Literature DB >> 23695928

Informal caregiving for cancer patients.

Francesca Romito1, Gil Goldzweig, Claudia Cormio, Mariët Hagedoorn, Barbara L Andersen.   

Abstract

According to the recent worldwide estimation by the GLOBOCAN project, in total, 12.7 million new cancer cases and 7.6 million cancer deaths occurred in 2008. The worldwide number of cancer survivors within 5 years of diagnosis has been estimated at be almost 28.8 million. Informal caregivers, such as family members and close friends, provide essential support to cancer patients. The authors of this report provide an overview of issues in the study of informal caregivers for cancer patients and long-term survivors in the United States and Europe, characterizing the caregivers commonly studied; the resources currently available to them; and their unmet needs, their psychosocial outcomes, and the psychosocial interventions tailored to their special circumstances. A broad overview of the state of research and knowledge, both in Europe and the United States, and observations on the directions for future research are provided.
Copyright © 2013 American Cancer Society.

Entities:  

Mesh:

Year:  2013        PMID: 23695928      PMCID: PMC3816360          DOI: 10.1002/cncr.28057

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  56 in total

1.  Cancer distress reduction with a couple-based skills training: a randomized controlled trial.

Authors:  Nina Heinrichs; Tanja Zimmermann; Birgit Huber; Peter Herschbach; Daniel W Russell; Donald H Baucom
Journal:  Ann Behav Med       Date:  2012-04

2.  Quality of life of family caregivers 5 years after a relative's cancer diagnosis: follow-up of the national quality of life survey for caregivers.

Authors:  Youngmee Kim; Rachel L Spillers; Daniel L Hall
Journal:  Psychooncology       Date:  2010-12-20       Impact factor: 3.894

Review 3.  How can informal caregivers in cancer and palliative care be supported? An updated systematic literature review of interventions and their effectiveness.

Authors:  Richard Harding; Sally List; Eleni Epiphaniou; Hannah Jones
Journal:  Palliat Med       Date:  2011-07-07       Impact factor: 4.762

Review 4.  End-of-life care across Southern Europe: a critical review of cultural similarities and differences between Italy, Spain and Portugal.

Authors:  Arantza Meñaca; Natalie Evans; Erin V W Andrew; Franco Toscani; Silvia Finetti; Xavier Gómez-Batiste; Irene J Higginson; Richard Harding; Robert Pool; Marjolein Gysels
Journal:  Crit Rev Oncol Hematol       Date:  2011-07-08       Impact factor: 6.312

5.  Does the cancer patient's disease stage matter? A comparative study of caregivers' mental health and health related quality of life.

Authors:  Ellen Karine Grov; Berit Taraldsen Valeberg
Journal:  Palliat Support Care       Date:  2012-03-22

6.  Is self-disclosure in couples coping with cancer associated with improvement in depressive symptoms?

Authors:  Mariët Hagedoorn; Eli Puterman; Robbert Sanderman; Theo Wiggers; Peter C Baas; Michiel van Haastert; Anita DeLongis
Journal:  Health Psychol       Date:  2011-06-20       Impact factor: 4.267

7.  Racial variation in the cancer caregiving experience: a multisite study of colorectal and lung cancer caregivers.

Authors:  Michelle Y Martin; Sara Sanders; Joan M Griffin; Robert A Oster; Christine Ritchie; Sean M Phelan; Audie A Atienza; Katherine Kahn; Michelle van Ryn
Journal:  Cancer Nurs       Date:  2012 Jul-Aug       Impact factor: 2.592

8.  Partners and close family members of long-term cancer survivors: health status, psychosocial well-being and unmet supportive care needs.

Authors:  Daniel Turner; Eike Adams; Mary Boulton; Sian Harrison; Nada Khan; Peter Rose; Alison Ward; Eila K Watson
Journal:  Psychooncology       Date:  2011-09-09       Impact factor: 3.894

9.  Global estimates of cancer prevalence for 27 sites in the adult population in 2008.

Authors:  Freddie Bray; Jian-Song Ren; Eric Masuyer; Jacques Ferlay
Journal:  Int J Cancer       Date:  2012-07-26       Impact factor: 7.396

Review 10.  Culture and end of life care: a scoping exercise in seven European countries.

Authors:  Marjolein Gysels; Natalie Evans; Arantza Meñaca; Erin Andrew; Franco Toscani; Sylvia Finetti; H Roeline Pasman; Irene Higginson; Richard Harding; Robert Pool
Journal:  PLoS One       Date:  2012-04-03       Impact factor: 3.240

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  66 in total

1.  The influence of dyadic symptom distress on threat appraisals and self-efficacy in advanced cancer and caregiving.

Authors:  Katrina R Ellis; Mary R Janevic; Trace Kershaw; Cleopatra H Caldwell; Nancy K Janz; Laurel Northouse
Journal:  Support Care Cancer       Date:  2016-09-08       Impact factor: 3.603

2.  Engagement in health-promoting behaviors and patient-caregiver interdependence in dyads facing advanced cancer: an exploratory study.

Authors:  Katrina R Ellis; Mary R Janevic; Trace Kershaw; Cleopatra H Caldwell; Nancy K Janz; Laurel Northouse
Journal:  J Behav Med       Date:  2017-01-11

3.  Social factors in informal cancer caregivers: The interrelationships among social stressors, relationship quality, and family functioning in the CanCORS data set.

Authors:  Kristin Litzelman; Erin E Kent; Julia H Rowland
Journal:  Cancer       Date:  2015-10-19       Impact factor: 6.860

4.  Prevalence of cardiovascular disease and risk factors, quality of life, and health behaviors of cancer survivors and their spouses: findings from MEPS.

Authors:  Lixin Song; Ting Guan; Peiran Guo; Thomas C Keyserling; Courtney Van Houtven; Xianming Tan
Journal:  J Cancer Surviv       Date:  2019-08-22       Impact factor: 4.442

5.  Long-Term Survivorship Care After Cancer Treatment - Summary of a 2017 National Cancer Policy Forum Workshop.

Authors:  Ronald M Kline; Neeraj K Arora; Cathy J Bradley; Eden R Brauer; Darci L Graves; Natasha Buchanan Lunsford; Mary S McCabe; Shelley Fuld Nasso; Larissa Nekhlyudov; Julia H Rowland; Rebekkah M Schear; Patricia A Ganz
Journal:  J Natl Cancer Inst       Date:  2018-12-01       Impact factor: 13.506

6.  Dyadic quality of life among heterosexual and sexual minority breast cancer survivors and their caregivers.

Authors:  Ulrike Boehmer; Jeffrey E Stokes; Angela R Bazzi; Melissa A Clark
Journal:  Support Care Cancer       Date:  2019-11-14       Impact factor: 3.603

7.  The role of medical/nursing skills training in caregiver confidence and burden: A CanCORS study.

Authors:  Michelle A Mollica; Kristin Litzelman; Julia H Rowland; Erin E Kent
Journal:  Cancer       Date:  2017-07-20       Impact factor: 6.860

8.  Spouse cancer caregivers' burden and distress at entry to home hospice: The role of relationship quality.

Authors:  Maija Reblin; Gary Donaldson; Lee Ellington; Kathi Mooney; Michael Caserta; Dale Lund
Journal:  J Soc Pers Relat       Date:  2015-06-04

9.  Post-diagnosis social networks, and lifestyle and treatment factors in the After Breast Cancer Pooling Project.

Authors:  Candyce H Kroenke; Yvonne L Michael; Xiao-Ou Shu; Elizabeth M Poole; Marilyn L Kwan; Sarah Nechuta; Bette J Caan; John P Pierce; Wendy Y Chen
Journal:  Psychooncology       Date:  2016-01-08       Impact factor: 3.894

Review 10.  Caring for caregivers and patients: Research and clinical priorities for informal cancer caregiving.

Authors:  Erin E Kent; Julia H Rowland; Laurel Northouse; Kristin Litzelman; Wen-Ying Sylvia Chou; Nonniekaye Shelburne; Catherine Timura; Ann O'Mara; Karen Huss
Journal:  Cancer       Date:  2016-03-17       Impact factor: 6.860

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