Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 May;162(5):942-8.e1-3.
doi: 10.1016/j.jpeds.2012.11.027. Epub 2013 Jan 5.

Early sepsis does not increase the risk of late sepsis in very low birth weight neonates

Collaborators, Affiliations

Early sepsis does not increase the risk of late sepsis in very low birth weight neonates

James L Wynn et al. J Pediatr. 2013 May.

Abstract

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.

PubMed Disclaimer

Figures

Figure
Figure
Neonatal Research Network VLBW cohort studied. Infants were followed to death, discharge/transfer, or 120 days. Limited information was collected for infants still in the hospital at 120 days, including final status up to one year of age. Final status after transfer (discharged to home, death) was recorded for infants transferred to another hospital if known. Transfers with incomplete status information included infants with unknown final status after transfer and infants known to have been discharged to home but with missing discharge date. The latter are shown with final status discharged home.

Similar articles

Cited by

References

    1. Wynn JL, Cvijanovich NZ, Allen GL, Thomas NJ, Freishtat RJ, Anas N, et al. The Influence of Developmental Age on the Early Transcriptomic Response of Children with Septic Shock. Molecular Medicine. 2011;17:1146–56. - PMC - PubMed
    1. Meakins JL, Pietsch JB, Bubenick O, Kelly R, Rode H, Gordon J, et al. Delayed hypersensitivity: indicator of acquired failure of host defenses in sepsis and trauma. Annals of Surgery. 1977;186:241–50. - PMC - PubMed
    1. Hall MW, Knatz NL, Vetterly C, Tomarello S, Wewers MD, Volk HD, et al. Immunoparalysis and nosocomial infection in children with multiple organ dysfunction syndrome. Intensive Care Medicine. 2011;37:525–32. - PMC - PubMed
    1. Frazier WJ, Hall MW. Immunoparalysis and adverse outcomes from critical illness. Pediatric Clinics of North America. 2008;55:647–68. xi. - PMC - PubMed
    1. Boomer JS, To K, Chang KC, Takasu O, Osborne DF, Walton AH, et al. Immunosuppression in patients who die of sepsis and multiple organ failure. JAMA. 2011;306:2594–605. - PMC - PubMed

Publication types

Grants and funding