Division of Medicine, KK Women's and Children's Hospital, Singapore; Duke-NUS Medical School, Singapore; Cancer and Stem Cell Biology Program, Duke-NUS Medical School, Singapore; Humphrey Oei Institute of Cancer Research, National Cancer Center, Singapore; Institute of Molecular and Cell Biology, A*STAR, Singapore; Pediatric Brain Tumor Research Office, SingHealth-Duke-NUS Academic Medical Center, Singapore.
Department of Neonatology, KK Women's and Children's Hospital, Singapore.
Pediatr Neonatol. 2020 Aug;61(4):385-392. doi: 10.1016/j.pedneo.2020.03.003. Epub 2020 Mar 13.
Congenital diaphragmatic hernia (CDH) is a common birth defect associated with significant mortality and morbidity. There is limited outcome data on CDH in the Southeast Asian region. Rapid accessibility to our CDH Perinatal Center, as a consequence of the small geographic size of our country and efficient land transportation system, has largely eliminated deaths of live outborn babies prior arrival at our center. We selected a study period when extracorporeal membrane oxygenation (ECMO) support was not available at our institution. The data will therefore be relevant in developing management guidelines and antenatal counselling for perinatal centers in this region managing CDH with limited resources, without ECMO facilities.
A retrospective study of antenatally or postnatally diagnosed CDH infants born between January 2002 and June 2005 was performed. We selected this study period as ECMO support was not available over this period. We studied the demographics, clinical characteristics, postnatal predictors of mortality and outcomes of CDH infants in a single tertiary institution.
A total of 24 patients with CDH were identified. Seventy-nine percent of liveborns with CDH survived to hospital discharge. Antenatal detection rate was 83.3%. Significant postnatal predictors of mortality were preoperative pneumothorax (p = 0.035), high CRIB score (p = 0.007), low one- and five-minute Apgar score (p = 0.011, p = 0.026 respectively) and high pCO2 on initial arterial blood gas (p = 0.007). At one-year follow-up, three patients had delayed gross motor milestones which resolved subsequently. Re-admissions were required for recurrent bronchiolitis (33%) and oesophageal reflux which resolved in all cases. Two (13.3%) infants had surgical complications and needed re-admission for probable adhesive intestinal obstruction; one required adhesiolysis and the other was managed conservatively with good outcome.
A single-center CDH outcome in Singapore, without ECMO use, was good. This is a cohort now with long-term survival outcome which will be valuable to the neonatology community.
先天性膈疝(CDH)是一种常见的出生缺陷,与较高的死亡率和发病率相关。东南亚地区关于 CDH 的结果数据有限。由于我国的国土面积较小,陆地交通系统高效,我们的 CDH 围产期中心能够快速接诊,这在很大程度上避免了在到达我们中心之前活产婴儿的死亡。我们选择了一个在我们机构没有体外膜肺氧合(ECMO)支持的研究时间段。因此,该数据将有助于为该地区没有 ECMO 设施的围产期中心制定管理指南和产前咨询,以管理 CDH 患儿。
对 2002 年 1 月至 2005 年 6 月期间出生的产前或产后诊断为 CDH 的婴儿进行了回顾性研究。我们选择了这段研究时间,因为在此期间没有 ECMO 支持。我们在一家三级医疗机构中研究了 CDH 婴儿的人口统计学、临床特征、出生后死亡率的预测因素和结局。
共确定了 24 例 CDH 患儿。79%的活产 CDH 患儿存活至出院。产前检出率为 83.3%。死亡率的显著预测因素为术前气胸(p=0.035)、高 CRIB 评分(p=0.007)、低 1 分钟和 5 分钟 Apgar 评分(p=0.011,p=0.026)以及初始动脉血气的高 pCO2(p=0.007)。在 1 年随访时,3 例患儿出现粗大运动发育迟缓,随后得到解决。因复发性细支气管炎(33%)和食管反流而再次入院,所有病例均得到解决。2 例(13.3%)患儿出现手术并发症,需要再次入院治疗可能的粘连性肠梗阻;1 例需要粘连松解,另 1 例经保守治疗效果良好。
新加坡单中心 CDH 患儿的结局(未使用 ECMO)良好。这是一个现在具有长期生存结局的队列,这对新生儿科社区将是有价值的。