E-Patient
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e-Patients (also known as Internet Patient, or Internet-savvy Patient) are health consumers who use the Internet to gather information about a medical condition of particular interest to them, and who use electronic communication tools (including Web 2.0 tools) in coping with medical conditions.[1] The term encompasses both those who seek online guidance for their own ailments and the friends and family members (e-Caregivers) who go online on their behalf. e-Patients report two effects of their online health research: "better health information and services, and different (but not always better) relationships with their doctors."[citation needed]
e-patients are increasingly active in their care and are demonstrating the power of the Participatory Medicine or Health 2.0 / Medicine 2.0[2]. model of care. They are equipped, enabled, empowered, engaged, equals, emancipated and experts.[citation needed]
- Equipped with the skills to manage their own condition.
- Enabled to make choices about self-care and those choices are respected.
- Empowered
- Engaged patients are engaged in their own care
- Equals in their partnerships with the various physicians involved in their care
- Emancipated
- Expert patients can improve their self-rated health status, cope better with fatigue and other generic features of chronic disease such as role limitation, and reduce disability and their dependence on hospital care.[citation needed]
Based on the current state of knowledge on the impact of e-Patients on the healthcare system and the quality of care received:
- A growing number of people say the internet has played a crucial or important role as they helped another person cope with a major illness.[3][4]
- Since the advent of the Internet, many clinicians have underestimated the benefits and overestimated the risks of online health resources for patients.[5][6][7]
- Medical online support groups have become an important healthcare resource.[citation needed]
- The net friendliness of clinicians and provider organizations—as rated by the e-patients they serve—is becoming an important new aspect of healthcare quality.[citation needed]
- This is one the most important cultural medical revolution of the past century, mediated and driven by technology.[citation needed]
- The impact of the e-Patient cannot be fully understood and appreciated in the context of pre-internet medical constructs.[citation needed] Research must combine expertise from specialties that are not used to work together.
- It is crucial for medical education to take the e-patient into account, and to prepare students for medical practice that encompasses the e-patient[8]
The proportion of e-Patients in selected patient populations seem to be highest in the US and Canada.[citation needed] European countries seem to lag.[citation needed]
See also
References
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- van Woerkum CM (1 April 2003). "The Internet and primary care physicians: coping with different expectations". Am. J. Clin. Nutr. 77 (4 Suppl): 1016S–1018S. PMID 12663310.
- Podiatry Online: Accommodating the Internet-Savvy Patient
- Susannah Fox, Pew Internet & American Life Project (2004-09-27). "Today's E-Patients: Hunters and Gatherers of Health Information Online".
- Laura Landro, Senior Editor, The Wall Street Journal (June 13, 2007). "The Growing Clout of Online Patient Groups" (PDF).
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- Meier A, Lyons EJ, Frydman G, Forlenza M, Rimer BK (2007). "How cancer survivors provide support on cancer-related Internet mailing lists". J. Med. Internet Res. 9 (2): e12. doi:10.2196/jmir.9.2.e12. PMC 1874721 Freely accessible. PMID 17513283.
- Feder J (2008). "A reader and author respond to "ePatients: engaging patients in their own care"". Medscape J Med. 10 (2): 46; author reply 46. PMC 2270894 Freely accessible. PMID 18382715.
External links
- The rise of the e-patient, Lee Rainie from the Pew Internet and American Life Project presentation at the Medical Library Association, Oct 7, 2009
- E-patients With a Disability or Chronic Disease, from the Pew Internet and American Life Project
- Association of Cancer Online Resources (ACOR), an aggregate of e-patient online communities for knowledge-sharing about cancer.
- E-Patients Prefer eGroups to Doctors for 10 of 12 Aspects of Health Care. 1999 article by Dr. Tom Ferguson.
- Time Magazine article: "When the patient is a Googler" - Mary Shomons response - Trisha Torreys response
- Who Cares Booklet by the Federal Trade Commission, a guide to health information
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