HOUSE OF REPRESENTATIVES STAFF ANALYSIS
BILL #: CS/HB 499 Congenital Cytomegalovirus Screenings
SPONSOR(S): Healthcare Regulation Subcommittee, Melo
TIED BILLS: IDEN./SIM. BILLS: SB 168
REFERENCE ACTION ANALYST STAFF DIRECTOR or
BUDGET/POLICY CHIEF
1) Healthcare Regulation Subcommittee 18 Y, 0 N, As CS Osborne McElroy
2) Health Care Appropriations Subcommittee 15 Y, 0 N Aderibigbe Clark
3) Health & Human Services Committee 19 Y, 0 N Osborne Calamas
SUMMARY ANALYSIS
Cytomegalovirus (CMV) is a common virus that infects people of all ages. Over half of adults are infected with
CMV by age 40, and approximately one of every 200 babies is born with congenital CMV (CCMV). Some
infants with CCMV infection have health problems that are apparent at birth or that develop later during infancy
or childhood. About one in five babies with CCMV have long-term health problems, including hearing loss.
Florida’s Newborn Screening Program (NSP), operated by the Department of Health (DOH), screens all
newborns for metabolic, hereditary, and congenital disorders known to result in significant impairment of health
or intellect, including hearing loss. In the event that a newborn screen has an abnormal result, the baby’s
health care provider, or a nurse or specialist from NSP’s Follow-up Program provides follow-up services and
referrals for the child and his or her family.
Current law requires all newborns be screened for hearing loss at birth, unless such screening is objected to by
the newborn’s parent or guardian; newborns who fail the hearing screening must also be screened for CCMV.
In 2021, 8,500 newborns did not pass their hearing screening, of which, 300 were diagnosed with hearing loss.
CS/HB 499 expands the population which must undergo mandatory CCMV testing beyond the current
population of infants who fail the required newborn hearing screening to include infants admitted to a neonatal
intensive care unit within 21 days of birth for specified reasons, and newborns who are transferred to another
facility for a higher level of care.
The bill also requires that children diagnosed with a congenital cytomegalovirus infection, with or without
hearing loss, be referred to the Children's Medical Services Early Intervention Program and be deemed eligible
for a baseline evaluation and any medically necessary follow-up reevaluations and monitoring.
The bill has an insignificant fiscal impact on the Department of Health that can be absorbed within existing
resources. The bill has no fiscal impact on local government.
The bill provides an effective date of July 1, 2024.
This docum ent does not reflect the intent or official position of the bill sponsor or House of Representatives .
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DATE: 2/22/2024
FULL ANALYSIS
I. SUBSTANTIVE ANALYSIS
A. EFFECT OF PROPOSED CHANGES:
Background
Florida Newborn Screening Program
The Legislature created the Florida Newborn Screening Program (NSP) within the Department of
Health (DOH), to promote the screening of all newborns for metabolic, hereditary, and congenital
disorders known to result in significant impairment of health or intellect. 1 The NSP also promotes the
identification and screening of all newborns in the state and their families for environmental risk factors
such as low income, poor education, maternal and family stress, emotional instability, substance
abuse, and other high-risk conditions associated with increased risk of infant mortality and morbidity to
provide early intervention, remediation, and prevention services. 2
The NSP involves coordination across several entities, including the Bureau of Public Health
Laboratories Newborn Screening Laboratory in Jacksonville (state laboratory), DOH Children’s Medical
Services (CMS) Newborn Screening Follow-up Program in Tallahassee, and referral centers, birthing
centers, and physicians throughout the state.3 Health care providers in hospitals, birthing centers,
perinatal centers, county health departments, and school health programs provide screening as part of
the multilevel NSP screening process.4 This includes a risk assessment for prenatal women, and risk
factor analysis and screening for postnatal women and newborns as well as laboratory screening for
select disorders in newborns.5 The NSP attempts to screen all newborns for hearing impairment and to
identify, diagnose, and manage newborns at risk for select disorders that, without detection and
treatment, can lead to permanent developmental and physical damage or death.6 The NSP is intended
to screen all prenatal women and newborns, however, parents and guardians may choose to decline
the screening.7
Health care providers perform non-laboratory NSP screening, such as hearing and risk factor analysis,
and report the results to the Office of Vital Statistics. If necessary, health care providers refer patients
to the appropriate health, education, and social services. 8 Health care providers in hospitals and
birthing centers perform specimen collection for laboratory NSP screening by collecting a few drops of
blood from the newborn’s heel on a standardized specimen collection card. 9 The specimen card is then
sent to the state laboratory for testing and the results are released to the newborn’s health care
provider. In the event that a newborn screen has an abnormal result, the baby’s health care provider, or
a nurse or specialist from NSP’s Follow-up Program provides follow-up services and referrals for the
child and his or her family.10
To administer the NSP, DOH is authorized to charge and collect a fee not to exceed $15 per live birth
occurring in a hospital or birth center.11 DOH must calculate the annual assessment for each hospital
and birth center, and then quarterly generate and mail each hospital and birth center a statement of the
1 S. 383.14(1), F.S.
2 Id.
3
S. 383.14, F.S.
4 Id.
5 Id.
6 Florida Department of Health, Florida Newb orn Screening Guidelines. Available at https://floridanewbornscreening.com/wp-
content/uploads/NBS-Protocols-2022-FINAL.pdf (last visited January 26, 2024).
7 S. 383.14(4), F.S.; Rule 64C-7.008, F.A.C.; The health care provider must attempt to get a written statement of objection to be placed
in the medical record.
8 Id.
9 Florida Newborn Screening, What is Newb orn Screening? Available at https://floridanewbornscreening.com/parents/what-is-newborn-
screening/ (last visited January 26, 2024). See also, Florida Newborn Screening, Specimen Collection Card,
http://floridanewbornscreening.com/wp-content/uploads/Order-Form.png (last visited January 26, 2024).
10 Id.
11 S. 383.145(3)(g)1., F.S.
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amount due.12 DOH bills hospitals and birth centers quarterly using vital statistics data to determine the
amount to be billed.13 DOH is authorized to bill third-party payers for the NSP tests and bills insurers
directly for the cost of the screening.14 DOH does not bill families that do not have insurance
coverage.15
The Legislature established the Florida Genetics and Newborn Screening Advisory Council to advise
DOH on disorders to be included in the NSP panel of screened disorders and the procedures for
collecting and transmitting specimens.16 Florida’s NSP currently screens for 58 conditions, 55 of which
are screened through the collection of blood spots. Screening of the other three conditions—hearing
screening, critical congenital heart defect (CCHD) or pulse oximetry, and congenital cytomegalovirus
(CCMV) targeted screening—are completed at the birthing facility through point of care (POC) testing.17
Congenital Cytomegalovirus
Cytomegalovirus (CMV) is a common virus for people of all ages; however, a healthy person’s immune
system usually keeps the virus from causing illness. 18 In the United States, nearly one in three children
are infected with CMV by age five. Over half of adults have been infected with CMV by age 40. Once
CMV is in a person’s body, it stays there for life and can reactivate. A person can also be re-infected
with a different strain of the virus. Most people with CMV infection have no symptoms and aren’t aware
that they have been infected.19
CMV that is present in a newborn at birth is known as congenital CMV (CCMV). Congenital CMV
occurs when the virus is present in a pregnant woman’s blood and crosses the placenta to the fetus.
This can happen if a woman is infected with CMV for the first time while she is pregnant, or is infected
with CMV again during pregnancy.20 In the most severe cases, a CMV infection can cause a woman to
lose her pregnancy.
Some infants with CCMV infection have health problems that are apparent at birth or that develop later
during infancy or childhood. CCMV is the most common infectious cause of birth defects in the United
States; approximately one in 200 infants are born with CCMV.21 Infants with CCMV infection may have
signs at birth, which include:22
Rash;
Jaundice (yellowing of the skin or whites of the eyes);
Microcephaly (small head);
Low birth weight;
Hepatosplenomegaly (enlarged liver and spleen);
Seizures; and
Retinitis (damaged eye retina).
Infants with signs of CCMV infection at birth may have long-term health problems, such as:23
Hearing loss;
12 Id.
13 S. 383.145(3)(g), F.S.
14 S. 383.145(3)(h), F.S.
15
S. 383.14, F.S.
16 S. 383.14(5), F.S.
17 Department of Health, Agency Analysis of HB 499 (2024). On file with the Health & Human Services Committee.
18 Centers for Disease Control and Prevention. Ab out Cytomegalovirus (CMV). Available at https://www.cdc.gov/cmv/overview.html (last
visited January 26, 2024).
19 Id.
20 Centers for Disease Control and Prevention. Bab ies Born with Congenital Cytomegalovirus (CMV). Available at
https://www.cdc.gov/cmv/congenital-infection.html, (last visited January 26, 2024).
21 Centers for Disease Control and Prevention. CMV Fact Sheet for Healthcare Providers. Available at https://www.cdc.gov/cmv/fact-
sheets/healthcare-providers.html#:~:text=Cytomegalovirus%20(CMV)%20is%20the%20most,Hearing%20loss (last visited January 26,
2024).
22 Supra, note 20.
23 Id.
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Developmental and motor delay;
Vision loss;
Microcephaly (small head); and
Seizures.
One out of five infants with CCMV will have symptoms or long-term health problems, such as hearing
loss. Approximately 15% of infants with CCMV will not have signs at birth, but will later develop hearing
loss.24 Infants may have hearing loss that may or may not be detected by newborn hearing test.
Hearing loss may be present at birth or may develop later, even in infants who passed the newborn
hearing test.25 Hearing loss may progress from mild to severe during the first two years of life, which is
a critical period for language learning. Over time, hearing loss can affect a child’s ability to develop
communication, language, and social skills.26
CCMV infection is diagnosed by detection of CCMV DNA in the urine, saliva (preferred specimens), or
blood, within three weeks after birth. Infection cannot be diagnosed using tests that detect antibodies to
CCMV. CCMV infection cannot be diagnosed using samples collected more than three weeks after
birth because testing after this time cannot distinguish between congenital infection and an infection
acquired during or after delivery.27 Infants who show signs of CCMV disease can be treated with
medicines called antivirals. Antivirals may decrease the severity of hearing loss. Infants who get treated
with antivirals should be closely monitored by their doctor for possible side effects.28
CCMV and the Newborn Screening Program
Section 383.145, F.S., requires a newborn hearing screening for all newborns in hospitals before
discharge. Before a newborn is discharged from a hospital or other state-licensed birthing facility, and
unless objected to by the parent or legal guardian, the newborn must be screened for the detection of
hearing loss to prevent the consequences of unidentified disorders. 29
In 2022, the Legislature enacted a law which established additional testing requirements for hearing
loss in newborns.30 Under current law, if a newborn fails the hearing screening, the hospital or birthing
facility is required to administer an FDA-approved test, or other diagnostically equivalent test, on the
newborn to screen for CCMV. The CCMV test must be administered before 21 days of age or before
discharge, whichever occurs earlier.31
For births occurring in a non-hospital setting, specifically a licensed birth center or private home, the
facility or attending health care provider is responsible for providing a referral to an audiologist, a
hospital, or other newborn hearing screening provider within 7 days after the birth or discharge from the
facility.32 All screenings must be conducted by a licensed audiologist, a licensed physician, or
appropriately supervised individual who has completed documented training specifically for newborn
hearing screening.33 When ordered by the treating physician, screening of a newborn's hearing must
include auditory brainstem responses, or evoked otoacoustic emissions, or appropriate technology as
approved by the United States Food and Drug Administration (FDA). 34
24 Supra, note 21.
25 Id.
26 Centers for Disease Control and Prevention. CMV Fact Sheet for Healthcare Providers. Available at https://www.cdc.gov/cmv/fact-
sheets/healthcare-providers.html#:~:text=Cytomegalovirus%20(CMV)%20is%20the%20most,Hearing%20loss (last visited January 26,
2024).
27 Centers for Disease Control and Prevention. Ab out Cytomegalovirus (CMV). Available at https://www.cdc.gov/cmv/overview.html (last
visited January 26, 2024).
28 Centers for Disease Control and Prevention. Congenital CMV and Hearing Loss. Available at https://www.cdc.gov/cmv/hearing-
loss.html, (last visited January 26, 2024).
29 S. 383.145(3), F.S. If the screening is not completed before discharge due to scheduling or temporary staffing limitations, the
screening must be completed within 21 days after the birth.
30 Ch. 2022-25, Laws of Fla.
31 S. 383.145(3)(a), F.S.
32 S. 383.145(3)(d), F.S.
33 S. 383.145(3)(f), F.S.
34 S. 383.145(3)(i), F.S.
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If an infant born in a licensed birth center or private home fails the hearing screening, the infant’s
primary care provider must refer the infant for the administration of an FDA-approved test, or other
diagnostically equivalent test, on the newborn to screen for CCMV.35
A child who is diagnosed as having a permanent hearing impairment must be referred by the licensee
or individual who conducted the screening to the primary care physician for medical management,
treatment, and follow-up services.36 Any child from birth to 36 months of age who is diagnosed as
having a hearing impairment that requires ongoing special hearing services must be referred to the
Early Steps Program for further screening and services.37
Annually, approximately 8,500 newborns fail the newborn hearing screening and are subsequently
tested for CCMV.38 In 2021, of the 8,500 newborns who did not pass their hearing screenings, 300
were diagnosed with hearing loss.39
Florida Early Steps Program
The Children's Medical Services Early Intervention Program, commonly known as Florida’s Early Steps
Program (Program), provides early intervention services to children ages birth to 36 months with
developmental delays and disabilities or who are at-risk for developmental delay based on a medical
condition.40 The Early Steps Program contracts with 15 Local Early Steps Programs to provide the
direct services infants, toddlers, and their families.41
A CCMV diagnosis is currently included on the Program’s list of at-risk conditions. Documentation of an
at-risk condition automatically makes a child eligible for at-risk enrollment, which includes the following
services: at-risk individualized family support plan support planning, service coordination,
developmental surveillance, and family support. If a developmental delay is suspected, an evaluation
can be completed to determine if the child’s delay meets the eligibility standard for the full scope of
Early Steps services. Approximately 120 infants with CCMV are referred to the Program annually. 42
Effect of the Bill
CS/HB 499 expands the population which must undergo mandatory CCMV testing beyond the current
population of infants who fail the required newborn hearing screening to include infants admitted to a
neonatal intensive care unit within 21 days of birth for any of the following