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Patients’ experiences of healthcare encounters in severe irritable bowel syndrome: an analysis based on narrative and feminist theory

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  • Ida Björkman
  • Magnus Simrén
  • Gisela Ringström
  • Eva Jakobsson Ung

Abstract

Aims and objectives This study aimed to explore patients’ experiences of healthcare encounters in severe irritable bowel syndrome. Background 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. Methods 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. Results 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. Conclusions 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. Relevance to clinical practice A deepened understanding of patients’ experiences of healthcare encounters in irritable bowel syndrome could enable more helpful and supporting interventions by healthcare professionals.

Suggested Citation

  • Ida Björkman & Magnus Simrén & Gisela Ringström & Eva Jakobsson Ung, 2016. "Patients’ experiences of healthcare encounters in severe irritable bowel syndrome: an analysis based on narrative and feminist theory," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(19-20), pages 2967-2978, October.
  • Handle: RePEc:wly:jocnur:v:25:y:2016:i:19-20:p:2967-2978
    DOI: 10.1111/jocn.13400
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    References listed on IDEAS

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    1. Kay I Penny & Graeme D Smith, 2012. "The use of data‐mining to identify indicators of health‐related quality of life in patients with irritable bowel syndrome," Journal of Clinical Nursing, John Wiley & Sons, vol. 21(19pt20), pages 2761-2771, October.
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    1. Elisabet Johannesson & Eva Jakobsson Ung & Gisela Ringström & Riadh Sadik, 2019. "The experiences of physical activity in irritable bowel syndrome—A qualitative study," Journal of Clinical Nursing, John Wiley & Sons, vol. 28(17-18), pages 3189-3199, September.

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