West Virginia 2022 Regular Session

West Virginia House Bill HB4276

Introduced
1/19/22  
Refer
1/19/22  
Engrossed
1/26/22  
Refer
1/27/22  
Refer
1/27/22  
Report Pass
2/7/22  
Enrolled
2/15/22  
Passed
2/23/22  

Caption

WVU to create a Parkinson’s disease registry

Impact

The bill considerably modifies the state’s approach to health data management by instituting a specialized registry. It provides legal backing for WVU to collect, maintain, and disseminate epidemiological data while ensuring strict confidentiality protocols to safeguard patient information. By establishing a central registry, the bill could facilitate better healthcare planning and resource allocation to address Parkinson's disease, which is increasingly prevalent in the aging population.

Summary

House Bill 4276 establishes a framework for the collection of data related to Parkinson's disease and related disorders in West Virginia. This legislation mandates the creation of a registry overseen by West Virginia University (WVU), which will compile data on the incidence of Parkinson's disease and related conditions. The bill aims to enhance understanding of these neurological disorders and their impact on the state’s population through systematic data collection and analysis.

Sentiment

The sentiment surrounding HB 4276 appears to be largely positive among health advocacy groups and researchers, who see value in systematic data collection as a means to improve patient care and treatment outcomes. Supporters argue that the registry will lead to improved awareness and research opportunities concerning Parkinson’s disease. However, there are concerns regarding patient consent and the ethical management of confidential data, which may invoke some skepticism from privacy advocates.

Contention

Notable points of contention include the balance between the need for valuable healthcare data and the rights of patients regarding their private health information. While the bill includes opt-out provisions for patients not wishing to participate in the registry, concerns remain about ensuring that patients are fully informed about their right to privacy. Additionally, the legislation allows for collaboration with out-of-state registries and health agencies, prompting discussions regarding the boundaries of data sharing and the robustness of confidentiality safeguards.

Companion Bills

No companion bills found.

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