Dimensions of living with emetophobia

IF 0.8 Q4 SOCIAL WORK Mental Health and Social Inclusion Pub Date : 2024-05-13 DOI:10.1108/mhsi-04-2024-0055
Hannah Jane Kerry, Russelll Gurbutt
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Abstract

Purpose This paper aims to present an examination of selected literature about the lived experiences of those with emetophobia. Its intention is to inform further empirical enquiry and subsequent approaches to treatment and care aimed at inclusive support for sufferers. To that end, it is important to bring the sufferers’ narrative into public and professional domains. Design/methodology/approach A systematic search of multiple databases using the search engine Discover@bolton and grey literature was undertaken to obtain evidence about the lived experiences of people with emetophobia. The search terms used were “emetophobia” and combinations of associated topic phrases using Boolean operators (AND / OR): “Emetophobia” OR “fear of vomiting” OR “fear of being sick”, Emetophobia AND “lived experiences” and finally Emetophobia OR “fear of vomiting” OR “fear of being sick” AND “lived experiences”. Eight papers were included in the review and five items of grey literature. Findings Several themes were identified in this literature including fear, escape and avoidance, other influences, consequences and medicalisation. The findings reveal that the experiences of those with emetophobia are subsumed beneath a focus on diagnosis and treatment. When it comes to understanding the actual lived experience of a person with emetophobia, the evidence presents the reader with what treatment may work and how they might respond to it, but largely omits the voice of the individual with emetophobia. This signals a need to undertake enquiry to bring this to the fore and so inform ways of greater inclusive practice for the public and professionals alike. Research limitations/implications The evidence reviewed in this paper can be noted for the limited discussion about the individual’s lived experience of emetophobia. Gaining insight into this would contribute to raising awareness in a wider public arena and inform carers and healthcare professionals’ understanding. It would also display the importance of an individual context and health journey. Practical implications Knowing this can inform approaches to helping an individual either to live with the phobia and manage its impact on daily living (positive rather than maladaptive coping mechanisms) or to overcome it with or without adjunct medical treatment (if this is possible). Social implications Knowing based on contemporary empirical enquiry will inform policy and guideline development. Whatever course is taken, it must contribute to steps being taken towards achieving a better quality of life for individual sufferers. The findings of this paper likewise inform the need for further study into the individual lived experience of emetophobia. Originality/value This paper is original in having identified a need to bring empirical evidence of the lived experience of sufferers with emetophobia into the public and professional domain.
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患呕吐恐惧症的生活层面
目的 本文旨在对有关恐吐症患者生活经历的部分文献进行研究。其目的是为进一步的实证调查以及随后的治疗和护理方法提供信息,以便为患者提供包容性的支持。为此,将患者的叙述带入公共和专业领域是非常重要的。设计/方法学/方法使用搜索引擎Discover@bolton对多个数据库和灰色文献进行了系统搜索,以获取有关恐吐症患者生活经历的证据。使用的搜索关键词是 "恐吐症 "以及使用布尔运算符(AND / OR)的相关主题短语组合:呕吐恐惧症 "或 "呕吐恐惧 "或 "生病恐惧"、"呕吐恐惧症 "和 "生活经历",最后是 "呕吐恐惧症 "或 "呕吐恐惧 "或 "生病恐惧 "和 "生活经历"。研究结果在这些文献中发现了几个主题,包括恐惧、逃避和回避、其他影响、后果和医疗化。研究结果表明,那些患有呕吐恐惧症的人的经历被归结为诊断和治疗。当涉及到了解恐吐症患者的实际生活经历时,这些证据向读者展示了哪些治疗方法可能有效,以及他们可能如何应对,但在很大程度上忽略了恐吐症患者的声音。这预示着我们有必要开展调查,将这一点凸显出来,从而为公众和专业人士提供更具包容性的实践方法。研究局限性/影响本文所回顾的证据中,关于恐吐症患者个人生活经历的讨论非常有限。对这一问题的深入研究将有助于提高更广泛的公众意识,并为护理人员和医疗保健专业人员的理解提供信息。社会影响基于当代实证调查的了解将为政策和指南的制定提供参考。无论采取何种方法,都必须有助于采取措施提高患者的生活质量。本文的研究结果同样表明,有必要对恐吐症患者的个人生活经历进行进一步研究。
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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CiteScore
1.80
自引率
25.00%
发文量
42
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