Senate Bill 1701 aims to enhance awareness and treatment options for uterine fibroids in Tennessee by establishing a comprehensive electronic database and educational resources. The bill mandates the Department of Health to create and maintain a database by January 1, 2027, which will include demographic information of women diagnosed with uterine fibroids and the treatments they receive. This database will be used solely for research purposes related to uterine fibroids and must comply with state and federal laws to protect patient confidentiality.

Additionally, the bill requires the Department of Health, in collaboration with the Tennessee Medical Association, to publish educational materials on its website by the same deadline. These resources will focus on raising public awareness about uterine fibroids, particularly highlighting the demographics of women at higher risk and outlining various treatment options, including non-hysterectomy alternatives. The act is set to take effect upon becoming law, emphasizing the importance of addressing this health issue for women in Tennessee.