2015
DOI: 10.1007/s13187-015-0814-3
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Medical Communication-related Informational Need and Resource Preferences Among Family Caregivers for Head and Neck Cancer Patients

Abstract: Introduction Despite advances in treatment, head and neck cancer (HNC) patients often experience considerable functional impairment during and following treatment. As a result, family caregivers are essential in a patient’s recovery; however, few caregivers are well-prepared to handle the extensive caregiving needs of this patient population. To date, little is known about HNC caregivers’ informational needs in this role. Thus, we surveyed a sample of HNC caregivers about their informational needs including th… Show more

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Cited by 45 publications
(55 citation statements)
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“…This study finds that medical professionals are the preferred method of receiving health information among TBI, SCI, and burn caregivers, similar to the preference of those caring for other conditions [27]. Nevertheless, the Internet was an integral health information resource for caregivers of persons with all three injuries.…”
Section: Discussionmentioning
confidence: 88%
“…This study finds that medical professionals are the preferred method of receiving health information among TBI, SCI, and burn caregivers, similar to the preference of those caring for other conditions [27]. Nevertheless, the Internet was an integral health information resource for caregivers of persons with all three injuries.…”
Section: Discussionmentioning
confidence: 88%
“…Also, results highlight factors that may place both dyad members at higher risk for compromised well-being and resulting potential targets for education and support. Because HNC caregivers prefer to receive informational support directly from health care providers (Longacre, Galloway, Parvanta, & Fang, 2015), results from this study highlight that oncology clinicians could target higher-risk HNC dyads (e.g., those facing more severe symptoms) who may especially benefit from screening and supportive resources before treatment. This research fits with recent national efforts by the American Association of Retired Persons (http://aarp.org) to pass state legislation requiring the systematic identification, documentation, and training of caregivers in the hospital setting [Caregiver Advise, Record, and Enable Act; (Coleman, 2016)].…”
Section: Resultsmentioning
confidence: 99%
“…It is common for carers to have unmet needs related to patients' diagnosis, prognosis, physical and psychological impacts of treatment, and how to manage care needs at home . While information needs decrease over time, some carers still experience unmet information needs throughout treatment and at the end of treatment . Carers have used a variety of sources to address their unmet needs, most commonly relying on healthcare professionals, family, friends, and the internet .…”
Section: Introductionmentioning
confidence: 99%