Literature DB >> 19936964

The use of human tissue in epidemiological research; ethical and legal considerations in two biobanks in Belgium.

Carla Truyers1, Eliane Kellen, Marc Arbyn, Leen Trommelmans, Herman Nys, Karen Hensen, Bert Aertgeerts, Stefaan Bartholomeeusen, Mats Hansson, Frank Buntinx.   

Abstract

This paper discusses the legal implications of setting up two new biobanks in Belgium. The first is hospital-based and will archive tissue from patients with haematologic cancer, whereas the second is linked to a general practice based morbidity registry and will involve storage of blood samples. To date, Belgium has no specific legislation that regulates storage of human tissue and related databases. Several issues concerning the protection of individuals with regard to the processing of personal medical data are discussed from the existing privacy legislation. We will address the principle of consent (broad versus specific) and the type of data recorded (anonymous, encoded and identifiable) for both biobanks.

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Year:  2010        PMID: 19936964     DOI: 10.1007/s11019-009-9230-y

Source DB:  PubMed          Journal:  Med Health Care Philos        ISSN: 1386-7423


  13 in total

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Authors: 
Journal:  Eur J Hum Genet       Date:  2003-12       Impact factor: 4.246

2.  Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.

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Review 3.  The social and ethical issues of post-genomic human biobanks.

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Review 4.  Should donors be allowed to give broad consent to future biobank research?

Authors:  Mats G Hansson; Joakim Dillner; Claus R Bartram; Joyce A Carlson; Gert Helgesson
Journal:  Lancet Oncol       Date:  2006-03       Impact factor: 41.316

Review 5.  One-time general consent for research on biological samples.

Authors:  David Wendler
Journal:  BMJ       Date:  2006-03-04

6.  Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?

Authors:  Asa Kettis-Lindblad; Lena Ring; Eva Viberth; Mats G Hansson
Journal:  Eur J Public Health       Date:  2005-10-05       Impact factor: 3.367

7.  Balancing the quality of consent.

Authors:  M O Hansson
Journal:  J Med Ethics       Date:  1998-06       Impact factor: 2.903

8.  Building on relationships of trust in biobank research.

Authors:  M G Hansson
Journal:  J Med Ethics       Date:  2005-07       Impact factor: 2.903

9.  Informed consent for population-based research involving genetics.

Authors:  L M Beskow; W Burke; J F Merz; P A Barr; S Terry; V B Penchaszadeh; L O Gostin; M Gwinn; M J Khoury
Journal:  JAMA       Date:  2001-11-14       Impact factor: 56.272

10.  The right to withdraw consent to research on biobank samples.

Authors:  Gert Helgesson; Linus Johnsson
Journal:  Med Health Care Philos       Date:  2005
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  5 in total

1.  Withdrawal from biobank research: considerations and the way forward.

Authors:  Kristina Hug; Göran Hermerén; Mats Johansson
Journal:  Stem Cell Rev Rep       Date:  2012-12       Impact factor: 5.739

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Review 4.  Ethical aspects of human biobanks: a systematic review.

Authors:  Danijela Budimir; Ozren Polasek; Ana Marusić; Ivana Kolcić; Tatijana Zemunik; Vesna Boraska; Ana Jeroncić; Mladen Boban; Harry Campbell; Igor Rudan
Journal:  Croat Med J       Date:  2011-06       Impact factor: 1.351

5.  The Intego database: background, methods and basic results of a Flemish general practice-based continuous morbidity registration project.

Authors:  Carla Truyers; Geert Goderis; Harrie Dewitte; Marjan vanden Akker; Frank Buntinx
Journal:  BMC Med Inform Decis Mak       Date:  2014-06-06       Impact factor: 2.796

  5 in total

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