Amanda R Kolmar, Daniela Bravo, Ricardo A Fonseca, Michael A Kramer, Jinli Wang, Kristin P Guilliams, Brian M Fuller
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We hypothesized that subjects receiving benzodiazepines for tolerance of mechanical ventilation will demonstrate worse clinical outcomes when compared with those not receiving benzodiazepines.</p><p><strong>Design: </strong>Single-center, retrospective cohort study.</p><p><strong>Setting and participants: </strong>PICU of a tertiary-care medical center. One thousand fifty-four pediatric participants requiring invasive mechanical ventilation between June 2018 and December 2022. Participants were categorized into those who received benzodiazepine-inclusive sedation regimens (n = 747) and those who received nonbenzodiazepine regimens (n = 307).</p><p><strong>Interventions: </strong>None.</p><p><strong>Main outcomes and measures: </strong>Subjects were sorted into groups of benzodiazepine-sedative regimens (midazolam and lorazepam, only lorazepam) or nonbenzodiazepine-sedation regimens. The primary outcome was ventilator-free days (VFDs). Statistical analysis was performed using multivariable linear regression and propensity-score matching.</p><p><strong>Results: </strong>Subjects receiving continuous and/or intermittent benzodiazepines had fewer VFDs compared with the nonbenzodiazepine group (median 21.0 vs. 26.7; p < 0.001). The benzodiazepine group had fewer ICU-free and hospital-free days, higher delirium scores, and a greater need for withdrawal-tapering medications. This was redemonstrated in subjects only receiving intermittent benzodiazepines as well. Younger subjects were more likely to receive benzodiazepines.</p><p><strong>Conclusions and relevance: </strong>Our study demonstrates an association between children receiving both continuous and intermittent benzodiazepine sedation and worse clinical outcomes. These patients have fewer VFDs and longer length of stay, higher doses of nonbenzodiazepine sedatives, and increased need for withdrawal tapering medications and antipsychotics. It is unclear in this retrospective study if the outcomes were worse because the subjects received benzodiazepines or because subjects receiving benzodiazepines were sicker and thus required benzodiazepines in their analgosedative regimen. Further investigation is warranted into the impact of benzodiazepines on patient outcomes, nonpharmacologic management of sedation, improvement in bedside assessment of analgosedation, and optimal balance between over- and under-sedation.</p>","PeriodicalId":93957,"journal":{"name":"Critical care explorations","volume":"7 5","pages":"e1255"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12040031/pdf/","citationCount":"0","resultStr":"{\"title\":\"Impact of Benzodiazepines on Outcomes of Mechanically Ventilated Pediatric Intensive Care Patients: A Retrospective Cohort Study.\",\"authors\":\"Amanda R Kolmar, Daniela Bravo, Ricardo A Fonseca, Michael A Kramer, Jinli Wang, Kristin P Guilliams, Brian M Fuller\",\"doi\":\"10.1097/CCE.0000000000001255\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Importance: </strong>Benzodiazepines are the most frequently used sedatives in PICUs, but they are increasingly associated with negative outcomes. Understanding their impact on patient outcomes is critical to provide better sedative management for patients.</p><p><strong>Objective: </strong>Our objective was to determine the impact of midazolam and lorazepam on clinical outcomes among subjects requiring mechanical ventilation in the PICU. We hypothesized that subjects receiving benzodiazepines for tolerance of mechanical ventilation will demonstrate worse clinical outcomes when compared with those not receiving benzodiazepines.</p><p><strong>Design: </strong>Single-center, retrospective cohort study.</p><p><strong>Setting and participants: </strong>PICU of a tertiary-care medical center. One thousand fifty-four pediatric participants requiring invasive mechanical ventilation between June 2018 and December 2022. Participants were categorized into those who received benzodiazepine-inclusive sedation regimens (n = 747) and those who received nonbenzodiazepine regimens (n = 307).</p><p><strong>Interventions: </strong>None.</p><p><strong>Main outcomes and measures: </strong>Subjects were sorted into groups of benzodiazepine-sedative regimens (midazolam and lorazepam, only lorazepam) or nonbenzodiazepine-sedation regimens. The primary outcome was ventilator-free days (VFDs). Statistical analysis was performed using multivariable linear regression and propensity-score matching.</p><p><strong>Results: </strong>Subjects receiving continuous and/or intermittent benzodiazepines had fewer VFDs compared with the nonbenzodiazepine group (median 21.0 vs. 26.7; p < 0.001). The benzodiazepine group had fewer ICU-free and hospital-free days, higher delirium scores, and a greater need for withdrawal-tapering medications. This was redemonstrated in subjects only receiving intermittent benzodiazepines as well. 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引用次数: 0
摘要
重要性:苯二氮卓类药物是picu中最常用的镇静剂,但它们越来越多地与不良结果相关。了解它们对患者预后的影响对于为患者提供更好的镇静管理至关重要。目的:我们的目的是确定咪达唑仑和劳拉西泮对PICU中需要机械通气的受试者临床结果的影响。我们假设接受苯二氮卓类药物治疗机械通气耐受性的受试者与未接受苯二氮卓类药物治疗的受试者相比,临床结果更差。设计:单中心、回顾性队列研究。地点和参与者:某三级医疗中心PICU。2018年6月至2022年12月期间需要有创机械通气的1254名儿科参与者。参与者被分为接受含苯二氮卓类药物镇静方案的组(n = 747)和接受非苯二氮卓类药物镇静方案的组(n = 307)。干预措施:没有。主要结局和措施:受试者被分为苯二氮卓-镇静方案组(咪达唑仑和劳拉西泮,仅劳拉西泮)或非苯二氮卓-镇静方案组。主要观察指标为无呼吸机天数(vfd)。采用多变量线性回归和倾向得分匹配进行统计分析。结果:与非苯二氮卓类药物组相比,接受持续和/或间歇性苯二氮卓类药物治疗的受试者vfd较少(中位数21.0 vs. 26.7;P < 0.001)。苯二氮卓类药物组无重症监护病房和住院天数更少,谵妄评分更高,更需要戒断药物。这在仅接受间歇性苯二氮卓类药物治疗的受试者中也得到了证实。年轻的受试者更有可能接受苯二氮卓类药物。结论和相关性:我们的研究表明,接受持续和间歇性苯二氮卓类镇静的儿童与较差的临床结果之间存在关联。这些患者的vfd较少,住院时间较长,非苯二氮卓类镇静剂的剂量较高,并且对戒断逐渐减少的药物和抗精神病药物的需求增加。在这项回顾性研究中,尚不清楚结果的恶化是因为受试者接受了苯二氮卓类药物,还是因为接受苯二氮卓类药物的受试者病情较重,因此在其镇痛镇静方案中需要苯二氮卓类药物。进一步研究苯二氮卓类药物对患者预后的影响,镇静的非药物管理,改善床边对镇静的评估,以及过度和不足镇静之间的最佳平衡。
Impact of Benzodiazepines on Outcomes of Mechanically Ventilated Pediatric Intensive Care Patients: A Retrospective Cohort Study.
Importance: Benzodiazepines are the most frequently used sedatives in PICUs, but they are increasingly associated with negative outcomes. Understanding their impact on patient outcomes is critical to provide better sedative management for patients.
Objective: Our objective was to determine the impact of midazolam and lorazepam on clinical outcomes among subjects requiring mechanical ventilation in the PICU. We hypothesized that subjects receiving benzodiazepines for tolerance of mechanical ventilation will demonstrate worse clinical outcomes when compared with those not receiving benzodiazepines.
Setting and participants: PICU of a tertiary-care medical center. One thousand fifty-four pediatric participants requiring invasive mechanical ventilation between June 2018 and December 2022. Participants were categorized into those who received benzodiazepine-inclusive sedation regimens (n = 747) and those who received nonbenzodiazepine regimens (n = 307).
Interventions: None.
Main outcomes and measures: Subjects were sorted into groups of benzodiazepine-sedative regimens (midazolam and lorazepam, only lorazepam) or nonbenzodiazepine-sedation regimens. The primary outcome was ventilator-free days (VFDs). Statistical analysis was performed using multivariable linear regression and propensity-score matching.
Results: Subjects receiving continuous and/or intermittent benzodiazepines had fewer VFDs compared with the nonbenzodiazepine group (median 21.0 vs. 26.7; p < 0.001). The benzodiazepine group had fewer ICU-free and hospital-free days, higher delirium scores, and a greater need for withdrawal-tapering medications. This was redemonstrated in subjects only receiving intermittent benzodiazepines as well. Younger subjects were more likely to receive benzodiazepines.
Conclusions and relevance: Our study demonstrates an association between children receiving both continuous and intermittent benzodiazepine sedation and worse clinical outcomes. These patients have fewer VFDs and longer length of stay, higher doses of nonbenzodiazepine sedatives, and increased need for withdrawal tapering medications and antipsychotics. It is unclear in this retrospective study if the outcomes were worse because the subjects received benzodiazepines or because subjects receiving benzodiazepines were sicker and thus required benzodiazepines in their analgosedative regimen. Further investigation is warranted into the impact of benzodiazepines on patient outcomes, nonpharmacologic management of sedation, improvement in bedside assessment of analgosedation, and optimal balance between over- and under-sedation.