A pilot study of the effect of diclofenac with B vitamins for the treatment of acute pain following lower-limb fracture and surgery.

Alexis F Garza, Raúl Monroy-Maya, Marisela Soto-Ríos, Gerardo Reyes-García, Lourdes Carrillo-Alarcón, Héctor Ponce-Monter, Eduardo Rangel-Flores, Mario I Ortiz
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Abstract

The aim of this pilot study was to compare the efficacy and tolerability of the non-steroidal anti-inflammatory drug (NSAID), diclofenac (2-(2,6-dichloranilino) phenylacetic acid), for treatment of acute pain originated by lower-limb fracture and surgery, with that of diclofenac plus B vitamins. This clinical trial was single-center, prospective randomized and double-blinded. After giving informed consent, patients with lower-limb closed fractures rated their pain on a 10-cm visual analog scale (VAS). Patients were then randomized to receive 75 mg diclofenac or 75 mg diclofenac plus B vitamins (thiamine, pyridoxine and cyanocobalamin) twice daily (all intramuscularly). Patient evaluations of pain intensity were recorded throughout two periods: twenty-four hours pre-surgically and twenty-four hours postsurgical. Twenty-four hours after the first drug administration, patients underwent elective lower-limb surgery. Standardized general anesthetic techniques were used for all patients. Fourteen patients completed the study. The subjects' assessments of limb pain on the visual analog scale showed a significant reduction from baseline values regardless of the treatment group when surveyed at 12, 24, 36 and 48 hr post operation. All treatments showed a similar profile in pain reduction. There were reports of pain in the administration site, but in general, all the regimens were well tolerated.

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双氯芬酸联合B族维生素治疗下肢骨折和手术后急性疼痛的初步研究。
本初步研究的目的是比较非甾体抗炎药(NSAID)双氯芬酸(2-(2,6-二氯苯胺)苯乙酸)与双氯芬酸加B族维生素治疗下肢骨折和手术引起的急性疼痛的疗效和耐受性。该临床试验为单中心、前瞻性、随机、双盲。在给予知情同意后,下肢闭合性骨折患者在10厘米视觉模拟量表(VAS)上对疼痛进行评分。然后,患者随机接受75 mg双氯芬酸或75 mg双氯芬酸加B族维生素(硫胺素、吡哆醇和氰钴胺素),每日两次(均为肌肉注射)。在术前24小时和术后24小时记录患者的疼痛强度评估。第一次给药24小时后,患者接受选择性下肢手术。所有患者均采用标准化全麻技术。14名患者完成了这项研究。在术后12、24、36和48小时进行调查时,受试者在视觉模拟量表上的肢体疼痛评估显示,与基线值相比,无论治疗组如何,受试者的肢体疼痛评估都有显著降低。所有的治疗方法在减轻疼痛方面都有相似的效果。在给药部位有疼痛的报告,但总的来说,所有的方案都是耐受性良好的。
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