Impact of healthcare-associated sepsis on mortality in critically ill infants

被引:15
|
作者
Verstraete, Evelien Hilde [1 ]
Mahieu, Ludo [2 ,3 ]
De Coen, Kris [4 ]
Vogelaers, Dirk [1 ,5 ]
Blot, Stijn [1 ,6 ]
机构
[1] Univ Ghent, Dept Internal Med, B-9000 Ghent, Belgium
[2] Univ Antwerp Hosp, Dept Neonatal Med, Antwerp, Belgium
[3] Univ Antwerp, Dept Pediat, B-2020 Antwerp, Belgium
[4] Ghent Univ Hosp, Dept Neonatal Med, Ghent, Belgium
[5] Ghent Univ Hosp, Dept Gen Internal Med Infect Dis & Psychosomat Di, Ghent, Belgium
[6] Univ Queensland, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld, Australia
关键词
Newborn; Cross infection; Sepsis; Mortality; Survival analysis; Logistic regression; BLOOD-STREAM INFECTIONS; BIRTH-WEIGHT INFANTS; LATE-ONSET SEPSIS; RISK-FACTORS; NOSOCOMIAL INFECTION; NEONATAL SEPSIS; SYSTEM; UNITS; STAY;
D O I
10.1007/s00431-016-2726-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Healthcare-associated sepsis (HAS) is a life-threatening complication in neonatal intensive care. Research into the impact of HAS on mortality adjusted for comorbidities is however limited. We conducted a historical cohort study to evaluate impact of HAS on mortality stratified by birth weight and risk factors for mortality in the HAS cohort. HAS was defined according to the National Institute of Child Health and Human Development criteria. Logistic regression was used to calculate adjusted odds of mortality. Of 5134 admissions, 342 infants developed HAS (6.7 %). Mortality in the total and HAS cohort was 5.6 and 10.5 %, respectively. The majority of HAS was caused by commensals (HAS-COM, 59.4 %) and 40.6 % by recognized pathogens (HAS-REC). Adjusted for comorbidities, "HAS-REC" is only a risk factor for mortality in newborns > 1500 g (adjusted odds ratio [aOR] 2.3, confidence interval [CI] 1.1-4.9). Post-hoc analysis identified HAS-REC as an independent risk factor for mortality in infants with gastrointestinal disease (aOR 4.8, CI 2.1-10.8). "Renal insufficiency," "focal intestinal perforation," and "necrotizing enterocolitis" are independent risk factors for mortality in the HAS cohort (aOR 13.5, CI 4.9-36.6; aOR 7.7, CI 1.5-39.2; aOR 2.1, CI 1.0-4.7, respectively). Conclusion: For very low birth weight infants (<= 1500 g), several comorbidities overrule the impact of HAS on mortality. After adjustment for comorbidities, HAS-REC independently predicts in-hospital mortality in heavier infants and in those with gastrointestinal disease.
引用
收藏
页码:943 / 952
页数:10
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