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ABSTRACT: Objective
To explore experience and prevalence of vulval lichen sclerosus (VLS) diagnosis in general practice using an anonymous patient survey.Design
Quantitative descriptive cross-sectional survey informed by previous qualitative interviews and developed with patient representatives, sent to people recorded in general practice as having a VLS diagnosis.Setting
General practices (n=24) in the UK (West Midlands).Participants
n=177 respondents.Results
One in five respondents reported that they had been misdiagnosed, and about a third reported that it was a struggle to get treatment. Only one third said they received regular check-ups, recommended in clinical guidelines. One-fifth reported they were not being treated with topical corticosteroids, the m
SUBMITTER: Rees S
PROVIDER: S-EPMC12414219 | biostudies-literature | 2025 Sep
REPOSITORIES: biostudies-literature