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基于算法的养老院痴呆患者疼痛管理。

Algorithm-based pain management for people with dementia in nursing homes.

机构信息

School of Public Health, Bielefeld University, Bielefeld, Germany.

German Center for Neurodegenerative Diseases (DZNE), Witten, Germany.

出版信息

Cochrane Database Syst Rev. 2022 Apr 1;4(4):CD013339. doi: 10.1002/14651858.CD013339.pub2.

Abstract

BACKGROUND

People with dementia in nursing homes often experience pain, but often do not receive adequate pain therapy. The experience of pain has a significant impact on quality of life in people with dementia, and is associated with negative health outcomes. Untreated pain is also considered to be one of the causes of challenging behaviour, such as agitation or aggression, in this population. One approach to reducing pain in people with dementia in nursing homes is an algorithm-based pain management strategy, i.e. the use of a structured protocol that involves pain assessment and a series of predefined treatment steps consisting of various non-pharmacological and pharmacological pain management interventions.

OBJECTIVES

To assess the effects of algorithm-based pain management interventions to reduce pain and challenging behaviour in people with dementia living in nursing homes. To describe the components of the interventions and the content of the algorithms.

SEARCH METHODS

We searched ALOIS, the Cochrane Dementia and Cognitive Improvement Group's register, MEDLINE, Embase, PsycINFO, CINAHL (Cumulative Index to Nursing and Allied Health Literature), Web of Science Core Collection (ISI Web of Science), LILACS (Latin American and Caribbean Health Science Information database), ClinicalTrials.gov and the World Health Organization's meta-register the International Clinical Trials Registry Portal on 30 June 2021.

SELECTION CRITERIA

We included randomised controlled trials investigating the effects of algorithm-based pain management interventions for people with dementia living in nursing homes. All interventions had to include an initial pain assessment, a treatment algorithm (a treatment plan consisting of at least two different non-pharmacological or pharmacological treatment steps to reduce pain), and criteria to assess the success of each treatment step. The control groups could receive usual care or an active control intervention. Primary outcomes for this review were pain-related outcomes, e.g. the number of participants with pain (self- or proxy-rated), challenging behaviour (we used a broad definition that could also include agitation or behavioural and psychological symptoms assessed with any validated instrument), and serious adverse events.

DATA COLLECTION AND ANALYSIS

Two authors independently selected the articles for inclusion, extracted data and assessed the risk of bias of all included studies. We reported results narratively as there were too few studies for a meta-analysis. We used GRADE methods to rate the certainty of the results.

MAIN RESULTS

We included three cluster-randomised controlled trials with a total of 808 participants (mean age 82 to 89 years). In two studies, participants had severe cognitive impairment and in one study mild to moderate impairment. The algorithms used in the studies varied in the number of treatment steps. The comparator was pain education for nursing staff in two studies and usual care in one study. We judged the risk of detection bias to be high in one study. The risk of selection bias and performance bias was unclear in all studies. Self-rated pain (i.e. pain rated by participants themselves) was reported in two studies. In one study, all residents in the nursing homes were included, but fewer than half of the participants experienced pain at baseline, and the mean values of self-rated and proxy-rated pain at baseline and follow-up in both study groups were below the threshold of pain that may require treatment. We considered the evidence from this study to be very low-certainty and therefore are uncertain whether the algorithm-based pain management intervention had an effect on self-rated pain intensity compared with pain education (MD -0.27, 95% CI -0.49 to -0.05, 170 participants; Verbal Descriptor Scale, range 0 to 3). In the other study, all participants had mild to moderate pain at baseline. Here, we found low-certainty evidence that an algorithm-based pain management intervention may have little to no effect on self-rated pain intensity compared with pain education (MD 0.4, 95% CI -0.58 to 1.38, 246 participants; Iowa Pain Thermometer, range 0 to 12). Pain was rated by proxy in all three studies. Again, we considered the evidence from the study in which mean pain scores indicated no pain, or almost no pain, at baseline to be very low-certainty and were uncertain whether the algorithm-based pain management intervention had an effect on proxy-rated pain intensity compared with pain education. For participants with mild to moderate pain at baseline, we found low-certainty evidence that an algorithm-based pain management intervention may reduce proxy-rated pain intensity in comparison with usual care (MD -1.49, 95% CI -2.11 to -0.87, 1 study, 128 participants; Pain Assessment in Advanced Dementia Scale-Chinese version, range 0 to 10), but may not be more effective than pain education (MD -0.2, 95% CI -0.79 to 0.39, 1 study, 383 participants; Iowa Pain Thermometer, range 0 to 12). For challenging behaviour, we found very low-certainty evidence from one study in which mean pain scores indicated no pain, or almost no pain, at baseline. We were uncertain whether the algorithm-based pain management intervention had any more effect than education for nursing staff on challenging behaviour of participants (MD -0.21, 95% CI -1.88 to 1.46, 1 study, 170 participants; Cohen-Mansfield Agitation Inventory-Chinese version, range 7 to 203). None of the studies systematically assessed adverse effects or serious adverse effects and no study reported information about the occurrence of any adverse effect. None of the studies assessed any of the other outcomes of this review.

AUTHORS' CONCLUSIONS: There is no clear evidence for a benefit of an algorithm-based pain management intervention in comparison with pain education for reducing pain intensity or challenging behaviour in people with dementia in nursing homes. We found that the intervention may reduce proxy-rated pain compared with usual care. However, the certainty of evidence is low because of the small number of studies, small sample sizes, methodological limitations, and the clinical heterogeneity of the study populations (e.g. pain level and cognitive status). The results should be interpreted with caution. Future studies should also focus on the implementation of algorithms and their impact in clinical practice.

摘要

背景

养老院中患有痴呆症的人常常经历疼痛,但往往得不到充分的疼痛治疗。疼痛对痴呆症患者的生活质量有重大影响,并与负面健康结果相关。未经治疗的疼痛也被认为是导致该人群出现激越或攻击等挑战性行为的原因之一。减少养老院中患有痴呆症的人疼痛的一种方法是基于算法的疼痛管理策略,即使用结构化的方案,包括疼痛评估和一系列预先设定的治疗步骤,其中包括各种非药物和药物疼痛管理干预措施。

目的

评估基于算法的疼痛管理干预措施对减少居住在养老院中的痴呆症患者的疼痛和挑战性行为的效果。描述干预措施的组成部分和算法的内容。

检索方法

我们于 2021 年 6 月 30 日在 ALOIS(Cochrane 痴呆症和认知改善组登记册)、MEDLINE、Embase、PsycINFO、CINAHL(护理与联合健康文献累积索引)、Web of Science 核心合集(ISI Web of Science)、LILACS(拉丁美洲和加勒比健康科学信息数据库)、ClinicalTrials.gov 和世界卫生组织的国际临床试验注册平台的元注册中心检索了随机对照试验。

纳入标准

我们纳入了针对居住在养老院中的痴呆症患者的基于算法的疼痛管理干预措施的影响的随机对照试验。所有干预措施都必须包括初始疼痛评估、治疗算法(包含至少两种不同的非药物或药物治疗步骤以减轻疼痛的治疗计划)以及评估每个治疗步骤成功的标准。对照组可以接受常规护理或积极对照干预。本综述的主要结局是疼痛相关结局,例如有疼痛的参与者人数(自我或代理评定)、挑战性行为(我们使用了广泛的定义,也可以包括使用任何经过验证的工具评定的激越或行为和心理症状)和严重不良事件。

数据收集和分析

两位作者独立选择纳入的文章、提取数据并对所有纳入研究的偏倚风险进行评估。由于研究数量太少,无法进行荟萃分析,因此我们以叙述性方式报告结果。我们使用 GRADE 方法来评估结果的确定性。

主要结果

我们纳入了三项包含 808 名参与者的聚类随机对照试验(平均年龄 82 至 89 岁)。两项研究中的参与者有严重认知障碍,一项研究中参与者有轻度至中度认知障碍。研究中使用的算法在治疗步骤的数量上有所不同。两项研究中的对照组是护理人员的疼痛教育,一项研究中的对照组是常规护理。我们认为一项研究存在高检测偏倚风险。所有研究的选择偏倚和实施偏倚风险均不明确。自我评定的疼痛(即参与者自己评定的疼痛)在两项研究中报告。在一项研究中,所有养老院的居民都被纳入,但只有不到一半的参与者在基线时有疼痛,且两组参与者在基线和随访时的自我评定和代理评定疼痛的平均值均低于可能需要治疗的疼痛阈值。我们认为这项研究的证据确定性非常低,因此不确定基于算法的疼痛管理干预措施与疼痛教育相比是否会对自我评定的疼痛强度产生影响(MD-0.27,95%CI-0.49 至-0.05,170 名参与者;言语描述量表,范围 0 至 3)。在另一项研究中,所有参与者在基线时都有轻度至中度疼痛。在这里,我们发现基于算法的疼痛管理干预措施与疼痛教育相比,可能对自我评定的疼痛强度几乎没有影响的低确定性证据(MD0.4,95%CI-0.58 至 1.38,246 名参与者;爱荷华州疼痛温度计,范围 0 至 12)。所有三项研究均通过代理评定疼痛。同样,我们认为在基线时平均疼痛评分表明无疼痛或几乎无疼痛的研究的证据确定性非常低,并且不确定基于算法的疼痛管理干预措施与疼痛教育相比是否会对代理评定的疼痛强度产生影响。对于基线时有轻度至中度疼痛的参与者,我们发现基于算法的疼痛管理干预措施与常规护理相比可能会降低代理评定的疼痛强度(MD-1.49,95%CI-2.11 至-0.87,1 项研究,128 名参与者;中文版疼痛评估在晚期痴呆症量表,范围 0 至 10),但可能不如疼痛教育有效(MD-0.2,95%CI-0.79 至 0.39,1 项研究,383 名参与者;爱荷华州疼痛温度计,范围 0 至 12)。对于挑战性行为,我们发现一项研究中的平均疼痛评分表明无疼痛或几乎无疼痛,证据确定性非常低。我们不确定基于算法的疼痛管理干预措施与护理人员的教育相比是否对参与者的挑战性行为有更多影响(MD-0.21,95%CI-1.88 至 1.46,1 项研究,170 名参与者;科恩-曼斯菲尔德激越量表-中文版,范围 7 至 203)。没有研究系统地评估不良影响或严重不良影响,也没有研究报告任何不良影响的发生信息。没有研究评估本综述的其他结局。

作者结论

目前尚无明确证据表明,与疼痛教育相比,基于算法的疼痛管理干预措施可降低养老院中痴呆症患者的疼痛强度或挑战性行为。我们发现该干预措施可能与常规护理相比,降低代理评定的疼痛程度。然而,由于研究数量较少、样本量小、方法学局限性以及研究人群的临床异质性(例如疼痛程度和认知状态),证据确定性较低。结果应谨慎解读。未来的研究还应关注算法的实施及其对临床实践的影响。

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