Display options
Share it on

J Multidiscip Healthc. 2015 Jun 03;8:271-7. doi: 10.2147/JMDH.S82239. eCollection 2015.

Being "on the alert" and "a forced volunteer": a qualitative study of the invisible care provided by the next of kin of patients with chronic heart failure.

Journal of multidisciplinary healthcare

Anita Strøm, Kirsti Lauvli Andersen, Kari Korneliussen, May Solveig Fagermoen

Affiliations

  1. Department of Masters and Continuing Education, Lovisenberg Diaconal University College, Oslo, Norway.
  2. Faculty of Health and Social Work Studies, Østfold University College, Halden, Norway.
  3. Heart Failure Clinic, Vestfold Hospital Trust, Tønsberg, Norway.
  4. Institute of Health and Society, University of Oslo, Oslo, Norway.

PMID: 26082643 PMCID: PMC4461135 DOI: 10.2147/JMDH.S82239

Abstract

BACKGROUND: Relatives' support is an important factor in how well people with chronic heart failure (CHF) manage their illness and everyday life. Deepening professionals' understanding of the content of relatives' invisible care activities, often characterized as care burden, is necessary to strengthen support services.

OBJECTIVE: To explore the next of kin's experiences of invisible care and the inherent responsibilities in caring for a relative with CHF.

DESIGN SETTING AND METHODS: Relatives were recruited from CHF outpatient clinics and home care services. Seventeen women and two men were interviewed, age range 45-83 years; 12 were partners, and seven were daughters. The qualitative interviews were taped and transcribed and thematic cross-case analyses were performed.

RESULTS: Two main themes were revealed. The first, "being on the alert", refers to a perceived need, real or assumed, to be aware day and night, whether present with the patient or not, that occupies the mind, emotions, and body. The second theme, "being a forced volunteer", refers to two different dimensions: relatives' own perceptions of responsibility with regard to the patient's needs; and voiced or silent expectations from the patient, family members, and health personnel that the relative will help the patient. Both findings appeared to have positive and negative impacts on the relationship with the patient.

CONCLUSION: The identified themes reflect how challenging being a next of kin of CHF patients can be. The results may deepen professionals' understanding of the relatives' invisible care burden and the importance of their subjective task-related feelings. More studies on invisible care and the attendant responsibilities are needed and also on relatives' inherent resources.

Keywords: care burden; informal caregivers; social support; task-related feelings

References

  1. Scand J Public Health. 2012 Feb;40(1):18-24 - PubMed
  2. Soc Sci Med. 2006 Nov;63(9):2429-39 - PubMed
  3. Ann Oncol. 2005 Jul;16(7):1185-91 - PubMed
  4. Dev Psychol. 2004 Mar;40(2):295-314 - PubMed
  5. Eur J Heart Fail. 2007 Jun-Jul;9(6-7):695-701 - PubMed
  6. Eur J Cardiovasc Nurs. 2008 Mar;7(1):3-9 - PubMed
  7. J Adv Nurs. 2009 Jul;65(7):1442-51 - PubMed
  8. Eur J Heart Fail. 2012 Aug;14(8):803-69 - PubMed
  9. J Cardiovasc Nurs. 2007 Mar-Apr;22(2):131-7 - PubMed
  10. J Pain Symptom Manage. 2003 Oct;26(4):922-53 - PubMed
  11. J Adv Nurs. 2008 Feb;61(4):373-83 - PubMed
  12. J Cardiovasc Nurs. 2005 May-Jun;20(3):162-9 - PubMed
  13. Eur J Cardiovasc Nurs. 2010 Dec;9(4):254-62 - PubMed
  14. Psychooncology. 2006 Jun;15(6):517-27 - PubMed
  15. Eur J Cardiovasc Nurs. 2011 Dec;10(4):234-40 - PubMed
  16. J Pers Soc Psychol. 2010 Jan;98(1):57-76 - PubMed
  17. J Clin Nurs. 2014 Oct;23(19-20):2928-38 - PubMed
  18. J Cardiovasc Nurs. 2011 Sep-Oct;26(5):386-94 - PubMed
  19. West J Nurs Res. 2008 Dec;30(8):943-59 - PubMed

Publication Types