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Prolotherapy Injections, Saline Injections, and Exercises for Chronic Low-Back Pain: A Randomized Trial.

机译:Prolotherapy注射液,盐水注射液和慢性腰背痛锻炼方法:随机试验。

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SUMMARY: OBJECTIVES To assess the efficacy of a prolotherapy injection and exercise protocol in the treatment of chronic nonspecific low back pain.DESIGN Randomized controlled trial with two-by-two factorial design, triple-blinded for injection status, and single-blinded for exercise status.SETTING General practice.PARTICIPANTS One hundred ten participants with nonspecific low-back pain of average 14 years duration were randomized to have repeated prolotherapy (20% glucose/0.2% lignocaine) or normal saline injections into tender lumbo-pelvic ligaments and randomized to perform either flexion/extension exercises or normal activity over 6 months.MAIN OUTCOME MEASURES Pain intensity (VAS) and disability scores (Roland-Morris) at 2.5, 4, 6, 12, and 24 months.RESULTS Follow-up was achieved in 96% at 12 months and 80% at 2 years. Ligament injections, with exercises and with normal activity, resulted in significant and sustained reductions in pain and disability throughout the trial, but no attributable effect was found for prolotherapy injections over saline injections or for exercises over normal activity. At 12 months, the proportions achieving more than 50% reduction in pain from baseline by injection group were glucose-lignocaine: 0.46 versus saline: 0.36. By activity group these proportions were exercise: 0.41 versus normal activity: 0.39. Corresponding proportions for >50% reduction in disability were glucose-lignocaine: 0.42 versus saline 0.36 and exercise: 0.36 versus normal activity: 0.38. There were no between group differences in any of the above measures.CONCLUSIONS In chronic nonspecific low-back pain, significant and sustained reductions in pain and disability occur with ligament injections, irrespective of the solution injected or the concurrent use of exercises.
机译:摘要:目的评估前言疗法和运动疗法在治疗慢性非特异性下腰痛中的疗效.DESIGN随机对照试验采用二乘二因子设计,注射方式为三盲,运动方式为单盲状况一般患者。一百一十名平均时间为14年的非特异性腰背痛参与者被随机分配至反复进行腰部骨盆韧带韧带注射(20%葡萄糖/0.2%利多卡因)或生理盐水注射,随机分配至主要的观察指标:在2.5、4、6、12和24个月时进行疼痛/伸展运动或正常活动超过6个月的疼痛强度(VAS)和残疾评分(Roland-Morris).96例患者进行了随访在12个月时为%,在2年时为80%。在整个试验过程中,进行运动并具有正常活动的韧带注射可显着且持续地减轻疼痛和残疾,但未发现因盐疗法或生理活动超出正常水平而进行的前路疗法注射。在第12个月时,注射组的疼痛比基线减轻50%以上的比例为葡萄糖-木酚卡因:0.46,而盐水:0.36。按活动组,这些比例是运动:0.41 vs正常活动:0.39。残疾减少> 50%的相应比例是葡萄糖-木酚卡因:0.42对盐水0.36;运动:0.36对正常活动:0.38。结论上述任何一种措施在组间均无差异。结论在慢性非特异性下腰痛中,韧带注射可显着且持续地减轻疼痛和致残性,而与注射溶液或同时进行运动无关。

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