Literature DB >> 31292753

Informal caregiver quality of life in a palliative oncology population.

Adele Duimering1, Jill Turner2, Karen Chu1, Fleur Huang1, Diane Severin1, Sunita Ghosh3, Don Yee1, Ericka Wiebe1, Nawaid Usmani1, Zsolt Gabos1, Samir Patel1, Brita Danielson1, John Amanie1, Wilson Roa1, Alysa Fairchild4.   

Abstract

PURPOSE: Many patients with advanced cancer receive primary supports from informal caregivers (IC). As patient health deteriorates, IC assume increasing responsibility, often accompanied by distress. We investigated the quality of life (QOL) of IC of patients referred to a palliative radiotherapy (PRT) program.
METHODS: IC accompanying patients to a dedicated PRT clinic completed a survey based on the validated Caregiver Quality of Life Index-Cancer (CQOLC). Demographics, burden, and engagement in support services were evaluated. Summary statistics were calculated, and parameters were assessed for association with CQOLC scores by a generalized linear model.
RESULTS: Two hundred one surveys were analyzed representing 197 unique patients. The mean age was 68.3 years, with predominantly lung (25.0%) and prostate (19.3%) malignancies. 24.4% had been in hospital/long-term care within the previous 7 days. IC were 60.8% female, and 60.6% were the patient's spouse. 69.5% lived with the patient and 38.3% were additionally employed. IC spent a daily mean of 6.6 h (SD 7) assisting with instrumental (72.5%) and basic (37.5%) activities of daily living. Mean CQOLC score was 82.1/140 (SD 20). 63.8% of IC had previously accessed support service(s), most commonly home care (37.2%) and pharmacy (29.1%). 55.9% indicated interest in services not yet accessed. Multivariate analysis revealed additional employment, cohabitation, poor patient performance status, and interest in accessing more support services significantly correlated with higher IC burden.
CONCLUSIONS: Employing the CQOLC to screen IC of patients referred to a PRT program permits early identification of vulnerable IC to facilitate linkage with appropriate supports.

Entities:  

Keywords:  Caregiver burden; Informal caregiver; Oncology; Palliative; Quality of life; Radiotherapy

Mesh:

Year:  2019        PMID: 31292753     DOI: 10.1007/s00520-019-04970-3

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  28 in total

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2.  The Caregiver Quality of Life Index-Cancer (CQOLC) Scale: revalidation in a home hospice setting.

Authors:  M A Weitzner; S C McMillan
Journal:  J Palliat Care       Date:  1999       Impact factor: 2.250

3.  Time costs associated with informal caregiving for cancer survivors.

Authors:  K Robin Yabroff; Youngmee Kim
Journal:  Cancer       Date:  2009-09-15       Impact factor: 6.860

4.  Increased risks of coronary heart disease and stroke among spousal caregivers of cancer patients.

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5.  Benefits of Early Versus Delayed Palliative Care to Informal Family Caregivers of Patients With Advanced Cancer: Outcomes From the ENABLE III Randomized Controlled Trial.

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6.  Burden, emotional distress and quality of life among informal caregivers of lung cancer patients: An exploratory study.

Authors:  J-Y Tan; A Molassiotis; M Lloyd-Williams; J Yorke
Journal:  Eur J Cancer Care (Engl)       Date:  2017-04-18       Impact factor: 2.520

7.  Cancer caregivers' quality of life: effects of gender, relationship, and appraisal.

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Review 8.  The psychological impact of cancer on patients' partners and other key relatives: a review.

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9.  Impact of early palliative care on caregivers of patients with advanced cancer: cluster randomised trial.

Authors:  J McDonald; N Swami; B Hannon; C Lo; A Pope; A Oza; N Leighl; M K Krzyzanowska; G Rodin; L W Le; C Zimmermann
Journal:  Ann Oncol       Date:  2017-01-01       Impact factor: 32.976

10.  Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

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  8 in total

1.  Reply to: "Informal caregiver quality of life in a palliative oncology population".

Authors:  Kohei Kajiwara; Jun Kako; Hiroko Noto; Yasufumi Oosono; Masamitsu Kobayashi
Journal:  Support Care Cancer       Date:  2019-08-10       Impact factor: 3.603

2.  Assessing the Reliability and Validity of a Brief Measure of Caregiver Quality of Life.

Authors:  Debra Parker Oliver; Robin L Kruse; Jamie Smith; Karla Washington; George Demiris
Journal:  J Pain Symptom Manage       Date:  2019-07-31       Impact factor: 3.612

3.  Study Protocol for the Evaluation of Individual Psychological Interventions for Family Caregivers of Advanced Cancer Patients.

Authors:  Min Yang; Rui Sun; Yanfeng Wang; Haiyan Xu; Baohua Zou; Yanmin Yang; Minghua Cong; Yadi Zheng; Lei Yu; Fei Ma; Tinglin Qiu; Jiang Li
Journal:  Front Psychol       Date:  2021-01-20

Review 4.  Family reported outcomes, an unmet need in the management of a patient's disease: appraisal of the literature.

Authors:  R Shah; F M Ali; A Y Finlay; M S Salek
Journal:  Health Qual Life Outcomes       Date:  2021-08-05       Impact factor: 3.186

Review 5.  Understanding and Supporting Informal Cancer Caregivers.

Authors:  Alex Molassiotis; Mian Wang
Journal:  Curr Treat Options Oncol       Date:  2022-03-14

6.  What patients with lung cancer with comorbidity tell us about interprofessional collaborative care across healthcare sectors: qualitative interview study.

Authors:  Jasmin Bossert; Johanna Forstner; Matthias Villalobos; Anja Siegle; Corinna Jung; Nicole Deis; Michael Thomas; Michel Wensing; Katja Krug
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Review 7.  Caring for the caregiver: a systematic review characterising the experience of caregivers of older adults with advanced cancers.

Authors:  Jacob J Adashek; Ishwaria M Subbiah
Journal:  ESMO Open       Date:  2020-09

8.  Self-care, resilience, and caregiver burden in relatives of patients with advanced cancer: results from the eQuiPe study.

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Journal:  Support Care Cancer       Date:  2021-07-03       Impact factor: 3.603

  8 in total

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