Pain management of patients with chronic pelvic pain syndrome (CPPS) is challenging, because pain is often refractory to conventional treatments. Botulinum toxin A (BTX-A) may represent a promising therapeutic strategy for these patients. This entry summarizes the literature for prospective studies evaluating the use of BTX-A in the treatment of CPPS. A pooled meta-analysis of the included studies was performed considering only patients underwent BTX-A injection and comparing pain scores evaluated at baseline and at the last available follow up. We found that BTX-A could be an efficacious treatment for some specific CPPS subtypes. Higher level studies are needed to assess the efficacy and safety of BTX-A and provide objective indications for its use in CPPS management.
We reviewed the literature for prospective studies evaluating the use of BTX-A in the treatment of CPPS. Comprehensive search in the PubMed, Scopus, Web of Science, and Cochrane Central Register of Controlled Trials databases was performed from English-language articles published between January 2000 and October 2021. The primary outcome was to evaluate pain improvement after BTX-A treatment. A pooled meta-analysis of the included studies was performed considering only patients underwent BTX-A injection and comparing pain scores evaluated at baseline and at the last available follow up.
After screening 1001 records, 18 full-text manuscripts were selected, comprising 13 randomised clinical trials and 5 comparative studies. They covered 896 patients and several subtypes of CPPS: interstitial cystitis/bladder pain syndrome (IC/BPS), chronic prostatitis/prostate pain syndrome (CP/PPS), chronic scrotal pain, gynecological pelvic pain (GPP) and myofascial pelvic pain. A narrative synthesis of the main findings for each studies was provided. However, the clinical and methodological heterogeneity of studies included regarding the study design, the definition of CPPS subtype, intervention and control groups, number and sexes of patients, type and dose of drug administered, number and location of injections delivered, outcome measured and time of follow up, make it difficult to do an overall estimation of the effect of BTX-A on pain and other functional outcomes of various CPPS subtypes.
For the pooled meta-analysis, we included 21 cohorts of BTX-A treated patients coming from 14 studies (447 patients). A significant reduction in pain scores, related to the scale adopted, was showed in the overall cohort (p<0.001). Considering treated patients grouped according to CPPS subtypes, we found a significant improvement in pain relief in IC/PBS (p<0.001, 192 patients), CP/PPS (p=0.005, 73 patients), and GPP (p<0.001, 120 patients), even if some studies did not reach a significant improvement when independently considering.
This entry is adapted from the peer-reviewed paper 10.3390/toxins14010025