Polymyxin B and the Pulmonary Peril: A Case Series of Acute Respiratory Failure.

Q3 Medicine
Case Reports in Critical Care Pub Date : 2026-09-21 eCollection Date: 2026-01-01 DOI:10.1155/crcc/5569011
Lovely Thomas, John Victor Peter, Binu Susan Mathew, Sara Jose, Lisa Merin Joseph, Jeethu Joseph Eapen, Sirish Chandra Srinath Patloori, Binila Chacko
{"title":"Polymyxin B and the Pulmonary Peril: A Case Series of Acute Respiratory Failure.","authors":"Lovely Thomas, John Victor Peter, Binu Susan Mathew, Sara Jose, Lisa Merin Joseph, Jeethu Joseph Eapen, Sirish Chandra Srinath Patloori, Binila Chacko","doi":"10.1155/crcc/5569011","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The neurotoxicity potential of polymyxin B is underrecognized.</p><p><strong>Results: </strong>Four critically ill patients treated with polymyxin B for suspected or confirmed nosocomial Gram-negative infections developed acute hypercapnic respiratory failure temporally associated with polymyxin B administration. Respiratory support escalated from room air or low-flow oxygen to noninvasive or invasive mechanical ventilation after one, two, five, and seven doses of polymyxin. No alternative explanation for the abrupt deterioration was identified after clinical evaluation. Following cessation of polymyxin (<i>n</i> = 3) or dose reduction (<i>n</i> = 1), all patients were liberated from ventilation within 60 h. Measured polymyxin concentrations were above the therapeutic range in all patients; however, the delayed timing of sampling, measured at variable intervals after the respiratory events, limits conclusions regarding causality and dose-dependent toxicity.</p><p><strong>Conclusion: </strong>Polymyxin B should be considered as a potential cause of acute hypercapnic respiratory failure in critically ill patients when no alternative explanation is apparent. Both idiosyncratic susceptibility and drug accumulation may contribute, although the delayed timing of drug concentration measurements precludes firm conclusions regarding dose-dependent toxicity. Further prospective studies are required to define the mechanisms and risk factors.</p>","PeriodicalId":52357,"journal":{"name":"Case Reports in Critical Care","volume":"2026 ","pages":"5569011"},"PeriodicalIF":0.0000,"publicationDate":"2026-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13594767/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Critical Care","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/crcc/5569011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The neurotoxicity potential of polymyxin B is underrecognized.

Results: Four critically ill patients treated with polymyxin B for suspected or confirmed nosocomial Gram-negative infections developed acute hypercapnic respiratory failure temporally associated with polymyxin B administration. Respiratory support escalated from room air or low-flow oxygen to noninvasive or invasive mechanical ventilation after one, two, five, and seven doses of polymyxin. No alternative explanation for the abrupt deterioration was identified after clinical evaluation. Following cessation of polymyxin (n = 3) or dose reduction (n = 1), all patients were liberated from ventilation within 60 h. Measured polymyxin concentrations were above the therapeutic range in all patients; however, the delayed timing of sampling, measured at variable intervals after the respiratory events, limits conclusions regarding causality and dose-dependent toxicity.

Conclusion: Polymyxin B should be considered as a potential cause of acute hypercapnic respiratory failure in critically ill patients when no alternative explanation is apparent. Both idiosyncratic susceptibility and drug accumulation may contribute, although the delayed timing of drug concentration measurements precludes firm conclusions regarding dose-dependent toxicity. Further prospective studies are required to define the mechanisms and risk factors.

多粘菌素B与肺危险:急性呼吸衰竭系列病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Case Reports in Critical Care
Case Reports in Critical Care Medicine-Critical Care and Intensive Care Medicine
CiteScore
2.10
自引率
0.00%
发文量
26
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书