Ankravs Melissa J, Udy Andrew, Bellomo Rinaldo, Presneill Jeffrey J, Adams Laura, Abdelhamid Yasmine Ali, Bailey Michael, Board Jasmin, Byrne Kathleen, Eastwood Glenn, Le Guen Maurice, Martin Emma-Leah, Plummer Mark P, Richardson Megan, Sharrock Lucy, Young Meredith, Deane Adam M
Department of Intensive Care, The Royal Melbourne Hospital, Melbourne, Australia.
Department of Pharmacy, The Royal Melbourne Hospital, Melbourne, Australia.
Crit Care Resusc. 2024 Nov 22;26(4):249-254. doi: 10.1016/j.ccrj.2024.08.003. eCollection 2024 Dec.
Patients in the intensive care unit (ICU) frequently develop hyperactive delirium, which may be accompanied by behaviour that increases clinical risks to themselves as well as other patients and staff. There is a paucity of evidence to inform the urgent enteral administration of antipsychotic drugs to treat such hyperactive delirium and behavioural disturbances.
The aim of this study is to test the efficacy and safety of administering enteral olanzapine when compared to quetiapine in critically ill patients with hyperactive delirium.
This is a cluster-randomised, double-crossover, clinical trial. Critically ill adult patients admitted to three tertiary Australian intensive care units over a 12-month period will be eligible. Randomisation will occur at the site level, with allocation to open-label olanzapine or quetiapine use over four treatment periods of 3-month duration.
The primary outcome and days alive and delirium-/coma-free (censored at 14 days post enrolment) will be analysed using median quantile regression accounting for clustering at sites' level and time period and treatment order.
This trial will compare the effect of enteral olanzapine to quetiapine in critically ill adults with hyperactive delirium on an important indicator of patient outcome.
重症监护病房(ICU)的患者经常出现多动性谵妄,可能伴有对自身以及其他患者和工作人员增加临床风险的行为。目前缺乏证据来指导紧急肠内给予抗精神病药物治疗此类多动性谵妄和行为障碍。
本研究的目的是比较在患有多动性谵妄的重症患者中,肠内给予奥氮平与喹硫平的疗效和安全性。
设计、设置、参与者和干预措施:这是一项整群随机、双交叉临床试验。在12个月期间入住澳大利亚三家三级重症监护病房的成年重症患者将符合条件。随机分组将在机构层面进行,在为期3个月的四个治疗期内分配使用开放标签的奥氮平或喹硫平。
主要结局以及存活且无谵妄/昏迷的天数(在入组后14天进行删失)将使用中位数分位数回归进行分析,同时考虑机构层面、时间段和治疗顺序的聚类情况。
本试验将比较肠内给予奥氮平与喹硫平对患有多动性谵妄的成年重症患者重要预后指标的影响。