Diabetes Education: the Experiences of Young Adults with Type 1 Diabetes

被引:10
|
作者
Wiley, Janice [1 ]
Westbrook, Mary [1 ]
Long, Janet [1 ]
Greenfield, Jerry R. [2 ]
Day, Richard O. [3 ]
Braithwaite, Jeffrey [1 ]
机构
[1] Univ New S Wales, Australian Inst Hlth Innovat, Ctr Clin Governance Res Hlth, Sydney, NSW, Australia
[2] Garvan Inst Med Res, Sydney, NSW, Australia
[3] Univ New S Wales, St Vincents Hosp, Dept Clin Pharmacol, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Diabetes education; Endocrinology; Patient-centered care; Patient education; Patient perspective; Qualitative research; Type; 1; diabetes; Young adults; SELF-MANAGEMENT; STRUCTURED EDUCATION; GLYCEMIC CONTROL; INSULIN THERAPY; CARE; CHILDREN; ADOLESCENTS; MELLITUS; OUTCOMES; PROGRAM;
D O I
10.1007/s13300-014-0056-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Clinician-led diabetes education is a fundamental component of care to assist people with Type 1 diabetes (T1D) self-manage their disease. Recent initiatives to incorporate a more patient-centered approach to diabetes education have included recommendations to make such education more individualized. Yet there is a dearth of research that identifies patients' perceptions of clinician-led diabetes education. We aimed to describe the experience of diabetes education from the perspective of young adults with T1D. Methods: We designed a self-reported survey for Australian adults, aged 18-35 years, with T1D. Participants (n = 150) were recruited by advertisements through diabetes consumer-organizations. Respondents were asked to rate aspects of clinician-led diabetes education and identify sources of self-education. To expand on the results of the survey we interviewed 33 respondents in focus groups. Results: Survey: The majority of respondents (56.0%) were satisfied with the amount of continuing clinician-led diabetes education; 96.7% sought further self-education; 73.3% sourced more diabetes education themselves than that provided by their clinicians; 80.7% referred to diabetes organization websites for further education; and 30.0% used online chat-rooms and blogs for education. Focus groups: The three key themes that emerged from the interview data were deficiencies related to the pedagogy of diabetes education; knowledge deficiencies arising from the gap between theoretical diabetes education and practical reality; and the need for and problems associated with autonomous and peer-led diabetes education. Conclusion: Our findings indicate that there are opportunities to improve clinician led-diabetes education to improve patient outcomes by enhancing autonomous health-literacy skills and to incorporate peer-led diabetes education and support with clinician-led education. The results provide evidence for the potential value of patient engagement in quality improvement and health-service redesign.
引用
收藏
页码:299 / 321
页数:23
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