Evidence map›Paper›PMID 42387410›Full record

Observational studyBMC infectious diseases2026

Effectiveness of conventional antimicrobial agents against carbapenem resistant non-carbapenem β-lactams susceptible Pseudomonas aeruginosa infection in critically ill patients: a multicentre retrospective study.

Sheng-Huei Wang, Wei-Cheng Chen, Ming-Cheng Chan, Kuang-Yao Yang, Chau-Chyun Sheu, Biing-Ru Wu, Wei-Hsuan Huang, Jia-Yih Feng, Chia-Min Chen, Tzu-Hsuan Weng and 4 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Sheng-Huei WangDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan.
Wei-Cheng ChenDivision of Pulmonary and Critical Care, Department of Internal Medicine, China Medical University Hospital, Taichung, Taiwan.
Ming-Cheng ChanDepartment of Critical Care Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Kuang-Yao YangDepartment of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Chau-Chyun SheuDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Biing-Ru WuDivision of Pulmonary and Critical Care, Department of Internal Medicine, China Medical University Hospital, Taichung, Taiwan.
Wei-Hsuan HuangDivision of Infectious Diseases, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Jia-Yih FengDepartment of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Chia-Min ChenDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Tzu-Hsuan WengDepartment of Medical Research, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Yi-Lin ChiuGraduate Institute of Biochemistry, College of Biomedical Sciences, National Defense Medical University, Taipei, Taiwan.
Chung-Kan PengDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan.
Chih-Hao ShenDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan. potato652@yahoo.com.tw.
T-CARE (Taiwan Critical Care and Infection) Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarbapenem resistant non-carbapenem β-lactam susceptible (CRBS) Pseudomonas aeruginosa (PA) is a unique phenotype of carbapenem-resistant Pseudomonas aeruginosa (CRPA). While guidelines suggest using conventional β-lactams, clinical evidence supporting their effectiveness in critically ill patients remains limited. This study evaluated the associations of conventional antimicrobial agents with clinical outcomes in CRBS PA infections in the intensive care unit (ICU).

methodsThis multicentre retrospective cohort study included 178 patients with CRPA-associated pneumonia or bloodstream infections, comprising 119 patients with CRBS PA and 59 patients with carbapenem-resistant non-carbapenem β-lactam resistant (CRBR) PA. Patient outcomes were compared between phenotypes. The primary endpoint was to evaluate the associations between specific antimicrobial agents and clinical outcomes in CRBS PA infections, using multivariable stepwise logistic regression analyses for in-hospital mortality, day-28 mortality, day-28 clinical failure, and day-28 microbiological eradication.

resultsThe CRBS PA group demonstrated significantly lower clinical failure rates compared to the CRBR PA group (45.4% vs. 62.7%, p = 0.034), suggesting potential clinical relevance of this phenotype. In the multivariable analysis of CRBS PA infections, treatment with piperacillin-tazobactam (OR: 0.52, p = 0.03) and ceftazidime (OR: 0.27, p = 0.01) was independently associated with lower in-hospital mortality. Levofloxacin was also associated with lower in-hospital mortality (OR: 0.40, p = 0.01), lower day-28 clinical failure, and higher day-28 microbiological eradication rates (OR: 4.87, p = 0.02), although this finding should be interpreted separately from the β-lactam-based CRBS phenotype.

conclusionsThis study suggests that piperacillin-tazobactam, ceftazidime, and levofloxacin may be reasonable definitive treatment options for critically ill patients with CRBS PA infections. These findings support the consideration of carbapenem-sparing approaches in this specific CRPA phenotype, in line with current therapeutic guidance.

Indexed as

Anti-Bacterial AgentsPseudomonas aeruginosaPseudomonas InfectionsAgedbeta-Lactam Resistancebeta-LactamsCarbapenemsCritical IllnessFemaleHumansIntensive Care UnitsMaleMicrobial Sensitivity TestsMiddle AgedPiperacillinPiperacillin, Tazobactam Drug CombinationAnti-Bacterial Agentsbeta-LactamsCarbapenemsPiperacillinPiperacillin, Tazobactam Drug CombinationBloodstream infectionCarbapenem resistant non-carbapenem β-lactams susceptible Pseudomonas aeruginosaClinical failureMicrobiological eradicationPneumonia

Identifiers

PMID42387410
PMCPMC13599225

What OpenQuestion holds

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Registered trials

None linked

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.