Literature DB >> 20207265

Enhancing the quality and efficiency of newborn screening programs through the use of health information technology.

Gregory J Downing1, Alan E Zuckerman, Constanze Coon, Michele A Lloyd-Puryear.   

Abstract

A variety of efforts are underway at national, state, regional, and local levels to enhance the performance of programs for early detection of inherited diseases and conditions of newborn infants. Newborn screening programs serve a vital purpose in identifying nonsymptomatic clinical conditions and enabling early intervention strategies that lessen morbidity and mortality. Currently, the programs of most intense focus are early hearing detection and intervention, using physiological techniques for audiology screening and use of newborn dried blood spots for detection of metabolites or proteins representing inherited disorders. One of the primary challenges to effective newborn screening programs to date has been the inability to provide information in a timely and easily accessible way to a variety of users. Other challenging communication issues being faced include the complexity introduced by the diversity of conditions for which testing is conducted and laboratory methods being used by each state's screening programs, lack of an electronic information infrastructure to facilitate information exchange, and variation in policies that enable access to information while protecting patient privacy and confidentiality. In this study, we address steps being taken to understand these challenges, outline progress made to date to overcome them, and provide examples of how electronic health information exchange will enhance the utility of newborn screening. It is likely that future advances in science and technology will bring many more opportunities to prevent and preempt disabilities among children through early detection programs. To take their advantage, effective communication strategies are needed among the public health, primary care practice, referral/specialty service, and consumer advocacy communities to provide continuity of information required for medical decision-making throughout prenatal, newborn, and early childhood periods of patient care. Published by Elsevier Inc.

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Year:  2010        PMID: 20207265     DOI: 10.1053/j.semperi.2009.12.005

Source DB:  PubMed          Journal:  Semin Perinatol        ISSN: 0146-0005            Impact factor:   3.300


  10 in total

1.  Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.

Authors:  Laurel K Willig; Josh E Petrikin; Laurie D Smith; Carol J Saunders; Isabelle Thiffault; Neil A Miller; Sarah E Soden; Julie A Cakici; Suzanne M Herd; Greyson Twist; Aaron Noll; Mitchell Creed; Patria M Alba; Shannon L Carpenter; Mark A Clements; Ryan T Fischer; J Allyson Hays; Howard Kilbride; Ryan J McDonough; Jamie L Rosterman; Sarah L Tsai; Lee Zellmer; Emily G Farrow; Stephen F Kingsmore
Journal:  Lancet Respir Med       Date:  2015-04-27       Impact factor: 30.700

Review 2.  An update on the use of health information technology in newborn screening.

Authors:  Swapna Abhyankar; Rebecca M Goodwin; Marci Sontag; Careema Yusuf; Jelili Ojodu; Clement J McDonald
Journal:  Semin Perinatol       Date:  2015-04-29       Impact factor: 3.300

3.  The use of model constructs to design collaborative health information technologies: A case study to support child development.

Authors:  Sean P Mikles; Hyewon Suh; Julie A Kientz; Anne M Turner
Journal:  J Biomed Inform       Date:  2018-09-05       Impact factor: 6.317

4.  [Quality of universal newborn hearing screening results : Multicenter analysis of data recorded between 2009 and 2012 in four German states].

Authors:  P Matulat; S Fabian; A Köhn; M Spormann-Lagodziski; R Lang-Roth; A Rissmann; M Gross; A am Zehnhoff-Dinnesen
Journal:  HNO       Date:  2014-03       Impact factor: 1.284

5.  Newborn Screening Programs and Sickle Cell Disease: A Public Health Services and Systems Approach.

Authors:  Cynthia S Minkovitz; Holly Grason; Marjory Ruderman; James F Casella
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

6.  [Transregional tracking in newborn hearing screening].

Authors:  P Matulat; S Stroe; A Am Zehnhoff-Dinnesen
Journal:  HNO       Date:  2017-12       Impact factor: 1.284

7.  Impact of an electronic medical record-based automated screening program for critical congenital heart disease: Emirates Health Services, United Arab Emirates.

Authors:  Sumaya Al Zarouni; Noor Majed Al Mheiri; Kalthoom Al Blooshi; Yousif Al Serkal; Neema Preman; Sadaf Ahsan Naqvi; Yasir Khan
Journal:  BMC Med Inform Decis Mak       Date:  2022-06-21       Impact factor: 3.298

8.  Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.

Authors:  Carol Jean Saunders; Neil Andrew Miller; Sarah Elizabeth Soden; Darrell Lee Dinwiddie; Aaron Noll; Noor Abu Alnadi; Nevene Andraws; Melanie LeAnn Patterson; Lisa Ann Krivohlavek; Joel Fellis; Sean Humphray; Peter Saffrey; Zoya Kingsbury; Jacqueline Claire Weir; Jason Betley; Russell James Grocock; Elliott Harrison Margulies; Emily Gwendolyn Farrow; Michael Artman; Nicole Pauline Safina; Joshua Erin Petrikin; Kevin Peter Hall; Stephen Francis Kingsmore
Journal:  Sci Transl Med       Date:  2012-10-03       Impact factor: 17.956

9.  The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.

Authors:  Josh E Petrikin; Julie A Cakici; Michelle M Clark; Laurel K Willig; Nathaly M Sweeney; Emily G Farrow; Carol J Saunders; Isabelle Thiffault; Neil A Miller; Lee Zellmer; Suzanne M Herd; Anne M Holmes; Serge Batalov; Narayanan Veeraraghavan; Laurie D Smith; David P Dimmock; J Steven Leeder; Stephen F Kingsmore
Journal:  NPJ Genom Med       Date:  2018-02-09       Impact factor: 8.617

10.  Preparing newborn screening for the future: a collaborative stakeholder engagement exploring challenges and opportunities to modernizing the newborn screening system.

Authors:  Sara M Andrews; Katherine Ackerman Porter; Donald B Bailey; Holly L Peay
Journal:  BMC Pediatr       Date:  2022-02-12       Impact factor: 2.125

  10 in total

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