Literature DB >> 16532486

Predictors of distress in caregivers of persons with a primary malignant brain tumor.

Paula R Sherwood1, Barbara A Given, Charles W Given, Rachel F Schiffman, Daniel L Murman, Mary Lovely, Alexander von Eye, Lisa R Rogers, Sandy Remer.   

Abstract

The purpose of this cross-sectional, descriptive study was to identify predictors of distress for family caregivers of persons with a primary malignant brain tumor (PMBT). The effect of the care recipient's functional, cognitive, and neuropsychiatric status on caregiver burden and depressive symptoms was examined through telephone interviews with 95 caregivers. Care recipients' neuropsychiatric status consistently affected caregivers' depressive symptoms and burden, and assisting with activities of daily living affected burden related to caregivers' schedules and health. The care recipient's cognitive status and need for assistance with instrumental activities of daily living did not affect any outcome variable. Results may help identify caregivers at risk for negative outcomes, and suggest interventions to improve caregivers' emotional health. Copyright 2006 Wiley Periodicals, Inc.

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Year:  2006        PMID: 16532486     DOI: 10.1002/nur.20116

Source DB:  PubMed          Journal:  Res Nurs Health        ISSN: 0160-6891            Impact factor:   2.228


  52 in total

Review 1.  Systematic review of supportive care needs in patients with primary malignant brain tumors.

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Journal:  Neuro Oncol       Date:  2012-02-03       Impact factor: 12.300

Review 2.  Neuro-oncology family caregiving: review and directions for future research.

Authors:  Paula R Sherwood; Maureen Cwiklik; Heidi S Donovan
Journal:  CNS Oncol       Date:  2015-12-17

Review 3.  The cancer family caregiving experience: an updated and expanded conceptual model.

Authors:  Barbara Swore Fletcher; Christine Miaskowski; Barbara Given; Karen Schumacher
Journal:  Eur J Oncol Nurs       Date:  2011-10-14       Impact factor: 2.398

4.  Predictors of employment and lost hours from work in cancer caregivers.

Authors:  Paula R Sherwood; Heidi S Donovan; Charles W Given; Xiaoli Lu; Barbara A Given; Allison Hricik; Sarah Bradley
Journal:  Psychooncology       Date:  2008-06       Impact factor: 3.894

5.  Effect of massage therapy on stress levels and quality of life in brain tumor patients--observations from a pilot study.

Authors:  Stephen Thomas Keir
Journal:  Support Care Cancer       Date:  2010-11-03       Impact factor: 3.603

6.  Needs of neuro-oncological patients and their caregivers during the hospitalization and after discharge: results from a longitudinal study.

Authors:  C Scaratti; M Leonardi; A Saladino; E Anghileri; M Broggi; E Lamperti; L Fariselli; R Ayadi; G Tringali; S Schiavolin
Journal:  Support Care Cancer       Date:  2017-02-15       Impact factor: 3.603

7.  Caring for the brain tumor patient: family caregiver burden and unmet needs.

Authors:  Jane R Schubart; Mable B Kinzie; Elana Farace
Journal:  Neuro Oncol       Date:  2007-11-09       Impact factor: 12.300

8.  Interaction of quality of life, mood and depression of patients and their informal caregivers after surgical treatment of high-grade glioma: a prospective study.

Authors:  Maxi Sacher; Jürgen Meixensberger; Wolfgang Krupp
Journal:  J Neurooncol       Date:  2018-08-02       Impact factor: 4.130

9.  The multidimensional burden of informal caregivers in primary malignant brain tumor.

Authors:  Eléonore Bayen; Florence Laigle-Donadey; Myrtille Prouté; Khê Hoang-Xuan; Marie-Eve Joël; Jean-Yves Delattre
Journal:  Support Care Cancer       Date:  2016-09-13       Impact factor: 3.603

10.  Caregiver-reported neuropsychiatric symptoms in patients undergoing treatment for head and neck cancer: a pilot study.

Authors:  Stewart M Bond; Deborah K Hawkins; Barbara A Murphy
Journal:  Cancer Nurs       Date:  2014 May-Jun       Impact factor: 2.592

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