Literature DB >> 16735260

Recommendations for effective newborn screening communication: results of focus groups with parents, providers, and experts.

Terry C Davis1, Sharon G Humiston, Connie L Arnold, Joseph A Bocchini, Pat F Bass, Estela M Kennen, Anna Bocchini, Penny Kyler, Michele Lloyd-Puryear.   

Abstract

OBJECTIVES: The aims of this study were to determine parent and provider knowledge and awareness of newborn screening; to gather opinions from parents, providers, and newborn screening professionals about the content and timing of newborn screening education; and to use consensus data to formulate recommendations and to develop educational materials for parents and providers.
METHODS: We conducted 22 focus groups and 3 individual interviews between October 2003 and May 2004, with English- and Spanish-speaking parents of infants <1 year of age who had experience with initial testing, retesting, or false-positive screenings; health professionals who provide prenatal care or health care for newborns; and state newborn screening program health professionals.
RESULTS: Parents and providers had limited knowledge and awareness about newborn screening practices. Parents wanted brief to-the-point information on newborn screening and its benefits, including the possible need for retesting and the importance of returning promptly for retesting if initial results are abnormal. Parents wanted the information orally from the primary care provider. Parents, providers, and newborn screening professionals all thought that an accompanying concise, easy-to-read brochure with contact information would be helpful. All focus group participants thought that parents should receive this information before the birth of the infant, preferably in the third trimester of pregnancy. Providers wanted a brief checklist of information and resources to prepare them to educate parents effectively.
CONCLUSIONS: We recommend prenatal and primary care providers be more involved in educating parents about newborn screening. Professional societies and state health officials should work together to encourage parent and provider education. User-friendly patient and provider education materials, such as those we developed, could form the basis for this educational approach.

Entities:  

Mesh:

Year:  2006        PMID: 16735260     DOI: 10.1542/peds.2005-2633M

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


  48 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.  Newborn screening education on the internet: a content analysis of North American newborn screening program websites.

Authors:  Makda H Araia; Beth K Potter
Journal:  J Community Genet       Date:  2011-04-15

3.  Public attitudes regarding the use of residual newborn screening specimens for research.

Authors:  Jeffrey R Botkin; Erin Rothwell; Rebecca Anderson; Louisa Stark; Aaron Goldenberg; Michelle Lewis; Matthew Burbank; Bob Wong
Journal:  Pediatrics       Date:  2012-01-16       Impact factor: 7.124

4.  Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study.

Authors:  Stuart G Nicholls; K W Southern
Journal:  J Community Genet       Date:  2012-02-16

5.  Design and evaluation of a decision aid for inviting parents to participate in a fragile X newborn screening pilot study.

Authors:  Donald B Bailey; Megan A Lewis; Shelly L Harris; Tracey Grant; Carla Bann; Ellen Bishop; Myra Roche; Sonia Guarda; Leah Barnum; Cynthia Powell; Bradford L Therrell
Journal:  J Genet Couns       Date:  2012-06-27       Impact factor: 2.537

6.  Parental views on informed consent for expanded newborn screening.

Authors:  Louise Moody; Kubra Choudhry
Journal:  Health Expect       Date:  2011-08-12       Impact factor: 3.377

7.  Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.

Authors:  Galen Joseph; Flavia Chen; Julie Harris-Wai; Jennifer M Puck; Charlotte Young; Barbara A Koenig
Journal:  Pediatrics       Date:  2016-01       Impact factor: 7.124

8.  Primary care role in expanded newborn screening: After the heel prick test.

Authors:  Robin Z Hayeems; Fiona A Miller; June C Carroll; Julian Little; Judith Allanson; Jessica P Bytautas; Pranesh Chakraborty; Brenda J Wilson
Journal:  Can Fam Physician       Date:  2013-08       Impact factor: 3.275

9.  Considering consent: a structural equation modelling analysis of factors influencing decisional quality when accepting newborn screening.

Authors:  Stuart G Nicholls; Kevin W Southern
Journal:  J Inherit Metab Dis       Date:  2013-09-17       Impact factor: 4.982

10.  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

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