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Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic Pelvic Pain Syndrome: A Nonrandomized Controlled Trial
This study aims to determine the effect of radial extracorporeal shock wave therapy (rESWT) versus drug when treating chronic pelvic pain syndrome (CPPS; type III B chronic prostatitis). The study included 45 participants with CPPS, divided into two groups: Group I comprised 25 participants, who wer...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775558/ https://www.ncbi.nlm.nih.gov/pubmed/30486723 http://dx.doi.org/10.1177/1557988318814663 |
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author | Zhang, Zhao-Xuan Zhang, Dai Yu, Xiao-Tong Ma, Yue-Wen |
author_facet | Zhang, Zhao-Xuan Zhang, Dai Yu, Xiao-Tong Ma, Yue-Wen |
author_sort | Zhang, Zhao-Xuan |
collection | PubMed |
description | This study aims to determine the effect of radial extracorporeal shock wave therapy (rESWT) versus drug when treating chronic pelvic pain syndrome (CPPS; type III B chronic prostatitis). The study included 45 participants with CPPS, divided into two groups: Group I comprised 25 participants, who were treated with rESWT (3,000 pulses each; pressure: 1.8–2.0 bar; frequency: 10 Hz) once a week; Group II consisted of 20 participants who received a combination of an α-blocker and an anti-inflammatory agent. Participants were treated for 8 weeks. The assessments were done before treatment, after the fourth and eighth rESWT, and 3 months after the end of treatment by Visual Analogue Scale (VAS) for pain, National Institutes of Health-developed Chronic Prostatitis Symptom Index (NIH-CPSI), International Prostate Symptom Score (IPSS), quality of life (QoL), and International Index of Erectile Function-5 (IIEF-5). Both groups of participants showed statistically significant improvement in all the assessments (p < .001) after the treatment, with significantly better results in Group I in NIH-CPSI (p < .001). The recurrence rate of symptoms in Group I at 3 months after end of treatment was much lower than that in Group II (4% vs. 50%, p < .001). This prospectively nonrandomized, control study revealed perineal rESWT as a new therapy option for CPPS with statistically significant effects in comparison to drugs at least for 3 months after cessation of treatment. |
format | Online Article Text |
id | pubmed-6775558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67755582019-10-16 Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic Pelvic Pain Syndrome: A Nonrandomized Controlled Trial Zhang, Zhao-Xuan Zhang, Dai Yu, Xiao-Tong Ma, Yue-Wen Am J Mens Health Original Article This study aims to determine the effect of radial extracorporeal shock wave therapy (rESWT) versus drug when treating chronic pelvic pain syndrome (CPPS; type III B chronic prostatitis). The study included 45 participants with CPPS, divided into two groups: Group I comprised 25 participants, who were treated with rESWT (3,000 pulses each; pressure: 1.8–2.0 bar; frequency: 10 Hz) once a week; Group II consisted of 20 participants who received a combination of an α-blocker and an anti-inflammatory agent. Participants were treated for 8 weeks. The assessments were done before treatment, after the fourth and eighth rESWT, and 3 months after the end of treatment by Visual Analogue Scale (VAS) for pain, National Institutes of Health-developed Chronic Prostatitis Symptom Index (NIH-CPSI), International Prostate Symptom Score (IPSS), quality of life (QoL), and International Index of Erectile Function-5 (IIEF-5). Both groups of participants showed statistically significant improvement in all the assessments (p < .001) after the treatment, with significantly better results in Group I in NIH-CPSI (p < .001). The recurrence rate of symptoms in Group I at 3 months after end of treatment was much lower than that in Group II (4% vs. 50%, p < .001). This prospectively nonrandomized, control study revealed perineal rESWT as a new therapy option for CPPS with statistically significant effects in comparison to drugs at least for 3 months after cessation of treatment. SAGE Publications 2018-11-28 /pmc/articles/PMC6775558/ /pubmed/30486723 http://dx.doi.org/10.1177/1557988318814663 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Zhang, Zhao-Xuan Zhang, Dai Yu, Xiao-Tong Ma, Yue-Wen Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic Pelvic Pain Syndrome: A Nonrandomized Controlled Trial |
title | Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic
Pelvic Pain Syndrome: A Nonrandomized Controlled Trial |
title_full | Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic
Pelvic Pain Syndrome: A Nonrandomized Controlled Trial |
title_fullStr | Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic
Pelvic Pain Syndrome: A Nonrandomized Controlled Trial |
title_full_unstemmed | Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic
Pelvic Pain Syndrome: A Nonrandomized Controlled Trial |
title_short | Efficacy of Radial Extracorporeal Shock Wave Therapy for Chronic
Pelvic Pain Syndrome: A Nonrandomized Controlled Trial |
title_sort | efficacy of radial extracorporeal shock wave therapy for chronic
pelvic pain syndrome: a nonrandomized controlled trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775558/ https://www.ncbi.nlm.nih.gov/pubmed/30486723 http://dx.doi.org/10.1177/1557988318814663 |
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