甘露醇热稳定ha配合物治疗膝关节病

M. N. Ryabova, A. Seleznev, I. A. Fokin, D. R. Shodiyev, M. N. Dmitriyeva
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MATERIALS AND METHODS: From September 2020 to April 2022 at settings of the orthopedic department of Ryazan Regional Clinical Hospital, an open prospective non-comparative study of the effectiveness and safety of Hyapro sterile biopolymer synovial fluid prosthesis at a concentration of 1.5% — 2 ml in 30 patients with 2 to 3 stage gonarthrosis according to Kellgren–Lawrence scale was carried out. Prior to the treatment, and also 3 and 6 months after, the severity of clinical symptoms on VAS, WOMAC, Leken scales, the quality of life according to SF-36 questionnaire were registered; the biochemical markers namely cartilaginous oligomatrix peptide (COMP), metal matrix proteinase 3 (MMR 3) were determined with the use of StatFax enzyme-linked plate analyzer (Awareness Technology, USA). RESULTS: In general, the studied drug was well tolerated by patients: there were no typical for intra-articular injections cases of clinically important adverse reactions like prolonged pain at the injection site, expansion-like sensation, an elevation of local temperature, and changes in the color of skin or changes of the shape of the knee joint. Just transient local tenderness in 6.7% of injection cases was noted. We revealed a statistically significant decrease in serum MMR-3 levels by 6 months of follow-up, which reflects a reduction of the inflammatory component in osteoarthritis of the joint studied. Besides, a gradual increase in COMP levels by the 6th month of the study was found, which may be an evidence of activation of the protein after the course of treatment to replenish the cartilage matrix. The results on VAS, WOMAC scales, and Leken algofunctional index demonstrated similar positive dynamics: a statistically reliable decrease in such parameters as pain, stiffness, and impaired functioning by the 3rd month of follow-up compared with the initial level; this trend was remaining in 6 months. After 3 months of treatment, there was a reliable improvement of the quality of life on the subscale of the physical component of health compared with the initial level, which persisted until the end of the study. On the subscale of the psychological component of health, no changes were found during the period. 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引用次数: 0

摘要

简介:透明质酸(HA)是一种天然糖胺聚糖,是关节软骨基质和滑膜液的组成部分,其独特的流变特性在关节病中丧失,导致滑膜粘弹性特性降低和软骨破坏。目的:评价Hyapro无菌生物聚合物滑膜液假体在一次性注射器内注射1.5% ~ 2ml用于关节内注射治疗膝关节病的有效性和安全性。材料与方法:于2020年9月至2022年4月,在梁赞地区临床医院骨科设置,对30例2 ~ 3期关节病患者采用浓度为1.5% ~ 2ml的Hyapro无菌生物聚合物滑膜液假体进行开放性前瞻性非比较研究。分别于治疗前、治疗后3、6个月对患者进行VAS、WOMAC、Leken量表的临床症状严重程度及SF-36问卷生活质量评分;生化指标为软骨寡基质肽(COMP)、金属基质蛋白酶3 (mmr3),采用StatFax酶联平板分析仪(Awareness Technology, USA)测定。结果:总体而言,患者对所研究药物的耐受性良好,关节内注射未出现典型的注射部位持续疼痛、扩张样感觉、局部温度升高、皮肤颜色改变或膝关节形状改变等临床重要不良反应。6.7%的注射病例仅出现短暂性局部压痛。我们发现,随访6个月后,血清MMR-3水平有统计学意义上的显著下降,这反映了所研究的关节骨关节炎炎症成分的减少。此外,在研究的第6个月,发现COMP水平逐渐增加,这可能是治疗过程后蛋白质激活以补充软骨基质的证据。VAS、WOMAC量表和Leken算法功能指数的结果显示出类似的积极动态:与初始水平相比,随访第3个月时,疼痛、僵硬和功能受损等参数在统计学上可靠地减少;这一趋势持续了6个月。治疗3个月后,与最初的水平相比,在健康的身体组成部分的亚量表上,生活质量有了可靠的改善,这种改善一直持续到研究结束。在健康心理成分的子量表上,在此期间没有发现任何变化。结论:在透明质酸和甘露醇热稳定的基础上使用Hyapro生物聚合物滑膜液假体,在症状性关节病的中期,可以安全有效地减轻疼痛和炎症反应,通过恢复滑膜液的粘弹性和保护特性改善患关节的功能,至少持续6个月,提高患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HA-Complexes Thermally–Stabilized with Mannitol in Treatment of Gonarthrosis
INTRODUCTION: Hyaluronic acid (HA) is a natural glycosaminoglycan which is an integral component of both the matrix of articular cartilage and synovial fluid with its unique rheological properties that are lost in gonarthrosis, which leads to a decrease of viscoelastic characteristics of the synovia and destruction of the cartilage. AIM: To evaluate the effectiveness and safety of the use of Hyapro sterile biopolymer synovial fluid prosthesis in a disposable syringe for intra-articular injection at a concentration of 1.5% — 2 ml in treatment of gonarthrosis. MATERIALS AND METHODS: From September 2020 to April 2022 at settings of the orthopedic department of Ryazan Regional Clinical Hospital, an open prospective non-comparative study of the effectiveness and safety of Hyapro sterile biopolymer synovial fluid prosthesis at a concentration of 1.5% — 2 ml in 30 patients with 2 to 3 stage gonarthrosis according to Kellgren–Lawrence scale was carried out. Prior to the treatment, and also 3 and 6 months after, the severity of clinical symptoms on VAS, WOMAC, Leken scales, the quality of life according to SF-36 questionnaire were registered; the biochemical markers namely cartilaginous oligomatrix peptide (COMP), metal matrix proteinase 3 (MMR 3) were determined with the use of StatFax enzyme-linked plate analyzer (Awareness Technology, USA). RESULTS: In general, the studied drug was well tolerated by patients: there were no typical for intra-articular injections cases of clinically important adverse reactions like prolonged pain at the injection site, expansion-like sensation, an elevation of local temperature, and changes in the color of skin or changes of the shape of the knee joint. Just transient local tenderness in 6.7% of injection cases was noted. We revealed a statistically significant decrease in serum MMR-3 levels by 6 months of follow-up, which reflects a reduction of the inflammatory component in osteoarthritis of the joint studied. Besides, a gradual increase in COMP levels by the 6th month of the study was found, which may be an evidence of activation of the protein after the course of treatment to replenish the cartilage matrix. The results on VAS, WOMAC scales, and Leken algofunctional index demonstrated similar positive dynamics: a statistically reliable decrease in such parameters as pain, stiffness, and impaired functioning by the 3rd month of follow-up compared with the initial level; this trend was remaining in 6 months. After 3 months of treatment, there was a reliable improvement of the quality of life on the subscale of the physical component of health compared with the initial level, which persisted until the end of the study. On the subscale of the psychological component of health, no changes were found during the period. CONCLUSION: The course use of Hyapro biopolymer synovial fluid prosthesis on the basis of hyaluronic acid thermally stabilized with mannitol, in symptomatic gonarthrosis of intermediate stages, permits safely and effectively reduce pain and the inflammatory response, improve the function of the affected joint through restoration of viscoelastic and protective properties of synovial fluid for up to at least 6 months, improving the quality of life of patients.
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