ArticleInternational journal of clinical pharmacy2026
Nephrotoxicity of polymyxin B and colistin sulfate in patients with multidrug-resistant gram-negative bacteria infections: a parametric time-to-event analysis.
Article in International journal of clinical pharmacy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
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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.
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.
Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- The outcomes in nephrotoxicity among therapies utilizing three distinct polymyxins: a systematic review and network meta-analysis.Frontiers in medicine · 2026Pooled it
- Predictors of In-Hospital Mortality Among Hospitalized Colistin-Treated Patients at a Tertiary Urology-Nephrology Referral Center.Antibiotics (Basel, Switzerland) · 2026Article
- Comparative efficacy and safety of colistin sulfate versus polymyxin B in critically ill patients with carbapenem-resistant gram-negative infections: a pilot inverse probability of treatment weighting-based retrospective cohort study.BMC infectious diseases · 2026Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
introductionMultidrug-resistant Gram-negative bacteria (MDR-GNB), especially carbapenem-resistant strains, pose a major therapeutic challenge in intensive care units and are associated with high morbidity and mortality. Polymyxin B (PMB) and colistin sulfate (CS) are the last-line agents for MDR-GNB infections; however, their clinical use is limited by nephrotoxicity. Although the steady-state 24-h area under the curve (AUC
aimThis study aimed to identify clinical and pharmacological factors influencing PMB- and CS-associated nephrotoxicity in critically ill patients with MDR-GNB infections and to establish AUC
methodWe retrospectively analyzed real-world data from 562 patients with MDR-GNB infections treated with PMB (n = 354) or CS (n = 208) at Xiangya Third Hospital, Central South University, between July 2018 and July 2023. Pharmacokinetic profiles were simulated using published models, and drug exposure parameters (AUC
resultsOverall, 39.4% of patients developed AKI, with a significantly higher incidence in the PMB group than in the CS group (51.7% vs. 18.4%). The final PMB model identified AUC
conclusionIn critically ill patients with MDR-GNB infections, higher plasma exposure to PMB and CS was strongly associated with increased nephrotoxicity. Exposure thresholds of AUC
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