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Related Experiment Video

Updated: Jun 24, 2026

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound (30/45MHZ) System

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Published on: May 5, 2018

Wisconsin Birth Defects Registry collecting data.

Elizabeth Oftedahl¹, Richard M Pauli, Sharon Fleischfresser

¹Children with Special Health Care Needs , Bureau of Community Health Promotion, Wisconsin Department of Health and Family Services, USA.

WMJ : Official Publication of the State Medical Society of Wisconsin

|November 24, 2004

Summary

Wisconsin established the Birth Defects Registry (WBDR) in 2000 to track birth defects. Since 2004, it has collected data on children up to age 2 with diagnosed conditions.

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Area of Science:

Public Health Surveillance
Pediatric Epidemiology
Reproductive Health

Background:

Wisconsin Statute 253.12, enacted in May 2000, established the Wisconsin Birth Defects Registry (WBDR).
The WBDR replaced the Birth and Developmental Outcome Monitoring Program, a system initiated in 1989.
This initiative aimed to improve the tracking and understanding of birth defects and developmental disabilities in Wisconsin.

Purpose of the Study:

To describe the development and implementation of the Wisconsin Birth Defects Registry (WBDR).
To outline the scope of data collection for children with birth defects.
To establish reporting expectations for healthcare providers regarding birth defects.

Main Methods:

The Wisconsin Birth Defects Registry (WBDR) began data collection in the summer of 2004.
The registry collects demographic, diagnostic, and identifying information.
Data focuses on children from birth to 2 years of age with reportable birth defects receiving healthcare in Wisconsin.

Main Results:

The registry successfully transitioned from its predecessor system.
Established a system for collecting comprehensive data on pediatric birth defects.
Defined the population and types of information to be collected for surveillance.

Conclusions:

The Wisconsin Birth Defects Registry (WBDR) provides a vital public health surveillance tool.
The registry enhances the ability to monitor and understand the burden of birth defects in Wisconsin's children.
Clear reporting expectations are crucial for the registry's effectiveness and ongoing data quality.