Larsen Josefine Beck, Østergaard Helle Kvistgaard, Thillemann Theis Muncholm, Falstie-Jensen Thomas, Reimer Lisa Cecilie Urup, Noe Sidsel, Jensen Steen Lund, Mechlenburg Inger
Department of Orthopaedic Surgery, Aarhus University Hospital, Aarhus N, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.
Pilot Feasibility Stud. 2022 Aug 3;8(1):168. doi: 10.1186/s40814-022-01127-8.
Little is known about the feasibility of progressive shoulder exercises (PSE) for patients with glenohumeral osteoarthritis (OA) or rotator cuff tear arthropathy (CTA). The aim of this study was to investigate whether 12 weeks of PSE is feasible in patients with glenohumeral OA or CTA eligible for shoulder arthroplasty. Moreover, to report changes in shoulder function and range of motion (ROM) following the exercise program.
Twenty patients were included. Eighteen patients (11 women, 15 with OA), mean age 70 years (range 57-80), performed 12 weeks of PSE with one weekly physiotherapist-supervised and two weekly home-based sessions. Feasibility was measured by dropout rate, adverse events, pain, and adherence to PSE. At baseline and end of intervention, patients completed the Western Ontario Osteoarthritis of the Shoulder (WOOS) score and Disabilities of the Arm, Shoulder and Hand (DASH). Data to assess feasibility were analyzed using descriptive statistics.
Two patients dropped out and no adverse events were observed. Sixteen of the eighteen patients (89%) had a high adherence (≥ 70%) to the physiotherapist-supervised sessions. Acceptable pain levels were reported; in 76% of all exercise sessions with no numeric rating scale (NRS) score over five for any exercise. WOOS improved with a mean of 23 points (95% CI 13;33), and DASH improved with a mean of 13 points (95% CI 6;19).
Adherence to PSE was high and dropout rates were low. PSE is feasible, safe and may relieve shoulder pain, improve function and ROM in patients with glenohumeral OA or CTA. The patient-experienced gains after PSE seem clinically relevant and should be compared to arthroplasty surgery in a RCT setting.
According to Danish law, this study did not need an approval by the Central Denmark Region Committee on Health Research Ethics. Approval from The Danish Data Protection Agency (journal number 1-16-02-15-20) was obtained.
对于盂肱关节骨关节炎(OA)或肩袖撕裂性关节病(CTA)患者进行渐进性肩部锻炼(PSE)的可行性知之甚少。本研究的目的是调查12周的PSE对于符合肩关节置换术条件的盂肱关节OA或CTA患者是否可行。此外,报告运动计划后肩部功能和活动范围(ROM)的变化。
纳入20名患者。18名患者(11名女性,15名患有OA),平均年龄70岁(范围57 - 80岁),进行了12周的PSE,每周有一次物理治疗师监督的训练课程和两次在家中进行的训练课程。通过退出率、不良事件、疼痛和对PSE的依从性来衡量可行性。在基线和干预结束时,患者完成了西 Ontario 肩部骨关节炎(WOOS)评分以及手臂、肩部和手部功能障碍(DASH)评估。使用描述性统计分析评估可行性的数据。
两名患者退出,未观察到不良事件。18名患者中有16名(89%)对物理治疗师监督的训练课程有高依从性(≥70%)。报告的疼痛水平可接受;在所有训练课程中,76%的课程在任何一项训练中数字评分量表(NRS)得分均未超过5分。WOOS平均提高了23分(95%CI 13;33),DASH平均提高了13分(95%CI 6;19)。
对PSE的依从性高且退出率低。PSE是可行、安全的,并且可能缓解盂肱关节OA或CTA患者的肩部疼痛,改善功能和ROM。PSE后患者体验到的改善在临床上似乎具有相关性,应在随机对照试验环境中与关节置换手术进行比较。
根据丹麦法律,本研究无需获得丹麦中部地区健康研究伦理委员会的批准。已获得丹麦数据保护局的批准(期刊编号1 - 16 - 02 - 15 - 20)。