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评估早期给予羟甲基戊二酰辅酶A还原酶抑制剂辛伐他汀预防和治疗重症机械通气患者谵妄(MoDUS试验):一项随机对照试验的研究方案

Evaluating early administration of the hydroxymethylglutaryl-CoA reductase inhibitor simvastatin in the prevention and treatment of delirium in critically ill ventilated patients (MoDUS trial): study protocol for a randomized controlled trial.

作者信息

Casarin Annalisa, McAuley Daniel F, Alce Timothy M, Zhao Xiaobei, Ely E Wesley, Jackson Jim C, McDowell Cliona, Agus Ashley, Murphy Lynn, Page Valerie J

机构信息

Intensive Care Unit, Watford General Hospital, West Hertfordshire Hospitals NHS Trust, Vicarage Road, Watford, WD18 0HB, UK.

Centre for Infection and Immunity, Queen's University of Belfast, Health Sciences Building, Lisburn Road, Belfast, BT9 7AE, UK.

出版信息

Trials. 2015 May 16;16:218. doi: 10.1186/s13063-015-0731-0.

Abstract

BACKGROUND

The incidence of delirium in ventilated patients is estimated at up to 82%, and it is associated with longer intensive care and hospital stays, and long-term cognitive impairment and mortality. The pathophysiology of delirium has been linked with inflammation and neuronal apoptosis. Simvastatin has pleiotropic properties; it penetrates the brain and, as well as reducing cholesterol, reduces inflammation when used at clinically relevant doses over the short term. This is a single centre randomised, controlled trial which aims to test the hypothesis that treatment with simvastatin will modify delirium incidence and outcomes.

METHODS/DESIGN: The ongoing study will include 142 adults admitted to the Watford General Hospital Intensive Care Unit who require mechanical ventilation in the first 72 hours of admission. The primary outcome is the number of delirium- and coma-free days in the first 14 days. Secondary outcomes include incidence of delirium, delirium- and coma-free days in the first 28 days, days in delirium and in coma at 14 and 28 days, number of ventilator-free days at 28 days, length of critical care and hospital stay, mortality, cognitive decline and healthcare resource use. Informed consent will be taken from patient's consultee before randomisation to receive either simvastatin (80 mg) or placebo once daily. Daily data will be recorded until day 28 after randomisation or until discharge from the ICU if sooner. Surviving patients will be followed up on at six months from discharge. Plasma and urine samples will be taken to investigate the biological effect of simvastatin on systemic markers of inflammation, as related to the number of delirium- and coma-free days, and the potential of cholinesterase activity and beta-amyloid as predictors of the risk of delirium and long-term cognitive impairment.

DISCUSSION

This trial will test the efficacy of simvastatin on reducing delirium in the critically ill. If patients receiving the statin show a reduced number of days in delirium compared with the placebo group, the inflammatory theory implicated in the pathogenesis of delirium will be strengthened.

TRIAL REGISTRATION

The trial was registered with the International Standard Randomised Controlled Trial Registry ( ISRCTN89079989 ) on 26 March 2013.

摘要

背景

据估计,接受机械通气患者的谵妄发生率高达82%,且与重症监护和住院时间延长、长期认知障碍及死亡率相关。谵妄的病理生理学与炎症和神经元凋亡有关。辛伐他汀具有多种特性;它可穿透血脑屏障,并且在短期内以临床相关剂量使用时,除降低胆固醇外,还可减轻炎症。这是一项单中心随机对照试验,旨在检验辛伐他汀治疗可改变谵妄发生率及转归的假设。

方法/设计:正在进行的这项研究将纳入142名入住沃特福德综合医院重症监护病房、在入院后72小时内需要机械通气的成年人。主要结局是前14天内无谵妄和昏迷的天数。次要结局包括谵妄发生率、前28天内无谵妄和昏迷的天数、第14天和第28天处于谵妄和昏迷状态的天数、第28天无呼吸机支持的天数、重症监护和住院时间、死亡率、认知功能减退及医疗资源使用情况。在随机分组前,将从患者的咨询人处获得知情同意,以便患者每日接受一次辛伐他汀(80毫克)或安慰剂治疗。每日记录数据,直至随机分组后第28天,或若更早则直至从重症监护病房出院。存活患者将在出院后6个月进行随访。将采集血浆和尿液样本,以研究辛伐他汀对全身炎症标志物的生物学效应,这与无谵妄和昏迷的天数相关,以及胆碱酯酶活性和β-淀粉样蛋白作为谵妄风险和长期认知障碍预测指标的可能性。

讨论

本试验将检验辛伐他汀在降低危重症患者谵妄发生率方面的疗效。如果接受他汀类药物治疗的患者与安慰剂组相比谵妄天数减少,那么与谵妄发病机制相关的炎症理论将得到加强。

试验注册

该试验于2013年3月26日在国际标准随机对照试验注册库(ISRCTN89079989)注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c380/4440514/bf566b5c0ae0/13063_2015_731_Fig1_HTML.jpg

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