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Effect of transcutaneous electrical nerve stimulation therapy for the treatment of primary dysmenorrheal

机译:经皮神经电刺激疗法治疗原发性痛经的效果

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摘要

Background: This study aimed to investigate the effect and safety of transcutaneous electrical nerve stimulation (TENS) therapy for relieving pain in women with primary dysmenorrhea (PD). Methods: In this study, 134 participants with PD were randomly divided into the intervention group and the sham group, with 67 participants in each group. Participants in the intervention group received TENS, whereas those in the sham group received sham TENS. The primary outcome was measured by the Numeric Rating Scale (NRS). The secondary outcomes were measured by the duration of relief from dysmenorrheal pain, number of ibuprofen tablets taken, and the World Health Organization quality of life (WHOQOL)-BREF score, as well as the adverse events. Results: A total of 122 participants completed the study. Compared to sham TENS, TENS showed a greater effect in pain relief with regard to the NRS ( P < .01), duration of relief from dysmenorrheal pain ( P < .01), and number of ibuprofen tablets taken ( P < .01). However, no significant differences in the quality of life, measured by the WHOQOL-BREF score, were found between 2 groups. The adverse event profiles were also similar between 2 groups. Conclusion: TENS was efficacious and safe in relieving pain in participants with PD.
机译:背景:本研究旨在探讨经皮神经电刺激(TENS)治疗减轻原发性痛经(PD)妇女疼痛的效果和安全性。方法:本研究将134名PD患者随机分为干预组和假手术组,每组67名。干预组的参与者接受了TENS,而假手术组的参与者接受了TENS。主要结果通过数字评分量表(NRS)进行衡量。次要结果由痛经缓解的持续时间,服用布洛芬片的数量,世界卫生组织的生活质量(WHOQOL)-BREF评分以及不良事件来衡量。结果:共有122位参与者完成了研究。与假TENS相比,TENS对NRS的疼痛缓解效果更好(P <.01),痛经疼痛缓解的持续时间(P <.01)和布洛芬片的服用量(P <.01) 。然而,两组之间的生活质量没有明显差异(通过WHOQOL-BREF评分衡量)。两组之间的不良事件特征也相似。结论:TENS可以有效减轻PD参与者的疼痛。

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