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Clinical effectiveness and dose response of image-guided intra-articular corticosteroid injection for hip osteoarthritis.

机译:图像引导关节内注射皮质类固醇激素治疗髋骨关节炎的临床疗效和剂量反应。

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OBJECTIVES: To assess symptomatic change after intra-articular corticosteroid (IAST) injection at 2 doses in hip osteoarthritis (OA), and to examine dose response and predictors of response. METHODS: Patients with hip OA (90 women and 30 men and median age 64 yrs) referred for IAST fluoroscopic injection were included in this longitudinal, clinical trial. WOMAC scores, body mass index (BMI), conventional radiographic grade (Kellgren and Lawrence scoring) and ultrasound measures (including capsular thickness and osteophyte assessments) were recorded at baseline. In the first phase of the study, 75 patients were injected with 40 mg methylprednisolone; another 45 patients were injected with 80 mg in the second phase. Change in WOMAC scores from baseline to weeks 6 and 12 were calculated for each dose and then dose comparisons were made. Clinical responders (>15% reduction in baseline pain score) were identified in order to establish predictors of response. RESULTS: For the 40 mg dose, there was a statistically significant improvement in pain (P < 0.001) and stiffness (P < 0.001) but not disability at week 6, and only the improvement in stiffness at week 12 was maintained (P = 0.041). For the 80 mg dose, there was significant improvement in pain (P < 0.001), stiffness (P < 0.001) and disability (P < 0.001) at week 6, which was maintained for all domains at week 12 (P = 0.002; P = 0.001; P < 0.001). When the doses were compared, the 80 mg dose demonstrated a significant improvement compared with the 40 mg group for stiffness at week 12 (P = 0.026) and disability at both weeks 6 and 12 (P = 0.026; P = 0.004). Imaging findings did not relate to severity of symptoms or response to IAST. CONCLUSIONS: In these two hip OA cohorts, both the 40 mg and 80 mg IAST doses had a beneficial effect at week 6, while the 80 mg dose maintained this improvement at week 12. Comparison of the two dose groups provided some evidence of a dose response. Randomized controlled trials of IAST for hip OA are now required.
机译:目的:评估髋骨关节炎(OA)中2剂关节内注射皮质类固醇(IAST)后的症状变化,并检查剂量反应和反应预测因子。方法:这项纵向临床试验包括接受IAST荧光镜检查转诊的髋骨OA患者(90名女性和30名男性,中位年龄64岁)。在基线记录WOMAC评分,体重指数(BMI),常规放射线照相成绩(Kellgren和Lawrence评分)和超声测量(包括包膜厚度和骨赘评估)。在研究的第一阶段,有75名患者注射了40 mg甲基强的松龙;在第二阶段,另外45名患者注射了80 mg。计算每个剂量从基线到第6周和第12周的WOMAC得分变化,然后进行剂量比较。确定临床反应者(基线疼痛评分降低> 15%),以建立反应的预测因子。结果:对于40 mg剂量,疼痛(P <0.001)和僵硬(P <0.001)有统计学上的显着改善,但第6周无残疾,只有第12周的僵硬得以保持(P = 0.041) )。对于80 mg剂量,第6周的疼痛(P <0.001),僵硬(P <0.001)和致残性(P <0.001)有显着改善,第12周的所有领域均得到改善(P = 0.002; P = 0.001; P <0.001)。当比较剂量时,与40 mg组相比,80 mg剂量组在第12周的刚度(P = 0.026)和第6周和第12周的残疾(P = 0.026; P = 0.004)方面有显着改善。影像学发现与症状的严重程度或对IAST的反应无关。结论:在这两个髋关节OA队列中,分别在第6周使用40 mg和80 mg IAST剂量均具有有益效果,而在第12周使用80 mg剂量的IAST则保持了这种改善。两个剂量组的比较提供了某种剂量的证据。响应。现在需要IAST治疗髋骨关节炎的随机对照试验。

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