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Birth Defects Home > Tracking > State Birth Defects Surveillance Systems > Virginia

Virginia Birth Defects Tracking Program

Program Title: Virginia Congenital Anomaly Reporting and Education System
Organization: Division of Child and Adolescent Health
Virginia Department of Health
Project Period: March 2005–February 2010
Project Director: Nancy Ford, RN, MPH
Grant Title: Population-Based Birth Defects Surveillance Programs and the Utilization of Surveillance Data by Public Health Programs
 

Project Summary

The Virginia Congenital Anomalies Reporting and Education System (VaCARES) is a statewide passive surveillance system that collects data on children younger than 2 years of age with a birth defect diagnosis identified by a hospital upon discharge or listed on the birth certificate. The Virginia Department of Health works with the Children with Special Health Care Needs (CSHCN) Program to promote the optimal health and development of children with special health care needs by partnering with families, service providers, and communities.
 

Project Goals and Activities

Surveillance

  • Broaden methodologies and approaches to improve and expand the capacity of the VaCARES.
  • Analyze and disseminate surveillance data generated by the system in a timely way, including rates and trends of major birth defects.
  • Evaluate the surveillance methodology used.
     
Prevention
  • Invite additional partners within Virginia to join in NTD prevention.
  • Start new NTD prevention programs based on epidemiologic and social marketing principles.
  • Expand partnerships to share results and integrate genetics into public health.
  • Evaluate progress made in preventing birth defects in Virginia, including evaluation of the quality of surveillance data used.
     
Referrals
  • Work with appropriate partners within Virginia to expand activities to improve the access of children with birth defects to comprehensive, community-based, family-centered care.
  • Evaluate the effectiveness of referral services and the outcomes of children and families who receive those services.
     

Date: January 03, 2008
Content source: National Center on Birth Defects and Developmental Disabilities

 

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