What Do People Affected by Cancer Think About Electronic Health Information Exchange? Results From the 2010 LIVESTRONG Electronic Health Information Exchange Survey and the 2008 Health Information National Trends Survey-Reference-Cited by-同舟云学术

What Do People Affected by Cancer Think About Electronic Health Information Exchange? Results From the 2010 LIVESTRONG Electronic Health Information Exchange Survey and the 2008 Health Information National Trends Survey

Published:2011-07 Issue:4 Volume:7 Page:237-241
ISSN:1554-7477
Container-title:Journal of Oncology Practice
language:en
Short-container-title:JOP

Author:

Beckjord Ellen B.¹,Rechis Ruth¹,Nutt Stephanie¹,Shulman Lawrence¹,Hesse Bradford W.¹

Affiliation:

1. University of Pittsburgh Cancer Institute, Pittsburgh, PA; LIVESTRONG, Austin, TX; Dana-Farber Cancer Institute, Boston, MA; National Cancer Institute, Bethesda, MD

Abstract

Responses to a 2010 survey by LIVESTRONG showed that, compared with the general population, persons affected by cancer had greater enthusiasm for electronic information exchange between patients and health care providers. Especially valued were security and privacy of communication.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Health Policy,Oncology (nursing),Oncology

Link

http://ascopubs.org/doi/pdfdirect/10.1200/JOP.2011.000324

Reference21 articles.

1. Launching HITECH

2. The “Meaningful Use” Regulation for Electronic Health Records

3. Demonstrating Meaningful Use of Health IT for 2011 and Beyond 2009 Markel Foundation New York, NY Markle Foundation, Center for American Progress, Engelberg Center for Health Care Reform at Brookings

4. Information Technology Comes to Medicine

5. Consumer empowerment versus consumer populism in healthcare IT

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