Vol 16, No 1 (2022)
Research paper
Published online: 2021-10-27

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Informational and supportive needs of the family caregivers of women with breast cancer in a low resource context: A cross-sectional study

Mozhgan Moshtagh1, Elahe Allahyari1
Palliat Med Pract 2022;16(1):59-65.

Abstract

Introduction: The present study was conducted to assess the needs of family caregivers in 2020 during
the COVID-19 pandemic.
Participants and methods: Data were collected through purposive sampling from 103 participants
and analysed by the Family Inventory of Needs (FIN) during the COVID-19 outbreak in 2020 (between
July and September).
Results: Informational and supportive needs were high for most caregivers (76%), but they were scored
unmet by higher than 30% of the family caregivers in items 8, 9, and 16 of informative dimensions and
items 15, 17, and 18 supportive dimensions. Also, the illness stage was significantly associated with the
score of unmet needs (p = 0.03).
Conclusions: Caregivers who live with women need more guidance and support. Considering the information
and psycho-social needs of cancer caregivers may increase the satisfaction of health services
and help improve the psychological well-being and quality of life of both patients and their caregivers.

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References

  1. Gauthier G, Gagnon-Sanschagrin P, Guérin A, et al. Economic Burden of HR+/HER2- Metastatic Breast Cancer Among Adult Premenopausal Women. Adv Ther. 2018; 35(4): 503–514.
  2. Koutrouli N, Anagnostopoulos F, Griva F, et al. Exploring the relationship between posttraumatic growth, cognitive processing, psychological distress, and social constraints in a sample of breast cancer patients. Women Health. 2016; 56(6): 650–667.
  3. Daroudi R, Akbari Sari A, Nahvijou A, et al. The Economic Burden of Breast Cancer in Iran. Iran J Public Health. 2015; 44(9): 1225–1233.
  4. Caruso R, Nanni MG, Riba MB, et al. The burden of psychosocial morbidity related to cancer: patient and family issues. Int Rev Psychiatry. 2017; 29(5): 389–402.
  5. Enstone A, Greaney M, Povsic M, et al. The Economic Burden of Small Cell Lung Cancer: A Systematic Review of the Literature. Pharmacoecon Open. 2018; 2(2): 125–139.
  6. Diem G, Brownson RC, Grabauskas V, et al. Prevention and control of noncommunicable diseases through evidence-based public health: implementing the NCD 2020 action plan. Glob Health Promot. 2016; 23(3): 5–13.
  7. Ashley L, O'Connor D, Jones F. Effects of Emotional Disclosure in Caregivers: Moderating Role of Alexithymia. Stress and Health. 2011; 27(5): 376–387.
  8. de Carvalho MW, da Nóbrega MM, Garcia TR. [Process and results of the development of an ICNP® Catalogue for Cancer Pain]. Rev Esc Enferm USP. 2013; 47(5): 1060–1068.
  9. Price ML, Surr CA, Gough B, et al. Experiences and support needs of informal caregivers of people with multimorbidity: a scoping literature review. Psychol Health. 2020; 35(1): 36–69.
  10. Litzelman K, Kent EE, Mollica M, et al. How Does Caregiver Well-Being Relate to Perceived Quality of Care in Patients With Cancer? Exploring Associations and Pathways. J Clin Oncol. 2016; 34(29): 3554–3561.
  11. Sanderson C, Lobb EA, Mowll J, et al. Signs of post-traumatic stress disorder in caregivers following an expected death: a qualitative study. Palliat Med. 2013; 27(7): 625–631.
  12. Stenberg U, Ruland CM, Miaskowski C. Review of the literature on the effects of caring for a patient with cancer. Psychooncology. 2010; 19(10): 1013–1025.
  13. Sørensen K. Health literacy is an emerging strategic priority in national cancer control plans in the EU. Journal of Cancer Policy. 2020; 26: 100255.
  14. Lund L, Ross L, Petersen MA, et al. The interaction between informal cancer caregivers and health care professionals: a survey of caregivers' experiences of problems and unmet needs. Support Care Cancer. 2015; 23(6): 1719–1733.
  15. Sklenarova H, Krümpelmann A, Haun MW, et al. When do we need to care about the caregiver? Supportive care needs, anxiety, and depression among informal caregivers of patients with cancer and cancer survivors. Cancer. 2015; 121(9): 1513–1519.
  16. Shin DW, Park JH, Shim EJ, et al. The development of a comprehensive needs assessment tool for cancer-caregivers in patient-caregiver dyads. Psychooncology. 2011; 20(12): 1342–1352.
  17. Oberoi DV, White V, Jefford M, et al. Caregivers' information needs and their 'experiences of care' during treatment are associated with elevated anxiety and depression: a cross-sectional study of the caregivers of renal cancer survivors. Support Care Cancer. 2016; 24(10): 4177–4186.
  18. Sun V, Raz DJ, Kim JY. Caring for the informal cancer caregiver. Curr Opin Support Palliat Care. 2019; 13(3): 238–242.
  19. Schur S, Neubauer M, Amering M, et al. Validation of the Family Inventory of Needs (FIN) for family caregivers in palliative care. Palliat Support Care. 2015; 13(3): 485–491.
  20. Fridriksdottir N, Sigurdardottir V, Gunnarsdottir S. Important needs of families in acute and palliative care settings assessed with the family inventory of needs. Palliat Med. 2006; 20(4): 425–432.
  21. Friðriksdóttir N, Saevarsdóttir T, Halfdánardóttir SÍ, et al. Family members of cancer patients: Needs, quality of life and symptoms of anxiety and depression. Acta Oncol. 2011; 50(2): 252–258.
  22. Miyashita M, Ohno S, Kataoka A, et al. Unmet Information Needs and Quality of Life in Young Breast Cancer Survivors in Japan. Cancer Nurs. 2015; 38(6): E1–11.
  23. Stenberg U, Ekstedt M, Olsson M, et al. Living close to a person with cancer: a review of the international literature and implications for social work practice. J Gerontol Soc Work. 2014; 57(6-7): 531–555.
  24. Ikels C. Filial piety: Practice and discourse in contemporary East Asia. Stanford University Press 2004.
  25. Holm M, Carlander I, Fürst CJ, et al. Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregivers. BMC Palliat Care. 2015; 14: 16.
  26. Lambert SD, Harrison JD, Smith E, et al. The unmet needs of partners and caregivers of adults diagnosed with cancer: a systematic review. BMJ Support Palliat Care. 2012; 2(3): 224–230.
  27. Ullrich A, Theochari M, Bergelt C, et al. Ethical challenges in family caregivers of patients with advanced cancer - a qualitative study. BMC Palliat Care. 2020; 19(1): 70.
  28. Hudson P, Payne S. Family caregivers and palliative care: current status and agenda for the future. J Palliat Med. 2011; 14(7): 864–869.
  29. Mayland CR, Doughty HC, Rogers SN, et al. A Qualitative Study Exploring Patient, Family Carer and Healthcare Professionals' Direct Experiences and Barriers to Providing and Integrating Palliative Care for Advanced Head and Neck Cancer. J Palliat Care. 2021; 36(2): 121–129.
  30. Røen I, Stifoss-Hanssen H, Grande G, et al. Supporting carers: health care professionals in need of system improvements and education - a qualitative study. BMC Palliat Care. 2019; 18(1): 58.



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