Attributable Mortality of Candida Bloodstream Infections in the Modern Era: A Propensity Score Analysis

Author:

Mazi Patrick B1ORCID,Olsen Margaret A1,Stwalley Dustin1,Rauseo Adriana M1,Ayres Chapelle1,Powderly William G1,Spec Andrej1ORCID

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Washington University in St Louis School of Medicine , St Louis, Missouri , USA

Abstract

Abstract Background This study quantifies the mortality attributable to Candida bloodstream infections (BSI) in the modern era of echinocandins. Methods We conducted a retrospective cohort study of adult patients admitted to Barnes Jewish Hospital, a 1368-bed tertiary care academic hospital, in Saint Louis, Missouri, from 1 February 2012 to 30 April 2019. We identified 626 adult patients with Candida BSI that were frequency-matched with 6269 control patients that had similar Candida BSI risk-factors. The 90-day all-cause mortality attributable to Candida BSI was calculated using three methods—propensity score matching, matching by inverse weighting of propensity score, and stratified analysis by quintile. Results The 90-day crude mortality was 42.4% (269 patients) for Candida BSI cases and 17.1% (1083 patients) for frequency-matched controls. Following propensity score-matching, the attributable risk difference for 90-day mortality was 28.4% with hazard ratio (HR) of 2.12 (95% confidence interval [CI], 1.98–2.25, P < .001). In the stratified analysis, the risk for mortality at 90 days was highest in patients in the lowest risk quintile to develop Candida BSI (hazard ratio [HR] 3.13 (95% CI, 2.33–4.19). Patients in this lowest risk quintile accounted for 81(61%) of the 130 untreated patients with Candida BSI. Sixty-nine percent of untreated patients (57/83) died versus 35% of (49/127) of treated patients (P < .001). Conclusions Patients with Candida BSI continue to experience high mortality. Mortality attributable to Candida BSI was more pronounced in patients at lowest risk to develop Candida BSI. A higher proportion of these low-risk patients went untreated, experienced higher mortality, and should be the target of aggressive interventions to ensure timely, effective treatment.

Funder

Astellas Global Development Pharma

Washington University Institute of Clinical and Translational Sciences

National Center for Advancing Translational Sciences

National Institutes of Health

Agency for Healthcare Research and Quality

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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