Kim Youlim, Kim Hyung-Sook, Park Jong Sun, Cho Young-Jae, Yoon Ho Il, Lee Sang-Min, Lee Jae Ho, Lee Choon-Taek, Lee Yeon Joo
Division of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Hallym University Chuncheon Sacred Heart Hospital, Chuncheon-si 24253, Gangwon-Do, Korea.
Department of Pharmacy, Seoul National University Bundang Hospital, Seongnam-si 13620, Gyeonggi-Do, Korea.
J Clin Med. 2019 Dec 27;9(1):69. doi: 10.3390/jcm9010069.
To evaluate the efficacy of short-term low-dose quetiapine for delirium prevention in critically ill patients.
In this prospective, a single-center, randomized, double-blind, placebo-controlled trial, adult patients who were admitted from July 2015 to July 2017 to a medical intensive care unit (ICU) of a tertiary teaching hospital affiliated to Seoul National University were included. Quetiapine (12.5 mg or 25 mg oral at night; = 16) or placebo ( = 21) was administered according to randomization until ICU discharge or the 10th ICU day. The primary endpoint was the incidence of delirium within the first 10 ICU days. Secondary endpoints included the rate of positive Confusion Assessment Method for the ICU (CAM-ICU) (the number of positive CAM-ICU counts/the number of total CAM-ICU counts), delirium duration, successful extubation, and overall mortality.
The incidence of delirium during the 10 days after ICU admission was 46.7% (7/15) in the quetiapine group and 55.0% (11/20) in the placebo group ( = 0.442). In the quetiapine group, the rate of positive CAM-ICU was significantly lower than in the placebo group (14.4% vs. 37.4%, = 0.048), delirium duration during the study period was significantly shorter (0.28 day vs. 1.83 days, = 0.018), and more patients in the quetiapine than in the placebo group were weaned from mechanical ventilation successfully (84.6% vs. 47.1%, = 0.040).
Our study suggests that prophylactic use of low-dose quetiapine could be helpful for preventing delirium in critically ill patients. A further large-scale prospective study is needed.
评估短期小剂量喹硫平预防重症患者谵妄的疗效。
在这项前瞻性、单中心、随机、双盲、安慰剂对照试验中,纳入了2015年7月至2017年7月入住首尔国立大学附属三级教学医院内科重症监护病房(ICU)的成年患者。根据随机分组,给予喹硫平(每晚口服12.5mg或25mg;n = 16)或安慰剂(n = 21),直至患者转出ICU或入住ICU第10天。主要终点是入住ICU的前10天内谵妄的发生率。次要终点包括ICU意识模糊评估法(CAM-ICU)阳性率(CAM-ICU阳性次数/总CAM-ICU次数)、谵妄持续时间、成功脱机和总体死亡率。
喹硫平组入住ICU后10天内谵妄的发生率为46.7%(7/15),安慰剂组为55.0%(11/20)(P = 0.442)。喹硫平组CAM-ICU阳性率显著低于安慰剂组(14.4%对37.4%,P = 0.048),研究期间谵妄持续时间显著缩短(0.28天对1.83天,P = 0.018),喹硫平组成功脱离机械通气的患者比安慰剂组更多(84.6%对47.1%,P = 0.040)。
我们的研究表明,预防性使用小剂量喹硫平可能有助于预防重症患者的谵妄。需要进一步开展大规模前瞻性研究。