Literature DB >> 21601142

Differences on psychosocial outcomes between male and female caregivers of children with life-limiting illnesses.

Monica Schneider1, Rose Steele, Susan Cadell, David Hemsworth.   

Abstract

This secondary analysis of data examined the psychosocial outcomes of meaning in caregiving, self-esteem, optimism, burden, depression, spirituality, and posttraumatic growth in 273 parents caring for children with life-limiting illnesses to (a) determine if there were gender differences and (b) identify gender-specific correlations among these outcomes. Findings suggest that significant gender differences exist. Women reported higher average scores compared with men for meaning in caregiving, depression, burden, and posttraumatic growth and lower average scores for optimism. Correlations also revealed some significant differences. Health care professionals need to be aware of gender differences and tailor their interventions appropriately.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21601142     DOI: 10.1016/j.pedn.2010.01.007

Source DB:  PubMed          Journal:  J Pediatr Nurs        ISSN: 0882-5963            Impact factor:   2.145


  7 in total

1.  Demographic, medical, and psychosocial predictors of benefit finding among caregivers of childhood cancer survivors.

Authors:  Molly H Gardner; Sylvie Mrug; David C Schwebel; Sean Phipps; Kimberly Whelan; Avi Madan-Swain
Journal:  Psychooncology       Date:  2015-10-22       Impact factor: 3.894

2.  Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?

Authors:  Allyn McConkie-Rosell; Stephen R Hooper; Loren D M Pena; Kelly Schoch; Rebecca C Spillmann; Yong-Hui Jiang; Heidi Cope; Christina Palmer; Vandana Shashi
Journal:  J Genet Couns       Date:  2018-01-02       Impact factor: 2.537

3.  Health Related Quality of Life in Family Caregivers of Patients Suffering from Mental Disorders.

Authors:  Fatemeh Noghani; Naiemeh Seyedfatemi; Mohammad-Reza Karimirad; Arash Akbarzadeh; Ali Hasanpour-Dehkordi
Journal:  J Clin Diagn Res       Date:  2016-11-01

Review 4.  Parents as informal caregivers of children and adolescents with spinal muscular atrophy: a systematic review of quantitative and qualitative data on the psychosocial situation, caregiver burden, and family needs.

Authors:  Maja Brandt; Lene Johannsen; Laura Inhestern; Corinna Bergelt
Journal:  Orphanet J Rare Dis       Date:  2022-07-19       Impact factor: 4.303

Review 5.  Designing and implementing a longitudinal study of children with neurological, genetic or metabolic conditions: charting the territory.

Authors:  Harold Siden; Rose Steele; Rollin Brant; Susan Cadell; Betty Davies; Lynn Straatman; Kimberley Widger; Gail S Andrews
Journal:  BMC Pediatr       Date:  2010-09-20       Impact factor: 2.125

6.  Burden among caregivers of people with mental illness at Jimma University Medical Center, Southwest Ethiopia: a cross-sectional study.

Authors:  Mohammed Ayalew; Abdulhalik Workicho; Elias Tesfaye; Hailemariam Hailesilasie; Mubarek Abera
Journal:  Ann Gen Psychiatry       Date:  2019-06-24       Impact factor: 3.455

7.  Differing needs of mothers and fathers during their child's end-of-life care: secondary analysis of the "Paediatric end-of-life care needs" (PELICAN) study.

Authors:  Tanja Leemann; Eva Bergstraesser; Eva Cignacco; Karin Zimmermann
Journal:  BMC Palliat Care       Date:  2020-08-04       Impact factor: 3.234

  7 in total

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