首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >The efficacy and safety of intra-articular injection of hyaluronic acid in the knee and physical therapy agents to treat Kashin-Beck disease: A prospective interventional study
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The efficacy and safety of intra-articular injection of hyaluronic acid in the knee and physical therapy agents to treat Kashin-Beck disease: A prospective interventional study

机译:膝关节腔内注射透明质酸和物理治疗剂治疗Kashin-Beck疾病的疗效和安全性:前瞻性干预研究

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摘要

The aim of the present study was to determine whether hyaluronic acid (HA) or physical therapy agents (PTA) can improve functional parameters in patients with knee Kashin-Beck disease (KBD). For 2 years, patients (n=55) were treated with HA weekly for 5 weeks, then received 6th and 7th injections on the 3rd and 6th month, respectively, for 7 injections in total. Patients (n=53) were treated with PTA five times a week for 3 weeks every month for 6 months. The patients were evaluated with the Western Ontario and McMaster University Osteoarthritis Index (WOMAC) and the visual analog pain scale (VAS). Trial registration, ChiCTR-TRC-12002189 (). During the study, following treatment interruption, pain increased in the PTA group (from a mean value of 85.7±83.8 mm at month 12 to 145.2±128.8 mm at month 18 and 201.3±150.5 mm at month 24), while it remained stable in the HA group (from a mean value of 80.7±70.6 mm at month 12 to 90.1±95.2 mm at month 18 and 82.6±85.3 mm at month 24), with a statistically significant difference in favor of HA at month 18 (P<0.05) and month 24 (P<0.05). Joint stiffness, physical function and total WOMAC showed the same trend as pain. The global efficacy judgments by the patients and the investigators showed a statistically significant difference in favor of HA at month 18 (P<0.05) and month 24 (P<0.05). In conclusion, although all the patients improved in terms of pain and function, HA was superior to PTA alone for pain relief and lasting effect.
机译:本研究的目的是确定透明质酸(HA)或物理治疗剂(PTA)是否可以改善膝关节Kashin-Beck病(KBD)患者的功能参数。在2年中,n例患者(n = 55)每周接受HA治疗5周,然后在第3和第6个月分别接受第6和第7针注射,总共进行7针注射。患者(n = 53)每周接受5次PTA治疗,每月3周,共6个月。用西安大略省和麦克马斯特大学的骨关节炎指数(WOMAC)和视觉模拟疼痛量表(VAS)对患者进行评估。试用注册,ChiCTR-TRC-12002189()。在研究期间,中断治疗后,PTA组疼痛增加(从第12个月的平均值85.7±83.8 mm升高到第18个月的145.2±128.8 mm和第24个月的201.3±150.5 mm),而在PTA组则保持稳定。 HA组(从第12个月的平均值80.7±70.6 mm到第18个月的平均值90.1±95.2 mm和第24个月的平均值82.6±85.3 mm),在第18个月对HA的支持率有统计学显着性差异(P <0.05 )和第24个月(P <0.05)。关节僵硬,身体机能和总WOMAC表现出与疼痛相同的趋势。患者和研究者的总体疗效判断显示,在第18个月(P <0.05)和第24个月(P <0.05),对HA的偏爱统计学差异有统计学意义。总之,尽管所有患者的疼痛和功能均得到改善,但HA在缓解疼痛和持续效果方面优于单独的PTA。

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