Association of Obesity With Sedative Dosing, Sedative Response, and Clinical Outcomes in Mechanically Ventilated Critically Ill Children.

Q4 Medicine
Critical care explorations Pub Date : 2025-02-10 eCollection Date: 2025-02-01 DOI:10.1097/CCE.0000000000001214
Shan L Ward, Onella S Dawkins-Henry, Lisa A Asaro, David Wypij, Martha A Q Curley
{"title":"Association of Obesity With Sedative Dosing, Sedative Response, and Clinical Outcomes in Mechanically Ventilated Critically Ill Children.","authors":"Shan L Ward, Onella S Dawkins-Henry, Lisa A Asaro, David Wypij, Martha A Q Curley","doi":"10.1097/CCE.0000000000001214","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to investigate the impact of obesity on the use of analgesics and sedatives, rates of iatrogenic withdrawal syndrome (IWS), and outcomes in mechanically ventilated pediatric patients. Additionally, it sought to assess whether a nurse-implemented sedation protocol would be equally effective for children with and without obesity.</p><p><strong>Design: </strong>Secondary analysis of the Randomized Evaluation of Sedation Titration for Respiratory Failure (RESTORE) pediatric multicenter clinical trial.</p><p><strong>Setting: </strong>Thirty-one U.S. PICUs.</p><p><strong>Patients: </strong>Children 1-17 years old, categorized as with or without obesity according to World Health Organization and Centers for Disease Control and Prevention criteria.</p><p><strong>Interventions: </strong>None.</p><p><strong>Measurements and main results: </strong>The study assessed various factors including medication exposure, adequacy of pain and sedation management, IWS rates, and clinical outcomes. Obesity occurred in 22% of patients. Obesity did not influence choice of opiate, but it led to extended exposure to these medications. There were no differences in dosing per kilogram of admission weight, resulting in significantly higher daily and cumulative doses in those with obesity. In the protocolized sedation arm, patients with obesity received significantly higher median opiate doses compared with the nonobesity protocolized sedation group. IWS rates did not differ; however, protocolized sedation obesity patients experienced more instances of inadequate sedation, longer time to extubation readiness, longer duration of mechanical ventilation and PICU stay, and higher 28-day in-hospital mortality than the protocolized sedation nonobesity group. These weight-based differences were not noted in the usual care arm.</p><p><strong>Conclusions: </strong>This study underscores the significance of accounting for body habitus when selecting and dosing opiates in children with acute respiratory failure. Obesity had substantial impact on medication exposure and clinical outcomes, particularly within a structured, protocolized sedation regimen. Further research is warranted to explore the intricate relationship between medication dosing and clinical outcomes in children with obesity.</p>","PeriodicalId":93957,"journal":{"name":"Critical care explorations","volume":"7 2","pages":"e1214"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11813009/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical care explorations","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/CCE.0000000000001214","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: This study aimed to investigate the impact of obesity on the use of analgesics and sedatives, rates of iatrogenic withdrawal syndrome (IWS), and outcomes in mechanically ventilated pediatric patients. Additionally, it sought to assess whether a nurse-implemented sedation protocol would be equally effective for children with and without obesity.

Design: Secondary analysis of the Randomized Evaluation of Sedation Titration for Respiratory Failure (RESTORE) pediatric multicenter clinical trial.

Setting: Thirty-one U.S. PICUs.

Patients: Children 1-17 years old, categorized as with or without obesity according to World Health Organization and Centers for Disease Control and Prevention criteria.

Interventions: None.

Measurements and main results: The study assessed various factors including medication exposure, adequacy of pain and sedation management, IWS rates, and clinical outcomes. Obesity occurred in 22% of patients. Obesity did not influence choice of opiate, but it led to extended exposure to these medications. There were no differences in dosing per kilogram of admission weight, resulting in significantly higher daily and cumulative doses in those with obesity. In the protocolized sedation arm, patients with obesity received significantly higher median opiate doses compared with the nonobesity protocolized sedation group. IWS rates did not differ; however, protocolized sedation obesity patients experienced more instances of inadequate sedation, longer time to extubation readiness, longer duration of mechanical ventilation and PICU stay, and higher 28-day in-hospital mortality than the protocolized sedation nonobesity group. These weight-based differences were not noted in the usual care arm.

Conclusions: This study underscores the significance of accounting for body habitus when selecting and dosing opiates in children with acute respiratory failure. Obesity had substantial impact on medication exposure and clinical outcomes, particularly within a structured, protocolized sedation regimen. Further research is warranted to explore the intricate relationship between medication dosing and clinical outcomes in children with obesity.

机械通气危重症儿童肥胖与镇静剂量、镇静反应和临床结果的关系
目的:本研究旨在探讨肥胖对儿童机械通气患者镇痛和镇静剂使用、医源性戒断综合征(IWS)发生率和预后的影响。此外,它还试图评估护士实施的镇静方案是否对肥胖儿童和非肥胖儿童同样有效。设计:对镇静滴定治疗呼吸衰竭(RESTORE)儿童多中心临床试验的随机评价进行二次分析。设置:31个美国picu。患者:1-17岁的儿童,根据世界卫生组织和疾病控制与预防中心的标准分为有或没有肥胖。干预措施:没有。测量和主要结果:该研究评估了各种因素,包括药物暴露、疼痛和镇静管理的充分性、IWS发生率和临床结果。22%的患者出现肥胖。肥胖并不影响阿片类药物的选择,但它会延长服用这些药物的时间。每公斤入院体重的剂量没有差异,导致肥胖患者的日剂量和累积剂量明显较高。在协议镇静组中,肥胖患者接受的阿片类药物中位数剂量明显高于非肥胖协议镇静组。IWS率没有差异;然而,与非肥胖组相比,接受镇静治疗的肥胖患者镇静不足的情况更多,拔管准备时间更长,机械通气时间更长,PICU住院时间更长,28天住院死亡率更高。在常规护理组中没有注意到这些基于体重的差异。结论:本研究强调了在急性呼吸衰竭儿童中选择和给药阿片类药物时考虑身体习惯的重要性。肥胖对药物暴露和临床结果有重大影响,特别是在一个有组织的、有协议的镇静方案中。需要进一步的研究来探索肥胖儿童药物剂量与临床结果之间的复杂关系。
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
CiteScore
5.70
自引率
0.00%
发文量
0
审稿时长
8 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:481959085
Book学术官方微信