§ 68-29-139 — Clinical laboratory testing advisory board

(a) As used in this section: (1) "Accountable care organization" or "ACO" means the term as defined by Section 3022 of the federal Patient Protection and Affordable Care Act (Pub. L. No. 111-148), as amended; and (2) "Clinical laboratory testing" means any test as defined under this section, or otherwise subject to Section 353 of the Public Health Service Act ( 42 U.S.C. § 263a ). (b) An accountable care organization that provides diagnosis and treatment for patients in this state shall establish a clinical laboratory testing advisory board to consider and recommend guidelines or protocols for clinical laboratory testing. (c) (1) The clinical laboratory testing advisory board may make recommendations to the ACO governance board for guidelines or protocol adoption for clinical laboratory testing used for diagnostic purposes, disease management, and pathologist consultation on episodes of care. (2) The ACO clinical laboratory testing advisory board may recommend guidelines or protocols for clinical laboratory testing to ensure appropriate use of testing. (3) The composition of an ACO clinical laboratory testing advisory board shall be determined by the ACO; provided, however, that the ACO clinical laboratory testing advisory board shall have at least one (1) physician who is a clinical laboratory director, as defined by Section 353 of the Public Health Service Act ( 42 U.S.C. § 263a ). (d) Notwithstanding the requirement of this section to establish a clinical laboratory testing advisory board, nothing contained in this section shall be construed to require an ACO governance board to adopt a clinical laboratory testing guideline or protocol recommended by its clinical laboratory testing advisory board.

Legislative History

Added by 2016 Tenn. Acts, ch. 913, s 1, eff. 7/1/2016.