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硫酸氨基葡聚糖注射治疗肱骨外上髁炎:一项安慰剂对照双盲试验

Glycosaminoglycan polysulfate injections in lateral humeral epicondylalgia: a placebo-controlled double-blind trial.

作者信息

Akermark C, Crone H, Elsasser U, Forsskåhl B

机构信息

Orthopaedic Outpatient Clinic Odenplan, Stockholm, Sweden.

出版信息

Int J Sports Med. 1995 Apr;16(3):196-200. doi: 10.1055/s-2007-972991.

Abstract

The purpose of this study was to investigate the therapeutic benefit of local Glycosaminoglycan polysulfate (GAGPS) injections in the treatment of chronic epicondylalgia. The study was conducted as a prospective, placebo-controlled double-blind trial. Sixty patients with a typical history of pain for at least 3 months who attended two private orthopaedic clinics in Stockholm received 50 mg GAGPS or placebo injections, one injection a week, for five weeks. The main outcome measures were the patients' evaluation of pain in connection with daily activities with a visual analogue scale and the number of treatment failures. The follow-up period was six months. The difference in reduction of painscore (VAS) ranging between 11.1 percentage units at the half-year follow-up and 20.9 percentage units 2 weeks after the treatment period is clinically good. The number of treatment failures in the GAGPS treatment groups at the 6 week follow-up was only 4 (13%) compared with 12 (40%) of the placebo treated patients. At the half-year follow-up 5 of those who received GAGPS had experienced a recurrency. The recurrency rate is thus smaller than most of those reported in controlled studies with corticosteroids. In the GAGPS treated group 13 patients reported on local pain after some injections, 2 cases combined with local haematomas, compared with 5 cases of local pain in the placebo group. The results confirm previous good results of GAGPS injection therapy in subchronic and chronic peritendinitis.

摘要

本研究的目的是探讨局部注射硫酸氨基葡聚糖(GAGPS)治疗慢性肱骨外上髁炎的疗效。该研究采用前瞻性、安慰剂对照双盲试验。60例有典型疼痛病史至少3个月的患者,来自斯德哥尔摩的两家私立骨科诊所,接受了50mg GAGPS或安慰剂注射,每周一次,共5周。主要观察指标是患者使用视觉模拟量表对日常活动相关疼痛的评估以及治疗失败的次数。随访期为6个月。疼痛评分(VAS)降低的差异在半年随访时为11.1个百分点,治疗期后2周为20.9个百分点,在临床上效果良好。在6周随访时,GAGPS治疗组的治疗失败次数仅为4例(13%),而安慰剂治疗组为12例(40%)。在半年随访时,接受GAGPS治疗的患者中有5例复发。因此,复发率低于大多数使用皮质类固醇的对照研究报告的复发率。在GAGPS治疗组中,13例患者在几次注射后报告有局部疼痛,2例伴有局部血肿,而安慰剂组有5例局部疼痛。结果证实了先前GAGPS注射疗法在亚慢性和慢性腱鞘炎中的良好效果。

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