Abstract
In general, use of the internet by patients in their healthcare is increasing. However,
its use specifically among those with head and neck cancer in the UK has not been
reported. The aims of this study were to report access to the internet by survivors
of head and neck cancer, to indicate where it fits within their information sources,
how they have used it, and how they might use it in future. A question on its use
has been included in annual surveys of patients since 2006. Patient-reported access
to the internet increased from 32% in 2006 to 54% in 2010. There were considerable
differences in access by age; currently (2010) 83% of those under 55 years, and 40%
of those aged 65–84 years. Binary logistic regression modelling involving age at survey
(p < 0.001), age leaving education (p < 0.001), and sex (p = 0.01), gave all three as independent predictors of access. In the 2010 survey 49%
(234/473) never used the internet, 10% (49/473) used it rarely, 15% (70/473) used
it occasionally, and 25% (120/473) used it often. The main reasons for its use for
head and neck cancer were to find information, learn about treatment, side effects,
and medication, and obtain advice from members of multidisciplinary teams. The findings
of this study show that the internet has an important role for patients in providing
information and support about their cancer, although other sources are still very
important. Data from the study will help inform those promoting e-health about the
type of resource that is wanted by patients.
Keywords
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Article info
Publication history
Published online: May 19, 2011
Accepted:
March 24,
2011
Identification
Copyright
© 2011 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Inc. All rights reserved.
