Catalog

Surveillance modernization efforts emphasize the potential use of electronic health record (EHR) data to inform public health surveillance and prevention. However, EHR data streams vary widely in their completeness, accuracy, and representativeness. This publication describes a validation process developed by the Multi-State EHR-Based Network for Disease Surveillance (MENDS) pilot project to identify and resolve data quality issues that could affect chronic disease prevalence estimates.

This presentation provides an overview of the Trusted Exchange Framework and Common Agreement (TEFCA) which has the overall goal to establish a floor of universal interoperability across the country. The Common Agreement will establish the infrastructure model and the governing approach for users in different networks to securely share basic clinical information with each other—all under commonly agreed-to expectations and rules.

In this presentation, we will define use case in an implementation guide, go over an HL7 v2 message, and review each of the newborn screening standards that exist today.

Guidance for initiating and sustaining this project and outlines steps needed to set up electronic messaging with partners