Hostname: page-component-6bf8c574d5-rwnhh Total loading time: 0 Render date: 2025-02-28T09:36:02.806Z Has data issue: false hasContentIssue false
  • English
  • Français

Providing Information to our Patients: Published and Personal Perspectives

Published online by Cambridge University Press:  23 September 2014

Joseph F. Megyesi
Joseph F. Megyesi*
Affiliation:
London, Ontario, Canada
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Editorial
Information
Canadian Journal of Neurological Sciences , Volume 41 , Issue 1 , January 2014 , pp. 3 - 4
Copyright
Copyright © The Canadian Journal of Neurological 2014

References

1. Bramall, AN, Bernstein, M. Improving information provision for neurosurgical patients: a qualitative study. Can Journal Neurol Sci. 2014;41(1):66–73.CrossRefGoogle ScholarPubMed
2. Axelrod, DA, Goold, SD. Maintaining trust in the surgeon-patient relationship: challenges for the new millennium. Arch Surg. 2000;135:55–61.CrossRefGoogle ScholarPubMed
3. Katz, JE, Roberge, D, Coulombe, G. The cancer patient’s use and appreciation of the internet and other modern means of communication. Technol Cancer Res Treat. 2013 Aug 31 [Epub ahead of print].CrossRefGoogle ScholarPubMed
4. Alba-Ruiz, R, Bermudez-Tamayo, C, Pernett, JJ, Garcia-Gutierrez, JF, Cozar-Olmo, JM, Valero-Aguilera, B. Adapting the content of cancer web sites to the information needs of patients: reliability and readability. Telemed J EHealth. 2013 Sep 27 [Epub ahead of print].CrossRefGoogle Scholar
5. Nielsen, M, Jull, G, Hodges, PW. Information needs of people with low back pain for an online resource: a qualitative study of consumer views. Disabil Rehabil. 2013 Sep 3 [Epub ahead of print].Google ScholarPubMed
6. Megyesi, J, Sahgal, A, Gorayeb, J, editors. Adult brain tumour handbook. London, ON (Canada): Brain Tumour Foundation of Canada; 2012.Google Scholar
7. Gorayeb, J, editor. Pediatric brain tumour handbook. London, ON (Canada): Brain Tumour Foundation of Canada; 2012.Google Scholar
8. Imran, SA, Sahgal, A, Gorayeb, J, editors. Non-malignant brain tumour handbook. London, ON (Canada): Brain Tumour Foundation of Canada; 2011.Google Scholar
9. McCarthy, J, editor. A manual for people living with ALS. Markham, ON (Canada): Amyotrophic Lateral Sclerosis Society of Canada; 2005.Google Scholar
10. Steinberg, JS, Koski, CL. Guillain-Barre Syndrome, CIDP and variants – an overview for the layperson. Narberth, PA (USA): GBS/CIDP Foundation International; 2010.Google Scholar
11. Heart and Stroke Foundation. Let’s talk about stroke – an information guide for survivors and their families. Last modified; May 2012.Google Scholar
12. Multiple sclerosis patient binder. London Health Sciences MS Clinic.Google Scholar
13. Salmon, P, Hall, GM. Patient empowerment and control: a psychological discourse in the service of medicine. Soc Sci Med. 2003;57:1969–80.CrossRefGoogle ScholarPubMed
14. Baker, LM. A new method for studying patient information needs and information-seeking patterns. Top Health Inf Manage. 1995; 16:19–28.Google ScholarPubMed
15. Rozmovits, L, Khu, KJ, Osman, S, Gentili, F, Guha, A, Bernstein, M. Information gaps for patients requiring craniotomy for benign brain lesions: a qualitative study. J Neurooncol. 2010;96:241–7.CrossRefGoogle ScholarPubMed