Literature DB >> 27573657

How Does Caregiver Well-Being Relate to Perceived Quality of Care in Patients With Cancer? Exploring Associations and Pathways.

Kristin Litzelman1, Erin E Kent1, Michelle Mollica1, Julia H Rowland1.   

Abstract

Purpose Perceived quality of care (QOC) is an increasingly important metric of care quality and can be affected by such factors among patients with cancer as quality of life and physician trust. This study sought to evaluate whether informal caregiver well-being was also associated with perceived QOC among patients with cancer and assessed potential pathways that link these factors. Methods This study used data from the Cancer Care Outcomes Research and Surveillance (CanCORS) consortium. Patients with lung and colorectal cancer enrolled in CanCORS (N = 689) nominated an informal caregiver to participate in a caregiving survey. Both groups self-reported sociodemographic, psychosocial, and caregiving characteristics; cancer characteristics were obtained from the CanCORS core data set. Multivariable logistic regression was used to assess the association between caregiver psychosocial factors and subsequent patient-perceived QOC, controlling for earlier patient-perceived QOC and covariates. Secondary analysis examined potential pathways that link these factors. Results Patients whose informal caregiver had higher levels of depressive symptoms were significantly more likely to report fair or poor QOC (odds ratio, 1.06; 95% CI, 1.01 to 1.13). When caregivers reported fair or poor self-rated health, patients were more than three times more likely to report fair or poor perceived QOC (odds ratio, 3.76; 95% CI, 1.76 to 9.55). Controlling for patient psychosocial factors and physician communication and coordination of medical care reduced the effect size and/or statistical significance of these relationships. Conclusion Informal caregivers are an important part of the care team and their well-being is associated with patient-perceived QOC. Engaging informal cancer caregivers as part of the care team and conducting ongoing risk stratification screening and intervention to optimize their health may improve patient-reported outcomes and QOC.

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Year:  2016        PMID: 27573657      PMCID: PMC5074348          DOI: 10.1200/JCO.2016.67.3434

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  33 in total

1.  Psychometric properties of the CAHPS 1.0 survey measures. Consumer Assessment of Health Plans Study.

Authors:  R D Hays; J A Shaul; V S Williams; J S Lubalin; L D Harris-Kojetin; S F Sweeny; P D Cleary
Journal:  Med Care       Date:  1999-03       Impact factor: 2.983

Review 2.  Family and caregiver needs over the course of the cancer trajectory.

Authors:  Barbara A Given; Charles W Given; Paula R Sherwood
Journal:  J Support Oncol       Date:  2012-01-04

3.  Evaluation of software for multiple imputation of semi-continuous data.

Authors:  L-M Yu; Andrea Burton; Oliver Rivero-Arias
Journal:  Stat Methods Med Res       Date:  2007-06       Impact factor: 3.021

4.  Meaning-Centered Psychotherapy for Cancer Caregivers (MCP-C): Rationale and Overview.

Authors:  Allison J Applebaum; Julia R Kulikowski; William Breitbart
Journal:  Palliat Support Care       Date:  2015-05-22

5.  The effects of caregiver emotional stress on the depressive symptomatology of the care recipient.

Authors:  Deborah B Ejem; Patricia Drentea; Olivio J Clay
Journal:  Aging Ment Health       Date:  2014-05-28       Impact factor: 3.658

6.  Cancer and quality of life in spousal dyads: spillover in couples with and without cancer-related health problems.

Authors:  Kristin Litzelman; Paige A Green; K Robin Yabroff
Journal:  Support Care Cancer       Date:  2015-07-05       Impact factor: 3.603

7.  Quality of breast cancer care: perception versus practice.

Authors:  Nina A Bickell; Jennifer Neuman; Kezhen Fei; Rebeca Franco; Kathie-Ann Joseph
Journal:  J Clin Oncol       Date:  2012-04-09       Impact factor: 44.544

8.  Population-based assessment of cancer survivors' financial burden and quality of life: a prospective cohort study.

Authors:  S Yousuf Zafar; Rebecca B McNeil; Catherine M Thomas; Christopher S Lathan; John Z Ayanian; Dawn Provenzale
Journal:  J Oncol Pract       Date:  2014-12-16       Impact factor: 3.840

9.  Patients' experiences with care for lung cancer and colorectal cancer: findings from the Cancer Care Outcomes Research and Surveillance Consortium.

Authors:  John Z Ayanian; Alan M Zaslavsky; Neeraj K Arora; Katherine L Kahn; Jennifer L Malin; Patricia A Ganz; Michelle van Ryn; Mark C Hornbrook; Catarina I Kiefe; Yulei He; Julie M Urmie; Jane C Weeks; David P Harrington
Journal:  J Clin Oncol       Date:  2010-08-16       Impact factor: 44.544

Review 10.  The impact of caregiving on the psychological well-being of family caregivers and cancer patients.

Authors:  Laurel L Northouse; Maria C Katapodi; Ann M Schafenacker; Denise Weiss
Journal:  Semin Oncol Nurs       Date:  2012-11       Impact factor: 2.315

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  33 in total

Review 1.  Caregiver Well-being and the Quality of Cancer Care.

Authors:  Kristin Litzelman
Journal:  Semin Oncol Nurs       Date:  2019-06-20       Impact factor: 2.315

2.  When chemotherapy fails: Emotionally charged experiences faced by family caregivers of patients with advanced cancer.

Authors:  Rachel A Rodenbach; Sally A Norton; Marsha N Wittink; Supriya Mohile; Holly G Prigerson; Paul R Duberstein; Ronald M Epstein
Journal:  Patient Educ Couns       Date:  2018-12-12

3.  Beyond care burden: associations between positive psychological appraisals and well-being among informal caregivers in Europe.

Authors:  Rebecca Maguire; Paul Hanly; Phil Maguire
Journal:  Qual Life Res       Date:  2019-02-04       Impact factor: 4.147

4.  Quality of Life of Caregivers of Older Patients with Advanced Cancer.

Authors:  Lee A Kehoe; Huiwen Xu; Paul Duberstein; Kah Poh Loh; Eva Culakova; Beverly Canin; Arti Hurria; William Dale; Megan Wells; Nikesha Gilmore; Amber S Kleckner; Jennifer Lund; Charles Kamen; Marie Flannery; Mike Hoerger; Judith O Hopkins; Jane Jijun Liu; Jodi Geer; Ron Epstein; Supriya G Mohile
Journal:  J Am Geriatr Soc       Date:  2019-03-29       Impact factor: 5.562

5.  Caring for the informal cancer caregiver.

Authors:  Virginia Sun; Dan J Raz; Jae Y Kim
Journal:  Curr Opin Support Palliat Care       Date:  2019-09       Impact factor: 2.302

6.  Who will care for the caregiver? Distress and depression among spousal caregivers of older patients undergoing treatment for cancer.

Authors:  Gil Goldzweig; L Schapira; L Baider; J M Jacobs; E Andritsch; Y Rottenberg
Journal:  Support Care Cancer       Date:  2019-03-06       Impact factor: 3.603

7.  Population-Based Profile of Mental Health and Support Service Need Among Family Caregivers of Adults With Cancer.

Authors:  Erin E Kent; J Nicholas Dionne-Odom
Journal:  J Oncol Pract       Date:  2018-11-29       Impact factor: 3.840

8.  Supporting cancer family caregivers: How can frontline oncology clinicians help?

Authors:  Laura S Porter; J Nicholas Dionne-Odom
Journal:  Cancer       Date:  2017-05-02       Impact factor: 6.860

9.  Lung cancer and family-centered patient concerns.

Authors:  Josephine Feliciano; Breanna Becker; Manish Shukla; Joann Bodurtha
Journal:  Support Care Cancer       Date:  2018-03-21       Impact factor: 3.603

10.  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

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