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先天性心脏缺陷手术后感染性心内膜炎的30年发病率。

Thirty-year incidence of infective endocarditis after surgery for congenital heart defect.

作者信息

Morris C D, Reller M D, Menashe V D

机构信息

Congenital Heart Disease Research Center, Division of Medical Informatics and Outcomes Research, Oregon Health Sciences University, Portland 97201, USA.

出版信息

JAMA. 1998 Feb 25;279(8):599-603. doi: 10.1001/jama.279.8.599.

Abstract

CONTEXT

The incidence of infective endocarditis after surgical repair of congenital heart defects is unknown.

OBJECTIVE

To determine the long-term incidence of endocarditis after repair of any of 12 congenital heart defects in childhood.

DESIGN

Population-based registry started in 1982.

SETTING

State of Oregon.

PARTICIPANTS

All Oregon residents who underwent surgical repair for 1 of 12 major congenital defects at the age of 18 years or younger from 1958 to the present.

MAIN OUTCOME MEASURE

Diagnosis of infective endocarditis confirmed by hospital or autopsy records.

RESULTS

Follow-up data were obtained from 88% of this cohort of 3860 individuals through 1993. At 25 years after surgery, the cumulative incidence of infective endocarditis was 1.3% for tetralogy of Fallot, 2.7% for isolated ventricular septal defect, 3.5% for coarctation of the aorta, 13.3% for valvular aortic stenosis, and 2.8% for primum atrial septal defect. In the cohorts with shorter follow-up, at 20 years after surgery the cumulative incidence was 4.0% for dextrotransposition of the great arteries; at 10 years, the cumulative incidence was 1.1% for complete atrioventricular septal defect, 5.3% for pulmonary atresia with an intact ventricular septum, and 6.4% for pulmonary atresia with ventricular septal defect. No children with secundum atrial septal defect, patent ductus arteriosus, or pulmonic stenosis have had infective endocarditis after surgery.

CONCLUSION

The continuing incidence of endocarditis after surgery for congenital heart defect, particularly valvular aortic stenosis, merits education about endocarditis prophylaxis for children and adults with repaired congenital heart defects.

摘要

背景

先天性心脏缺陷手术修复后感染性心内膜炎的发病率尚不清楚。

目的

确定儿童期12种先天性心脏缺陷中任何一种修复后心内膜炎的长期发病率。

设计

始于1982年的基于人群的登记。

地点

俄勒冈州。

参与者

1958年至现在,俄勒冈州所有18岁及以下接受过12种主要先天性缺陷之一手术修复的居民。

主要观察指标

通过医院或尸检记录确诊的感染性心内膜炎。

结果

截至1993年,从这3860名个体的队列中88%的人获得了随访数据。术后25年,法洛四联症感染性心内膜炎的累积发病率为1.3%,孤立性室间隔缺损为2.7%,主动脉缩窄为3.5%,瓣膜性主动脉狭窄为13.3%,原发孔房间隔缺损为2.8%。在随访时间较短的队列中,术后20年大动脉转位的累积发病率为4.0%;术后10年,完全性房室间隔缺损的累积发病率为1.1%,室间隔完整的肺动脉闭锁为5.3%,室间隔缺损的肺动脉闭锁为6.4%。继发孔房间隔缺损、动脉导管未闭或肺动脉狭窄的儿童术后均未发生感染性心内膜炎。

结论

先天性心脏缺陷手术后心内膜炎的持续发病率,尤其是瓣膜性主动脉狭窄,值得对先天性心脏缺陷修复后的儿童和成人进行心内膜炎预防教育。

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