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首页> 外文期刊>Pain. >A multicenter randomized controlled trial on the efficacy of intradiscal methylene blue injection for chronic discogenic low back pain: the IMBI study
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A multicenter randomized controlled trial on the efficacy of intradiscal methylene blue injection for chronic discogenic low back pain: the IMBI study

机译:关于体内亚甲基蓝注射效果对慢性致畸腰痛的多中心随机对照试验:IMBI研究

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A study published in PAIN in 2010 showed remarkable effects of intradiscal methylene blue (MB) injections compared with placebo on pain intensity in patients with chronic discogenic low back pain (CD-LBP). Both groups received lidocaine hydrochloride injections for pain associated with the procedure. We replicated the design of the previously published study and performed a multicenter, double-blind, randomized, placebo-controlled trial to assess whether the extraordinary effects of MB on pain intensity could be confirmed. The primary outcomes were treatment success defined as at least 30% reduction in pain intensity and the Patients' Global Impression of Change 6 months after the intervention. We included 84 patients with CD-LBP of which 14 (35%) in the MB plus lidocaine group showed treatment success compared with 11 (26.8%) in the control group who received placebo plus lidocaine (P = 0.426). Twenty-seven percent of all participants treated with MB stated that their overall health improved much or very much (Patients' Global Impression of Change), vs 25.6% in the placebo group (P = 0.958). We were unable to confirm that intradiscal MB injections are better capable of significantly reducing pain in patients with CD-LBP 6 months after treatment compared with placebo. We observed that over one-quarter of patients receiving only lidocaine injections reported treatment success, which is in contrast with the previously published study. Our results do not support the recommendation of using intradiscal MB injections for patients with CD-LBP.
机译:在2010年痛苦中发表的一项研究表明,与慢性致畸低腰疼痛(CD-LBP)患者的疼痛强度相比,对体内亚甲基蓝(MB)注射的显着影响。两组均接受Lidocaine盐酸盐注射液,用于与该程序相关的疼痛。我们复制了先前发表的研究的设计,并进行了多中心,双盲,随机,安慰剂对照试验,以评估MB对疼痛强度的非凡效应是否可以得到证实。主要结果是治疗成功定义为疼痛强度降低至少30%,患者在干预后6个月内的变化的全球印象。我们包括84名CD-LBP患者,其中MB Plus Lidocaine组中的14(35%)显示治疗成功与接受安慰剂Plus Lidocaine的对照组(P = 0.426)相比。所有与MB治疗的参与者中的27%表示,它们的整体健康状况越来越多地(患者全球变化印象),安慰剂集团的25.6%(P = 0.958)。我们无法确认,在与安慰剂相比,治疗后6个月后,患有体内MB注射能够更好地减少患有CD-LBP患者的疼痛。我们观察到,超过四分之一的患者只接受利多卡因注射报告的治疗成功,这与先前公布的研究相反。我们的结果不支持使用CD-LBP患者使用脑内MB注射的建议。

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