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Mucosal barrier injury-associated bloodstream infections in pediatric oncology patients.
Hakim, Hana; Billett, Amy L; Xu, Jiahui; Tang, Li; Richardson, Troy; Winkle, Cynthia; Werner, Eric J; Hord, Jeffrey D; Bundy, David G; Gaur, Aditya H.
Afiliação
  • Hakim H; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Billett AL; Department of Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
  • Xu J; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Tang L; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Richardson T; Children's Hospital Association, Lenexa, Kansas.
  • Winkle C; Nursing Department, Children's Medical Center, Dallas, Texas.
  • Werner EJ; Department of Oncology, Children's Specialty Group, Norfolk, Virginia.
  • Hord JD; Department of Oncology, Akron Children's Hospital, Akron, Ohio.
  • Bundy DG; Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina.
  • Gaur AH; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee.
Pediatr Blood Cancer ; 67(8): e28234, 2020 08.
Article em En | MEDLINE | ID: mdl-32386095
ABSTRACT

BACKGROUND:

Single-center reports of central line-associated bloodstream infection (CLABSI) and the subcategory of mucosal barrier injury laboratory-confirmed bloodstream infection (MBI-LCBI) in pediatric hematology oncology transplant (PHO) patients have focused on the inpatient setting. Characterization of MBI-LCBI across PHO centers and management settings (inpatient and ambulatory) is urgently needed to inform surveillance and prevention strategies.

METHODS:

Prospectively collected data from August 1, 2013, to December 31, 2015, on CLABSI (including MBI-LCBI) from a US PHO multicenter quality improvement network database was analyzed. CDC National Healthcare Safety Network definitions were applied for inpatient events and adapted for ambulatory events.

RESULTS:

Thirty-five PHO centers reported 401 ambulatory and 416 inpatient MBI-LCBI events. Ambulatory and inpatient MBI-LCBI rates were 0.085 and 1.01 per 1000 line days, respectively. Fifty-three percent of inpatient CLABSIs were MBI-LCBIs versus 32% in the ambulatory setting (P  <  0.01). Neutropenia was the most common criterion defining MBI-LCBI in both settings, being present in ≥90% of events. The most common organisms isolated in MBI-LCBI events were Escherichia coli (in 28% of events), Klebsiella spp. (23%), and viridans streptococci (12%) in the ambulatory setting and viridans streptococci (in 29% of events), E. coli (14%), and Klebsiella spp. (14%) in the inpatient setting.

CONCLUSION:

In this largest study of PHO MBI-LCBI inpatient events and the first such study in the ambulatory setting, the burden of MBI-LCBI across the continuum of care of PHO patients was substantial. These data should raise awareness of MBI-LCBI among healthcare providers for PHO patients, help benchmarking across centers, and help inform prevention and treatment strategies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Bases de Dados Factuais / Neoplasias / Neutropenia Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Bases de Dados Factuais / Neoplasias / Neutropenia Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article