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Shiga Toxin-Producing Escherichia coli Infection, Antibiotics, and Risk of Developing Hemolytic Uremic Syndrome: A Meta-analysis.
Freedman, Stephen B; Xie, Jianling; Neufeld, Madisen S; Hamilton, William L; Hartling, Lisa; Tarr, Phillip I; Nettel-Aguirre, Alberto; Chuck, Anderson; Lee, Bonita; Johnson, David; Currie, Gillian; Talbot, James; Jiang, Jason; Dickinson, Jim; Kellner, Jim; MacDonald, Judy; Svenson, Larry; Chui, Linda; Louie, Marie; Lavoie, Martin; Eltorki, Mohamed; Vanderkooi, Otto; Tellier, Raymond; Ali, Samina; Drews, Steven; Graham, Tim; Pang, Xiao-Li.
Afiliação
  • Freedman SB; Section of Gastroenterology, Alberta Children's Hospital, Alberta Children's Hospital Research Institute.
  • Xie J; Section of Pediatric Emergency Medicine, Alberta Children's Hospital, University of Calgary, Canada.
  • Neufeld MS; Section of Pediatric Emergency Medicine, Alberta Children's Hospital, University of Calgary, Canada.
  • Hamilton WL; Section of Pediatric Emergency Medicine, Alberta Children's Hospital, University of Calgary, Canada.
  • Hartling L; University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, United Kingdom.
  • Tarr PI; Alberta Research Centre for Health Evidence, Department of Pediatrics, University of Alberta, Edmonton, Canada.
Clin Infect Dis ; 62(10): 1251-1258, 2016 05 15.
Article em En | MEDLINE | ID: mdl-26917812
ABSTRACT

BACKGROUND:

Antibiotic administration to individuals with Shiga toxin-producing Escherichia coli (STEC) infection remains controversial. We assessed if antibiotic administration to individuals with STEC infection is associated with development of hemolytic uremic syndrome (HUS).

METHODS:

The analysis included studies published up to 29 April 2015, that provided data from patients (1) with STEC infection, (2) who received antibiotics, (3) who developed HUS, and (4) for whom data reported timing of antibiotic administration in relation to HUS. Risk of bias was assessed; strength of evidence was adjudicated. HUS was the primary outcome. Secondary outcomes restricted the analysis to low-risk-of-bias studies employing commonly used HUS criteria. Pooled estimates of the odds ratio (OR) were obtained using random-effects models.

RESULTS:

Seventeen reports and 1896 patients met eligibility; 8 (47%) studies were retrospective, 5 (29%) were prospective cohort, 3 (18%) were case-control, and 1 was a trial. The pooled OR, including all studies, associating antibiotic administration and development of HUS was 1.33 (95% confidence interval [CI], .89-1.99; I(2) = 42%). The repeat analysis including only studies with a low risk of bias and those employing an appropriate definition of HUS yielded an OR of 2.24 (95% CI, 1.45-3.46; I(2) = 0%).

CONCLUSIONS:

Overall, use of antibiotics was not associated with an increased risk of developing HUS; however, after excluding studies at high risk of bias and those that did not employ an acceptable definition of HUS, there was a significant association. Consequently, the use of antibiotics in individuals with STEC infections is not recommended.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por Escherichia coli / Escherichia coli Shiga Toxigênica / Síndrome Hemolítico-Urêmica / Antibacterianos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por Escherichia coli / Escherichia coli Shiga Toxigênica / Síndrome Hemolítico-Urêmica / Antibacterianos Idioma: En Ano de publicação: 2016 Tipo de documento: Article