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养老院痴呆症患者的疼痛干预(PID):一项准实验性护士干预的研究方案

Pain Intervention for people with Dementia in nursing homes (PID): study protocol for a quasi-experimental nurse intervention.

作者信息

Koppitz Andrea, Bosshard Georg, Blanc Geneviève, Hediger Hannele, Payne Sheila, Volken Thomas

机构信息

Zurich University of Applied Sciences, School of Health Professions, Institute of Nursing, Technikumstrasse 81, 8401, Winterthur, Switzerland.

University Hospital Zurich, Clinic for Geriatric Medicine and Centre on Aging and Mobility at the University of Zurich, Gloriastrasse 25, 8091, Zurich, Switzerland.

出版信息

BMC Palliat Care. 2017 Apr 21;16(1):27. doi: 10.1186/s12904-017-0200-5.

Abstract

BACKGROUND

It is estimated that 19 to 83% of people with dementia suffer from pain that is inadequately treated in the last months of life. A large number of healthcare workers who care for these people in nursing homes lack appropriate expertise and may therefore not always recognise, assess and treat pain in those with dementia who have complex problems on time, properly and efficiently. The aim of this intervention trial is to identify care needs of people with dementia suffering from pain living in a nursing home.

METHODS

A quasi-experimental nurse-led intervention trial based on a convenience sample of four nursing homes in the Swiss Canton of Zurich examines the effects on dementia patients (n = 411), the healthcare institution and the qualification level of the healthcare workers compared to historical controls, using an event analysis and a multilevel analysis. Healthcare workers will be individually trained how to assess, intervene and evaluate acute and chronic pain. There are three data-monitoring cycles (T0, T1, T2) and two intervention cycles (I1, I2) with a total study duration of 425 days. There is also a process evaluation based on Dobbins analyses that analyse in particular the potentials for change in clinical practice of change agents.

DISCUSSION

The aim of the intervention trial is to improve pain management strategies in older people with dementia in nursing homes. Clinically significant findings will be expected that will help reduce suffering in the sense of "total pain" for people with dementia. The joint intra- and interdisciplinary collaboration between practice and supply-oriented (nursing) research will have both a lasting effect on the efficiency measurement and provide scientifically sound results. Nursing homes can integrate the findings from the intervention trial into their internal quality control process. The potential for improvements can be directly influenced by the nursing home itself.

TRIAL REGISTRATION

Registration trial number: DRKS00009726 on DRKS, registered 10 January 2017, retrorespectively registered. Clearance certificate is available of the ethics committees of the canton of Thurgau, Switzerland, number: TG K201-02, and Zurich, Switzerland, number: ZH 01-2016.

摘要

背景

据估计,19%至83%的痴呆症患者在生命的最后几个月遭受疼痛折磨,且疼痛未得到充分治疗。大量在养老院照顾这些患者的医护人员缺乏适当的专业知识,因此可能无法始终及时、正确且有效地识别、评估和治疗患有复杂问题的痴呆症患者的疼痛。这项干预试验的目的是确定住在养老院的痴呆症疼痛患者的护理需求。

方法

一项基于瑞士苏黎世州四家养老院便利样本的由护士主导的准实验性干预试验,使用事件分析和多层次分析,将痴呆症患者(n = 411)、医疗机构以及医护人员的资质水平与历史对照组进行比较,研究其效果。医护人员将接受关于如何评估、干预和评估急性和慢性疼痛的个体培训。有三个数据监测周期(T0、T1、T2)和两个干预周期(I1、I2),总研究时长为425天。还将基于多宾斯分析进行过程评估,该分析特别分析变革推动者临床实践中的变革潜力。

讨论

干预试验的目的是改善养老院中患有痴呆症的老年人的疼痛管理策略。预计将得出具有临床意义的结果,这将有助于减轻痴呆症患者“全面疼痛”意义上的痛苦。实践与以供应为导向(护理)的研究之间的联合内部和跨学科合作将对效率衡量产生持久影响,并提供科学合理的结果。养老院可将干预试验结果纳入其内部质量控制流程。改善的潜力可直接受养老院自身影响。

试验注册

注册试验编号:DRKS上的DRKS00009726,于2017年1月10日注册,追溯注册。可获得瑞士图尔高州伦理委员会的批准证书,编号:TG K201 - 02,以及瑞士苏黎世伦理委员会的批准证书,编号:ZH 01 - 2016。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a08/5399861/d230224a1097/12904_2017_200_Fig1_HTML.jpg

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