Premium
‘To Suddenly Have a Name for this Thing… Was Wonderful’: The Patient's Experience of Receiving a Diagnosis of Systemic Lupus Erythematosus
Author(s) -
Waldron Nicola,
Brown Sue J.,
Hewlett Sarah,
Elliott Barbara,
McHugh Neil,
McCabe Candy S.
Publication year - 2012
Publication title -
musculoskeletal care
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.628
H-Index - 28
eISSN - 1557-0681
pISSN - 1478-2189
DOI - 10.1002/msc.1010
Subject(s) - medicine , feeling , thematic analysis , systemic lupus erythematosus , health professionals , patient experience , perception , focus group , dermatology , qualitative research , disease , health care , pathology , psychology , social psychology , social science , business , marketing , neuroscience , sociology , economics , economic growth
Objectives The aim of this study was to explore the patient's perception of receiving a diagnosis of systemic lupus erythematosus (lupus) and reports on their experience of the period between onset of symptoms and receiving a definitive diagnosis. Methods Focus groups were conducted in seven rheumatology centres. Forty‐three participants were purposively selected and data were subjected to thematic deductive analysis. Results Focus group data generated three major themes. ‘Diagnostic uncertainty and misdiagnosis’ describes the frustration for many of experiencing years of often debilitating symptoms that have gone unacknowledged by health professionals and misunderstood by themselves. Some experienced the trauma of being misdiagnosed, which impacted on how they adjusted to their final diagnosis of lupus. ‘Consequences of receiving a diagnosis’ highlights the feelings of relief for participants at finally having a diagnosis, despite its implications. However, the manner in which this knowledge was delivered was often inappropriate and unsupported, affecting how they adjusted to future management of their condition. ‘Impact on individuals' lives’ explores how many felt empowered by finally receiving recognition for their symptoms, but the diagnosis of a relatively unknown condition with often invisible symptoms impacted on the response and support they received from those around them. Conclusion It is essential health professionals have a greater understanding of the patient experience prior to receiving a diagnosis of lupus. The individual experience from symptom onset to diagnosis has a direct impact on the patient's subsequent acceptance of their diagnosis and response to management and therefore justifies the need for further research in this field. Copyright © 2012 John Wiley & Sons, Ltd.