Literature DB >> 12016192

Consent, confidentiality, and the threat to public health surveillance.

Chris Verity1, Angus Nicoll.   

Abstract

Keywords:  Health Care and Public Health; National Health Service; Professional Patient Relationship

Mesh：

Year:  2002        PMID： 12016192      PMCID： PMC1123166          DOI： 10.1136/bmj.324.7347.1210

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


× No keyword cloud information.
  10 in total

1.  Health protection in the next millennium: from tactics to strategy?

Authors:  M Regan
Journal:  J Epidemiol Community Health       Date:  1999-09       Impact factor: 3.710

2.  Undermining data privacy in health information.

Authors:  R Anderson
Journal:  BMJ       Date:  2001-02-24

Review 3.  Public health outputs from the British Paediatric Surveillance Unit and similar clinician-based systems.

Authors:  A Nicoll; R Lynn; J Rahi; C Verity; L Haines
Journal:  J R Soc Med       Date:  2000-11       Impact factor: 5.344

4.  Using patient-identifiable data for observational research and audit.

Authors:  R Al-Shahi; C Warlow
Journal:  BMJ       Date:  2000-10-28

5.  Consent to cancer registration--an unnecessary burden.

Authors:  I C Paterson
Journal:  BMJ       Date:  2001-05-05

6.  Why the human rights act matters to doctors.

Authors:  B Hewson
Journal:  BMJ       Date:  2000-09-30

7.  Potential effect of authorization bias on medical record research.

Authors:  S J Jacobsen; Z Xia; M E Campion; C H Darby; M F Plevak; K D Seltman; L J Melton
Journal:  Mayo Clin Proc       Date:  1999-04       Impact factor: 7.616

8.  The surveillance of communicable diseases of national importance.

Authors:  A D LANGMUIR
Journal:  N Engl J Med       Date:  1963-01-24       Impact factor: 91.245

9.  The threat to medical-records research.

Authors:  L J Melton
Journal:  N Engl J Med       Date:  1997-11-13       Impact factor: 91.245

10.  Developing a district diabetic register.

Authors:  S D Burnett; C M Woolf; J S Yudkin
Journal:  BMJ       Date:  1992-09-12
  10 in total
  30 in total

1.  Patient privacy and confidentiality.

Authors:  Jim Chalmers; Rod Muir
Journal:  BMJ       Date:  2003-04-05

2.  Genomics and health care. How genomics medicine is translated into better health care largely depends on how physicians handle this information.

Authors:  Vicki Brower
Journal:  EMBO Rep       Date:  2004-02       Impact factor: 8.807

Review 3.  Why we should not seek individual informed consent for participation in health services research.

Authors:  J Cassell; A Young
Journal:  J Med Ethics       Date:  2002-10       Impact factor: 2.903

4.  Surveillance in occupational health.

Authors:  D Koh; T-C Aw
Journal:  Occup Environ Med       Date:  2003-09       Impact factor: 4.402

5.  Public opinions about participating in health research.

Authors:  Kay Teschke; Suhail Marino; Rong Chu; Joseph K C Tsui; M Anne Harris; Stephen A Marion
Journal:  Can J Public Health       Date:  2010 Mar-Apr

6.  Children, rights, and responsibilities.

Authors:  D M B Hall
Journal:  Arch Dis Child       Date:  2005-02       Impact factor: 3.791

7.  Of genomics and public health: Building public "goods"?

Authors:  Bartha Maria Knoppers
Journal:  CMAJ       Date:  2005-11-08       Impact factor: 8.262

8.  Survey of informed consent for registration of congenital anomalies in Europe.

Authors:  Araceli Busby; Annukka Ritvanen; Helen Dolk; Nicola Armstrong; Hermien De Walle; Isolina Riaño-Galán; Miriam Gatt; Robert McDonnell; Vera Nelen; David Stone
Journal:  BMJ       Date:  2005-07-16

9.  Preventing recurrent rheumatic fever: the role of register based programmes.

Authors:  M McDonald; A Brown; S Noonan; J R Carapetis
Journal:  Heart       Date:  2005-09       Impact factor: 5.994

10.  Using personal health information in medical research.

Authors:  Tom Walley
Journal:  BMJ       Date:  2006-01-21
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.