Liu Tai-Xiang, Du Li-Zhong, Ma Xiao-Lu, Chen Zheng, Shi Li-Ping
Department of NICU, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Hangzhou, China.
Front Pediatr. 2022 Sep 9;10:940289. doi: 10.3389/fped.2022.940289. eCollection 2022.
Omphalocele is a common congenital defect of the abdominal wall, management of giant omphalocele (GO) is particularly for pediatric surgeons and neonatologists worldwide. The current study aimed to review and summarize the clinical features and prognosis in neonates with GO complicated with pulmonary hypertension (PH), which is associated with increased mortality, while in hospital.
Medical records of infants with GO between July 2015 and June 2020 were retrospectively analyzed. The patients enrolled were divided into PH and non-PH groups based on the presence or absence of PH, and patients with PH were divided into death and survival groups based on survival status. Clinical characteristics and outcomes were compared between groups, respectively. The risk factors for PH were analyzed by binary logistic regression.
In total, 67 neonates were identified as having GO and 24 (35.8%) were complicated with PH. Infants with PH were associated with intubation within 24 h after birth ( = 0.038), pulmonary dysplasia ( = 0.020), presence of patent ductus arteriosus (PDA; = 0.028), a staged operation ( = 0.002), longer mechanical ventilation days ( < 0.001), oxygen requirement days ( < 0.001), parenteral nutrition (PN) days ( < 0.001), length of neonatal intensive care unit (NICU) or hospital stay ( = 0.001 and 0.002, respectively), and mortality ( = 0.001). The results of multivariable logistic regression analysis revealed that a staged operation was independently associated with PH. In addition, PH patients with lower birth weight, higher peak of pulmonary arterial systolic pressure, and refractory to pulmonary vasodilators (PVD) had increased mortality.
Pulmonary hypertension is a serious complication and significantly increases the mortality and morbidities in infants with a GO. In addition, early and serial assessment of PH by echocardiography should be a routine screening scheme, especially in the neonatal omphalocele population who required a staged surgical repair. Clinicians should be aware that infants with PH who had low weight, severe and refractory PH have a higher risk of death.
脐膨出是一种常见的腹壁先天性缺陷,巨大脐膨出(GO)的治疗尤其困扰着全球的小儿外科医生和新生儿科医生。本研究旨在回顾和总结合并肺动脉高压(PH)的GO新生儿的临床特征和预后,PH与住院期间死亡率增加相关。
回顾性分析2015年7月至2020年6月期间患有GO的婴儿的病历。根据是否存在PH将纳入的患者分为PH组和非PH组,根据生存状态将PH患者分为死亡组和存活组。分别比较两组的临床特征和结局。采用二元逻辑回归分析PH的危险因素。
总共67例新生儿被诊断为患有GO,其中24例(35.8%)合并PH。合并PH的婴儿与出生后24小时内插管(P = 0.038)、肺发育不良(P = 0.020)、动脉导管未闭(PDA;P = 0.028)、分期手术(P = 0.002)、机械通气天数延长(P < 0.001)、吸氧天数(P < 0.001)、肠外营养(PN)天数(P < 0.001)、新生儿重症监护病房(NICU)住院时间或住院时间(分别为P = 0.001和0.002)以及死亡率(P = 0.001)相关。多变量逻辑回归分析结果显示,分期手术与PH独立相关。此外,出生体重较低、肺动脉收缩压峰值较高且对肺血管扩张剂(PVD)难治的PH患者死亡率增加。
肺动脉高压是一种严重的并发症,显著增加GO婴儿的死亡率和发病率。此外,通过超声心动图对PH进行早期和系列评估应成为常规筛查方案,尤其是在需要分期手术修复的新生儿脐膨出人群中。临床医生应意识到,体重低、PH严重且难治的PH婴儿死亡风险更高。