Infectious disease consultation for Staphylococcus aureus bacteremia - A systematic review and meta-analysis
- PMID: 26453841
- DOI: 10.1016/j.jinf.2015.09.037
Infectious disease consultation for Staphylococcus aureus bacteremia - A systematic review and meta-analysis
Abstract
Objective: Mortality and morbidity of Staphylococcus aureus bacteremia (SAB) still remains considerably high. We aimed to evaluate the impact of infectious disease consultation (IDC) on the management and outcomes of patients with SAB.
Methods: We systematically searched 3 publication databases from inception to 31st May 2015 and reference lists of identified primary studies.
Results: Our search returned 2874 reports, of which 18 fulfilled the inclusion criteria, accounting for 5337 patients. Overall 30-day mortality was 19.95% [95% CI 14.37-27.02] with a significant difference in favour of the IDC group (12.39% vs 26.07%) with a relative risk (RR) of 0.53 [95% CI 0.43-0.65]. 90-day mortality and relapse risk for SAB were also reduced significantly with RRs of 0.77 [95% CI 0.64-0.92] and 0.62 [95% CI 0.39-0.99], respectively. Both, the appropriateness of antistaphylococcal agent and treatment duration was improved by IDC (RR 1.14 [95% CI 1.08-1.20] and 1.85 [95% CI 1.39-2.46], respectively). Follow-up blood cultures and echocardiography were performed more frequently following IDC (RR 1.35 [95% CI 1.25-1.46] and 1.98 [95% CI 1.66-2.37], respectively).
Conclusions: Evidence-based clinical management enforced by IDC may improve outcome of patients with SAB. Well-designed cluster-randomized controlled trials are needed to confirm this finding from observational studies.
Keywords: Bacteremia; Infectious disease medicine; Meta-analysis; Mortality; Quality of health care; Staphylococcus aureus.
Copyright © 2015 The British Infection Association. Published by Elsevier Ltd. All rights reserved.
Comment in
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Personal microbiological consultations improve the therapeutic management of Staphylococcus aureus bacteremia.J Infect. 2018 Oct;77(4):349-356. doi: 10.1016/j.jinf.2018.07.011. Epub 2018 Jul 29. J Infect. 2018. PMID: 30067944 No abstract available.
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