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Demographics, epidemiology, mortality and difficult-to-treat resistance patterns of bacterial bloodstream infections in the global US Military Health System from 2010 to 2019: a retrospective cohort study

  1. Author:
    Vostal, Alexander C [ORCID]
    Grance, Melissa
    Powers,John
    Kadri, Sameer S
    Warner, Sarah
    Chukwuma, Uzo
    Morales, Carlos
    Lanteri, Charlotte
    Carson, M Leigh
    Poitras, Beth
    Seliga, Nicholas
    Follmann, Dean
    Wang,Jing
    Parmelee, Edward
    Mende, Katrin
  2. Author Address

    Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA alexander.vostal@nih.gov., Infectious Disease Clinical Research Program, Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA., Henry M Jackson Foundation for the Advancement of Military Medicine, Inc, Bethesda, Maryland, USA., Clinical Research Directorate, National Cancer Institute Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA., Critical Care Medicine Department, National Institutes of Health Clinical Center, Bethesda, Maryland, USA., Critical Care Medicine Branch, National Heart Lung and Blood Institute, Bethesda, Maryland, USA., Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA., Defense Centers for Public Health-Portsmouth, Portsmouth, Virginia, USA., Indian Health Services, Rockville, Maryland, USA., Office of Biostatistics Research, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA., Clinical Monitoring Research Program Directorate, National Cancer Institute Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA., Brooke Army Medical Center, Fort Sam Houston, Texas, USA.,
    1. Year: 2025
    2. Date: Mar 03
    3. Epub Date: 2025 03 03
  1. Journal: BMJ Open
    1. 15
    2. 3
    3. Pages: e094861
  2. Type of Article: Article
  3. Article Number: e094861
  1. Abstract:

    To describe demographics, causative pathogens, hospitalisation, mortality and antimicrobial resistance (AMR) of bacterial bloodstream infections (BSIs) among beneficiaries in the global US Military Health System (MHS), a single-provider healthcare system with 10-year longitudinal follow-up. Retrospective cohort study. Clinical and demographic data collected from the MHS Data Repository and collated with microbiological data obtained from the Defense Centers for Public Health-Portsmouth. Participants: 12?748 MHS beneficiaries diagnosed with 15?357 bacterial BSIs (2010-2019). Demographic data and diagnosis codes preceding BSI episodes and during hospitalisations were collected. Inpatient admission data identified acute clinical diagnoses, intensive care unit (ICU) admission and mortality. BSI pathogens were evaluated for AMR, including difficult-to-treat resistance (DTR). Crude mortality trends were assessed. The decade analysed included 15?357 BSI episodes in 12?748 patients; 6216 patients (48.8%) were=65 years and 83.7% of episodes had=1 comorbidity (12?856 of 15 357). Approximately 29% of episodes with hospitalisation required ICU admission and~34% had concurrent urinary tract infections. Pathogen distribution was 53% and 47% for Gram-positive bacteria and Gram-negative bacilli (GNB), respectively. Inpatient mortality was 4.4%, and at 1 year was 23.4%; 0.5% (16 of 2977) of deaths were associated with DTR GNB. Among an average 8?145?778 individuals receiving care annually in the MHS, annual rates of overall BSI, methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus spp and DTR GNB BSI were 18.9, 1.30, 0.25 and 0.05 per 100?000 beneficiaries, respectively. Over the decade, annual mortality did not significantly increase for any pathogen and decreased by~2% for overall BSI (p=0.024) and~3% for lactose-fermenting GNB BSI (p=0.048). In the global US MHS, the mortality burden associated with BSI was substantial (approximately one in four dying at 1 year), relatively unchanged over a decade, and associated with older age and comorbidities. First-line treatment options remained available for 99.7% of BSIs. Population-level improvements in BSI survival might be maximally influenced by focusing on prevention, early detection, prompt antibiotics and other novel therapies not contingent on in vitro activity. © Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.

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External Sources

  1. DOI: 10.1136/bmjopen-2024-094861
  2. PMID: 40032367
  3. PMCID: PMC11877242
  4. PII : bmjopen-2024-094861

Library Notes

  1. Fiscal Year: FY2024-2025
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