The needs of persons with lupus and health care providers: a qualitative study aimed toward the development of the Lupus Interactive Navigator™
| Autor: | Davy Eng, D. Da Costa, Carolyn Neville, Aviña-Zubieta Ja, Paul R. Fortin, Christian A. Pineau, Murray Rochon, Christopher Mill |
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| Rok vydání: | 2013 |
| Předmět: |
Adult
Male Coping (psychology) medicine.medical_specialty Canada Adolescent Health Personnel Allied Health Personnel Grounded theory Young Adult Rheumatology immune system diseases Physicians Health care Outcome Assessment Health Care medicine Humans Lupus Erythematosus Systemic Patient Navigation skin and connective tissue diseases Aged Internet Systemic lupus erythematosus Lupus erythematosus business.industry Focus Groups Middle Aged medicine.disease Focus group Self Care Family medicine Physical therapy Female Outcomes research business Qualitative research |
| Zdroj: | Lupus. 23(2) |
| ISSN: | 1477-0962 |
| Popis: | Objective Systemic lupus erythematosus is an inflammatory autoimmune disease associated with high morbidity and unacceptable mortality. A major challenge for persons with lupus is coping with their illness and complex care. Our objective was to identify the informational and resource needs of persons with lupus, rheumatologists, and allied health professionals treating lupus. Our findings will be applied toward the development of an innovative web-based technology, the Lupus Interactive Navigator (LIN™), to facilitate and support engagement and self-management for persons with lupus. Methods Eight focus groups were conducted: four groups of persons with lupus ( n = 29), three groups of rheumatologists ( n = 20), and one group of allied health professionals ( n = 8). The groups were held in British Columbia, Ontario, and Quebec. All sessions were audio-recorded and transcribed verbatim. Qualitative analysis was performed using grounded theory. The transcripts were reviewed independently and coded by the moderator and co-moderator using 1) qualitative data analysis software developed by Provalis Research, Montreal, Canada, and 2) manual coding. Results Four main themes emerged: 1) specific information and resource needs; 2) barriers to engagement in health care; 3) facilitators of engagement in health care; and 4) tools identified as helpful for the self-management of lupus. Conclusion These findings will help guide the scope of LIN™ with relevant information topics and specific tools that will be most helpful to the diverse needs of persons with lupus and their health care providers. |
| Databáze: | OpenAIRE |
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