Literature DB >> 22538260

The burdensome and depressive experience of caring: what cancer, schizophrenia, and Alzheimer's disease caregivers have in common.

Evridiki Papastavrou1, Andreas Charalambous, Haritini Tsangari, George Karayiannis.   

Abstract

BACKGROUND: Family members of patients with chronic illnesses experience distress as a result of caregiving roles, which can be manifested as burden and depression, but cross-disease studies on how caring is experienced are limited.
OBJECTIVE: The present study was designed to examine the burden and psychiatric morbidity in the form of depression experienced by Cypriot families caring for a relative with one of the following: cancer, Alzheimer's disease, or schizophrenia.
METHODS: This study was cross-sectional, descriptive, and correlational. A total of 410 caregivers were recruited from the community. The research instruments included the Greek version of the Burden Interview and the Center of Epidemiological Studies-Depression Scale. Descriptive statistics, 1-way analysis of variance, and post hoc Tukey pairwise comparisons were used to examine significant differences between the 3 groups.
RESULTS: The results indicate a high level of burden and depression among all caregivers. Significant differences (P < .001, F = 26.11) between the 3 caregiving groups were detected in terms of burden, with the highest reported for Alzheimer's disease caregivers. One-way analysis of variance showed significant differences (P = .008, F = 4.85) between the 3 caregiving groups in terms of depression, with the highest depression levels being for cancer caregivers.
CONCLUSIONS: The findings increase our understanding about burden and emotional well-being in family caring for relatives with cancer and other chronic illnesses. IMPLICATIONS FOR PRACTICE: The findings may be useful for health professionals to plan intervention strategies focusing on each domain of burden. The lessons learned from the caregiving role of family caregivers of patients with Alzheimer's disease or schizophrenia can be used to improve the caregiving process of patients with cancer.

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Year:  2012        PMID: 22538260     DOI: 10.1097/NCC.0b013e31822cb4a0

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  15 in total

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

2.  Cross-national differences in the prevalence and correlates of burden among older family caregivers in the World Health Organization World Mental Health (WMH) Surveys.

Authors:  V Shahly; S Chatterji; M J Gruber; A Al-Hamzawi; J Alonso; L H Andrade; M C Angermeyer; R Bruffaerts; B Bunting; J M Caldas-de-Almeida; G de Girolamo; P de Jonge; S Florescu; O Gureje; J M Haro; H R Hinkov; C Hu; E G Karam; J-P Lépine; D Levinson; M E Medina-Mora; J Posada-Villa; N A Sampson; J K Trivedi; M C Viana; R C Kessler
Journal:  Psychol Med       Date:  2012-08-09       Impact factor: 7.723

3.  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

4.  Stressors and common mental disorder in informal carers--an analysis of the English Adult Psychiatric Morbidity Survey 2007.

Authors:  Stephen Stansfeld; Melanie Smuk; Juliana Onwumere; Charlotte Clark; Cleo Pike; Sally McManus; Jenny Harris; Paul Bebbington
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5.  Are Disagreements in Caregiver and Patient Assessment of Patient Health Associated with Increased Caregiver Burden in Caregivers of Older Adults with Cancer?

Authors:  Tina Hsu; Matthew Loscalzo; Rupal Ramani; Stephen Forman; Leslie Popplewell; Karen Clark; Vani Katheria; Rex Strowbridge; Redmond Rinehart; Dan Smith; Keith Matthews; Jeff Dillehunt; Tao Feng; David Smith; Canlan Sun; Arti Hurria
Journal:  Oncologist       Date:  2017-08-14

6.  Review and Selection of Online Resources for Carers of Frail Adults or Older People in Five European Countries: Mixed-Methods Study.

Authors:  Roberta Papa; Areti Efthymiou; Giovanni Lamura; Flavia Piccinini; Giulia Onorati; Evridiki Papastavrou; Theologia Tsitsi; Giulia Casu; Licia Boccaletti; Alessandra Manattini; Rita Seneca; Carlos Vaz de Carvalho; Rita Durão; Francesco Barbabella; Frida Andréasson; Lennart Magnusson; Elizabeth Hanson
Journal:  JMIR Mhealth Uhealth       Date:  2020-06-17       Impact factor: 4.773

7.  Dementia as a predictor of care-related quality of life in informal caregivers: a cross-sectional study to investigate differences in health-related outcomes between dementia and non-dementia caregivers.

Authors:  Nina Karg; Elmar Graessel; Ottilie Randzio; Anna Pendergrass
Journal:  BMC Geriatr       Date:  2018-08-23       Impact factor: 3.921

8.  Comparison of the lived experiences of family caregivers of patients with dementia and of patients with cancer in Indonesia.

Authors:  Martina Sinta Kristanti; Yvonne Engels; Christantie Effendy; Adi Utarini; Myrra Vernooij-Dassen
Journal:  Int Psychogeriatr       Date:  2017-09-05       Impact factor: 3.878

9.  Family burden, family health and personal mental health.

Authors:  Edel Ennis; Brendan P Bunting
Journal:  BMC Public Health       Date:  2013-03-21       Impact factor: 3.295

10.  Mediators Linking Childhood Adversities and Trauma to Suicidality in Individuals at Risk for Psychosis.

Authors:  Stefanie J Schmidt; Frauke Schultze-Lutter; Sarah Bendall; Nicola Groth; Chantal Michel; Nadja Inderbitzin; Benno G Schimmelmann; Daniela Hubl; Barnaby Nelson
Journal:  Front Psychiatry       Date:  2017-11-20       Impact factor: 4.157

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