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Characterization of gram-negative bloodstream infections in hospitalised Australian children and their clinical outcomes.
Wen, Sophie Ch; Harris, Patrick N A; Forde, Brian; Permana, Budi; Chatfield, Mark D; Lau, Colleen L; Spurling, Geoffrey; Bauer, Michelle J; Balch, Ross; Chambers, Henry; Schlapbach, Luregn J; Clark, Julia E; Dougherty, Sonia; Blyth, Christopher C; Britton, Philip N; Clifford, Vanessa; Haeusler, Gabrielle M; McMullan, Brendan; Wadia, Ushma; Paterson, David L; Irwin, Adam D.
Afiliação
  • Wen SC; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Harris PNA; Children's Health Queensland, Brisbane, Australia.
  • Forde B; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Permana B; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Chatfield MD; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Lau CL; Herston Infectious Diseases Institute, Metro North Health, Brisbane, Australia.
  • Spurling G; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Bauer MJ; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Balch R; The University of Queensland, General Practice Clinical Unit, Brisbane, Australia.
  • Chambers H; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Schlapbach LJ; The University of Queensland, Centre for Clinical Research, Brisbane, Australia.
  • Clark JE; University of California San Francisco, San Francisco, United States of America.
  • Dougherty S; The University of Queensland, Child Health Research Centre, Brisbane, Australia.
  • Blyth CC; Children's Health Queensland, Brisbane, Australia.
  • Britton PN; Children's Health Queensland, Brisbane, Australia.
  • Clifford V; Wesfarmer Centre of Vaccines and Infectious Diseases, Perth, Australia.
  • Haeusler GM; Perth Children's Hospital, Perth, Australia.
  • McMullan B; PathWest Laboratory Network, Perth, Australia.
  • Wadia U; University of Western Australia, Perth, Australia.
  • Paterson DL; The Children's Hospital Westmead, Sydney, Australia.
  • Irwin AD; Sydney Medical School and Sydney Infectious Diseases, University of Sydney, Australia.
Clin Infect Dis ; 2024 Jun 25.
Article em En | MEDLINE | ID: mdl-38917034
ABSTRACT

BACKGROUND:

Gram-negative bloodstream infections (GNBSI) more commonly occur in children with comorbidities and are increasingly associated with antimicrobial resistance. There are few large studies of GNBSI in children that relate the clinical presentation, pathogen characteristics and outcomes.

METHODS:

A 3-year prospective study of GNBSI in children aged <18 years was conducted in five Australian children's hospitals between 2019-2021. The clinical characteristics, disease severity and outcomes were recorded. Causative pathogens underwent antibiotic susceptibility testing and whole genome sequencing.

RESULTS:

There were 931 GNBSI episodes involving 818 children. Median age was 3 years (IQR 0.6-8.5). 576/931 episodes (62%) were community onset though 661/931 (71%) occurred in children with comorbidities and a central venous catheter (CVC) was present in 558/931 (60%). CVC (145/931) and urinary tract (149/931) were the most common sources (16% each). 100/931 (11%) children required Intensive Care Unit (ICU) admission and a further 11% (105/931) developed GNBSI in ICU. 659/927 (71%) isolates were Enterobacterales of which 22% (138/630) were third generation cephalosporin resistant (3GCR). Extended spectrum beta-lactamase genes (ESBL) were confirmed in 65/138 (47%) 3GCR-Enterobacterales. Most common ESBL genes were blaCTX-M-15 (34/94, 36%) and blaSHV-12 (10/94, 11%). There were 48 deaths overall and 30-day in-hospital mortality was 3% (32/931). Infections with 3GCR Enterobacterales were independently associated with higher mortality (adjusted OR 3.2, 95%CI 1.6-6.4).

CONCLUSION:

GNBSI in children are frequently healthcare-associated and affect children under 5 years. Infections with 3GCR Enterobacterales were associated with worse outcomes. These findings will inform optimal management guidelines and help prioritise future antimicrobial clinical trials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Infect Dis Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Infect Dis Ano de publicação: 2024 Tipo de documento: Article