Improving Newborn Screening Through Interoperability

Overview

Newborn screening programs are a vital public health resource that enable millions of infants to benefit from early detection and intervention of genetic, endocrine, metabolic, hearing, and critical congenital heart conditions. Yet in many jurisdictions across the country newborn screening data is fragmented, siloed, and subject to different screening procedures, turnaround times, and methods of interpreting results.

Approach

Altarum helps jurisdictions address these gaps, creating a more streamlined and uniform system of newborn screening and reporting. We built processes to facilitate the exchange of knowledge with experts and peers, providing interoperability training, assessing state interoperability readiness, and creating customized roadmaps for states to help them reach specific interoperability objectives.

This builds on our two decades of experience advancing state health information exchange and interoperability, which includes developing solutions using a variety of products including Fast Healthcare Interoperability Resources (FHIR), CDA and HL7 Version 2; building applications that support information exchange for disease surveillance and care coordination; and helping to create national standards for electronic birth defect reporting, newborn screening early hearing detection and intervention, and critical congenital heart defects and disease.