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  81R3506 ALB-D
 
  By: Deuell S.B. No. 946
 
 
 
A BILL TO BE ENTITLED
 
AN ACT
  relating to the Medicaid Drug Utilization Review Program and
  prescription drug use under the Medicaid program.
         BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:
         SECTION 1.  Subchapter B, Chapter 531, Government Code, is
  amended by adding Sections 531.0691, 531.0692, and 531.0693 to read
  as follows:
         Sec. 531.0691.  MEDICAID DRUG UTILIZATION REVIEW PROGRAM:  
  DRUG USE REVIEWS AND ANNUAL REPORT. (a) In this section:
               (1)  "Medicaid Drug Utilization Review Program" means
  the program operated by the vendor drug program to improve the
  quality of pharmaceutical care under the Medicaid program.
               (2)  "Prospective drug use review" means the review of
  a patient's drug therapy and prescription drug order or medication
  order before dispensing or distributing a drug to the patient.
               (3)  "Retrospective drug use review" means the review
  of prescription drug claims data to identify patterns of
  prescribing.
         (b)  The commission shall provide for an increase in the
  number and types of retrospective drug use reviews performed each
  year under the Medicaid Drug Utilization Review Program, in
  comparison to the number and types of reviews performed in the state
  fiscal year ending August 31, 2009.
         (c)  In determining the number and types of drug use reviews
  to be performed, the commission shall:
               (1)  allow for the repeat of retrospective drug use
  reviews that address ongoing drug therapy problems and that, in
  previous years, improved client outcomes and reduced Medicaid
  spending;
               (2)  consider implementing disease-specific
  retrospective drug use reviews that address ongoing drug therapy
  problems in this state and that reduced Medicaid prescription drug
  use expenditures in other states; and
               (3)  regularly examine Medicaid prescription drug
  claims data to identify occurrences of potential drug therapy
  problems that may be addressed by repeating successful
  retrospective drug use reviews performed in this state and other
  states.
         (d)  In addition to any other information required by federal
  law, the commission shall include the following information in the
  annual report regarding the Medicaid Drug Utilization Review
  Program:
               (1)  a detailed description of the program's
  activities; and
               (2)  estimates of cost savings anticipated to result
  from the program's performance of prospective and retrospective
  drug use reviews.
         (e)  The cost-saving estimates for prospective drug use
  reviews under Subsection (d) must include savings attributed to
  drug use reviews performed through the vendor drug program's
  electronic claims processing system and clinical edits screened
  through the prior authorization system implemented under Section
  531.073.
         (f)  The commission shall post the annual report regarding
  the Medicaid Drug Utilization Review Program on the commission's
  website.
         Sec. 531.0692.  MEDICAID DRUG UTILIZATION REVIEW BOARD:
  CONFLICTS OF INTEREST.  (a) A member of the board of the Medicaid
  Drug Utilization Review Program may not have a contractual
  relationship, ownership interest, or other conflict of interest
  with a pharmaceutical manufacturer or labeler or with an entity
  engaged by the commission to assist in the administration of the
  Medicaid Drug Utilization Review Program.
         (b)  The executive commissioner may implement this section
  by adopting rules that identify prohibited relationships and
  conflicts or requiring the board to develop a conflict-of-interest
  policy that applies to the board.
         Sec. 531.0693.  PRESCRIPTION DRUG USE AND EXPENDITURE
  PATTERNS. (a) The commission shall monitor and analyze
  prescription drug use and expenditure patterns in the Medicaid
  program.  The commission shall identify the therapeutic
  prescription drug classes and individual prescription drugs that
  are most often prescribed to patients or that represent the
  greatest expenditures.  The analysis must consider the number of
  claims, the total cost of paid claims, and the average cost per paid
  claim after any prescription drug rebates.
         (b)  The commission shall post the data determined by the
  commission under Subsection (a) on the commission's website and
  update the information on a quarterly basis.
         SECTION 2.  If before implementing any provision of this Act
  a state agency determines that a waiver or authorization from a
  federal agency is necessary for implementation of that provision,
  the agency affected by the provision shall request the waiver or
  authorization and may delay implementing that provision until the
  waiver or authorization is granted.
         SECTION 3.  This Act takes effect September 1, 2009.