...
首页> 外文期刊>Early human development >Very low birth weight neonates who survive early-onset sepsis do not have an increased risk of developing late-onset sepsis
【24h】

Very low birth weight neonates who survive early-onset sepsis do not have an increased risk of developing late-onset sepsis

机译:幸存于早发性败血症的极低出生体重的新生儿并没有增加发生晚发性败血症的风险

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background: Very low birth weight neonates (≤ 1500 g, VLBWs) have a high rate of infection and distinct baseline immune function compared with more mature populations. In critically ill children and adults, sepsis increases subsequent infection risk. It is unknown whether sepsis modifies the risk of subsequent infection in VLBWs. Methods: We conducted a retrospective cohort study of VLBWs ≤ 32. weeks of gestation at birth cared for in 312 neonatal intensive care units in the United States from 1997 to 2011 (n = 103,376). Early-onset sepsis (EOS, culture-positive only) and late-onset sepsis (LOS, culture-positive or clinical) cases were identified. Cox proportional hazard models were used to control for clinical variables between neonates with and without EOS to determine if EOS modified risk of LOS, necrotizing enterocolitis (NEC), or death. Results: LOS occurred in 12,112/102,317 (11.8%) neonates without EOS and in 133/1059 (12.6%) of those with EOS. After adjustment for clinical variables, the risk of LOS was not different between neonates with or without a history of EOS (hazard ratio [HR] = 0.92; 95% confidence interval [CI] 0.74, 1.16). EOS increased the risk of 120-day mortality (HR = 1.78; 95% CI 1.49, 2.13). Conclusions: In contrast to findings in children and adults, EOS was not associated with an increased risk of LOS in this cohort. Age-specific investigations are needed to determine if post-sepsis immunologic alterations are present.
机译:背景:与较成熟的人群相比,极低出生体重的新生儿(≤1500 g,VLBWs)感染率高,基线免疫功能独特。在重症儿童和成人中,败血症会增加随后的感染风险。脓毒症是否会改变VLBWs后续感染的风险尚不清楚。方法:1997年至2011年,我们在美国312个新生儿重症监护病房中对出生时妊娠≤32周的VLBW进行了回顾性队列研究(n = 103,376)。确定了早发性败血症(EOS,仅培养阳性)和晚发性败血症(LOS,培养阳性或临床)病例。使用Cox比例风险模型控制有和没有EOS的新生儿之间的临床变量,以确定EOS是否可以改善LOS,坏死性小肠结肠炎(NEC)或死亡的风险。结果:LOS发生在没有EOS的12,112 / 102,317(11.8%)新生儿和有EOS的133/1059(12.6%)中。调整临床变量后,有或没有EOS病史的新生儿之间LOS的风险无差异(危险比[HR] = 0.92; 95%置信区间[CI] 0.74,1.16)。 EOS增加了120天死亡的风险(HR = 1.78; 95%CI 1.49,2.13)。结论:与儿童和成人的发现相反,在这个队列中,EOS与LOS风险增加无关。需要进行针对年龄的调查,以确定是否存在脓毒症后免疫学改变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号