在支持骨关节炎自我管理计划后,赋权和启用及其与健康相关生活质量变化的关系——一项前瞻性观察性研究。

IF 2.1 Q1 REHABILITATION Archives of physiotherapy Pub Date : 2023-09-22 DOI:10.1186/s40945-023-00172-7
Karin Sturesdotter Åkesson, Anne Sundén, Kjerstin Stigmar, Frida Eek, Teresa Pawlikowska, Eva Ekvall Hansson
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引用次数: 0

摘要

背景:骨关节炎是世界范围内致残的主要原因。目前的治疗支持改善健康相关生活质量的应对策略。预测治疗反应的需求已被提升为个性化护理。本研究旨在检查参与支持性骨关节炎自我管理计划(SOASP)后从基线到三个月和九个月随访的HRQoL变化,并检查授权和/或启用是否与SOASP后HRQoL的变化有关。方法:在2016年4月至2018年6月期间连续招募参与SOASP的患者。EQ-5D用于测量HRQoL,瑞典风湿病授权量表(SWE-RES-23)(评分范围1-5)用于测量授权,患者授权工具(PEI)(评分区间0-12)用于测量启用。在SOASP之前(EQ-5D,SWE-RES-23)和之后(EQ-5D,SWE-RS-23,PEI)对仪器进行应答。一位患者伙伴参与了研究过程,以增强患者的视角。采用配对样本t检验和标准化效应大小(Cohen s d)检验结果的变化。进行多元线性回归分析以评估潜在的相关性。结果:143名患者参与了基线测量。平均EQ-5D-5L指数得分从基线到三个月显著增加,对应于d的标准化效应大小(Cohen s d) = 0.43,95%置信区间[0.24,0.63](n = 109),从基线到9个月d = 0.19,95%可信区间[0.0.37](n = 119)。平均EQ VAS评分从基线到三个月显著增加,对应于d的标准化效应大小 = 0.26,95%置信区间[0.07,0.45](n = 109),从基线到9个月d = 0.18,95%置信区间[0.003](n = 119)。三个月随访时的SWE-RES-23和PEI,以及从基线到三个月的SWE-RES-23评分的变化都与EQ-5D-5L指数的变化无关(p > 0.05)或EQ VAS(p > 0.05)。结论:参与SOASP后,与健康相关的生活质量提高。SWE-RES-23和PEI测量的授权和启用与参与SOASP的患者的HRQoL变化无关。试验注册:ClinicalTrials.gov。识别号:NCT02974036。2016年11月28日首次注册,追溯注册。
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Empowerment and enablement and their associations with change in health-related quality of life after a supported osteoarthritis self-management programme - a prospective observational study.

Background: Osteoarthritis is a leading cause of disability worldwide. Current treatment supports coping strategies to improve health-related quality of life (HRQoL). The need to predict response to treatment has been raised to personalise care. This study aims to examine change in HRQoL from baseline to three and nine months follow-up after participating in a Supported Osteoarthritis Self-Management Programme (SOASP) and to examine if empowerment and/or enablement were associated with change in HRQoL after a SOASP.

Methods: Patients participating in a SOASP were recruited consecutively between April 2016 and June 2018. The EQ-5D was used to measure HRQoL, the Swedish Rheumatic Disease Empowerment Scale (SWE-RES-23) (score range 1-5) to measure empowerment and the Patient Enablement Instrument (PEI) (score range 0-12) to measure enablement. The instruments were answered before (EQ-5D, SWE-RES-23) and after (EQ-5D, SWE-RES-23, PEI) the SOASP. A patient partner was involved in the research process to enhance the patient perspective. Changes in outcome were examined with paired sample t-test and standardized effect sizes (Cohen´s d). Multiple linear regression analysis was performed to assess potential associations.

Results: One hundred forty-three patients participated in baseline measurement. Mean EQ-5D-5 L index score increased significantly from baseline to three months corresponding to a standardised effect size (Cohen´s d) of d = 0.43, 95% CI [0.24, 0.63] (n = 109), and from baseline to nine months d = 0.19, 95% CI [0.01, 0.37] (n = 119). The average EQ VAS score increased significantly from baseline to three months corresponding to a standardised effect size of d = 0.26, 95% CI [0.07, 0.45] (n = 109), and from baseline to nine months d = 0.18, 95% CI [0.00, 0.36] (n = 119). Neither SWE-RES-23 nor PEI at three months follow-up nor the change in the SWE-RES-23 score from baseline to three months follow-up were associated with change in either EQ-5D-5 L index (p > 0.05) or the EQ VAS (p > 0.05).

Conclusions: Health-related quality of life increased after participating in a SOASP. Empowerment and enablement as measured with the SWE-RES-23 and the PEI were not associated with change in HRQoL among patients participating in a SOASP.

Trial registration: ClinicalTrials.gov. Identification number: NCT02974036. First registration 28/11/2016, retrospectively registered.

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