HLS 22RS-1922 REENGROSSED
2022 Regular Session
HOUSE BILL NO. 968
BY REPRESENTATIVES PHELPS, ADAMS, BOYD, ROBBY CARTER, CORMIER,
DUPLESSIS, FISHER, GLOVER, GREEN, HUGHES, JEFFERSON, JENKINS,
JORDAN, LAFLEUR, LANDRY, LYONS, NEWELL, PIERRE, SELDERS,
WHITE, AND WILLARD
HEALTH/SICKLE CELL ANEM: Establishes a state sickle cell disease registry
1 AN ACT
2To amend and reenact R.S. 36:259(B)(13) and R.S. 44:4.1(B)(26) and to enact Part XIII of
3 Chapter 5-B of Title 40 of the Louisiana Revised Statutes of 1950, to be comprised
4 of R.S. 40:1125.1, 1125.11 through 1125.16, 1125.21, and 1125.31 through 1125.33,
5 relative to sickle cell disease; to provide for the establishment of a state sickle cell
6 disease registry; to provide for the purpose of the registry; to provide for duties of
7 the Louisiana Department of Health with respect to operation of the registry; to
8 authorize access to data in the registry; to provide for a public records exception; to
9 require promulgation of administrative rules with respect to the registry; to provide
10 for the redesignation and reorganization of certain laws pertaining to sickle cell
11 disease; to provide for a short title; and to provide for related matters.
12Be it enacted by the Legislature of Louisiana:
13 Section 1. R.S. 36:259(B)(13) is hereby amended and reenacted to read as follows:
14 §259. Transfer of agencies and functions to Louisiana Department of Health
15 * * *
16 B. The following agencies, as defined in R.S. 36:3, are placed within the
17 Louisiana Department of Health and shall perform and exercise their powers, duties,
18 functions, and responsibilities as otherwise provided by law:
19 * * *
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1 (13) Louisiana Sickle Cell Commission (R.S. 40:2018.3 R.S. 40:1125.1).
2 * * *
3 Section 2. Part XIII of Chapter 5-B of Title 40 of the Louisiana Revised Statutes of
41950, comprised of R.S. 40:1125.1, 1125.11 through 1125.16, 1125.21, and 1125.31 through
51125.33, is hereby enacted to read as follows:
6 PART XIII. SICKLE CELL DISEASE
7 SUBPART A. LOUISIANA SICKLE CELL COMMISSION
8 §1125.1. Louisiana Sickle Cell Commission
9 [Section redesignated from R.S. 40:2018.3]
10 SUBPART B. SICKLE CELL DISEASE REGISTRY
11 §1125.11. Definitions
12 As used in this Subpart, the following terms have the meanings ascribed to
13 them in this Section:
14 (1) "Department" means the Louisiana Department of Health.
15 (2) "Registry" means the sickle cell disease registry established by the
16 provisions of this Subpart.
17 §1125.12. Sickle cell disease registry; purpose
18 A. The department shall establish and maintain, in accordance with the
19 provisions of this Subpart, a registry of individuals diagnosed with sickle cell disease
20 which shall be known as the "Skylar-Cooper Database". The purpose of the registry
21 shall be to function as a single repository of accurate, complete records to aid in the
22 cure and treatment of sickle cell disease in this state.
23 B. The registry shall encompass, without limitation, all of the following:
24 (1) A record of individuals in this state who have been diagnosed with sickle
25 cell disease.
26 (2) All data and other information associated with individuals who have been
27 diagnosed with sickle cell disease that the secretary of the department deems
28 necessary and appropriate for inclusion in the registry.
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1 §1125.13. Healthcare facilities; reporting of data
2 Upon making a diagnosis of sickle cell disease, a healthcare provider shall
3 provide to the department data regarding the individual who has been diagnosed with
4 the disease. The form and manner of the data shall be prescribed by the department
5 by rule duly promulgated in accordance with the Administrative Procedure Act.
6 §1125.14. Use of registry data
7 A. The secretary of the department shall facilitate access to data in the
8 registry as provided for in rule.
9 B. Notwithstanding any other provision of law to the contrary, the
10 department or its agent may access medical and vital records in the custody of
11 physicians, hospitals, clinics, other healthcare providers, and the office of public
12 health in order that it may conduct sickle cell disease studies. The data contained in
13 the registry as well as all such medical and vital records obtained by the department
14 or its agent in accordance with the provisions of this Subsection, as well as the
15 results of any sickle cell disease study, shall be confidential and shall not be
16 available for subpoena, nor shall such information be disclosed, discoverable, or
17 compelled to be produced in any civil, criminal, administrative, or other proceeding
18 nor shall such records be deemed admissible as evidence in any civil, criminal,
19 administrative, or other tribunal or court for any reason. Nothing in this Subsection
20 shall prohibit the publishing by the department of statistical compilations relating to
21 sickle cell disease which do not identify individual cases or individual physicians,
22 hospitals, clinics, or other healthcare providers.
23 §1125.15. Healthcare needs of persons with sickle cell disease; legislative findings;
24 use of registry data in care coordination
25 The legislature hereby finds that sickle cell patients who need care for sickle
26 cell disease and other health conditions often face lengthy wait times for that care,
27 and that these wait times contribute to poor health outcomes and excess morbidity
28 and mortality among populations that are impacted by sickle cell disease. The
29 legislature further finds that sickle cell patients may face greater barriers in accessing
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1 the necessary care for their disease after reaching the age of majority or aging out of
2 health coverage furnished through the Louisiana Children's Health Insurance
3 Program. Therefore, the secretary of the department shall take such actions as are
4 necessary to support the facilitation of care coordination for sickle cell patients,
5 assist in reducing the wait times to access healthcare services, and assist in
6 promoting continuity of care for young people who age out of Louisiana Children's
7 Health Insurance Program coverage.
8 §1125.16. Administrative rules
9 A. The department shall promulgate in accordance with the Administrative
10 Procedure Act all such rules as are necessary to implement the provisions of this
11 Subpart.
12 B. The rules required by this Section shall include but not be limited to the
13 following:
14 (1) Data elements to be included in the registry.
15 (2) Guidelines and procedures for obtaining from healthcare providers
16 information regarding individuals diagnosed with sickle cell disease.
17 (3) Standards for ensuring that the registry is developed and operated in a
18 manner that comports with all applicable requirements of the Health Insurance
19 Portability and Accountability Act of 1996 (Pub. L. 104-191); regulations adopted
20 pursuant to that Act including but not limited to the HIPAA Privacy Rule, 45 CFR
21 Part 164; and other applicable laws and regulations governing disclosure of health
22 information.
23 SUBPART C. PATIENT NAVIGATOR PROGRAM
24 §1125.21. Sickle cell patient navigator program
25 [Section redesignated from R.S. 40:1081.8]
26 SUBPART D. CLINICS AND LOCAL PROGRAMS
27 §1125.31. Sickle cell anemia; clinic established
28 [Section redesignated from R.S. 40:1081.5]
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1 §1125.32. Sickle cell anemia; clinics established statewide
2 [Section redesignated from R.S. 40:1081.6]
3 §1125.33. Sickle cell anemia; local programs
4 [Section redesignated from R.S. 40:1081.7]
5 Section 3. R.S. 44:4.1(B)(26) is hereby amended and reenacted to read as follows:
6 §4.1. Exceptions
7 * * *
8 B. The legislature further recognizes that there exist exceptions, exemptions,
9 and limitations to the laws pertaining to public records throughout the revised
10 statutes and codes of this state. Therefore, the following exceptions, exemptions, and
11 limitations are hereby continued in effect by incorporation into this Chapter by
12 citation:
13 * * *
14 (26) R.S. 40:3.1, 31.14, 31.27, 39.1, 41, 73, 95, 96, 526, 528, 973.1, 978.2.1,
15 1007, 1061.21, 1079.18, 1081.10, 1105.6, 1105.8, 1125.14, 1133.8, 1168.3, 1171.4,
16 1203.4, 1231.4, 1379.1.1(D), 1379.3, 2009.8, 2009.14, 2010.5, 2017.9, 2018, 2018.5,
17 2019, 2020, 2106, 2109.1, 2138, 2175.7(B)(1), 2532, 2845.1
18 * * *
19 Section 4.(A) The Louisiana State Law Institute is hereby authorized and directed
20to redesignate R.S. 40:2018.3 as R.S. 40:1125.1 within Part XIII of Chapter 5-B of Title 40
21of the Louisiana Revised Statutes of 1950, as enacted by Section 2 of this Act. The
22redesignated section shall comprise Subpart A, entitled "Louisiana Sickle Cell Commission",
23of Part XIII of Chapter 5-B of Title 40 of the Louisiana Revised Statutes of 1950.
24 (B) The Louisiana State Law Institute is hereby authorized and directed to
25redesignate R.S. 40:1081.8 as R.S. 40:1125.21 within Part XIII of Chapter 5-B of Title 40
26of the Louisiana Revised Statutes of 1950, as enacted by Section 2 of this Act. The
27redesignated section shall comprise Subpart C, entitled "Patient Navigator Program", of Part
28XIII of Chapter 5-B of Title 40 of the Louisiana Revised Statutes of 1950.
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1 (C) The Louisiana State Law Institute is hereby authorized and directed to
2redesignate R.S. 40:1081.5, 1081.6, and 1081.7, respectively, as R.S. 40:1125.31, 1125.32,
3and 1125.33 within Part XIII of Chapter 5-B of Title 40 of the Louisiana Revised Statutes
4of 1950, as enacted by Section 2 of this Act. The redesignated sections shall comprise
5Subpart D, entitled "Clinics and Local Programs", of Part XIII of Chapter 5-B of Title 40 of
6the Louisiana Revised Statutes of 1950.
7 (D) The Louisiana State Law Institute is hereby authorized and directed to revise the
8citations appearing within R.S. 40:1081.7(C) and 2018.3(D)(5) to reflect the redesignation
9of the laws cited therein, and to make any other changes and technical corrections
10throughout the statutes and codes as may be necessary to reflect the redesignation of laws
11effected by this Section.
12 Section 5. This Act shall be known and may be cited as the "Remington Skylar
13Watts and Betty Cooper Phelps Act".
DIGEST
The digest printed below was prepared by House Legislative Services. It constitutes no part
of the legislative instrument. The keyword, one-liner, abstract, and digest do not constitute
part of the law or proof or indicia of legislative intent. [R.S. 1:13(B) and 24:177(E)]
HB 968 Reengrossed 2022 Regular Session Phelps
Abstract: Requires the La. Dept. of Health to establish and maintain a sickle cell disease
registry to be known as the "Skylar-Cooper Database" which shall function as a
repository of accurate, complete records to aid in the cure and treatment of sickle cell
disease.
Proposed law requires the La. Dept. of Health (LDH) to establish and maintain a registry of
individuals diagnosed with sickle cell disease which shall be known as the "Skylar-Cooper
Database". Provides that the purpose of the registry shall be to function as a single
repository of accurate, complete records to aid in the cure and treatment of sickle cell disease
in this state.
Proposed law requires that the sickle cell disease registry encompass, without limitation, all
of the following:
(1)A record of individuals in this state who have been diagnosed with sickle cell
disease.
(2)All data and other information associated with individuals who have been diagnosed
with sickle cell disease that the secretary of LDH deems necessary and appropriate
for inclusion in the registry.
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Proposed law requires that upon making a diagnosis of sickle cell disease, a healthcare
provider shall provide to LDH data regarding the individual who has been diagnosed with
the disease.
Proposed law requires LDH to facilitate access to data in the registry through administrative
rules. Stipulates that registry data as well as medical and vital records obtained by LDH or
its agent in accordance with proposed law, as well as the results of any sickle cell disease
study, shall be confidential and shall not be available for subpoena, nor shall such
information be disclosed, discoverable, or compelled to be produced in any civil, criminal,
administrative, or other proceeding nor shall such records be deemed admissible as evidence
in any civil, criminal, administrative, or other tribunal or court for any reason.
Proposed law requires the secretary of LDH to take such actions as are necessary to support
the facilitation of care coordination for sickle cell patients, assist in reducing wait times to
access healthcare services, and assist in promoting continuity of care for young people who
age out of La. Children's Health Insurance Program coverage.
Proposed law requires the secretary of LDH to promulgate all such rules as are necessary to
implement the provisions of proposed law. Provides that these rules shall include but not
be limited to the following:
(1)Data elements to be included in the registry.
(2)Guidelines and procedures for obtaining from healthcare providers information
regarding individuals diagnosed with sickle cell disease.
(3)Standards for ensuring that the registry is developed and operated in a manner that
comports with all applicable requirements of the Health Insurance Portability and
Accountability Act (HIPAA), the HIPAA Privacy Rule, and other applicable laws
and regulations governing disclosure of health information.
Proposed law establishes an exception to present law relative to public records, R.S. 44:1 et
seq., exempting data in the registry from disclosure pursuant to present law.
Proposed law consolidates certain sections of present law relative to sickle cell disease (R.S.
40:1081.5 through 1081.8 and 2018.3) within the new part of law established by proposed
law which pertains exclusively to sickle cell disease.
Proposed law provides that proposed law shall be known as the "Remington Skylar Watts
and Betty Cooper Phelps Act".
(Amends R.S. 36:259(B)(13) and R.S. 44:4.1(B)(26); Adds R.S. 40:1125.1, 1125.11-
1125.16, 1125.21, and 1125.31-1125.33)
Summary of Amendments Adopted by House
The Committee Amendments Proposed by House Committee on Health and Welfare to
the original bill:
1. Delete proposed law requiring healthcare facilities to provide to LDH data
regarding individuals who have been diagnosed with sickle cell disease; add in
lieu thereof a requirement that upon making a diagnosis of sickle cell disease, a
healthcare provider shall provide to LDH data regarding the individual who has
been diagnosed with the disease.
2. Delete proposed law authorizing access to data in the sickle cell disease registry
by certain specifically identified entities; add in lieu thereof a requirement that
LDH facilitate access to data in the registry through administrative rules.
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3. Authorize LDH or its agent to access medical and vital records in the custody of
physicians, hospitals, clinics, other healthcare providers, and the office of public
health in order that it may conduct sickle cell disease studies.
4. Stipulate that the data contained in the sickle cell disease registry as well as
medical and vital records obtained by LDH or its agent in accordance with
proposed law, as well as the results of any sickle cell disease study, shall be
confidential and shall not be available for subpoena, nor shall such information
be disclosed, discoverable, or compelled to be produced in any civil, criminal,
administrative, or other proceeding nor shall such records be deemed admissible
as evidence in any civil, criminal, administrative, or other tribunal or court for
any reason.
5. Establish an exception to present law relative to public records, R.S. 44:1 et seq.,
exempting data in the sickle cell disease registry from disclosure pursuant to that
law.
6. Make technical changes.
The House Floor Amendments to the engrossed bill:
1. Delete a definition from proposed law for consistency with changes effected
through committee amendments to the original bill.
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