Østerås N, Hagen K B, Grotle M, Sand-Svartrud A-L, Mowinckel P, Kjeken I
National Advisory Unit on Rehabilitation in Rheumatology, Department of Rheumatology, Diakonhjemmet Hospital, PO Box 23 Vinderen, N-0319 Oslo, Norway.
National Advisory Unit on Rehabilitation in Rheumatology, Department of Rheumatology, Diakonhjemmet Hospital, PO Box 23 Vinderen, N-0319 Oslo, Norway; Department of Health Sciences, Institute of Health and Society, Faculty of Medicine, University of Oslo, Norway.
Osteoarthritis Cartilage. 2014 Sep;22(9):1224-33. doi: 10.1016/j.joca.2014.06.036. Epub 2014 Jul 5.
To determine the clinical effectiveness of an exercise programme on self-reported hand activity performance in people with hand osteoarthritis (OA).
In this randomized, controlled trial, participants with physician-confirmed hand OA were randomly allocated to a 12-week exercise intervention (group- and home-based) or usual care. The primary outcome was self-reported hand activity performance at 3 months measured by the Functional Index for Hand Osteoarthritis (FIHOA) and a patient-generated measure of disability, the Patient-Specific Functional Scale (PSFS).
Of 130 randomized participants (mean age 66 (standard deviation (SD) 9); female 90%), 120 (92%) and 119 (92%) completed the 3- and 6-month follow-ups. The adjusted mean difference for the exercise vs control group was -0.5 points (95% confidence interval (CI) -1.6, 0.6) for the FIHOA score (0-30 scale, 0 = best) and 0.9 points (95% CI 0.1, 1.7) for the PSFS score (0-10 scale, 10 = best). Small significant mean differences in favour of the intervention group were found for hand pain, hand stiffness and disease activity, whereas no mean differences were observed in hand dexterity or maximal grip strength. A significantly larger proportion in the intervention (46%) vs control group (16%) fulfilled the Outcome Measures in Rheumatological Clinical Trials-Osteoarthritis Research Society International (OMERACT-OARSI) responder criteria at 3 months (OR = 4.4, 95% CI 1.9, 10.2). At the 6-month follow-up, there were no significant group differences in any outcome.
The exercise programme was well tolerated among people with hand OA, but resulted only in small, beneficial short-term improvements on self-reported measures and not on most performance-based tests. Future studies should address optimal grip strength exercises and dosage.
ClinicalTrials.gov registration number: NCT01245842.
确定一项运动计划对手部骨关节炎(OA)患者自我报告的手部活动表现的临床效果。
在这项随机对照试验中,经医生确诊为手部OA的参与者被随机分配至为期12周的运动干预组(包括小组和居家运动)或常规护理组。主要结局指标是在3个月时通过手部骨关节炎功能指数(FIHOA)和患者自行制定的残疾衡量指标——患者特定功能量表(PSFS)来评估的自我报告手部活动表现。
130名随机分组的参与者(平均年龄66岁(标准差(SD)9);女性占90%)中,120名(92%)和119名(92%)分别完成了3个月和6个月的随访。运动组与对照组相比,FIHOA评分(0 - 30分制,0分表示最佳)的调整后平均差异为 -0.5分(95%置信区间(CI) -1.6, 0.6),PSFS评分(0 - 10分制,10分表示最佳)的调整后平均差异为0.9分(95% CI 0.1, 1.7)。在手部疼痛、手部僵硬和疾病活动方面发现了有利于干预组的小幅度显著平均差异,而在手部灵活性或最大握力方面未观察到平均差异。在3个月时,干预组(46%)达到风湿病临床试验 - 国际骨关节炎研究学会(OMERACT - OARSI)反应标准的比例显著高于对照组(16%)(比值比(OR) = 4.4,95% CI 1.9, 10.2)。在6个月随访时,各结局指标在两组间均无显著差异。
手部OA患者对该运动计划耐受性良好,但仅在自我报告指标上带来了小幅度的短期有益改善,而在大多数基于表现的测试中未产生改善。未来研究应关注最佳握力锻炼方法和剂量。
ClinicalTrials.gov注册号:NCT01245842。