Literature DB >> 12801132

Disease-related distress in parents of children with cancer at various stages after the time of diagnosis.

Krister Boman1, Annika Lindahl, Olle Björk.   

Abstract

This study evaluates and describes disease-related distress in parents, with particular focus on the association between the time elapsed since the child's cancer diagnosis and a number of indicators of distress. In a cross-sectional design, 264 mothers and fathers of children with various malignancies completed a multidimensional questionnaire focusing on 11 illness-specific and general indicators of distress. Parents were assessed from 4 weeks to 14 years after the child's diagnosis, and age of children at onset of illness ranged from newly born to 21 years (mean approximately 6 years). The levels of distress related to loss of control, self-esteem, anxiety, depression, sleep disturbances, and psychological and physical distress were lower among parents for whom a longer period of time had elapsed from the time of diagnosis. However, the time elapsed could not explain all of the variation in these stress reactions, or any of the variation in uncertainty, disease-related fear and loneliness. The child's age at diagnosis and treatment situation at assessment were surpassed by time elapsed since diagnosis as predictors of variance in parental distress. The pattern observed indicates the presence of disease-related distress even years after the completion of medical treatment. The findings point to the need for research to identify parents at particular risk of suffering long-term harmful consequences from the prolonged stress of parenting a child with cancer. The necessity of longitudinal studies to evaluate the proportion of acute stress in relation to chronic or cumulative parental stress is emphasized.

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Year:  2003        PMID: 12801132     DOI: 10.1080/02841860310004995

Source DB:  PubMed          Journal:  Acta Oncol        ISSN: 0284-186X            Impact factor:   4.089


  23 in total

1.  Barriers to the enrollment of children in the Children's Oncology Group study of very low risk Wilms tumor: a report from the Children's Oncology Group.

Authors:  Conrad V Fernandez; Ning Li; Elizabeth A Mullen; Paul E Grundy; Elizabeth J Perman; Robert C Shamberger; Peter F Ehrlich; Jeffrey S Dome
Journal:  J Pediatr Hematol Oncol       Date:  2011-10       Impact factor: 1.289

2.  Quality of life among parents of children with cancer or brain tumors: the impact of child characteristics and parental psychosocial factors.

Authors:  Kristin Litzelman; Kris Catrine; Ronald Gangnon; Whitney P Witt
Journal:  Qual Life Res       Date:  2011-02-02       Impact factor: 4.147

3.  Stress-mediated quality of life outcomes in parents of childhood cancer and brain tumor survivors: a case-control study.

Authors:  Whitney P Witt; Kristin Litzelman; Lauren E Wisk; Hilary A Spear; Kris Catrine; Nataliya Levin; Carissa A Gottlieb
Journal:  Qual Life Res       Date:  2010-05-15       Impact factor: 4.147

4.  Sleep quality of mother-caregivers of Duchenne muscular dystrophy patients.

Authors:  Karen T Nozoe; Daniel N Polesel; Gustavo A Moreira; Gabriel N Pires; Ricardo T Akamine; Sergio Tufik; Monica L Andersen
Journal:  Sleep Breath       Date:  2015-05-24       Impact factor: 2.816

5.  Understanding psychological distress among pediatric cancer caregivers.

Authors:  Gina E Nam; Echo L Warner; Deborah K Morreall; Anne C Kirchhoff; Anita Y Kinney; Mark Fluchel
Journal:  Support Care Cancer       Date:  2016-03-01       Impact factor: 3.603

6.  Childhood Cancer and Brain Tumor Late Effects: Relationships with Family Burden and Survivor Psychological Outcomes.

Authors:  Melissa K Cousino; Rebecca Hazen; Katherine Leigh Josie; Kelly Laschinger; Peter de Blank; H Gerry Taylor
Journal:  J Clin Psychol Med Settings       Date:  2017-12

7.  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

8.  Perceptions of changes in clinical, informational, and supportive relationships after end of treatment among parents of young childhood cancer survivors.

Authors:  Justin G Wilford; Suellen Hopfer; Lari Wenzel
Journal:  Psychooncology       Date:  2019-03-14       Impact factor: 3.894

9.  Psychological outcomes in Swedish and Icelandic parents following a child's cancer-in the light of site-related differences.

Authors:  Eygló Gudmundsdóttir; Lina Hörnquist; Krister K Boman
Journal:  Support Care Cancer       Date:  2013-02-05       Impact factor: 3.603

10.  Specificity of problem-solving skills training in mothers of children newly diagnosed with cancer: results of a multisite randomized clinical trial.

Authors:  Olle Jane Z Sahler; Michael J Dolgin; Sean Phipps; Diane L Fairclough; Martha A Askins; Ernest R Katz; Robert B Noll; Robert W Butler
Journal:  J Clin Oncol       Date:  2013-01-28       Impact factor: 44.544

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