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重症监护病房护理谵妄预防干预措施的影响(UNDERPIN-ICU):一项多中心阶梯楔形随机对照试验的研究方案

The impact of nUrsiNg DEliRium Preventive INnterventions in the Intensive Care Unit (UNDERPIN-ICU): A study protocol for a multi-centre, stepped wedge randomized controlled trial.

作者信息

Wassenaar Annelies, Rood Paul, Schoonhoven Lisette, Teerenstra Steven, Zegers Marieke, Pickkers Peter, van den Boogaard Mark

机构信息

Department of Intensive Care Medicine, Radboud Institute for Health Sciences, Radboud University Medical Center, P.O. Box 9101, 6500HB Nijmegen, The Netherlands.

Faculty of Health Sciences, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK; Scientific Institute for Quality of Healthcare, Radboud Institute for Health Sciences, Radboud University Medical Center, P.O. Box 9101, 6500HB Nijmegen, The Netherlands.

出版信息

Int J Nurs Stud. 2017 Mar;68:1-8. doi: 10.1016/j.ijnurstu.2016.11.018. Epub 2016 Dec 8.

Abstract

BACKGROUND

Delirium is a common disorder in Intensive Care Unit (ICU) patients and is associated with serious short- and long-term consequences, including re-intubations, ICU readmissions, prolonged ICU and hospital stay, persistent cognitive problems, and higher mortality rates. Considering the high incidence of delirium and its consequences, prevention of delirium is imperative. This study focuses on a program of standardized nursing and physical therapy interventions to prevent delirium in the ICU, called UNDERPIN-ICU (nUrsiNg DEliRium Preventive INterventions in the ICU).

OBJECTIVE

To determine the effect of the UNDERPIN-ICU program on the number of delirium-coma-free days in 28days and several secondary outcomes, such as delirium incidence, the number of days of survival in 28 and 90days and delirium-related outcomes.

DESIGN AND SETTING

A multicenter stepped wedge cluster randomized controlled trial.

METHODS

Eight to ten Dutch ICUs will implement the UNDERPIN-ICU program in a randomized order. Every two months the UNDERPIN-ICU program will be implemented in an additional ICU following a two months period of staff training. UNDERPIN-ICU consists of standardized protocols focusing on several modifiable risk factors for delirium, including cognitive impairment, sleep deprivation, immobility and visual and hearing impairment.

PARTICIPANTS

ICU patients aged ≥18years (surgical, medical, or trauma) and at high risk for delirium, E-PRE-DELIRIC ≥35%, will be included, unless delirium was detected prior ICU admission, expected length of ICU stay is less then one day or when delirium assessment is not possible.

DISCUSSION

For every intervention the balance between putative benefit and potential unwanted side effects needs to be considered. In non-ICU patients, it has been shown that a similar program resulted in a significant reduction of delirium incidence and duration. Recent small studies using multi component interventions to prevent delirium in ICU patients have also shown beneficial effect, without unwanted side effects. We therefore feel that the proportionality of potential positive effects of the UNDERPIN-ICU program, weighed against potential unwanted side effects is favourable. Since this has not been rigorously proven in ICU patients, we will study the effects of this program in ICU patients using a stepped wedge design.

TRIAL REGISTRATION

The study is registered in the clinical trials registry: https://clinicaltrials.gov/.

REPORTING METHOD

Standard Protocol Items: Recommendations for Interventional Trails (SPIRIT).

摘要

背景

谵妄是重症监护病房(ICU)患者常见的病症,与严重的短期和长期后果相关,包括再次插管、再次入住ICU、ICU和住院时间延长、持续的认知问题以及更高的死亡率。鉴于谵妄的高发病率及其后果,预防谵妄势在必行。本研究聚焦于一项标准化护理和物理治疗干预方案,以预防ICU中的谵妄,称为UNDERPIN-ICU(ICU谵妄预防护理干预)。

目的

确定UNDERPIN-ICU方案对28天内无谵妄昏迷天数以及若干次要结局的影响,如谵妄发生率、28天和90天的生存天数以及与谵妄相关的结局。

设计与设置

一项多中心阶梯式楔形整群随机对照试验。

方法

8至10家荷兰ICU将按随机顺序实施UNDERPIN-ICU方案。每两个月,在经过两个月的工作人员培训后,UNDERPIN-ICU方案将在另外一家ICU实施。UNDERPIN-ICU包括针对谵妄若干可改变风险因素的标准化方案,这些因素包括认知障碍、睡眠剥夺、活动减少以及视力和听力障碍。

参与者

年龄≥18岁(外科、内科或创伤)且谵妄风险高(E-PRE-DELIRIC≥35%)的ICU患者将被纳入,除非在入住ICU前已检测到谵妄、预计ICU住院时间少于一天或无法进行谵妄评估。

讨论

对于每一项干预措施,都需要考虑假定益处与潜在不良副作用之间的平衡。在非ICU患者中,已表明类似方案可显著降低谵妄发生率和持续时间。最近使用多成分干预措施预防ICU患者谵妄的小型研究也显示出有益效果,且无不良副作用。因此,我们认为UNDERPIN-ICU方案潜在积极效果与潜在不良副作用的比例是有利的。由于在ICU患者中尚未得到严格证实,我们将采用阶梯式楔形设计研究该方案在ICU患者中的效果。

试验注册

该研究已在临床试验注册库注册:https://clinicaltrials.gov/。

报告方法

标准方案项目:干预试验推荐(SPIRIT)。

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