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    v1.0.31
    OpenPayerPolicy UpdatesPlastic/Reconstructive SurgeryKaiser Permanente Dermal Filler Coverage | OpenPay…
    Ask Trek AI about this page
    ModifiedKaiser PermanentePolicy N/A

    Dermal Fillers for Facial Lipoatrophy

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    Coverage of FDA-approved dermal filler injections for HIV- or HAART-associated facial lipodystrophy/lipoatrophy, subject to applicable plan benefits and coverage criteria.

    Policy Summary
    PayerKaiser Permanente
    PolicyDermal Fillers for Facial Lipoatrophy
    Policy CodePolicy N/A
    Change TypeModified
    Effective DateDecember 1, 2026
    Last ReviewMar 3, 2026
    Next Review DateN/A
    Key ActionSubmit dermal filler injection requests for clinical review with the required clinical documentation.
    SourceLink
    POLICY UPDATE CHANGES

    Effective December 1, 2026, coverage eligibility expands from Carruthers grades 3-4 to grades 2-4 facial lipodystrophy/lipoatrophy.

    The policy adds grade-specific quantity limits of up to 2 sessions for grade 2, up to 4 sessions for grade 3, and up to 8 sessions for grade 4.

    Kaiser Permanente adopted Kaiser Permanente National clinical criteria for Dermal Fillers for Facial Lipoatrophy effective December 1, 2026.

    The policy adopts Kaiser Permanente National clinical criteria for Dermal Fillers for Facial Lipoatrophy.

    Coverage criteria were approved for non-Medicare members.

    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.

    Grades 2-4Covered facial lipoatrophy severity range
    Grade 1Severity grade not covered
    2 / 4 / 8Maximum sessions for grades 2 / 3 / 4
    1-2 yearsRepeat treatment interval
    3Applicable filler codes

    Coverage Criteria

    Initial coverage criteria

    Covered when ALL of the following are met:

    • Eligible condition

      • The member has a diagnosis of human immunodeficiency virus (HIV).
      • The member has facial lipodystrophy/lipoatrophy, grades 2-4, related to HIV or highly active antiretroviral therapy (HAART).Grades 2-4
    • Approved product: The dermal filler is approved by the Food and Drug Administration for Facial Lipodystrophy Syndrome (LDS), such as Sculptra or Radiesse.FDA approval for Facial Lipodystrophy Syndrome

    Grading and quantity limits

    Quantity limits depend on the patient’s Carruthers Lipoatrophy Severity Scale grade.

    Grade-specific session limits

    • Grade 2: For grade 2 facial lipoatrophy, up to 2 sessions are covered.Grade 2; up to 2 sessions
    • Grade 3: For grade 3 facial lipoatrophy, up to 4 sessions are covered.Grade 3; up to 4 sessions
    • Grade 4: For grade 4 facial lipoatrophy, up to 8 sessions are covered.Grade 4; up to 8 sessions

    Repeat treatment

    Repeat treatment may be considered when the following condition is met:

    Repeat treatment consideration: Repeat treatment is typically necessary one to two years after initial therapy when the patient has regressed to grade 2 or greater lipoatrophy.Grade 2 or greater; typically 1-2 years after initial therapy

    For additional treatment, the treating provider must reevaluate the patient or provide repeat facial photographs to determine whether further treatment is warranted.

    Medical necessity for applicable codes

    Applicable codes are considered medically necessary when the following requirement is met:

    Applicable policy criteria: The criteria in the applicable policy statements listed above must be met for the listed dermal filler services to be considered medically necessary.

    Applicable services include dermal filler injection(s) for facial lipodystrophy syndrome and the listed Radiesse and Sculptra injection codes.

    Coverage is excluded in the presence of coagulopathy, active infection whether or not it is related to HIV disease, or inadequate immune function as determined by the HIV provider.

    The use of injectable poly-L-lactic acid for treatment of facial lipoatrophy does not meet the Kaiser Permanente Medical Technology Assessment Criteria.

    Grade 1 facial lipoatrophy is not covered. Grade 1 represents mild facial fat loss under the Carruthers Lipoatrophy Severity Scale.

    Injectable poly-L-lactic acid treatment for facial lipoatrophy is not considered to meet the Kaiser Permanente Medical Technology Assessment Criteria.

    Applicable Codes and Quantity Limits

    Covered HCPCS CodesHCPCSCovered
    G0429Dermal filler injection(s) for the treatment of facial lipodystrophy syndrome (LDS) (e.g., as a result of highly active antiretroviral therapy).
    Q2026Injection, Radiesse, 0.1 ml.
    Q2028Injection, Sculptra, 0.5 mg.
    Covered HCPCS CodesHCPCSCovered
    G0429Dermal filler injection(s) for the treatment of facial lipodystrophy syndrome (LDS) (e.g., as a result of highly active antiretroviral therapy).
    Q2026Injection, Radiesse, 0.1 ml.
    Q2028Injection, Sculptra, 0.5 mg.
    Grade 2 quantity limit
    Severity gradeGrade 2 facial lipoatrophy
    Maximum covered sessionsUp to 2 sessions
    Clinical descriptionDeeper concavity of the cheeks; facial lipoatrophy visible to others
    Grade 3 quantity limit
    Severity gradeGrade 3 facial lipoatrophy
    Maximum covered sessionsUp to 4 sessions
    Clinical description

    Authorization and Documentation Requirements

    Prior Authorization

    Submit for Authorization Review

    Submit the service for authorization review before treatment. Verify authorization requirements for the member’s plan using the Pre-authorization Code Check; applicable codes are considered medically necessary only when the policy criteria are met.

    • G0429 — Dermal filler injection(s) for treatment of facial lipodystrophy syndrome (LDS), such as from highly active antiretroviral therapy
    • Q2026 — Injection, Radiesse, 0.1 mL
    • Q2028 — Injection, Sculptra, 0.5 mg
    Documentation Required

    Submit Six Months of Clinical Notes

    For a review request, submit the last six months of clinical notes from the requesting provider and/or specialist.

    Clinical Background

    HIV-associated lipodystrophy can involve loss of subcutaneous fat in the face, including the nasolabial regions, temples, and eye sockets. Facial lipoatrophy is distinct from HIV wasting syndrome, which primarily involves loss of muscle mass. Dermal fillers such as Sculptra and Radiesse may be used to restore facial volume in eligible patients with HIV-associated Facial Lipodystrophy Syndrome.

    Definitions and Severity Scale

    Carruthers Lipoatrophy Severity Scale (CLSS)
    Scale rangeGrade 1 through Grade 4
    InterpretationHigher scores indicate greater severity of facial fat loss
    Grade 1Mild severity
    Grade 2Moderate severity
    Grade 3Severe severity
    Grade 4Very severe severity
    Facial lipodystrophy/lipoatrophy
    Policy Summary
    PayerKaiser Permanente
    PolicyDermal Fillers for Facial Lipoatrophy
    Policy CodePolicy N/A
    Change TypeModified
    Effective DateDecember 1, 2026
    Last ReviewMar 3, 2026
    Next Review DateN/A
    Key ActionSubmit dermal filler injection requests for clinical review with the required clinical documentation.
    SourceLink
    On This Page
    Coverage CriteriaApplicable Codes and Quantity LimitsAuthorization and Documentation RequirementsClinical BackgroundDefinitions and Severity Scale
    Deep concavity with prominent facial skeletal landmarks
    Grade 4 quantity limit
    Severity gradeGrade 4 facial lipoatrophy
    Maximum covered sessionsUp to 8 sessions
    Clinical descriptionNear-total or total loss of facial fat, with severe skeletal prominence
    Grade 1 coverage threshold
    Severity gradeGrade 1 facial lipoatrophy
    Coverage statusNot covered
    Clinical descriptionMild facial flattening or shallow concavity, typically noticeable only to the patient or trained observer
    Documentation Required

    Support Additional Treatment Requests

    For additional treatment sessions, reevaluate the patient or repeat facial photographs to establish that further treatment is warranted. Treatment limits depend on Carruthers Lipoatrophy Severity Scale (CLSS) grade, and repeat treatment is typically needed one to two years after initial therapy when lipoatrophy has regressed to Grade 2 or greater.

    • Grade 1: treatment is not covered
    • Grade 2: up to 2 sessions
    • Grade 3: up to 4 sessions
    • Grade 4: up to 8 sessions
    Denial Risk

    Watch for Coverage Denial Conditions

    Coverage may be denied when the member does not meet all coverage criteria or has an applicable exclusion. The member must have HIV and Grade 2–4 facial lipodystrophy/lipoatrophy related to HIV or HAART, and the filler must be FDA-approved for Facial Lipodystrophy Syndrome.

    • Exclusions include coagulopathy, active infection whether or not related to HIV disease, and inadequate immune function as determined by the HIV provider
    • Grade 1 facial lipoatrophy is not covered
    • Examples of FDA-approved fillers include Sculptra® and Radiesse®
    Denial Risk

    PLA Fails Technology Assessment Criteria

    Poly-L-lactic acid (PLA) treatment for facial lipoatrophy does not meet Kaiser Permanente Medical Technology Assessment Criteria and may be denied or considered non-covered.

    Definition
    Loss of facial subcutaneous fat
    Associated conditionHuman immunodeficiency virus (HIV) infection
    Associated treatmentHighly active antiretroviral therapy (HAART)
    Facial Lipodystrophy Syndrome (LDS)
    DefinitionFacial Lipodystrophy Syndrome (LDS)
    Filler requirementThe dermal filler must be approved by the Food and Drug Administration for Facial Lipodystrophy Syndrome
    ExamplesSculptra® and Radiesse®