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mGem: Sepsis and antimicrobial resistance in the context of advanced HIV disease

Wake, RM; Govender, NP (2025) mGem: Sepsis and antimicrobial resistance in the context of advanced HIV disease. mBio, 16 (5). ISSN 2150-7511 https://doi.org/10.1128/mbio.00769-24
SGUL Authors: Wake, Rachel Marie

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Abstract

Sepsis triggered by bloodstream infections (BSI) is a significant driver of HIV-related mortality, particularly among in-patients with advanced HIV disease (AHD). Currently, the incidence, etiology, and outcomes of BSI in this population are poorly defined. We review the existing evidence, which shows an increased risk of BSI, particularly with antimicrobial-resistant (AMR) organisms, and higher BSI-associated mortality in patients with AHD. Causative bacterial and fungal pathogens are often unknown, but when identified, limited data show etiology has shifted probably owing to increasing coverage of antiretroviral treatment, antimicrobial prophylaxis, and rising global AMR trends. Further research is crucial to design and refine interventions before, during, and after hospital admission to reduce sepsis-related mortality in patients with AHD.

Item Type: Article
Additional Information: © 2025 Wake and Govender. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/).
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: mBio
Editors: Rodrigues, Marcio
ISSN: 2150-7511
Language: en
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
NIHR 134342National Institute for Health and Care Researchhttps://doi.org/10.13039/501100000272
NIHR 303140National Institute for Health and Care Researchhttps://doi.org/10.13039/501100000272
INV077442Bill and Melinda Gates Foundationhttp://dx.doi.org/10.13039/100000865
URI: https://openaccess.sgul.ac.uk/id/eprint/117609
Publisher's version: https://doi.org/10.1128/mbio.00769-24

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