TY - JOUR
T1 - Severe health-care-associated infections and antimicrobial resistance in an Asian Surveillance Network (ACORN-HAI)
T2 - a multicentre, prospective cohort study
AU - ACORN-HAI investigators
AU - Mo, Yin
AU - Hao, Xinxin
AU - Ding, Ying
AU - Cao, Yang
AU - Cai, Yiying
AU - Kitsaran, Suwatthiya
AU - Chua, Hock Hin
AU - Bory, Sotharith
AU - Sri La Sri Ponnampalavanar, Sasheela
AU - Anunnatsiri, Siriluck
AU - Mazlan, Mohd Zulfakar
AU - Dhiloo, Azizullah Khan
AU - Plongla, Rongpong
AU - Kwa, Andrea Lay Hoon
AU - Mahmood, Syed Faisal
AU - Roman, Arthur Dessi
AU - Thwaites, Louise
AU - Tho, Phan Vinh
AU - Wu, Sheng
AU - Chotiprasitsakul, Darunee
AU - Wong, Ke Juin
AU - Wijaya, Hendri
AU - Abad, Cybele L.
AU - Khalid, Muhammad Osama Rehman
AU - Mamun, Gazi Md Salahuddin
AU - Rajahram, Giri Shan
AU - Guterres, Helio
AU - Hon, Huynh Ngoc
AU - Pham, Ngoc Thach
AU - Tran, Van Giang
AU - Karkey, Abhilasha
AU - Gunasekara, Samanmalee
AU - Hamers, Raph L.
AU - Sinto, Robert
AU - Lubis, Inke Nadia D.
AU - Wang, Minggui
AU - Moni, Merlin
AU - Liu, Po Yu
AU - Xiao, Yonghong
AU - Khanal, Basudha
AU - Priya, N. Lakshmi
AU - Doi, Yohei
AU - Honda, Hitoshi
AU - Baljin, Bayaraa
AU - Asli, Rosmonaliza
AU - Gurjav, Ulziijargal
AU - Ling, Lowell
AU - Dhungana, Ashesh
AU - Hsu, Li Yang
AU - Paterson, David Leslie
N1 - Publisher Copyright:
© 2026 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
PY - 2026
Y1 - 2026
N2 - Background: Antimicrobial resistance (AMR) poses a major global health threat, with health-care-associated infections contributing substantially to mortality. Attributable disease burden remains poorly quantified by relying on cross-sectional and microbiology data. We aimed to characterise AMR epidemiology and disease burden associated with ventilator-associated pneumonia and bloodstream infection in a network of hospitals in Asia. Methods: This large-scale, prospective, multinational, multicentre cohort study consecutively enrolled patients of any age with microbiologically-confirmed ventilator-associated pneumonia, hospital-acquired bloodstream infections, or health-care-associated bloodstream infections from 41 selected hospitals capable of standardised prospective data collection in 19 Asian countries and regions. Patients with pathogens typically associated with community-acquired infection or not recognised causes of health-care-associated infection were excluded according to predefined protocol criteria, and patients were followed for 28 days. The primary outcome was 28-day mortality from infection onset. Pathogen profiles, antimicrobial prescriptions, attributable mortality, and health-related quality-of-life outcomes were analysed. Findings: Between Sept 1, 2022, and Feb 28, 2025, 10 111 patients were enrolled, and after exclusions, 9496 patients were included in the final analysis. 9642 infection episodes were analysed, comprising 6597 (68·4%) bloodstream infections and 3045 (31·6%) ventilator-associated pneumonia. Of these infections, 7102 (73·7%) of 9642 infection episodes were associated with AMR bacteria, and Gram-negative bacteria were predominant (7599 [78·8%]). Crude 28-day mortality was 2674 (37·7%) of 7102 AMR infection episodes and 1900 (40·6%) of 4683 multidrug resistance infection episodes, with the highest for carbapenem-resistant Acinetobacter spp (CRA; 51·3%) and carbapenem-resistant Enterobacterales (CRE; 48·4%). AMR-attributable mortality was the highest in ventilator-associated pneumonia (16·9%, 95% CI 13·0–20·9), individuals aged 5–14 years (11·7%, 95% CI 1·6–21·8), individuals aged 15–49 years (11·2%, 95% CI 7·2–15·2), and lower-middle-income countries (10·7%, 95% CI 7·0–14·4). By pathogens, CRA and CRE had the highest attributable mortality (19·4%, 95% CI 14·1–24·7 vs 16·2%, 95% CI 12·8–19·6) and also had the poorest quality-of-life outcomes. Most carbapenem-resistant Gram-negative infections were treated with carbapenems (57·8%) or polymyxins (35·6%). Interpretation: AMR bacterial bloodstream infections and ventilator-associated pneumonia were common and associated with high mortality and reduced quality of life in Asia, particularly in infections due to carbapenem-resistant Acinetobacter spp and CRE, and among children and younger adults. The widespread use of suboptimal antimicrobial regimens highlights the urgent need for equitable access to effective therapies and context-specific evidence to guide antimicrobial stewardship. Funding: Wellcome Trust, National University of Singapore, Yong Loo Lin School of Medicine, Duke-NUS Medical School, Nanyang Technological University (Lee Kong Chian School of Medicine), Singapore National Centre for Infectious Diseases, and Singapore Medical Research Council.
AB - Background: Antimicrobial resistance (AMR) poses a major global health threat, with health-care-associated infections contributing substantially to mortality. Attributable disease burden remains poorly quantified by relying on cross-sectional and microbiology data. We aimed to characterise AMR epidemiology and disease burden associated with ventilator-associated pneumonia and bloodstream infection in a network of hospitals in Asia. Methods: This large-scale, prospective, multinational, multicentre cohort study consecutively enrolled patients of any age with microbiologically-confirmed ventilator-associated pneumonia, hospital-acquired bloodstream infections, or health-care-associated bloodstream infections from 41 selected hospitals capable of standardised prospective data collection in 19 Asian countries and regions. Patients with pathogens typically associated with community-acquired infection or not recognised causes of health-care-associated infection were excluded according to predefined protocol criteria, and patients were followed for 28 days. The primary outcome was 28-day mortality from infection onset. Pathogen profiles, antimicrobial prescriptions, attributable mortality, and health-related quality-of-life outcomes were analysed. Findings: Between Sept 1, 2022, and Feb 28, 2025, 10 111 patients were enrolled, and after exclusions, 9496 patients were included in the final analysis. 9642 infection episodes were analysed, comprising 6597 (68·4%) bloodstream infections and 3045 (31·6%) ventilator-associated pneumonia. Of these infections, 7102 (73·7%) of 9642 infection episodes were associated with AMR bacteria, and Gram-negative bacteria were predominant (7599 [78·8%]). Crude 28-day mortality was 2674 (37·7%) of 7102 AMR infection episodes and 1900 (40·6%) of 4683 multidrug resistance infection episodes, with the highest for carbapenem-resistant Acinetobacter spp (CRA; 51·3%) and carbapenem-resistant Enterobacterales (CRE; 48·4%). AMR-attributable mortality was the highest in ventilator-associated pneumonia (16·9%, 95% CI 13·0–20·9), individuals aged 5–14 years (11·7%, 95% CI 1·6–21·8), individuals aged 15–49 years (11·2%, 95% CI 7·2–15·2), and lower-middle-income countries (10·7%, 95% CI 7·0–14·4). By pathogens, CRA and CRE had the highest attributable mortality (19·4%, 95% CI 14·1–24·7 vs 16·2%, 95% CI 12·8–19·6) and also had the poorest quality-of-life outcomes. Most carbapenem-resistant Gram-negative infections were treated with carbapenems (57·8%) or polymyxins (35·6%). Interpretation: AMR bacterial bloodstream infections and ventilator-associated pneumonia were common and associated with high mortality and reduced quality of life in Asia, particularly in infections due to carbapenem-resistant Acinetobacter spp and CRE, and among children and younger adults. The widespread use of suboptimal antimicrobial regimens highlights the urgent need for equitable access to effective therapies and context-specific evidence to guide antimicrobial stewardship. Funding: Wellcome Trust, National University of Singapore, Yong Loo Lin School of Medicine, Duke-NUS Medical School, Nanyang Technological University (Lee Kong Chian School of Medicine), Singapore National Centre for Infectious Diseases, and Singapore Medical Research Council.
UR - https://www.scopus.com/pages/publications/105048582902
UR - https://www.scopus.com/pages/publications/105048582902#tab=citedBy
U2 - 10.1016/S1473-3099(26)00357-9
DO - 10.1016/S1473-3099(26)00357-9
M3 - Article
C2 - 42628558
AN - SCOPUS:105048582902
SN - 1473-3099
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
ER -