Literature DB >> 22669411

Quality of life and coping of women treated for breast cancer and their caregiver. What are the interactions?

Angélique Bonnaud-Antignac1, Jean-Benoit Hardouin, Julie Leger, François Dravet, Véronique Sebille.   

Abstract

This longitudinal study analyzed the interactions between the quality of life and the coping strategies of 100 patients treated for breast cancer and their caregivers. Data were collected after diagnosis, at the end of treatment, and 6 months after treatment with the Quality of Life Questionnaire-C30 (QLQ-C30), Duke Health Profile and Ways of Coping Checklist for both patients and caregivers. The theoretical model was tested using a typology of patients and mixed model analyses. The quality of life of patients changed over time and no cluster effect was found. The influence of the sociodemographic characteristics, coping strategies (patients and caregivers) and the quality of life of caregivers on patient's quality of life were different according to the quality of life dimensions considered. To understand the adaptation of patients to their disease, it is therefore essential to look at whether the caregiver is capable of playing a supporting role.

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Year:  2012        PMID: 22669411     DOI: 10.1007/s10880-012-9300-9

Source DB:  PubMed          Journal:  J Clin Psychol Med Settings        ISSN: 1068-9583


  22 in total

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Journal:  CMAJ       Date:  2004-06-08       Impact factor: 8.262

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Journal:  Nurs Res       Date:  1987 Jul-Aug       Impact factor: 2.381

Review 10.  Outcomes and quality of life following breast cancer treatment in older women: when, why, how much, and what do women want?

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Journal:  Health Qual Life Outcomes       Date:  2003-09-17       Impact factor: 3.186

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  5 in total

1.  Addressing psychosocial needs of partners of breast cancer patients: a pilot program using social workers to improve communication and psychosocial support.

Authors:  Rondi Kauffmann; Courtney Bitz; Karen Clark; Matthew Loscalzo; Laura Kruper; Courtney Vito
Journal:  Support Care Cancer       Date:  2015-04-28       Impact factor: 3.603

2.  Caregiving for patients in vegetative and minimally conscious states: perceived burden as a mediator in caregivers' expression of needs and symptoms of depression and anxiety.

Authors:  M Pagani; A M Giovannetti; V Covelli; D Sattin; M Leonardi
Journal:  J Clin Psychol Med Settings       Date:  2014-09

3.  Longitudinal dyadic interdependence in psychological distress among Latinas with breast cancer and their caregivers.

Authors:  Chris Segrin; Terry A Badger; Alla Sikorskii; Alice Pasvogel; Karen Weihs; Ana Maria Lopez; Pavani Chalasani
Journal:  Support Care Cancer       Date:  2019-11-09       Impact factor: 3.359

4.  Linguistic Markers of Processing Trauma Experience in Women's Written Narratives During Different Breast Cancer Phases: Implications for Clinical Interventions.

Authors:  Maria Luisa Martino; Raffaella Onorato; Maria Francesca Freda
Journal:  Eur J Psychol       Date:  2015-11-27

Review 5.  Coping Assessment Tools in the Family Caregivers of Patients with Breast Cancer: A Systematic Review.

Authors:  Marzieh Jahani Sayad Noveiri; Farshid Shamsaei; Masoud Khodaveisi; Zohreh Vanaki; Lily Tapak
Journal:  Breast Cancer (Dove Med Press)       Date:  2020-02-05
  5 in total

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