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在谵妄的药物治疗中停用药物:重症监护病房的一项随机试验。

Deprescribing in the Pharmacologic Management of Delirium: A Randomized Trial in the Intensive Care Unit.

机构信息

Purdue University College of Pharmacy, West Lafayette, Indiana.

Indiana University Center for Aging Research, Indianapolis, Indiana.

出版信息

J Am Geriatr Soc. 2019 Apr;67(4):695-702. doi: 10.1111/jgs.15751. Epub 2019 Jan 21.

Abstract

OBJECTIVE

Benzodiazepines and anticholinergics are risk factors for delirium in the intensive care unit (ICU). We tested the impact of a deprescribing intervention on short-term delirium outcomes.

DESIGN

Multisite randomized clinical trial.

SETTING

ICUs of three large hospitals.

PARTICIPANTS

Two hundred adults aged 18 years or older and admitted to an ICU with delirium, according to the Richmond Agitation-Sedation Scale and the Confusion Assessment Method for the ICU (CAM-ICU). Participants had a contraindication to haloperidol (seizure disorder or prolonged QT interval) or preference against haloperidol as a treatment for delirium, and were excluded for serious mental illness, stroke, pregnancy, or alcohol withdrawal. Participants were randomized to a deprescribing intervention or usual care. The intervention included electronic alerts combined with pharmacist support to deprescribe anticholinergics and benzodiazepines.

MEASUREMENTS

Primary outcomes were delirium duration measured by the CAM-ICU and severity measured by the Delirium Rating Scale Revised-98 (DRS-R-98) and the CAM-ICU-7; secondary outcomes included adverse events and mortality.

RESULTS

Participants had a mean age of 61.8 (SD = 14.3) years, 59% were female, and 52% were African American, with no significant differences in baseline characteristics between groups. No differences between groups were identified in the number exposed to anticholinergics (P = .219) or benzodiazepines (P = .566), the median total anticholinergic score (P = .282), or the median total benzodiazepine dose in lorazepam equivalents (P = .501). Neither median delirium/coma-free days (P = .361) nor median change in delirium severity scores (P = .582 for DRS-R-98; P = .333 for CAM-ICU-7) were different between groups. No differences in adverse events or mortality were identified.

CONCLUSIONS

When added to state-of-the-art clinical services, this deprescribing intervention had no impact on medication use in ICU participants. Given the age of the population, results of clinical outcomes may not be easily extrapolated to older adults. Nonetheless, improved approaches for deprescribing or preventing anticholinergics and benzodiazepines should be developed to determine the impact on delirium outcomes. J Am Geriatr Soc 67:695-702, 2019.

摘要

目的

苯二氮䓬类药物和抗胆碱能药物是重症监护病房(ICU)谵妄的危险因素。我们测试了去处方干预对短期谵妄结局的影响。

设计

多地点随机临床试验。

地点

三家大医院的 ICU。

参与者

年龄在 18 岁或以上,根据 Richmond 激越-镇静量表和 ICU 意识模糊评估法(CAM-ICU)诊断为谵妄,并入住 ICU 的 200 名成年人。参与者有抗精神病药物(如氟哌啶醇)使用禁忌(癫痫发作或 QT 间期延长)或不接受氟哌啶醇作为谵妄治疗,或因严重精神疾病、中风、妊娠或酒精戒断而被排除。参与者被随机分配到去处方干预组或常规护理组。干预措施包括电子警示与药剂师支持相结合,以减少抗胆碱能药物和苯二氮䓬类药物的使用。

测量

主要结局是通过 CAM-ICU 测量的谵妄持续时间和通过 Delirium Rating Scale Revised-98(DRS-R-98)和 CAM-ICU-7 测量的严重程度;次要结局包括不良事件和死亡率。

结果

参与者的平均年龄为 61.8(SD=14.3)岁,59%为女性,52%为非裔美国人,两组间基线特征无显著差异。两组间抗胆碱能药物(P=0.219)或苯二氮䓬类药物(P=0.566)、抗胆碱能药物总评分中位数(P=0.282)或劳拉西泮等效剂量的苯二氮䓬类药物总剂量中位数(P=0.501)均无差异。去处方干预组与常规护理组相比,无谵妄/昏迷天数的中位数(P=0.361)或谵妄严重程度评分的中位数变化(DRS-R-98:P=0.582;CAM-ICU-7:P=0.333)也无差异。两组间不良事件或死亡率无差异。

结论

在加入最先进的临床服务后,这种去处方干预措施对 ICU 参与者的药物使用没有影响。鉴于人群的年龄,临床结局的结果可能不容易外推到老年人。尽管如此,仍应开发改善去处方或预防抗胆碱能药物和苯二氮䓬类药物的方法,以确定其对谵妄结局的影响。美国老年医学会 67:695-702,2019 年。

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