Literature DB >> 21678188

'It's as if PBC didn't exist': the illness experience of women affected by primary biliary cirrhosis.

L Montali1, A Frigerio, P Riva, P Invernizzi.   

Abstract

This study investigates the illness experience of women who are affected by primary biliary cirrhosis (PBC), a rare chronic liver disease which mostly affects women. Despite the fact that PBC is medically recognised, it shares many characteristics with other chronic and controversial conditions which may lead to delegitimation of the patient's experience of illness, impacting on the construction of the patient's self-identity. Twenty three women took part in semi-structured interviews. Data were analysed using interpretative phenomenological analysis and the analysis identified three themes that are interrelated and characterised by a dynamic of normalisation. The first theme, the delegitimation of women's experience, implies denial of patients' sick-role, trivialisation of fatigue and lack of consideration of patients' needs. The second theme, PBC as a challenge to women's social identity refers to how patients face delegitimation and manage the illness's consequences for relationships and social roles. The third theme, the need for biographical continuity, focuses on how patients construct their ill identities as a consequence of both the delegitimation and the challenges posed by PBC. Results are discussed in a gender perspective, highlighting how delegitimation and identity construction processes are influenced by women's social roles and conditions.

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Year:  2011        PMID: 21678188     DOI: 10.1080/08870446.2011.565876

Source DB:  PubMed          Journal:  Psychol Health        ISSN: 0887-0446


  5 in total

1.  Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma.

Authors:  Charlotte Lloyd; Jessica Leighton; Lin Lee Wong; Anna Goulding; Ann Brownlee; Penney Gray; Emma Culver; Neil Halliday; Doug Thorburn; Michael A Heneghan; David E J Jones; Catherine Exley; Jessica K Dyson
Journal:  Dig Dis Sci       Date:  2022-05-17       Impact factor: 3.487

2.  Making sense of the delegitimation experiences of people suffering from indoor air problems in their homes.

Authors:  Tuija Seppälä; Eerika Finell; Suvi Kaikkonen
Journal:  Int J Qual Stud Health Well-being       Date:  2022-12

3.  Prospective Validation of the Decalogue, a Set of Doctor-Patient Communication Recommendations to Improve Patient Illness Experience and Mood States within a Hospital Cardiologic Ambulatory Setting.

Authors:  Piercarlo Ballo; Massimo Milli; Carly Slater; Fabrizio Bandini; Federico Trentanove; Giulia Comper; Alfredo Zuppiroli; Stefania Polvani
Journal:  Biomed Res Int       Date:  2017-11-21       Impact factor: 3.411

4.  Quality of life and unmet needs in patients with chronic liver disease: A mixed-method systematic review.

Authors:  Lea Ladegaard Grønkjær; Mette Munk Lauridsen
Journal:  JHEP Rep       Date:  2021-09-28

5.  Health-related quality of life in patients with autoimmune hepatitis.

Authors:  Maurice Michel; Francesca Spinelli; Annette Grambihler; Christian Labenz; Michael Nagel; Leonard Kaps; Yvonne Huber; Peter R Galle; Marcus-Alexander Wörns; Jörn M Schattenberg
Journal:  Qual Life Res       Date:  2021-05-12       Impact factor: 4.147

  5 in total

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