Association between treatment duration and mortality or relapse in adult patients with Staphylococcus aureus bacteraemia: a retrospective cohort study.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
May 2020
Historique:
received: 07 12 2018
revised: 15 07 2019
accepted: 17 07 2019
pubmed: 30 7 2019
medline: 5 1 2021
entrez: 30 7 2019
Statut: ppublish

Résumé

The aim was to evaluate the effect of duration of therapy (DOT) on mortality and relapse for patients with Staphylococcus aureus bacteraemia (SAB). We performed a retrospective single-centre cohort study including adult patients with SAB. We determined the association between DOT (≤14 days versus >14 days) and mortality by adjusted hazard ratios (aHR) and 95% confidence intervals through Cox regression adjusted for immortal-time bias and confounding by indication, stratified by presence of complicated SAB (any of: endocarditis, implant, duration of SAB >2 days, fever >3 days). The primary outcome was 90-day all-cause mortality, and the secondary outcome was 90-day relapse. Between January 2010 and December 2015, we included 530 patients, of whom 94 out of 530 (17.7%) had methicillin-resistant SAB and 305 out of 530 (57.6%) had complicated SAB. Ninety-day mortality was 27.0% (143/530), with no significant trend across the study period; median time to death was 17 days (interquartile range (IQR) 8-30) after onset of SAB. Median DOT was 20 days (IQR 13-39). Patients with complicated SAB had significantly reduced mortality with DOT >14 days (aHR 0.32, 95% CI 0.16-0.64). DOT was not associated with mortality in patients with uncomplicated SAB (aHR 0.85; 0.41-1.78). Eighteen (18/530) patients (3.4%) relapsed; on univariate analysis, DOT was not associated with relapse (HR 1.01; 0.97-1.06). DOT >14 days is associated with higher survival in patients with complicated SAB, but not for patients with uncomplicated SAB. No association was found for relapse, but 90-day relapse was very low in this cohort. Importantly, 90-day mortality remained high across the study period.

Identifiants

pubmed: 31357013
pii: S1198-743X(19)30411-2
doi: 10.1016/j.cmi.2019.07.019
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

626-631

Informations de copyright

Copyright © 2019 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

M Abbas (M)

Infection Control Programme, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland; Service of Infectious Diseases, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland. Electronic address: Mohamed.abbas@hcuge.ch.

A Rossel (A)

Service of General Internal Medicine, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

M E A de Kraker (MEA)

Infection Control Programme, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

E von Dach (E)

Infection Control Programme, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland; Clinical Trials Unit, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

C Marti (C)

Service of General Internal Medicine, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

S Emonet (S)

Service of Infectious Diseases, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland; Bacteriology Laboratory, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

S Harbarth (S)

Infection Control Programme, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland; Service of Infectious Diseases, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

L Kaiser (L)

Service of Infectious Diseases, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

I Uçkay (I)

Infection Control Programme, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland; Service of Infectious Diseases, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland; Balgrist University Hospital, Zurich, Switzerland.

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Classifications MeSH