Literature DB >> 23369110

Expectations and values about expanded newborn screening: a public engagement study.

Robin Z Hayeems1, Fiona A Miller, Yvonne Bombard, Denise Avard, June Carroll, Brenda Wilson, Julian Little, Pranesh Chakraborty, Jessica Bytautas, Yves Giguere, Judith Allanson, Renata Axler.   

Abstract

OBJECTIVES: Newborn bloodspot screening (NBS) panels have expanded to include conditions for which treatment effects are less certain, creating debate about population-based screening criteria. We investigated Canadian public expectations and values regarding the types of conditions that should be included in NBS and whether parents should provide consent.
METHODS: Eight focus groups (FG; n = 60) included education, deliberative discussion and pre-/post-questionnaires. Data were analysed quantitatively and qualitatively.
RESULTS: Quantitatively, the majority supported NBS for serious disorders for which treatment is not available (95-98, 82%). A majority endorsed screening without explicit consent (77-88%) for treatable disorders, but 62% supported unpressured choice for screening for untreatable disorders. Qualitatively, participants valued treatment-related benefits for infants and informational benefits for families. Concern for anxiety, stigma and unwanted knowledge depended upon disease context and strength of countervailing benefits.
CONCLUSIONS: Anticipated benefits of expanded infant screening were prioritized over harms, with information provision perceived as a mechanism for mitigating harms and enabling choice. However, we urge caution around the potential for public enthusiasm to foster unlimited uptake of infant screening technologies.
© 2013 Blackwell Publishing Ltd.

Entities:  

Keywords:  expanded newborn screening; mixed methods; public engagement; public expectations

Mesh:

Year:  2013        PMID: 23369110      PMCID: PMC5060787          DOI: 10.1111/hex.12047

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  45 in total

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Authors:  Jeffrey S Wagener; Edith T Zemanick; Marci K Sontag
Journal:  Curr Opin Pediatr       Date:  2012-06       Impact factor: 2.856

2.  Parental support for newborn screening for cystic fibrosis.

Authors:  Isabelle de Monestrol; Agneta Bergsten Brucefors; Birgitta Sjöberg; Lena Hjelte
Journal:  Acta Paediatr       Date:  2010-10-15       Impact factor: 2.299

3.  Screening mammography--a long run for a short slide?

Authors:  H Gilbert Welch
Journal:  N Engl J Med       Date:  2010-09-23       Impact factor: 91.245

4.  Does familiarity breed acceptance? The influence of policy on physicians' attitudes toward newborn screening programs.

Authors:  Joy Koopmans; Lainie Friedman Ross
Journal:  Pediatrics       Date:  2006-05       Impact factor: 7.124

5.  Newborn screening: toward a uniform screening panel and system--executive summary.

Authors: 
Journal:  Pediatrics       Date:  2006-05       Impact factor: 7.124

6.  Bringing 'the public' into health technology assessment and coverage policy decisions: from principles to practice.

Authors:  Julia Abelson; Mita Giacomini; Pascale Lehoux; Francois-Pierre Gauvin
Journal:  Health Policy       Date:  2006-09-22       Impact factor: 2.980

7.  From public health emergency to public health service: the implications of evolving criteria for newborn screening panels.

Authors:  Scott D Grosse; Coleen A Boyle; Aileen Kenneson; Muin J Khoury; Benjamin S Wilfond
Journal:  Pediatrics       Date:  2006-03       Impact factor: 7.124

8.  Fostering deliberations about health innovation: what do we want to know from publics?

Authors:  Pascale Lehoux; Genevieve Daudelin; Olivier Demers-Payette; Antoine Boivin
Journal:  Soc Sci Med       Date:  2009-04-10       Impact factor: 4.634

9.  Evidence-based path to newborn screening for Duchenne muscular dystrophy.

Authors:  Jerry R Mendell; Chris Shilling; Nancy D Leslie; Kevin M Flanigan; Roula al-Dahhak; Julie Gastier-Foster; Kelley Kneile; Diane M Dunn; Brett Duval; Alexander Aoyagi; Cindy Hamil; Maha Mahmoud; Kandice Roush; Lauren Bird; Chelsea Rankin; Heather Lilly; Natalie Street; Ram Chandrasekar; Robert B Weiss
Journal:  Ann Neurol       Date:  2012-03       Impact factor: 10.422

10.  Pediatricians' attitudes about screening newborns for infectious diseases.

Authors:  Hanna Schittek; Joy Koopmans; Lainie Friedman Ross
Journal:  Matern Child Health J       Date:  2008-12-09
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  9 in total

1.  Public views on participating in newborn screening using genome sequencing.

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Carolyn Barg; Celine Cressman; June C Carroll; Brenda J Wilson; Julian Little; Denise Avard; Michael Painter-Main; Judith Allanson; Yves Giguere; Pranesh Chakraborty
Journal:  Eur J Hum Genet       Date:  2014-02-19       Impact factor: 4.246

2.  Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice.

Authors:  Holly Etchegary; Stuart G Nicholls; Laure Tessier; Charlene Simmonds; Beth K Potter; Jamie C Brehaut; Daryl Pullman; Robyn Hayeems; Sari Zelenietz; Monica Lamoureux; Jennifer Milburn; Lesley Turner; Pranesh Chakraborty; Brenda Wilson
Journal:  Eur J Hum Genet       Date:  2016-06-15       Impact factor: 4.246

3.  Parental intentions to enroll children in a voluntary expanded newborn screening program.

Authors:  Ryan S Paquin; Holly L Peay; Lisa M Gehtland; Megan A Lewis; Donald B Bailey
Journal:  Soc Sci Med       Date:  2016-07-29       Impact factor: 4.634

4.  Framing optional genetic testing in the context of mandatory newborn screening tests.

Authors:  Sarah E Lillie; Beth A Tarini; Nancy K Janz; Brian J Zikmund-Fisher
Journal:  BMC Med Inform Decis Mak       Date:  2015-06-27       Impact factor: 2.796

5.  Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocol.

Authors:  S G Nicholls; L Tessier; H Etchegary; J C Brehaut; B K Potter; R Z Hayeems; P Chakraborty; J Marcadier; J Milburn; D Pullman; L Turner; B J Wilson
Journal:  BMJ Open       Date:  2014-11-24       Impact factor: 2.692

Review 6.  Policy Making in Newborn Screening Needs a Structured and Transparent Approach.

Authors:  Marleen E Jansen; Karla J Lister; Henk J van Kranen; Martina C Cornel
Journal:  Front Public Health       Date:  2017-03-21

7.  Parents' views on accepting, declining, and expanding newborn bloodspot screening.

Authors:  Sylvia M van der Pal; Sophie Wins; Jasmijn E Klapwijk; Tessa van Dijk; Adriana Kater-Kuipers; Catharina P B van der Ploeg; Suze M P J Jans; Stephan Kemp; Rendelien K Verschoof-Puite; Lion J M van den Bosch; Lidewij Henneman
Journal:  PLoS One       Date:  2022-08-18       Impact factor: 3.752

8.  Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents' Perspective on Ataxia Telangiectasia.

Authors:  Maartje Blom; Michiel H D Schoenaker; Myrthe Hulst; Martine C de Vries; Corry M R Weemaes; Michèl A A P Willemsen; Lidewij Henneman; Mirjam van der Burg
Journal:  Front Immunol       Date:  2019-11-06       Impact factor: 7.561

9.  Queensland Consumers' Awareness and Understanding of Clinical Genetics Services.

Authors:  Courtney K Wallingford; Katrina Cutler; Satrio Nindyo Istiko; Lindsay F Fowles; Rachel Lamb; Jessica Bean; Louise Healy; Gary Hondow; Gregory Pratt; Miranda E Vidgen; Nicola Waddell; Erin Evans; David Bunker; Aideen M McInerney-Leo
Journal:  Front Genet       Date:  2020-10-15       Impact factor: 4.599

  9 in total

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