Management of Chronic Prostatitis/Chronic Pelvic Pain Syndrome A Systematic Review and Network Meta-analysis

被引:166
|
作者
Anothaisintawee, Thunyarat [1 ,2 ]
Attia, John [3 ,4 ]
Nickel, J. Curtis [5 ]
Thammakraisorn, Sangsuree [2 ]
Numthavaj, Pawin [1 ]
McEvoy, Mark [3 ]
Thakkinstian, Ammarin [1 ]
机构
[1] Mahidol Univ, Ramathibodi Hosp, Fac Med, Sect Clin Epidemiol & Biostat, Bangkok 10400, Thailand
[2] Mahidol Univ, Ramathibodi Hosp, Fac Med, Dept Family Med, Bangkok 10400, Thailand
[3] Univ Newcastle, Sch Med & Publ Hlth, Ctr Clin Epidemiol & Biostat, Newcastle, NSW 2308, Australia
[4] Hunter Med Res Inst, Newcastle, NSW, Australia
[5] Queens Univ, Dept Urol, Kingston, ON, Canada
来源
基金
美国国家卫生研究院;
关键词
PLACEBO-CONTROLLED MULTICENTER; DOUBLE-BLIND; MEN; SYMPTOMS; THERAPY; CIPROFLOXACIN; LEVOFLOXACIN; FINASTERIDE; TAMSULOSIN; DIAGNOSIS;
D O I
10.1001/jama.2010.1913
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) is common, but trial evidence is conflicting and therapeutic options are controversial. Objective To conduct a systematic review and network meta-analysis comparing mean symptom scores and treatment response among alpha-blockers, antibiotics, antiinflammatory drugs, other active drugs (phytotherapy, glycosaminoglycans, finasteride, and neuromodulators), and placebo. Data Sources We searched MEDLINE from 1949 and EMBASE from 1974 to November 16, 2010, using the PubMed and Ovid search engines. Study Selection Randomized controlled trials comparing drug treatments in CP/CPPS patients. Data Extraction Two reviewers independently extracted mean symptom scores, quality-of-life measures, and response to treatment between treatment groups. Standardized mean difference and random-effects methods were applied for pooling continuous and dichotomous outcomes, respectively. A longitudinal mixed regression model was used for network meta-analysis to indirectly compare treatment effects. Data Synthesis Twenty-three of 262 studies identified were eligible. Compared with placebo, alpha-blockers were associated with significant improvement in symptoms with standardized mean differences in total symptom, pain, voiding, and quality-of-life scores of -1.7 (95% confidence interval [CI], -2.8 to -0.6), -1.1 (95% CI, -1.8 to -0.3), -1.4 (95% CI, -2.3 to -0.5), and -1.0 (95% CI, -1.8 to -0.2), respectively. Patients receiving alpha-blockers or anti-inflammatory medications had a higher chance of favorable response compared with placebo, with pooled RRs of 1.6 (95% CI, 1.1-2.3) and 1.8 (95% CI, 1.2-2.6), respectively. Contour-enhanced funnel plots suggested the presence of publication bias for smaller studies of alpha-blocker therapies. The network meta-analysis suggested benefits of antibiotics in decreasing total symptom scores (-9.8; 95% CI, -15.1 to -4.6), pain scores (-4.4; 95% CI, -7.0 to -1.9), voiding scores (-2.8; 95% CI, -4.1 to -1.6), and quality-of-life scores (-1.9; 95% CI, -3.6 to -0.2) compared with placebo. Combining alpha-blockers and antibiotics yielded the greatest benefits compared with placebo, with corresponding decreases of -13.8 (95% CI, -17.5 to -10.2) for total symptom scores, -5.7 (95% CI, -7.8 to -3.6) for pain scores, -3.7 (95% CI, -5.2 to -2.1) for voiding, and -2.8 (95% CI, -4.7 to -0.9) for quality-of-life scores. Conclusions alpha-Blockers, antibiotics, and combinations of these therapies appear to achieve the greatest improvement in clinical symptom scores compared with placebo. Antiinflammatory therapies have a lesser but measurable benefit on selected outcomes. However, beneficial effects of alpha-blockers may be overestimated because of publication bias. JAMA. 2011;305(1):78-86 www.jama.com
引用
收藏
页码:78 / 86
页数:9
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