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Clinical Features and Outcomes of Infections Caused by Metallo-β-Lactamase–Producing Enterobacterales: A 3-Year Prospective Study From an Endemic Area.
Document Type
Article
Source
Clinical Infectious Diseases. 5/15/2024, Vol. 78 Issue 5, p1111-1119. 9p.
Subject
*URINARY tract infections
*SOFT tissue infections
*ANTIBIOTICS
*IN vitro studies
*ENTEROBACTERIACEAE diseases
*ACADEMIC medical centers
*CROSS infection
*INFECTION control
*SCIENTIFIC observation
*MULTIPLE regression analysis
*BLOODBORNE infections
*CATHETER-related infections
*HOSPITAL mortality
*MULTIVARIATE analysis
*DESCRIPTIVE statistics
*VENTILATOR-associated pneumonia
*INTRA-abdominal infections
*COLISTIN
*LONGITUDINAL method
*BETA lactamases
*CONFIDENCE intervals
*CEFTAZIDIME
*AZTREONAM
*COMPARATIVE studies
*PROPORTIONAL hazards models
*SYMPTOMS
Language
ISSN
1058-4838
Abstract
Background Metallo-β-lactamase (MBL)–producing Enterobacterales are increasing worldwide. Our aim was to describe clinical features, treatments, and outcomes of infections by MBL-Enterobacterales. Methods A prospective observational study conducted in the Pisa University Hospital (January 2019 to October 2022) included patients with MBL-producing Enterobacterales infections. The primary outcome measure was the 30-day mortality rate. Multivariable Cox regression analysis was performed to identify factors associated with that mortality rate, and adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) were calculated. Results The study's 343 patients included 15 with Verona integron-encoded MBL (VIM)- and 328 with New Delhi MBL (NDM)–producing Enterobacterales infections; there were 199 patients (58%) with bloodstream infections, 60 (17.5%) with hospital-acquired or ventilator-associated pneumonia, 60 (17.5%) with complicated urinary tract infections, 13 (3.8%) with intra-abdominal infections, and 11 (3.2%) with skin and soft-tissue infections. The 30-day mortality rate was 29.7%. Of 343 patients, 32 did not receive in vitro active antibiotic therapy, 215 (62.7%) received ceftazidime-avibactam plus aztreonam, 33 (9.6%) received cefiderocol-containing regimens, 26 (7.6%) received colistin-containing regimens, and 37 (10.8%) received other active antibiotics. On multivariable analysis, septic shock (aHR, 3.57 [95% CI, 2.05–6.23]; P <.001) and age (1.05 [1.03–1.08]; P <.001) were independently associated with the 30-day mortality rate, while in vitro active antibiotic therapy within 48 hours after infection (0.48 [.26–.8]; P =.007) and source control (0.43 [.26–.72]; P =.001) were protective factors. Sensitivity analysis showed that ceftazidime-avibactam plus aztreonam, compared with colistin, was independently associated with a reduced 30-day mortality rate (aHR, 0.39 [95% CI,.18–.86]; P =.02). Propensity score analyses confirmed these findings. Conclusions MBL-producing carbapenem-resistant Enterobacterales infections are associated with high 30-day mortality rates. Patients with MBL-producing Enterobacterales infections should receive early active antibiotic therapy. [ABSTRACT FROM AUTHOR]