Evidence map›Paper›PMID 41496730›Full record

ArticleInternational health2026

Antimicrobial resistance analysis of Klebsiella pneumoniae bloodstream infections based on a random forest algorithm: a longitudinal study based on data from tertiary hospitals in China from 2012 to 2023.

Na Wang, AiLing Hu, Zexin Wang, Xiaojie Yu, Ying Wei, PingPing Song

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Article in International health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Na WangDepartment of Pharmacy, The First Hospital of Qinhuangdao, Qinhuangdao 066000, China.ORCID 0009-0009-5022-1649
AiLing HuDepartment of Pharmacy, The First Hospital of Qinhuangdao, Qinhuangdao 066000, China.
Zexin WangDepartment of Pharmacy, The First Hospital of Qinhuangdao, Qinhuangdao 066000, China.
Xiaojie YuDepartment of Pharmacy, The First Hospital of Qinhuangdao, Qinhuangdao 066000, China.
Ying WeiDepartment of Pharmacy, The First Hospital of Qinhuangdao, Qinhuangdao 066000, China.
PingPing SongDepartment of Pharmacy, The First Hospital of Qinhuangdao, Qinhuangdao 066000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBloodstream infections (BSIs) caused by Klebsiella pneumoniae pose a significant global health burden, complicated by rising antimicrobial resistance (AMR). This study aimed to characterize resistance patterns, identify predictors of carbapenem resistance, and develop a machine learning model to predict patient outcomes.

methodsIn a retrospective analysis of 109 279 K. pneumoniae BSIs from tertiary hospitals in China (2012-2023), 11 000 isolates underwent whole-genome sequencing (WGS) and antimicrobial susceptibility testing. Cox proportional hazards and logistic regression models identified predictors of 30-day mortality and carbapenem-resistant K. pneumoniae (CRKP), respectively. A random forest model predicted AMR trends and outcomes, evaluated by accuracy, precision, recall, and ROC-AUC using R Studio (R Studio, Inc., Boston, MA, USA).

resultsCarbapenem resistance occurred in 32.3% of isolates, with rates of 41.9% for third-generation cephalosporins and 41.2% for fluoroquinolones. Among sequenced isolates, ST11 with blaKPC was the dominant CRKP genotype (12.0%). blaKPC (OR 3.97, 95% CI 3.10-5.11) and blaNDM (OR 2.80, 95% CI 2.07-3.71) strongly predicted carbapenem resistance; ICU admission predicted 30-day mortality (HR 2.10, 95% CI 1.80-2.46, p<0.001). Mortality was higher in CRKP (40.2%) vs. susceptible cases (21.5%). The random forest model achieved 89.2% accuracy and 0.92 ROC-AUC, with drug share, age, and CRKP status as top predictors.

conclusionsCRKP, especially ST11-blaKPC, drives excess mortality. Key predictors highlight the urgency for enhanced AMR surveillance and targeted therapy.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialKlebsiella InfectionsKlebsiella pneumoniaeCarbapenemsChinaFemaleHumansLongitudinal StudiesMachine LearningMicrobial Sensitivity TestsRandom ForestRetrospective StudiesTertiary Care CentersWhole Genome SequencingAnti-Bacterial AgentsCarbapenemsantimicrobial resistancebloodstream infectionscarbapenem resistanceKlebsiella pneumoniaemachine learningwhole-genome sequencing

Identifiers

PMID41496730
PMCPMC13530284

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.