创新链/学科链/研发链/产业链

新药研发前沿动态 / 医药领域趋势进展

益气活血温肾利水方联合穴位敷贴对良性前列腺增生术后尿潴留的治疗效果研究

Effect of Yiqi Huoxue Wenshen Lishui Formula Combined with Acupoint Application on Postoperative Urinary Retention in Patients with Benign Prostatic Hyperplasia

  • 摘要: 目的 探讨益气活血温肾利水方联合穴位敷贴对良性前列腺增生术后尿潴留的疗效。方法 按照随机数字表法将2022年6月至2023年7月丽水市中心医院收治的200例良性前列腺增生术后尿潴留患者分为对照组(n=100,接受穴位敷贴治疗)与观察组(n=100,接受益气活血温肾利水方联合穴位敷贴治疗)。对比2组的临床效果。结果 治疗7 d后,观察组的临床总有效率高于对照组(P < 0.05);治疗3 d、7 d后,观察组的最大尿流率高于对照组,残余尿量、各单项症状评分、国际前列腺症状评分(International Prostate Symptom Score,IPSS)低于对照组(P < 0.05),组间效应、时间效应,以及时间和组间交互作用均显著(P < 0.05);2组不良反应发生率无显著差异(P > 0.05)。结论 益气活血温肾利水方联合穴位敷贴治疗良性前列腺增生术后尿潴留疗效显著,安全性良好。

     

    Abstract: Objective To investigate the efficacy of the Yiqi Huoxue Wenshen Lishui Formula combined with acupoint application in treating postoperative urinary retention in patients with benign prostatic hyperplasia (BPH). Methods According to the random number table method, 200 BPH patients with postoperative urinary retention in Lishui City Central Hospital from June 2022 to July 2023 were divided into a control group (n = 100, receiving acupoint application) and an intervention group (n = 100, receiving Yiqi Huoxue Wenshen Lishui Formula combined with acupoint application). The clinical outcomes of the two groups were compared. Results After 7 days of treatment, the total clinical effectiveness rate of the intervention group was higher than that of the control group (P < 0.05). After 3 and 7 days of treatment, the maximum urinary flow rate in the intervention group was higher than that in the control group, while the residual urine volume, symptom-specific scores, and the International Prostate Symptom Score (IPSS) were lower than those in the control group (P < 0.05). Significant between-group, time, and time-by-group interaction effects were observed (P < 0.05). There was no significant difference in the incidence of adverse reactions between the two groups (P > 0.05). Conclusion Yiqi Huoxue Wenshen Lishui Formula combined with acupoint application demonstrates significant efficacy and clinical safety in the treatment of postoperative urinary retention in BPH patients.

     

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