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

Florida Birth Defects Tracking Program

Program Title: Florida Birth Defects Registry
Organization: Florida Department of Health
Project Period: September 2003–June 2008
Project Director: Prakash S. Patel, MBBS, MPH
Grant Title: Population-Based Birth Defects Surveillance Programs and the Utilization of Surveillance Data by Public Health Programs
 

Project Summary

The Florida Birth Defects Registry (FBDR) works with state and local programs serving children with special health care needs to improve access to health services and early intervention programs. Through this project, the FBDR will enhance, expand, and evaluate public health initiatives related to statewide population-based birth defects surveillance in Florida. The project will focus on prevention and referral programs targeted to women of childbearing age, children with special health care needs and their families, and families with a history of birth defects.

Project Goals and Activities

Surveillance

  • Expand current rapid identification of birth defects to include all central nervous system defects, anotia, microtia, orofacial clefts, gastroschisis/omphalocele, chromosomal abnormalities, and fetal alcohol syndrome.
  • Investigate and develop new sources of data to identify birth defects in Florida.
Prevention
  • Work with the Florida Folic Acid Coalition to continue effective programs to raise awareness and increase use of folic acid. Develop and launch new programs.
  • Educate health care providers about birth defects recurrence to improve prevention.
  • Counsel women who have an NTD-affected pregnancy within 6 months of birth, pregnancy loss, or termination.
  • Participate in the Fetal Alcohol Spectrum Disorders Action Group.
  • Prepare and distribute a series of public health briefs about conditions identified through active medical records review.
     
Referrals
  • Evaluate the feasibility of linking the FBDR to other appropriate data sets.
  • Support the use of birth defects data in making decisions about health services planning, prevention efforts, secondary disabilities prevention, and service coordination.
  • Improve data linkages, collaboration, and referrals among the department’s programs serving families and children with special health care needs, including the Children’s Medical Services and Healthy Start Programs.
     

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

 

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