Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-13T02:20:10.191Z Has data issue: false hasContentIssue false

Protection against perceptions of powerlessness and helplessness during palliative care: The family members' perspective

Published online by Cambridge University Press:  15 August 2011

Anna Milberg*
Affiliation:
Department of Social and Welfare Studies, Linköping University, LAH/Unit of Palliative Care, University Hospital, Linköping, and Palliative Education and Research Centre in the County of Östergötland, Östergötland, Sweden
Peter Strang
Affiliation:
Karolinska Institutet, FoUU, Stockholms Sjukhem, Stockholm, Sweden
*
Address correspondence and reprint requests to: Anna Milberg, LAH Öst, Vrinnevisjukhuset, 601 82 Norrköping, Sweden. E-mail: anna.milberg@isv.liu.se

Abstract

Objective:

Resilience in relation to coping with stress, loss, and bereavement has recently received increased attention. The aim of the current study was to describe aspects that are experienced as a protection against powerlessness and/or helplessness during advanced palliative home care (APHC) or as a help when coping with such perceptions.

Method:

Both family members during ongoing APHC and family members 3–9 months after the patient's death responded (in total, N = 233; response rate 72%) to a postal questionnaire with mainly open-ended questions. The text responses were analyzed using Manifest Content Analysis.

Results:

Protection against powerlessness and helplessness had been facilitated by a stable patient condition, the patient coping well, a trusting relationship with the patient, practical and emotional support from family and friends, access to palliative expertise, and staff support that was both individually-focused and cooperative. Other aspects that had helped or protected family members against powerlessness and helplessness were a belief that they had their own reliable knowledge to manage the difficult situation, talking to someone, doing good for the patient, distracting activities, acceptance, meaning and hope, and an inner feeling of security.

Significance of results:

The findings are discussed in relation to existential psychology, the dual process model of coping with bereavement, and repressive coping. Clinical implications are suggested.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Andershed, B. & Ternestedt, B.M. (2001). Development of a theoretical framework describing relatives' involvement in palliative care. Journal of Advanced Nursing, 34, 554562.CrossRefGoogle ScholarPubMed
Anderson, B.A. & Kralik, D. (2008). Palliative care at home: carers and medication management. Palliative & Supportive Care, 6, 349356.Google Scholar
Antonovsky, A. (1987). Unravelling the Mystery of Health: How People Manage Stress and Stay Well. San Fransisco: Jossey–Bass Publishers.Google Scholar
Beck-Friis, B. & Strang, P. (1993). The organization of hospital-based home care for terminally ill cancer patients: the Motala model. Palliative Medicine, 7, 93100.CrossRefGoogle Scholar
Block, S.D. (2000). Assessing and managing depression in the terminally ill patient. ACP-ASIM End-of-Life Care Consensus Panel. American College of Physicians – American Society of Internal Medicine. Annals of Internal medicine, 132, 209218.Google Scholar
Bonanno, G.A. & Keltner, D. (1997). Facial expressions of emotion and the course of conjugal bereavement. Journal of Abnormal Psychology, 106, 126137.Google Scholar
Bonanno, G.A., Keltner, D., Holen, A., et al. (1995). When avoiding unpleasant emotions might not be such a bad thing: verbal-autonomic response dissociation and midlife conjugal bereavement. Journal of Personality and Social Psychology, 69, 975989.Google Scholar
Bonanno, G.A., Moskowitz, J.T., Papa, A., et al. (2005). Resilience to loss in bereaved spouses, bereaved parents, and bereaved gay men. Journal of Personality and Social Psychology, 88, 827843.Google Scholar
Bonanno, G.A., Papa, A., Lalande, K., et al. (2004a). The importance of being flexible: The ability to both enhance and suppress emotional expression predicts long-term adjustment. Psychological Science, 15, 482487.Google Scholar
Bonanno, G.A., Wortman, C.B., Lehman, D.R., et al. (2002). Resilience to loss and chronic grief: a prospective study from preloss to 18-months postloss. Journal of Personality and Social Psychology, 83, 11501164.Google Scholar
Bonanno, G.A., Wortman, C.B. & Nesse, R.M. (2004b). Prospective patterns of resilience and maladjustment during widowhood. Psychology and Aging, 19, 260271.CrossRefGoogle ScholarPubMed
Booth, S., Silvester, S. & Todd, C. (2003). Breathlessness in cancer and chronic obstructive pulmonary disease: Using a qualitative approach to describe the experience of patients and carers. Palliative and Supportive Care, 1, 337344.Google Scholar
Bowlby, J. (1969). Attachment and Loss: Vol. 1. Attachment, London: Pimlico.Google Scholar
Bowlby, J. (1980). Attachment and Loss: Vol. 3. Loss: Sadness and Depression, New York: Basic Books.Google Scholar
Breitbart, W. (2002). Spirituality and meaning in supportive care: spirituality- and meaning-centered group psychotherapy interventions in advanced cancer. Supportive Care in Cancer, 10, 272280.CrossRefGoogle ScholarPubMed
Carlsson, M.E. & Strang, P.M. (1998). Educational support programme for gynaecological cancer patients and their families. Acta Oncologica, 37, 269275.Google Scholar
Chochinov, H.M., Hack, T., Hassard, T., et al. (2005). Dignity therapy: a novel psychotherapeutic intervention for patients near the end of life. Journal of Clinical Oncology, 23, 55205525.CrossRefGoogle ScholarPubMed
Clayton, J.M., Butow, P.N., Arnold, R.M., et al. (2005). Fostering coping and nurturing hope when discussing the future with terminally ill cancer patients and their caregivers. Cancer, 103, 19651975.CrossRefGoogle ScholarPubMed
Clements, S. & Cummings, S. (1991). Helplessness and powerlessness: caring for clients in pain. Holistic Nursing Practice, 6, 7685.Google Scholar
Coifman, K.G., Bonanno, G.A., Ray, R.D., et al. (2007). Does repressive coping promote resilience? Affective-autonomic response discrepancy during bereavement. Journal of Personality and Social Psychology, 92, 745758.CrossRefGoogle ScholarPubMed
Drew, B.L. (1990). Differentiation of hopelessness, helplessness, and powerlessness using Erik Erikson's “Roots of virtue.” Archives of Psychiatric Nursing, 4, 332337.Google Scholar
Esterling, B., Antoni, M., Kumar, M., et al. (1993). Defensiveness, trait anxiety, and Epstein–Barr viral capsid antigen antibody titers in healthy college students. Health Psychology, 12, 132139.Google Scholar
Ferrell, B., Ervin, K., Smith, S., et al. (2002). Family perspectives of ovarian cancer. Cancer Practice, 10, 269276.Google Scholar
Folkman, S. (2002). Revised coping theory and the process of bereavement. In Handbook of Bereavement Research: Consequences, Coping, and Care. Stroebe, M.S., Hansson, R.O., Stroebe, W. & Schut, H. (eds). Washington: American Psychological Association. 563584.Google Scholar
Folkman, S. & Greer, S. (2000). Promoting psychological well-being in the face of serious illness: when theory, research and practice inform each other. Psycho-oncology, 9, 1119.3.0.CO;2-Z>CrossRefGoogle ScholarPubMed
Fraley, R.C. & Bonanno, G.A. (2004). Attachment and loss: a test of three competing models on the association between attachment-related avoidance and adaptation to bereavement. Personality & Social Psychology Bulletin, 30, 878890.Google Scholar
Frasure-Smith, N., Lesperance, F., Gravel, G., et al. (2002). Long-term survival differences among low-anxious, high-anxious and repressive copers enrolled in the Montreal heart attack readjustment trial. Psychosomatic Medicine, 64, 571579.Google Scholar
Giese-Davis, J., Sephton, S., Abercorombie, H., et al. (2004). Repression and high anxiety are associated with diurnal cortisol rhytms in women with metastatic breast cancer. Health Psychology, 23, 645660.CrossRefGoogle Scholar
Glaser, B.G. & Strauss, A.L. (1965). Awareness of Dying. New York: Aldine Publishing Company.Google Scholar
Goldschmidt, D., Schmidt, L., Krasnik, A., et al. (2006). Expectations to and evaluation of a palliative home-care team as seen by patients and carers. Supportive Care in Cancer, 14, 12321240.CrossRefGoogle ScholarPubMed
Graneheim, U.H. & Lundman, B. (2004). Qualitative content analysis in nursing research: concepts, procedures and measures to achieve trustworthiness. Nurse Education Today, 24, 105112.CrossRefGoogle ScholarPubMed
Greenberg, J., Koole, S.L. & Pyszczynski, T. (eds). (2004). Handbook of Experimental Existential Psychology. New York: Guilford Press.Google Scholar
Gysels, M.H. & Higginson, I.J. (2009). Caring for a person in advanced illness and suffering from breathlessness at home: Threats and resources. Palliative & Supportive Care, 7, 153162.Google Scholar
Harding, R. & Higginson, I.J. (2003). What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliative Medicine, 17, 6374.Google Scholar
Herbert, R., Prigerson, H.G., Schulz, R., et al. (2006). Preparing caregivers for the death of a loved one: A theoretical framework and suggestions for future research. Journal of Palliative Medicine, 9, 11641171.Google Scholar
Hickey, G. & Kipping, C. (1996). Issues in research. A multi-stage approach to the coding of data from open-ended questions. Nurse Researcher, 4, 8191.Google Scholar
Hodgson, C., Higginson, I., McDonnell, M., et al. (1997). Family anxiety in advanced cancer: a multicentre prospective study in Ireland. British Journal of Cancer, 76, 12111214.CrossRefGoogle Scholar
Holtslander, L.F., Duggleby, W., Williams, A.M., et al. (2005). The experience of hope for informal caregivers of palliative patients. Journal of Palliative Care, 21, 285291.Google Scholar
Ingleton, C., Payne, S., Nolan, M., et al. (2003). Respite in palliative care: A review and discussion of the literature. Palliative Medicine, 17, 567575.Google Scholar
Kelly, B., Edwards, P., Synott, R., et al. (1999). Predictors of bereavement outcome for family carers of cancer patients. Psycho-oncology, 8, 237249.3.0.CO;2-C>CrossRefGoogle ScholarPubMed
Kissane, D.W., Clarke, D.M. & Street, A.F. (2001). Demoralization syndrome—A relevant psychiatric diagnosis for palliative care. Journal of Palliative Care, 17, 1221.Google Scholar
Krippendorff, K. (1980). Content Analysis: An Introduction to its Methodology. London: Sage Publications Ltd.Google Scholar
Kurtz, M.E., Kurtz, J.C., Given, C.W., et al. (1995). Relationship of caregiver reactions and depression to cancer patients' symptoms, functional states and depression—A longitudinal view. Social Science & Medicine, 40, 837846.CrossRefGoogle ScholarPubMed
Kurtz, M.E., Kurtz, J.C., Given, C.W., et al. (1997). Predictors of post bereavement depressive symptomatology among family caregivers of cancer patients. Supportive Care in Cancer, 5, 5360.Google Scholar
Kvale, S. (1996). Interviews: An Introduction to Qualitative Research Interviewing. Thousand Oaks: SAGE.Google Scholar
Lethborg, C., Aranda, S., Cox, S., et al. (2007). To what extent does meaning mediate adaptation to cancer? The relationship between physical suffering, meaning in life, and connection to others in adjustment to cancer. Palliative & Supportive Care, 5, 377388.Google Scholar
Malterud, K. (2001). Qualitative research: Standards, challenges, and guidelines. Lancet, 358, 483488.Google Scholar
Mikulincer, M. & Shaver, P.R. (2007). Attachment in Adulthood: Structure, Dynamics, and Change. New York: Guildford Press.Google Scholar
Milberg, A. & Strang, P. (2000). Met and unmet needs in hospital-based home care: qualitative evaluation through open-ended questions. Palliative Medicine, 14, 533534.Google Scholar
Milberg, A. & Strang, P. (2003). Meaningfulness in palliative home care: An interview study of dying cancer patients' next of kin. Palliative & Supportive Care, 1, 171180.Google Scholar
Milberg, A. & Strang, P. (2004). Exploring comprehensibility and manageability in palliative home care: An interview study of dying cancer patients' informal carers. Psycho-oncology, 13, 605618.CrossRefGoogle ScholarPubMed
Milberg, A. & Strang, P. (2007). What to do when ‘there is nothing more to do'? A study within a salutogenic framework of family members' experience of palliative home care staff. Psycho-oncology, 16, 741751.CrossRefGoogle Scholar
Milberg, A., Olsson, E.C., Jakobsson, M., et al. (2008). Family members' perceived needs for bereavement follow-up. Journal of Pain and Symptom Management, 35, 5869.Google Scholar
Milberg, A., Strang, P. & Jakobsson, M. (2004). Next of kin's experience of powerlessness and helplessness in palliative home care. Supportive Care in Cancer, 12, 120128.Google Scholar
Moskowitz, J.T., Folkman, S. & Acree, M. (2003). Do positive psychological states shed light on recovery from bereavement? Findings from a 3-year longitudinal study. Death Studies, 27, 471500.Google Scholar
Myers, L., Vetere, A. & Derakshan, N. (2004). Are suppression and repressive coping related? Personality and Individual Differences, 36, 10091013.CrossRefGoogle Scholar
Neimeyer, R.A. (2000). Searching för the meaning of meaning: Grief therapy and the process of reconstruction. Death Studies, 24, 541558.Google Scholar
Parkes, C. & Weiss, R. (1983). Recovery from Bereavement, New York: Basic Books.Google Scholar
Phelps, C., Bennett, P., Iredale, R., et al. (2006). The development of distraction-based coping intervention for women waiting for genetic information: A phase I qualitative study. Psycho-oncology, 15, 169173.CrossRefGoogle Scholar
Safer, M.A., Bonanno, G.A. & Field, N.P. (2001). “It was never that bad”: Biased recall of grief and long-term adjustment to the death of a spouse. Memory, 9, 195204.Google Scholar
Salander, P. & Spetz, A. (2002). How do patients and spouses deal with the serious facts of malignant glioma? Palliative Medicine, 16, 305313.Google Scholar
Sand, L., Strang, P. & Milberg, A. (2008). Dying cancer patients' experiences of powerlessness and helplessness. Supportive Care in Cancer, 16, 853862.Google Scholar
Schut, H. & Stroebe, M.S. (2005). Interventions to enhance adaptation to bereavement. Journal of Palliative Medicine, 8 (Suppl. 1), S140147.Google Scholar
Seale, C., Addington–Hall, J. & McCarthy, M. (1997). Awareness of dying: prevalence, causes and consequences. Social Science & Medicine, 45, 477484.Google Scholar
Sherman, D.W., Ye, X.Y., McSherry, C., et al. (2005). Spiritual well-being as a dimension of quality of life for patients with advanced cancer and AIDS and their family caregivers: Results of a longitudinal study. American Journal of Hospice & Palliative Care, 22, 349362.Google Scholar
Smith, S.H. (2005). Anticipatory grief and psychological adjustment to grieving in middle-aged children. American Journal of Hospice and Palliative Medicine, 22, 283286.CrossRefGoogle ScholarPubMed
Spinelli, E. (1997/2006). Tales of Un-knowing. Therapeutic Encounters from an Existential Perspective. Ross-on-Wye: PCCS Books.Google Scholar
Strang, S. & Strang, P. (2001). Spiritual thoughts, coping and ‘sense of coherence' in brain tumour patients and their spouses. Palliative Medicine, 15, 127134.Google Scholar
Stroebe, M. & Schut, H. (1999). The dual process model of coping with bereavement: Rationale and description. Death Studies, 23, 197224.Google ScholarPubMed
Stroebe, M., Schut, H. & Stroebe, W. (2005a). Attachment in coping with bereavement: A theoretical intergration. Review of General Psychology, 9, 4866.Google Scholar
Stroebe, M., Schut, H. & Stroebe, W. (2006). Who benefits from disclosure? Exploration of attachment style differences in the effects of expressing emotions. Clinical Psychology Review, 26, 6685.Google Scholar
Stroebe, W., Schut, H. & Stroebe, M.S. (2005b). Grief work, disclosure and counseling: Do they help the bereaved? Clinical Psychology Review, 25, 395414.Google Scholar
Tillich, P. (1952/2000). The Courage to Be. New Haven: Yale University Press.Google Scholar
Walden–Galuszko, K.D., Majkowicz, M., et al. (1995). The psychic problems of family-caregivers. New Trends in Experimental & Clinical Psychiatry, 11, 6366.Google Scholar
Valdimarsdottir, U., Helgason, A.R., Furst, C.J., et al. (2004). Awareness of husband's impending death from cancer and long-term anxiety in widowhood: A national follow-up. Palliative Medicine, 18, 432443.Google Scholar
van Deurzen, E. (1997/2006). Everyday Mysteries: Existential Dimensions of Psychotherapy. London: Routledge.Google Scholar
Worden, J.W. (2002). Grief Counseling and Grief Therapy. New York: Springer Publishing Company.Google Scholar
Yalom, I.D. (1980). Existential Psychotherapy. New York: Basic Books.Google Scholar