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

被引:26
作者
Campbell, Noll L. [1 ,2 ,3 ,4 ,5 ,6 ]
Perkins, Anthony J. [4 ,5 ]
Khan, Babar A. [2 ,3 ,4 ,5 ,6 ,7 ]
Gao, Sujuan [2 ,3 ,7 ]
Farber, Mark O. [7 ]
Khan, Sikandar [2 ,3 ,7 ]
Wang, Sophia [7 ,8 ]
Boustani, Malaz A. [2 ,3 ,4 ,5 ,6 ,7 ]
机构
[1] Purdue Univ, Coll Pharm, W Lafayette, IN 47907 USA
[2] Indiana Univ, Ctr Aging Res, Indianapolis, IN 46204 USA
[3] Regenstrief Inst Inc, Indianapolis, IN USA
[4] Indiana Univ, Ctr Hlth Innovat & Implementat Sci, Indianapolis, IN 46204 USA
[5] Indiana Clin & Translat Sci Inst, Indianapolis, IN 46204 USA
[6] Eskenazi Hlth, Sandra Eskenazi Ctr Brain Care Innovat, Indianapolis, IN USA
[7] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN USA
[8] Richard L Roudebush Vet Adm Med Ctr, Indianapolis, IN USA
关键词
delirium; deprescribing; anticholinergic; benzodiazepine; CONFUSION ASSESSMENT METHOD; MECHANICALLY VENTILATED PATIENTS; COGNITIVE IMPAIRMENT; INFORMANT QUESTIONNAIRE; ELDERLY IQCODE; RATING-SCALE; SEVERITY; RELIABILITY; VALIDITY; IMPACT;
D O I
10.1111/jgs.15751
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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.
引用
收藏
页码:695 / 702
页数:8
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