Literature DB >> 29226997

Participation and interest in support services among family caregivers of older adults with cancer.

J Nicholas Dionne-Odom1, Allison J Applebaum2, Katherine A Ornstein3, Andres Azuero1, Paula P Warren4, Richard A Taylor1, Gabrielle B Rocque4,5, Elizabeth A Kvale6,7, Wendy Demark-Wahnefried8, Maria Pisu9, Edward E Partridge4, Michelle Y Martin10, Marie A Bakitas1,6.   

Abstract

OBJECTIVE: The purpose of this study was to describe distressed and underprepared family caregiver's use of and interest in formal support services (eg, professional counseling, education, organizational assistance).
METHOD: Cross-sectional mail survey conducted in communities of 8 cancer centers in Tennessee, Alabama, and Florida (response rate: 42%). Family caregivers of Medicare beneficiaries with pancreatic, lung, brain, ovarian, head and neck, hematologic, and stage IV cancers reported support service use and completed validated measures of depression, anxiety, burden, preparedness, and health.
RESULTS: Caregivers (n = 294) were on average age 65 years and mostly female (73%), White (91%), and care recipients' spouse/partner (60%); patients averaged 75 years were majority male (54%) with lung cancer (39%). Thirty-two percent of caregivers reported accessing services while 28% were "mostly" or "extremely" interested. Thirty-five percent of caregivers with high depressive symptoms (n = 122), 33% with high anxiety symptoms (n = 100), and 25% of those in the lowest quartile of preparedness (n = 77) accessed services. Thirty-eight percent of those with high depressive symptoms, 47% with high anxiety symptoms, and 36% in the lowest quartile of preparedness were "mostly" or "extremely" interested in receiving services. Being interested in support services was significantly associated with being a minority, shorter durations of caregiving, and with higher stress burden.
CONCLUSIONS: A large proportion of family caregivers, including those experiencing depression and anxiety symptoms and who were underprepared, are not using formal support services but have a strong interest in services. Strategies to increase service use may include targeting distressed caregivers early in their caregiving experience.
Copyright © 2017 John Wiley & Sons, Ltd.

Entities:  

Keywords:  cancer; family caregiver; palliative care; support services

Mesh:

Year:  2017        PMID: 29226997      PMCID: PMC5840039          DOI: 10.1002/pon.4603

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  30 in total

1.  Mutuality and preparedness as predictors of caregiver role strain.

Authors:  P G Archbold; B J Stewart; M R Greenlick; T Harvath
Journal:  Res Nurs Health       Date:  1990-12       Impact factor: 2.228

2.  Dementia Caregivers' Use of Services for Themselves.

Authors:  Jennifer Martindale-Adams; Linda O Nichols; Jeffrey Zuber; Robert Burns; Marshall J Graney
Journal:  Gerontologist       Date:  2015-09-08

Review 3.  A review of distress and its management in couples facing end-of-life cancer.

Authors:  Linda M McLean; Jennifer M Jones
Journal:  Psychooncology       Date:  2007-07       Impact factor: 3.894

4.  Barriers to mental health service use among distressed family caregivers of lung cancer patients.

Authors:  C E Mosher; B A Given; J S Ostroff
Journal:  Eur J Cancer Care (Engl)       Date:  2014-04-25       Impact factor: 2.520

5.  The self-care practices of family caregivers of persons with poor prognosis cancer: differences by varying levels of caregiver well-being and preparedness.

Authors:  J Nicholas Dionne-Odom; Wendy Demark-Wahnefried; Richard A Taylor; Gabrielle B Rocque; Andres Azuero; Aras Acemgil; Michelle Y Martin; Meka Astin; Deborah Ejem; Elizabeth Kvale; Karen Heaton; Maria Pisu; Edward E Partridge; Marie A Bakitas
Journal:  Support Care Cancer       Date:  2017-03-01       Impact factor: 3.603

6.  Quantifying the burden of informal caregiving for patients with cancer in Europe.

Authors:  Amir Goren; Isabelle Gilloteau; Michael Lees; Marco DaCosta Dibonaventura
Journal:  Support Care Cancer       Date:  2014-02-05       Impact factor: 3.603

7.  Revisiting the behavioral model and access to medical care: does it matter?

Authors:  R M Andersen
Journal:  J Health Soc Behav       Date:  1995-03

8.  Revisiting the Surveillance Epidemiology and End Results Cancer Registry and Medicare Health Outcomes Survey (SEER-MHOS) Linked Data Resource for Patient-Reported Outcomes Research in Older Adults with Cancer.

Authors:  Erin E Kent; Rochelle Malinoff; Heather M Rozjabek; Anita Ambs; Steven B Clauser; Marie A Topor; Gigi Yuan; James Burroughs; Anne B Rodgers; Kimberly DeMichele
Journal:  J Am Geriatr Soc       Date:  2016-01       Impact factor: 5.562

9.  Preliminary study of themes of meaning and psychosocial service use among informal cancer caregivers.

Authors:  Allison J Applebaum; Carol J Farran; Allison M Marziliano; Anna R Pasternak; William Breitbart
Journal:  Palliat Support Care       Date:  2013-08-07

10.  Psychological distress, health, and socio-economic factors in caregivers of terminally ill patients: a nationwide population-based cohort study.

Authors:  Mette Kjaergaard Nielsen; Mette Asbjoern Neergaard; Anders Bonde Jensen; Flemming Bro; Mai-Britt Guldin
Journal:  Support Care Cancer       Date:  2016-02-18       Impact factor: 3.603

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  12 in total

1.  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

2.  Factors Associated with Family Caregivers' Confidence in Future Surrogate Decision Making for Persons with Cancer.

Authors:  J Nicholas Dionne-Odom; Deborah Ejem; Andres Azuero; Richard A Taylor; Gabrielle B Rocque; Yasemin Turkman; Moneka A Thompson; Sara J Knight; Michelle Y Martin; Marie A Bakitas
Journal:  J Palliat Med       Date:  2018-08-21       Impact factor: 2.947

3.  Cancer in the context of aging: Health characteristics, function and caregiving needs prior to a new cancer diagnosis in a national sample of older adults.

Authors:  Katherine A Ornstein; Bian Liu; Rebecca M Schwartz; Cardinale B Smith; Naomi Alpert; Emanuela Taioli
Journal:  J Geriatr Oncol       Date:  2019-04-02       Impact factor: 3.599

4.  Multimodal psychosocial intervention for family caregivers of patients undergoing hematopoietic stem cell transplantation: A randomized clinical trial.

Authors:  Areej El-Jawahri; Jamie M Jacobs; Ashley M Nelson; Lara Traeger; Joseph A Greer; Showly Nicholson; Lauren P Waldman; Alyssa L Fenech; Annemarie D Jagielo; Jennifer D'Alotto; Nora Horick; Thomas Spitzer; Zachariah DeFilipp; Yi-Bin A Chen; Jennifer S Temel
Journal:  Cancer       Date:  2020-01-03       Impact factor: 6.860

5.  Trajectories of social resource use among informal lung cancer caregivers.

Authors:  Kristin Litzelman; Maija Reblin; Helene E McDowell; Lori L DuBenske
Journal:  Cancer       Date:  2019-10-18       Impact factor: 6.860

6.  Caregiver Eligibility for Support Services: Correlates and Consequences for Resource Utilization.

Authors:  Kristin Litzelman; Autumn Harnish
Journal:  J Appl Gerontol       Date:  2020-11-06

7.  Caregiver engagement practices in National Cancer Institute Clinical Oncology Research Program settings: Implications for research to advance the field.

Authors:  Chandylen L Nightingale; Katherine R Sterba; Laurie E McLouth; Erin E Kent; Emily V Dressler; Alexandra Dest; Anna C Snavely; Christian S Adonizio; Mark Wojtowicz; Heather B Neuman; Anne E Kazak; Ruth C Carlos; Matthew F Hudson; Joseph M Unger; Charles S Kamen; Kathryn E Weaver
Journal:  Cancer       Date:  2020-11-02       Impact factor: 6.860

8.  Care for the Cancer Caregiver: a Qualitative Study of Facilitators and Barriers to Caregiver Integration and Support.

Authors:  Maija Reblin; Dana Ketcher; Susan T Vadaparampil
Journal:  J Cancer Educ       Date:  2021-03-30       Impact factor: 1.771

9.  Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care.

Authors:  Karin Oechsle; Anneke Ullrich; Gabriella Marx; Gesine Benze; Julia Heine; Lisa-Marie Dickel; Youyou Zhang; Feline Wowretzko; Kim Nikola Wendt; Friedemann Nauck; Carsten Bokemeyer; Corinna Bergelt
Journal:  BMC Palliat Care       Date:  2019-11-18       Impact factor: 3.234

10.  Supportive care needs and service use during palliative care in family caregivers of patients with advanced cancer: a prospective longitudinal study.

Authors:  Anneke Ullrich; Gabriella Marx; Corinna Bergelt; Gesine Benze; Youyou Zhang; Feline Wowretzko; Julia Heine; Lisa-Marie Dickel; Friedemann Nauck; Carsten Bokemeyer; Karin Oechsle
Journal:  Support Care Cancer       Date:  2020-07-06       Impact factor: 3.603

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