Barriers to diagnosing and treating vulval lichen sclerosus: a survey study.

IF 5.3 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
British Journal of General Practice Pub Date : 2025-03-27 Print Date: 2025-04-01 DOI:10.3399/BJGP.2024.0360
Arabella Crew, Rheanne Leatherland, Louise Clarke, Caroline Owen, Rosalind C Simpson
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引用次数: 0

Abstract

Background: Vulval lichen sclerosus (VLS) is a chronic inflammatory condition that is frequently misdiagnosed and under-recognised. To date, qualitative research has focused on lived experience of VLS, with women attributing diagnostic delay to poor interactions with healthcare professionals (HCPs), often due to lack of knowledge. In the UK, women with VLS are most likely to present to primary care.

Aim: To establish HCPs' perspectives on the identification, management, and education of vulval skin disease, with a focus on VLS.

Design and setting: A mixed-methods study survey undertaken across the UK.

Method: HCPs were recruited through opportunistic sampling. The survey was distributed via email and WhatsApp through professional networks and in hard-copy format at events, and completed between 1 November 2023 and 14 December 2023. Data were analysed using descriptive statistics, Spearman's rank correlations, and thematic analysis.

Results: Of 122 responders, most were GPs (n = 53) and GP trainees (n = 59). In total, 37.7% of responders had never participated in teaching or learning on vulval skin disease. Confidence in the identification of vulval skin disease positively correlated with experience, exposure, and female gender, although this last correlation was weak. The top identified barriers to diagnosis and treatment included lack of knowledge, embarrassment, and absence of VLS diagnostic criteria. Almost all participants (97.5%) felt that VLS diagnostic criteria would be helpful in clinical practice.

Conclusion: This study provides insight into the barriers to diagnosing and treating VLS in primary care. HCPs recognise deficiencies in training and referral pathways, and a lack of tools to support VLS diagnosis. Training should include skills to address stigma and embarrassment. This study highlights the importance of developing interventions, such as reproducible diagnostic criteria, to overcome barriers, thereby expediting diagnosis and treatment.

诊断和治疗外阴硬皮病的障碍:一项调查研究。
背景外阴硬皮病(VLS)是一种慢性炎症,经常被误诊,而且认识不足。迄今为止,定性研究主要集中在 VLS 患者的生活体验方面,女性患者往往由于缺乏相关知识而将诊断延误归咎于与医疗保健专业人员(HCPs)的不良互动。在英国,患有 VLS 的妇女最有可能向初级保健机构求诊。目的 确定医护人员对外阴皮肤病的识别、管理和教育的看法,重点是 VLS。设计和设置 向从事初级保健工作的保健医生发放调查问卷。方法 通过专业网络和活动分发调查问卷。分析包括描述性统计、斯皮尔曼等级相关性和主题分析。结果 在 122 名受访者中,53 名是全科医生(GP),59 名是全科医生实习生。37.7%的受访者从未参加过有关外阴皮肤病的教学或学习。识别外阴皮肤病的信心与经验、接触和女性性别呈正相关。诊断和治疗的主要障碍包括缺乏知识、尴尬和缺乏外阴皮肤病诊断标准。几乎所有参与者(97.5%)都认为 VLS 诊断标准有助于临床实践。结论 本研究深入探讨了在初级保健中诊断和治疗 VLS 的障碍。初级保健人员认识到在培训、转诊途径和缺乏支持 VLS 诊断的工具方面存在不足。培训应包括解决耻辱感和尴尬的技能。本研究强调了制定干预措施以克服障碍、加快诊断和治疗的重要性,例如可重复的诊断标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
British Journal of General Practice
British Journal of General Practice 医学-医学:内科
CiteScore
5.10
自引率
10.20%
发文量
681
期刊介绍: The British Journal of General Practice is an international journal publishing research, editorials, debate and analysis, and clinical guidance for family practitioners and primary care researchers worldwide. BJGP began in 1953 as the ‘College of General Practitioners’ Research Newsletter’, with the ‘Journal of the College of General Practitioners’ first appearing in 1960. Following the change in status of the College, the ‘Journal of the Royal College of General Practitioners’ was launched in 1967. Three editors later, in 1990, the title was changed to the ‘British Journal of General Practice’. The journal is commonly referred to as the ''BJGP'', and is an editorially-independent publication of the Royal College of General Practitioners.
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