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首页> 外文期刊>The journal of knee surgery >Clinical experience with the effectiveness and tolerability of hylan G-F 20 in 1047 patients with osteoarthritis of the knee.
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Clinical experience with the effectiveness and tolerability of hylan G-F 20 in 1047 patients with osteoarthritis of the knee.

机译:Hylan G-F 20在1047例膝关节骨关节炎患者中的疗效和耐受性的临床经验。

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摘要

This retrospective review evaluates the effectiveness and tolerability of hylan G-F 20 for relief of pain due to knee osteoarthritis in a large orthopedic practice over a 5-year period. Prospectively collected data from patients who initiated intra-articular hylan G-F 20 (3 weekly injections) for osteoarthritis knee pain treatment were analyzed. Efficacy variables included physician visual analogue scale (VAS: 100 mm), and patient rating of pain, mobility, and amount of pain medication taken after treatment. Patients (n=1047; 1489 knees) were an average age of 65.3 years, 60% female, and 71% had radiologic osteoarthritis grade IV. Mean VAS scores significantly improved with hylan G-F 20 compared to baseline at all time points (P<.0001). Most knees (62%-89%) responded positively with hylan G-F 20. Pain and mobility improved and less pain medication was needed after therapy. The incidences of local adverse events were 5.2% per patient and 1.2% per injection; most local adverse events were mild or moderate, with severe local events in 0.3% of injections. Our clinical experience shows that hylan G-F 20 effectively relieves osteoarthritis knee pain (as indicated) and reduces pain medication needed for up to 6 months with a low incidence of local adverse events.
机译:这项回顾性评估评估了Hylan G-F 20在5年的大型整形外科实践中缓解膝部骨关节炎引起的疼痛的有效性和耐受性。分析了从开始进行关节内hylan G-F 20(每周3次注射)治疗骨关节炎膝盖疼痛的患者收集的前瞻性数据。疗效变量包括医师视觉模拟量表(VAS:100毫米)以及患者对疼痛,活动性的评价,以及治疗后服用的止痛药的量。患者(n = 1047; 1489膝)的平均年龄为65.3岁,女性为60%,而放射性放射性骨关节炎为IV级,占71%。与基线相比,hylan G-F 20的平均VAS评分在所有时间点均显着改善(P <.0001)。多数膝关节(62%-89%)对Hylan G-F的反应为阳性。治疗后疼痛和活动性得到改善,所需的止痛药更少。局部不良事件的发生率是每位患者5.2%,每次注射1.2%。大多数局部不良事件为轻度或中度,注射率为0.3%时出现严重的局部事件。我们的临床经验表明,Hylan G-F 20可有效缓解骨关节炎膝盖疼痛(如所示)并减少长达6个月所需的止痛药,且局部不良事件的发生率较低。

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