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Hyaluronic acid injections for osteoarthritis of the knee: predictors of successful treatment

机译:透明质酸注射膝关节骨关节炎:成功治疗的预测因子

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Abstract Purpose This study aimed to identify patient and treatment factors that predict a favourable response to intra-articular hyaluronic acid (HA) treatment to better guide patient and treatment selection. Methods This prospective, observational study evaluated patients with mild-to-moderate (Kellgren–Lawrence grades 1–3) primary knee osteoarthritis treated between March 2013 and May 2016. Patient function and pain scores were assessed by the Western Ontario and McMaster Universities Arthritis Index/Knee Injury and Osteoarthritis Outcome Score (WOMAC/KOOS) and visual analogue scale (VAS) surveys, with response to treatment defined according to the Osteoarthritis Research Society International (OARSI) 2004 criteria. Surveys were completed at each injection and three?months post-treatment. Patients were followed an average of 27?months. Results Of 102 patients, 57% had a positive response. Those at least twice as likely to respond were patients with grades 1–2 osteoarthritis or a positive response to the first injection and those who were ≥60?years. Gender, race, body mass index (BMI), smoking status, HA brand, and initial VAS and WOMAC/KOOS scores were not significant predictors of success. Mean time to arthroplasty following injection series was 11?months (30% of nonresponders, 12% of responders). The VAS strongly correlated with KOOS pain scores and successful outcomes. Conclusion Patients with mild-to-moderate osteoarthritis (grades 1–2) and those responding positively to the first injection were twice as likely to respond positively to the injection series, as were patients ≥60?years. Patients who did not respond positively were more likely to proceed to arthroplasty. The VAS appears to be a reliable method of defining and monitoring treatment success. Judicious patient selection and counseling may improve outcomes associated with intra-articular HA injections.
机译:摘要目的本研究旨在鉴定预测对关节内透明质酸(HA)处理的患者和治疗因素,以更好地指导患者和治疗选择。方法评估2013年3月至2016年3月间患有轻度至中度(Kellgren-Lawrence年级1-3)初级膝关节骨关节炎的患者的患者。由西部的安大略省和麦克马斯特大学关节炎指数评估患者功能和疼痛评分/膝盖损伤和骨关节炎结果评分(Womac / Koos)和视觉模拟量表(VAS)调查,响应根据骨关节炎研究协会国际(OARSI)2004标准定义的治疗。调查在每次注射时完成,并治疗后三个月。患者平均遵循27个月。结果102例患者,57%患阳性反应。那些至少两次反应的患者是1-2°骨关节炎患者或对第一次注射的积极反应以及≥60的患者。性别,种族,体重指数(BMI),吸烟地​​位,HA品牌和最初的VAS和WOMAC / KOOS分数并不重要的成功预测因素。注射系列后关节成形术的平均时间为11?月(30%的无回复者,12%的响应者)。 VAS与KOOS疼痛评分和成功的结果强烈相关。结论患有轻度至中度骨关节炎(等级1-2)的患者及其对第一次注射的响应的患者对注射系列响应的可能性是响应的两倍,≥60岁患者≥60岁。没有积极反应的患者更有可能进行关节成形术。 VAS似乎是定义和监测治疗成功的可靠方法。明智的患者选择和咨询可以改善与关节内注射内部注射相关的结果。

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