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1996 年至 2003 年,德克萨斯州功能性单心室婴儿出生后头 5 年的死亡率。

Mortality in first 5 years in infants with functional single ventricle born in Texas, 1996 to 2003.

机构信息

Department of Pediatrics, University of Texas Health Science Center, Dallas, USA.

出版信息

Circulation. 2010 Feb 9;121(5):644-50. doi: 10.1161/CIRCULATIONAHA.109.881904. Epub 2010 Jan 25.

Abstract

BACKGROUND

Infants with functional single ventricle have a high risk of death during the early years of life. Studies have reported improvement in postoperative survival, but they do not include preoperative deaths or those occurring before transfer. The purpose of this population-based study was to estimate 5-year survival in infants with functional single ventricle, to define factors associated with survival, and to estimate improvement in outcome.

METHODS AND RESULTS

Patients with hypoplastic left heart syndrome, pulmonary atresia intact ventricular septum, single ventricle, and tricuspid atresia born in 1996 to 2003 were identified from the Texas Birth Defects Registry and linked to state and national birth and death vital records. We examined the effects of defect type, birth era, birth weight, gestational age, maternal race/ethnicity, extracardiac anomalies, sex, and maternal age and education on survival. Five-year survival varied by defect type: hypoplastic left heart syndrome, 38.0% (95% confidence interval, 32.6 to 43.5); single ventricle, 56.1% (95% confidence interval, 49.9 to 61.7); pulmonary atresia intact ventricular septum, 55.7% (95% confidence interval, 45.8 to 64.4); and tricuspid atresia, 74.6% (95% confidence interval, 62.4 to 83.4). The presence of extracardiac defects increased the adjusted risk of death by 84%. Non-Hispanic blacks had an adjusted risk of death that was 41% higher than that for non-Hispanic whites, and Hispanics had a 26% higher risk. Patients born in 2001 to 2003 had a 47% lower risk than those born in 1996 to 2000.

CONCLUSIONS

This population-based study demonstrates significant improvement in overall 5-year survival, particularly in cases of hypoplastic left heart syndrome and single ventricle. Additional studies are needed to determine the factors causing racial/ethnic and regional differences in outcome.

摘要

背景

功能性单心室婴儿在生命早期死亡的风险很高。研究报告称术后生存率有所提高,但这些研究并未包括术前死亡或转移前死亡。本基于人群的研究旨在估计功能性单心室婴儿的 5 年生存率,确定与生存率相关的因素,并评估结果的改善情况。

方法和结果

从德克萨斯州出生缺陷登记处确定了 1996 年至 2003 年期间患有左心发育不全综合征、肺动脉闭锁伴完整室间隔、单心室和三尖瓣闭锁的患者,并与州和国家出生和死亡生命记录相联系。我们检查了缺陷类型、出生时代、出生体重、胎龄、母亲种族/民族、心脏外畸形、性别以及母亲年龄和教育对生存率的影响。5 年生存率因缺陷类型而异:左心发育不全综合征为 38.0%(95%置信区间,32.6 至 43.5);单心室为 56.1%(95%置信区间,49.9 至 61.7);肺动脉闭锁伴完整室间隔为 55.7%(95%置信区间,45.8 至 64.4);三尖瓣闭锁为 74.6%(95%置信区间,62.4 至 83.4)。存在心脏外畸形会使死亡风险增加 84%。非西班牙裔黑人的死亡风险比非西班牙裔白人高 41%,西班牙裔的死亡风险高 26%。2001 年至 2003 年出生的患者比 1996 年至 2000 年出生的患者死亡风险低 47%。

结论

本基于人群的研究表明,总体 5 年生存率显著提高,尤其是左心发育不全综合征和单心室患者。需要进一步研究以确定导致种族/民族和地区间结果差异的因素。

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