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Bill

HB 3655

Health; Oklahoma Blood Clot Registry Act of 2026; effective date.

2026 Regular Session Introduced by Preston Stinson

Oklahoma establishes statewide blood clot registry to track clotting disorder cases for public health surveillance and research purposes.

Second Reading referred to Rules
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Bill Summary · HB 3655

Legislative bill overview

HB 3655 establishes the Oklahoma Blood Clot Registry Act of 2026, which would create a statewide registry to track and monitor blood clot cases and related health outcomes. The bill appears designed to collect epidemiological data on venous thromboembolism (VTE) and other clotting disorders across Oklahoma's healthcare system.

Why is this important

Blood clots pose significant public health risks, causing conditions like deep vein thrombosis and pulmonary embolism that can be fatal if untreated. A comprehensive registry would help public health officials identify trends, risk factors, and potentially preventable cases, while also supporting research into prevention and treatment protocols.

Potential points of contention

  • Privacy and data security concerns: Registry systems collecting personal health information on blood clot diagnoses raise questions about patient privacy protections, data storage security, and potential misuse of sensitive medical records.
  • Healthcare provider compliance burden: Mandatory reporting requirements could impose administrative costs on hospitals and clinics, particularly smaller facilities with limited resources.
  • Scope and funding ambiguity: The bill's current description doesn't clarify which facilities must report, reporting thresholds, or how the registry will be funded and maintained long-term.

Compiled from official sources — confirm details with the bill’s official record.

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