Literature DB >> 23208850

Head and neck cancer and dysphagia; caring for carers.

J M Patterson1, T Rapley, P N Carding, J A Wilson, E McColl.   

Abstract

OBJECTIVES: A diagnosis of head and neck cancer (HNC) is a profound event for patients and family members who play a crucial role in their care. Eating and drinking difficulties affect patients' quality of life (QOL), but the impact on the carers' QOL has not been explored. This preliminary mixed method study reports on carer QOL over time and investigates the relationship with dysphagia.
METHODS: Two hundred and eight HNC patients referred for (chemo)radiotherapy were asked to identify a carer and complete a health-related QOL and a swallowing QOL questionnaire at pre-treatment, 3 and 12 months post-treatment. Carers were given the Caregiver QOL-Cancer (CQOL-C) questionnaire at the same time points. A purposive sample of patient and carer dyads was observed over mealtimes and interviewed.
RESULTS: Seventy per cent of carers returned a questionnaire at least once. There was no change in CQOL-C scores between pre-treatment and 3 months, but a significant improvement was found between 3 and 12 months post-treatment (p = 0.012). Patient-reported outcomes accounted for 52% of variance in carer QOL measurements (R(2) = 0.52, p < 0.001). Four themes emerged from the qualitative data food provision, monitoring, motivation and changes to lifestyle.
CONCLUSIONS: Findings suggest a relationship between carer and patient QOL. Elsewhere, these two characteristics have been associated such that the greater the patients' physical care needs, the poorer the carers' and patients' QOL. Living with someone with dysphagia not only involves managing the physical swallowing difficulties but is also likely to impact on social activities such as participation in shared meals, leading to permanent lifestyle changes.
Copyright © 2012 John Wiley & Sons, Ltd.

Entities:  

Keywords:  caregiver; deglutition; head and neck cancer; oncology; quality of life

Mesh:

Year:  2012        PMID: 23208850     DOI: 10.1002/pon.3226

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


  22 in total

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7.  Application of the International Classification of Functioning, Disability and Health (ICF) to people with dysphagia following non-surgical head and neck cancer management.

Authors:  Rebecca L Nund; Nerina A Scarinci; Bena Cartmill; Elizabeth C Ward; Pim Kuipers; Sandro V Porceddu
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8.  A Prospective Biopsychosocial Investigation Into Head and Neck Cancer Caregiving.

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9.  Burden, quality of life, and social support in caregivers of patients undergoing radiotherapy for head and neck cancer: A pilot study.

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10.  Quality of life of family caregivers of cancer patients in Singapore and globally.

Authors:  Haikel A Lim; Joyce Ys Tan; Joanne Chua; Russell Kl Yoong; Siew Eng Lim; Ee Heok Kua; Rathi Mahendran
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