Higher incidence of neurotoxicity and skin hyperpigmentation in renal transplant patients treated with polymyxin B
- PMID: 35508710
- DOI: 10.1111/bcp.15384
Higher incidence of neurotoxicity and skin hyperpigmentation in renal transplant patients treated with polymyxin B
Abstract
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 < .0001), and the presence of SH (OR 1.98, 95% CI 1.13-3.46, P = .016) was also an independent risk factor.
Conclusions: Neurotoxicity and SH are the two major adverse effects of polymyxin B in renal transplant patients, which may limit its clinical use.
Keywords: neurotoxicity; polymyxin B; renal transplant patients; safety; skin hyperpigmentation.
© 2022 British Pharmacological Society.
References
REFERENCES
-
- Velkov T, Thompson PE, Azad MAK, Roberts KD, Bergen PJ. History, Chemistry and antibacterial spectrum. Adv Exp Med Biol. 2019;1145:15-36. doi:10.1007/978-3-030-16373-0_3
-
- Tsuji BT, Pogue JM, Zavascki AP, et al. International Consensus Guidelines for the Optimal Use of the Polymyxins: Endorsed by the American College of Clinical Pharmacy (ACCP), European Society of Clinical Microbiology and Infectious Diseases (ESCMID), Infectious Diseases Society of America (IDSA), International Society for Anti-infective Pharmacology (ISAP), Society of Critical Care Medicine (SCCM), and Society of Infectious Diseases Pharmacists (SIDP). Pharmacotherapy. 2019;39(1):10-39. doi:10.1002/phar.2209
-
- Justo JA, Bosso JA. Adverse reactions associated with systemic polymyxin therapy. Pharmacotherapy. 2015;35(1):28-33. doi:10.1002/phar.1493
-
- Falagas ME, Kasiakou SK. Toxicity of polymyxins: a systematic review of the evidence from old and recent studies. Crit Care. 2006;10(1):R27. doi:10.1186/cc3995
-
- Nelson BC, Eiras DP, Gomez-Simmonds A, et al. Clinical outcomes associated with polymyxin B dose in patients with bloodstream infections due to carbapenem-resistant Gram-negative rods. Antimicrob Agents Chemother. 2015;59(11):7000-7006. doi:10.1128/AAC.00844-15
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical