Functional Status After Delirium in the ICU: A 1-Year Follow-Up of the Agents Intervening Against Delirium in the ICU (AID-ICU) Trial.

IF 6 1区 医学 Q1 CRITICAL CARE MEDICINE
Lone M Poulsen, Camilla B Mortensen, Nina C Andersen-Ranberg, Anders Granholm, Marie O Collet, Lars P K Andersen, Stine Estrup, Bodil S Rasmussen, Ole Mathiesen
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引用次数: 0

Abstract

Objectives: To assess the effect of haloperidol compared with placebo on functional status in adult ICU patients with delirium, 1 year after inclusion in the Agents Intervening against Delirium in the ICU (AID-ICU) trial.

Design: This was a preplanned 1-year follow-up of the randomized, placebo-controlled, blinded AID-ICU trial.

Setting and patients: A total of 632 Danish patients enrolled in the AID-ICU trial at three selected Danish sites.

Interventions: None.

Measurements and main results: Functional status was evaluated using the Lawton-Brody Instrumental Activities of Daily Living (IADL) score, the Barthel-20 Activities of Daily Living (ADL) score, the Clinical Frailty Scale (CFS), and grip strength. Nonsurvivors were assigned the worst possible values, and missing data were managed with multiple imputation. Results were presented as mean differences and ratios of means with 95% CIs, adjusted for age, and sex. Of the original cohort of 632 patients enrolled in the AID-ICU trial at the three Danish sites, 75 participants in the haloperidol group, and 69 in the placebo group were available for follow-up. In 28.5% of responders (41/144), follow-up was performed by telephone. The proportion of relatives answering the questionnaire at 1-year follow-up on behalf of the participants was 4.2% (6/144). At 1 year, the adjusted mean differences between IADL, ADL, CFS, and grip strength in the haloperidol and placebo group were 0.1 (95% CI, -0.5 to 0.7; p = 0.687), 0.2 (95% CI, -1.3 to 1.7; p = 0.773), 0.0 (95% CI, -0.4 to 0.5; p = 0.862), and -2.9 (95% CI, -7.1 to 1.2; p = 0.175), respectively.

Conclusions: Among adult ICU patients with delirium, treatment with haloperidol vs. placebo did not result in statistically significant differences in functional status at 1-year follow-up. However, due to the uncertainty of the estimates, clinically important differences cannot be excluded.

ICU患者谵妄后的功能状态:干预ICU患者谵妄的药物1年随访(aids -ICU)试验。
目的:评价氟哌啶醇与安慰剂在ICU干预谵妄药物(aids -ICU)试验1年后对谵妄成人ICU患者功能状态的影响。设计:这是一项预先计划的1年随访的随机、安慰剂对照、盲法艾滋病- icu试验。环境和患者:共有632名丹麦患者在三个选定的丹麦地点参加了艾滋病- icu试验。干预措施:没有。测量方法和主要结果:使用劳顿-布罗迪日常生活工具活动(IADL)评分、Barthel-20日常生活活动(ADL)评分、临床虚弱量表(CFS)和握力评估功能状态。非幸存者被分配最坏的可能值,缺失的数据被多次输入处理。结果显示为95% ci的平均差异和平均比率,并根据年龄和性别进行了调整。在丹麦三个地点的艾滋病- icu试验中,最初的632名患者中,氟哌啶醇组的75名参与者和安慰剂组的69名参与者可进行随访。28.5%的应答者(41/144)通过电话进行随访。1年随访时,亲属代表参与者回答问卷的比例为4.2%(6/144)。1年时,氟哌啶醇组和安慰剂组的IADL、ADL、CFS和握力校正后的平均差异分别为0.1 (95% CI, -0.5 ~ 0.7; p = 0.687)、0.2 (95% CI, -1.3 ~ 1.7; p = 0.773)、0.0 (95% CI, -0.4 ~ 0.5; p = 0.862)和-2.9 (95% CI, -7.1 ~ 1.2; p = 0.175)。结论:在成年ICU谵妄患者中,氟哌啶醇治疗与安慰剂治疗在1年随访时功能状态无统计学差异。然而,由于估计的不确定性,不能排除临床上重要的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Critical Care Medicine
Critical Care Medicine 医学-危重病医学
CiteScore
16.30
自引率
5.70%
发文量
728
审稿时长
2 months
期刊介绍: Critical Care Medicine is the premier peer-reviewed, scientific publication in critical care medicine. Directed to those specialists who treat patients in the ICU and CCU, including chest physicians, surgeons, pediatricians, pharmacists/pharmacologists, anesthesiologists, critical care nurses, and other healthcare professionals, Critical Care Medicine covers all aspects of acute and emergency care for the critically ill or injured patient. Each issue presents critical care practitioners with clinical breakthroughs that lead to better patient care, the latest news on promising research, and advances in equipment and techniques.
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