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F I S C A L I M P A C T R E P O R T
SPONSOR Komadina
ORIGINAL DATE
LAST UPDATED
02/09/07
HB
SHORT TITLE Birth Defects Registry
SB 667
ANALYST Geisler
APPROPRIATION (dollars in thousands)
Appropriation
Recurring
or Non-Rec
Fund
Affected
FY07
FY08
$250.0
Recurring
General
(Parenthesis ( ) Indicate Expenditure Decreases)
SOURCES OF INFORMATION
LFC Files
Responses Received From
Department of Health (DOH)
SUMMARY
Synopsis of Bill
Senate Bill 667, for the Legislative Health and Human Services Committee, would appropriate
$250,000 from the general fund to the Public Health division of the Department of Health (DOH)
for the purposes of supporting a birth defects registry. Any unexpended funds remaining at the
end of FY08 shall revert to the general fund.
FISCAL IMPLICATIONS
DOH notes that the funding in SB 667 is not part of the Executive Budget Request.
DOH notes that in order to implement an effective birth defects registry, $150,000 of the funding
would be used for two FTEs to support data management and referral of identified children to
appropriate programs for follow up. The remaining $100,000 would be used for other costs as-
sociated with developing the registry. As this is a long term project, recurring funding may be
needed to sustain the registry.
pg_0002
Senate Bill 667 – Page
2
SIGNIFICANT ISSUES
Each year in New Mexico, approximately 600 infants (about 1 out of every 45 births) are born
with a major birth defect. Birth defects were the second leading cause of infant mortality in
New Mexico (New Mexico Selected Health Statistics Annual Report for 2004, NMDOH). Since
2000, birth defects have been a reportable condition in New Mexico. Babies born with birth de-
fects have a greater chance of illness and long term disability than babies without birth defects.
By identifying these children early in their life, we have the opportunity to assure that they re-
ceive the medical care and early intervention services to allow them to be productive adults and
fulfill their potential.
NM had a Birth Defects Registry between 1995 and 2005 that was federally funded by the Cen-
ter for Disease Control (CDC). The state’s proposal for continued support from CDC was ap-
proved but not funded in 2005. There is currently no state or other funding to support this activ-
ity. The goal of the birth defects registry is to 1) monitor the prevalence of birth defects in the
state, 2) provide data for the planning for services needed by these children and their families, 3)
assess the impact of screening and prevention activities, and 4) to link children to necessary ser-
vices such as case management for those that have complex medical needs and early intervention
services to support the child’s development.
GG/mt