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    v1.0.28
    OpenPayerPolicy UpdatesReproductive Health & FertilityAmbetter Nevada ART Coverage & Prior Auth Update |…
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    ModifiedAmbetter NevadaPolicy CP.MP.55

    Assisted Reproductive Technology (ART) Coverage Criteria

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    Defines medical necessity, covered services, and exclusions for assisted reproductive technologies (ART) for members whose benefit plans include infertility coverage. Applies to clinical treatments and laboratory procedures handling gametes and embryos for establishing pregnancy.

    Policy Summary
    PayerAmbetter Nevada
    PolicyAssisted Reproductive Technology (ART) Coverage Criteria
    Policy CodePolicy CP.MP.55
    Change TypeCriteria clarifications and structural editsICSI indications revisedFET added to description
    Effective Date
    Next Review Date
    Key ActionObtain prior authorization per the member's benefit plan before providing listed infertility services.
    SourceLink
    POLICY UPDATE CHANGES

    Frozen Embryo Transfer (FET) added under Description with no impact to criteria.

    ICSI indications clarified to include patients with previously failed fertilization and those with very low sperm concentration or motility; counseling regarding outcomes and small potential neonatal risks recommended.

    Numerous eligibility and procedural criteria reorganized and clarified across sections (examples: embryo transfer limits, updated fertility indications, added FET and oocyte in vitro maturation references).

    AddedFET status
    10+Listed procedure types
    ~30Codes listed
    43+References
    IncludedMedicaid/Medicare notes

    Coverage Criteria for Assisted Reproductive Technology

    Basic criteria

    Covered when ALL of the following basic criteria are met:

    Basic criteria: 1. No untreatable anatomic cause of infertility and modifiable causes of infertility have been considered and addressed when possible.
    Basic criteria: 2. Documented inability to conceive during a period of cycles exposed to sperm: 12 months for members with female reproductive systems < 35 years of age, or 6 months for those ≥ 35 years of age.
    Basic criteria: 3. For members with female reproductive systems ≥ 40 years attempting conception using their own oocytes, documentation that the treating provider has evaluated age, infertility risk factors, measure of ovarian reserve, prior treatment and response, and considers use of the member's own oocytes a viable strategy.
    Basic criteria:
    Policy Summary
    PayerAmbetter Nevada
    PolicyAssisted Reproductive Technology (ART) Coverage Criteria
    Policy CodePolicy CP.MP.55
    Change TypeCriteria clarifications and structural editsICSI indications revisedFET added to description
    Effective Date
    Next Review Date
    Key ActionObtain prior authorization per the member's benefit plan before providing listed infertility services.
    SourceLink
    On This Page
    Coverage Criteria for Assisted Reproductive TechnologyCPT, HCPCS and Coding GuidanceProvider Actions, Prior Authorization and DocumentationBackground on Assisted Reproductive TechnologyKey Definitions
    4. Infertility is unrelated to voluntary sterilization or failed reversal of voluntary sterilization of either partner.

    Treatment-specific criteria

    Treatment-specific covered indications — the requested treatment is covered when the listed criteria for that treatment are met:

    Artificial Insemination (ICI/IUI): Unilateral or bilateral tubal patency, and one of: mild male reproductive system factor infertility; cervical factors (e.g., stenosis, chronic cervicitis); ovulatory dysfunction treated with medications (e.g., clomiphene); unexplained infertility; sperm antibodies; endometriosis; use of cryopreserved sperm obtained for fertility preservation prior to gonadotoxic treatment; or situations that waive the timing requirement such as inability to have intercourse due to a physical disability or psychosexual problem, HIV-positive partner undergoing sperm washing, or single persons using donor sperm.

    Some listed factors waive the usual 6–12 month infertility timing requirement.

    In Vitro Fertilization with Embryo Transfer (IVF-ET): Meets one of: bilateral tubal absence/obstruction (not due to voluntary sterilization); endometriosis-associated infertility that failed treatment; severe male reproductive system infertility failing conservative treatments (sperm concentration <10 million/mL and/or normal morphology ≤1% by Krüger or ≤5% by WHO); prior IVF with failed or poor fertilization; unexplained infertility after failure of ≥3 IUI cycles with oral agents; high response to a medicated IUI cycle (both estradiol >1000 pg/mL AND production of ≥3 follicles ≥16 mm or 4–8 follicles >14 mm) requiring conversion to IVF; utilization of cryopreserved gametes/oocytes/embryos obtained for fertility preservation; or inadequate number of frozen embryos from prior IVF (fewer than 3 if age <35; fewer than 4 if age ≥35).

    Refer to Table 1 for embryo transfer guidance and ASRM limits.

    Frozen Embryo Transfer (FET): Meets both: (a) number of embryos to transfer per attempt meets Table 1 requirements; and (b) frozen embryos must be used prior to authorization of additional IVF cycles in specified circumstances (e.g., <35 with at least three embryos available for transfer; ≥35 with at least four embryos available for transfer), except when member continues to meet infertility diagnosis criteria.

    See FET-specific embryo availability thresholds in policy.

    GIFT/ZIFT: Member has at least one patent fallopian tube, AND one of: utilization of cryopreserved gametes/embryos obtained for fertility preservation, or unexplained infertility with failure of IUI (for <38 years: failure of 3 IUI cycles with oral agents; for ages 38–42: failure of at least 1 IUI cycle); AND justification that GIFT/ZIFT is preferable to standard IVF.
    Intracytoplasmic Sperm Injection (ICSI): Meets one of: fewer than two million motile spermatozoa per ejaculate; anti-sperm antibodies contributing to infertility; prior or repeated fertilization failure with standard IVF (<50% fertilization); washed sperm limited in number/quality; male tract obstruction not amenable to repair requiring MESA/TESE; abnormal sperm morphology (≤1% normal forms by Krüger or ≤5% by WHO); specific sperm defects impairing sperm-oocyte interaction; fertilization of previously frozen oocytes or oocytes that underwent in vitro maturation; utilization of cryopreserved gametes for fertility preservation; HIV or hepatitis-discordant couples; need for PGT-M where contamination from other sperm must be avoided; selected female infertility with oocyte/zona anomalies.

    Policy recommends counseling regarding outcomes and small potential neonatal risks for ICSI.

    Donor egg/sperm and TESE/MESA: Donor egg covered for indications including congenital or surgical absence of ovaries, primary ovarian insufficiency, diminished ovarian reserve, ovarian failure after radiation/chemotherapy, prior failed IVF in those >40, gonadal dysgenesis, high genetic transmission risk, or hypergonadotropic hypogonadism. TESE/micro-TESE/epididymal extraction covered for obstructive or non-obstructive azoospermia. Donor sperm covered for bilateral congenital absence of vas deferens, ejaculatory dysfunction, obstructive azoospermia/severe oligozoospermia or other significant sperm abnormalities, single persons without male partner, high infectious/genetic transmission risk, prior abnormal semen analyses, prior radiation/chemotherapy effects, or failure of ≥3 cycles of IVF/ICSI.

    Selected Procedural Indications and Authorization-related criteria

    Selected coverage-relevant procedural statements, clarifications, and authorization-related requirements extracted from the policy:

    ICSI indications and counseling: ICSI should be available to patients with previously failed fertilization and to patients with sperm concentration and motility too low for expected success with conventional IVF; patients should be counseled regarding outcomes and small potential neonatal risks.

    Supported by policy clinical discussion and references.

    ZIFT clinical role: ZIFT may be considered for patients with difficult trans-cervical embryo transfer, uterine abnormalities (e.g., DES exposure), or recurrent failure with standard IVF; success rates are similar to IVF and ZIFT may be chosen when trans-cervical embryo transfer is problematic.
    Prior authorization requirement: Multiple listed infertility CPT and HCPCS procedure codes require prior authorization if the service is a covered benefit; providers must obtain prior authorization per the member's benefit plan before rendering services.

    See coding sections and prior authorization callouts for the specific CPT/HCPCS codes subject to prior authorization.

    The following items are explicitly excluded or not medically necessary under this policy: surrogacy; reversal of voluntary sterilization; any experimental infertility procedure; commercially available over-the-counter home test kits (including ovulation prediction and pregnancy test kits); infertility treatment required as a result of prior voluntary sterilization or unsuccessful sterilization reversal; a partner's infertility services when the partner is not the enrollee (unless mandated by benefits); menopausal members with a female reproductive system who are ≤54 years of age (unless using a donor egg for premature diminished ovarian reserve or premature ovarian failure) and members with a female reproductive system who are >55 years of age; and services for sex selection or chromosomal studies of donor gametes.

    Administrative update: CPT-89253 was removed from the policy's table of CPT Codes that Support Medical Necessity (the CPT code table header and contents were updated as part of revision reviews).

    Coverage under this policy is a medical necessity guide and is subject to the terms, conditions, exclusions and limitations of the member's benefit plan. This policy does not guarantee payment; coverage decisions and benefit administration are governed by the member's specific coverage documents and applicable state or federal requirements.

    Restating non-covered or redundant items for clarity: the policy deems any experimental infertility procedure, surrogacy, and reversal of voluntary sterilization as not medically necessary. Also excluded are commercially available OTC home test kits, infertility treatment resulting from prior voluntary sterilization or unsuccessful reversal, partner infertility services when the partner is not enrolled (unless benefits mandate), and age-based menopause exclusions as specified in the policy.

    Editorial notes: prior language referencing experimental infertility procedures was revised and streamlined during recent policy restructuring. Several statements were removed or reworded as part of the update to align this policy with other Centene clinical policies and to clarify criteria; these editorial changes include removal of certain procedural authorizations and reformatting of exclusions.

    CPT, HCPCS and Coding Guidance

    Infertility CPT Codes that Support Medical Necessity (group 1)CPT
    58321Artificial insemination; intra-cervical.
    58322Artificial insemination; intra-uterine.
    58323Sperm washing for artificial insemination.
    58970Follicle puncture for oocyte retrieval, any method.
    58974Embryo transfer, intrauterine.
    58976Gamete, zygote, or embryo intrafallopian tube transfer; any method.
    89250Culture of oocyte(s)/embryo(s), less than 4 days.
    89251Culture of oocyte(s)/embryo(s), less than 4 days; with co-culture of oocyte(s)/ embryo(s).
    89254Oocyte identification from follicular fluid.
    89255Preparation of embryo for transfer (any method).
    1–10 of 16
    1/2
    Infertility CPT Codes that Support Medical Necessity (group 2)CPT
    89268Insemination of oocytes.
    89272Extended culture of oocyte(s)/embryo(s), 4-7 days.
    89280Assisted oocyte fertilization, microtechnique, less than or equal to 10 oocytes.
    89281Assisted oocyte fertilization, microtechniques; greater than 10 oocytes..
    89290Biopsy, oocyte polar body or embryo blastomere, microtechnique (for pre- implantation genetic diagnosis); less than or equal to 5 embryos.
    89291Biopsy, oocyte polar body or embryo blastomere, microtechnique (for pre- implantation genetic diagnosis); greater than 5 embryos.
    89337Cryopreservation, mature oocyte(s).
    89352Thawing of cryopreserved; embryo(s).
    89353Thawing of cryopreserved; sperm/semen, each aliquot.
    89356Thawing of cryopreserved; oocytes, each aliquot
    Infertility HCPCS/CMS S-codes (case rates and procedures)HCPCS
    S4011In vitro fertilization; including but not limited to identification and incubation of mature oocytes, fertilization with sperm, incubation of embryo(s), and subsequent visualization for determination.
    S4013Complete cycle, gamete intrafallopian transfer (GIFT), case rate.
    S4014Complete cycle, zygote intrafallopian transfer (ZIFT), case rate.
    S4015Complete in vitro fertilization cycle, not otherwise specified, case rate.
    S4016Frozen in vitro fertilization cycle, case rate.
    S4017Incomplete cycle, treatment canceled prior to stimulation, case rate.
    S4018Frozen embryo transfer procedure canceled before transfer, case rate.
    S4020In vitro fertilization procedure canceled before aspiration, case rate.
    S4021In vitro fertilization procedure canceled after aspiration, case rate.
    S4022Assisted oocyte fertilization, case rate.
    1–10 of 16
    1/2
    Severe male factor sperm concentration
    Severe male factor sperm concentrationSperm concentration less than 10 million per mL
    Context of useThreshold applied when severe male reproductive system infertility has failed conservative treatments and supports IVF indication
    Related requirementMay be combined with other semen abnormalities (e.g., morphology/motility) to indicate ICSI or IVF pathway
    Abnormal morphology thresholds (Kruger and WHO)
    Kruger morphology threshold≤ 1% normal forms by Kruger criteria
    WHO morphology threshold≤ 5% normal forms by WHO criteria
    ApplicationAbnormal morphology thresholds used as indications for ICSI or other assisted fertilization techniques
    High estradiol for IUI-to-IVF conversion
    High estradiol threshold for IUI-to-IVF conversion> 1000 pg/ml
    Action when threshold metMedicated IUI cycle with estradiol >1000 pg/ml should be converted to IVF
    DocumentationEstradiol level must be recorded in cycle monitoring to justify conversion to IVF and prior authorization
    Follicle counts for high IUI response
    High IUI response — follicle criteria AProduction of at least 3 follicles ≥ 16 mm
    High IUI response — follicle criteria BOr production of 4–8 follicles > 14 mm in diameter
    Resulting actionMedicated IUI cycles meeting these follicle counts (with estradiol threshold) should be converted to IVF
    Embryo culture days and oocyte counts
    Culture duration categoriesCulture of oocyte(s)/embryo(s) noted as: less than 4 days and extended culture 4–7 days
    Microtechnique stratification by oocyte countAssisted oocyte fertilization (microtechnique) coded and described as ≤10 oocytes (89280) or >10 oocytes (89281)
    PGT biopsy stratificationBiopsy for PGT described separately for ≤5 embryos (89290) and >5 embryos (89291)
    Coding implicationCulture days and oocyte-count stratifications map to specific CPT codes that require prior authorization when covered
    Step Therapy

    Step therapy per plan administrative policy

    Any step therapy requirements (e.g., required sequence of conservative treatments before advanced procedures) are defined by the member's administrative plan policies; use this clinical policy as guidance but follow plan‑specific step therapy rules.

    • Plan administrative policies may specify step therapy sequences and prior authorization workflows.
    • Confirm plan‑level step therapy requirements before proceeding with higher‑level ART interventions.

    Provider Actions, Prior Authorization and Documentation

    Prior Authorization

    Authorization required when medical necessity criteria are met

    Obtain authorization per the member's benefit plan before providing ART services. The policy makes ART medically necessary only when both the basic criteria and the applicable treatment-specific criteria are met and authorized benefits are based on the member's benefit plan contract.

    Prior Authorization

    Prior authorization required for listed procedure codes

    Prior authorization is required for the listed CPT and HCPCS procedure codes when the service is a covered benefit. The policy provides a list of infertility CPT and HCPCS/S-codes that require prior authorization if covered.

    Prior Authorization

    Prior authorization required per plan administrative rules

    Obtain prior authorization in accordance with plan rules: the policy serves as a medical necessity guide and standard Health Plan administrative procedures require providers to secure authorization per the member's plan before services are rendered.

    Step Therapy

    Document failure of prior, less invasive therapies when required

    Some treatment pathways require documented failure of less invasive therapies before advancing. For example, IVF eligibility can require failure of at least three IUI cycles for unexplained infertility or specified failed IUI counts for GIFT/ZIFT depending on age.

    • IVF: unexplained infertility requires failure of ≥3 IUI cycles with oral agents.
    • GIFT/ZIFT: <38 years requires failure of 3 IUI cycles; 38–42 years requires failure of at least 1 IUI cycle.
    Note
    Step Therapy

    Step therapy requirements governed by plan administrative policy

    The policy is a guideline; any step therapy requirements are defined by the member's plan administrative policies. Use this clinical policy to inform medical necessity determinations but verify plan-level step therapy rules.

    Documentation Required

    Required clinical documentation to support authorization

    Maintain clinical documentation that supports medical necessity: include infertility duration (12 months if <35; 6 months if ≥35), assessment of ovarian reserve and, for those ≥40 using own oocytes, prior treatment and response, as well as condition-specific evidence such as semen analysis and tubal patency when relevant.

    • Infertility timing: 12 months (<35) or 6 months (≥35).
    • For ≥40 using own oocytes: document ovarian reserve, prior treatments and responses.
    • Treatment-specific evidence: semen analysis results, tubal patency, failed IUI cycles, etc.
    Documentation Required

    Align documentation with plan and regulatory requirements

    Ensure documentation and submissions comply with the member's plan coverage documents and applicable state or federal requirements. The policy emphasizes that providers should follow plan coverage documents and regulatory requirements when documenting medical necessity.

    Note

    Verify member benefit plan includes infertility/ART coverage

    Confirm that the member's benefit plan includes infertility/ART coverage before providing services. The policy states services are covered only when specific coverage exists under the member/enrollee's benefit plan and refers providers to benefit guidelines for coverage limitations.

    Prior Authorization

    Obtain prior authorization for listed infertility services

    Prior authorization is required for the infertility services listed in the policy when those services are a covered benefit; failure to obtain PA when required may lead to denial.

    Denial Risk

    Denial risk if services fall outside plan terms, exclusions, or limits

    Coverage is subject to all terms, conditions, exclusions and limitations of the member's coverage documents; services outside plan terms, exclusions or limitations risk denial of payment.

    Background on Assisted Reproductive Technology

    Background: Assisted reproductive technology (ART) encompasses clinical treatments and laboratory procedures that handle oocytes, sperm, or embryos to establish pregnancy. In vitro fertilization (IVF) involves ovarian stimulation, egg retrieval, sperm preparation, fertilization of oocytes in the laboratory, and subsequent embryo transfer (including use of cryopreserved embryos for frozen embryo transfer). Procedures such as GIFT and ZIFT require laparoscopy to place gametes or zygotes into the fallopian tube, and ICSI is a microtechnique to inject sperm directly into an egg when indicated.

    Key Definitions

    inv-30: In vitro fertilization (IVF) — definition and one-cycle scope
    DefinitionFertilization of an egg with sperm in a laboratory with subsequent embryo transfer to the uterus
    One-cycle scopeOne IVF-ET cycle includes ovarian stimulation and monitoring, oocyte retrieval, sperm preparation/capacitation, and embryo transfer (including frozen embryo transfer)
    Timing of embryo transferEmbryo transfer (including FET) may occur any time between one to six days after egg retrieval, or after cryopreservation in FET
    inv-31: GIFT — Gamete intra-fallopian transfer definition
    DefinitionGamete intra-fallopian transfer (GIFT) — laparoscopic aspiration of oocytes; oocytes are mixed with sperm and transferred to the fallopian tube via catheter
    Indications/contextMay be chosen for religious/personal reasons or after failed donor insemination; requires laparoscopy and at least one patent tube
    Success ratesSuccess rates are similar to those undergoing IVF
    inv-32: ZIFT — Zygote intra-fallopian transfer definition (placement of zygotes/embryos into fallopian tube)
    DefinitionZygote intra-fallopian transfer (ZIFT) — placement of fertilized eggs (zygotes) or embryos into the fallopian tube, requiring laparoscopy
    Clinical roleMay be considered for difficult trans-cervical embryo transfer, uterine abnormalities (e.g., DES exposure), or recurrent IVF failure
    Success comparisonOverall success rates are similar to IVF
    inv-33: ICSI — Intracytoplasmic sperm injection definition and indications
    DefinitionIntracytoplasmic sperm injection (ICSI) — injection of a single sperm into the egg in the laboratory to achieve fertilization
    IndicationsIndicated for previously failed fertilization, very low sperm concentration or motility, antisperm antibodies, prior fertilization failure (<50%), washed sperm limited in number/quality, and abnormal morphology (Kruger ≤1% or WHO ≤5%)
    Counseling notePatients should be counseled regarding outcomes and small potential neonatal risks associated with ICSI
    inv-34: ZIFT (duplicate inventory entry) — alternate ZIFT definition preserved
    Alternate definition preservedZygote Intra-Fallopian Transfer (ZIFT) — placement of fertilized eggs (zygotes) or embryos into the fallopian tube typically via laparoscopy
    NoteEntry preserved as alternate wording consistent with main ZIFT definition and clinical use for difficult trans-cervical transfers
    inv-35: ICSI (duplicate inventory entry) — laboratory microinjection definition preserved
    Alternate wordingICSI — laboratory microinjection of sperm into an egg to achieve fertilization, followed by embryo transfer or cryopreservation
    Indication overlapICSI indications include severe male factor, prior fertilization failure, specific sperm defects, and use with cryopreserved/IVM oocytes
    inv-36: Infertility definitions — infertility and recurrent pregnancy loss informed by ASRM guidance
    Infertility definition by ageFailure to achieve pregnancy after 1 year if <35 years, after 6 months if ≥35 years, or more immediately if age 40 and over
    Recurrent pregnancy loss and terminologyDefinitions and related terminology are informed by ASRM committee opinions and guideline documents referenced in the policy
    Use of guidanceASRM practice committee documents and related guidelines inform infertility and recurrent pregnancy loss definitions used in the policy