Population Name
Population Size
Report for 12 months ending
Number of practices in the population
Participating practices - number (%)
Total number of patients from participating practices
Total number of patients identified with PP
% of total patients identified with PP (prevalence):
Was a Pelvic Pain questionnaire (e.g. IPPS) use for patients?
% of PP patients identified in primary care
% of urgent or semi-urgent patients referred within one month of presentation by their GP (urgent/semi urgent patients=severe undiagnosed or progressive pain with the risk of increasing functional impairment, generally of 6 months duration or more)
% of routine or regular patients referred with 8 weeks of presentation by their GP (routine=persistent long term pain without significant progression)
Number of follow up PP patients in gynaecology, urology, psychology/counseling (IAPT, CBT), gastro-enterology, colo-rectal, pain/physiotherapy
% of PP patients for whom a multidisciplinary meetings was held
Average time from presentation to multidisciplinary meeting being held
% of PP patients with a named co-ordinator of care
% of PP patients for whom patient outcomes are reviewed every 6 months (being mindful of whether the patient should be monitored or discharged as self-managing)
% of PP patients who feel they have adequate methods to manage their pain
Is there direct access to psychological services? If so, please describe.
Are patients given access to decision support tools (e.g. map of medicine, releavent websites, leaflets, local buddying and peer support groups)? If so, please describe.
Are experiences of PP patients monitored? If so, please describe.
Are local support groups or materials (e.g. shared decision aids, youtube videos, leaflets, etc.) developed with PP patient/care involvement? If so, please describe?
Estimated cost of your service
Contact Person
Contact email address:
