Literature DB >> 23147970

Informed choice for newborn blood spot screening in the United Kingdom: a survey of parental perceptions.

Stuart G Nicholls1, Kevin W Southern.   

Abstract

OBJECTIVE: In the United Kingdom, newborn blood spot screening proceeds on the basis of consent based on an informed choice. However, little is known about parent experiences of this process. This study was intended to explore parents' understanding of newborn screening and their experience of the consent process using a structured survey.
METHODS: A mail survey exploring key components of consent was sent to parents whose children had been screened in the year before the study. A descriptive analysis of responses together with logistic regression was performed to identify variables that predicted parental likelihood to agree that they had made an informed choice to screening.
RESULTS: Most parents indicated they understood why the heel prick was done, but only a third understood how conditions would be dealt with if found. Almost a third of parents reported that they did not feel they had a choice to decline screening, yet >70% felt they had made an informed choice. Logistic regression indicated previous children, understanding why the heel prick was done, having time to make a decision, and feeling they had a choice were significant predictors of feeling an informed choice had been made.
CONCLUSIONS: The findings support previous studies that screening may be seen as a fait accompli. Analyses indicated that allowing time to make a decision (eg, by providing information during pregnancy, emphasizing the decision-making aspect, and clearly articulating the reasons behind screening) may help parents feel that they have made an informed choice.

Entities:  

Mesh:

Year:  2012        PMID: 23147970     DOI: 10.1542/peds.2012-1479

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  5 in total

1.  Pediatric data sharing in genomic research: attitudes and preferences of parents.

Authors:  Matthew D Burstein; Jill Oliver Robinson; Susan G Hilsenbeck; Amy L McGuire; Ching C Lau
Journal:  Pediatrics       Date:  2014-03-10       Impact factor: 7.124

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.  Genomic newborn screening: public health policy considerations and recommendations.

Authors:  Jan M Friedman; Martina C Cornel; Aaron J Goldenberg; Karla J Lister; Karine Sénécal; Danya F Vears
Journal:  BMC Med Genomics       Date:  2017-02-21       Impact factor: 3.063

4.  Mothering a population: How Danish mothers experience newborn dried blood spot samples and their considerations about re-use of samples for research purposes.

Authors:  Francisca Nordfalk; Anja M B Jensen
Journal:  Eur J Midwifery       Date:  2022-09-05

5.  Parents' Experiences of Receiving the Initial Positive Newborn Screening (NBS) Result for Cystic Fibrosis and Sickle Cell Disease.

Authors:  Jane Chudleigh; Sarah Buckingham; Jo Dignan; Sandra O'Driscoll; Kemi Johnson; David Rees; Hilary Wyatt; Alison Metcalfe
Journal:  J Genet Couns       Date:  2016-04-20       Impact factor: 2.537

  5 in total

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