Center for Regenerative Medicine, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, Ohio; Department of General Surgery, Indiana University, Indianapolis, Indiana.
Center for Regenerative Medicine, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, Ohio.
J Surg Res. 2023 Aug;288:166-171. doi: 10.1016/j.jss.2023.02.020. Epub 2023 Mar 27.
Certain congenital cardiac lesions are at increased risk for the development of necrotizing enterocolitis (NEC). These patients are often reliant on pulmonary and systemic vasomodulators to maintain adequate perfusion and oxygenation. This study sought to determine whether pulmonary or systemic vasodilator treatment is protective against the development of NEC in this population.
We utilized International Classification of Diseases (ICD) codes to identify high risk congenital cardiac disease patients ≤6 mo of age, cared for at a tertiary children's hospital between January 2011 and January 2021. Cardiac anomalies were stratified into ductal dependent (pulmonary DD-P or systemic DD-S) or independent lesions. The rate of NEC development in those who received vasodilators (inhaled nitric oxide [iNO], pulmonary vasodilators, systemic vasodilators) was compared to controls in a multivariate analysis.
Of the 352 patients, who met inclusion criteria, 77.6% had ductal dependent lesions (DD-S 41.9%, DD-P 35.7%), 19.5% received iNO, and 37.5% received other vasodilatory drugs. The overall NEC rate was 15.1%. On univariate analysis, DD-S, iNO use, and systemic vasodilators was associated with a significantly higher risk of NEC, while DD-P was associated with lower NEC risk. On multivariate analysis, only iNO (odds ratio 2.725, confidence interval [1.36-5.44]) and DD-S (odds ratio 2.279, confidence interval [1.02-5.11]) were independent risk factors for NEC.
In patients with at-risk congenital cardiac disease lesions, a ductus dependent systemic circulation or iNO treatment is associated with an increased risk of developing NEC. The presence of iNO or DD-S should be utilized as markers of increased risk both in the prevention and workup of suspected NEC.
某些先天性心脏病变发生坏死性小肠结肠炎(NEC)的风险增加。这些患者通常依赖于肺和全身血管扩张剂来维持足够的灌注和氧合。本研究旨在确定在这一人群中,肺或全身血管扩张剂治疗是否能预防 NEC 的发生。
我们利用国际疾病分类(ICD)代码,确定了 2011 年 1 月至 2021 年 1 月期间在一家三级儿童医院接受治疗的≤6 月龄、患有高危先天性心脏病的患者。心脏畸形分为依赖导管(肺 DD-P 或全身 DD-S)或独立病变。在多变量分析中,比较了接受血管扩张剂(吸入一氧化氮(iNO)、肺血管扩张剂、全身血管扩张剂)治疗的患者与对照组 NEC 发展的发生率。
在符合纳入标准的 352 名患者中,77.6%患有导管依赖性病变(DD-S 41.9%,DD-P 35.7%),19.5%接受了 iNO 治疗,37.5%接受了其他血管扩张药物治疗。总的 NEC 发生率为 15.1%。在单变量分析中,DD-S、iNO 应用和全身血管扩张剂与 NEC 风险显著增加相关,而 DD-P 与 NEC 风险降低相关。在多变量分析中,只有 iNO(比值比 2.725,置信区间 [1.36-5.44])和 DD-S(比值比 2.279,置信区间 [1.02-5.11])是 NEC 的独立危险因素。
在患有高危先天性心脏病病变的患者中,依赖导管的全身循环或 iNO 治疗与发生 NEC 的风险增加相关。存在 iNO 或 DD-S 应作为预防和疑似 NEC 检查中增加风险的标志物。