An agency of the Texas Health and Human Services System.
Vision: A Healthy Texas
Mission: To improve health and well-being in Texas
The Texas Birth Defects Registry - Enabling Law and Rules
The Texas Birth Defects Registry
Disease surveillance is a core public health function that allows epidemiologists to better understand differences in the way disease occurs among groups of people, different places, and across time.
Enabling Law and Rules
Texas Health and Safety Code, Title 2, Subtitle D, Chapter 87. Effective September 1, 1993.
Texas Administrative Code, Title 25, Part 1, Chapter 37, Subchapter P. Revised November 4, 2009.
Recent changes to the Texas Administrative Code permit the passive reporting of specific laboratory information to the Birth Defects Epidemiology and Surveillance Branch. Beginning in 2010, fetal and infant chromosomal test results for ICD 9-CM codes of 758 (Chromosomal anomalies) and 759 (Other and unspecified congenital anomalies) will become a notifiable condition through the National Electronic Disease Surveillance System (NEDSS). The chromosomal results will be used to clarify those genetic conditions of birth defects cases that have not been definitively diagnosed in the Registry.
Passive Reporting of Specific Laboratory Information to the Birth Defects Epidemiology and Surveillance Branch.
What to Report:
Pertinent excerpts of the Texas Health and Safety Code and Texas Administrative Code:
TEXAS HEALTH AND SAFETY CODE, TITLE 2, SUBTITLE D, CHAPTER 87,
SUBCHAPTER B. BIRTH DEFECTS MONITORING PROGRAM
Sec. 87.021. SURVEILLANCE PROGRAM; REGISTRY ESTABLISHED.
(a) The board shall establish in the department a program to:
(1) identify and investigate certain birth defects in children; and
(2) maintain a central registry of cases of birth defects.
(b) The board may authorize the department to implement a statewide program
(f) In addition to providing for the active collection of birth defects information under Subsection (c)(7), the board and
the department may design the program to also provide for the passive collection of that information.
Sec. 87.022. DATA COLLECTION.
(a) To ensure an accurate source of data necessary to investigate the incidence, prevalence, and trends of birth defects, the board may require a health facility, health professional, or midwife to make available for review by the department or by an authorized agent medical records or other information that is in the facility's, professional's, or midwife's custody or control and that relates to the occurrence of a birth defect specified by the board.
(b) The board by rule shall prescribe the manner in which records and other information are made available to the department.
(c) The board shall adopt procedural rules to facilitate cooperation between the health care facility, health professional, or midwife and a department employee or authorized agent, including rules for notice, requests for medical records, times for record reviews, and record management during review.
Texas Administrative Code
TITLE 25 HEALTH SERVICES
PART 1 DEPARTMENT OF STATE HEALTH SERVICES
CHAPTER 37 MATERNAL AND INFANT HEALTH SERVICES
SUBCHAPTER P SURVEILLANCE AND CONTROL OF BIRTH DEFECTS
RULE §37.303 Definitions
(10) Health facility--Any of the following types of facility:
(14) Surveillance--The systematic collection, analysis, interpretation, and dissemination of health data on an ongoing basis.
RULE §37.305Surveillance of Birth Defects: Central Registry
(a) The central registry shall use a birth defects coding scheme used by the Centers for Disease Control and Prevention (CDC) of the United States Public Health Service in their birth defects monitoring programs.
(b) In order for information related to a child to be included in the central registry, the following conditions must be met.
(2) The child must have a structural or genetic birth defect or other specified outcome that can adversely affect his or her health and development as defined in subsection (a) of this section.
(3) The defect must be diagnosed prenatally or within one year after delivery. In certain circumstances (e.g., the diagnosis of fetal alcohol syndrome, special studies and childhood genetic disorders diagnosed after infancy), the upper age limit will be extended to age six.
(c) A reportable defect as defined in subsection (a) of this section occurring in a fetal death or pregnancy termination shall be included in the central registry.
(d) Interaction between department staff and health facility staff is detailed below:
(2) Potential cases are obtained by department staff through review of medical and health records, logs, indices, appointment rosters, and other records. Cases may also be obtained through passive reporting from health facilities and health professionals.
For more information, contact the Birth Defects Epidemiology and Surveillance Branch via email or by phone at 512-776-7232.
NEDSS Project Office Contact:
For NEDSS access or NEDSS training opportunities, contact Pamela Stuart:
Last Updated April 14, 2016