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用于治疗肩部骨关节炎的NASHA透明质酸:一项前瞻性单臂临床试验。

NASHA hyaluronic acid for the treatment of shoulder osteoarthritis: a prospective, single-arm clinical trial.

作者信息

McKee Michael D, Litchfield Robert, Hall Jeremy A, Wester Tawana, Jones John, Harrison Andrew J

机构信息

Department of Orthopaedic Surgery, University of Arizona College of Medicine, Phoenix, AZ, USA.

Department of Surgery, Fowler Kennedy Sport Medicine Clinical, London, ON, Canada.

出版信息

Med Devices (Auckl). 2019 Jun 12;12:227-234. doi: 10.2147/MDER.S189522. eCollection 2019.

Abstract

Osteoarthritis of the shoulder or glenohumeral joint is a painful condition that can be debilitating. Intra-articular injection with hyaluronic acid should be considered for patients not responding adequately to physical therapy or anti-inflammatory medication. This was a single-arm, open-label, prospective study of a single intra-articular injection of NASHA (non-animal hyaluronic acid) in patients with symptomatic glenohumeral osteoarthritis. Patients were followed up for 26 weeks post-treatment, during which time rescue medication with acetaminophen was permissible. The study objective was to demonstrate that a single injection of NASHA is well tolerated with an over-6-month 25% reduction in shoulder pain on movement, assessed using a 100-mm visual analog scale. Forty-one patients were enrolled, all of whom received study treatment. The mean decrease in shoulder pain on movement score over the 6-month study period was -20.1 mm (95% CI: -25.2, -15.0 mm), corresponding to a mean reduction of 29.5% (22.0, 37.0%). Statistically significant improvements were also observed in shoulder pain at night and patient global assessment. There was no clear change over time in the percentage of patients using rescue medication and mean weekly doses were below 3500 mg. Seventeen patients (41.5%) experienced adverse events, all of which were mild or moderate. Two adverse events (both shoulder pain) were deemed related to study treatment. This study provides preliminary evidence that a single injection of NASHA may be efficacious over 6 months and well tolerated in patients with symptomatic glenohumeral osteoarthritis. Larger studies are needed for confirmation.

摘要

肩部或盂肱关节骨关节炎是一种会导致疼痛的疾病,可能使人虚弱无力。对于对物理治疗或抗炎药物反应不佳的患者,可考虑进行关节内注射透明质酸。这是一项单臂、开放标签的前瞻性研究,对有症状的盂肱关节骨关节炎患者单次关节内注射非动物源性透明质酸(NASHA)。对患者进行治疗后26周的随访,在此期间允许使用对乙酰氨基酚作为急救药物。研究目的是证明单次注射NASHA耐受性良好,使用100毫米视觉模拟量表评估,治疗后6个月以上肩部运动时疼痛减轻25%。共纳入41例患者,所有患者均接受了研究治疗。在6个月的研究期间,肩部运动疼痛评分的平均降低为-20.1毫米(95%置信区间:-25.2,-15.0毫米),相当于平均降低29.5%(22.0,37.0%)。夜间肩部疼痛和患者整体评估也有统计学上的显著改善。使用急救药物的患者百分比随时间没有明显变化,平均每周剂量低于3500毫克。17例患者(41.5%)出现不良事件,所有不良事件均为轻度或中度。两项不良事件(均为肩部疼痛)被认为与研究治疗有关。本研究提供了初步证据,表明单次注射NASHA可能在6个月内有效,且对有症状的盂肱关节骨关节炎患者耐受性良好。需要更大规模的研究来证实这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd0/6573776/03e525c57c0a/MDER-12-227-g0001.jpg

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