Alaa Almagthali, Khalid Al Sulaiman, Samiah Alsohimi, Kholoud Al Aamer, Alaa Naser Kurdi, Alwaleed Nasser Al Qurashi, Nawaf Shalih Alqahtani, Aljoharah Khaled Alqub, Waad A Alnami, Abdullah M Alhammad, Fatimah Abudayah, Ohoud Aljuhani
{"title":"Montelukast and Delirium Risk During Intensive Care Unit (ICU) Stay: Findings from a Cohort Study.","authors":"Alaa Almagthali, Khalid Al Sulaiman, Samiah Alsohimi, Kholoud Al Aamer, Alaa Naser Kurdi, Alwaleed Nasser Al Qurashi, Nawaf Shalih Alqahtani, Aljoharah Khaled Alqub, Waad A Alnami, Abdullah M Alhammad, Fatimah Abudayah, Ohoud Aljuhani","doi":"10.2147/CPAA.S586979","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Delirium is a frequent complication in critically ill patients and is associated with increased mortality, prolonged hospitalization, and long-term cognitive impairment. Montelukast, a leukotriene receptor antagonist commonly used in respiratory diseases, has been associated with neuropsychiatric adverse effects, including delirium. Evidence regarding its safety in critically ill adults is limited. This study aimed to investigate the association between montelukast use during ICU stay and the development of delirium and further evaluate its safety in the ICU.</p><p><strong>Methods: </strong>This retrospective cohort study was conducted at King Abdulaziz Medical City, Saudi Arabia, between January 2018 and December 2021. Adult critically ill patients (18-79 years) who were admitted to ICUs for respiratory symptoms and categorized based on montelukast exposure during ICU stay. The primary outcome was assessing the incidence of delirium during ICU stay. Secondary outcomes included delirium duration, recurrence of delirium, delirium-free days, ventilator-free days, length of stay (LOS), safety outcomes (liver and kidney injury), 30-day and in-hospital mortality. Propensity score (PS) matching with a 1:4 ratio was performed to minimize baseline differences between the groups.</p><p><strong>Results: </strong>Out of 1590 screened patients, 1469 were included, and 44 received montelukast during ICU stay. After PS matching (1:4), montelukast use was associated with a significantly higher incidence of delirium (OR 4.66, 95% CI 1.63 to 13.34; <i>P</i> < 0.004). Among patients who developed delirium, mixed delirium was the most frequent subtype in the montelukast group (50% vs 12.5% in controls). There were no notable differences found in terms of delirium-free days, recurrence of delirium, liver or kidney injury, length of stay, ventilator-free days, or overall mortality.</p><p><strong>Conclusion: </strong>Our study demonstrates an association between montelukast use during ICU admission and a higher incidence of delirium. Prospective randomized studies are needed to confirm these findings.</p>","PeriodicalId":10406,"journal":{"name":"Clinical Pharmacology : Advances and Applications","volume":"18 ","pages":"586979"},"PeriodicalIF":2.5000,"publicationDate":"2026-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13003959/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Pharmacology : Advances and Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/CPAA.S586979","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Delirium is a frequent complication in critically ill patients and is associated with increased mortality, prolonged hospitalization, and long-term cognitive impairment. Montelukast, a leukotriene receptor antagonist commonly used in respiratory diseases, has been associated with neuropsychiatric adverse effects, including delirium. Evidence regarding its safety in critically ill adults is limited. This study aimed to investigate the association between montelukast use during ICU stay and the development of delirium and further evaluate its safety in the ICU.
Methods: This retrospective cohort study was conducted at King Abdulaziz Medical City, Saudi Arabia, between January 2018 and December 2021. Adult critically ill patients (18-79 years) who were admitted to ICUs for respiratory symptoms and categorized based on montelukast exposure during ICU stay. The primary outcome was assessing the incidence of delirium during ICU stay. Secondary outcomes included delirium duration, recurrence of delirium, delirium-free days, ventilator-free days, length of stay (LOS), safety outcomes (liver and kidney injury), 30-day and in-hospital mortality. Propensity score (PS) matching with a 1:4 ratio was performed to minimize baseline differences between the groups.
Results: Out of 1590 screened patients, 1469 were included, and 44 received montelukast during ICU stay. After PS matching (1:4), montelukast use was associated with a significantly higher incidence of delirium (OR 4.66, 95% CI 1.63 to 13.34; P < 0.004). Among patients who developed delirium, mixed delirium was the most frequent subtype in the montelukast group (50% vs 12.5% in controls). There were no notable differences found in terms of delirium-free days, recurrence of delirium, liver or kidney injury, length of stay, ventilator-free days, or overall mortality.
Conclusion: Our study demonstrates an association between montelukast use during ICU admission and a higher incidence of delirium. Prospective randomized studies are needed to confirm these findings.
背景:谵妄是危重症患者的常见并发症,与死亡率增加、住院时间延长和长期认知障碍有关。孟鲁司特是一种白三烯受体拮抗剂,通常用于呼吸系统疾病,与神经精神不良反应有关,包括谵妄。关于其在危重成人中的安全性的证据有限。本研究旨在探讨孟鲁司特在ICU住院期间使用与谵妄发生的关系,并进一步评估其在ICU的安全性。方法:本回顾性队列研究于2018年1月至2021年12月在沙特阿拉伯阿卜杜勒阿齐兹国王医疗城进行。因呼吸道症状入住ICU并根据ICU住院期间孟鲁司特暴露程度进行分类的成人危重患者(18-79岁)。主要结果是评估ICU住院期间谵妄的发生率。次要结局包括谵妄持续时间、谵妄复发、无谵妄天数、无呼吸机天数、住院时间(LOS)、安全性结局(肝和肾损伤)、30天和住院死亡率。以1:4的比例进行倾向评分(PS)匹配,以尽量减少组间基线差异。结果:在1590例筛选患者中,1469例纳入,其中44例在ICU住院期间接受孟鲁司特治疗。PS匹配(1:4)后,孟鲁司特的使用与谵妄的发生率显著升高相关(OR 4.66, 95% CI 1.63至13.34;P结论:我们的研究表明,在ICU入院期间孟鲁司特的使用与谵妄的发生率升高有关。需要前瞻性随机研究来证实这些发现。