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Contribution of Concurrent Comorbidities to Sepsis-Related Mortality in Preterm Infants ≤32 Weeks of Gestation at an Academic Neonatal Intensive Care Network.
Barnette, Brian W; Schumacher, Benjamin T; Armenta, Richard F; Wynn, James L; Richardson, Andrew; Bradley, John S; Lazar, Sarah; Lawrence, Shelley M.
Afiliação
  • Barnette BW; Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of California, San Diego, College of Medicine, San Diego, California.
  • Schumacher BT; Department of Public Heath, Herbert Wertheim School of Public Health and Longevity Science, UC San Diego School of Medicine, San Diego, California.
  • Armenta RF; Department of Kinesiology, College of Education, Health, and Human Services, California State University, San Marco, San Diego, California.
  • Wynn JL; Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Florida, College of Medicine, Gainesville, Florida.
  • Richardson A; Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, Florida.
  • Bradley JS; Department of Pediatrics, Clinical Research Informatics, Rady Children's Hospital San Diego, San Diego, California.
  • Lazar S; Division of Infectious Disease, Department of Pediatrics, University of California, San Diego, College of Medicine, San Diego, California.
  • Lawrence SM; Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of California, San Diego, College of Medicine, San Diego, California.
Am J Perinatol ; 2021 Dec 31.
Article em En | MEDLINE | ID: mdl-34674193
ABSTRACT

OBJECTIVE:

This study sought to identify concurrent major comorbidities in preterm infants ≤32 weeks of gestation that may have contributed to sepsis-related mortality following a diagnosis of bacteremia or blood culture-negative sepsis within the neonatal period (≤28 days of life). STUDY

DESIGN:

This is a retrospective chart review of infants ≤32 weeks of gestation who were admitted to a single academic network of multiple neonatal intensive care units between January 1, 2012, and December 31, 2015, to determine the primary cause(s) and timing of death in those diagnosed with bacteremia or blood culture-negative sepsis. Direct comparisons between early-onset sepsis (EOS; ≤72 hours) and late-onset sepsis (LOS; >72 hours) were made.

RESULTS:

In our study cohort, of 939 total patients with ≤32 weeks of gestation, 182 infants were diagnosed with 198 episodes of sepsis and 7.7% (14/182) died. Mortality rates did not significantly differ between neonates with bacteremia or blood culture-negative sepsis (7/14 each group), and those diagnosed with EOS compared with LOS (6/14 vs. 8/14). Nearly 80% (11/14) of infants were transitioned to comfort care prior to their death secondary to a coinciding diagnosis of severe grade-3 or -4 intraventricular hemorrhage, periventricular leukomalacia, necrotizing enterocolitis, and/or intestinal perforation.

CONCLUSION:

Preexisting comorbidities commonly associated with extreme preterm birth contributed to sepsis-related mortality in our patient cohort. KEY POINTS · Concurrent comorbidities contribute to, and may artificially inflate, sepsis-related mortality.. · Absence of a consensus definition for neonatal sepsis complicates the investigation of infection.. · Accurate assessment of the incidence of sepsis in very low birth weight infants is vital for future investigations.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Perinatol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Perinatol Ano de publicação: 2021 Tipo de documento: Article