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A randomised controlled trial evaluating a rehabilitation complex intervention for patients following intensive care discharge:the RECOVER study

机译:一项评估重症监护病人出院后康复综合干预措施的随机对照试验:RECOVER研究

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摘要

Introduction: Patients who survive an intensive care unit admission frequently suffer physical and psychological morbidity for many months after discharge. Current rehabilitation pathways are often fragmented and little is known about the optimum method of promoting recovery. Many patients suffer reduced quality of life. Methods and analysis: The authors plan a multicentre randomised parallel group complex intervention trial with concealment of group allocation from outcome assessors. Patients who required more than 48 h of mechanical ventilation and are deemed fit for intensive care unit discharge will be eligible. Patients with primary neurological diagnoses will be excluded. Participants will be randomised into one of the two groups: the intervention group will receive standard ward-based care delivered by the NHS service with additional treatment by a specifically trained generic rehabilitation assistant during ward stay and via telephone contact after hospital discharge and the control group will receive standard ward-based care delivered by the current NHS service. The intervention group will also receive additional information about their critical illness and access to a critical care physician. The total duration of the intervention will be from randomisation to 3 months postrandomisation. The total duration of follow-up will be 12 months from randomisation for both groups. The primary outcome will be the Rivermead Mobility Index at 3 months. Secondary outcomes will include measures of physical and psychological morbidity and function, quality of life and survival over a 12-month period. A health economic evaluation will also be undertaken. Groups will be compared in relation to primary and secondary outcomes; quantitative analyses will be supplemented by focus groups with patients, carers and healthcare workers. Ethics and dissemination: Consent will be obtained from patients and relatives according to patient capacity. Data will be analysed according to a predefined analysis plan.
机译:简介:重症监护病房幸存下来的患者出院后数月经常患有身体和心理疾病。当前的康复途径通常是零散的,对促进康复的最佳方法知之甚少。许多患者的生活质量下降。方法和分析:作者计划进行一项多中心随机平行分组复杂干预试验,其中不向结果评估者分配分组。需要超过48小时的机械通气并且被认为适合重症监护病房出院的患者将符合资格。具有初级神经系统诊断的患者将被排除在外。参与者将被随机分为两组:干预组将接受由NHS服务提供的基于病房的标准护理,并在病房期间以及经过出院后通过电话联系与对照组进行特殊训练的通用康复助手的额外治疗。将接受当前NHS服务提供的基于病房的标准护理。干预小组还将获得有关其危重疾病的更多信息以及就医的机会。干预的总持续时间为随机化至随机后3个月。两组患者的随访总时间为12个月。主要结果将是3个月时的Rivermead流动性指数。次要结果将包括身体和心理的发病率和功能,在12个月内的生活质量和生存率的量度。还将进行卫生经济评估。将根据主要和次要结果比较各组;与患者,护理人员和医护人员的焦点小组将补充定量分析。道德与传播:将根据患者的能力从患者和亲戚那里获得同意。数据将根据预定义的分析计划进行分析。

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