首页> 美国卫生研究院文献>The Indian Journal of Surgery >A Randomized Controlled Trial to Assess the Efficacy of Arthroscopic Debridement in Combination with Oral Medication Versus Oral Medication in Patients with Gouty Knee Arthritis
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A Randomized Controlled Trial to Assess the Efficacy of Arthroscopic Debridement in Combination with Oral Medication Versus Oral Medication in Patients with Gouty Knee Arthritis

机译:评估膝痛风性关节炎患者关节镜清创术与口服药物与口服药物联合疗效的随机对照试验

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摘要

Gouty knee arthritis refers to a form of inflammatory diseases caused by deposits of needle-like crystals of uric acid in knee joint. The aim of this study was to assess the efficacy and safety of arthroscopic debridement in combination with oral medication versus oral medication alone for the treatment of gouty knee arthritis. A total of 60 patients with gouty knee arthritis were randomized to receive either arthroscopic surgery in combination with oral medication or oral medication alone. Efficacy was assessed with the angle of motion, functions, and visual analog scale (VAS). These indices were measured prior to treatment and at 2, 4, 12, 24, and 48 weeks posttreatment. Surgery- and medication-related complications were observed. Significant differences in flexion and extension of the knee joint, lymphoma scores, and VAS were detected between the two groups at 2, 4, and 12 weeks posttreatment (P < 0.05) but not at weeks 24 and 48 posttreatment (P > 0.05) . Significant differences in these indices were detected at different time points in each group (P < 0.05), except between weeks 24 and 48 (P > 0.05). Arthroscopic surgery in combination with oral medication is superior to single oral medication in the flexion and extension of the knee joint, lymphoma scores, and pain relief (VAS) before 24 weeks, although no statistical differences were detected in the efficacy after 24 weeks, and in medication-related safety between the two groups. Although arthroscopic debridement cannot replace systemic uric acid-lowering treatments such as medication and dietary control, it is still an effective approach.
机译:痛风性膝关节炎是指由尿酸的针状晶体沉积在膝关节引起的一种炎症性疾病。这项研究的目的是评估关节镜清创术联合口服药物与单独口服药物治疗痛风性膝关节炎的疗效和安全性。总共60例痛风性膝关节炎患者被随机分配接受联合口服药物或单独口服药物的关节镜手术。通过运动角度,功能和视觉模拟量表(VAS)评估疗效。这些指数是在治疗前和治疗后2、4、12、24和48周测量的。观察到与手术和药物相关的并发症。两组在治疗后第2、4和12周发现膝关节屈伸,淋巴瘤评分和VAS有显着差异(P <)0.05),但在治疗后第24和48周未见差异(P> 0.05)。除第24周和第48周之间(P(> 0.05)外,各组在不同时间点均检测到这些指标的显着差异(P <0.05)。关节镜手术联合口服药物在24周之前的膝关节屈伸,膝关节淋巴瘤评分和疼痛缓解(VAS)方面优于单一口服药物,尽管24周后的疗效没有统计学差异,并且两组之间与药物相关的安全性。尽管关节镜下清创术不能替代药物和饮食控制等全身性降低尿酸的疗法,但这仍然是一种有效的方法。

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