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    OpenPayerPolicy UpdatesObstetrics/GynecologyColorado Rocky Mountain AUB Policy Update | OpenPa…
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    CurrentColorado Rocky Mountain Health PlansPolicy 2026T0442WW

    Abnormal Uterine Bleeding and Uterine Fibroids

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    Coverage and medical necessity for selected treatments of abnormal uterine bleeding, menorrhagia, and symptomatic uterine fibroids, including endometrial ablation, levonorgestrel-releasing intrauterine devices, uterine artery embolization, and magnetic resonance-guided focused ultrasound.

    Policy Summary
    PayerColorado Rocky Mountain Health Plans
    PolicyAbnormal Uterine Bleeding and Uterine Fibroids
    Policy CodePolicy 2026T0442WW
    Change TypeReference and supporting-information update
    Effective DateNovember 1, 2026
    Next Review DateNot specified
    Key ActionApply InterQual criteria for endometrial ablation used to treat abnormal uterine bleeding in premenopausal individuals.
    SourceLink

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    POLICY UPDATE CHANGES

    The Clinical Evidence and References sections were updated to reflect current information.

    16Policy pages
    4Treatment categories
    2Unproven services
    28LNG-IUS review studies

    Medical Necessity and Coverage Criteria

    Endometrial Ablation

    Covered when medically necessary for treating abnormal uterine bleeding in premenopausal individuals and applicable clinical criteria are met.

    Abnormal uterine bleeding is present in a premenopausal individual.
    Medical necessity clinical coverage criteria are met under InterQual® CP: Procedures, Hysteroscopy, Operative.

    Refer to the InterQual® criteria.

    Levonorgestrel-Releasing Intrauterine Device

    Covered when medically necessary for treating menorrhagia.

    Menorrhagia is present.
    Treatment with a levonorgestrel-releasing intrauterine device is medically necessary for the stated indication.

    Examples include Mirena®, Skyla®, Liletta®, and Kyleena™. Refer to the FDA section for additional information.

    Uterine Artery Embolization

    Covered when medically necessary for symptomatic uterine fibroids, postpartum or posthysterectomy bleeding, or uterine arteriovenous malformation, and applicable clinical criteria are met.

    ONE of the following indications

    • Symptomatic uterine fibroids.
    • Postpartum bleeding.
    • Posthysterectomy bleeding.
    • Uterine arteriovenous malformation.
    Medical necessity clinical coverage criteria are met under InterQual® CP: Procedures, Uterine Artery Embolization (UAE).

    Refer to the InterQual® criteria.

    Initial Therapy When Fertility Preservation Is Desired

    ACR considers the following equivalent alternatives usually appropriate for initial therapy; in most cases, medical management should be trialed before more invasive therapies.

    ALL of the following

    • The patient is of reproductive age and has uterine fibroids.
    • The patient is symptomatic with heavy uterine bleeding or bulk symptoms, such as pressure, pain, fullness, bladder symptoms, or bowel symptoms.
    • The patient desires to preserve fertility.
    • ONE usually appropriate initial therapy

      • Laparoscopic myomectomy.
      • Open myomectomy.

    Initial Therapy When Future Fertility Is Not Desired

    ACR considers the following equivalent alternatives usually appropriate for initial therapy; in most cases, medical management should be trialed before more invasive therapies.

    ALL of the following

    • The patient is of reproductive age and has uterine fibroids.
    • The patient is symptomatic with heavy uterine bleeding or bulk symptoms, such as pressure, pain, fullness, bladder symptoms, or bowel symptoms.
    • The patient has no desire for future fertility.
    • ONE usually appropriate initial therapy

      • Laparoscopic myomectomy.
      • Open myomectomy.

    Initial Therapy for Fibroids With Concurrent Adenomyosis

    ACR considers medical management or UAE usually appropriate for initial therapy; in most cases, medical management should be trialed before more invasive therapy.

    ALL of the following

    • The patient is of reproductive age and has uterine fibroids with concurrent adenomyosis.
    • The patient is symptomatic with heavy uterine bleeding or bulk symptoms, such as pressure, pain, fullness, bladder symptoms, or bowel symptoms.
    • The patient has no desire for future fertility.
    • ONE usually appropriate initial therapy

      • Medical management.

    Initial Therapy for Pedunculated Submucosal Fibroids

    ACR considers hysteroscopic myomectomy or medical management usually appropriate for initial therapy; in most cases, medical management should be trialed before more invasive therapy.

    ALL of the following

    • The patient is of reproductive age.
    • The patient has pedunculated submucosal uterine fibroids.
    • The fibroids are symptomatic with heavy uterine bleeding.
    • ONE usually appropriate initial therapy

      • Hysteroscopic myomectomy.
      • Medical management.

    Next-Step Therapy After Negative Biopsy in Postmenopause

    ACR considers hysterectomy usually appropriate as the next step in this clinical scenario.

    ALL of the following

    • The patient is postmenopausal.
    • The patient has uterine fibroids.
    • The patient is symptomatic with heavy uterine bleeding or bulk symptoms, such as pressure, pain, fullness, bladder symptoms, or bowel symptoms.
    • Endometrial biopsy is negative.
    • Hysterectomy is selected as the next-step therapy.

    Initial Therapy for Fibroid-Related Reproductive Dysfunction

    ACR considers hysteroscopic myomectomy or laparoscopic or open myomectomy usually appropriate initial therapy; these are equivalent alternatives, and the panel did not agree that medical management should be recommended for this scenario.

    ALL of the following

    • The patient is of reproductive age.
    • The patient has uterine fibroids.
    • The patient desires pregnancy.
    • The patient is experiencing reproductive dysfunction.
    • ONE usually appropriate initial therapy

      • Hysteroscopic myomectomy.

    Medical Management of Abnormal Uterine Bleeding

    ACOG recommendations for medical management of abnormal uterine bleeding include the following options and considerations.

    Medical management options or considerations

    • Levonorgestrel-releasing intrauterine device may be considered for treatment of abnormal uterine bleeding; evidence is insufficient to support its use for uterine leiomyoma symptoms other than bleeding.
    • Combined oral contraceptives may regulate and reduce menstrual bleeding, treat dysmenorrhea, reduce premenstrual dysphoric disorder symptoms, and ameliorate acne.

      ACOG evidence level A.

    • Hormonal contraception should be considered for menorrhagia in individuals who may desire future pregnancies.

      ACOG evidence level B.

    NICE Management of Heavy Menstrual Bleeding

    NICE recommendations for assessment and management of heavy menstrual bleeding include the following treatment pathways.

    For no identified pathology, fibroids less than 3 cm, or suspected or diagnosed adenomyosis

    • Offer levonorgestrel-releasing intrauterine system (LNG-IUS) as first treatment.
    • If treatment is unsuccessful, the patient declines pharmacological treatment, or symptoms are severe, refer to a specialist to discuss additional options.

    For fibroids greater than 3 cm

    • LNG-IUS may be considered as a pharmacological option.
    • Uterine artery embolization may be considered when fibroids are 3 cm or more in diameter.

    Uterine Artery Embolization: Indications and Fertility Counseling

    SIR states that UAE is indicated for uterine leiomyomata causing significant symptoms. Fertility counseling and individualized treatment selection are required when future pregnancy is relevant.

    ONE or more significant symptoms

    • Heavy or prolonged menstrual bleeding.
    • Severe menstrual cramping.
    • Pelvic pressure, discomfort, excessive bloating, or fullness, particularly perimenstrual, or bothersome abdominal wall distortion caused by an enlarged uterus.
    • Pelvic pain related to identified leiomyomas, including dyspareunia.
    • Urinary urgency, frequency, nocturia, or retention related to an enlarged leiomyomatous uterus.

    Focused Ultrasound Safeguards

    NICE recommends ultrasound-guided high-intensity transcutaneous focused ultrasound for symptomatic uterine fibroids only with special arrangements for clinical governance, consent, and audit or research.

    ALL of the following

    • Inform the clinical governance leads in the applicable health service trust.
    • Explain the procedure's recognized complications, including skin burns, limited-quality efficacy evidence, and uncertainties about safety and effectiveness.
    • Provide clear written information to support shared decision-making, including relevant NICE public information.
    • Audit and review clinical outcomes for all treated patients using relevant audit criteria or an audit tool.
    • During consent, explain that symptoms may not be completely relieved, may return, and may require further procedures.

    Uterine Artery Embolization for Symptomatic Leiomyomata

    SIR quality improvement guidance indicates UAE for uterine leiomyomata causing significant symptoms.

    ONE or more significant leiomyoma-related symptoms

    • Heavy or prolonged menstrual bleeding.
    • Severe menstrual cramping.
    • Pelvic pressure, discomfort, excessive bloating, or fullness, particularly perimenstrual, or bothersome abdominal wall distortion caused by an enlarged uterus.
    • Pelvic pain related to identified leiomyomas, including dyspareunia.
    • Urinary urgency, frequency, nocturia, or retention related to an enlarged leiomyomatous uterus.

    FDA approval alone is not a basis for coverage. This FDA section is for informational purposes only.

    Coding and Clinical Parameters

    Uterine FibroidsCPT
    0071TFocused ultrasound ablation of uterine leiomyomata, including MR guidance; total leiomyomata volume less than 200 cc of tissue.
    0072TFocused ultrasound ablation of uterine leiomyomata, including MR guidance; total leiomyomata volume greater or equal to 200 cc of tissue.
    37243Vascular embolization or occlusion, inclusive of all radiological supervision and interpretation, intraprocedural roadmapping, and imaging guidance necessary to complete the intervention; for tumors, organ ischemia, or infarction.
    58563Hysteroscopy, surgical; with endometrial ablation (e.g., endometrial resection, electrosurgical ablation, thermoablation).
    Levonorgestrel-Releasing Intrauterine DeviceHCPCS
    J7296Levonorgestrel-Releasing Intrauterine Device; levonorgestrel-releasing intrauterine contraceptive system (Kyleena), 19.5 mg.
    J7297Levonorgestrel-releasing intrauterine contraceptive system (Liletta), 52 mg.
    J7298Levonorgestrel-releasing intrauterine contraceptive system (Mirena), 52 mg.
    J7301Levonorgestrel-releasing intrauterine contraceptive system (Skyla), 13.5 mg.
    J7306Levonorgestrel (contraceptive) implant system, including implants and supplies.
    S4981Insertion of levonorgestrel-releasing intrauterine system.
    Fibroid volume in MR-HIFU versus US-HIFU analysis
    AnalysisComparative analysis of MR-HIFU and US-HIFU for symptomatic uterine fibroids
    Fibroid volume criterionFibroid volume less than 300 cm3
    Included studies48 studies: 28 addressing MR-HIFU and 20 addressing US-HIFU
    Successful nonperfused volume rate
    ParameterNonperfused volume rate (NPVR)
    Successful resultNPVR greater than 80%
    Reported group values

    Provider Requirements and Action Items

    Prior Authorization

    Apply InterQual hysteroscopy criteria

    For endometrial ablation to treat abnormal uterine bleeding in premenopausal individuals, apply the InterQual CP: Procedures, Hysteroscopy, Operative medical necessity clinical coverage criteria.

    Prior Authorization

    Apply InterQual UAE criteria

    For uterine artery embolization for symptomatic uterine fibroids, postpartum or posthysterectomy bleeding, or uterine arteriovenous malformation, apply the InterQual CP: Procedures, Uterine Artery Embolization (UAE) medical necessity clinical coverage criteria.

    Documentation Required

    Submit records for clinical review

    Clinical Background

    Abnormal uterine bleeding (AUB) includes changes in menstrual frequency, duration, or flow, as well as bleeding between cycles. In postmenopausal individuals, it includes bleeding occurring at least 12 months after menstruation has ceased or unpredictable bleeding during long-term hormone therapy. Uterine fibroids, also called leiomyomata, are benign uterine tumors that may cause heavy bleeding, uterine enlargement, pelvic pain or pressure, urinary frequency, and abdominal distension. Management may include observation, pharmacologic treatment, or procedural therapy; hysterectomy may be considered when symptoms cannot be controlled conservatively.

    Definitions and Terminology

    Abnormal uterine bleeding (AUB)
    Menstrual timingAUB includes any change in menstrual period frequency or duration
    Flow changesAUB includes a change in the amount of menstrual flow
    Bleeding between cyclesAUB includes bleeding between cycles; after menopause, it includes vaginal bleeding 12 months or more after cessation of menstruation or unpredictable bleeding during hormone therapy for 12 months or more
    Menorrhagia
    IntervalBleeding occurs at normal intervals
    FlowThe bleeding has heavy flow
    Duration
    Policy Summary
    PayerColorado Rocky Mountain Health Plans
    PolicyAbnormal Uterine Bleeding and Uterine Fibroids
    Policy CodePolicy 2026T0442WW
    Change TypeReference and supporting-information update
    Effective DateNovember 1, 2026
    Next Review DateNot specified
    Key ActionApply InterQual criteria for endometrial ablation used to treat abnormal uterine bleeding in premenopausal individuals.
    SourceLink
    On This Page
    Medical Necessity and Coverage CriteriaCoding and Clinical ParametersProvider Requirements and Action ItemsClinical BackgroundDefinitions and Terminology
  1. Medical management.
  2. Magnetic resonance-guided focused ultrasound (MRgFUS).
  3. Uterine artery embolization (UAE).
  4. Medical management.
  5. Magnetic resonance-guided focused ultrasound (MRgFUS).
  6. Uterine artery embolization (UAE).
  7. Uterine artery embolization (UAE).
  8. Laparoscopic myomectomy.
  9. Open myomectomy.
  10. Medical management is not recommended by the ACR panel for this clinical scenario because there is insufficient medical literature to conclude whether patients would benefit from it; intervention is controversial but may be appropriate.
    Assess the uterus and fibroids by ultrasound before UAE.
  11. Consider magnetic resonance imaging when further information about fibroid position, size, number, or vascularity is needed.
  12. Hydronephrosis caused by an enlarged uterus.

    Fertility counseling when pregnancy is desired or possible

    • Explore the patient's interest in pregnancy, including age, previous interventions, pregnancies, and interest in assisted-reproductive technologies.
    • Assess current fertility status, including evaluation by a reproductive endocrinologist when appropriate.
    • Discuss that evidence regarding fertility outcomes is limited and that myomectomy may be associated with better fertility outcomes than UAE, although evidence is very weak.
    • For patients without prior surgery, with resectable leiomyomas, and with a reasonable likelihood of pregnancy, discuss that myomectomy may be preferred while respecting informed patient preference.
    • For patients with prior myomectomy, discuss that high-quality reproductive-outcome data are lacking and UAE may be preferred because repeat surgery can be difficult.
    • For patients who are poor surgical candidates because of comorbidity, body habitus, or leiomyoma extent or location, UAE is an acceptable choice for those seeking pregnancy.
  13. Discuss the risk of skin burns.
  14. Tell patients considering pregnancy that effects on fertility and future pregnancy are uncertain.
  15. Use a multidisciplinary team, including a gynecologist and appropriate imaging specialist, for patient selection.
  16. Perform the procedure only in a specialized center by clinicians with specific training in the technique.
  17. Hydronephrosis caused by an enlarged uterus.
    MR-HIFU: 58.92%; US-HIFU: 81.07%
    Reduced HIFU reintervention risk parameter
    Treatment modalityHigh-intensity focused ultrasound (HIFU) ablation of uterine fibroids
    NPVR associated with lower reintervention riskNPVR at least 50%
    Reintervention rates with NPVR above 50%1% at 12 months, 5% at 36 months, and 15% at 60 months
    NICE heavy menstrual bleeding treatment threshold
    Fibroids less than 3 cmNICE recommends an LNG-IUS as the first treatment when fibroids are less than 3 cm in diameter, absent identified pathology, or with suspected or diagnosed adenomyosis
    Fibroids 3 cm or moreNICE lists UAE as an option for fibroids 3 cm or more in diameter
    Assessment before UAEAssess the uterus and fibroids by ultrasound; consider MRI when additional information about position, size, number, or vascularity is needed

    Medical records documentation may be required to assess whether the member meets the clinical criteria for coverage. Documentation does not guarantee coverage; coverage remains subject to the member-specific benefit plan and applicable laws.

    Documentation Required

    Complete pre-UFE evaluation

    Prior to uterine fibroid embolization, obtain or document an endometrial biopsy as recommended to rule out malignancy or hyperplasia.

    Denial Risk

    Avoid excluded or unproven indications

    Uterine artery embolization is unproven and not medically necessary when requested solely to preserve childbearing potential in individuals with symptomatic uterine fibroids. Magnetic resonance-guided focused ultrasound ablation for treating uterine fibroids is also unproven and not medically necessary due to insufficient evidence of efficacy.

    Denial Risk

    Document the LNG-IUD treatment purpose

    For benefit plans that exclude contraception, an intrauterine device, including an LNG-IUD, is excluded when used for contraceptive purposes. Coverage exists for an LNG-IUD used for a non-contraceptive purpose, including medically necessary treatment of abnormal uterine bleeding.

    Bleeding lasts more than 7 days
    Menometrorrhagia
    IntervalBleeding occurs at irregular, noncyclic intervals
    FlowThe bleeding has heavy flow
    DurationBleeding lasts more than 7 days
    Uterine fibroids
    NatureUterine fibroids are benign tumors of the uterus
    Alternate terminologyAlso known as leiomyomata
    Potential effectsThey may cause excessive uterine bleeding, uterine enlargement or mass, pelvic pain or pressure, urinary frequency, and abdominal distension
    Uterine artery embolization
    ProcedureParticles are injected via the uterine arteries
    MechanismThe particles block the blood supply to uterine fibroids
    ResultBlocking the blood supply causes the fibroids to shrink
    Levonorgestrel-releasing intrauterine system (LNG-IUS)
    Device typeContinuous-release intrauterine progesterone system
    Levonorgestrel contentContains 52 mg of levonorgestrel
    Release rateReleases approximately 20 micrograms per day during the first year
    Uterine artery embolization (UAE)
    Treatment typeMinimally invasive treatment for symptomatic uterine fibroids
    Evidence outcomesEvidence evaluates fertility, pregnancy, symptom, and reintervention outcomes
    Fertility evidenceA 2025 meta-analysis reported a pooled pregnancy rate of 52.1% and a pooled mean time to conception of 14.7 months
    Magnetic resonance-guided focused ultrasound (MRgFUS)
    ProcedureFocused ultrasound ablation
    GuidancePerformed with magnetic resonance guidance
    Treatment targetUsed for treatment of uterine fibroids
    HIFU
    MeaningHIFU means high-intensity focused ultrasound ablation of uterine fibroids
    Modalities distinguishedThe document distinguishes magnetic resonance-guided and ultrasound-guided approaches
    Clinical parameterNPVR is associated with clinical success; NPVR of at least 50% was associated with reduced intervention in subgroup analysis
    NPVR
    DefinitionNPVR means nonperfused volume rate
    Clinical significanceNPVR is a treatment parameter positively associated with clinical success when sufficiently high
    Relevant thresholdsNPVR of at least 50% was associated with reduced intervention; greater than 80% was considered successful in a comparative analysis
    MRgFUS
    Full termMagnetic resonance imaging-guided focused ultrasound ablation
    Treatment targetUsed for uterine leiomyomas
    Comparative evidenceCompared with UAE, limited comparative data associate MRgFUS with less symptom improvement and a higher rate of reintervention
    UAE
    Full termUterine artery embolization
    IndicationUsed for symptomatic uterine leiomyomas causing significant symptoms
    Examples of symptomsSymptoms may include heavy or prolonged bleeding, severe cramping, pelvic pressure or pain, urinary symptoms, or hydronephrosis