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HB 2750

Missouri HouseIntroduced

Summary

HB 2750, which modifies provisions relating to testing performed by the department of health and senior services laboratories, was introduced in the House on Jan 6, 2026 by Rep. Bishop Davidson (R) with 1 co-sponsor. It was referred to Health and Mental Health, and last saw action on Jan 8, 2026: Referred: Health and Mental Health(H).


Record

Text

HB 2750 has 1 co-sponsor.

hb2750/introduced.txt
SECOND REGULAR SESSION
HOUSE BILL NO. 2750
103RD GENERAL ASSEMBLY
INTRODUCED BY REPRESENTATIVE DAVIDSON.
4026H.01I JOSEPH ENGLER, Chief Clerk
AN ACT
To repeal sections 191.317, 191.331, 191.332, and 191.333, RSMo, and to enact in lieu
thereof four new sections relating to testing performed by the department of health
and senior services laboratories.
Be it enacted by the General Assembly of the state of Missouri, as follows:
Section A. Sections 191.317, 191.331, 191.332, and 191.333, RSMo, are repealed
and four new sections enacted in lieu thereof, to be known as sections 191.317, 191.331,
191.332, and 191.333, to read as follows:
191.317. 1. All testing results and personal information obtained from any
individual, or from specimens from any individual, shall be held confidential and be
considered a confidential medical record, except for such information as the individual,
parent or guardian consents to be released; but the individual must first be fully informed of
the scope of the information [requests] requested to be released, of the risks, benefits and
purposes for such release, and of the identity of those to whom the information will be
released. Statistical data compiled without reference to the identity of any individual shall not
be declared confidential. Notwithstanding any other provision of law to the contrary, the
department may release the results of newborn screening tests to a child's health care
professional. The department shall destroy the results of newborn screening tests after
one year from the date the results were finalized.
2. The specimen shall be retained for [five years] one year after initial submission to
the department. After [five years] one year, the specimen shall be destroyed. [Unless
otherwise directed under this section, a biological specimen may be released for purposes of
EXPLANATION — Matter enclosed in bold-faced brackets [thus] in the above bill is not enacted and is
intended to be omitted from the law. Matter in bold-face type in the above bill is proposed language.
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anonymous scientific study. At the time of collection, the parent or legal guardian of the child
from whom a biological specimen was obtained may direct the department to:
(1) Return a biological specimen that remains after all screening tests have been
performed;
(2) Destroy a biological specimen in a scientifically acceptable manner after all
screening tests required under section 191.331 or rule promulgated thereunder have been
performed; or
(3) Store a biological specimen but not release the biological specimen for
anonymous scientific study.
3. A biological specimen released for anonymous study under this section shall not
contain information that may be used to determine the identity of the donor.]
191.331. 1. Every infant who is born in this state shall be tested for phenylketonuria
and such other metabolic or genetic diseases as are prescribed by the department if the parent
or guardian of the infant consented to such testing in the manner provided under
subsection 4 of this section. The test used by the department shall be dictated by accepted
medical practice and such tests shall be of the types approved by the department. All
newborn screening tests [required] for the diseases prescribed by the department shall be
performed by the department of health and senior services laboratories. The attending
physician, certified nurse midwife, public health facility, ambulatory surgical center or
hospital shall assure that appropriate specimens are collected and submitted to the department
of health and senior services laboratories.
2. All physicians, certified nurse midwives, public health nurses and administrators of
ambulatory surgical centers or hospitals shall report to the department all diagnosed cases of
phenylketonuria and other metabolic or genetic diseases as designated by the department.
The department shall prescribe and furnish all necessary reporting forms.
3. The department shall develop and institute educational programs concerning
phenylketonuria and other metabolic and genetic diseases and assist parents, physicians,
hospitals and public health nurses in the management and basic treatment of these diseases.
4. [The provisions of this section shall not apply if the parents of such child object to
the tests or examinations provided in this section on the grounds that such tests or
examinations conflict with their religious tenets and practices.] An infant shall not be tested
in accordance with the provisions of this section unless the parent or guardian of the
infant consented to such testing as described in this subsection. The following criteria
shall be required for any consent to be deemed valid:
(1) The consent shall be voluntary and informed and given freely and without
coercion;
(2) The consent shall be given in writing;
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(3) The parent or guardian giving consent shall have the capacity to understand
the risks and benefits of testing; and
(4) The consent shall be provided before the birth of the infant but not during
any active labor immediately preceding such birth.
5. [As provided in subsection 4 of this section, the parents of any child who fail to
have such test or examination administered after notice of the requirement for such test or
examination shall be required to document in writing such refusal.] All physicians, certified
nurse midwives, public health nurses and administrators of ambulatory surgical centers or
hospitals seeking the consent of the parent or guardian under subsection 4 of this section
shall provide to the [parents] parent or [guardians] guardian a written packet of educational
information developed and supplied by the department of health and senior services
describing the type of specimen, how it is obtained, the nature of diseases being screened, and
the consequences of treatment and nontreatment. [The attending physician, certified nurse
midwife, public health facility, ambulatory surgical center or hospital shall obtain the written
refusal and make such refusal part of the medical record of the infant.]
6. Notwithstanding the provisions of section 192.015 to the contrary, the department
may, by rule, annually determine and impose a reasonable fee for each newborn screening test
made in any of its laboratories. The department may collect the fee from any entity or
individual described in subsection 1 of this section in a form and manner established by the
department. Such fee shall be considered as a cost payable to such entity by a health care
third-party payer, including, but not limited to, a health insurer operating pursuant to chapter
376, a domestic health services corporation or health maintenance organization operating
pursuant to chapter 354, and a governmental or entitlement program operating pursuant to
state law. Such fee shall not be considered as part of the internal laboratory costs of the
persons and entities described in subsection 1 of this section by such health care third-party
payers. No individual shall be denied screening because of inability to pay. Such fees shall
be deposited in a separate account in the public health services fund created in section
192.900, and funds in such account shall be used for the support of the newborn screening
program and activities related to the screening, diagnosis, and treatment, including special
dietary products, of persons with metabolic and genetic diseases; and follow-up activities that
ensure that diagnostic evaluation, treatment and management is available and accessible once
an at-risk family is identified through initial screening; and for no other purpose. These
programs may include education in these areas and the development of new programs related
to these diseases.
7. Subject to appropriations provided for formula for the treatment of inherited
diseases of amino acids and organic acids, the department shall provide such formula to
persons with inherited diseases of amino acids and organic acids subject to the conditions
HB 2750 4
described in this subsection. State assistance pursuant to this subsection shall be available to
an applicant only after the applicant has shown that the applicant has exhausted all benefits
from third-party payers, including, but not limited to, health insurers, domestic health services
corporations, health maintenance organizations, Medicare, Medicaid and other government
assistance programs.
8. Assistance under subsection 7 of this section shall be provided to the following:
(1) Applicants ages birth to five years old meeting the qualifications under subsection
7 of this section;
(2) Applicants between the ages of six to eighteen meeting the qualifications under
subsection 7 of this section and whose family income is below three hundred percent of the
federal poverty level;
(3) Applicants between the ages of six to eighteen meeting the qualifications under
subsection 7 of this section and whose family income is at three hundred percent of the
federal poverty level or above. For these applicants, the department shall establish a sliding
scale of fees and monthly premiums to be paid in order to receive assistance under subsection
7 of this section; and
(4) Applicants age nineteen and above meeting the qualifications under subsection 7
of this section and who are eligible under an income-based means test established by the
department to determine eligibility for the assistance under subsection 7 of this section.
9. The department shall have authority over the use, retention, and disposal of
biological specimens and all related information collected in connection with newborn
screening tests conducted under subsection 1 of this section. The use of such specimens and
related information shall only be made for public health purposes and shall comply with all
applicable provisions of federal law. [The department may charge a reasonable fee for the use
of such specimens for public health research and preparing and supplying specimens for
research proposals approved by the department.]
191.332. 1. By January 1, 2002, the department of health and senior services shall,
subject to appropriations, expand the newborn screening [requirements] tests in section
191.331 to include potentially treatable or manageable disorders, which may include but are
not limited to cystic fibrosis, galactosemia, biotinidase deficiency, congenital adrenal
hyperplasia, maple syrup urine disease (MSUD) and other amino acid disorders, glucose-6-
phosphate dehydrogenase deficiency (G-6-PD), MCAD and other fatty acid oxidation
disorders, methylmalonic acidemia, propionic acidemia, isovaleric acidemia and glutaric
acidemia Type I.
2. By January 1, 2017, the department of health and senior services shall, subject to
appropriations, expand the newborn screening [requirements] tests in section 191.331 to
include severe combined immunodeficiency (SCID), also known as bubble boy disease. The
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department may increase the fee authorized under subsection 6 of section 191.331 to cover
any additional costs of the expanded newborn screening [requirements] tests under this
subsection.
3. By January 1, 2019, the department of health and senior services shall, subject to
appropriations, expand the newborn screening [requirements] tests in section 191.331 to
include spinal muscular atrophy (SMA) and Hunter syndrome (MPS II). The department may
increase the fee authorized under subsection 6 of section 191.331 to cover any additional
costs of the expanded newborn screening [requirements] tests under this subsection. To help
fund initial costs incurred by the state, the department shall apply for available newborn
screening grant funding specific to screening for spinal muscular atrophy and Hunter
syndrome. The department shall have discretion in accepting the terms of such grants.
4. The department of health and senior services may promulgate rules to implement
the provisions of this section. No rule or portion of a rule promulgated pursuant to the
authority of this section shall become effective unless it has been promulgated pursuant to
chapter 536.
191.333. 1. This section shall be known and may be cited as the "Brady Alan
Cunningham Newborn Screening Act".
2. By July 1, 2012, the department of health and senior services shall expand the
newborn screening [requirements] tests in section 191.331 to include the following lysosomal
storage diseases: Krabbe disease, Pompe disease, Gaucher disease, Niemann-Pick disease,
and Fabry disease. The department may by rule screen for additional lysosomal storage
disorders when the following occurs:
(1) The registration of the necessary reagents with the federal Food and Drug
Administration;
(2) The availability of the necessary reagents from the Centers for Disease Control
and Prevention;
(3) The availability of quality assurance testing methodology for such processes; and
(4) The acquisition and installment by the department of equipment necessary to
implement the expanded screening tests.
3. The department may promulgate rules to implement the provisions of this section.
Any rule or portion of a rule, as that term is defined in section 536.010, that is created under
the authority delegated in this section shall become effective only if it complies with and is
subject to all of the provisions of chapter 536 and, if applicable, section 536.028. This section
and chapter 536 are nonseverable and if any of the powers vested with the general assembly
pursuant to chapter 536 to review, to delay the effective date, or to disapprove and annul a
rule are subsequently held unconstitutional, then the grant of rulemaking authority and any
rule proposed or adopted after August 28, 2009, shall be invalid and void.
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4. The department may increase the fee authorized in subsection 6 of section 191.331
24 to cover the additional cost of the expanded newborn screening [test required in] tests under
25 this section.

Modifies provisions relating to testing performed by the department of health and senior services laboratories

Sponsors

Rep. Bishop Davidson (R) sponsors HB 2750, and 1 member has co-sponsored it.

Committees

HB 2750 went before 1 committee: Health and Mental Health.

Health and Mental Health
Health and Mental Health
Referred to · Jan 8, 2026 · 17 Bills

History

HB 2750 has taken 4 actions since Jan 6, 2026, the latest on Jan 8, 2026.

ChamberAction
Jan 8, 2026
House
Read Second Time (H)
Jan 8, 2026
House
Referred: Health and Mental Health(H)
Jan 7, 2026
House
Read First Time (H)
Jan 6, 2026
House
Prefiled (H)

Votes

HB 2750 has not gone to a roll call.


Source: house.mo.gov · legiscan.com