Efficacy of acupuncture on drinkers with chronic prostatitis / chronic pelvic pain syndrome: secondary analysis of a randomized clinical trial

医学 慢性前列腺炎/慢性盆腔疼痛综合征 针灸科 前列腺炎 随机对照试验 盆腔疼痛 慢性疼痛 物理疗法 临床试验 替代医学 内科学 外科 前列腺 病理 癌症
作者
Lili Zhu,Yuanjie Sun,Shiyan Yan,Xiaoxu Liu,Xinlu Wang,Zhishun Liu
出处
期刊:Acupuncture in Medicine [SAGE Publishing]
卷期号:42 (5): 243-250
标识
DOI:10.1177/09645284241274158
摘要

Objective: To evaluate the efficacy of acupuncture in drinkers with chronic prostatitis / chronic pelvic pain syndrome (CP/CPPS). Methods: We conducted a secondary analysis of a randomized controlled trial across multiple centers, involving 224 drinkers. Patients received either acupuncture or sham acupuncture treatment. The primary outcome was the proportion of responders, defined as participants who had a reduction of 6 points or more from baseline in the National Institute of Health—Chronic Prostatitis Symptom Index (NIH-CPSI) total score at weeks 8 and 32. Secondary outcomes measures included the Global Response Assessment (GRA), International Prostate Symptom Score (IPSS) and International Index of Erectile Function 5 (IIEF-5). Results: One hundred and twelve drinkers were included in each group (n = 224 in total). The proportion of responders in terms of NIH-CPSI was 58.9% versus 40.3% in the acupuncture group (AG) and sham acupuncture group (SAG), respectively, with a statistically significant difference of 18.6% ( p = 0.002) at week 8. Higher proportions of responders with respect to NIH-CPSI ( p < 0.001 at week 32) and GRA ( p < 0.001 at week 8 and p = 0.01 at week 32) were observed in the AG compared with the SAG. No between-group differences were found in the changes in IPSS at any assessment time point. Changes in IIEF-5 score were significantly higher in the AG than in the SAG at weeks 20 and 32, while the difference was not statistically significant at week 8. Conclusion: Acupuncture appeared to alleviate the symptoms of pain among drinkers with CP/CPPS and improve their quality of life, but had no demonstrable effect on urinary tract symptoms or erectile function among these patients. Trial registration number: NCT03213938 (ClinicalTrials.gov)
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