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Increased mortality in hospital- compared to community-onset carbapenem-resistant enterobacterales infections

  • MDRO Network Investigators and the Antibacterial Resistance Leadership Group
  • Duke University
  • Division of Infectious Diseases
  • University of North Carolina
  • The Biostatistics Center
  • George Washington University
  • Hackensack Meridian Health
  • University of Pittsburgh
  • Departments of Microbiology and Infectious Diseases
  • Fujita Health University School of Medicine
  • Division of Infectious Diseases
  • Cornell University
  • Division of Infectious Diseases and Center for Infectious Diseases Research
  • Houston Methodist
  • Department of Medicine
  • Institute of Antibiotics
  • Fudan University
  • Department of Health Services Research and Policy
  • London School of Hygiene and Tropical Medicine
  • Department of Medicine
  • Henry Ford Health System
  • Department of Infectious Diseases
  • Cleveland Clinic Foundation
  • Division of Infectious Diseases
  • Montefiore Health System
  • Division of Clinical Microbiology
  • Mayo Clinic Rochester, MN
  • Department of Medicine
  • Louis Stokes Cleveland Department of Veterans Affairs Medical Center
  • Case Western Reserve University
  • Departments of Pharmacology
  • Division of Infectious Diseases
  • American University of Beirut
  • Capital Medical University
  • Boston University
  • Case Western
  • Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno
  • Hospital Universitario San Ignacio
  • Universidad El Bosque

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

Background: The CDC reported a 35% increase in hospital-onset (HO) carbapenem-resistant Enterobacterales (CRE) infections during the COVID-19 pandemic. We evaluated patient outcomes following HO and community-onset (CO) CRE bloodstream infections (BSI). Methods: Patients prospectively enrolled in CRACKLE-2 from 56 hospitals in 10 countries between 30 April 2016 and 30 November 2019 with a CRE BSI were eligible. Infections were defined as CO or HO by CDC guidelines, and clinical characteristics and outcomes were compared. The primary outcome was desirability of outcome ranking (DOOR) 30 days after index culture. Difference in 30-day mortality was calculated with 95% CI. Results: Among 891 patients with CRE BSI, 65% were HO (582/891). Compared to those with CO CRE, patients with HO CRE were younger [median 60 (Q1 42, Q3 70) years versus 65 (52, 74); P< 0.001], had fewer comorbidities [median Charlson comorbidity index 2 (1, 4) versus 3 (1, 5); P= 0.002] and were more acutely ill (Pitt bacteraemia score ≥4: 47% versus 32%; P< 0.001). The probability of a better DOOR outcome in a randomly selected patient with CO BSI compared to a patient with HO BSI was 60.6% (95% CI: 56.8%–64.3%). Mortality at 30-days was 12% higher in HO BSI (192/582; 33%) than CO BSI [66/309 (21%); P< 0.001]. Conclusion: We found a disproportionately greater impact on patient outcomes with HO compared to CO CRE BSIs; thus, the recently reported increases in HO CRE infections by CDC requires rigorous surveillance and infection prevention methods to prevent added mortality.

Original languageEnglish
Pages (from-to)2916-2922
Number of pages7
JournalJournal of Antimicrobial Chemotherapy
Volume79
Issue number11
DOIs
StatePublished - 01 Nov 2024
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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