Literature DB >> 25533753

Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities.

Shannon Cunningham1, Kieran C O'Doherty, Karine Sénécal, David Secko, Denise Avard.   

Abstract

Recently, public concerns have been expressed regarding the non-consented storage and secondary research uses of residual newborn bloodspot (RBS) samples. The purpose of this paper is to examine public responses to the storage and secondary uses of RBS that can be identified through analysis of media, legal cases, and documented public engagement activities. Coverage in the examined print media confirmed the importance of RBS to journalists and those people who expressed their concerns to these journalists. Several lawsuits, brought by parents concerned about the storage of newborn bloodspots, placed the practice of storing NBS into the spotlight. This resulted in controversial debates and the mandatory destruction of millions of samples. Analysis of public engagement activities across several jurisdictions indicated that across (inter)national boundaries there are common elements to what is perceived as inappropriate governance of RBS. Public concerns were grouped into five main themes: trust, transparency, confidentiality, ownership, and stigmatization/discrimination. The results of our analysis help to make a compelling case for placing citizens at the center of the debate and developing policy about the storage and secondary uses of newborn bloodspots.

Entities:  

Year:  2014        PMID: 25533753      PMCID: PMC4356669          DOI: 10.1007/s12687-014-0206-0

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  30 in total

1.  Policy issues and stakeholder concerns regarding the storage and use of residual newborn dried blood samples for research.

Authors:  Erin Rothwell; Rebecca Anderson; Jeffrey Botkin
Journal:  Policy Polit Nurs Pract       Date:  2010-05-10

2.  Citizens' values regarding research with stored samples from newborn screening in Canada.

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; June C Carroll; Denise Avard; Brenda J Wilson; Julian Little; Jessica P Bytautas; Judith Allanson; Renata Axler; Yves Giguere; Pranesh Chakraborty
Journal:  Pediatrics       Date:  2012-01-16       Impact factor: 7.124

3.  Universal Draft Declaration on Bioethics and Human Rights.

Authors: 
Journal:  Dev World Bioeth       Date:  2005-09       Impact factor: 2.294

4.  From newborn screening to population health research: implementation of the Michigan BioTrust for health.

Authors:  Carrie Langbo; Janice Bach; Mary Kleyn; Frances Pouch Downes
Journal:  Public Health Rep       Date:  2013 Sep-Oct       Impact factor: 2.792

5.  The Michigan BioTrust for Health: using dried bloodspots for research to benefit the community while respecting the individual.

Authors:  Denise Chrysler; Harry McGee; Janice Bach; Ed Goldman; Peter D Jacobson
Journal:  J Law Med Ethics       Date:  2011-03       Impact factor: 1.718

6.  Newborn screening: a spot of trouble.

Authors:  Mary Carmichael
Journal:  Nature       Date:  2011-07-13       Impact factor: 49.962

7.  DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study.

Authors:  Mads Vilhelm Hollegaard; Jonas Grauholm; Bent Nørgaard-Pedersen; David Michael Hougaard
Journal:  Mol Genet Metab       Date:  2013-02-01       Impact factor: 4.797

8.  Assessing public attitudes on the retention and use of residual newborn screening blood samples: a focus group study.

Authors:  Erin Rothwell; Rebecca Anderson; Aaron Goldenberg; Michelle H Lewis; Louisa Stark; Matthew Burbank; Bob Wong; Jeffrey R Botkin
Journal:  Soc Sci Med       Date:  2012-02-18       Impact factor: 4.634

9.  The use of newborn screening dried blood spots for research: the parental perspective.

Authors:  Li-Ming Gong; Wen-Jun Tu; Jian He; Xiao-Dong Shi; Xin-Yu Wang; Ying Li
Journal:  J Bioeth Inq       Date:  2012-03-21       Impact factor: 1.352

10.  Research use of leftover newborn bloodspots: attitudes of Canadian geneticists regarding storage and informed consent requirements.

Authors:  Julie Richer; Musie S Ghebremichael; Albert E Chudley; Walter M Robinson; Benjamin S Wilfond; Mildred Z Solomon
Journal:  Genet Med       Date:  2011-04       Impact factor: 8.822

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  4 in total

1.  Engaging a state: Facebook comments on a large population biobank.

Authors:  Tevah Platt; Jodyn Platt; Daniel Thiel; Sharon L R Kardia
Journal:  J Community Genet       Date:  2017-04-05

Review 2.  If you build it, they will come: unintended future uses of organised health data collections.

Authors:  Kieran C O'Doherty; Emily Christofides; Jeffery Yen; Heidi Beate Bentzen; Wylie Burke; Nina Hallowell; Barbara A Koenig; Donald J Willison
Journal:  BMC Med Ethics       Date:  2016-09-06       Impact factor: 2.652

3.  Parental perspectives on retention and secondary use of neonatal dried bloodspots: a Dutch mixed methods study.

Authors:  Marleen E Jansen; Lion J M van den Bosch; Marjolein J Hendriks; Mariska M J Scheffer; Marie-Louise Heijnen; Conor M W Douglas; Carla G van El
Journal:  BMC Pediatr       Date:  2019-07-09       Impact factor: 2.125

Review 4.  Lessons from HeLa Cells: The Ethics and Policy of Biospecimens.

Authors:  Laura M Beskow
Journal:  Annu Rev Genomics Hum Genet       Date:  2016-03-03       Impact factor: 8.929

  4 in total

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