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Higher incidence of neurotoxicity and skin hyperpigmentation in renal transplant patients treated with polymyxin B
Background Toxicity is a major concern related to the clinical use of polymyxin B, and available safety data for renal transplant patients are limited. Aims We investigated the safety of polymyxin B and toxicity risk factors in renal transplant patients. Methods A prospective study was performed on...
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Published in: | British journal of clinical pharmacology 2022-11, Vol.88 (11), p.4742-4750 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
Toxicity is a major concern related to the clinical use of polymyxin B, and available safety data for renal transplant patients are limited.
Aims
We investigated the safety of polymyxin B and toxicity risk factors in renal transplant patients.
Methods
A prospective study was performed on a group of renal transplant patients who received intravenous polymyxin B between January 2018 and August 2021. Polymyxin B treatment was monitored to evaluate toxicity and risk factors.
Results
A total of 235 courses of polymyxin B were administered to 213 patients. Of these, 121 (51.5%) developed skin hyperpigmentation (SH), 149 (63.4%) developed neurotoxicity and 10 (5.5%) developed acute kidney injury of which 80% was reversible. Risk factors for developing SH included a high total dose by weight (odds ration [OR] 1.31, 95% confidence interval [CI] 1.08–1.60, P = .008) and the presence of neurotoxicity (OR 2.86, 95% CI 1.56–5.26, P = .001). Neurotoxicity manifested during the first 2 days of treatment. Neurotoxicity occurred most commonly in women (OR 3.84, 95% CI 1.82–8.10, P |
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ISSN: | 0306-5251 1365-2125 |
DOI: | 10.1111/bcp.15384 |