高分子量透明质酸治疗肩关节关节炎相关的慢性肩关节疼痛。

IF 1.3 Q4 ENGINEERING, BIOMEDICAL Medical Devices-Evidence and Research Pub Date : 2011-01-01 Epub Date: 2011-07-26 DOI:10.2147/MDER.S22423
Arnold J Weil
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引用次数: 9

摘要

背景:没有足够的证据来确定关节内注射是否可以有效治疗盂肱骨关节炎。Euflexxa(®)(高分子量透明质酸)是一种生物工程高分子量透明质酸,已被证明是一种安全有效的治疗膝关节骨关节炎的药物。也有研究支持使用透明质酸注射治疗与骨关节炎或肩袖损伤相关的慢性肩痛。这项小规模的探索性研究旨在评估高分子量透明质酸治疗骨关节炎相关慢性肩痛的安全性和有效性。方法:患有盂肱骨关节炎和慢性疼痛的受试者(n = 27)每周注射一次高分子量透明质酸,持续3周,并在26周内评估疼痛变化(100 mm视觉模拟量表[VAS])、活动范围以及受试者和医生的整体评估。受试者还使用西安大略和麦克马斯特大学关节炎指数(WOMAC)评估疼痛、僵硬和身体功能。最后,使用类风湿关节炎临床试验(OMERACT)-国际骨关节炎研究协会(OARSI)提案D标准对反应进行评估。通过记录不良事件来评估安全性。结果:高分子量透明质酸显著改善疼痛(VAS、WOMAC)、活动范围、僵硬度和身体功能评分;77.8%的受试者被评为OMERACT-OARSI命题D高反应。没有严重的不良事件,也没有被认为与治疗有关。结论:高分子量透明质酸治疗可改善疼痛、僵硬和活动范围,并且可能具有可接受的安全性和耐受性。一项随机、双盲、安慰剂对照的临床试验可能有必要进一步研究关节内高分子量透明质酸治疗肩关节骨性关节炎患者慢性肩痛的有效性和安全性。
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High molecular weight hyaluronan for treatment of chronic shoulder pain associated with glenohumeral arthritis.

Background: There is insufficient evidence to determine whether intra-articular injections may be effective for treatment of glenohumeral osteoarthritis. Euflexxa(®) (high molecular weight hyaluronate), a bioengineered high molecular weight hyaluronan, has been shown to be a safe and effective treatment for patients with knee osteoarthritis. There is also support for the use of hyaluronate injection for the treatment of chronic shoulder pain associated with osteoarthritis or rotator cuff damage. This small-scale exploratory study was conducted to evaluate the safety and efficacy of high molecular weight hyaluronate for the treatment of chronic shoulder pain associated with osteoarthritis.

Methods: Subjects with glenohumeral osteoarthritis and chronic pain (n = 27) received one injection per week for 3 weeks of high molecular weight hyaluronate and were assessed for changes in pain (100 mm visual analog scale [VAS]), range of motion, and the subject's and physician's global assessment over 26 weeks. Subjects were also assessed for pain, stiffness, and physical functioning using the Western Ontario and McMaster Universities Arthritis Index (WOMAC). Finally, responses were evaluated using modified Outcome Measures in Rheumatoid Arthritis Clinical Trials (OMERACT)-Osteoarthritis Research Society International (OARSI) Proposition D criteria. Safety was assessed by recording adverse events.

Results: High molecular weight hyaluronate significantly improved pain (VAS, WOMAC), range of motion, stiffness, and physical functioning scores; 77.8% of subjects were rated as having an OMERACT-OARSI Proposition D high response. There were no serious adverse events, and none were considered to be related to treatment.

Conclusion: Treatment with high molecular weight hyaluronate improves pain, stiffness, and range of motion, and may have an acceptable safety and tolerability profile. A randomized, double-blind, placebo-controlled clinical trial may be warranted to investigate further the efficacy and safety of intra-articular high molecular weight hyaluronate for treatment of chronic shoulder pain in patients with glenohumeral osteoarthritis.

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来源期刊
Medical Devices-Evidence and Research
Medical Devices-Evidence and Research ENGINEERING, BIOMEDICAL-
CiteScore
2.80
自引率
0.00%
发文量
41
审稿时长
16 weeks
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