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    v1.0.30
    OpenPayerPolicy UpdatesPharmacy & Specialty DrugsOklahoma Medicaid Plavix Effient Coverage | OpenPa…
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    CurrentOklahoma Health Care AuthorityPolicy N/A

    Current Prior Authorization of Plavix and Effient

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    This policy governs Oklahoma Medicaid prior authorization requirements for Plavix (clopidogrel) and Effient (prasugrel), including covered cardiovascular indications, exclusions, approval durations, and continuation requirements. The first 90 days of therapy do not require prior authorization.

    Policy Summary
    PayerOklahoma Health Care Authority
    PolicyCurrent Prior Authorization of Plavix and Effient
    Policy CodePolicy N/A
    Change TypeNo material clinical or coverage changes
    Effective DateN/A
    Next Review DateN/A
    Key ActionAfter the initial 90-day period, submit authorization requests using the applicable drug-specific diagnostic criteria.
    SourceLink
    POLICY UPDATE CHANGES

    No material clinical or coverage changes in this revision.

    90 daysInitial therapy without prior authorization
    1 yearStandard approval length
    15 monthsContinuation supporting information required after
    2,623Prior authorization requests processed in FY 2011

    OpenPayer is powered by Trek Health's payer performance platform. Trek continuously ingests, validates, and normalizes Transparency in Coverage data alongside payer policies and other commercial payer data to create a structured payer intelligence foundation. OpenPayer uses this foundation to deliver personalized search results, dynamically generated policy pages, and tailored policy monitoring based on each user's payers, specialties, billing codes, and areas of interest. The same intelligence powers broader payer performance workflows, including reimbursement benchmarking, contract evaluation, payer negotiations, and financial decision-making.

    Drug-Specific Coverage Criteria

    Plavix covered indications

    Plavix therapy will be approved when the member has at least one of the following diagnoses or clinical situations.

    ONE of the following

    • Member has a recent stroke.
    • Member has a recent myocardial infarction.
    • Member has established peripheral artery disease.
    • Member has acute coronary syndrome consisting of unstable angina or non-Q-wave myocardial infarction.
    • Member has undergone percutaneous coronary intervention with stent placement.
    • Member has a transient ischemic attack, CVA, or stroke.

    Effient covered indications

    Effient therapy will be approved when the member meets an approved diagnostic criterion.

    ONE of the following

    • Member has unstable angina or non-ST-segment elevated myocardial infarction and is to be managed with primary or delayed percutaneous coronary intervention (PCI).
    • Member has ST-segment elevated myocardial infarction and is to be managed with primary or delayed percutaneous coronary intervention (PCI).

    Effient exclusion criteria

    Effient is not approved when any listed exclusion applies.

    ANY of the following exclusions

    • Member is undergoing coronary artery bypass graft surgery.
    • Member has a history of transient ischemic attack or stroke.

    Effient age-related review

    Members older than 75 years generally require supporting information for Effient approval.

    All of the following

    • Member is older than 75 years.
    • Supporting information is submitted.

    Plavix 300 mg criteria

    Plavix 300 mg is approved only for the specified acute coronary syndrome or myocardial infarction diagnosis and limited dosing.

    All of the following

    • Member has an FDA-approved diagnosis of non-ST-segment elevated acute coronary syndrome or ST-segment elevated acute myocardial infarction.
    • Use is limited to one 300 mg dose.one 300 mg dose

    Effient is not approved for members undergoing coronary artery bypass graft surgery or for members with a history of transient ischemic attack or stroke.

    Prior Authorization and Documentation Actions

    Note

    Initial 90-day exemption

    The first 90 days of therapy with Plavix or Effient do not require prior authorization.

    Prior Authorization

    Prior authorization after 90 days

    After the initial 90-day period, obtain authorization based on the applicable drug-specific diagnostic criteria. Standard approval is for 1 year.

    Billing Rule

    Plavix 300 mg single dose

    Plavix 300 mg is approved for only one dose when used for an FDA-approved diagnosis of non-ST-segment elevated acute coronary syndrome or ST-segment elevated acute myocardial infarction.

    • Approval is limited to one 300 mg dose.
    Documentation Required

    Support continuation after 15 months

    Provide supporting information for continuation of Plavix or Effient after 15 months of therapy.

    Documentation Required

    Document Effient use in older members

    Supporting information is required for Effient approval in members older than 75 years.

    Denial Risk

    Effient exclusion conditions

    Effient will not be approved for members undergoing coronary artery bypass graft surgery or members with a history of transient ischemic attack or stroke.

    • Coronary artery bypass graft surgery
    • History of transient ischemic attack or stroke
    Denial Risk

    Effient approval for members older than 75

    Members older than 75 years generally will not be approved for Effient without supporting information. Submit the required supporting information with the approval request.

    Therapy Overview

    Plavix (clopidogrel) and Effient (prasugrel) are antiplatelet therapies used in conditions such as acute coronary syndromes, myocardial infarction, cerebrovascular disease, peripheral artery disease, and selected coronary interventions. The policy includes broader covered indications for Plavix, while Effient coverage is focused on acute coronary syndrome or myocardial infarction managed with percutaneous coronary intervention (PCI), with additional safety exclusions.

    Initial Therapy Requirements

    Plavix initial therapy

    Plavix therapy is approved when at least one approved diagnosis is present.

    ONE of the following

    • Member has a recent stroke.
    • Member has a recent myocardial infarction.
    • Member has established peripheral artery disease.
    • Member has acute coronary syndrome consisting of unstable angina or non-Q-wave myocardial infarction.
    • Member has undergone percutaneous coronary intervention with stent placement.
    • Member has a transient ischemic attack, CVA, or stroke.

    Effient initial therapy

    Effient therapy is approved when an approved PCI-managed diagnosis is present.

    ONE of the following

    • Member has unstable angina or non-ST-segment elevated myocardial infarction managed with primary or delayed percutaneous coronary intervention (PCI).
    • Member has ST-segment elevated myocardial infarction managed with primary or delayed percutaneous coronary intervention (PCI).

    Continuation Therapy Requirements

    Continuation therapy

    After 15 months of therapy, prescribers should provide supporting information for continuation.

    All of the following

    • Member is continuing Plavix or Effient after 15 months of therapy.
    • Prescriber provides supporting information.

    Dose and Quantity Limits

    Quantity Limits
    MedicationPlavix 300 mg
    Approved diagnosisFDA-approved diagnosis of non-ST-segment elevated acute coronary syndrome or ST-segment elevated acute myocardial infarction
    Quantity limitOne dose of 300 mg
    Policy Summary
    PayerOklahoma Health Care Authority
    PolicyCurrent Prior Authorization of Plavix and Effient
    Policy CodePolicy N/A
    Change TypeNo material clinical or coverage changes
    Effective DateN/A
    Next Review DateN/A
    Key ActionAfter the initial 90-day period, submit authorization requests using the applicable drug-specific diagnostic criteria.
    SourceLink
    On This Page
    Drug-Specific Coverage CriteriaPrior Authorization and Documentation ActionsTherapy OverviewInitial Therapy RequirementsContinuation Therapy RequirementsDose and Quantity Limits