Literature DB >> 22661096

Walking a mile in their shoes: anxiety and depression among partners and caregivers of cancer survivors at 6 and 12 months post-diagnosis.

Sylvie D Lambert1, Afaf Girgis, Christophe Lecathelinais, Fiona Stacey.   

Abstract

PURPOSE: This study aims to examine the prevalence of psychosocial variables associated with anxiety and depression among partners and caregivers of cancer survivors, compare prevalence with community norms and report differences across cancer diagnosis.
METHODS: A prospective survey of partners and caregivers was undertaken to assess anxiety and depression and potential psychosocial variables associated with these outcomes at 6 and 12 months post-survivor diagnosis (N = 436).
RESULTS: Although the proportion of anxious participants decreased over time (p = 0.01), the percentage of those depressed remained stable (p = 0.68). Most participants who were depressed were also anxious. To a certain extent, the prevalence of anxiety and depression exceeded community norms and varied across cancer types. Partners and caregivers particularly vulnerable included those of lung, haematological or head and neck survivors. High use of avoidant coping and interference in regular activities were associated with both anxiety and depression across time points. Of the different types of support measured, only lower emotional/informational support was associated with anxiety and depression at 6 months, whereas lower positive social interaction was associated with depression at 12 months. Additional variables associated with anxiety and depression at 12 months included higher unmet needs and involvement in personal and medical tasks, respectively.
CONCLUSIONS: Even at 12 months post-survivor diagnosis, almost a third of participants reported anxiety, a result partially predicted by high use of avoidant coping and interference in regular activities. Understanding variables associated with partners' and caregivers' anxiety and depression can lead to optimal referral to supportive care services and inform the tailoring of interventions to address those variables contributing to anxiety and depression at particular time points.

Entities:  

Mesh:

Year:  2012        PMID: 22661096     DOI: 10.1007/s00520-012-1495-7

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


  41 in total

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4.  Depressive symptoms in lung cancer patients and their family caregivers and the influence of family environment.

Authors:  Laura A Siminoff; Maureen Wilson-Genderson; Sherman Baker
Journal:  Psychooncology       Date:  2010-12       Impact factor: 3.894

5.  Psychiatric disorders and mental health service use among caregivers of advanced cancer patients.

Authors:  Lauren C Vanderwerker; Rachel E Laff; Nina S Kadan-Lottick; Suzanne McColl; Holly G Prigerson
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6.  The psychosocial impact of prostate cancer on patients and their partners.

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7.  Prevalence and predictors of anxiety and depression in women with invasive ovarian cancer and their caregivers.

Authors:  Melanie A Price; Phyllis N Butow; Daniel S J Costa; Madeleine T King; Lynley J Aldridge; Joanna E Fardell; Anna DeFazio; Penelope M Webb
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8.  Normative data for the HADS from a large non-clinical sample.

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9.  Interdependent anxiety and psychological distress in women with breast cancer and their partners.

Authors:  Chris Segrin; Terry Badger; Sybilla M Dorros; Paula Meek; Ana Maria Lopez
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10.  Hidden morbidity in cancer: spouse caregivers.

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  37 in total

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Authors:  Sylvie D Lambert; Hyojin Yoon; Katrina R Ellis; Laurel Northouse
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2.  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

3.  Improving information to caregivers of cancer patients: the Herlev Hospital Empowerment of Relatives through More and Earlier information Supply (HERMES) randomized controlled trial.

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Journal:  Support Care Cancer       Date:  2019-06-08       Impact factor: 3.603

4.  A pilot, multisite, randomized controlled trial of a self-directed coping skills training intervention for couples facing prostate cancer: accrual, retention, and data collection issues.

Authors:  Sylvie D Lambert; Patrick McElduff; Afaf Girgis; Janelle V Levesque; Tim W Regan; Jane Turner; Hayley Candler; Cathrine Mihalopoulos; Sophy T F Shih; Karen Kayser; Peter Chong
Journal:  Support Care Cancer       Date:  2015-07-17       Impact factor: 3.603

5.  How are spousal depressed mood, distress, and quality of life associated with risk of depressed mood in cancer survivors? Longitudinal findings from a national sample.

Authors:  Kristin Litzelman; K Robin Yabroff
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2015-06       Impact factor: 4.254

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

Authors:  J Nicholas Dionne-Odom; Allison J Applebaum; Katherine A Ornstein; Andres Azuero; Paula P Warren; Richard A Taylor; Gabrielle B Rocque; Elizabeth A Kvale; Wendy Demark-Wahnefried; Maria Pisu; Edward E Partridge; Michelle Y Martin; Marie A Bakitas
Journal:  Psychooncology       Date:  2017-12-28       Impact factor: 3.894

8.  Longitudinal associations between caregiver burden and patient and spouse distress in couples coping with lung cancer.

Authors:  Kathrin Milbury; Hoda Badr; Frank Fossella; Katherine M Pisters; Cindy L Carmack
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9.  "You need something like this to give you guidelines on what to do": patients' and partners' use and perceptions of a self-directed coping skills training resource.

Authors:  Sylvie D Lambert; Afaf Girgis; Jane Turner; Tim Regan; Hayley Candler; Ben Britton; Suzanne Chambers; Catalina Lawsin; Karen Kayser
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10.  A telephone outcall program to support caregivers of people diagnosed with cancer: utility, changes in levels of distress, and unmet needs.

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Journal:  Support Care Cancer       Date:  2018-05-15       Impact factor: 3.603

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