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理解身体感觉:癌症共同叙事是否会影响症状评估?

Making sense of bodily sensations: Do shared cancer narratives influence symptom appraisal?

机构信息

Institute of Health & Wellbeing, University of Glasgow, Glasgow, G12 8QQ, UK.

Institute of Health & Wellbeing, University of Glasgow, Glasgow, G12 8QQ, UK.

出版信息

Soc Sci Med. 2019 Feb;223:31-39. doi: 10.1016/j.socscimed.2018.12.034. Epub 2019 Jan 10.

Abstract

Though new or altered bodily sensations are a common occurrence they rarely transition to biomedically defined symptoms. When they do, sensations are subject to an appraisal process that can culminate in help-seeking. The transition has particular relevance for cancer diagnoses. Studies of 'symptom appraisal' in cancer patients typically conclude that failure to regard sensations as serious or 'symptom misattribution' results in lengthier help-seeking intervals. Though multiple influences on appraisal processes are acknowledged, including the socio-cultural context, detailed description and analyses of how socio-cultural factors shape appraisal is lacking. In this paper we explore one substantial component of the sociocultural context, namely, publicly recognised shared cancer narratives, and their impact on appraisal. We undertook a secondary analysis of 24 interviews with Scottish colorectal cancer patients originally completed in 2006-2007. Our analysis showed that fear, death and severity dominated cancer narratives and were frequently restated throughout interviews. Yet, early bodily changes were often mild and vague, were commonly experienced in the context of 'feeling well' and failed to match preconceived ideas of what cancer 'feels like'. Moreover, few perceived themselves to be 'at risk' of cancer and diagnoses were characterised as 'shocking' events. Participants engaged in self-monitoring strategies and severe or painful changes prompted help-seeking. Far from misattributing symptoms, responses to bodily changes were sensible and measured; responses are particularly apt in relation to current policy rhetoric, which urges measured use of services. Our findings have resonance across healthcare settings as patients are required to negotiate a narrow and challenging space when making decisions to seek help. There is a pressing need for a more realistic approach to symptom appraisal in order to reduce help-seeking intervals. Future awareness campaigns should emphasise the importance of vague/minor bodily changes although this will necessitate discussions with health professionals on referral thresholds to achieve earlier detection.

摘要

虽然新的或改变的身体感觉是很常见的,但它们很少会转化为医学定义的症状。当它们确实转化为症状时,这些感觉会经历一个评估过程,最终可能会寻求帮助。这种转变对于癌症诊断尤其重要。对癌症患者“症状评估”的研究通常得出结论,即未能将感觉视为严重或“症状归因错误”会导致更长的寻求帮助的间隔。尽管人们承认评估过程受到多种因素的影响,包括社会文化背景,但缺乏对社会文化因素如何塑造评估的详细描述和分析。在本文中,我们探讨了社会文化背景的一个重要组成部分,即公众认可的共同癌症叙述及其对评估的影响。我们对 2006-2007 年间最初完成的 24 名苏格兰结直肠癌患者的访谈进行了二次分析。我们的分析表明,恐惧、死亡和严重性主导着癌症叙述,并在访谈中经常被重复。然而,早期的身体变化通常很轻微和模糊,常常发生在“感觉良好”的背景下,与对癌症“感觉如何”的先入为主的观念不匹配。此外,很少有人认为自己有患癌症的风险,而且诊断结果被描述为“令人震惊”的事件。参与者采取了自我监测策略,只有严重或疼痛的变化才会促使他们寻求帮助。他们对身体变化的反应远非归因错误,而是明智和适度的;这些反应特别适合当前政策言论,该言论敦促适度使用服务。由于患者在决定寻求帮助时需要在一个狭窄而具有挑战性的空间中进行协商,因此我们的发现与医疗保健环境有关。为了减少寻求帮助的间隔,迫切需要对症状评估采取更现实的方法。未来的宣传活动应强调模糊/轻微身体变化的重要性,尽管这需要与卫生专业人员讨论转诊阈值,以实现更早的检测。

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