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A BILL TO BE ENTITLED
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AN ACT
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relating to the reimbursement of prescription drugs under Medicaid |
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and the child health plan program. |
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BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: |
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SECTION 1. Section 533.005(a), Government Code, is amended |
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to read as follows: |
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(a) A contract between a managed care organization and the |
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commission for the organization to provide health care services to |
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recipients must contain: |
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(1) procedures to ensure accountability to the state |
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for the provision of health care services, including procedures for |
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financial reporting, quality assurance, utilization review, and |
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assurance of contract and subcontract compliance; |
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(2) capitation rates that ensure the cost-effective |
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provision of quality health care; |
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(3) a requirement that the managed care organization |
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provide ready access to a person who assists recipients in |
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resolving issues relating to enrollment, plan administration, |
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education and training, access to services, and grievance |
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procedures; |
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(4) a requirement that the managed care organization |
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provide ready access to a person who assists providers in resolving |
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issues relating to payment, plan administration, education and |
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training, and grievance procedures; |
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(5) a requirement that the managed care organization |
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provide information and referral about the availability of |
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educational, social, and other community services that could |
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benefit a recipient; |
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(6) procedures for recipient outreach and education; |
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(7) a requirement that the managed care organization |
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make payment to a physician or provider for health care services |
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rendered to a recipient under a managed care plan on any claim for |
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payment that is received with documentation reasonably necessary |
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for the managed care organization to process the claim: |
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(A) not later than: |
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(i) the 10th day after the date the claim is |
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received if the claim relates to services provided by a nursing |
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facility, intermediate care facility, or group home; |
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(ii) the 30th day after the date the claim |
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is received if the claim relates to the provision of long-term |
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services and supports not subject to Subparagraph (i); and |
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(iii) the 45th day after the date the claim |
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is received if the claim is not subject to Subparagraph (i) or (ii); |
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or |
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(B) within a period, not to exceed 60 days, |
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specified by a written agreement between the physician or provider |
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and the managed care organization; |
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(7-a) a requirement that the managed care organization |
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demonstrate to the commission that the organization pays claims |
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described by Subdivision (7)(A)(ii) on average not later than the |
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21st day after the date the claim is received by the organization; |
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(8) a requirement that the commission, on the date of a |
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recipient's enrollment in a managed care plan issued by the managed |
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care organization, inform the organization of the recipient's |
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Medicaid certification date; |
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(9) a requirement that the managed care organization |
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comply with Section 533.006 as a condition of contract retention |
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and renewal; |
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(10) a requirement that the managed care organization |
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provide the information required by Section 533.012 and otherwise |
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comply and cooperate with the commission's office of inspector |
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general and the office of the attorney general; |
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(11) a requirement that the managed care |
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organization's usages of out-of-network providers or groups of |
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out-of-network providers may not exceed limits for those usages |
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relating to total inpatient admissions, total outpatient services, |
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and emergency room admissions determined by the commission; |
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(12) if the commission finds that a managed care |
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organization has violated Subdivision (11), a requirement that the |
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managed care organization reimburse an out-of-network provider for |
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health care services at a rate that is equal to the allowable rate |
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for those services, as determined under Sections 32.028 and |
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32.0281, Human Resources Code; |
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(13) a requirement that, notwithstanding any other |
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law, including Sections 843.312 and 1301.052, Insurance Code, the |
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organization: |
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(A) use advanced practice registered nurses and |
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physician assistants in addition to physicians as primary care |
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providers to increase the availability of primary care providers in |
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the organization's provider network; and |
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(B) treat advanced practice registered nurses |
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and physician assistants in the same manner as primary care |
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physicians with regard to: |
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(i) selection and assignment as primary |
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care providers; |
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(ii) inclusion as primary care providers in |
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the organization's provider network; and |
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(iii) inclusion as primary care providers |
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in any provider network directory maintained by the organization; |
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(14) a requirement that the managed care organization |
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reimburse a federally qualified health center or rural health |
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clinic for health care services provided to a recipient outside of |
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regular business hours, including on a weekend day or holiday, at a |
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rate that is equal to the allowable rate for those services as |
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determined under Section 32.028, Human Resources Code, if the |
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recipient does not have a referral from the recipient's primary |
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care physician; |
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(15) a requirement that the managed care organization |
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develop, implement, and maintain a system for tracking and |
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resolving all provider appeals related to claims payment, including |
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a process that will require: |
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(A) a tracking mechanism to document the status |
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and final disposition of each provider's claims payment appeal; |
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(B) the contracting with physicians who are not |
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network providers and who are of the same or related specialty as |
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the appealing physician to resolve claims disputes related to |
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denial on the basis of medical necessity that remain unresolved |
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subsequent to a provider appeal; |
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(C) the determination of the physician resolving |
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the dispute to be binding on the managed care organization and |
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provider; and |
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(D) the managed care organization to allow a |
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provider with a claim that has not been paid before the time |
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prescribed by Subdivision (7)(A)(ii) to initiate an appeal of that |
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claim; |
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(16) a requirement that a medical director who is |
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authorized to make medical necessity determinations is available to |
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the region where the managed care organization provides health care |
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services; |
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(17) a requirement that the managed care organization |
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ensure that a medical director and patient care coordinators and |
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provider and recipient support services personnel are located in |
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the South Texas service region, if the managed care organization |
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provides a managed care plan in that region; |
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(18) a requirement that the managed care organization |
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provide special programs and materials for recipients with limited |
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English proficiency or low literacy skills; |
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(19) a requirement that the managed care organization |
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develop and establish a process for responding to provider appeals |
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in the region where the organization provides health care services; |
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(20) a requirement that the managed care organization: |
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(A) develop and submit to the commission, before |
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the organization begins to provide health care services to |
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recipients, a comprehensive plan that describes how the |
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organization's provider network complies with the provider access |
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standards established under Section 533.0061; |
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(B) as a condition of contract retention and |
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renewal: |
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(i) continue to comply with the provider |
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access standards established under Section 533.0061; and |
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(ii) make substantial efforts, as |
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determined by the commission, to mitigate or remedy any |
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noncompliance with the provider access standards established under |
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Section 533.0061; |
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(C) pay liquidated damages for each failure, as |
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determined by the commission, to comply with the provider access |
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standards established under Section 533.0061 in amounts that are |
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reasonably related to the noncompliance; and |
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(D) regularly, as determined by the commission, |
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submit to the commission and make available to the public a report |
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containing data on the sufficiency of the organization's provider |
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network with regard to providing the care and services described |
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under Section 533.0061(a) and specific data with respect to access |
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to primary care, specialty care, long-term services and supports, |
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nursing services, and therapy services on the average length of |
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time between: |
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(i) the date a provider requests prior |
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authorization for the care or service and the date the organization |
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approves or denies the request; and |
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(ii) the date the organization approves a |
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request for prior authorization for the care or service and the date |
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the care or service is initiated; |
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(21) a requirement that the managed care organization |
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demonstrate to the commission, before the organization begins to |
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provide health care services to recipients, that, subject to the |
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provider access standards established under Section 533.0061: |
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(A) the organization's provider network has the |
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capacity to serve the number of recipients expected to enroll in a |
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managed care plan offered by the organization; |
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(B) the organization's provider network |
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includes: |
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(i) a sufficient number of primary care |
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providers; |
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(ii) a sufficient variety of provider |
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types; |
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(iii) a sufficient number of providers of |
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long-term services and supports and specialty pediatric care |
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providers of home and community-based services; and |
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(iv) providers located throughout the |
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region where the organization will provide health care services; |
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and |
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(C) health care services will be accessible to |
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recipients through the organization's provider network to a |
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comparable extent that health care services would be available to |
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recipients under a fee-for-service or primary care case management |
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model of Medicaid managed care; |
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(22) a requirement that the managed care organization |
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develop a monitoring program for measuring the quality of the |
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health care services provided by the organization's provider |
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network that: |
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(A) incorporates the National Committee for |
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Quality Assurance's Healthcare Effectiveness Data and Information |
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Set (HEDIS) measures; |
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(B) focuses on measuring outcomes; and |
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(C) includes the collection and analysis of |
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clinical data relating to prenatal care, preventive care, mental |
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health care, and the treatment of acute and chronic health |
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conditions and substance abuse; |
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(23) subject to Subsection (a-1), a requirement that |
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the managed care organization develop, implement, and maintain an |
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outpatient pharmacy benefit plan for its enrolled recipients: |
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(A) that exclusively employs the vendor drug |
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program formulary and preserves the state's ability to reduce |
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waste, fraud, and abuse under Medicaid; |
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(B) that adheres to the applicable preferred drug |
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list adopted by the commission under Section 531.072; |
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(C) that includes the prior authorization |
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procedures and requirements prescribed by or implemented under |
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Sections 531.073(b), (c), and (g) for the vendor drug program; |
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(D) for purposes of which the managed care |
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organization: |
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(i) may not negotiate or collect rebates |
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associated with pharmacy products on the vendor drug program |
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formulary; and |
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(ii) may not receive drug rebate or pricing |
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information that is confidential under Section 531.071; |
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(E) that complies with the prohibition under |
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Section 531.089; |
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(F) under which the managed care organization may |
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not prohibit, limit, or interfere with a recipient's selection of a |
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pharmacy or pharmacist of the recipient's choice for the provision |
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of pharmaceutical services under the plan through the imposition of |
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different copayments; |
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(G) that allows the managed care organization or |
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any subcontracted pharmacy benefit manager to contract with a |
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pharmacist or pharmacy providers separately for specialty pharmacy |
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services, except that: |
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(i) the managed care organization and |
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pharmacy benefit manager are prohibited from allowing exclusive |
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contracts with a specialty pharmacy owned wholly or partly by the |
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pharmacy benefit manager responsible for the administration of the |
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pharmacy benefit program; and |
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(ii) the managed care organization and |
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pharmacy benefit manager must adopt policies and procedures for |
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reclassifying prescription drugs from retail to specialty drugs, |
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and those policies and procedures must be consistent with rules |
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adopted by the executive commissioner and include notice to network |
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pharmacy providers from the managed care organization; |
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(H) under which the managed care organization may |
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not prevent a pharmacy or pharmacist from participating as a |
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provider if the pharmacy or pharmacist agrees to comply with the |
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financial terms and conditions of the contract as well as other |
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reasonable administrative and professional terms and conditions of |
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the contract; |
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(I) under which the managed care organization may |
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include mail-order pharmacies in its networks, but may not require |
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enrolled recipients to use those pharmacies, and may not charge an |
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enrolled recipient who opts to use this service a fee, including |
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postage and handling fees; |
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(J) under which the managed care organization or |
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pharmacy benefit manager, as applicable, must pay claims in |
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accordance with Section 843.339, Insurance Code; and |
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(K) under which the managed care organization or |
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pharmacy benefit manager, as applicable: |
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(i) must comply with Section 533.00514 as a |
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condition of contract retention and renewal [to place a drug on a
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maximum allowable cost list, must ensure that:
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[(a)
the drug is listed as "A" or "B"
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rated in the most recent version of the United States Food and Drug
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Administration's Approved Drug Products with Therapeutic
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Equivalence Evaluations, also known as the Orange Book, has an "NR"
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or "NA" rating or a similar rating by a nationally recognized
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reference; and
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[(b)
the drug is generally available
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for purchase by pharmacies in the state from national or regional
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wholesalers and is not obsolete]; |
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(ii) must [provide to a network pharmacy
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provider, at the time a contract is entered into or renewed with the
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network pharmacy provider, the sources used to determine the
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maximum allowable cost
pricing for the maximum allowable cost list
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specific to that provider;
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[(iii) must] review and update drug |
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reimbursement [maximum allowable cost] price information at least |
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once every seven days to reflect any modification of [maximum
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allowable cost] pricing under the vendor drug program; |
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(iii) [(iv)
must, in formulating the
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maximum allowable cost price for a drug, use only the price of the
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drug and drugs listed as therapeutically equivalent in the most
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recent version of the United States Food and Drug Administration's
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Approved Drug Products with Therapeutic Equivalence Evaluations,
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also known as the Orange Book;
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[(v)
must establish a process for
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eliminating products from the maximum allowable cost list or
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modifying maximum allowable cost prices in a timely manner to
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remain consistent with pricing changes and product availability in
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the marketplace;
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[(vi)] must: |
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(a) provide a procedure under which a |
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network pharmacy provider may challenge the reimbursement [a listed
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maximum allowable cost] price for a drug; |
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(b) respond to a challenge not later |
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than the 15th day after the date the challenge is made; |
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(c) if the challenge is successful, |
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make an adjustment in the drug price effective on the date the |
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challenge is resolved, and make the adjustment applicable to all |
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similarly situated network pharmacy providers, as determined by the |
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managed care organization or pharmacy benefit manager, as |
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appropriate; |
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(d) if the challenge is denied, |
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provide the reason for the denial; and |
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(e) report to the commission every 90 |
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days the total number of challenges that were made and denied in the |
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preceding 90-day period for each [maximum allowable cost list] drug |
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for which a challenge was denied during the period; and |
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(iv) [(vii)
must notify the commission not
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later than the 21st day after implementing a practice of using a
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maximum allowable cost list for drugs dispensed at retail but not by
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mail; and
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[(viii)] must provide a process for each of |
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its network pharmacy providers to readily access the drug |
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reimbursement price [maximum allowable cost] list specific to that |
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provider; |
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(24) a requirement that the managed care organization |
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and any entity with which the managed care organization contracts |
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for the performance of services under a managed care plan disclose, |
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at no cost, to the commission and, on request, the office of the |
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attorney general all discounts, incentives, rebates, fees, free |
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goods, bundling arrangements, and other agreements affecting the |
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net cost of goods or services provided under the plan; |
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(25) a requirement that the managed care organization |
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not implement significant, nonnegotiated, across-the-board |
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provider reimbursement rate reductions unless: |
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(A) subject to Subsection (a-3), the |
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organization has the prior approval of the commission to make the |
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reductions [reduction]; or |
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(B) the rate reductions are based on changes to |
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the Medicaid fee schedule or cost containment initiatives |
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implemented by the commission; and |
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(26) a requirement that the managed care organization |
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make initial and subsequent primary care provider assignments and |
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changes. |
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SECTION 2. Subchapter A, Chapter 533, Government Code, is |
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amended by adding Section 533.00514 to read as follows: |
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Sec. 533.00514. REIMBURSEMENT METHODOLOGY FOR PRESCRIPTION |
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DRUGS. (a) In accordance with rules adopted by the executive |
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commissioner, a managed care organization that contracts with the |
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commission under this chapter or a pharmacy benefit manager |
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administering a pharmacy benefit program on behalf of the managed |
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care organization shall reimburse a pharmacy or pharmacist, |
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including a Texas retail pharmacy or a Texas specialty pharmacy, |
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that: |
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(1) dispenses a prescribed prescription drug, other |
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than a drug obtained under Section 340B, Public Health Service Act |
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(42 U.S.C. Section 256b), to a recipient for not less than the |
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lesser of: |
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(A) the reimbursement amount for the drug under |
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the vendor drug program, including a dispensing fee that is not less |
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than the dispensing fee for the drug under the vendor drug program; |
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or |
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(B) the amount claimed by the pharmacy or |
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pharmacist, including the gross amount due or the usual and |
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customary charge to the public for the drug; or |
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(2) dispenses a prescribed prescription drug obtained |
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at a discounted price under Section 340B, Public Health Service Act |
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(42 U.S.C. Section 256b) to a recipient for not less than the |
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reimbursement amount for the drug under the vendor drug program, |
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including a dispensing fee that is not less than the dispensing fee |
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for the drug under the vendor drug program. |
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(b) The methodology adopted by rule by the executive |
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commissioner to determine Texas pharmacies' actual acquisition |
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cost (AAC) for purposes of the vendor drug program must be |
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consistent with the actual prices Texas pharmacies pay to acquire |
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prescription drugs marketed or sold by a specific manufacturer and |
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must be based on the National Average Drug Acquisition Cost |
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published by the Centers for Medicare and Medicaid Services or |
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another publication approved by the executive commissioner. |
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(c) The executive commissioner shall develop a process for |
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the periodic study of Texas retail pharmacies' actual acquisition |
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cost (AAC) for prescription drugs, Texas specialty pharmacies' |
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actual acquisition cost (AAC) for prescription drugs, retail |
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professional dispensing costs, and specialty pharmacy professional |
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dispensing costs and publish the results of each study on the |
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commission's Internet website. |
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(d) The dispensing fees adopted by the executive |
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commissioner for purposes of: |
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(1) Subsection (a)(1) must be based on, as |
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appropriate: |
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(A) Texas retail pharmacies' professional |
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dispensing costs for retail prescription drugs; or |
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(B) Texas specialty pharmacies' professional |
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dispensing costs for specialty prescription drugs; or |
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(2) Subsection (a)(2) must be based on Texas |
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pharmacies' professional dispensing costs for those drugs. |
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(e) Not less frequently than once every two years, the |
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commission shall conduct a study of Texas pharmacies' dispensing |
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costs for retail prescription drugs, specialty prescription drugs, |
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and drugs obtained under Section 340B, Public Health Service Act |
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(42 U.S.C. Section 256b). Based on the results of the study, the |
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executive commissioner shall adjust the minimum amount of the |
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retail professional dispensing fee and specialty pharmacy |
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professional dispensing fee under Subsection (a)(1) and the |
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dispensing fee for drugs obtained under Section 340B, Public Health |
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Service Act (42 U.S.C. Section 256b). |
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SECTION 3. Subchapter D, Chapter 62, Health and Safety |
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Code, is amended by adding Section 62.160 to read as follows: |
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Sec. 62.160. REIMBURSEMENT METHODOLOGY FOR PRESCRIPTION |
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DRUGS. A managed care organization providing pharmacy benefits |
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under the child health plan program or a pharmacy benefit manager |
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administering a pharmacy benefit program on behalf of the managed |
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care organization shall comply with Section 533.00514, Government |
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Code. |
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SECTION 4. Section 533.005(a-2), Government Code, is |
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repealed. |
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SECTION 5. If before implementing any provision of this Act |
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a state agency determines that a waiver or authorization from a |
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federal agency is necessary for implementation of that provision, |
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the agency affected by the provision shall request the waiver or |
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authorization and may delay implementing that provision until the |
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waiver or authorization is granted. |
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SECTION 6. This Act takes effect March 1, 2020. |