IDEAS home Printed from https://ideas.repec.org/a/eee/socmed/v70y2010i7p1035-1041.html
   My bibliography  Save this article

Which carers of family members at the end of life need more support from health services and why?

Author

Listed:
  • McNamara, Beverley
  • Rosenwax, Lorna

Abstract

With end of life care a national priority in many countries, and the main place of care the family home, informal family carers are now considered the frontline of primary care. Yet we are insufficiently informed about the needs of carers, both during the time of caring and during bereavement. This study identifies which carers believed they did not get enough support from health services when caring for a terminally ill family member, what factors influenced perceptions of support, and whether inadequate support influenced the carer's health following the death of a family member. Unlike previous survey designs that explore end-of-life concerns, we were able to triangulate interview data from semi-structured telephone interviews (August 2005-June 2006) with a relatively large group of 1071 carers in Western Australia, with administrative records from death registrations, hospital morbidity and community care records from the 1071 deceased family members. The addition of administrative data allowed us to quantify hospital and community care service use. Data analysis consisted of summary statistics and logistic regressions for two groups of carers during the first few months of bereavement: those whose health got a bit/lot worse, and those who were not coping on most/all days. We found that carers were more likely to have poor health if they perceived they did not get enough support from health services and if the deceased family member did not die in the carer's preferred place of death. Additionally, carers were more likely to be not coping if they were aged 60 years or less, female, had lost a spouse/partner and the deceased family member did not die in the carer's preferred place. By identifying which carers are more vulnerable than others, carer education and practical support can be targeted to specific groups. Ideally resources for bereavement support should be extended into the months following the relative's death.

Suggested Citation

  • McNamara, Beverley & Rosenwax, Lorna, 2010. "Which carers of family members at the end of life need more support from health services and why?," Social Science & Medicine, Elsevier, vol. 70(7), pages 1035-1041, April.
  • Handle: RePEc:eee:socmed:v:70:y:2010:i:7:p:1035-1041
    as

    Download full text from publisher

    File URL: http://www.sciencedirect.com/science/article/pii/S0277-9536(09)00845-4
    Download Restriction: Full text for ScienceDirect subscribers only
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    References listed on IDEAS

    as
    1. Exley, Catherine & Allen, Davina, 2007. "A critical examination of home care: End of life care as an illustrative case," Social Science & Medicine, Elsevier, vol. 65(11), pages 2317-2327, December.
    2. O'Reilly, Dermot & Connolly, Sheelah & Rosato, Michael & Patterson, Chris, 2008. "Is caring associated with an increased risk of mortality? A longitudinal study," Social Science & Medicine, Elsevier, vol. 67(8), pages 1282-1290, October.
    3. Grov, Ellen Karine & Fosså, Sophie D. & Sørebø, Øystein & Dahl, Alv A., 2006. "Primary caregivers of cancer patients in the palliative phase: A path analysis of variables influencing their burden," Social Science & Medicine, Elsevier, vol. 63(9), pages 2429-2439, November.
    4. Moorin, Rachael Elizabeth & Holman, Cashel D'Arcy James, 2008. "The cost of in-patient care in Western Australia in the last years of life: A population-based data linkage study," Health Policy, Elsevier, vol. 85(3), pages 380-390, March.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Terence V McCann & John Bamberg, 2016. "Carers of older adults' satisfaction with public mental health service clinicians: a qualitative study," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(11-12), pages 1634-1643, June.

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Giesbrecht, Melissa & Crooks, Valorie A. & Castleden, Heather & Schuurman, Nadine & Skinner, Mark & Williams, Allison, 2016. "Palliating inside the lines: The effects of borders and boundaries on palliative care in rural Canada," Social Science & Medicine, Elsevier, vol. 168(C), pages 273-282.
    2. Lowton, Karen, 2009. "'A bed in the middle of nowhere': Parents' meanings of place of death for adults with cystic fibrosis," Social Science & Medicine, Elsevier, vol. 69(7), pages 1056-1062, October.
    3. Kaschowitz, Judith & Brandt, Martina, 2017. "Health effects of informal caregiving across Europe: A longitudinal approach," Social Science & Medicine, Elsevier, vol. 173(C), pages 72-80.
    4. Claudia Geue & Paula Lorgelly & James Lewsey & Carole Hart & Andrew Briggs, 2015. "Hospital Expenditure at the End-of-Life: What Are the Impacts of Health Status and Health Risks?," PLOS ONE, Public Library of Science, vol. 10(3), pages 1-14, March.
    5. Rapp, Thomas & Grand, Alain & Cantet, Christelle & Andrieu, Sandrine & Coley, Nicola & Portet, Florence & Vellas, Bruno, 2011. "Public financial support receipt and non-medical resource utilization in Alzheimer's disease results from the PLASA study," Social Science & Medicine, Elsevier, vol. 72(8), pages 1310-1316, April.
    6. Claudia Geue & Andrew Briggs & James Lewsey & Paula Lorgelly, 2014. "Population ageing and healthcare expenditure projections: new evidence from a time to death approach," The European Journal of Health Economics, Springer;Deutsche Gesellschaft für Gesundheitsökonomie (DGGÖ), vol. 15(8), pages 885-896, November.
    7. Rebecca E Lacey & Anne McMunn & Elizabeth Webb, 2018. "Informal caregiving and markers of adiposity in the UK Household Longitudinal Study," PLOS ONE, Public Library of Science, vol. 13(7), pages 1-15, July.
    8. Miyawaki, Atsushi & Tanaka, Hirokazu & Kobayashi, Yasuki & Kawachi, Ichiro, 2019. "Informal caregiving and mortality―Who is protected and who is not? A prospective cohort study from Japan," Social Science & Medicine, Elsevier, vol. 223(C), pages 24-30.
    9. Cohen-Mansfield, Jiska & Brill, Shai, 2016. "Trajectories at the end of life: A controlled investigation of longitudinal Health Services Consumption data," Health Policy, Elsevier, vol. 120(12), pages 1395-1403.
    10. Eliza Lai-Yi Wong & Janice Ying-Chui Lau & Patsy Yuen-Kwan Chau & Roger Yat-Nork Chung & Samuel Yeung-Shan Wong & Jean Woo & Eng-Kiong Yeoh, 2022. "Caregivers’ Experience of End-of-Life Stage Elderly Patients: Longitudinal Qualitative Interview," IJERPH, MDPI, vol. 19(4), pages 1-12, February.
    11. Patrick Janson & Kristina Willeke & Lisa Zaibert & Andrea Budnick & Anne Berghöfer & Sarah Kittel-Schneider & Peter U. Heuschmann & Andreas Zapf & Manfred Wildner & Carolin Stupp & Thomas Keil, 2022. "Mortality, Morbidity and Health-Related Outcomes in Informal Caregivers Compared to Non-Caregivers: A Systematic Review," IJERPH, MDPI, vol. 19(10), pages 1-25, May.
    12. Chandoevwit, Worawan & Phatchana, Phasith, 2018. "Inpatient care expenditure of the elderly with chronic diseases who use public health insurance: Disparity in their last year of life," Social Science & Medicine, Elsevier, vol. 207(C), pages 64-70.
    13. Rolden, Herbert J.A. & van Bodegom, David & Westendorp, Rudi G.J., 2014. "Variation in the costs of dying and the role of different health services, socio-demographic characteristics, and preceding health care expenses," Social Science & Medicine, Elsevier, vol. 120(C), pages 110-117.
    14. Jacobs, Josephine C. & Lilly, Meredith B. & Ng, Carita & Coyte, Peter C., 2013. "The fiscal impact of informal caregiving to home care recipients in Canada: How the intensity of care influences costs and benefits to government," Social Science & Medicine, Elsevier, vol. 81(C), pages 102-109.
    15. Masahiro Yamaguchi & Keiko Yamada & Masako Iseki & Yusuke Karasawa & Yasuko Murakami & Tatsuya Enomoto & Nobuko Kikuchi & Satoko Chiba & Atsuko Hara & Keisuke Yamaguchi & Eiichi Inada, 2020. "Insomnia and caregiver burden in chronic pain patients: A cross-sectional clinical study," PLOS ONE, Public Library of Science, vol. 15(4), pages 1-10, April.
    16. Irene Magaña & Pablo Martínez & María‐Soledad Loyola, 2020. "Health outcomes of unpaid caregivers in low‐ and middle‐income countries: A systematic review and meta‐analysis," Journal of Clinical Nursing, John Wiley & Sons, vol. 29(21-22), pages 3950-3965, November.
    17. Bruni, Attila & Miele, Francesco & Piras, Enrico Maria, 2019. "‘Homemade’: Building, mending, and coordinating a care network," Social Science & Medicine, Elsevier, vol. 237(C), pages 1-1.
    18. Tessa Morgan & Aamena Bharmal & Robbie Duschinsky & Stephen Barclay, 2020. "Experiences of oldest-old caregivers whose partner is approaching end-of-life: A mixed-method systematic review and narrative synthesis," PLOS ONE, Public Library of Science, vol. 15(6), pages 1-18, June.
    19. Sandrine Juin, 2019. "Formal home care, informal support and caregiver health: should other people care?," Erudite Working Paper 2019-21, Erudite.
    20. Bauer, Jan Michael & Sousa-Poza, Alfonso, 2015. "Impacts of Informal Caregiving on Caregiver Employment, Health, and Family," IZA Discussion Papers 8851, Institute of Labor Economics (IZA).

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:eee:socmed:v:70:y:2010:i:7:p:1035-1041. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Catherine Liu (email available below). General contact details of provider: http://www.elsevier.com/wps/find/journaldescription.cws_home/315/description#description .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.