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Treatment of Chronic Prostatitis/Chronic Pelvic Pain Syndrome—Reply

Ammarin Thakkinstian, PhD; John Attia, MD, PhD, FRCPC, FRACP
JAMA. 2011;305(13):1298-1299. doi:10.1001/jama.2011.400.
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In Reply: Dr Jackson and colleagues are concerned that our meta-analysis alternated between fixed and random effects for pooling. The majority of outcomes in our review were heterogeneous, so we did use a random-effects model. The exceptions to this were pain and voiding scores between phytotherapy and placebo groups and treatment responsiveness between anti-inflammatory drugs and placebo where mild heterogeneity was found (ie, I2 = 0%, 0%, and 24.4%, respectively). Applying fixed- or random-effects models for these first 2 pooled effects obviously yields identical results. For the last outcome, the pooled risk ratio for treatment responsiveness was 1.8 (95% confidence interval [CI], 1.2-2.6) for the random-effects model compared with 1.8 (95% CI, 1.3-2.4) for the fixed-effects model. As Jackson et al point out, the tests for heterogeneity are weak, and that is why we set the threshold P value for this test at .10 rather than .05 and why we also calculated I2 statistics.12

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April 6, 2011
Jeffrey L. Jackson, MD; Jeffrey M. Cohen; Jordan Dimitrakoff, MD, PhD
JAMA. 2011;305(13):1298-1299. doi:10.1001/jama.2011.399.
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