Bagdure Dayanand, Torres Natalie, Walker L Kyle, Waddell Jaylyn, Bhutta Adnan, Custer Jason W
Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland, United States.
Department of Pediatrics, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware, United States.
J Pediatr Intensive Care. 2017 Sep;6(3):188-193. doi: 10.1055/s-0037-1598036. Epub 2017 Feb 6.
Congenital anomalies of the kidney and urinary tract constitute up to 30% of anomalies identified in the neonatal period. In utero oligohydramnios is often associated with pulmonary hypoplasia and respiratory failure in the neonate who may not be responsive to mechanical ventilation. Placement of these neonates on extracorporeal membrane oxygenation (ECMO) remains controversial and is considered in most centers to be a relative contraindication. The objective of this study is to use the Extracorporeal Life Support Organization (ELSO) database to describe the outcomes and complications of patients with congenital renal and urogenital anomalies with pulmonary hypoplasia who underwent ECMO in the neonatal period. Data from the ELSO registry were retrospectively reviewed for all patients with congenital renal and urogenital anomalies with pulmonary hypoplasia treated with ECMO support between 1990 and November 2014 using ICD-9 diagnosis codes. We identified 45 patients. The average age of the patient at the time of ECMO was 1.7 days (range: 0-14 days) and weight was 3.1 kg (interquartile range [IQR]: 2.5-3.3). Patients spent an average of 162 hours on ECMO (IQR: 81-207). The majority of patients were managed with venoarterial ECMO (60%), and the overall survival of this cohort was 42%. Survivors had higher weights (3.4 vs. 2.8 kg; < 0.019) and were more likely to be male (90 vs. 44%; < 0.002). Patients with obstructive urogenital lesions had an overall survival of 71 versus 16.6% in patients with a primary intrinsic renal diagnosis ( = 0.004). Renal replacement therapy was required in 51% of the patients during their ECMO support. Neonates with renal or urogenital disease and pulmonary hypoplasia have an overall survival rate of 42%. Patients with a diagnosis of urogenital obstruction have much more favorable outcomes when compared with those with intrinsic renal disease such as polycystic kidney disease.
先天性肾和尿路异常占新生儿期发现的异常的30%。宫内羊水过少常与新生儿肺发育不全和呼吸衰竭相关,这些新生儿可能对机械通气无反应。将这些新生儿置于体外膜肺氧合(ECMO)治疗仍存在争议,在大多数中心被视为相对禁忌证。本研究的目的是利用体外生命支持组织(ELSO)数据库描述新生儿期接受ECMO治疗的先天性肾和泌尿生殖系统异常合并肺发育不全患者的治疗结果和并发症。
使用ICD-9诊断编码对1990年至2014年11月期间接受ECMO支持治疗的所有先天性肾和泌尿生殖系统异常合并肺发育不全患者的ELSO登记数据进行回顾性分析。
我们确定了45例患者。ECMO治疗时患者的平均年龄为1.7天(范围:0 - 14天),体重为3.1 kg(四分位间距[IQR]:2.5 - 3.3)。患者接受ECMO治疗的平均时间为162小时(IQR:81 - 207)。大多数患者采用静脉 - 动脉ECMO治疗(60%),该队列的总体生存率为42%。存活者体重更高(3.4 vs. 2.8 kg;P < 0.019),且更可能为男性(90% vs. 44%;P < 0.002)。泌尿生殖系统梗阻性病变患者的总体生存率为71%,而原发性肾内疾病患者为16.6%(P = 0.004)。51%的患者在ECMO支持期间需要肾脏替代治疗。
患有肾或泌尿生殖系统疾病及肺发育不全的新生儿总体生存率为42%。与患有诸如多囊肾病等原发性肾内疾病的患者相比,诊断为泌尿生殖系统梗阻的患者预后要好得多。