首页> 外文期刊>The journal of knee surgery >Comparison of Efficacy and Tolerability of HylanG-F 20 in Patients with and without Effusions atthe Time of Initial Injection
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Comparison of Efficacy and Tolerability of HylanG-F 20 in Patients with and without Effusions atthe Time of Initial Injection

机译:初次注射时有无积液的HylanG-F 20疗效和耐受性比较

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An effusion at the onset of viscosupplementation has been thought to diminish the efficacyand increase adverse event rates. This study compares efficacy of hylan G-F 20 in patientswith and without an effusion. Patients with knee osteoarthritis (OA) received three weeklyinjections of hylan G-F 20. A total of 50 patients with an effusion requiring aspiration werecompared with 50 matched patients without an effusion. Outcome measurementsincluded Western Ontario and McMaster's Universities Osteoarthritis index (WOMAC)and visual analog scale (VAS). Patients were followed for 26 weeks. Both effusion andcontrol group VAS was significantly lowered at all time points. WOMAC scores improved(p < 0.025) at all visits in the effusion group except for WOMAC A-1 week 14. ControlWOMAC scores also significantly improved at all visits (p < 0.027), except for full WOMACand WOMAC A-1 at week 1. Neither group experienced an adverse event. Presence of aneffusion at onset of viscosupplementation requiring aspiration does not negatively impactefficacy of hylan G-F 20 or increase adverse event rates.
机译:粘液补充开始时的积液被认为会降低疗效并增加不良事件发生率。这项研究比较了hylan G-F 20在有或没有积液的患者中的疗效。膝骨性关节炎(OA)患者每周接受3次hylan G-F 20注射。将50例需要抽吸的积液患者与50例无积液的匹配患者进行比较。结果测量包括安大略省西部和麦克马斯特大学的骨关节炎指数(WOMAC)和视觉模拟量表(VAS)。随访患者26周。在所有时间点,渗出液和对照组的VAS均显着降低。除WOMAC A-1第14周外,积液组中所有访视的WOMAC得分均得到改善(p <0.025),除第1周时的WOMAC和WOMAC A-1完全得分外,对照WOMAC得分在所有访视中均得到了显着改善(p <0.027)。两组均未发生不良事件。需要抽吸的粘液补充开始时出现血流并不会负面影响Hylan G-F 20的疗效或增加不良事件发生率。

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