Non-pharmacological interventions for treating chronic prostatitis/chronic pelvic pain syndrome

被引:62
作者
Franco, Juan V. A. [1 ,2 ]
Turk, Tarek [3 ]
Jung, Jae Hung [4 ,5 ]
Xiao, Yu-Tian [6 ]
Iakhno, Stanislav [7 ]
Garrote, Virginia [8 ]
Vietto, Valeria [1 ,2 ]
机构
[1] Inst Univ Hosp Italiano, Argentine Cochrane Ctr, C1199ACL, RA-4234 Potosi, Buenos Aires, Argentina
[2] Hosp Italiano Buenos Aires, Family & Community Med Serv, Buenos Aires, DF, Argentina
[3] Damascus Univ, Fac Med, Damascus, Syria
[4] Yonsei Univ, Wonju Coll Med, Dept Urol, Wonju, South Korea
[5] Yonsei Univ, Wonju Coll Med, Inst Evidence Based Med, Wonju, South Korea
[6] Second Mil Med Univ, Changhai Hosp, Dept Urol, Shanghai, Peoples R China
[7] Univ Tromso, Tromsdalen, Norway
[8] Inst Univ Hosp Italiano, Biblioteca Cent, Buenos Aires, DF, Argentina
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2018年 / 05期
关键词
QUALITY-OF-LIFE; SHOCK-WAVE THERAPY; TRANSURETHRAL MICROWAVE THERMOTHERAPY; CHRONIC ABACTERIAL PROSTATITIS; CATEGORY III PROSTATITIS; DOUBLE-BLIND; NONBACTERIAL PROSTATITIS; IMPORTANT DIFFERENCE; NERVE-STIMULATION; BOTULINUM TOXIN;
D O I
10.1002/14651858.CD012551.pub3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) is a common disorder in which the two main clinical features are pelvic pain and lower urinary tract symptoms. There are currently many approaches for its management, using both pharmacological and non-pharmacological interventions. The National Institute of Health - Chronic Prostatitis Symptom Index (NIH-CPSI) score is a validated measure commonly used to measure CP/CPPS symptoms. Objectives To assess the effects of non-pharmacological therapies for chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS). Search methods We performed a comprehensive search using multiple databases, trial registries, grey literature and conference proceedings with no restrictions on the language of publication or publication status. The date of the latest search of all databases was August 2017. Selection criteria We included randomised controlled trials. Inclusion criteria were men with a diagnosis of CP/CPPS. We included all available nonpharmacological interventions. Data collection and analysis Two review authors independently classified studies and abstracted data from the included studies, performed statistical analyses and rated quality of evidence (QoE) according to the GRADE methods. Main results We included 38 unique studies with 3290 men with CP/CPPS across 23 comparisons. 1. Acupuncture: (three studies, 204 participants) based on short-term follow-up, acupuncture probably leads to clinically meaningful reduction in prostatitis symptoms compared with sham procedure (mean difference (MD) in total NIH-CPSI score -5.79, 95% confidence interval (CI) -7.32 to -4.26, high QoE). Acupuncture may result in little to no difference in adverse events (low QoE). Acupuncture may not reduce sexual dysfunction when compared with sham procedure (MD in the International Index of Erectile Function (IIEF) Scale -0.50, 95% CI -3.46 to 2.46, low QoE). Acupuncture may also lead to a clinically meaningful reduction in prostatitis symptoms compared with standard medical therapy (MD -6.05, 95% CI -7.87 to -4.24, two studies, 78 participants, low QoE). We found no information regarding quality of life, depression or anxiety. 2. Lifestyle modifications: (one study, 100 participants) based on short-term follow-up, lifestyle modifications may be associated with a reduction in prostatitis symptoms compared with control (risk ratio (RR) for improvement in NIH-CPSI scores 3.90, 95% CI 2.20 to 6.92, very low QoE). We found no information regarding adverse events, sexual dysfunction, quality of life, depression or anxiety. 3. Physical activity: (one study, 85 participants) based on short-term follow-up, a physical activity programme may cause a small reduction in prostatitis symptoms compared with control (NIH-CPSI score MD -2.50, 95% CI -4.69 to -0.31, low QoE). This programme may not reduce anxiety or depression (low QoE). We found no information regarding adverse events, sexual dysfunction or quality of life. 4. Prostatic massage: (two studies, 115 participants) based on short-term follow-up, we are uncertain whether the prostatic massage reduces or increases prostatitis symptoms compared with control (very low QoE). We found no information regarding adverse events, sexual dysfunction, quality of life, depression or anxiety. 5. Extracorporeal shockwave therapy: (three studies, 157 participants) based on short-term follow-up, extracorporeal shockwave therapy reduces prostatitis symptoms compared with control (NIH-CPSI score MD 6.18, 95% CI -7.46 to -4.89, high QoE). These results may not be sustained at medium-term follow-up (low QoE). This treatment may not be associated with a greater incidence of adverse events (low QoE). This treatment probably improves sexual dysfunction (MD in the IIEF Scale MD 3.34, 95% CI 2.68 to 4.00, one study, 60 participants, moderate QoE). We found no information regarding quality of life, depression or anxiety. 6. Transrectal thermotherapy compared tomedical therapy: (two studies, 237 participants) based on short-termfollow-up, transrectal thermotherapy alone or in combination with medical therapy may decrease prostatitis symptoms slightly when compared with medical therapy alone (NIH-CPSI score MD -2.50, 95% CI -3.82 to -1.18, low QoE). One included study reported that participants may experience transient adverse events. We found no information regarding sexual dysfunction, quality of life, depression or anxiety. 7. Other interventions: there is uncertainty about the effects of most of the other interventions included in this review. We found no information regarding psychological support or prostatic surgery. Authors' conclusions Based on the findings of moderate quality evidence, this review found that some non-pharmacological interventions such as acupuncture and extracorporeal shockwave therapy are likely to result in a decrease in prostatitis symptoms and may not be associated with a greater incidence of adverse event. The QoE for most other comparisons was predominantly low. Future clinical trials should include a full report of their methods including adequate masking, consistent assessment of all patient-important outcomes including potential treatment-related adverse events and appropriate sample sizes.
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