Greenberg Rachel G, Kandefer Sarah, Do Barbara T, Smith P Brian, Stoll Barbara J, Bell Edward F, Carlo Waldemar A, Laptook Abbot R, Sánchez Pablo J, Shankaran Seetha, Van Meurs Krisa P, Ball M Bethany, Hale Ellen C, Newman Nancy S, Das Abhik, Higgins Rosemary D, Cotten C Michael
From the *Department of Pediatrics, Duke University School of Medicine, †Duke Clinical Research Institute, Duke University School of Medicine, and ‡Social, Statistical and Environmental Sciences Unit, RTI International, Research Triangle Park, Durham, North Carolina; §Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, Georgia; ¶Department of Pediatrics, University of Iowa, Iowa City, Iowa; ‖Division of Neonatology, University of Alabama at Birmingham, Birmingham, Alabama; **Department of Pediatrics, Women & Infants Hospital, Brown University, Providence, Rhode Island; ††Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas; ‡‡Department of Pediatrics, Wayne State University, Detroit, Michigan; §§Department of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University School of Medicine, Lucile Packard Children's Hospital, Palo Alto, California; ¶¶Department of Pediatrics, Rainbow Babies & Children's Hospital, Case Western Reserve University, Cleveland, Ohio; ‖‖Social, Statistical and Environmental Sciences Unit, RTI International, Rockville, Maryland; and ***Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
Pediatr Infect Dis J. 2017 Aug;36(8):774-779. doi: 10.1097/INF.0000000000001570.
Late-onset sepsis (LOS) is an important cause of death and neurodevelopmental impairment in premature infants. The purpose of this study was to assess overall incidence of LOS, distribution of LOS-causative organisms and center variation in incidence of LOS for extremely premature infants over time.
In a retrospective analysis of infants 401-1000 g birth weight and 22-28 6/7 weeks of gestational age born at 12 National Institute of Child Health and Human Development Neonatal Research Network centers in the years 2000-2005 (era 1) or 2006-2011 (era 2) who survived >72 hours, we compared the incidence of LOS and pathogen distribution in the 2 eras using the χ test. We also examined the effect of birth year on the incidence of LOS using multivariable regression to adjust for nonmodifiable risk factors and for center. To assess whether the incidence of LOS was different among centers in era 2, we used a multivariable regression model to adjust for nonmodifiable risk factors.
Ten-thousand one-hundred thirty-one infants were studied. LOS occurred in 2083 of 5031 (41%) infants in era 1 and 1728 of 5100 (34%) infants in era 2 (P < 0.001). Birth year was a significant predictor of LOS on adjusted analysis, with birth years 2000-2009 having a significantly higher odds of LOS than the reference year 2011. Pathogens did not differ, with the exception of decreased fungal infection (P < 0.001). In era 2, 9 centers had significantly higher odds of LOS compared with the center with the lowest incidence.
The incidence of LOS decreased over time. Further investigation is warranted to determine which interventions have the greatest impact on infection rates.
晚发性败血症(LOS)是早产儿死亡和神经发育障碍的重要原因。本研究的目的是评估极早产儿LOS的总体发病率、LOS致病微生物的分布以及LOS发病率随时间的中心差异。
对2000 - 2005年(第1阶段)或2006 - 2011年(第2阶段)在12个国家儿童健康与人类发展研究所新生儿研究网络中心出生、出生体重401 - 1000g且胎龄22 - 28又6/7周、存活超过72小时的婴儿进行回顾性分析。我们使用χ检验比较了两个阶段LOS的发病率和病原体分布。我们还使用多变量回归分析出生年份对LOS发病率的影响,以调整不可改变的风险因素和中心因素。为了评估第2阶段各中心LOS发病率是否存在差异,我们使用多变量回归模型调整不可改变的风险因素。
共研究了1131名婴儿。第1阶段5031名婴儿中有2083名(41%)发生LOS,第2阶段5100名婴儿中有1728名(34%)发生LOS(P < 0.001)。经调整分析,出生年份是LOS的显著预测因素,2000 - 2009年出生的婴儿发生LOS的几率显著高于参考年份2011年。除真菌感染减少外(P < 0.001),病原体无差异。在第2阶段,9个中心发生LOS的几率显著高于发病率最低的中心。
LOS的发病率随时间下降。有必要进一步调查以确定哪些干预措施对感染率影响最大。