PPT-Newborn Screening for

Critical Congenital Heart Diseases CCHD Lazaros Kochilas MD Associate Professor of Pediatrics University of Minnesota Disclosures and Support I will not discuss off label use andor investigational use in my presentation. . Strategy Summit and Awareness Campaign. Newborn screening is rapidly changing. Number of Conditions Screened. # of. States. But…. . We in this room are intimately aware of these changes, the complexities inherent making these changes happen in a rational way across all states, and magnitude of effort involved in implementing a comprehensive program of screening, follow-up, and treatment. Newborn Screening Diagnosis and Follow-up Work Group Harvey L. Levy, MD (Chair) Children WA Newborn Screening ProgramYour newborn baby’s screening testA blood test to screen for genetic conditions GEN-009372 MAY’14 a person with a disability. Produced by the WA Newborn Screening SACHDNC Advisory Committee Meeting. May 17-18, 2012. Subcommittee Charge. Review existing educational and training resources, identify gaps, and make recommendations regarding five groups:. Parents and the public. Screening: . National and International. Hurdles . and Progress. R. Rodney Howell, M. D.. Professor of Pediatrics, Chairman Emeritus. Member, Hussman Institute for Human Genomics. Miller School of Medicine, University of Miami. Diana Kimbal, RNC-NIC. Disclosure. I have no relevant financial or nonfinancial relationships to disclose.. Objectives. Identify nursing interventions to keep newborns safe. Defend the necessity of recommended newborn screenings and protocols. Refreshers, Best Practices, and Program Updates. Mission of ISDH Newborn Screening Program. Ensure that every newborn in Indiana receives state-mandated screening for all designated genetic conditions. Erin Burnette, NP-C. Emily Freeman, CPNP. Jamie Haushalter, CPNP. Objectives. Recognize the important factors in the maternal history and labor/delivery process which may affect the newborn. These factors include: pertinent social issues, chronic medical conditions in the mother, genetic risk factors, maternal/infant . 1Programme Newborn Pulse Oximetry Screening BackgroundCongenital heart defects CHD are the most common group of congenital malformations and one of the leading causes of infant death in the developed FINAL FEB16MaternityGCorporate GovernanceCompliance TeamPolicies Procedural DocumentsPublished Policy DatabaseMaternitynewborn Infant physical examination guidelinesNewborn Infant Physical Examinatio Newborn Screening Goals:. Sondi Aponte. QI, Education & Outreach Manager. Office of Newborn Screening. s. ondi.aponte@azdhs.gov. . O: 602-364-1642. www.aznewborn.com. . To identify newborns with certain, rare disorders . Key Points. Newborn screening involves the collection of a blood sample, transport of the sample to a state laboratory, and reporting of the results to the health care provider.. Newborn screening protocols are not uniform across the states and as such there are inconsistencies in timely results reporting.. Spinal Muscular Atrophy (SMA) Exon 7 Deletion (Pathogenic Variant) in Survival Motor Neuron Gene ( SMN1 ) Condition Description: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerati Robert Clark. Clinical Ethics and Law Group . Faculty of Medicine . University of Southampton . Newborn Screening. Modern Advancements?. Fragile X Syndrome?. Lymphoblastic Leukaemia?. Hereditary . Haemochromatosis.