Literature DB >> 22095338

Ethical justification for conducting public health surveillance without patient consent.

Lisa M Lee1, Charles M Heilig, Angela White.   

Abstract

Public health surveillance by necessity occurs without explicit patient consent. There is strong legal and scientific support for maintaining name-based reporting of infectious diseases and other types of public health surveillance. We present conditions under which surveillance without explicit patient consent is ethically justifiable using principles of contemporary clinical and public health ethics. Overriding individual autonomy must be justified in terms of the obligation of public health to improve population health, reduce inequities, attend to the health of vulnerable and systematically disadvantaged persons, and prevent harm. In addition, data elements collected without consent must represent the minimal necessary interference, lead to effective public health action, and be maintained securely.

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Year:  2011        PMID: 22095338      PMCID: PMC3490562          DOI: 10.2105/AJPH.2011.300297

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  28 in total

Review 1.  Autonomy, paternalism, and justice: ethical priorities in public health.

Authors:  David R Buchanan
Journal:  Am J Public Health       Date:  2007-11-29       Impact factor: 9.308

2.  Accurate monitoring of the HIV epidemic in the United States: case duplication in the national HIV/AIDS surveillance system.

Authors:  M Kathleen Glynn; Qiang Ling; Ruby Phelps; Jianmin Li; Lisa M Lee
Journal:  J Acquir Immune Defic Syndr       Date:  2008-03-01       Impact factor: 3.731

Review 3.  Looking ahead: addressing ethical challenges in public health practice.

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Journal:  MMWR Morb Mortal Wkly Rep       Date:  1998-01-09       Impact factor: 17.586

6.  The genesis of public health ethics.

Authors:  Ronald Bayer; Amy L Fairchild
Journal:  Bioethics       Date:  2004-11       Impact factor: 1.898

7.  Impracticability of informed consent in the Registry of the Canadian Stroke Network.

Authors:  Jack V Tu; Donald J Willison; Frank L Silver; Jiming Fang; Janice A Richards; Andreas Laupacis; Moira K Kapral
Journal:  N Engl J Med       Date:  2004-04-01       Impact factor: 91.245

8.  Indicators for chronic disease surveillance.

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Journal:  MMWR Recomm Rep       Date:  2004-09-10

9.  The basis of privacy and autonomy in medical practice. A model.

Authors:  W J Friedlander
Journal:  Soc Sci Med       Date:  1982       Impact factor: 4.634

10.  Pandemic influenza preparedness: an ethical framework to guide decision-making.

Authors:  Alison K Thompson; Karen Faith; Jennifer L Gibson; Ross E G Upshur
Journal:  BMC Med Ethics       Date:  2006-12-04       Impact factor: 2.652

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  23 in total

1.  Legal Authority for Infectious Disease Reporting in the United States: Case Study of the 2009 H1N1 Influenza Pandemic.

Authors:  Richard N Danila; Ellen S Laine; Franci Livingston; Kathryn Como-Sabetti; Lauren Lamers; Kelli Johnson; Anne M Barry
Journal:  Am J Public Health       Date:  2015-01       Impact factor: 9.308

2.  Expert stakeholders' perspectives on a Data-to-Care strategy for improving care among HIV-positive individuals incarcerated in jails.

Authors:  Mara Buchbinder; Colleen Blue; Eric Juengst; Lauren Brinkley-Rubinstein; Stuart Rennie; David L Rosen
Journal:  AIDS Care       Date:  2020-03-11

3.  Expected ethical competencies of public health professionals and graduate curricula in accredited schools of public health in North America.

Authors:  Lisa M Lee; Brandy Wright; Salaam Semaan
Journal:  Am J Public Health       Date:  2012-09-20       Impact factor: 9.308

Review 4.  Enhanced use of phylogenetic data to inform public health approaches to HIV among men who have sex with men.

Authors:  Danielle German; Mary Kate Grabowski; Chris Beyrer
Journal:  Sex Health       Date:  2017-02       Impact factor: 2.706

5.  Addressing Ethical Challenges in US-Based HIV Phylogenetic Research.

Authors:  Liza Dawson; Nanette Benbow; Faith E Fletcher; Seble Kassaye; Amy Killelea; Stephen R Latham; Lisa M Lee; Thomas Leitner; Susan J Little; Sanjay R Mehta; Omar Martinez; Brian Minalga; Art Poon; Stuart Rennie; Jeremy Sugarman; Patricia Sweeney; Lucia V Torian; Joel O Wertheim
Journal:  J Infect Dis       Date:  2020-11-13       Impact factor: 5.226

6.  Community and Provider Perspectives on Molecular HIV Surveillance and Cluster Detection and Response for HIV Prevention: Qualitative Findings From King County, Washington.

Authors:  Alic G Shook; Susan E Buskin; Matthew Golden; Julia C Dombrowski; Joshua Herbeck; Richard J Lechtenberg; Roxanne Kerani
Journal:  J Assoc Nurses AIDS Care       Date:  2021-10-26       Impact factor: 1.809

7.  Getting Data Right - and Righteous to Improve Hispanic or Latino Health.

Authors:  Alfonso Rodríguez-Lainz; Mariana McDonald; Ana Penman-Aguilar; Drue H Barrett
Journal:  J Healthc Sci Humanit       Date:  2016

8.  COVID-19 and collective responsibility: a lesson from the Smallpox outbreak in Moscow in 1960.

Authors:  Yana G Grigoryan; Nikolay N Krylov
Journal:  J Med Ethics Hist Med       Date:  2020-12-28

9.  Using typing techniques in a specific outbreak: the ethical reflection of public health professionals.

Authors:  B Rump; C Cornelis; F Woonink; J VAN Steenbergen; M Verweij; M Hulscher
Journal:  Epidemiol Infect       Date:  2017-02-13       Impact factor: 4.434

10.  The informed consent in Southern Italy does not adequately inform parents about infant vaccination.

Authors:  Francesco Attena; Amanda Valdes Abuadili; Sara Marino
Journal:  BMC Public Health       Date:  2014-02-28       Impact factor: 3.295

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