High vancomycin MICs predict the development of infective endocarditis in patients with catheter-related bacteraemia due to methicillin-resistant Staphylococcus aureus

No Thumbnail Available

Date

2017-07-01

Authors

San-Juan, Rafael
Fernandez-Ruiz, Mario
Gasch, Oriol
Camoez, Mariana
Lopez-Medrano, Francisco
Angeles Dominguez, Maria
Almirante, Benito
Padilla, Belen
Pujol, Miquel
Maria Aguado, Jose

Advisors

Journal Title

Journal ISSN

Volume Title

Publisher

Oxford univ press
Metrics
Google Scholar
Export

Research Projects

Organizational Units

Journal Issue

Abstract

Background: It has been suggested that there is an increased risk of treatment failure in episodes of MRSA bloodstream infection (BSI) caused by strains with high vancomycin MICs. However, it is unknown if this phenomenon may also act as a risk factor for the development of infective endocarditis (IE).Methods: We analysed 207 episodes of catheter-related (CR)-BSI recruited from June 2008 to December 2009 within a prospective study on MRSA BSI in 21 Spanish hospitals. Vancomycin susceptibility was centrally tested. The impact of high vancomycin MIC values (a parts per thousand1.5 mg/L by Etest) on the subsequent development of IE was investigated by Cox regression.Results: High vancomycin MIC values were observed in 46.9% of the isolates. Initial therapy consisted of vancomycin [99 episodes (44.7%)], daptomycin [25 (12.1%)], linezolid [18 (8.7%)] and other antistaphylococcal agents [16 (7.7%)]. Haematogenous complications occurred in 41 patients (19.8%), including 10 episodes complicated by IE. Early (48 h) and late (30 day) all-cause mortality were 3.4% and 25.1%, respectively. High vancomycin MIC isolates were more common among patients that developed IE compared with those free from this complication [90.9% (9/10) versus 44.7% (88/197); P = 0.007]. This association remained significant after adjusting for multiple confounders (including initial antibiotic therapy and catheter removal) in different models (minimum hazard ratio: 9.18; 95% CI: 1.16-72.78; P = 0.036). There were no differences in mortality according to vancomycin MIC values.Conclusions: Decreased susceptibility to vancomycin acted as a predictor of the development of IE complicating MRSA CR-BSI.

Description

MeSH Terms

DeCS Terms

CIE Terms

Keywords

Minimum inhibitory concentration, Blood-stream infections, Field gel-electrophoresis, Endothelial-cells, In-vitro, Susceptibility, Persistent, Mortality, Association, Criteria

Citation