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评估纳洛西戈在危重症阿片类药物所致便秘患者中的安全性和有效性。

Evaluating the Safety and Efficacy of Naloxegol in Critically Ill Opioid-Induced Constipation Patients.

作者信息

Rizwan M Zeeshan, Garcia Rodney, Mara Kristin, Nei Scott

机构信息

Department of Pharmacy, Mayo Clinic, Rochester, USA.

Department of Nursing, Mayo Clinic, Rochester, USA.

出版信息

Cureus. 2023 Jul 5;15(7):e41422. doi: 10.7759/cureus.41422. eCollection 2023 Jul.

Abstract

Background Opioid-induced constipation (OIC) has become more common in the intensive care unit (ICU) due to increased opioid utilization. Traditional laxatives often prove ineffective against OIC, leading to the increased utilization of naloxegol. However, further research is needed to confirm naloxegol's effectiveness and safety in critical care. This study aimed to explore the safety and efficacy of this intervention in critically ill OIC patients. Methods A single-center retrospective study was conducted on 353 patients who received one or more doses of naloxegol from January 1, 2019, to June 30, 2020, for OIC at a tertiary care center. The primary endpoint of this study was to evaluate serious adverse events such as reduced analgesic effect, gastrointestinal perforation, seizure, acute myocardial infarction (AMI), or ventricular arrhythmias using Naranjo Scale in critically ill patients. The secondary goal was to assess the efficacy of naloxegol, measured by the time of the first bowel movement. Results The average duration of naloxegol use was three days, with the first bowel movement occurring at an average of 11.3 hours. Furthermore, 59.8% of individuals had their first bowel movement within 20 hours of receiving naloxegol. There was a low level of causality between naloxegol use and adverse events such as gastrointestinal perforation, seizures, AMI, cardiovascular mortality, stroke, and ventricular arrhythmia. Additionally, reduction in analgesia showed no strong relationship with naloxegol use indicated by the Naranjo Scale assessment. Conclusion Naloxegol showed promising safety and efficacy profiles in treating OIC amongst critically ill patients, though our findings require further validation through prospective studies. This research paves the way for further investigation into naloxegol's role in OIC management, emphasizing the necessity of personalized treatment strategies in critical care settings.

摘要

背景

由于阿片类药物使用增加,阿片类药物引起的便秘(OIC)在重症监护病房(ICU)中变得更加常见。传统泻药往往对OIC无效,导致纳洛西醇的使用增加。然而,需要进一步研究以确认纳洛西醇在重症监护中的有效性和安全性。本研究旨在探讨这种干预措施在重症OIC患者中的安全性和有效性。方法:在一家三级医疗中心,对2019年1月1日至2020年6月30日期间因OIC接受一剂或多剂纳洛西醇治疗的353例患者进行了单中心回顾性研究。本研究的主要终点是使用Naranjo量表评估重症患者中严重不良事件,如镇痛效果降低、胃肠道穿孔、癫痫发作、急性心肌梗死(AMI)或室性心律失常。次要目标是评估纳洛西醇的疗效,以首次排便时间衡量。结果:纳洛西醇的平均使用时间为三天,首次排便平均发生在11.3小时。此外,59.8%的个体在接受纳洛西醇后20小时内首次排便。纳洛西醇使用与胃肠道穿孔、癫痫发作、AMI、心血管死亡率、中风和室性心律失常等不良事件之间的因果关系较低。此外,Naranjo量表评估表明,镇痛效果降低与纳洛西醇使用之间没有密切关系。结论:纳洛西醇在治疗重症患者的OIC方面显示出有前景的安全性和有效性,尽管我们的研究结果需要通过前瞻性研究进一步验证。本研究为进一步研究纳洛西醇在OIC管理中的作用铺平了道路,强调了重症监护环境中个性化治疗策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/506b/10403335/8d47b3eb9f31/cureus-0015-00000041422-i01.jpg

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