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Published on: August 30, 2018
Clinical features and mortality of patients on renal replacement therapy receiving polymyxin B
Maria Helena Rigatto1, Diego R Falci2, Natane T Lopes3
1Infectious Diseases Service, Hospital São Lucas da Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil; Infectious Diseases Service, Hospital de Clínicas de Porto Alegre, 2350 Ramiro Barcelos St., Porto Alegre 90.035-903, Brazil.
Abstract:
There are no clinical data for polymyxin B (PMB) in patients on renal replacement therapy (RRT). The aim of this study was to evaluate the characteristics of patients on RRT receiving PMB and to identify predictors of 30-day mortality, with special focus on dosage. A multicentre prospective cohort study including patients aged ≥18 years treated with PMB for ≥48h while on any type of RRT was performed. In total, 88 patients were evaluated, including 34 (38.6%) on continuous venovenous haemodialysis (CVVH) and 54 (61.4%) on intermittent haemodialysis. Most patients (81.8%) received recommended doses between 1.5mg/kg/day and 3.0mg/kg/day. The 30-day mortality was 51.1% (45/88 patients). There was no significant association of dose (in mg/kg) with mortality. A PMB average daily dose ≥200mg was predictive of decreased 30-day mortality in the multivariate model (hazard ratio=0.35, 95% confidence interval 0.14-0.90; P=0.03), whilst CVVH (P=0.04), higher Charlson co-morbidity index (P=0.02) and Acute Physiology and Chronic Health Evaluation (APACHE) II score (P=0.04), and Pseudomonas aeruginosa infection (P=0.001) were independent risk factors for mortality. The results were not changed by the inclusion of patient weight or dose (in mg/kg) in the model, although the latter was significantly correlated with total daily dose. This is the first clinical study to show that higher doses of PMB are associated with lower mortality in patients on RRT.
Insights
Polymyxin B (PMB) dosing in renal replacement therapy (RRT) patients is unclear. Higher daily PMB doses (≥200mg) were linked to reduced 30-day mortality in this RRT patient cohort.
Area of Science:
- Nephrology
- Infectious Diseases
- Clinical Pharmacology
Background:
- Limited clinical data exists for polymyxin B (PMB) use in patients undergoing renal replacement therapy (RRT).
- Optimal PMB dosing strategies in RRT patients remain undefined, impacting treatment efficacy and patient outcomes.
Purpose of the Study:
- To characterize patients on RRT receiving PMB.
- To identify predictors of 30-day mortality in this population, with a focus on PMB dosage.
Main Methods:
- A multicenter prospective cohort study involving 88 adult patients on RRT receiving PMB for at least 48 hours.
- Data collected included RRT modality (continuous venovenous haemodialysis or intermittent haemodialysis), PMB dosage, comorbidities (Charlson index), and severity scores (APACHE II).
- Statistical analysis identified predictors of 30-day mortality.
Main Results:
- The 30-day mortality rate was 51.1%.
- While the dose in mg/kg was not associated with mortality, a higher average daily PMB dose (≥200mg) predicted decreased 30-day mortality (HR=0.35).
- Independent risk factors for mortality included continuous venovenous haemodialysis, higher Charlson and APACHE II scores, and Pseudomonas aeruginosa infection.
Conclusions:
- This is the first clinical study to suggest that higher daily doses of polymyxin B may be associated with lower 30-day mortality in patients on renal replacement therapy.
- Further research is warranted to establish definitive dosing guidelines for PMB in RRT patients to optimize survival outcomes.
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