on repeated surgery were included in the analysis if the duration of follow-up was at least 5 years.

RESULTS

The group comprised 148 children: 75 girls and 73 boys. The median age at time of surgery was 20 weeks (range: 6 weeks to 3.7 years) and showed a statistically significant decrease during the period under investigation. Of 4 children lost to clinical follow-up actual data could be obtained. The median duration offollow-up was 6 years and 7 months (range: 38 days to 23 years and 11 months). 28 children (19%) died. The mortality within 30 days after the operation decreased from 0-38% in the period 1980-1989 via 0-30% in the period 1990-1999 to 0% in 2000-2003. The percentage ofreoperations related to the correction ofcAVSD (14%; 14/98) did not seem to increase. Of the correction-related reoperations, 14% (2/14) were followed by a second reoperation. Conclusion. In the period 1980-2003, children with Down's syndrome and a cAVSD were corrected surgically at a younger and younger age. The early mortality decreased to 0% in the years 2000-2003. Echocardiography in the first weeks of life for all children with Down's syndrome makes it possible to diagnose those with a cAVSD early enough for surgical repair.

摘要

目的

评估唐氏综合征合并完全性房室间隔缺损(cAVSD)患儿的心脏外科治疗效果。

设计

回顾性研究。

方法

收集1980年至2003年期间在荷兰莱顿接受cAVSD一期矫正手术的所有唐氏综合征患者的记录。排除标准为:合并法洛四联症或主动脉弓中断以及肺动脉姑息性束带术。心室形态异常无法进行双心室矫正的患儿未纳入本研究。如果随访时间至少为5年,则将术后30天以上的死亡率数据和再次手术数据纳入分析。

结果

该组包括148名儿童:75名女孩和73名男孩。手术时的中位年龄为20周(范围:6周至3.7岁),且在研究期间呈统计学显著下降。4名失访儿童可获得实际数据。中位随访时间为6年7个月(范围:38天至23年11个月)。28名儿童(19%)死亡。术后30天内的死亡率从1980 - 1989年期间的0 - 38%降至1990 - 1999年期间的0 - 30%,并在2000 - 2003年降至0%。与cAVSD矫正相关的再次手术百分比(14%;14/98)似乎并未增加。在与矫正相关的再次手术中,14%(2/14)之后进行了第二次再次手术。结论:在1980 - 2003年期间,唐氏综合征合并cAVSD的患儿接受手术矫正的年龄越来越小。2000 - 2003年早期死亡率降至0%。对所有唐氏综合征患儿在出生后第一周进行超声心动图检查,有可能足够早地诊断出患有cAVSD的患儿以便进行手术修复。

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