The efficacy and safety of low-intensity extracorporeal shock wave treatment combined with or without medications in Chronic prostatitis/chronic pelvic pain syndrome: a systematic review and meta-analysis

被引:6
|
作者
Kong, Xiangbin [1 ]
Hu, Weiwei [2 ]
Dong, Zhilong [1 ]
Tian, Junqiang [1 ]
Wang, Yuhan [1 ]
Jin, Chen [3 ]
Liang, Chaozhao [3 ]
Hao, Zongyao [3 ]
Wang, Zhiping [1 ]
机构
[1] Lanzhou Univ, Res Inst Urol, Key Lab Gansu Prov Urol Dis, Clin Ctr Gansu Prov Urol Dis,Hosp 2, Lanzhou, Gansu, Peoples R China
[2] Lanzhou Univ, Dept Nephrol, Hosp 2, Lanzhou, Gansu, Peoples R China
[3] Anhui Med Univ, Dept Urol, Affiliated Hosp 1, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
DOUBLE-BLIND; THERAPY; SYMPTOMS; IMPACT;
D O I
10.1038/s41391-022-00571-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background We performed this systematic review and meta-analysis to investigate the efficacy and safety of Li-ESWT combined with or without medications for patients with Chronic prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS). Methods A comprehensive search was conducted of PUBMED, Cochrane Library, and Web of Science databases from inception to February 2022 for randomized controlled trials (RCTs) assessing the efficacy and safety of Li-ESWT with or without the combination of medications compared with the control group. The National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI), Visual Analogue Scale/Score (VAS), International Index of Erectile Function (IIEF), and International prostate symptom score (IPSS) were used to assess the improvements of symptoms in CP/CPPS patients. Results 651 patients from 12 randomized controlled studies were included in this study. The total NIH-CPSI scores, pain domain scores, and quality of life (QOL) scores were significantly lower in the Li-ESWT group than those in the control group at the termination of treatment, and 1, 4, 12, and 24 weeks after treatment. And these scores were significantly reduced in the Li-ESWT group than in baselines. In the subgroup analysis, reductions of these scores lasted longer and were greater in Li-ESWT combined with medications than in Li-ESWT alone. In the Li-ESWT group, the VAS score; IIEF score; and IPSS score were significant improvements than those in control group at the termination of treatment, and 1, 4, and 12 weeks after treatment; 4, 12, and 24 weeks after treatment; and 1, 4, and 12 weeks after treatment, respectively. Conclusions Li-ESWT is a safe, non-invasive, and effective option for patients with CP/CPPS, whether combined with medications or not, should be recommended for widespread use in clinical practice.
引用
收藏
页码:483 / 494
页数:12
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