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The lived experience of Sjögren’s Syndrome
BACKGROUND: Sjögren’s Syndrome is an autoimmune exocrinopathy characterised by lymphocytic infiltration of exocrine glands in multiple sites, with dry mouth as a primary presenting symptom. Although quantitative studies have shown the negative impact of both dry mouth and Sjögren’s Syndrome on patie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736702/ https://www.ncbi.nlm.nih.gov/pubmed/26831141 http://dx.doi.org/10.1186/s12903-016-0165-4 |
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author | Ngo, Di Ying J. Thomson, William M. Nolan, Anita Ferguson, Shelagh |
author_facet | Ngo, Di Ying J. Thomson, William M. Nolan, Anita Ferguson, Shelagh |
author_sort | Ngo, Di Ying J. |
collection | PubMed |
description | BACKGROUND: Sjögren’s Syndrome is an autoimmune exocrinopathy characterised by lymphocytic infiltration of exocrine glands in multiple sites, with dry mouth as a primary presenting symptom. Although quantitative studies have shown the negative impact of both dry mouth and Sjögren’s Syndrome on patients’ quality of life, no qualitative diary and interview study has been undertaken to examine the lived experience of dry mouth for Sjögren’s Syndrome sufferers. The aim of this qualitative study was to provide clinicians with insight into how dry mouth can impact on the daily lives of Sjögren’s Syndrome patients. METHODS: The American-European Consensus Group (AECG) Revised International Classification criteria were used to identify participants from patients seen in an oral medicine clinic. After pilot study work to test the approach, the 10 main study participants were recruited. Diary entries and semi-structured interviews were used to explore how dry mouth affects their lives. Owing to the exploratory nature of the research, thematic content analysis was applied, allowing the themes to arise naturalistically from the data without bias or elicitation. RESULTS: The data showed that it is unrealistic to understand the experience of a single symptom, but that the disease as a whole needs to be taken into perspective. The empirical evidence supported four main themes that depicted the lived experience of Sjögren’s Syndrome. These included: (1) the journey to diagnosis; (2) disease impact spectrum (of dry mouth amid other symptoms); (3) interactions with healthcare professionals; and (4) the positive coping process. CONCLUSIONS: The findings revealed patients’ perspectives on diagnosis, coping with dry mouth and Sjögren’s Syndrome, and interaction with healthcare professionals. Dry mouth is not a trivial symptom for Sjögren’s Syndrome sufferers; it has considerable impact on their day-to-day lives. Healthcare professionals need to understand patients as individuals in their environment in order to be part of the Sjögren’s journey. |
format | Online Article Text |
id | pubmed-4736702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47367022016-02-03 The lived experience of Sjögren’s Syndrome Ngo, Di Ying J. Thomson, William M. Nolan, Anita Ferguson, Shelagh BMC Oral Health Research Article BACKGROUND: Sjögren’s Syndrome is an autoimmune exocrinopathy characterised by lymphocytic infiltration of exocrine glands in multiple sites, with dry mouth as a primary presenting symptom. Although quantitative studies have shown the negative impact of both dry mouth and Sjögren’s Syndrome on patients’ quality of life, no qualitative diary and interview study has been undertaken to examine the lived experience of dry mouth for Sjögren’s Syndrome sufferers. The aim of this qualitative study was to provide clinicians with insight into how dry mouth can impact on the daily lives of Sjögren’s Syndrome patients. METHODS: The American-European Consensus Group (AECG) Revised International Classification criteria were used to identify participants from patients seen in an oral medicine clinic. After pilot study work to test the approach, the 10 main study participants were recruited. Diary entries and semi-structured interviews were used to explore how dry mouth affects their lives. Owing to the exploratory nature of the research, thematic content analysis was applied, allowing the themes to arise naturalistically from the data without bias or elicitation. RESULTS: The data showed that it is unrealistic to understand the experience of a single symptom, but that the disease as a whole needs to be taken into perspective. The empirical evidence supported four main themes that depicted the lived experience of Sjögren’s Syndrome. These included: (1) the journey to diagnosis; (2) disease impact spectrum (of dry mouth amid other symptoms); (3) interactions with healthcare professionals; and (4) the positive coping process. CONCLUSIONS: The findings revealed patients’ perspectives on diagnosis, coping with dry mouth and Sjögren’s Syndrome, and interaction with healthcare professionals. Dry mouth is not a trivial symptom for Sjögren’s Syndrome sufferers; it has considerable impact on their day-to-day lives. Healthcare professionals need to understand patients as individuals in their environment in order to be part of the Sjögren’s journey. BioMed Central 2016-02-01 /pmc/articles/PMC4736702/ /pubmed/26831141 http://dx.doi.org/10.1186/s12903-016-0165-4 Text en © Ngo et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ngo, Di Ying J. Thomson, William M. Nolan, Anita Ferguson, Shelagh The lived experience of Sjögren’s Syndrome |
title | The lived experience of Sjögren’s Syndrome |
title_full | The lived experience of Sjögren’s Syndrome |
title_fullStr | The lived experience of Sjögren’s Syndrome |
title_full_unstemmed | The lived experience of Sjögren’s Syndrome |
title_short | The lived experience of Sjögren’s Syndrome |
title_sort | lived experience of sjögren’s syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736702/ https://www.ncbi.nlm.nih.gov/pubmed/26831141 http://dx.doi.org/10.1186/s12903-016-0165-4 |
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