Siffel Csaba, Riehle-Colarusso Tiffany, Oster Matthew E, Correa Adolfo
National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia; College of Allied Health Sciences, Georgia Regents University, Augusta, Georgia;
National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia;
Pediatrics. 2015 Oct;136(4):e864-70. doi: 10.1542/peds.2014-1427. Epub 2015 Sep 21.
To examine the survival of infants with hypoplastic left heart syndrome (HLHS) and potential influence of demographic and clinical characteristics on survival using population-based data.
Infants with nonsyndromic HLHS (n = 212) born between 1979 and 2005 were identified through the Metropolitan Atlanta Congenital Defects Program. Vital status was ascertained through 2009 based on linkage with vital records. We estimated Kaplan-Meier survival probabilities stratified by select demographic and clinical characteristics.
The overall survival probability to 2009 was 24% and significantly improved over time: from 0% in 1979-1984 to 42% in 1999-2005. Survival probability was 66% during the first week, 27% during the first year of life, and 24% during the first 10 years. Survival of very low and low birth weight or preterm infants and those born in high-poverty neighborhoods was significantly poorer. For children with information on surgical intervention (n = 88), the overall survival was 52%, and preterm infants had significantly poorer survival (31%) compared with term infants (56%). For children who survived to 1 year of age, long-term survival was ∼90%.
Survival to adolescence of children with nonsyndromic HLHS born in metropolitan Atlanta has significantly improved in recent years, with those born full term, with normal birth weight, or in a low-poverty neighborhood having a higher survival probability. Survival beyond infancy to adolescence is high. A better understanding of the growing population of survivors with HLHS is needed to inform resource planning.
利用基于人群的数据,研究左心发育不全综合征(HLHS)患儿的生存率以及人口统计学和临床特征对生存率的潜在影响。
通过大亚特兰大先天性缺陷项目确定1979年至2005年期间出生的非综合征性HLHS患儿(n = 212)。根据与生命记录的关联确定截至2009年的生命状态。我们估计了按选定的人口统计学和临床特征分层的Kaplan-Meier生存概率。
到2009年的总体生存概率为24%,且随时间显著提高:从1979 - 1984年的0%提高到1999 - 2005年的42%。第一周的生存概率为66%,一岁时为27%,前10年为24%。极低和低出生体重或早产婴儿以及出生在高贫困社区的婴儿生存率明显较差。对于有手术干预信息的儿童(n = 88),总体生存率为52%,与足月儿(56%)相比,早产儿的生存率明显较差(31%)。对于存活至1岁的儿童,长期生存率约为90%。
近年来,在大亚特兰大出生的非综合征性HLHS患儿到青春期的生存率有显著提高,足月、出生体重正常或出生在低贫困社区的患儿生存率更高。婴儿期后至青春期的生存率较高。需要更好地了解HLHS存活者不断增加的人群情况,以为资源规划提供信息。