Literature DB >> 17277616

Distress in spouses and patients after treatment for head and neck cancer.

Irma M Verdonck-de Leeuw1, Simone E Eerenstein, Mecheline H Van der Linden, Dirk J Kuik, Remco de Bree, C Rene Leemans.   

Abstract

BACKGROUND: The objective of this study is to obtain insight into distress in spouses and patients treated for head and neck cancer.
METHODS: Forty-one patient-spouse pairs completed the Hospital Anxiety and Depression Scale (HADS). Inclusion criteria included curative treatment for head and neck cancer. Exclusion criteria were visiting the clinic without a spouse, bad news at the routine follow-up examination, diseases causing cognitive dysfunction, and poor understanding of the Dutch language. Next to the HADS, the assessment protocol included age, gender, health status, coping strategy, time since cancer treatment, tumor stage and site, treatment modality, functional and social impairment, and caregiving burden.
RESULTS: A clinical level of distress was noted in 20% of the spouses and in 27% of the patients. Distress in spouses was related to the presence of a feeding tube in patients, a passive coping style, less vitality, and a disrupted daily life schedule resulting from caregiving. Distress in patients was related to the presence of a feeding tube, speech and swallowing problems, less social contacts, a passive style of coping, and nonexpression of emotions.
CONCLUSION: Distress is often present in spouses and patients treated for head and neck cancer. Routine screening for psychologic distress is recommended.

Entities:  

Mesh:

Year:  2007        PMID: 17277616     DOI: 10.1097/01.mlg.0000250169.10241.58

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  45 in total

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3.  Illness perceptions and coping predict post-traumatic stress in caregivers of patients with head and neck cancer.

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4.  Psychological distress and need for psycho-oncological support in spouses of total laryngectomised cancer patients-results for the first 3 years after surgery.

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5.  Validity of patient-reported swallowing and speech outcomes in relation to objectively measured oral function among patients treated for oral or oropharyngeal cancer.

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6.  Posttraumatic stress disorder symptoms in newly diagnosed patients with head and neck cancer and their partners.

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Review 8.  Psychological factors associated with head and neck cancer treatment and survivorship: evidence and opportunities for behavioral medicine.

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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.  Psychosocial adjustment of family caregivers of head and neck cancer survivors.

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