What is important for you? A qualitative interview study of living with diabetes and experiences of diabetes care to establish a basis for a tailored Patient-Reported Outcome Measure for the Swedish National Diabetes Register

Maria Svedbo Engström, Janeth Leksell, Unn-Britt Johansson, Soffia Gudbjörnsdottir, Maria Svedbo Engström, Janeth Leksell, Unn-Britt Johansson, Soffia Gudbjörnsdottir

Abstract

Objectives: There is a growing emphasis on the perspective of individuals living with diabetes and the need for a more person-centred diabetes care. At present, the Swedish National Diabetes Register (NDR) lacks patient-reported outcome measures (PROMs) based on the perspective of the patient. As a basis for a new PROM, the aim of this study was to describe important aspects in life for adult individuals with diabetes.

Design: Semistructured qualitative interviews analysed using content analysis.

Setting: Hospital-based outpatient clinics and primary healthcare clinics in Sweden.

Participants: 29 adults with type 1 diabetes mellitus (DM) (n=15) and type 2 DM (n=14).

Inclusion criteria: Swedish adults (≥ 18 years) living with type 1 DM or type 2 DM (duration ≥ 5 years) able to describe their situation in Swedish. Purposive sampling generated heterogeneous characteristics.

Results: To live a good life with diabetes is demanding for the individual, but experienced barriers can be eased by support from others in the personal sphere, and by professional support from diabetes care. Diabetes care was a crucial resource to nurture the individual's ability and knowledge to manage diabetes, and to facilitate life with diabetes by supplying support, guidance, medical treatment and technical devices tailored to individual needs. The analysis resulted in the overarching theme 'To live a good life with diabetes' constituting the two main categories 'How I feel and how things are going with my diabetes' and 'Support from diabetes care in managing diabetes' including five different categories.

Conclusions: Common aspects were identified including the experience of living with diabetes and support from diabetes care. These will be used to establish a basis for a tailored PROM for the NDR.

Keywords: QUALITATIVE RESEARCH.

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

References

    1. International Diabetes Federation. IDF DIABETES ATLAS 2014 update poster. Secondary IDF DIABETES ATLAS 2014 update poster 2014.
    1. Eeg-Olofsson K, Cederholm J, Nilsson PM et al. . New aspects of HbA1c as a risk factor for cardiovascular diseases in type 2 diabetes: an observational study from the Swedish National Diabetes Register (NDR). J Intern Med 2010;268:471–82. 10.1111/j.1365-2796.2010.02265.x
    1. Lind M, Svensson AM, Kosiborod M et al. . Glycemic control and excess mortality in type 1 diabetes. N Engl J Med 2014;371:1972–82. 10.1056/NEJMoa1408214
    1. Roy T, Lloyd CE. Epidemiology of depression and diabetes: a systematic review. J Affect Disord 2012;142(Suppl):S8–21. 10.1016/S0165-0327(12)70004-6
    1. McKnight JA, Wild SH, Lamb MJ et al. . Glycaemic control of type 1 diabetes in clinical practice early in the 21st century: an international comparison. Diabet Med 2015;32:1036–50. 10.1111/dme.12676
    1. Ahola AJ, Groop PH. Barriers to self-management of diabetes. Diabet Med 2013;30:413–20. 10.1111/dme.12105
    1. Barendse S, Singh H, Frier BM et al. . The impact of hypoglycaemia on quality of life and related patient-reported outcomes in type 2 diabetes: a narrative review. Diabet Med 2012;29:293–302. 10.1111/j.1464-5491.2011.03416.x
    1. Barnard KD, Peyrot M, Holt RI. Psychosocial support for people with diabetes: past, present and future. Diabet Med 2012;29:1358–60. 10.1111/j.1464-5491.2012.03727.x
    1. Chen CM, Chang Yeh M. The experiences of diabetics on self-monitoring of blood glucose: a qualitative metasynthesis. J Clin Nurs 2015;24:614–26. 10.1111/jocn.12691
    1. Frost J, Garside R, Cooper C et al. . A qualitative synthesis of diabetes self-management strategies for long term medical outcomes and quality of life in the UK. BMC Health Serv Res 2014;14:348 10.1186/1472-6963-14-348
    1. Gask L, Macdonald W, Bower P. What is the relationship between diabetes and depression? A qualitative meta-synthesis of patient experience of co-morbidity. Chronic Illn 2011;7:239–52.
    1. Gomersall T, Madill A, Summers LK. A metasynthesis of the self-management of type 2 diabetes. Qual Health Res 2011;21:853–71. 10.1177/1049732311402096
    1. Ho AY, Berggren I, Dahlborg-Lyckhage E. Diabetes empowerment related to Pender's Health Promotion Model: a meta-synthesis. Nurs Health Sci 2010;12:259–67. 10.1111/j.1442-2018.2010.00517.x
    1. IDF Clinical Guidelines Task Force. Global guideline for type 2: diabetes. Brussels: International Diabetes Federation, 2005.
    1. Nicolucci A, Kovacs Burns K, Holt RI et al. . Diabetes Attitudes, Wishes and Needs second study (DAWN2): cross-national benchmarking of diabetes-related psychosocial outcomes for people with diabetes. Diabet Med 2013;30:767–77. 10.1111/dme.12245
    1. Paterson BL, Thorne S, Dewis M. Adapting to and managing diabetes. Image J Nurs Sch 1998;30:57–62. 10.1111/j.1547-5069.1998.tb01237.x
    1. Wilkinson A, Whitehead L, Ritchie L. Factors influencing the ability to self-manage diabetes for adults living with type 1 or 2 diabetes. Int J Nurs Stud 2014;51:111–22. 10.1016/j.ijnurstu.2013.01.006
    1. Rankin D, Barnard K, Elliott J et al. . Type 1 diabetes patients' experiences of, and need for, social support after attending a structured education programme: a qualitative longitudinal investigation. J Clin Nurs 2014;23:2919–27. 10.1111/jocn.12539
    1. Rankin D, Cooke DD, Elliott J et al. . Supporting self-management after attending a structured education programme: a qualitative longitudinal investigation of type 1 diabetes patients' experiences and views. BMC Public Health 2012;12:652 10.1186/1471-2458-12-652
    1. Rankin D, Cooke DD, Heller S et al. . Experiences of using blood glucose targets when following an intensive insulin regimen: a qualitative longitudinal investigation involving patients with type 1 diabetes. Diabet Med 2012;29:1079–84. 10.1111/j.1464-5491.2012.03670.x
    1. Rankin D, Elliott J, Heller S et al. . Experiences of hypoglycaemia unawareness amongst people with type 1 diabetes: a qualitative investigation. Chronic Illn 2014;10:180–91. 10.1177/1742395313513911
    1. Rankin D, Heller S, Lawton J. Understanding information and education gaps among people with type 1 diabetes: a qualitative investigation. Patient Educ Couns 2011;83:87–91. 10.1016/j.pec.2010.04.026
    1. Bramberg EB, Dahlborg-Lyckhage E, Maatta S. Lack of individualized perspective: a qualitative study of diabetes care for immigrants in Sweden. Nurs Health Sci 2012;14:244–9. 10.1111/j.1442-2018.2012.00684.x
    1. Oftedal B, Karlsen B, Bru E. Perceived support from healthcare practitioners among adults with type 2 diabetes. J Adv Nurs 2010;66:1500–9. 10.1111/j.1365-2648.2010.05329.x
    1. Svenningsson I, Gedda B, Marklund B. Experiences of the encounter with the diabetes team-a comparison between obese and normal-weight type 2 diabetic patients. Patient Educ Couns 2011;82:58–62. 10.1016/j.pec.2010.04.003
    1. Gunn KL, Seers K, Posner N et al. . ‘Somebody there to watch over you’: the role of the family in everyday and emergency diabetes care. Health Soc Care Community 2012;20:591–8. 10.1111/j.1365-2524.2012.01073.x
    1. Garmo A, Hornsten A, Leksell J. ‘The pump was a saviour for me.’ Patients' experiences of insulin pump therapy. Diabet Med 2013;30:717–23. 10.1111/dme.12155
    1. Lawton J, Kirkham J, Rankin D et al. . Perceptions and experiences of using automated bolus advisors amongst people with type 1 diabetes: a longitudinal qualitative investigation. Diabetes Res Clin Pract 2014;106:443–50. 10.1016/j.diabres.2014.09.011
    1. Lawton J, Rankin D, Cooke D et al. . Patients' experiences of adjusting insulin doses when implementing flexible intensive insulin therapy: a longitudinal, qualitative investigation. Diabetes Res Clin Pract 2012;98:236–42. 10.1016/j.diabres.2012.09.024
    1. Lawton J, Rankin D, Cooke DD et al. . Self-treating hypoglycaemia: a longitudinal qualitative investigation of the experiences and views of people with type 1 diabetes. Diabet Med 2013;30:209–15. 10.1111/dme.12007
    1. Peel E, Douglas M, Parry O et al. . Type 2 diabetes and dog walking: patients' longitudinal perspectives about implementing and sustaining physical activity. Br J Gen Pract 2010;60:570–7. 10.3399/bjgp10X515061
    1. Peel E, Douglas M, Lawton J. Self monitoring of blood glucose in type 2 diabetes: longitudinal qualitative study of patients' perspectives. BMJ 2007;335:493 10.1136/
    1. Mathew R, Gucciardi E, De Melo M et al. . Self-management experiences among men and women with type 2 diabetes mellitus: a qualitative analysis. BMC Fam Pract 2012;13:122 10.1186/1471-2296-13-122
    1. Brod M, Pohlman B, Wolden M et al. . Non-severe nocturnal hypoglycemic events: experience and impacts on patient functioning and well-being. Qual Life Res 2013;22:997–1004. 10.1007/s11136-012-0234-3
    1. Kneck A, Klang B, Fagerberg I. Learning to live with illness: experiences of persons with recent diagnoses of diabetes mellitus. Scand J Caring Sci 2011;25:558–66. 10.1111/j.1471-6712.2010.00864.x
    1. Kneck A, Klang B, Fagerberg I. Learning to live with diabetes—integrating an illness or objectifying a disease. J Adv Nurs 2012;68:2486–95. 10.1111/j.1365-2648.2012.05947.x
    1. Kneck A, Fagerberg I, Eriksson LE et al. . Living with diabetes—development of learning patterns over a 3-year period. Int J Qual Stud Health Well-being 2014;9:24375 10.3402/qhw.v9.24375
    1. Barnard KD, Lloyd CE, Dyson PA et al. . Kaleidoscope model of diabetes care: time for a rethink? Diabet Med 2014;31:522–30. 10.1111/dme.12400
    1. Coulter A, Entwistle VA, Eccles A et al. . Personalised care planning for adults with chronic or long-term health conditions. Cochrane Database Syst Rev 2015;3:CD010523 10.1002/14651858.CD010523.pub2
    1. American Diabetes Association Standards of medical care in diabetes—2015: summary of revisions. Diabetes Care 2015;38(Suppl):S4 10.2337/dc15-S003
    1. Glasgow RE, Peeples M, Skovlund SE. Where is the patient in diabetes performance measures? The case for including patient-centered and self-management measures. Diabetes Care 2008;31:1046–50.
    1. Jones A, Vallis M, Pouwer F. If it does not significantly change HbA1c levels why should we waste time on it? A plea for the prioritization of psychological well-being in people with diabetes. Diabet Med 2015;32:155–63. 10.1111/dme.12620
    1. Eliasson B, Gudbjornsdottir S. Diabetes care—improvement through measurement. Diabetes Res Clin Pract 2014;106(Suppl 2):S291–4. 10.1016/S0168-8227(14)70732-6
    1. Calvert M, Blazeby J, Altman DG et al. . Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension. JAMA 2013;309:814–22. 10.1001/jama.2013.879
    1. Amsberg S, Wredling R, Lins PE et al. . The psychometric properties of the Swedish version of the Problem Areas in Diabetes Scale (Swe-PAID-20): scale development. Int J Nurs Stud 2008;45:1319–28. 10.1016/j.ijnurstu.2007.09.010
    1. Anderbro T, Amsberg S, Wredling R et al. . Psychometric evaluation of the Swedish version of the Hypoglycaemia Fear Survey. Patient Educ Couns 2008;73:127–31. 10.1016/j.pec.2008.03.022
    1. Eigenmann CA, Colagiuri R, Skinner TC et al. . Are current psychometric tools suitable for measuring outcomes of diabetes education? Diabet Med 2009;26:425–36. 10.1111/j.1464-5491.2009.02697.x
    1. El Achhab Y, Nejjari C, Chikri M et al. . Disease-specific health-related quality of life instruments among adults diabetic: a systematic review. Diabetes Res Clin Pract 2008;80:171–84. 10.1016/j.diabres.2007.12.020
    1. Garratt AM, Schmidt L, Fitzpatrick R. Patient-assessed health outcome measures for diabetes: a structured review. Diabet Med 2002;19:1–11. 10.1046/j.1464-5491.2002.00650.x
    1. Gibbons E, Fitzpatrick R. Patient Reported Outcome Measurement Group. A structured review of patient-reported outcome measures (PROMs) for diabetes. University of Oxford, 2009.
    1. Leksell J, Funnell M, Sandberg G et al. . Psychometric properties of the Swedish Diabetes Empowerment Scale. Scand J Caring Sci 2007;21:247–52. 10.1111/j.1471-6712.2007.00463.x
    1. Speight J, Reaney MD, Barnard KD. Not all roads lead to Rome—a review of quality of life measurement in adults with diabetes. Diabet Med 2009;26:315–27.
    1. Wikblad K, Smide B, Leksell JK. Check your health validity and reliability of a measure of health and burden of diabetes. Scand J Caring Sci 2014;28:139–45. 10.1111/scs.12042
    1. Wikblad KF, Wibell LB, Montin KR. The patient's experience of diabetes and its treatment: construction of an attitude scale by a semantic differential technique. J Adv Nurs 1990;15:1083–91. 10.1111/j.1365-2648.1990.tb01990.x
    1. Wredling R, Stalhammar J, Adamson U et al. . Well-being and treatment satisfaction in adults with diabetes: a Swedish population-based study. Qual Life Res 1995;4:515–22. 10.1007/BF00634746
    1. Peyrot M, Burns KK, Davies M et al. . Diabetes Attitudes Wishes and Needs 2 (DAWN2): a multinational, multi-stakeholder study of psychosocial issues in diabetes and person-centred diabetes care. Diabetes Res Clin Pract 2013;99:174–84. 10.1016/j.diabres.2012.11.016
    1. Borg S, Palaszewski B, Gerdtham UG et al. . Patient-reported outcome measures and risk factors in a quality registry: a basis for more patient-centered diabetes care in Sweden. Int J Environ Res Public Health 2014;11:12223–46. 10.3390/ijerph111212223
    1. Streiner DL, Norman GR. Health measurement scales: a practical guide to their development and use. Oxford: Oxford University Press, 2008.
    1. Patrick DL, Burke LB, Gwaltney CJ et al. . Content validity—establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO good research practices task force report: part 1—eliciting concepts for a new PRO instrument. Value Health 2011;14:967–77. 10.1016/j.jval.2011.06.014
    1. Food and Drug Administration. Guidance for industry patient reported outcome measures: use in medical product development to support labeling claims. U.S. Department of Health and Human Services, 2009.
    1. Nussbaum MC, Sen AK. The quality of life. Oxford: Clarendon Press, 1993.
    1. Robeyns I. Sen's capability approach and gender inequality: selecting relevant capabilities. Feminist Econ 2003;9:61–92. 10.1080/1354570022000078024
    1. Alkire S. Why the capability approach? J Hum Dev 2005;6: 115–33. 10.1080/146498805200034275
    1. Robeyns I. Selecting capabilities for quality of life measurement. Soc Indicators Res 2005;74:191–215. 10.1007/s11205-005-6524-1
    1. Sen A. Human rights and capabilities. J Hum Dev 2005;6:151–66. 10.1080/14649880500120491
    1. Polit DF, Beck CT. Nursing research: generating and assessing evidence for nursing practice. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins, 2012.
    1. Graneheim UH, Lundman B. Qualitative content analysis in nursing research: concepts, procedures and measures to achieve trustworthiness. Nurse Educ Today 2004;24:105–12. 10.1016/j.nedt.2003.10.001
    1. Campbell R, Pound P, Pope C et al. . Evaluating meta-ethnography: a synthesis of qualitative research on lay experiences of diabetes and diabetes care. Soc Sci Med 2003;56:671–84. 10.1016/S0277-9536(02)00064-3
    1. Howell D, Molloy S, Wilkinson K et al. . Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors. Ann Oncol 2015;26:1846–58. 10.1093/annonc/mdv181
    1. Ekman I, Swedberg K, Taft C et al. . Person-centered care—ready for prime time. Eur J Cardiovasc Nurs 2011;10:248–51. 10.1016/j.ejcnurse.2011.06.008
    1. Ivers N, Jamtvedt G, Flottorp S et al. . Audit and feedback: effects on professional practice and healthcare outcomes. Cochrane Database Syst Rev 2012;6:CD000259 10.1002/14651858.CD000259.pub3
    1. Boyce MB, Browne JP. Does providing feedback on patient-reported outcomes to healthcare professionals result in better outcomes for patients? A systematic review. Qual Life Res 2013;22:2265–78. 10.1007/s11136-013-0390-0
    1. Kotronoulas G, Kearney N, Maguire R et al. . What is the value of the routine use of patient-reported outcome measures toward improvement of patient outcomes, processes of care, and health service outcomes in cancer care? A systematic review of controlled trials. J Clin Oncol 2014;32:1480–501.
    1. Mesbah M, Kreiner S, Christensen KB. Rasch models in health. London: Wiley, 2013.
    1. Robeyns I. The Capability Approach in Practice*. J Polit Philos 2006;14:351–76. 10.1111/j.1467-9760.2006.00263.x
    1. Sveriges framtida befolkning 2015-2060 [Elektronisk resurs]: Statistiska centralbyrån, 2015.

Source: PubMed

3
Subscribe