Abstract
This is the official guideline endorsed by the specialty associations involved in the care of head and neck cancer patients in the UK. It provides recommendations on the assessment and interventions for the psychological management in this patient group. Recommendations • Audit of information supplied to patients and carers should be conducted on an annual basis to update and review content and media presentation. (G) • Patients and carers should be invited to discuss treatment options and relate possible outcomes to functional retention or loss to provide a patient-centred approach. (G) • Clinical staff should inspect their systems of assessment to make them sensitive enough to identify patients with psychological difficulties. (G) • Flexibility, rather than rigid formulation is required to assess patients frequently, and to allow for change in circumstances to be noted. (G) • Multidisciplinary teams should determine the supportive care services available and commission extra assistance to provide patients and carers with timely information, education or brief supportive advice. (G) • Multidisciplinary teams need to inspect specialist services for mental health interventions at structured and complex levels for the small proportion of patients with more serious, but rarer, psychological difficulties. (G) • Clinical staff at all levels should receive communication skills training to raise and maintain consultation expertise with difficult patient and/or carer interactions. (G).
Highlights
The head and neck cancer patient and their carers have considerable challenges to overcome.[1]
Clinical staff should inspect their systems of assessment to make them sensitive enough to identify patients with psychological difficulties. (G)
The psychological experience of the patient with head and neck cancer has been closely described in a recent systematic review and meta-synthesis.[2]
Summary
The head and neck cancer patient and their carers have considerable challenges to overcome.[1]. Delivering information about treatment and recovery Considerable efforts have been expended to determine the information needs of head and neck cancer patients.[9,10] Poor satisfaction with information supplied by the team was predictive of patient lowered mood and quality of life (QoL) in the longer term.[11] More information was required on financial advice, support groups and ability to return to work.
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