Skip to main content
Top
Published in: BMC Palliative Care 1/2019

Open Access 01-12-2019 | Care | Research article

Caregiver exposure to critical events and distress in home-based palliative care in Germany a cross-sectional study using the Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) scale

Authors: Michael Galatsch, Holly G. Prigerson, Wilfried Schnepp, Friederike zu Sayn-Wittgenstein, Jian Li

Published in: BMC Palliative Care | Issue 1/2019

Login to get access

Abstract

Background

Lay family caregivers of patients receiving palliative care often confront stressful situations in the care of their loved ones. This is particularly true for families in the home-based palliative care settings, where the family caregivers are responsible for a substantial amount of the patient’s care. Yet, to our knowledge, no study to date has examined the family caregivers’ exposure to critical events and distress with home-based palliative care has been reported from Germany. Therefore, we attempt to assess family caregiver exposure to the dying patient’s critical health events and relate that to the caregiver’s own psychological distress to examine associations with general health within a home-based palliative care situation in Germany.

Methods

A cross-sectional study was conducted among 106 family caregivers with home-based palliative care in the Federal State of North Rhine Westphalia, Germany. We administered the Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) Scale. Descriptive statistics and linear regression models relating general health (SF-36) were used to analyze the data.

Results

The frequency of the caregiver’s exposure, or witness of, critical health events of the patient ranged from 95.2% “pain/discomfort” to 20.8% “family caregiver thought patient was dead”. The highest distress scores assessing fear and helpfulness were associated with “family caregiver felt patient had enough’” and “family caregiver thought patient was dead”. Linear regression analyses revealed significant inverse associations between SCARED critical health event exposure frequency (beta = .408, p = .025) and total score (beta = .377, p = .007) with general health in family caregivers.

Conclusions

Family caregivers with home-based palliative care in Germany frequently experience exposure to a large number of critical health events in caring for their family members who are terminally ill. These exposures are associated with the family caregiver’s degree of fear and helplessness and are associated with their worse general health. Thus the SCARED Scale, which is brief and easy to administer, appears able to identify these potentially upsetting critical health events among family caregivers of palliative care patients receiving care at home. Because it identified commonly encountered critical events in these patients and related them to adverse general health of family caregivers, the SCARED may add to clinically useful screens to identify family caregivers who may be struggling.
Literature
1.
go back to reference Rossi Ferrario S, Cardillo V, Vicario F, Balzarini E, Zotti AM. Advanced cancer at home: caregiving and bereavement. Palliat Med. 2004;18:129–36.CrossRef Rossi Ferrario S, Cardillo V, Vicario F, Balzarini E, Zotti AM. Advanced cancer at home: caregiving and bereavement. Palliat Med. 2004;18:129–36.CrossRef
2.
go back to reference Ringdal GI, Jordhoy MS, Kaasa S. Measuring quality of palliative care: psychometric properties of the FAMCARE scale. Qual Life Res. 2003;12:167–76.CrossRef Ringdal GI, Jordhoy MS, Kaasa S. Measuring quality of palliative care: psychometric properties of the FAMCARE scale. Qual Life Res. 2003;12:167–76.CrossRef
3.
go back to reference Hudson P, Payne S. Family caregivers and palliative care: current status and agenda for the future. J Palliat Med. 2011;14:864–9.CrossRef Hudson P, Payne S. Family caregivers and palliative care: current status and agenda for the future. J Palliat Med. 2011;14:864–9.CrossRef
4.
go back to reference Canadian Hospice Palliative Care Assiociation, editor. The role of informal carers in hospice palliative and end-of-life care in Canada: a discussion of the legal, ethical and moral challenges. Ottawa: (Canadian hospice palliative care Assiociation ed; 2004. Canadian Hospice Palliative Care Assiociation, editor. The role of informal carers in hospice palliative and end-of-life care in Canada: a discussion of the legal, ethical and moral challenges. Ottawa: (Canadian hospice palliative care Assiociation ed; 2004.
5.
go back to reference Stajduhar K, Cohen R. Family caregiving in the home. In Family Carers in Palliative Care. Edited by Hudson P, Payne S. New York: Oxford University Press; 2011. Stajduhar K, Cohen R. Family caregiving in the home. In Family Carers in Palliative Care. Edited by Hudson P, Payne S. New York: Oxford University Press; 2011.
6.
go back to reference Payne S. and the colleagues from the EAPC Task Force on Family Carers: White paper on improving support for family carers in palliative care: part 1. Eur J Palliat Care. 2010;17:238–45. Payne S. and the colleagues from the EAPC Task Force on Family Carers: White paper on improving support for family carers in palliative care: part 1. Eur J Palliat Care. 2010;17:238–45.
7.
go back to reference Hudson P, Aranda S, McMurray N. Intervention development for enhanced lay palliative caregiver support - the use of focus groups. Eur J Cancer Care (Engl). 2002;11:262–70.CrossRef Hudson P, Aranda S, McMurray N. Intervention development for enhanced lay palliative caregiver support - the use of focus groups. Eur J Cancer Care (Engl). 2002;11:262–70.CrossRef
8.
go back to reference Prigerson HG, Cherlin E, Chen JH, Kasl SV, Hurzeler R, Bradley EH. The stressful caregiving adult reactions to experiences of dying (SCARED) scale: a measure for assessing caregiver exposure to distress in terminal care. Am J Geriatr Psychiatry. 2003;11:309–19.CrossRef Prigerson HG, Cherlin E, Chen JH, Kasl SV, Hurzeler R, Bradley EH. The stressful caregiving adult reactions to experiences of dying (SCARED) scale: a measure for assessing caregiver exposure to distress in terminal care. Am J Geriatr Psychiatry. 2003;11:309–19.CrossRef
9.
go back to reference Hudson PL, Hayman-White K, Aranda S, Kristjanson LJ. Predicting family caregiver psychosocial functioning in palliative care. J Palliat Care. 2006;22:133–40.PubMed Hudson PL, Hayman-White K, Aranda S, Kristjanson LJ. Predicting family caregiver psychosocial functioning in palliative care. J Palliat Care. 2006;22:133–40.PubMed
10.
go back to reference Carlander I, Sahlberg-Blom E, Hellstrom I, Ternestedt BM. The modified self: family caregivers' experiences of caring for a dying family member at home. J Clin Nurs. 2011;20:1097–105.CrossRef Carlander I, Sahlberg-Blom E, Hellstrom I, Ternestedt BM. The modified self: family caregivers' experiences of caring for a dying family member at home. J Clin Nurs. 2011;20:1097–105.CrossRef
11.
go back to reference Rabow MW, Hauser JM, Adams J. Supporting family caregivers at the end of life: "they don't know what they don't know". JAMA. 2004;291:483–91.CrossRef Rabow MW, Hauser JM, Adams J. Supporting family caregivers at the end of life: "they don't know what they don't know". JAMA. 2004;291:483–91.CrossRef
12.
go back to reference Waldrop DP, Kusmaul N. The living-dying interval in nursing home-based end-of-life care: family caregivers' experiences. J Gerontol Soc Work. 2011;54:768–87.CrossRef Waldrop DP, Kusmaul N. The living-dying interval in nursing home-based end-of-life care: family caregivers' experiences. J Gerontol Soc Work. 2011;54:768–87.CrossRef
13.
go back to reference Hirdes JP, Freeman S, Smith TF, Stolee P. Predictors of caregiver distress among palliative home care clients in Ontario: evidence based on the interRAI palliative care. Palliat Support Care. 2012;10:155–63.CrossRef Hirdes JP, Freeman S, Smith TF, Stolee P. Predictors of caregiver distress among palliative home care clients in Ontario: evidence based on the interRAI palliative care. Palliat Support Care. 2012;10:155–63.CrossRef
14.
go back to reference Thomas K, Hudson P, Oldham L, Kelly B, Trauer T. Meeting the needs of family carers: an evaluation of three home-based palliative care services in Australia. Palliat Med. 2010;24:183–91.CrossRef Thomas K, Hudson P, Oldham L, Kelly B, Trauer T. Meeting the needs of family carers: an evaluation of three home-based palliative care services in Australia. Palliat Med. 2010;24:183–91.CrossRef
15.
go back to reference Longman AJ, Atwood JR, Sherman JB, Benedict J, Shang TC. Care needs of home-based cancer patients and their caregivers. Quantitative findings. Cancer Nurs. 1992;15:182-190.CrossRef Longman AJ, Atwood JR, Sherman JB, Benedict J, Shang TC. Care needs of home-based cancer patients and their caregivers. Quantitative findings. Cancer Nurs. 1992;15:182-190.CrossRef
16.
go back to reference Deutscher Hospiz- und PalliativVerband e.V.: Hospiz- und Palliativversorgung- Entwicklung in Deutschland. 2016. Deutscher Hospiz- und PalliativVerband e.V.: Hospiz- und Palliativversorgung- Entwicklung in Deutschland. 2016.
17.
go back to reference Statistisches Bundesamt: Bevölkerung: Bundesländer, Stichtag 31.12.2015. Wiesbaden: Statistisches Bundesamt,; 2015. Statistisches Bundesamt: Bevölkerung: Bundesländer, Stichtag 31.12.2015. Wiesbaden: Statistisches Bundesamt,; 2015.
18.
go back to reference Galatsch M, Schlarmann JG, FZS W, Schnepp W. development of a screening-tool utilizing relevant research to measure the burden and the needs of families receiving home-based palliative care in Germany. Pflegewissenschaft. 2015;1:46–61. Galatsch M, Schlarmann JG, FZS W, Schnepp W. development of a screening-tool utilizing relevant research to measure the burden and the needs of families receiving home-based palliative care in Germany. Pflegewissenschaft. 2015;1:46–61.
19.
go back to reference Maneesriwongul W, Dixon JK. Instrument translation process: a methods review. J Adv Nurs. 2004;48:175–86.CrossRef Maneesriwongul W, Dixon JK. Instrument translation process: a methods review. J Adv Nurs. 2004;48:175–86.CrossRef
20.
go back to reference Ware CF, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I Conceptual framework and item selection. Med Care. 1992;30:473–83.CrossRef Ware CF, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I Conceptual framework and item selection. Med Care. 1992;30:473–83.CrossRef
21.
go back to reference Grande G, Rowland C, van den Berg B, Hanratty B. Psychological morbidity and general health among family caregivers during end-of-life cancer care: a retrospective census survey. Palliat Med. 2018;32:1605–14.CrossRef Grande G, Rowland C, van den Berg B, Hanratty B. Psychological morbidity and general health among family caregivers during end-of-life cancer care: a retrospective census survey. Palliat Med. 2018;32:1605–14.CrossRef
22.
go back to reference Doorenbos AZ, Given B, Given CW, Wyatt G, Gift A, Rahbar M, Jeon S. The influence of end-of-life cancer care on caregivers. Res Nurs Health. 2007;30:270–81.CrossRef Doorenbos AZ, Given B, Given CW, Wyatt G, Gift A, Rahbar M, Jeon S. The influence of end-of-life cancer care on caregivers. Res Nurs Health. 2007;30:270–81.CrossRef
23.
go back to reference Ellert U, Kurth BM. health related quality of life in adults in Germany: results of the German health interview and examination survey for adults (DEGS1). Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013;56:643–9.CrossRef Ellert U, Kurth BM. health related quality of life in adults in Germany: results of the German health interview and examination survey for adults (DEGS1). Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013;56:643–9.CrossRef
24.
go back to reference Hudson P. Positive aspects and challenges associated with caring for a dying relative at home. Int J Palliat Nurs. 2004;10:58–65 discussion 65.CrossRef Hudson P. Positive aspects and challenges associated with caring for a dying relative at home. Int J Palliat Nurs. 2004;10:58–65 discussion 65.CrossRef
25.
go back to reference Hudson PL, Aranda S, Kristjanson LJ. Meeting the supportive needs of family caregivers in palliative care: challenges for health professionals. J Palliat Med. 2004;7:19–25.CrossRef Hudson PL, Aranda S, Kristjanson LJ. Meeting the supportive needs of family caregivers in palliative care: challenges for health professionals. J Palliat Med. 2004;7:19–25.CrossRef
26.
go back to reference Singer Y, Bachner YG, Shvartzman P, Carmel S. Home death--the caregivers' experiences. J Pain Symptom Manag. 2005;30:70–4.CrossRef Singer Y, Bachner YG, Shvartzman P, Carmel S. Home death--the caregivers' experiences. J Pain Symptom Manag. 2005;30:70–4.CrossRef
27.
go back to reference Teno JM, Gozalo PL, Bynum JP, Leland NE, Miller SC, Morden NE, Scupp T, Goodman DC, Mor V. Change in end-of-life care for Medicare beneficiaries: site of death, place of care, and health care transitions in 2000, 2005, and 2009. JAMA. 2013;309:470–7.CrossRef Teno JM, Gozalo PL, Bynum JP, Leland NE, Miller SC, Morden NE, Scupp T, Goodman DC, Mor V. Change in end-of-life care for Medicare beneficiaries: site of death, place of care, and health care transitions in 2000, 2005, and 2009. JAMA. 2013;309:470–7.CrossRef
28.
go back to reference Kwietniewski L, Blankart CR, Schneider AM. J S: Inanspruchnahme von Gesundheitsleistungen und Ressourceneinsatz während der letzten Lebensmonate in Deutschland im internationalen Vergleich Gesundheitswesen aktuell, vol. 2016; 2016. p. 128–55. Kwietniewski L, Blankart CR, Schneider AM. J S: Inanspruchnahme von Gesundheitsleistungen und Ressourceneinsatz während der letzten Lebensmonate in Deutschland im internationalen Vergleich Gesundheitswesen aktuell, vol. 2016; 2016. p. 128–55.
29.
go back to reference Givens JL, Prigerson HG, Jones RN, Mitchell SL. Mental health and exposure to patient distress among families of nursing home residents with advanced dementia. J Pain Symptom Manag. 2011;42:183–91.CrossRef Givens JL, Prigerson HG, Jones RN, Mitchell SL. Mental health and exposure to patient distress among families of nursing home residents with advanced dementia. J Pain Symptom Manag. 2011;42:183–91.CrossRef
30.
go back to reference Hudson P, Collins A, Bostanci A, Willenberg L, Stephanov N, Phillip J. Toward a systematic approach to assessment and care planning in palliative care: a practical review of clinical tools. Palliat Support Care. 2016;14:161–73.CrossRef Hudson P, Collins A, Bostanci A, Willenberg L, Stephanov N, Phillip J. Toward a systematic approach to assessment and care planning in palliative care: a practical review of clinical tools. Palliat Support Care. 2016;14:161–73.CrossRef
31.
go back to reference Ferris FD, Balfour HM, Bowen K, Farley J, Hardwick M, Lamontagne C, Lundy M, Syme A, West PJ. A model to guide patient and family care: based on nationally accepted principles and norms of practice. J Pain Symptom Manage. 2002;24:106–23.CrossRef Ferris FD, Balfour HM, Bowen K, Farley J, Hardwick M, Lamontagne C, Lundy M, Syme A, West PJ. A model to guide patient and family care: based on nationally accepted principles and norms of practice. J Pain Symptom Manage. 2002;24:106–23.CrossRef
32.
go back to reference Weissman DE, Meier DE. Identifying patients in need of a palliative care assessment in the hospital setting: a consensus report from the center to advance palliative care. J Palliat Med. 2011;14:17–23.CrossRef Weissman DE, Meier DE. Identifying patients in need of a palliative care assessment in the hospital setting: a consensus report from the center to advance palliative care. J Palliat Med. 2011;14:17–23.CrossRef
33.
go back to reference Antunes B, Harding R, Higginson IJ. Euroimpact: implementing patient-reported outcome measures in palliative care clinical practice: a systematic review of facilitators and barriers. Palliat Med. 2014;28:158–75.CrossRef Antunes B, Harding R, Higginson IJ. Euroimpact: implementing patient-reported outcome measures in palliative care clinical practice: a systematic review of facilitators and barriers. Palliat Med. 2014;28:158–75.CrossRef
34.
go back to reference Bausewein C, Daveson BA, Currow DC, Downing J, Deliens L, Radbruch L, Defilippi K, Lopes Ferreira P, Costantini M, Harding R, Higginson IJ. EAPC White paper on outcome measurement in palliative care: improving practice, attaining outcomes and delivering quality services - recommendations from the European Association for Palliative Care (EAPC) task force on outcome measurement. Palliat Med. 2016;30:6–22.CrossRef Bausewein C, Daveson BA, Currow DC, Downing J, Deliens L, Radbruch L, Defilippi K, Lopes Ferreira P, Costantini M, Harding R, Higginson IJ. EAPC White paper on outcome measurement in palliative care: improving practice, attaining outcomes and delivering quality services - recommendations from the European Association for Palliative Care (EAPC) task force on outcome measurement. Palliat Med. 2016;30:6–22.CrossRef
35.
go back to reference Aoun S, Slatyer S, Deas K, Nekolaichuk C. Family caregiver participation in palliative care research: challenging the myth. J Pain Symptom Manag. 2017;53:851–61.CrossRef Aoun S, Slatyer S, Deas K, Nekolaichuk C. Family caregiver participation in palliative care research: challenging the myth. J Pain Symptom Manag. 2017;53:851–61.CrossRef
36.
go back to reference Higginson I, Wade A, McCarthy M. Palliative care: views of patients and their families. BMJ. 1990;301:277–81.CrossRef Higginson I, Wade A, McCarthy M. Palliative care: views of patients and their families. BMJ. 1990;301:277–81.CrossRef
Metadata
Title
Caregiver exposure to critical events and distress in home-based palliative care in Germany a cross-sectional study using the Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) scale
Authors
Michael Galatsch
Holly G. Prigerson
Wilfried Schnepp
Friederike zu Sayn-Wittgenstein
Jian Li
Publication date
01-12-2019
Publisher
BioMed Central
Keywords
Care
Anxiety
Published in
BMC Palliative Care / Issue 1/2019
Electronic ISSN: 1472-684X
DOI
https://doi.org/10.1186/s12904-019-0395-8

Other articles of this Issue 1/2019

BMC Palliative Care 1/2019 Go to the issue