Björkman Ida, Simrén Magnus, Ringström Gisela, Jakobsson Ung Eva
Department of Internal Medicine & Clinical Nutrition, Institute of Medicine and the Centre for Person-Centred Care (GPCC), Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Institute of Health and Care Sciences and the Centre for Person-Centred Care (GPCC), Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
J Clin Nurs. 2016 Oct;25(19-20):2967-78. doi: 10.1111/jocn.13400. Epub 2016 Jul 25.
This study aimed to explore patients' experiences of healthcare encounters in severe irritable bowel syndrome.
Irritable bowel syndrome is a common functional disorder with symptoms such as abdominal pain and disturbed bowel habits, the cause of which is not completely known. Treatments options are limited, and healthcare encounters in irritable bowel syndrome have been described as unsatisfying and frustrating for both patients and professional healthcare providers. Furthermore, the influence of power on healthcare encounters has long been recognised, especially regarding the disadvantaged position of those suffering from functional illness which cannot be identified by commonly used tests or investigations.
We interviewed 10 patients during 2014, all attending an outpatient clinic and suffering from severe irritable bowel syndrome. Relying on narrative and feminist theory, we explored how they actively negotiate professional discourse communicated to them in the clinical encounter.
The patients' experiences of healthcare encounters in irritable bowel syndrome were mostly described as negative, and often induced feelings of confusion and self-doubt. Positive encounters were described as being listened to, believed and taken seriously. Narrators found it especially problematic when healthcare professionals described irritable bowel syndrome as a minor disorder with primarily stress or psychological aetiology and put the responsibility for recovery onto the patient. Patients' actively negotiated such professional discourse by presenting a counternarrative describing their own suffering and strengths, experienced healthcare shortcomings and possible organic aetiology of irritable bowel syndrome.
Patients suffering from severe irritable bowel syndrome described how they often felt a need to protect their positive identities in the face of trivialisation and disbelief by healthcare professionals.
A deepened understanding of patients' experiences of healthcare encounters in irritable bowel syndrome could enable more helpful and supporting interventions by healthcare professionals.
本研究旨在探索重症肠易激综合征患者的就医体验。
肠易激综合征是一种常见的功能性疾病,症状包括腹痛和排便习惯紊乱,其病因尚未完全明确。治疗选择有限,肠易激综合征患者的就医体验对患者和专业医疗服务提供者而言都不尽人意且令人沮丧。此外,权力对就医体验的影响早已得到认可,尤其是对于那些患有功能性疾病的弱势群体而言,他们处于劣势地位,因为常用的检查或检测无法识别其病情。
2014年,我们对10名患者进行了访谈,这些患者均前往门诊就诊,且患有重症肠易激综合征。基于叙事和女性主义理论,我们探究了他们在临床诊疗过程中如何积极应对专业话语。
肠易激综合征患者的就医体验大多被描述为负面的,且常常引发困惑和自我怀疑的情绪。积极的就医体验被描述为被倾听、被信任和被认真对待。讲述者发现,当医疗专业人员将肠易激综合征描述为一种主要由压力或心理病因引起的小疾病,并将康复的责任推给患者时,问题尤其严重。患者通过讲述自己的痛苦与优势、就医过程中的不足以及肠易激综合征可能的器质性病因等反叙事来积极应对这种专业话语。
患有重症肠易激综合征的患者描述了他们在面对医疗专业人员的轻视和怀疑时,如何常常感到需要维护自己的正面形象。
深入了解肠易激综合征患者的就医体验,有助于医疗专业人员采取更有益和支持性的干预措施。