relative to improving screening for and treatment of blood clots, or venous thromboembolism, and establishing a statewide venous thromboembolism registry.

SB 609 requires hospitals, ambulatory surgical centers, and emergency medical care centers to develop evidence-based screening and treatment plans for venous thromboembolism (VTE), including annual training for nonphysician staff. It mandates these facilities to report specific patient data - such as age, race, zip code, diagnosis method, and treatment - to a statewide VTE registry starting July 2027. The Department of Health must contract with a qualified nonprofit entity to maintain the registry, using nationally recognized data collection standards. The registry will track VTE incidence, outcomes, and treatment patterns to improve care systems and ensure compliance with national guidelines. This bill directly affects healthcare facilities and patients treated for blood clots, focusing on standardized screening and data-driven care improvements.