Literature DB >> 15580734

Using tandem mass spectrometry for metabolic disease screening among newborns. A report of a work group.

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Abstract

Increasingly, tandem mass spectrometry (MS/MS) is being used for newborn screening because this laboratory testing technology substantially increases the number of metabolic disorders that can be detected from dried blood-spot specimens. In June 2000, the National Newborn Screening and Genetics Resource Center, in collaboration with CDC and the Health Resources and Services Administration, convened a workshop in San Antonio, Texas. Workshop participants examined programmatic concerns for health providers choosing to integrate MS/MS technology into their newborn screening activities. Representatives from approximately 50 public and private health agencies and universities participated in the workshop. The workshop participants and work group focused on laboratory methodology, decision criteria, quality assurance, diagnostic protocols, patient case management, and program evaluation for using MS/MS to analyze dried blood spots routinely collected from newborns. This work group report contains proposals for planning, operating, and evaluating MS/MS technology in newborn screening and maternal and child health programs. As a supplement to these proposals, this report contains synopses of selected presentations made at the 2000 workshop regarding integration of MS/MS technology into newborn screening programs. The proposals contained in this report should assist policymakers, program managers, and laboratorians in making informed decisions regarding the process of including MS/MS technology in their newborn screening and maternal and child health programs.

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Mesh:

Year:  2001        PMID: 15580734

Source DB:  PubMed          Journal:  MMWR Recomm Rep        ISSN: 1057-5987


  11 in total

1.  Screening for inherited metabolic disease in newborn infants using tandem mass spectrometry.

Authors:  James V Leonard; Carol Dezateux
Journal:  BMJ       Date:  2002-01-05

2.  Legal issues in newborn screening: implications for public health practice and policy.

Authors:  Jennifer Kraszewski; Taylor Burke; Sara Rosenbaum
Journal:  Public Health Rep       Date:  2006 Jan-Feb       Impact factor: 2.792

3.  Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors.

Authors:  Robin L Bennett; Arno G Motulsky; Alan Bittles; Louanne Hudgins; Stefanie Uhrich; Debra Lochner Doyle; Kerry Silvey; C Ronald Scott; Edith Cheng; Barbara McGillivray; Robert D Steiner; Debra Olson
Journal:  J Genet Couns       Date:  2002-04       Impact factor: 2.537

Review 4.  Current situation and prospects of newborn screening and treatment for Phenylketonuria in China - compared with the current situation in the United States, UK and Japan.

Authors:  Lin Mei; Peipei Song; Norihiro Kokudo; Lingzhong Xu; Wei Tang
Journal:  Intractable Rare Dis Res       Date:  2013-11

5.  The heritability of metabolic profiles in newborn twins.

Authors:  F Y Alul; D E Cook; O A Shchelochkov; L G Fleener; S L Berberich; J C Murray; K K Ryckman
Journal:  Heredity (Edinb)       Date:  2012-11-14       Impact factor: 3.821

6.  Clinical and environmental influences on metabolic biomarkers collected for newborn screening.

Authors:  Kelli K Ryckman; Stanton L Berberich; Oleg A Shchelochkov; Daniel E Cook; Jeffrey C Murray
Journal:  Clin Biochem       Date:  2012-09-23       Impact factor: 3.281

7.  Expanded Newborn Screening Program in Slovenia using Tandem Mass Spectrometry and Confirmatory Next Generation Sequencing Genetic Testing.

Authors:  Barbka Repič Lampret; Žiga Iztok Remec; Ana Drole Torkar; Mojca Žerjav Tanšek; Andraz Šmon; Vanesa Koračin; Vanja Čuk; Daša Perko; Blanka Ulaga; Ana Marija Jelovšek; Maruša Debeljak; Jernej Kovač; Tadej Battelino; Urh Grošelj
Journal:  Zdr Varst       Date:  2020-10-18

8.  Practical aspects of genetic testing in ambulatory paediatrics and child health care.

Authors:  Philip R Wyatt
Journal:  Paediatr Child Health       Date:  2003-01       Impact factor: 2.253

9.  Frequency of inborn errors of metabolism screening for children with unexplained acute encephalopathy at an emergency department.

Authors:  Mamdouh Abdel Maksoud; Solaf Mohamed ELsayed; Rania H Shatla; Abdulbasit Abdulhalim Imam; Riad M Elsayed; Amira Aa Mosabah; Ashraf M Sherif
Journal:  Neuropsychiatr Dis Treat       Date:  2018-06-29       Impact factor: 2.570

Review 10.  The Use of Whole Genome and Exome Sequencing for Newborn Screening: Challenges and Opportunities for Population Health.

Authors:  Audrey C Woerner; Renata C Gallagher; Jerry Vockley; Aashish N Adhikari
Journal:  Front Pediatr       Date:  2021-07-19       Impact factor: 3.418

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