Kentucky 2025 Regular Session

Kentucky Senate Bill SB27

Introduced
1/7/25  
Refer
1/7/25  
Refer
1/9/25  
Report Pass
2/26/25  
Engrossed
3/4/25  
Refer
3/4/25  
Refer
3/11/25  
Report Pass
3/12/25  
Refer
3/14/25  
Enrolled
3/14/25  
Enrolled
3/14/25  
Chaptered
3/25/25  

Caption

AN ACT relating to health care.

Impact

The bill's enactment will have significant implications for state laws related to health care reporting and patient data management. By designating Parkinson's disease as a reportable condition, the legislation is expected to enhance surveillance and lead to better health outcomes through more informed public health strategies. Additionally, the introduction of a formal registry is anticipated to facilitate research opportunities, allowing data sharing between states and researchers while maintaining patient confidentiality.

Summary

SB27 establishes the Kentucky Parkinson's Disease Research Registry, aimed at systematically collecting data on the incidence and prevalence of Parkinson's disease and related conditions in the state. This registry will operate under the guidance of the Cabinet for Health and Family Services, which is tasked with creating and maintaining a comprehensive database of Parkinson's disease cases. The legislation mandates participation from movement disorder centers and health care providers, ensuring they periodically report diagnoses and other relevant data to the registry.

Sentiment

There is a generally positive sentiment surrounding SB27, especially among health professionals, researchers, and advocacy groups invested in Parkinson's disease awareness and treatment. They recognize the registry as a vital tool for understanding the disease's effects on the population and the need for targeted health resources. However, there are reservations among some stakeholders regarding the data collection processes and concerns about patients' privacy.

Contention

Notable points of contention include the procedures for obtaining patient consent for reporting, as some stakeholders worry about potential hurdles that may arise from patients opting out of data sharing. There may also be debates regarding the adequacy of funding and resources needed for the necessary administration of the registry and compliance with reporting requirements. Overall, while the bill is seen as a positive step towards addressing Parkinson's disease in Kentucky, ensuring that it remains patient-centric and well-funded is crucial to its success.

Companion Bills

No companion bills found.

Previously Filed As

KY HB387

AN ACT relating to reorganization.

KY SB74

AN ACT relating to public health.

KY HB829

AN ACT relating to medicinal cannabis and declaring an emergency.

KY SB337

AN ACT relating to medicinal cannabis and declaring an emergency.

KY SB367

AN ACT relating to health care to provide for an all-payer claims database and making an appropriation therefor.

KY SB38

AN ACT relating to health care to provide for an all-payer claims database and making an appropriation therefor.

KY SB275

AN ACT relating to health care to provide for an all-payer claims database and making an appropriation therefor.

KY HB10

AN ACT relating to maternal and child health.

KY SB261

AN ACT relating to state employee health insurance.

KY HB428

AN ACT relating to reproductive privacy.

Similar Bills

WV HB4276

WVU to create a Parkinson’s disease registry

NJ A3693

Establishes State Parkinson's disease registry.

NJ S2339

Establishes State Parkinson's disease registry.

HI SB447

Relating To Parkinson's Disease Research.

HI SB447

Relating To Parkinson's Disease Research.

HI SB1049

Relating To Parkinson's Disease Research.

HI HB952

Relating To Parkinson's Disease Research.

MO SB553

Establishes the "Missouri Parkinson's Disease Registry Act"