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Using the life course perspective to study the entry into the illness trajectory: The perspective of caregivers of people with Alzheimer's disease

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  • Carpentier, Normand
  • Bernard, Paul
  • Grenier, Amanda
  • Guberman, Nancy

Abstract

The research community is showing increasing interest in the analysis of the care trajectory of people with chronic health problems, especially dementias such as Alzheimer's disease. However, despite this interest, there is little research on the initial phases of the care trajectory. The fact that the first symptoms of dementia are generally noticed by those surrounding the elderly person suggests that the recognition of the disease is intimately linked to interactions not only amongst family members but also amongst friends, neighbours and health professionals. This study focuses on the period beginning with the first manifestations of cognitive difficulties and ending with the diagnosis of Alzheimer-type dementia. Interviews with 60 caregivers in Montreal, Canada were used to reconstruct how older people with Alzheimer-type dementia enter into the care trajectory. Our methods consisted of the analysis of social networks, social dynamics and action sequences. Our findings are presented in the form of a typology comprised of 5 pathways of entries into the care trajectory that are structured around the following four principles of the Life Course Perspective: family history, linked lives, human agency and organisational effects. We believe that analyses of the initial phases of the care trajectory, such as this one, are essential for the application of effective early detection and intervention policies. They are also central to informing future studies that seek to understand the care experience in its entirety.

Suggested Citation

  • Carpentier, Normand & Bernard, Paul & Grenier, Amanda & Guberman, Nancy, 2010. "Using the life course perspective to study the entry into the illness trajectory: The perspective of caregivers of people with Alzheimer's disease," Social Science & Medicine, Elsevier, vol. 70(10), pages 1501-1508, May.
  • Handle: RePEc:eee:socmed:v:70:y:2010:i:10:p:1501-1508
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    References listed on IDEAS

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    1. Birditt, Kira & Antonucci, Toni C., 2008. "Life sustaining irritations? Relationship quality and mortality in the context of chronic illness," Social Science & Medicine, Elsevier, vol. 67(8), pages 1291-1299, October.
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    Cited by:

    1. Altomonte, Guillermina, 2022. "Coordinating illness and insurance trajectories: Evidence from a post-acute care unit," Social Science & Medicine, Elsevier, vol. 308(C).
    2. Rapp, Thomas & Apouey, Bénédicte H. & Senik, Claudia, 2018. "The impact of institution use on the wellbeing of Alzheimer's disease patients and their caregivers," Social Science & Medicine, Elsevier, vol. 207(C), pages 1-10.
    3. Wyke, Sally & Adamson, Joy & Dixon, Diane & Hunt, Kate, 2013. "Consultation and illness behaviour in response to symptoms: A comparison of models from different disciplinary frameworks and suggestions for future research directions," Social Science & Medicine, Elsevier, vol. 86(C), pages 79-87.
    4. Super, Sabina & Verkooijen, Kirsten & Koelen, Maria, 2021. "A salutogenic perspective on sport-for-development research," Social Science & Medicine, Elsevier, vol. 268(C).
    5. Munson, Michelle R. & Jaccard, James & Smalling, Susan E. & Kim, Hyunsoo & Werner, James J. & Scott, Lionel D., 2012. "Static, dynamic, integrated, and contextualized: A framework for understanding mental health service utilization among young adults," Social Science & Medicine, Elsevier, vol. 75(8), pages 1441-1449.
    6. Smith, Robert Courtney, 2021. "Analytic autoethnography of familial and institutional social identity construction of My Dad with Alzheimer's: In the emergency room with Erving Goffman and Oliver Sacks," Social Science & Medicine, Elsevier, vol. 277(C).
    7. Rapp, Thomas, 2014. "Patients' diagnosis decisions in Alzheimer's disease: The influence of family factors," Social Science & Medicine, Elsevier, vol. 118(C), pages 9-16.

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