Literature DB >> 27185021

Burden and happiness in head and neck cancer carers: the role of supportive care needs.

Paul Hanly1, Rebecca Maguire2, Myles Balfe3, Philip Hyland2, Aileen Timmons3, Eleanor O'Sullivan4, Phyllis Butow5, Linda Sharp6.   

Abstract

PURPOSE: Our study aimed to investigate the relationship between unmet supportive care needs and carer burden and happiness, in head and neck cancer (HNC).
METHODS: Two hundred eighty-five HNC informal carers were sent a postal questionnaire between January and June 2014, which included the supportive care needs survey for partners and caregivers of cancer survivors (SCNS-P&C) and the CarerQol, which assesses burden and happiness. Multiple regression analysis was conducted to examine the association of (i) carer characteristics, (ii) carer situation, and (iii) unmet supportive care needs, with carer burden and happiness
RESULTS: One hundred ninety-seven carers completed the questionnaire (response rate = 69 %), 180 of whom were included in the analysis. The majority were female (76 %), not in paid employment (68 %) and caring for their spouse (67 %). On average, carers reported relatively low levels of burden and relatively high levels of happiness. Carer factors explained 42 % of variance in levels of burden and 24 % of variance in levels of happiness. Healthcare service needs were associated with carer burden (β = .28, p = .04), while psychological needs (β = -.38, p = .028), health care service needs (β = -.30, p = .049), information needs (β = .29, p = .028), carer comorbidity (β = -.18, p = .030), and gender (β = -.16, p = .045) were associated with happiness.
CONCLUSIONS: Our results indicate that different aspects of carer characteristics and unmet needs are associated with carer burden and happiness. Efforts directed at reducing unmet healthcare service needs in particular are merited given their associations with both aspects of carer quality of life.

Entities:  

Keywords:  Carer burden; Happiness; Head and neck cancer carer burden; Quality of life; Unmet needs

Mesh:

Year:  2016        PMID: 27185021     DOI: 10.1007/s00520-016-3261-8

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


  42 in total

1.  The supportive care needs survey for partners and caregivers of cancer survivors: development and psychometric evaluation.

Authors:  Afaf Girgis; Sylvie Lambert; Christophe Lecathelinais
Journal:  Psychooncology       Date:  2010-04-05       Impact factor: 3.894

2.  A family-based model to predict fear of recurrence for cancer survivors and their caregivers.

Authors:  Suzanne Mellon; Trace S Kershaw; Laurel L Northouse; Laurie Freeman-Gibb
Journal:  Psychooncology       Date:  2007-03       Impact factor: 3.894

3.  Validation of the Care-Related Quality of Life Instrument in different study settings: findings from The Older Persons and Informal Caregivers Survey Minimum DataSet (TOPICS-MDS).

Authors:  J E Lutomski; N J A van Exel; G I J M Kempen; E P Moll van Charante; W P J den Elzen; A P D Jansen; P F M Krabbe; B Steunenberg; E W Steyerberg; M G M Olde Rikkert; R J F Melis
Journal:  Qual Life Res       Date:  2014-11-08       Impact factor: 4.147

4.  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

Review 5.  Psychological functioning of caregivers for head and neck cancer patients.

Authors:  Margaret L Longacre; John A Ridge; Barbara A Burtness; Thomas J Galloway; Carolyn Y Fang
Journal:  Oral Oncol       Date:  2011-12-09       Impact factor: 5.337

6.  Examining the role of subjective and objective burden in carer health-related quality of life: the case of colorectal cancer.

Authors:  Paul Hanly; Rebecca Maguire; Philip Hyland; Linda Sharp
Journal:  Support Care Cancer       Date:  2014-12-12       Impact factor: 3.603

7.  When do we need to care about the caregiver? Supportive care needs, anxiety, and depression among informal caregivers of patients with cancer and cancer survivors.

Authors:  Halina Sklenarova; Arne Krümpelmann; Markus W Haun; Hans-Christoph Friederich; Johannes Huber; Michael Thomas; Eva C Winkler; Wolfgang Herzog; Mechthild Hartmann
Journal:  Cancer       Date:  2015-02-11       Impact factor: 6.860

8.  Cancer caregivers information needs and resource preferences.

Authors:  Margaret L Longacre
Journal:  J Cancer Educ       Date:  2013-06       Impact factor: 2.037

9.  Social inequality and incidence of and survival from cancers of the mouth, pharynx and larynx in a population-based study in Denmark, 1994-2003.

Authors:  Zorana Jovanovic Andersen; Christina Funch Lassen; Inge Haunstrup Clemmensen
Journal:  Eur J Cancer       Date:  2008-07-25       Impact factor: 9.162

10.  How much does it cost to care for survivors of colorectal cancer? Caregiver's time, travel and out-of-pocket costs.

Authors:  Paul Hanly; Alan Ó Céilleachair; Mairead Skally; Eamonn O'Leary; Kanika Kapur; Patricia Fitzpatrick; Anthony Staines; Linda Sharp
Journal:  Support Care Cancer       Date:  2013-05-07       Impact factor: 3.603

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  8 in total

1.  A qualitative comparison of the nutrition care experiences of carers supporting patients with head and neck cancer throughout surgery and radiation treatment and survivorship.

Authors:  Joanne Hiatt; Adrienne Young; Teresa Brown; Merrilyn Banks; Bronwyn Segon; Judith Bauer
Journal:  Support Care Cancer       Date:  2022-09-16       Impact factor: 3.359

2.  Quality of Life Among Informal Caregivers of Patients With Degenerative Cervical Myelopathy: Cross-Sectional Questionnaire Study.

Authors:  Oliver Daniel Mowforth; Benjamin Marshall Davies; Mark Reinhard Kotter
Journal:  Interact J Med Res       Date:  2019-11-07

3.  Informal caregiving for adults, loneliness and social isolation: a study protocol for a systematic review.

Authors:  André Hajek; Benedikt Kretzler; Hans-Helmut König
Journal:  BMJ Open       Date:  2021-05-04       Impact factor: 2.692

4.  Disparity of perception of quality of life between head and neck cancer patients and caregivers.

Authors:  Zachary M Kassir; Jinhong Li; Christine Harrison; Jonas T Johnson; Marci L Nilsen
Journal:  BMC Cancer       Date:  2021-10-20       Impact factor: 4.430

5.  The Role of Associations in Reducing the Emotional and Financial Impact on Parents Caring for Children with Duchenne Muscular Dystrophy: A Cross-Cultural Study.

Authors:  Alicia Aurora Rodríguez; Imanol Amayra; Juan Francisco López-Paz; Oscar Martínez; Maitane García; Mónika Salgueiro; Mohammad Al-Rashaida; Paula María Luna; Paula Pérez-Nuñez; Nicole Passi; Irune García; Javiera Ortega
Journal:  Int J Environ Res Public Health       Date:  2022-09-28       Impact factor: 4.614

6.  The quality of life of regional and remote cancer caregivers in Australia.

Authors:  Belinda C Goodwin; Fiona Crawford-Williams; Michael Ireland; Sonja March; Suzanne K Chambers; Joanne F Aitken; Jeff Dunn
Journal:  Eur J Cancer Care (Engl)       Date:  2022-04-11       Impact factor: 2.328

7.  An explorative analysis of the differences in levels of happiness between cancer patients, informal caregivers and the general population.

Authors:  Mayara Goulart de Camargos; Bianca Sakamoto Ribeiro Paiva; Marco Antônio de Oliveira; Paula de Souza Ferreira; Vinicius Tolentino Nardoto de Almeida; Sandra de Andrade Cadamuro; Carla Simone Leite de Almeida; Carlos Eduardo Paiva
Journal:  BMC Palliat Care       Date:  2020-07-11       Impact factor: 3.234

8.  Diseases Costs and Impact of the Caring Role on Informal Carers of Children with Neuromuscular Disease.

Authors:  Alicia Aurora Rodríguez; Óscar Martínez; Imanol Amayra; Juan Francisco López-Paz; Mohammad Al-Rashaida; Esther Lázaro; Patricia Caballero; Manuel Pérez; Sarah Berrocoso; Maitane García; Paula María Luna; Paula Pérez-Núñez; Nicole Passi
Journal:  Int J Environ Res Public Health       Date:  2021-03-15       Impact factor: 3.390

  8 in total

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