Hodgson Kate, Togo Andrea, Moore Aideen M, Moody Amanda, King Sebastian K, Zani Augusto
Division of Neonatology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Neonatal Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.
J Paediatr Child Health. 2018 Aug;54(8):872-874. doi: 10.1111/jpc.13905. Epub 2018 Mar 30.
Isolated oesophageal perforation in neonates is a rare but potentially life-threatening condition. Although management has historically been operative, conservative management (antibiotics, bowel rest, parenteral nutrition) is now more routinely used. The aim of this study was to evaluate the management of this condition in two large neonatal surgical centres.
A retrospective cohort study was conducted for neonates admitted to The Hospital for Sick Children (Toronto, Canada) or The Royal Children's Hospital (Melbourne, Australia) with a diagnosis of oesophageal perforation, from 2006 to 2016. Patients with oesophageal atresia or tracheo-oesophageal fistula were excluded. Data were collected from chart review regarding demographics, clinical course, management and outcomes.
Eleven neonates with oesophageal perforation were identified over a 10-year period at the two centres. Median gestational age at birth was 25.3 weeks (interquartile range 24.2-28.8) and the majority (7/11, 64%) of neonates were extremely low birthweight. Diagnosis was made on day 1 of life for 9 of 11 (81%) neonates and was secondary to nasogastric tube insertion in 10 of 11 (91%) neonates. Only four (36%) neonates had symptomatic complications. All neonates were managed with bowel rest and intravenous antibiotics for a median of 7 days (interquartile range 7-10); two patients required operative intervention. Three neonates (27%) developed chronic lung disease and two (19%) died prior to discharge.
Oesophageal perforation is severe complication secondary to instrumentation of the upper gastrointestinal tract in neonates. Prompt and accurate diagnosis is crucial. Non-operative management is effective for the majority, though morbidity is common.
新生儿孤立性食管穿孔是一种罕见但可能危及生命的疾病。虽然过去一直采用手术治疗,但现在更常规地使用保守治疗(抗生素、肠道休息、肠外营养)。本研究的目的是评估两个大型新生儿外科中心对这种疾病的治疗情况。
对2006年至2016年期间入住加拿大多伦多病童医院或澳大利亚墨尔本皇家儿童医院且诊断为食管穿孔的新生儿进行回顾性队列研究。排除食管闭锁或气管食管瘘患者。通过查阅病历收集有关人口统计学、临床过程、治疗和结局的数据。
在这两个中心的10年期间共确定了11例食管穿孔新生儿。出生时的中位胎龄为25.3周(四分位间距24.2 - 28.8),大多数(7/11,64%)新生儿为极低出生体重儿。11例新生儿中有9例(81%)在出生第1天确诊,11例中有10例(91%)是鼻胃管插入继发穿孔。只有4例(36%)新生儿出现有症状的并发症。所有新生儿均进行肠道休息并静脉使用抗生素,中位时间为7天(四分位间距7 - 10);2例患者需要手术干预。3例新生儿(27%)发生慢性肺病,2例(19%)在出院前死亡。
食管穿孔是新生儿上消化道器械操作继发的严重并发症。及时准确的诊断至关重要。非手术治疗对大多数患者有效,尽管发病率很常见。