Literature DB >> 23625020

Association between hope and burden reported by family caregivers of patients with advanced cancer.

Inger Utne1, Christine Miaskowski, Steven M Paul, Tone Rustøen.   

Abstract

PURPOSE: The aim of this study, in a sample of family caregivers (FCs) of patients with advanced cancer, was to describe the level of FC burden using the Caregiver Reaction Assessment (CRA). In addition, the effects of select FC and patient characteristics on each of the CRA subscales were evaluated.
METHODS: FCs and patients (n = 112) completed a demographic questionnaire, and Herth Hope Index, and the Hospital Anxiety and Depression Scale. FCs completed the CRA. Data were analyzed using multiple linear regression analyses.
RESULTS: For three of the five CRA subscales (i.e., "impact on finances", "impact on daily schedule", and "impact on health"), the mean scores were comparable to a Norwegian sample of FCs caring for patients in the late palliative phase. The variance in each of the CRA subscales was explained by different factors. Total explained variance ranged from 5.5% ("lack of family support") to 31.8% ("impact on daily schedule"). FC characteristics, such as being female and lower educational level, distress regarding the patient's pain, anxiety, depression, and level of hope, as well as the patients' number of comorbidities, depression, and hope contributed to an increase in various domains of FC burden. FCs' level of hope was a significant predictor for three of the CRA subscales (i.e., "self-esteem", "lack of family support", and "impact on health").
CONCLUSIONS: Findings suggest that FCs' and patients' level of hope are important determinants of caregiver burden and that FCs with lower levels of hope represent a high-risk group for higher levels of caregiver burden.

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Year:  2013        PMID: 23625020     DOI: 10.1007/s00520-013-1824-5

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  51 in total

1.  Measuring both negative and positive reactions to giving care to cancer patients: psychometric qualities of the Caregiver Reaction Assessment (CRA).

Authors:  C Nijboer; M Triemstra; R Tempelaar; R Sanderman; G A van den Bos
Journal:  Soc Sci Med       Date:  1999-05       Impact factor: 4.634

2.  The Norwegian version of the Herth Hope Index (HHI-N): a psychometric study.

Authors:  Astrid K Wahl; Tone Rustøen; Anners Lerdal; Berit R Hanestad; Oistein Knudsen; Torbjørn Moum
Journal:  Palliat Support Care       Date:  2004-09

3.  Hope and optimism: latent structures and influences on grade expectancy and academic performance.

Authors:  Kevin L Rand
Journal:  J Pers       Date:  2008-12-10

4.  Primary caregivers of cancer patients in the palliative phase: a path analysis of variables influencing their burden.

Authors:  Ellen Karine Grov; Sophie D Fosså; Oystein Sørebø; Alv A Dahl
Journal:  Soc Sci Med       Date:  2006-08-01       Impact factor: 4.634

5.  Anxiety, depression, and quality of life in caregivers of patients with cancer in late palliative phase.

Authors:  E K Grov; A A Dahl; T Moum; S D Fosså
Journal:  Ann Oncol       Date:  2005-04-22       Impact factor: 32.976

6.  Hope in the family caregiver of terminally ill people.

Authors:  K Herth
Journal:  J Adv Nurs       Date:  1993-04       Impact factor: 3.187

7.  The Norwegian brief pain inventory questionnaire: translation and validation in cancer pain patients.

Authors:  Pål Klepstad; Jon Håvard Loge; Petter C Borchgrevink; Tito R Mendoza; Charles S Cleeland; Stein Kaasa
Journal:  J Pain Symptom Manage       Date:  2002-11       Impact factor: 3.612

8.  Metasynthesis of the hope experience of family caregivers of persons with chronic illness.

Authors:  Wendy Duggleby; Lorraine Holtslander; Jari Kylma; Vicky Duncan; Chad Hammond; Allison Williams
Journal:  Qual Health Res       Date:  2010-02

9.  Effect of cancer pain on performance status, mood states, and level of hope among Taiwanese cancer patients.

Authors:  Chia-Chin Lin; Yuen-Liang Lai; Sandra E Ward
Journal:  J Pain Symptom Manage       Date:  2003-01       Impact factor: 3.612

10.  Advanced home care for cancer patients at the end of life: a qualitative study of hopes and expectations of family caregivers.

Authors:  Agneta Wennman-Larsen; Carol Tishelman
Journal:  Scand J Caring Sci       Date:  2002-09
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  17 in total

1.  "Oh, yeah, I'm getting closer to god": spirituality and religiousness of family caregivers of cancer patients undergoing palliative care.

Authors:  Bianca Sakamoto Ribeiro Paiva; André Lopes Carvalho; Giancarlo Lucchetti; Eliane Marçon Barroso; Carlos Eduardo Paiva
Journal:  Support Care Cancer       Date:  2015-01-16       Impact factor: 3.603

2.  Predictors of burden and quality of sleep among family caregivers of patients with cancer.

Authors:  Laila I Al-Daken; Muayyad M Ahmad
Journal:  Support Care Cancer       Date:  2018-05-26       Impact factor: 3.603

3.  Examining the role of subjective and objective burden in carer health-related quality of life: the case of colorectal cancer.

Authors:  Paul Hanly; Rebecca Maguire; Philip Hyland; Linda Sharp
Journal:  Support Care Cancer       Date:  2014-12-12       Impact factor: 3.603

4.  Ultimate journey of the terminally ill: Ways and pathways of hope.

Authors:  Serge Daneault; Véronique Lussier; Suzanne Mongeau; Louise Yelle; Andréanne Côté; Claude Sicotte; Pierre Paillé; Dominique Dion; Manon Coulombe
Journal:  Can Fam Physician       Date:  2016-08       Impact factor: 3.275

5.  Burden, quality of life, and social support in caregivers of patients undergoing radiotherapy for head and neck cancer: A pilot study.

Authors:  Chandylen L Nightingale; Barbara A Curbow; John R Wingard; Deidre B Pereira; Giselle D Carnaby
Journal:  Chronic Illn       Date:  2016-04-10

6.  Documenting stress in caregivers of transplantation patients: initial evidence of HPA dysregulation.

Authors:  Margaret F Bevans; Alyson Ross; Leslie Wehrlen; Stephen D Klagholz; Li Yang; Richard Childs; Sharon L Flynn; Alan T Remaley; Michael Krumlauf; Robert N Reger; Gwenyth R Wallen; Robert Shamburek; Karel Pacak
Journal:  Stress       Date:  2016-03-07       Impact factor: 3.493

7.  Caregiver-oncologist prognostic concordance, caregiving esteem, and caregiver outcomes.

Authors:  Kah Poh Loh; Erin Watson; Eva Culakova; Marie Flannery; Michael Sohn; Huiwen Xu; Sindhuja Kadambi; Allison Magnuson; Colin McHugh; Chandrika Sanapala; Lee Kehoe; Victor G Vogel; Brian L Burnette; Vincent Vinciguerra; Supriya G Mohile; Paul R Duberstein
Journal:  J Geriatr Oncol       Date:  2022-03-08       Impact factor: 3.929

8.  Assessing health status in informal schizophrenia caregivers compared with health status in non-caregivers and caregivers of other conditions.

Authors:  Shaloo Gupta; Gina Isherwood; Kevin Jones; Kristel Van Impe
Journal:  BMC Psychiatry       Date:  2015-07-21       Impact factor: 3.630

9.  Assessing cancer-related distress in cancer patients and caregivers receiving outpatient psycho-oncological counseling.

Authors:  Sabrina Gröpper; Elke van der Meer; Tom Landes; Hubert Bucher; Anna Stickel; Ute Goerling
Journal:  Support Care Cancer       Date:  2015-12-02       Impact factor: 3.359

Review 10.  Psychometric properties of carer-reported outcome measures in palliative care: A systematic review.

Authors:  Charlotte T J Michels; Mary Boulton; Astrid Adams; Bee Wee; Michele Peters
Journal:  Palliat Med       Date:  2015-09-25       Impact factor: 4.762

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