HB1580: Parkinson's disease registry.
Legislative Summary
Parkinson's disease registry. Requires the Indiana University School of Medicine to collect data on the incidence of Parkinson's disease and establish a Parkinson's disease registry. Requires health care providers to report a diagnosis of Parkinson's disease and a related condition to the registry, and, if a patient agrees to the reporting, additional information concerning the medical treatment. Requires the health care provider to provide certain information to a patient diagnosed with Parkinson's disease or a related condition and to receive either permission or a denial to provide other information concerning the diagnosis and treatment. Requires that the information be confidential. Provides immunity to a person that provides information for the registry. Specifies persons that can obtain information from the registry.
Demographic Impact
Overall analysis of equity impact
Unlock Full Demographic Insights
Go beyond the overall score.
Gain a deeper understanding of this bill's potential impact across diverse communities, including detailed breakdowns by category and subgroup. Access to this granular analysis helps ensure equitable outcomes.
Enable full analysis features for your organization.
Contact Sales to Learn MoreOr email us directly at sales@legiequity.us.