Literature DB >> 17597274

Complex syndromes, ambivalent diagnosis, and existential uncertainty: the case of Systemic Lupus Erythematosus (SLE).

Andrea Stockl1.   

Abstract

Systemic Lupus Erythematosus (SLE), also known as lupus, is an autoimmune disorder which is difficult to diagnose due to its manifold symptoms. Its complexity is part and parcel of the epistemological changes that scientific biomedicine is undergoing which in turn influence clinical practice. These changes lead to the well known and often-discussed frustration of patients who suffer from elusive disorders, long-term or chronic illnesses, and medically unexplained symptoms. Using ethnographic observations in combination with grounded theory methods this study explores SLE as one example of complex syndromes that the clinical practice of late modernity seems to bring about. It concentrates on the difficulties of diagnosing complex disorders from a medical point of view, then goes on to describe the impact this has on patients' lives, and their reaction to this situation. I argue that ambivalent diagnosis leads to existential uncertainty amongst patients which in turn influence the doctor-patient relationship. In concluding, I suggest that medical sociology has to move from merely describing and analysing this emerging situation to suggesting strategies for integrating experiential knowledge into clinical practice, especially when it comes to medical and personal management of chronic disorders such as SLE.

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Mesh:

Year:  2007        PMID: 17597274     DOI: 10.1016/j.socscimed.2007.05.016

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  8 in total

1.  Development of a digital toolkit to improve quality of life of patients with systemic lupus erythematosus.

Authors:  Jerik Leung; Laura Kloos; Alfred Hj Kim; Elizabeth A Baker
Journal:  Digit Health       Date:  2021-08-10

2.  Living with encapsulating peritoneal sclerosis (EPS): the patient's perspective.

Authors:  Helen Hurst; Angela Summers; Kinta Beaver; Ann-Louise Caress
Journal:  Perit Dial Int       Date:  2014-02-04       Impact factor: 1.756

3.  Individuals living with lupus: findings from the LUPUS UK Members Survey 2014.

Authors:  C Morgan; A R Bland; C Maker; J Dunnage; I N Bruce
Journal:  Lupus       Date:  2018-01-08       Impact factor: 2.911

4.  "…Not Having the Real Support That We Need": Patients' Experiences with Ambiguity of Systemic Lupus Erythematosus and Erosion of Social Support.

Authors:  Jerik Leung; Jennifer Ra; Elizabeth A Baker; Alfred H J Kim
Journal:  ACR Open Rheumatol       Date:  2019-04-22

5.  Exploring intentional medication non-adherence in patients with systemic lupus erythematosus: the role of physician-patient interactions.

Authors:  Jerik Leung; Elizabeth A Baker; Alfred H J Kim
Journal:  Rheumatol Adv Pract       Date:  2021-01-24

6.  Topic Modeling and User Network Analysis on Twitter during World Lupus Awareness Day.

Authors:  Salvatore Pirri; Valentina Lorenzoni; Gianni Andreozzi; Marta Mosca; Giuseppe Turchetti
Journal:  Int J Environ Res Public Health       Date:  2020-07-28       Impact factor: 3.390

7.  Is it me? The impact of patient-physician interactions on lupus patients' psychological well-being, cognition and health-care-seeking behaviour.

Authors:  Melanie Sloan; Felix Naughton; Rupert Harwood; Elliott Lever; David D'Cruz; Stephen Sutton; Chanpreet Walia; Paul Howard; Caroline Gordon
Journal:  Rheumatol Adv Pract       Date:  2020-07-22

8.  'But you don't look sick': a qualitative analysis of the LUPUS UK online forum.

Authors:  Melanie Sloan; Michael Bosley; Moira Blane; Lynn Holloway; Colette Barrere; David D'Cruz; Chanpreet Walia; Felix Naughton; Paul Howard; Stephen Sutton; Caroline Gordon
Journal:  Rheumatol Int       Date:  2020-10-26       Impact factor: 2.631

  8 in total

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