Literature DB >> 22127385

Understanding the health impact of caregiving: a qualitative study of immigrant parents and single parents of children with cancer.

Anne F Klassen1, Sonia Gulati, Leeat Granek, Zahava R S Rosenberg-Yunger, Lisa Watt, Lillian Sung, Robert Klaassen, David Dix, Nicola T Shaw.   

Abstract

PURPOSE: Research looking at the health of parents of children with cancer typically uses outcome measures focused on symptoms of anxiety, depression, or post-traumatic stress. Our team builds on this literature to provide a more comprehensive understanding of the health impact of caregiving.
METHODS: Interviews were conducted with 79 Canadian parents of children with cancer at least 6 months post-diagnosis. Line-by-line coding was used to establish categories and themes. Constant comparison was used to examine relationships within and across codes and categories. Interviewing continued until no new themes emerged.
RESULTS: Parents described health concerns as including sleep disturbance, daytime fatigue, anxiety, depression, social isolation, and changes in social roles. Parents described the positive impacts of caregiving as including gaining a greater appreciation for child and family and developing compassion, empathy, patience, inner strength, and new perspectives on life.
CONCLUSION: Parents of children with cancer can experience a range of health problems due to the emotional impact of a cancer diagnosis and the intensive and often prolonged nature of treatment and aftercare. Given the central role parents play as caregivers, it is crucial to understand the health impact of caregiving so that supportive interventions can be implemented as necessary.

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Year:  2011        PMID: 22127385     DOI: 10.1007/s11136-011-0072-8

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  27 in total

1.  Positive aspects of caregiving: rounding out the caregiver experience.

Authors:  Carole A Cohen; Angela Colantonio; Lee Vernich
Journal:  Int J Geriatr Psychiatry       Date:  2002-02       Impact factor: 3.485

Review 2.  Adjustment and coping by parents of children with cancer: a review of the literature.

Authors:  M A Grootenhuis; B F Last
Journal:  Support Care Cancer       Date:  1997-11       Impact factor: 3.603

3.  Cultural beliefs and coping strategies related to childhood cancer: the perceptions of South Asian immigrant parents in Canada.

Authors:  Ananya Tina Banerjee; Lisa Watt; Sonia Gulati; Lillian Sung; David Dix; Robert Klassen; Anne F Klassen
Journal:  J Pediatr Oncol Nurs       Date:  2011-06-06       Impact factor: 1.636

4.  Common themes and ethnic differences in family caregiving the first year after diagnosis of childhood cancer: Part II.

Authors:  M Leavitt; I M Martinson; C Y Liu; V Armstrong; L Hornberger; J Q Zhang; X P Han
Journal:  J Pediatr Nurs       Date:  1999-04       Impact factor: 2.145

5.  Positive perceptions in families of children with developmental disabilities.

Authors:  Richard P Hastings; Helen M Taunt
Journal:  Am J Ment Retard       Date:  2002-03

6.  Immigrant women's health.

Authors:  L M Meadows; W E Thurston; C Melton
Journal:  Soc Sci Med       Date:  2001-05       Impact factor: 4.634

7.  The experience of South American mothers who have a child being treated for malignancy in the United States.

Authors:  D B Crom
Journal:  J Pediatr Oncol Nurs       Date:  1995-07       Impact factor: 1.636

8.  PRO development: rigorous qualitative research as the crucial foundation.

Authors:  Kathryn Eilene Lasch; Patrick Marquis; Marc Vigneux; Linda Abetz; Benoit Arnould; Martha Bayliss; Bruce Crawford; Kathleen Rosa
Journal:  Qual Life Res       Date:  2010-05-30       Impact factor: 4.147

9.  Qualitative analysis of the role of culture in coping themes of Latina and European American mothers of children with cancer.

Authors:  Alexis L Johns; Alyssa A Oland; Ernest R Katz; Olle Jane Z Sahler; Martha A Askins; Robert W Butler; Michael J Dolgin
Journal:  J Pediatr Oncol Nurs       Date:  2009-04-27       Impact factor: 1.636

10.  Psychological distress and socioeconomic status in single mothers and their children in a German city.

Authors:  M Franz; H Lensche; N Schmitz
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2003-02       Impact factor: 4.328

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  9 in total

1.  Information-sharing challenges between adolescents with cancer, their parents and health care providers: a qualitative study.

Authors:  Masoud Bahrami; Mahboobeh Namnabati; Fariborz Mokarian; Parastoo Oujian; Paul Arbon
Journal:  Support Care Cancer       Date:  2017-01-11       Impact factor: 3.603

2.  Prevalence and Levels of Depression Among Parents of Children with Cancer in Basrah, Iraq.

Authors:  Shukrya K Al-Maliki; Jasim Al-Asadi; Akeel Al-Waely; Sabah Agha
Journal:  Sultan Qaboos Univ Med J       Date:  2016-08-19

3.  Feasibility and Preliminary Efficacy of an Internet Support Group for Parents of a Child with Neurofibromatosis Type 1: a Pilot Study.

Authors:  S Martin; M C Roderick; R Lockridge; M A Toledo-Tamula; A Baldwin; P Knight; P Wolters
Journal:  J Genet Couns       Date:  2016-11-07       Impact factor: 2.537

4.  The psychosocial profile of family caregivers of children with chronic diseases: a cross-sectional study.

Authors:  Filiberto Toledano-Toledano; David Luna
Journal:  Biopsychosoc Med       Date:  2020-10-22

5.  Power of Religious Beliefs and Coping with Cancer: Opinions of Iranian Parents.

Authors:  Fariba Mazhari; Masoud Rayyani; Sedigheh Iranmanesh; Shahin Heidari; Sakineh Sabzevari
Journal:  J Relig Health       Date:  2021-08

Review 6.  Disutility of illness for caregivers and families: a systematic review of the literature.

Authors:  Eve Wittenberg; Lisa A Prosser
Journal:  Pharmacoeconomics       Date:  2013-06       Impact factor: 4.981

7.  Measuring hemophilia caregiver burden: validation of the Hemophilia Caregiver Impact measure.

Authors:  Carolyn E Schwartz; Victoria E Powell; Adi Eldar-Lissai
Journal:  Qual Life Res       Date:  2017-04-25       Impact factor: 4.147

8.  Cross-Diagnostic Validity of the Congenital Glaucoma Caregiver's Quality of Life Questionnaire (CarCGQoL).

Authors:  Vijaya K Gothwal; Sujata Sharma; Anil K Mandal
Journal:  Transl Vis Sci Technol       Date:  2020-12-07       Impact factor: 3.283

9.  Interplay of disability, caregiver impact, and out-of-pocket expenditures in Duchenne muscular dystrophy: a cohort study.

Authors:  Carolyn E Schwartz; Roland B Stark; Katrina Borowiec; Ivana F Audhya; Katherine L Gooch
Journal:  J Patient Rep Outcomes       Date:  2022-03-10
  9 in total

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