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Summary of findings 10

Transrectal thermotherapy (add‐on) compared to medical treatment alone for chronic prostatitis/chronic pelvic pain syndrome
Transrectal thermotherapy (add‐on) compared to medical treatment alone for chronic prostatitis/chronic pelvic pain syndrome
Patient or population: participants with chronic prostatitis/chronic pelvic pain syndrome
Setting: outpatient, China and Korea
Intervention: transrectal thermotherapy in addition to medical therapy
Comparison: medical treatment alone
Outcomes№ of participants
(studies)
Follow‐up
Quality of the evidence
(GRADE)
Relative effect
(95% CI)
Anticipated absolute effects* (95% CI)
Risk with medical treatment aloneRisk difference with transrectal thermotherapy (add‐on)
Prostatitis symptoms
assessed with: NIH‐CPSI score
Scale from: 0 to 43
follow‐up: 6 to 12 weeks
Benefit is indicated by lower scores
145
(2 RCTs)
⊕⊕⊝⊝
Low1
The mean prostatitis symptom score ranged from 14.33 to 17.19MD 4.34 lower
(5.65 lower to 3.04 lower)
Adverse events ‐ not reported
Sexual dysfunction ‐ not reported
Quality of life ‐ not reported
Depression and anxiety ‐ not reported
*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; MD: mean difference; NIH‐CPSI: National Institutes of Health ‐ Chronic Prostatitis Symptom Index; RCT: randomised controlled trial.
GRADE Working Group grades of evidence
High quality: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate quality: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low quality: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect.
Very low quality: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect.

1Downgraded 2 levels due to high risk of allocation concealment bias, performance and detection bias (study not blinded) and high risk of attrition bias.

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