Literature DB >> 19853341

"Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose.

Carlo Petrini1.   

Abstract

An important ethical issue regarding biological samples stored in biobanks is unforeseen future sample use, when no or limited subject consent is obtained. Biobanks of biological samples have significant future research potential, but may cause conflicts of interest regarding the consent obtained. Indeed, ethics, deontology, and jurisprudence generally advise that consent must be specific and circumstantiated. However, it is not possible to foresee all of the future circumstances in which the samples might be useful, nor is it possible to re-contact all subjects in order to gain consent for a new use. The main arguments for the use of "broad" consent are presented with a brief discussion of the conditions where it may be legitimate not to obtain consent. Particular attention is given to the expressed positions of national and international bioethics bodies. Copyright 2009 Elsevier Ltd. All rights reserved.

Mesh:

Year:  2009        PMID: 19853341     DOI: 10.1016/j.socscimed.2009.10.004

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  44 in total

1.  Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach.

Authors:  Menno Mostert; Annelien L Bredenoord; Monique C I H Biesaart; Johannes J M van Delden
Journal:  Eur J Hum Genet       Date:  2015-11-11       Impact factor: 4.246

2.  Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.

Authors:  S Trent Rosenbloom; Jennifer L Madison; Kyle B Brothers; Erica A Bowton; Ellen Wright Clayton; Bradley A Malin; Dan M Roden; Jill Pulley
Journal:  J Am Med Inform Assoc       Date:  2013-07-25       Impact factor: 4.497

Review 3.  The Bio-PIN: a concept to improve biobanking.

Authors:  J J Nietfeld; Jeremy Sugarman; Jan-Eric Litton
Journal:  Nat Rev Cancer       Date:  2011-03-17       Impact factor: 60.716

4.  Ethical, Legal, and Social Issues (ELSI) in Clinical Genetics Research.

Authors:  Daryl Pullman; Holly Etchegary
Journal:  Methods Mol Biol       Date:  2021

5.  Can our understanding of informed consent be strengthened using the idea of cluster concepts?

Authors:  Wayne Xavier Shandera
Journal:  Med Health Care Philos       Date:  2013-11

6.  Biobanks, consent and claims of consensus.

Authors:  Zubin Master; Erin Nelson; Blake Murdoch; Timothy Caulfield
Journal:  Nat Methods       Date:  2012-09       Impact factor: 28.547

7.  'Cool! and creepy': engaging with college student stakeholders in Michigan's biobank.

Authors:  Tevah Platt; Jodyn Platt; Daniel B Thiel; Nicole Fisher; Sharon L R Kardia
Journal:  J Community Genet       Date:  2014-06-12

8.  Secondary Use of Patient Tissue in Cancer Biobanks.

Authors:  Debra J H Mathews; Julia T Rabin; Katharine Quain; Eric Campbell; Deborah Collyar; Fay J Hlubocky; Steven Isakoff; Jeffrey Peppercorn
Journal:  Oncologist       Date:  2019-06-10

9.  "As Long as You Ask": A Qualitative Study of Biobanking Consent-Oncology Patients' and Health Care Professionals' Attitudes, Motivations, and Experiences-the B-PPAE Study.

Authors:  Sonia Yip; Jennifer Fleming; Heather L Shepherd; Adam Walczak; Jonathan Clark; Phyllis Butow
Journal:  Oncologist       Date:  2018-11-09

10.  'Born in Michigan? You're in the biobank': engaging population biobank participants through Facebook advertisements.

Authors:  J E Platt; T Platt; D Thiel; S L R Kardia
Journal:  Public Health Genomics       Date:  2013-06-21       Impact factor: 2.000

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