The association of breast surgery ASPIRE: breast pain pathway rapid evaluation project – study protocol

Author:

Hubbard Thomas J. E.1,Isaac Anna T.2,Cui Alice34,Cutress Ramsey I.5,Dave Rajiv6,Ellis Katy6,Fields Jo7,Halliday Suzanne8,Hu Jennifer9,Potter Shelley10,Chagla Leena11,Cox Karina12,Holcombe Christopher13

Affiliation:

1. Faculty of Health and Life Sciences, University of Exeter, Exeter

2. School of Medicine, Dentistry and Biomedical Sciences, Queen’s University Belfast, Belfast, Northern Ireland

3. Manchester University NHS Foundation Trust

4. Faculty of Medicine, Biology and Health, University of Manchester, Manchester

5. University of Southampton and University Hospital Southampton, Hampshire

6. Manchester University Foundation Trust, Manchester

7. University of Southampton and Hampshire Hospitals NHS Foundation Trust

8. Surrey and Sussex Healthcare NHS Trust

9. Barts Health NHS Trust, London

10. Bristol Medical School and Bristol Breast Care Centre, North Bristol NHS Trust, Bristol

11. Mersey and West Lancashire Teaching Hospitals NHS Trust, President ABS

12. Maidstone and Tunbridge Wells NHS Trust, Kent, UK

13. Emeritus Professor of Surgery (Retired)

Abstract

Background: Breast pain accounts for 20–40% of new referrals to breast units in the UK and these patients have a very low risk of breast cancer. Patients have previously been assessed in resource-intensive, cancer-exclusion, one stop clinics, which are now failing to meet government targets due to excessive demand. UK Breast units are increasingly piloting Breast Pain-only Pathways (BPP) to assess these patients, and there is no consensus for the optimal pathway. The aim of this prospective multicentre study is to assess the safety and patient satisfaction of different BPPs to inform future BPP design and implementation. Methods: All UK breast units will be invited to join the ASPIRE study between January 2023 and December 2023. Units with a BPP are invited to submit their pathway for evaluation; and those without a BPP who see patients with breast pain-only in a one stop clinics setting are also invited to join the study to evaluate the traditional pathway model concurrently. Patient satisfaction assessments will be collected after their initial consultation and patient outcomes, including subsequent cancer diagnosis, will be followed up at 12 months to determine if they have cancer diagnosis after discharge to assess pathway safety.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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