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Gepubliceerd in: Quality of Life Research 5/2015

01-05-2015 | Patient Engagement Special Section

Engaging patients to recover life projectuality: an Italian cross-disease framework

Auteurs: Serena Barello, Guendalina Graffigna

Gepubliceerd in: Quality of Life Research | Uitgave 5/2015

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Abstract

Purpose

Chronic disease is recognized as having a large impact on patient quality of life (QoL), which can be defined as an individual’s satisfaction or happiness with life in domains he or she considers important. Policy makers and clinicians recognize increasingly that patients can safeguard their QoL by making healthy lifestyle choices and being actively engaged in their health care. However, in the emphasis on promoting patient engagement to enhance patients’ QoL, there is no consensus regarding the relationship between QOL and patient engagement, resulting in a lack of shared guidelines among clinicians on interventions. Furthermore, no studies have provided an in-depth exploration of the perspective of patients with chronic conditions who are engaged in their health care and their requirements to achieve an improved QoL. Given this theoretical gap, the present study attempted to explore the patient engagement experience and its relationship with patient QoL in the context of the Italian healthcare system and in relation to different chronic diseases.

Methods

In-depth qualitative interviews on a sample of 99 patients with a wide variety of chronic conditions (heart failure, chronic obstructive pulmonary disease, stroke, diabetes, and cancer).

Results

Patient engagement in health care can be defined as a context-based and cross-disease process that appears to enable patients to recover their life projectuality, which had been impaired by the onset of chronic disease. Successful patient engagement may also be related to a positive shift in the ways in which patients perceive self and life and experience empowerment to realize their life potential, thus improving quality of life. Patient engagement is a powerful concept capable of reflecting significant psychosocial changes that promote patient QoL along the care process. There appears to be theoretical and empirical justification for a broad definition of QoL.

Conclusions

QoL deeply depends on the patient ability to engage in their care and on the health expectations they have. We propose a model of the relation between patient engagement and patients’ trajectories in critical event responses and use it to illustrate a new perspective on QoL. This research showed the heuristic value patient engagement as a is a key concept in the promotion of a patients’ experience-sensitive QoL interventions and assessment measures.
Voetnoten
1
According to the patient engagement model by Graffigna et al. [16, 17], patient engagement is a process featuring four sequential phases. In the phase of “blackout”, patients fall in an initial state of emotional, behavioral and cognitive blackout determined by the critical event, which is described as unexpected and out of their control. In the subsequent phase of “arousal”, patients are hyper attentive to every symptom produced by their body. Symptoms during this phase are perceived as an “alarm bell” that worries the patient and may instigate dysregulated emotional responses. The “adhesion” phase arrives when patients have acquired sufficient knowledge and behavioral skills to effectively adhere to medical prescriptions and feel sufficiently confident in their own emotional strength to cope with their condition. Finally, in the “eudaimonic project” phase, patients have fully accepted their condition and that the patient self is only one of their possible selves. They are also able to recognize internal resources that are useful for projecting satisfactory life trajectories for their future.
 
Literatuur
2.
go back to reference Rothrock, N. E., Hays, R. D., Spritzer, K., Yount, S. E., Riley, W., & Cella, D. (2010). Relative to the general US population, chronic diseases are associated with poorer health-related quality of life as measured by the patient-reported outcomes measurement information system (PROMIS). Journal of Clinical Epidemiology, 63(11), 1195–1204. doi:10.1016/j.jclinepi.2010.04.012.CrossRefPubMedCentralPubMed Rothrock, N. E., Hays, R. D., Spritzer, K., Yount, S. E., Riley, W., & Cella, D. (2010). Relative to the general US population, chronic diseases are associated with poorer health-related quality of life as measured by the patient-reported outcomes measurement information system (PROMIS). Journal of Clinical Epidemiology, 63(11), 1195–1204. doi:10.​1016/​j.​jclinepi.​2010.​04.​012.CrossRefPubMedCentralPubMed
3.
go back to reference Öztürk, A., Şimşek, T. T., Yümin, E. T., Sertel, M., & Yümin, M. (2011). The relationship between physical, functional capacity and quality of life (QoL) among elderly people with a chronic disease. Archives of Gerontology and Geriatrics, 53(3), 278–283. doi:10.1016/j.archger.2010.12.011.CrossRefPubMed Öztürk, A., Şimşek, T. T., Yümin, E. T., Sertel, M., & Yümin, M. (2011). The relationship between physical, functional capacity and quality of life (QoL) among elderly people with a chronic disease. Archives of Gerontology and Geriatrics, 53(3), 278–283. doi:10.​1016/​j.​archger.​2010.​12.​011.CrossRefPubMed
5.
go back to reference Graffigna, G., Vegni, E., Barello, S., Olson, K., & Bosio, C. A. (2011). Studying the social construction of cancer-related fatigue experience: The heuristic value of Ethnoscience. Patient Education and Counseling, 82(3), 402–409. doi:10.1016/j.pec.2010.12.017.CrossRefPubMed Graffigna, G., Vegni, E., Barello, S., Olson, K., & Bosio, C. A. (2011). Studying the social construction of cancer-related fatigue experience: The heuristic value of Ethnoscience. Patient Education and Counseling, 82(3), 402–409. doi:10.​1016/​j.​pec.​2010.​12.​017.CrossRefPubMed
6.
go back to reference Barello, S., Graffigna, G., Lamiani, G., Luciani, A., Vegni, E., Saita, E., et al. (2013). How patients experience and give meaning to their cancer-related fatigue? A qualitative research in the Italian context. International Journal of Social Science Studies, 1(2), 8–19. doi:10.11114/ijsss.v1i2.44.CrossRef Barello, S., Graffigna, G., Lamiani, G., Luciani, A., Vegni, E., Saita, E., et al. (2013). How patients experience and give meaning to their cancer-related fatigue? A qualitative research in the Italian context. International Journal of Social Science Studies, 1(2), 8–19. doi:10.​11114/​ijsss.​v1i2.​44.CrossRef
7.
go back to reference Frisch, M. B. (2014). Quality-of-life-inventory. Encyclopedia of Quality of Life and Well-Being Research, 5374–5377. Frisch, M. B. (2014). Quality-of-life-inventory. Encyclopedia of Quality of Life and Well-Being Research, 5374–5377.
8.
go back to reference Phillips, D. (2012). Quality of life: Concept, policy and practice. Hibbard: Routledge. Phillips, D. (2012). Quality of life: Concept, policy and practice. Hibbard: Routledge.
11.
go back to reference Graffigna, G., Barello, S., Wiederhold, B. K., Bosio, A. C., & Riva, G. (2013). Positive Technology as a Driver for Health Engagement. Annual Review of Cybertherapy and Telemedicine 2013, 9. (A). doi:10.3233/978-1-61499-282-0-9. Graffigna, G., Barello, S., Wiederhold, B. K., Bosio, A. C., & Riva, G. (2013). Positive Technology as a Driver for Health Engagement. Annual Review of Cybertherapy and Telemedicine 2013, 9. (A). doi:10.​3233/​978-1-61499-282-0-9.
12.
go back to reference Barello, S., Graffigna, G.,Meyer, E.C. (2014) Ethics and etiquette in neonatal intensive care. A comment on the value of parents’ engagement in everyday ethics, and recommendations for further advancing the field. JAMA Pediatrics (in press). Barello, S., Graffigna, G.,Meyer, E.C. (2014) Ethics and etiquette in neonatal intensive care. A comment on the value of parents’ engagement in everyday ethics, and recommendations for further advancing the field. JAMA Pediatrics (in press).
13.
go back to reference Graffigna, G., Barello, S., & Riva, G. (2013). How to make health information technology effective: The challenge of patient engagement. Archives of Physical Medicine and Rehabilitation, 94(10), 2034-2035. (B). doi:10.1016/j.apmr.2013.04.024. Graffigna, G., Barello, S., & Riva, G. (2013). How to make health information technology effective: The challenge of patient engagement. Archives of Physical Medicine and Rehabilitation, 94(10), 2034-2035. (B). doi:10.​1016/​j.​apmr.​2013.​04.​024.
14.
go back to reference Wiederhold, B. K., Riva, G., & Graffigna, G. (2013). Ensuring the best care for our increasing aging population: Health engagement and positive technology can help patients achieve a more active role in future healthcare. Cyberpsychology, Behavior, and Social Networking, 16(6), 411–412. doi:10.1089/cyber.2013.1520.CrossRef Wiederhold, B. K., Riva, G., & Graffigna, G. (2013). Ensuring the best care for our increasing aging population: Health engagement and positive technology can help patients achieve a more active role in future healthcare. Cyberpsychology, Behavior, and Social Networking, 16(6), 411–412. doi:10.​1089/​cyber.​2013.​1520.CrossRef
16.
go back to reference Barello, S., Graffigna, G., Vegni, E., Savarese, M., Lombardi, F., & Bosio, A. C. (2014). Engage me in taking care of my heart”: A grounded theory study on patient–cardiologist relationship in the hospital management of heart failure BMJ Open (in press). Barello, S., Graffigna, G., Vegni, E., Savarese, M., Lombardi, F., & Bosio, A. C. (2014). Engage me in taking care of my heart”: A grounded theory study on patient–cardiologist relationship in the hospital management of heart failure BMJ Open (in press).
17.
go back to reference Graffigna, G., Barello, S., Libreri, C., & Bosio, C. A. (2014). How to engage type-2 diabetic patients in their own health management: implications for clinical practice. BMC Public Health, 14(1), 648.CrossRefPubMedCentralPubMed Graffigna, G., Barello, S., Libreri, C., & Bosio, C. A. (2014). How to engage type-2 diabetic patients in their own health management: implications for clinical practice. BMC Public Health, 14(1), 648.CrossRefPubMedCentralPubMed
18.
go back to reference Barello, S., Graffigna, G., Savarese, M., & Bosio, A. C. (2014). Engaging patients in health management: Towards a preliminary theoretical conceptualization. Psicologia della Salute (in press). Barello, S., Graffigna, G., Savarese, M., & Bosio, A. C. (2014). Engaging patients in health management: Towards a preliminary theoretical conceptualization. Psicologia della Salute (in press).
19.
go back to reference Graffigna, G., Barello, S., Triberti, S., Wiederhold, B. K., Bosio, A. C., Riva, G. (2014). Enabling eHealth as a pathway for patient engagement: A toolkit for medical practice. Cyberpsychology, Behavior, and Social Networking (submitted). Graffigna, G., Barello, S., Triberti, S., Wiederhold, B. K., Bosio, A. C., Riva, G. (2014). Enabling eHealth as a pathway for patient engagement: A toolkit for medical practice. Cyberpsychology, Behavior, and Social Networking (submitted).
20.
go back to reference Wagner, E. H., Austin, B. T., Davis, C., Hindmarsh, M., Schaefer, J., & Bonomi, A. (2001). Improving chronic illness care: Translating evidence into action. Health Affairs (Millwood), 20, 64–78.CrossRef Wagner, E. H., Austin, B. T., Davis, C., Hindmarsh, M., Schaefer, J., & Bonomi, A. (2001). Improving chronic illness care: Translating evidence into action. Health Affairs (Millwood), 20, 64–78.CrossRef
23.
go back to reference Gibbs, G. R. (2002). Qualitative data analysis: Explorations with NVivo. Open University. Gibbs, G. R. (2002). Qualitative data analysis: Explorations with NVivo. Open University.
24.
go back to reference Morse, J. M., Barrett, M., Mayan, M., Olson, K., & Spiers, J. (2002). Verification strategies for establishing reliability and validity in qualitative research. International Journal of Qualitative Methods, 1(2). Morse, J. M., Barrett, M., Mayan, M., Olson, K., & Spiers, J. (2002). Verification strategies for establishing reliability and validity in qualitative research. International Journal of Qualitative Methods, 1(2).
26.
go back to reference Carr, A. J., Gibson, B., & Robinson, P. G. (2001). Is quality of life determined by expectations or experience? British Medical Journal, 322(7296), 1240–1243.CrossRefPubMedCentralPubMed Carr, A. J., Gibson, B., & Robinson, P. G. (2001). Is quality of life determined by expectations or experience? British Medical Journal, 322(7296), 1240–1243.CrossRefPubMedCentralPubMed
27.
go back to reference Park, C. L. (2010). Making sense of the meaning literature: An integrative review of meaning making and its effects on adjustment to stressful life events. Psychological Bulletin, 136(2), 257. doi:10.1037/a0018301.CrossRefPubMed Park, C. L. (2010). Making sense of the meaning literature: An integrative review of meaning making and its effects on adjustment to stressful life events. Psychological Bulletin, 136(2), 257. doi:10.​1037/​a0018301.CrossRefPubMed
28.
go back to reference Theofilou, P. (2012). Health-related quality of life and illness perceptions in patients with chronic obstructive pulmonary disease. Journal of Pulmonary & Respiratory Medicine. doi:10.4172/2161-105X.1000e103. Theofilou, P. (2012). Health-related quality of life and illness perceptions in patients with chronic obstructive pulmonary disease. Journal of Pulmonary & Respiratory Medicine. doi:10.​4172/​2161-105X.​1000e103.
29.
go back to reference Bury, M., & Gabe, J. (Eds.). (2013). The sociology of health and illness: A reader. London: Routledge. Bury, M., & Gabe, J. (Eds.). (2013). The sociology of health and illness: A reader. London: Routledge.
31.
go back to reference Ahmed, S., Mayo, N. E., Corbiere, M., Wood-Dauphinee, S., Hanley, J., & Cohen, R. (2005). Change in quality of life of people with stroke over time: true change or response shift? Quality of Life Research, 14, 611–627.CrossRefPubMed Ahmed, S., Mayo, N. E., Corbiere, M., Wood-Dauphinee, S., Hanley, J., & Cohen, R. (2005). Change in quality of life of people with stroke over time: true change or response shift? Quality of Life Research, 14, 611–627.CrossRefPubMed
32.
go back to reference Schwartz, C. E., Sprangers, M. A. G., Carey, A., & Reed, G. (2004). Exploring response shift in longitudinal data. Psychology & Health, 19, 51–69.CrossRef Schwartz, C. E., Sprangers, M. A. G., Carey, A., & Reed, G. (2004). Exploring response shift in longitudinal data. Psychology & Health, 19, 51–69.CrossRef
33.
go back to reference Sprangers, M. A. G., van Dam, F. S. A. M., Broersen, J., et al. (1999). Revealing response shift in longitudinal research on fatigue. The use of the thentest approach. Acta Oncologica, 38, 709–718.CrossRefPubMed Sprangers, M. A. G., van Dam, F. S. A. M., Broersen, J., et al. (1999). Revealing response shift in longitudinal research on fatigue. The use of the thentest approach. Acta Oncologica, 38, 709–718.CrossRefPubMed
34.
go back to reference Schwartz, C. E., & Rapkin, B. D. (2004). Reconsidering the psychometrics of quality of life assessment in light of response shift and appraisal. Health and Quality of Life Outcomes, 2(1), 16.CrossRefPubMedCentralPubMed Schwartz, C. E., & Rapkin, B. D. (2004). Reconsidering the psychometrics of quality of life assessment in light of response shift and appraisal. Health and Quality of Life Outcomes, 2(1), 16.CrossRefPubMedCentralPubMed
35.
go back to reference Rapkin, B. D., & Schwartz, C. E. (2004). Toward a theoretical model of quality-of-life appraisal: Implications of findings from studies of response shift. Health and Quality of Life Outcomes, 2(1), 14.CrossRefPubMedCentralPubMed Rapkin, B. D., & Schwartz, C. E. (2004). Toward a theoretical model of quality-of-life appraisal: Implications of findings from studies of response shift. Health and Quality of Life Outcomes, 2(1), 14.CrossRefPubMedCentralPubMed
36.
go back to reference Schwartz, C. E., Bode, R., Repucci, N., Becker, J., Sprangers, M. A., & Fayers, P. M. (2006). The clinical significance of adaptation to changing health: A meta-analysis of response shift. Quality of Life Research, 15(9), 1533–1550.CrossRefPubMed Schwartz, C. E., Bode, R., Repucci, N., Becker, J., Sprangers, M. A., & Fayers, P. M. (2006). The clinical significance of adaptation to changing health: A meta-analysis of response shift. Quality of Life Research, 15(9), 1533–1550.CrossRefPubMed
37.
go back to reference Sharpe, L., Butow, P., Smith, C., McConnell, D., & Clarke, S. (2005). Changes in quality of life in patients with advanced cancer: evidence of response shift and response restriction. Journal of Psychosomatic Research, 58(6), 497–504.CrossRefPubMed Sharpe, L., Butow, P., Smith, C., McConnell, D., & Clarke, S. (2005). Changes in quality of life in patients with advanced cancer: evidence of response shift and response restriction. Journal of Psychosomatic Research, 58(6), 497–504.CrossRefPubMed
38.
go back to reference WHOQOL group. (1995). The World Health Organization quality of life assessment (WHOQOL): Position paper from the World Health Organization. Social Science and Medicine, 41(10), 1403–1409.CrossRef WHOQOL group. (1995). The World Health Organization quality of life assessment (WHOQOL): Position paper from the World Health Organization. Social Science and Medicine, 41(10), 1403–1409.CrossRef
Metagegevens
Titel
Engaging patients to recover life projectuality: an Italian cross-disease framework
Auteurs
Serena Barello
Guendalina Graffigna
Publicatiedatum
01-05-2015
Uitgeverij
Springer International Publishing
Gepubliceerd in
Quality of Life Research / Uitgave 5/2015
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-014-0846-x

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