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首页> 外文期刊>Frontiers in Pediatrics >Risk Factors for Necrotizing Enterocolitis in Infants With Patent Arterial Duct. A Retrospective Matched Paired Analysis
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Risk Factors for Necrotizing Enterocolitis in Infants With Patent Arterial Duct. A Retrospective Matched Paired Analysis

机译:婴幼儿动脉管道中坏死性小肠结肠炎的危险因素。 回顾性匹配配对分析

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Background: The development of necrotizing enterocolitis (NEC) in neonates with patent ductus arteriosus (PDA) is not well-understood. Our aim was to find risk factors for NEC in children with a significant PDA and to assess differences in mortality and duration of hospital stay between patients with PDA and those with PDA and NEC. Methods: We performed a retrospective single center case control study including infants with PDA scheduled for treatment. We compared multiple patient data between patients with PDA and those with PDA and NEC from 2004 to 2018 using 1:2 and 1:1 matching. Results: We used 1:2 matching with 26 NEC patients (cases) and 52 PDA patients without NEC (controls) and 1:1 matching with 5 NEC patients and 5 PDA patients without NEC. NEC patients had lower Apgar score (1′), more congenital malformations, more suspected sepsis, less hypotension, higher minimum platelet count and higher CRP-values during the week before NEC ( P 0.05, respectively). The mortality was higher in NEC cases [29% (9/31)] compared to the control patients [2% (1/57), P 0.001]. Lower Apgar score (1′) was correlated with an increased risk of NEC stage III. Hypotension was inversely correlated with the odds of NEC (OR 0.3). Conclusions: NEC increased mortality in infants with PDA. Hypotension did not increase the risk of NEC in infants with PDA. Routine clinical parameters were not able to predict NEC in infants who suffer from PDA.
机译:背景:具有专利导管术(PDA)的新生儿中坏死性肠腐殖炎(NEC)的发展尚未得到很好的理解。我们的目标是发现有重大PDA儿童的NEC的风险因素,并评估PDA患者与PDA和NEC患者之间死亡率和住院时间持续时间的差异。方法:我们进行了回顾性单中心案例控制研究,包​​括预定PDA进行治疗的婴儿。我们将PDA患者的多重患者数据与PDA和NEC的患者使用1:2和1:1:1匹配比较了PDA和NEC之间的多重患者数据。结果:我们使用了1:2与26名NEC患者(病例)和52名没有NEC(对照)的PDA患者和1:1与5个NEC患者的患者和52名没有NEC的患者匹配。 NEC患者的APGAR评分(1')较低,更新的畸形,更具疑似脓毒症,较少的低血压,在NEC之前的一周内的最低血小板计数和更高的CRP值(P <0.05分别)。与对照患者相比,NEC病例的死亡率较高[29%(9/31)] [2%(1/57),P& 0.001]。较低的APGAR评分(1')与NEC阶段III的风险增加相关。低血压与NEC的几率(或0.3)相反。结论:NEC在PDA的婴儿增加死亡率。低血压没有增加婴儿用PDA的NEC的风险。常规临床参数无法预测患有PDA的婴儿的NEC。

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