LEGISLATIVE BUDGET BOARD Austin, Texas FISCAL NOTE, 87TH LEGISLATIVE REGULAR SESSION April 20, 2021 TO: Honorable Stephanie Klick, Chair, House Committee on Public Health FROM: Jerry McGinty, Director, Legislative Budget Board IN RE: HB3673 by Johnson, Jarvis (Relating to the establishment of a sickle cell disease registry.), As Introduced Estimated Two-year Net Impact to General Revenue Related Funds for HB3673, As Introduced : a negative impact of ($1,973,497) through the biennium ending August 31, 2023. The bill would make no appropriation but could provide the legal basis for an appropriation of funds to implement the provisions of the bill. General Revenue-Related Funds, Five- Year Impact: Fiscal Year Probable Net Positive/(Negative) Impact toGeneral Revenue Related Funds2022($1,362,893)2023($610,604)2024($611,308)2025($612,032)2026($612,780)All Funds, Five-Year Impact: Fiscal Year Probable Savings/(Cost) fromGeneral Revenue Fund1 Change in Number of State Employees from FY 20212022($1,362,893)4.02023($610,604)4.02024($611,308)4.02025($612,032)4.02026($612,780)4.0 Fiscal AnalysisThe bill would require the Department of State Health Services (DSHS) to establish and maintain a registry of individuals diagnosed with sickle cell disease. Health care facilities would be required to provide data regarding individuals who have been diagnosed with sickle cell disease to DSHS and the Health and Human Services Commission (HHSC) would be required to develop guidelines by rule related to the registry. The bill would require DSHS to publish an annual report on information in the registry and DSHS would be authorized to publish other reports in cooperation with other sickle cell disease reporting organizations and research institutions.
LEGISLATIVE BUDGET BOARD
Austin, Texas
FISCAL NOTE, 87TH LEGISLATIVE REGULAR SESSION
April 20, 2021
TO: Honorable Stephanie Klick, Chair, House Committee on Public Health FROM: Jerry McGinty, Director, Legislative Budget Board IN RE: HB3673 by Johnson, Jarvis (Relating to the establishment of a sickle cell disease registry.), As Introduced
TO: Honorable Stephanie Klick, Chair, House Committee on Public Health
FROM: Jerry McGinty, Director, Legislative Budget Board
IN RE: HB3673 by Johnson, Jarvis (Relating to the establishment of a sickle cell disease registry.), As Introduced
Honorable Stephanie Klick, Chair, House Committee on Public Health
Honorable Stephanie Klick, Chair, House Committee on Public Health
Jerry McGinty, Director, Legislative Budget Board
Jerry McGinty, Director, Legislative Budget Board
HB3673 by Johnson, Jarvis (Relating to the establishment of a sickle cell disease registry.), As Introduced
HB3673 by Johnson, Jarvis (Relating to the establishment of a sickle cell disease registry.), As Introduced
Estimated Two-year Net Impact to General Revenue Related Funds for HB3673, As Introduced : a negative impact of ($1,973,497) through the biennium ending August 31, 2023. The bill would make no appropriation but could provide the legal basis for an appropriation of funds to implement the provisions of the bill.
Estimated Two-year Net Impact to General Revenue Related Funds for HB3673, As Introduced : a negative impact of ($1,973,497) through the biennium ending August 31, 2023. The bill would make no appropriation but could provide the legal basis for an appropriation of funds to implement the provisions of the bill.
The bill would make no appropriation but could provide the legal basis for an appropriation of funds to implement the provisions of the bill.
General Revenue-Related Funds, Five- Year Impact:
2022 ($1,362,893)
2023 ($610,604)
2024 ($611,308)
2025 ($612,032)
2026 ($612,780)
All Funds, Five-Year Impact:
2022 ($1,362,893) 4.0
2023 ($610,604) 4.0
2024 ($611,308) 4.0
2025 ($612,032) 4.0
2026 ($612,780) 4.0
Fiscal Analysis
The bill would require the Department of State Health Services (DSHS) to establish and maintain a registry of individuals diagnosed with sickle cell disease. Health care facilities would be required to provide data regarding individuals who have been diagnosed with sickle cell disease to DSHS and the Health and Human Services Commission (HHSC) would be required to develop guidelines by rule related to the registry. The bill would require DSHS to publish an annual report on information in the registry and DSHS would be authorized to publish other reports in cooperation with other sickle cell disease reporting organizations and research institutions.
Methodology
The analysis assumes DSHS would require 4.0 additional full-time equivalents (FTEs) to establish and maintain the registry. This includes an epidemiologist to perform data analysis and reporting, an information specialist to prepare and disseminate reports and training, a research specialist to collect data and respond to data requests, and a program specialist to oversee the program and serve as a subject matter expert.
Technology
The analysis assumes DSHS would have $0.2 million in costs related to Data Center Services each fiscal year for servers, storage, security, and other needs for the database. It is assumed that there would also be costs for Technology Solution Services (TSS) development of $0.7 million in fiscal year 2022. DSHS would also be required to pay related Department of Information Resources (DIR) fees, which are estimated to be $0.1 million in fiscal year 2022. It is assumed that DSHS would work with the Health and Human Services Commission (HHSC) on project oversight and that HHSC could absorb the related costs. Including technology costs related to 4.0 additional FTEs, total technology costs are estimated to be $1.0 million in fiscal year 2022 and $0.2 million in subsequent fiscal years.
Local Government Impact
No significant fiscal implication to units of local government is anticipated.
Source Agencies: b > td > 529 Hlth & Human Svcs Comm, 537 State Health Services
529 Hlth & Human Svcs Comm, 537 State Health Services
LBB Staff: b > td > JMc, AKI, JLI, NDA
JMc, AKI, JLI, NDA