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首页> 外文期刊>BMC Musculoskeletal Disorders >Hand therapy or not following collagenase treatment for Dupuytren’s contracture? Protocol for a randomised controlled trial
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Hand therapy or not following collagenase treatment for Dupuytren’s contracture? Protocol for a randomised controlled trial

机译:手工疗法或不遵循胶原酶治疗Dupuytren的挛缩吗?随机对照试验的协议

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摘要

Dupuytren's contracture (DC) is a fibrotic hand condition in which one or more fingers develop progressive flexion deformities. Quality of life is diminished due to disabling limitations in performing everyday activities. For DC patients treated with collagenase, referral for subsequent hand therapy is inconsistent. It is unknown whether subsequent hand therapy is beneficial compared to no therapy. The purpose of this study is to determine whether hand therapy improves DC patients' performance of and satisfaction with performing everyday activities one year after collagenase treatment. We will conduct a randomised controlled trial with two treatment groups (hand therapy vs. control) of DC patients who have received collagenase treatment. DC patients with contracted metacarpophalangeal joint(s) (MCPJ) (hand therapy, n?=?40; control, n?=?40) and those with proximal interphalangeal joint(s) (PIPJ) involvement (hand therapy, n?=?40; control, n?=?40) comprise two subgroups, and we will study if the treatment effect will be different between both groups (n?=?160). Patients with a previous injury or treatment for DC in the treatment finger are excluded. Hand therapy includes oedema and scar management, splinting, movement exercises, and practice of everyday activities. The main outcome variable is patients' performance of and satisfaction with performing everyday activities, as assessed with the Canadian Occupational Performance Measure. Secondary outcomes are DC-specific activity problems, as assessed with the Unité Rhumatologique des Affections de la Main scale, and active/passive flexion/extension of treated joints and grip force using standard measuring tools, and self-reported pain level. Demographic and clinical variables, degree of scarring, cold hypersensitivity, number of occupational sick-leave days are collected. Self-reported global impression of change will be used to assess patient satisfaction with change in hand function. Assessments are done pre-injection and 6?weeks, 4?months, and 1?year later. Standard univariate and multivariate statistical analyses will be used to evaluate group differences. This study aims to assess whether hand therapy is beneficial for activity-related, biomechanical, and clinical outcomes in DC patients after collagenase treatment. The results will provide an objective basis for determining whether hand therapy should be conducted after collagenase treatment. This study has been registered at ClinicalTrials.gov as NCT03580213 (April 5, 2018).
机译:Dupuytren的挛缩(DC)是一种纤维化的手工条件,其中一个或多个手指发展渐进屈曲畸形。由于在执行日常活动方面禁用限制,生活质量减少。对于用胶原酶治疗的DC患者,随后的手工疗法转诊是不一致的。与无治疗相比,随后的手疗是否有益,尚不清楚。本研究的目的是确定手工治疗是否提高了直流患者的表现和满足,在胶原酶治疗后一年进行日常活动。我们将进行随机对照试验,其两种治疗组(手工治疗与控制)的DC患者接受胶原酶治疗。直流患者患有患者患者(MCPJ)(MCPJ)(手工疗法,N?= 40;控制,N?=?40)和近端间关节接头(PIPJ)的参与(手疗,N?= ?40;控制,n?=?40)包括两个亚组,如果治疗效果在两个组之间存在不同(n?=Δ160)。在治疗手指中以前损伤或治疗的患者被排除在外。手工疗法包括水肿和疤痕管理,夹板,运动锻炼和日常活动的实践。主要成果变量是患者的表现和满意于执行日常活动,如加拿大职业绩效措施的评估。二次结果是直流特定的活动问题,如统一rhumatologique des富级评估,以及使用标准测量工具的经处理的关节和握力的主动/被动屈曲/延伸,以及自我报告的疼痛水平。收集人口统计学和临床​​变量,瘢痕,冷超敏反应,职业病休假日的数量。自我报告的全球变革印象将用于评估患者对手动变化的满意度。评估进行预注射,6?周,4个月,1年后1个月。标准单变量和多变量统计分析将用于评估组差异。本研究旨在评估胶原酶治疗后DC患者的活动相关,生物力学和临床结果是否有益。结果将提供目标基础,用于确定是否应在胶原酶治疗后进行手工治疗。本研究已在ClinicalTrials.gov注册为NCT03580213(2018年4月5日)。

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