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A plaster containing DHEP and heparin for mild to moderate contusions and sprains with haematoma: a double-blind randomized study.

机译:含DHEP和肝素的膏药用于轻度至中度挫伤和血肿扭伤:一项双盲随机研究。

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OBJECTIVE: This prospective, randomized, double-blind, three-arm study was performed to investigate the efficacy of a medicated plaster containing the combination of diclofenac epolamine (DHEP) 180 mg and heparin 5600 IU in the treatment of unilateral blunt soft tissue injuries involving the upper or lower limb, complicated by severe local haematoma. RESEARCH DESIGN AND METHODS: Patients with mild-to-moderate injuries complicated by local haematoma (< or =140 cm(2)) were included and randomly treated once daily with plasters containing DHEP/heparin, DHEP only, or placebo. Plasters were applied for at least 12 hours daily for 10 consecutive days. MAIN OUTCOME MEASURES: The time to complete haematoma dissolution was the primary efficacy endpoint; secondary endpoints were spontaneous pain reduction, pain on movement, muscle swelling and use of rescue analgesia. RESULTS: A total of 185 patients (90 males and 95 females, aged 18-80 years) were evaluated for efficacy. Baseline clinical and demographic characteristics were similar across the treatment groups. The time to complete haematoma dissolution was significantly shorter with the DHEP/heparin plaster compared with both the DHEP and placebo plasters (p < 0.05). Patients in the DHEP/heparin group had a 60% probability of achieving complete haematoma dissolution within the 10-day treatment period compared with patients receiving either DHEP or placebo plasters. Patient-rated reductions in pain on movement were significantly (p < 0.05) greater in the two active treatment groups compared with placebo. Overall, the DHEP/heparin, DHEP and placebo plasters were well-tolerated. While a reliance on patient self-reporting had the potential to limit the usefulness of some data obtained in this study, the investigators accounted for this accordingly. CONCLUSIONS: The plaster formulation combining DHEP and heparin relieves pain and induces faster dissolution of superficial haematomas, and may therefore contribute to a more rapid and complete recovery.
机译:目的:进行这项前瞻性,随机,双盲,三臂研究,以研究含180 mg双氯芬酸依波明(DHEP)和肝素5600 IU的药物组合对单侧钝性软组织损伤的治疗效果上肢或下肢,并发严重的局部血肿。研究设计与方法:纳入轻度至中度损伤并发局部血肿(<或= 140 cm(2))的患者,并每天用含DHEP /肝素,仅DHEP或安慰剂的膏药随机治疗一次。每天连续至少10天每天涂石膏至少12个小时。主要观察指标:完成血肿溶解的时间是主要的疗效终点。次要终点是自发性疼痛减轻,运动疼痛,肌肉肿胀和使用抢救性镇痛。结果:共评估了185例患者的疗效(男90例,女95例,年龄18-80岁)。各治疗组的基线临床和人口统计学特征相似。与DHEP和安慰剂膏药相比,DHEP /肝素膏药使血肿完全溶解的时间明显缩短(p <0.05)。与接受DHEP或安慰剂膏药的患者相比,DHEP /肝素组的患者在10天的治疗期内达到完全血肿溶解的可能性为60%。与安慰剂相比,在两个有效治疗组中,患者评定的运动疼痛减轻明显(p <0.05)。总体而言,DHEP /肝素,DHEP和安慰剂膏药耐受性良好。虽然依赖患者的自我报告可能会限制本研究中获得的某些数据的有用性,但研究者对此做出了相应的解释。结论:DHEP和肝素相结合的膏药可减轻疼痛并促使浅部血肿更快地溶解,因此可能有助于更快,更完全的康复。

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