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Literature DB >> 16809714

Patients should have to opt out of national electronic care records: FOR.

Nigel Watson¹.

Abstract

Entities: Species

Mesh：

Year: 2006 PMID： 16809714 PMCID： PMC1494772 DOI： 10.1136/bmj.333.7557.39

Source DB: PubMed Journal: BMJ ISSN： 0959-8138

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4 in total

1. Lessons from the central Hampshire electronic health record pilot project: issues of data protection and consent.

Authors: Trina Adams; Martin Budden; Chris Hoare; Hugh Sanderson
Journal: BMJ Date: 2004-04-10

2. Regulatory and policy barriers to effective clinical data exchange: lessons learned from MedsInfo-ED.

Authors: Lawrence K Gottlieb; Elliot M Stone; Diane Stone; Lynne A Dunbrack; John Calladine
Journal: Health Aff (Millwood) Date: 2005 Sep-Oct Impact factor: 6.301

3. Health care IT collaboration in Massachusetts: the experience of creating regional connectivity.

Authors: John Halamka; Meg Aranow; Carl Ascenzo; David Bates; Greg Debor; John Glaser; Allan Goroll; Jim Stowe; Micky Tripathi; Gordon Vineyard
Journal: J Am Med Inform Assoc Date: 2005-07-27 Impact factor: 4.497

4. The electronic patient record in primary care--regression or progression? A cross sectional study.

Authors: Julia Hippisley-Cox; Mike Pringle; Ruth Cater; Alison Wynn; Vicky Hammersley; Carol Coupland; Rhydian Hapgood; Peter Horsfield; Sheila Teasdale; Christine Johnson
Journal: BMJ Date: 2003-06-28

4 in total

7 in total

7. Individuals appreciate having their medication record on the web: a survey of attitudes to a national pharmacy register.

Authors: Emelie Montelius; Bengt Astrand; Bo Hovstadius; Göran Petersson
Journal: J Med Internet Res Date: 2008-11-11 Impact factor: 5.428

7 in total

Patients should have to opt out of national electronic care records: FOR.

1. Lessons from the central Hampshire electronic health record pilot project: issues of data protection and consent.

2. Regulatory and policy barriers to effective clinical data exchange: lessons learned from MedsInfo-ED.

3. Health care IT collaboration in Massachusetts: the experience of creating regional connectivity.

4. The electronic patient record in primary care--regression or progression? A cross sectional study.

1. Rights and responsibilities of users of electronic health records.

2. To opt in or opt out of electronic patient records? Isle of Wight and Scottish projects are not opt out schemes.

3. To opt in or opt out of electronic patient records? Integration technology is key to success.

4. The state of play in the battle against antimicrobial resistance: a general practitioner perspective.

5. A trial of consent procedures for future research with clinically derived biological samples.

6. Pharmaceutical information systems and possible implementations of informed consent -- developing an heuristic.

7. Individuals appreciate having their medication record on the web: a survey of attitudes to a national pharmacy register.