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Pediatric Staphylococcus aureus Bacteremia: Clinical Spectrum and Predictors of Poor Outcome.
Campbell, Anita J; Al Yazidi, Laila S; Phuong, Linny K; Leung, Clare; Best, Emma J; Webb, Rachel H; Voss, Lesley; Athan, Eugene; Britton, Philip N; Bryant, Penelope A; Butters, Coen T; Carapetis, Jonathan R; Ching, Natasha S; Coombs, Geoffrey W; Daley, Denise A; Francis, Joshua R; Hung, Te-Yu; Mowlaboccus, Shakeel; Nourse, Clare; Ojaimi, Samar; Tai, Alex; Vasilunas, Nan; McMullan, Brendan; Blyth, Christopher C; Bowen, Asha C.
Affiliation
  • Campbell AJ; Department of Infectious Diseases, Perth Children's Hospital, Perth, Australia.
  • Al Yazidi LS; Wesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, Australia.
  • Phuong LK; School of Medicine, University of Western Australia, Perth, Australia.
  • Leung C; Child Health Department, Sultan Qaboos University Hospital, Muscat, Oman.
  • Best EJ; Department of Immunology and Infectious Diseases, Sydney Children's Hospital, Randwick, Sydney, Australia.
  • Webb RH; Children's Department of Infectious Diseases and Microbiology, Children's Hospital at Westmead, New South Wales, Australia.
  • Voss L; Department of General Medicine, Infectious Diseases Unit, Royal Children's Hospital, Melbourne, Australia.
  • Athan E; Infection and Immunity Group, Murdoch Children's Research Institute, Melbourne, Australia.
  • Britton PN; Department of Paediatrics, Wagga Wagga Base Hospital, Wagga Wagga, Australia.
  • Bryant PA; Department of Paediatrics, Child and Youth Health, University of Auckland, Auckland, New Zealand.
  • Butters CT; National Immunisation Advisory Centre, University of Auckland, Auckland, New Zealand.
  • Carapetis JR; Department of Infectious Diseases, Starship Children's Hospital, Auckland, New Zealand.
  • Ching NS; Department of Paediatrics, Child and Youth Health, University of Auckland, Auckland, New Zealand.
  • Coombs GW; Department of Infectious Diseases, Starship Children's Hospital, Auckland, New Zealand.
  • Daley DA; Department of Paediatrics, Kidz First Hospital, Auckland, New Zealand.
  • Francis JR; Department of Paediatrics, Child and Youth Health, University of Auckland, Auckland, New Zealand.
  • Hung TY; Department of Infectious Diseases, Starship Children's Hospital, Auckland, New Zealand.
  • Mowlaboccus S; Department of Infectious Disease, Barwon Health, Geelong, Australia.
  • Nourse C; School of Medicine, Deakin University, Geelong, Australia.
  • Ojaimi S; Children's Department of Infectious Diseases and Microbiology, Children's Hospital at Westmead, New South Wales, Australia.
  • Tai A; Sydney Medical School and Marie Bashir Institute, University of Sydney, Sydney, Australia.
  • Vasilunas N; Department of General Medicine, Infectious Diseases Unit, Royal Children's Hospital, Melbourne, Australia.
  • McMullan B; Infection and Immunity Group, Murdoch Children's Research Institute, Melbourne, Australia.
  • Blyth CC; Department of General Medicine, Infectious Diseases Unit, Royal Children's Hospital, Melbourne, Australia.
  • Bowen AC; Department of Infectious Diseases, Perth Children's Hospital, Perth, Australia.
Clin Infect Dis ; 74(4): 604-613, 2022 03 01.
Article in En | MEDLINE | ID: mdl-34089594
ABSTRACT

BACKGROUND:

Staphylococcus aureus is a common cause of bacteremia, yet the epidemiology and predictors of poor outcome remain inadequately defined in childhood.

METHODS:

ISAIAH (Invasive Staphylococcus aureus Infections and Hospitalizations in children) is a prospective, cross-sectional study of S. aureus bacteremia (SAB) in children hospitalized in Australia and New Zealand over 24 months (2017-2018).

RESULTS:

Overall, 552 SABs were identified (incidence 4.4/100 000/year). Indigenous children, those from lower socioeconomic areas and neonates were overrepresented. Although 90-day mortality was infrequent, one-third experienced the composite of length of stay >30 days (26%), intensive care unit admission (20%), relapse (4%), or death (3%). Predictors of mortality included prematurity (adjusted odds ratio [aOR],16.8; 95% confidence interval [CI], 1.6-296.9), multifocal infection (aOR, 22.6; CI, 1.4-498.5), necrotizing pneumonia (aOR, 38.9; CI, 1.7-1754.6), multiorgan dysfunction (aOR, 26.5; CI, 4.1-268.8), and empiric vancomycin (aOR, 15.7; CI, 1.6-434.4); while infectious diseases (ID) consultation (aOR, 0.07; CI .004-.9) was protective. Neither MRSA nor vancomycin trough targets impacted survival; however, empiric vancomycin was associated with nephrotoxicity (OR, 3.1; 95% CI 1.3-8.1).

CONCLUSIONS:

High SAB incidence was demonstrated and for the first time in a pediatric setting, necrotizing pneumonia and multifocal infection were predictors of mortality, while ID consultation was protective. The need to reevaluate pediatric vancomycin trough targets and limit unnecessary empiric vancomycin exposure to reduce poor outcomes and nephrotoxicity is highlighted. One in 3 children experienced considerable SAB morbidity; therefore, pediatric inclusion in future SAB comparator trials is paramount to improve outcomes.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Staphylococcal Infections / Bacteremia / Methicillin-Resistant Staphylococcus aureus Type of study: Observational_studies / Prevalence_studies / Prognostic_studies Limits: Child / Humans / Newborn Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2022 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Staphylococcal Infections / Bacteremia / Methicillin-Resistant Staphylococcus aureus Type of study: Observational_studies / Prevalence_studies / Prognostic_studies Limits: Child / Humans / Newborn Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2022 Type: Article Affiliation country: Australia