Exploring the healthcare journey of patients with rheumatoid arthritis: A mapping project – implications for practice

医学 医疗保健 谈判 护理部 家庭医学 定性研究 医学教育 政治学 社会科学 经济增长 社会学 经济 法学
作者
Susan Oliver
出处
期刊:Musculoskeletal Care [Wiley]
卷期号:6 (4): 247-266 被引量:41
标识
DOI:10.1002/msc.139
摘要

Abstract Objective: Consumers of healthcare can reveal important insights into the personal challenges they experience when negotiating their health needs. The National Rheumatoid Arthritis Society (NRAS) wanted to explore the experiences of those with rheumatoid arthritis (RA) in order to understand the impact on the individual and on healthcare resources and benchmark care against published standards and guidelines. Methods: A project was designed to explore the experiences of individuals with sero‐positive RA who had been diagnosed for three years or less. Qualitative semi‐structured interviews were used and combined with process mapping to explore the experiences of a purposeful sample of individuals with RA. The information generated was mapped and variances explored. Ethical approval was not required as the data were collected outside the National Health Service. Results: Twenty‐two participants' stories were mapped. Fifty per cent of participants sought a medical opinion within three weeks of symptom onset and the majority received a disease‐modifying anti‐rheumatic drug within six months from first presenting symptoms. Work‐related issues were highlighted by 13 participants, and seven of these experienced job losses directly attributed to their diagnosis. Conclusions: This unique mapping approach used qualitative research and process mapping to compare patient experiences against recognized standards and guidelines. These twenty‐two stories reveal important insights into the challenges experienced in negotiating these healthcare journeys and the impact upon the individual as a result of variances in standards of care received. The participants in this study were chiefly self‐motivated, informed and articulate, and did not reflect the broad ethnic, social or cultural diversity in the UK. Limitations must also be considered in relation to perceptions and recall of participants over a three‐year period, as these may have altered over time and illness experience. Copyright © 2008 John Wiley & Sons, Ltd.
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