4.6 Article

Early Sepsis Does Not Increase the Risk of Late Sepsis in Very Low Birth Weight Neonates

Journal

JOURNAL OF PEDIATRICS
Volume 162, Issue 5, Pages 942-U92

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jpeds.2012.11.027

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Funding

  1. NCATS NIH HHS [UL1 TR000454, UL1 TR000041, UL1 TR001449] Funding Source: Medline
  2. NCRR NIH HHS [M01 RR7122, M01 RR44, UL1 RR24139, M01 RR750, M01 RR997, M01 RR54, M01 RR16587, M01 RR80, M01 RR39, M01 RR64, M01 RR633, M01 RR125, M01 RR70, M01 RR6022, M01 RR59, M01 RR32] Funding Source: Medline
  3. NIAAA NIH HHS [HHSN275201000003C] Funding Source: Medline
  4. NICHD NIH HHS [U10 HD053109, U10 HD27880, U10 HD27904, 1K24HD058735-01, U10 HD40689, U10 HD53109, U10 HD40498, 1R01HD057956-02, U10 HD53089, U10 HD27871, U10 HD27881, U10 HD27856, U10 HD40461, U10 HD27853, U10HD21415, U10 HD27851, U10 HD21397, U10 HD34216, U10 HD21364, U10 HD53124, UG1 HD053109, U10 HD21373, U10 HD53119, U10 HD40492, U10 HD021364, HHSN267200700051C, U10 HD21385, 1U10-HD45962-06, HHSN275201000003I, U10 HD40521, U10 HD36790] Funding Source: Medline
  5. FDA HHS [1R01FD003519-01] Funding Source: Medline

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Objective To examine whether preterm very low birth weight (VLBW) infants have an increased risk of late-onset sepsis (LOS) following early-onset sepsis (EOS). Study design Retrospective analysis of VLBW infants (401-1500 g) born September 1998 through December 2009 who survived >72 hours and were cared for within the National Institute of Child Health and Human Development Neonatal Research Network. Sepsis was defined by growth of bacteria or fungi in a blood culture obtained <= 72 hours of birth (EOS) or >72 hours (LOS) and antimicrobial therapy for >= 5 days or death <5 days while receiving therapy. Regression models were used to assess risk of death or LOS by 120 days and LOS by 120 days among survivors to discharge or 120 days, adjusting for gestational age and other covariates. Results Of 34 396 infants studied, 504 (1.5%) had EOS. After adjustment, risk of death or LOS by 120 days did not differ overall for infants with EOS compared with those without EOS [risk ratio (RR): 0.99 (0.89-1.09)] but was reduced in infants born at <25 weeks gestation [RR: 0.87 (0.76-0.99), P = .048]. Among survivors, no difference in LOS risk was found overall for infants with versus without EOS [RR: 0.88 (0.75-1.02)], but LOS risk was reduced in infants with birth weight 401-750 g who had EOS [RR: 0.80 (0.64-0.99), P = .047]. Conclusions Risk of LOS after EOS was not increased in VLBW infants. Surprisingly, risk of LOS following EOS appeared to be reduced in the smallest, most premature infants, underscoring the need for age-specific analyses of immune function. (J Pediatr 2013;162:942-8).

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