• Sophie Rees, Matthew Ridd, Lorelei Hunt, Hazel Everitt, Anna Gilbertson, Robert Johnson, Anthony E Pickering, Oliver van Hecke, Vikki Wylde, Sian Wells, and Jonathan P Banks.
• Bristol Trials Centre, Population Health Sciences, University of Bristol, Bristol, UK.
• Br J Gen Pract. 2025 Feb 1; 75 (751): e137e142e137-e142.

BackgroundShingles (herpes zoster), caused by reactivation of the varicella-zoster virus, is usually diagnosed and managed in primary care. The lifetime risk of shingles in the general population is approximately 30%, and it can have a detrimental effect on quality of life. There has been little qualitative research about patient experience and understanding of shingles.AimTo explore patient experiences and understanding of shingles.Design And SettingQualitative interviews with people with shingles recruited from primary care in England.MethodQualitative semi-structured remote interviews were undertaken with 29 participants in a randomised controlled trial in primary care in England (ATHENA, ISRCTN14490832). Participants were aged >49 years and were diagnosed within 6 days of shingles rash onset. Interviewees were sampled for diversity in terms of pain, intervention adherence, age, gender, and ethnicity. Data were analysed using reflexive thematic analysis.ResultsInterviews took place in November 2022 to April 2023. Participants' understanding of shingles was limited, particularly pre-diagnosis. A common theme was that 'everyone has heard of it, but no one knows what it is'. Television campaigns about the shingles vaccination programme helped some to recognise the rash. Shingles was understood as a disease with a variable prognosis, resulting in a sense of uncertainty about the significance when diagnosed. Participants reported a range of symptoms, which impacted on everyday life. Some people thought their diagnosis was caused by poor mental health or challenging life circumstances, a perception sometimes reinforced by healthcare professionals. Many participants sought meaning in their diagnosis, reflecting on, and sometimes changing, their life and circumstances.ConclusionPrimary care practitioners should be aware of the broad spectrum of patient knowledge, and the potential for better understanding to promote early attendance and treatment to reduce the impact of shingles.© The Authors.

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