Presented as a poster at the 9th Annual Meeting of the National Birth Defects Prevention Network, Arlington, VA, January 29–February 1, 2006.
Birth defects interstate data exchange: A battle worth fighting?†
Article first published online: 7 NOV 2007
Copyright © 2007 Wiley-Liss, Inc.
Birth Defects Research Part A: Clinical and Molecular Teratology
Special Issue: Special Issue: 2007 Congenital Malformations Surveillance Report, Part I
Volume 79, Issue 11, pages 806–810, November 2007
How to Cite
Cassell, C., Mai, C. and Rickard, R. (2007), Birth defects interstate data exchange: A battle worth fighting?. Birth Defects Research Part A: Clinical and Molecular Teratology, 79: 806–810. doi: 10.1002/bdra.20413
The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention.
- Issue published online: 7 NOV 2007
- Article first published online: 7 NOV 2007
- Manuscript Revised: 6 SEP 2007
- Manuscript Accepted: 6 SEP 2007
- Manuscript Received: 13 AUG 2007
- interstate data exchange;
- data exchange agreements;
- birth defects;
Regardless of where infants and children are delivered, diagnosed, or treated, an important aspect of population-based birth defects surveillance is ensuring the inclusion of children with birth defects in the catchment area. However, little is known as to how the lack of interstate birth defects data exchange affects program surveillance, monitoring, prevention, and referral activities. The study objectives were to determine the status of interstate birth defects data exchange agreements and to quantify statewide data on resident births occurring in nonresident states.
In 2004, surveys were distributed to all population-based birth defects programs in the United States to determine: 1) the types of interstate birth defects data exchange agreements that exist among birth defects programs, 2) perceived barriers in establishing exchange agreements, and 3) the extent to which out-of-state births affect a program's catchment area. The National Center for Health Statistics (NCHS) data for 2002 on live birth residency were used to determine the actual frequency of out-of-state live birth occurrence.
Of the 52 states and territories that were surveyed, 65% (n = 34) responded. Approximately 21% (n = 7) of those that responded had an interstate data exchange agreement that allowed sharing of birth defects data with another state or a facility within another state. Approximately 53% (n = 18) of responding states indicated plans to develop an interstate birth defects data exchange agreement with other states, hospitals, or both. The NCHS data showed that the actual percentage of resident out-of-state live births ranged from 0.16 to 11.51. NCHS data also reveal that 78% of states would be able to capture >75% of their out-of-state births by sharing data on out-of-state births with the three neighboring states ranking highest in terms of such occurrences.
Few states have interstate birth defects data exchange agreements, though all states have resident births occurring out of state. While suggestive, data beyond residency of live births are needed to quantify the degree to which the objectives of state-based birth defects programs are compromised. Resources exist to guide programs in establishing interstate data exchange agreements. Efforts to establish such agreements with only a few neighboring states could be a large step toward improving birth defects surveillance on a state, regional, and national level. Birth Defects Research (Part A) 79:806–810, 2007. © 2007 Wiley-Liss, Inc.