Literature DB >> 16510336

Should donors be allowed to give broad consent to future biobank research?

Mats G Hansson1, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson.   

Abstract

Large international biobank studies can make substantial contributions to scientific research by validation of the biological importance of previous research and by identification of previously unknown causes of disease. However, regulations for patient consent that are too strict and discrepancies in national policies on informed consent might hinder progress. Therefore, establishment of common ground for ethical review of biobank research is essential. In this essay, broad consent is defined on a scale between strictly specified (eg, for a specific study) and blanket consent (ie, with no restrictions regarding the purpose of the research). Future research includes that which might not be planned or even conceptualised when consent is obtained. In conclusion, broad consent and consent for future research are valid ethically and should be recommended for biobank research provided that: personal information related to research is handled safely; donors of biological samples are granted the right to withdraw consent; and new research studies or changes to the legal or ethical authority of a biobank are approved by an ethics-review board.

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Year:  2006        PMID: 16510336     DOI: 10.1016/S1470-2045(06)70618-0

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  106 in total

1.  Can Broad Consent be Informed Consent?

Authors:  Mark Sheehan
Journal:  Public Health Ethics       Date:  2011-08-03       Impact factor: 1.940

2.  Biobank governance: heterogeneous modes of ordering and democratization.

Authors:  Herbert Gottweis; Georg Lauss
Journal:  J Community Genet       Date:  2011-12-07

3.  Broad consent and biorepositories for molecular epidemiology and genomics research.

Authors:  Steven S Coughlin
Journal:  Int J Mol Epidemiol Genet       Date:  2011-11-25

4.  Structural requirements of research tissue banks derived from standardized project surveillance.

Authors:  E Herpel; N Koleganova; B Schreiber; B Walter; C V Kalle; P Schirmacher
Journal:  Virchows Arch       Date:  2012-06-01       Impact factor: 4.064

Review 5.  Biobanks: importance, implications and opportunities for genetic counselors.

Authors:  Alice K Hawkins
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537

Review 6.  Integrating biobanks: addressing the practical and ethical issues to deliver a valuable tool for cancer research.

Authors:  R William G Watson; Elaine W Kay; David Smith
Journal:  Nat Rev Cancer       Date:  2010-08-12       Impact factor: 60.716

7.  Regulating biobanking with children's tissue: a legal analysis and the experts' view.

Authors:  Elcke J Kranendonk; M Corrette Ploem; Raoul C M Hennekam
Journal:  Eur J Hum Genet       Date:  2015-04-15       Impact factor: 4.246

Review 8.  Handling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countries.

Authors:  Nola M Ries; Jane LeGrandeur; Timothy Caulfield
Journal:  BMC Med Ethics       Date:  2010-03-23       Impact factor: 2.652

9.  Health Research with Big Data: Time for Systemic Oversight.

Authors:  Effy Vayena; Alessandro Blasimme
Journal:  J Law Med Ethics       Date:  2018-03-27       Impact factor: 1.718

10.  Researchers' Perspectives on Informed Consent and Ethical Review of Biobank Research in South Africa: A Cross-Sectional Study.

Authors:  Erisa Mwaka; Lyn Horn
Journal:  J Empir Res Hum Res Ethics       Date:  2019-08-05       Impact factor: 1.742

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