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    v1.0.28
    OpenPayerPolicy UpdatesOtorhinolaryngology (ENT)EmblemHealth OAE Coverage & Prior Auth | OpenPayer
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    CurrentEmblemHealthPolicy MG.MM.ME.33bC2

    Otoacoustic Emissions Testing

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    Clinical coverage criteria and coding guidance for otoacoustic emissions (OAE) screening and diagnostic testing for EmblemHealth members, including indications, limitations, and applicable procedure and diagnosis codes; intended for providers requesting authorization or submitting claims.

    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.

    Policy Summary
    PayerEmblemHealth
    PolicyOtoacoustic Emissions Testing
    Policy CodePolicy MG.MM.ME.33bC2
    Change TypeNo material changes
    Effective Date
    Last ReviewApr 11, 2025
    Next Review DateApr 11, 2025
    Key ActionProviders must submit clinical documentation that the member meets the policy criteria when requesting authorization for CPT codes 92558, 92587, and 92588.
    SourceLink
    POLICY UPDATE CHANGES

    No material clinical or coverage changes in this revision.

    3CPT codes addressed
    ~70+ICD-10 codes listed
    90 daysNeonatal screening age threshold
    3 yearsScreening age when audiometry not feasible
    ExtensiveCode coverage scope

    Coverage Criteria for OAE Screening and Diagnostic Testing

    inv-01: Screening indications (92558) — covered indications

    Covered when ALL of the following are met:

    Screening (CPT 92558): Neonatal hearing screening using otoacoustic emissions (OAE) is medically necessary for infants 90 days of age or younger.age <= 90 days for neonatal screening

    Use CPT 92558 for OAE screening

    Screening (CPT 92558) — alternate pediatric indication: Evoked OAE is medically necessary to screen children 3 years of age and younger who did not have initial neonatal screening and/or cannot be effectively measured or monitored through conventional audiometry.age <= 3 years when audiometry not feasible

    Use CPT 92558 for OAE screening

    inv-02: Diagnostic indications (92587, 92588) — diagnostic evaluations

    Covered diagnostic evaluations (use CPT 92587 for limited and CPT 92588 for comprehensive testing):

    Diagnostic indications (CPT 92587, 92588): Infants over 90 days and children up to 4 years of age.

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Children and adults who are unable to cooperate with other methods of hearing testing (for example, individuals with autism or stroke).

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Children with developmental or delayed speech or language disorders.

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Individuals with tinnitus, acoustic trauma, noise-induced hearing loss, or sudden hearing loss.

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Routine evoked otoacoustic emissions screening (CPT 92558) performed at well‑child visits for children age 3 years who have passed the newborn hearing screen is not medically necessary unless the child has a documented risk factor for hearing loss, demonstrated impairment of speech or auditory skills, or abnormal middle ear status. This limitation applies to screening OAE performed solely as part of routine well‑child care in the absence of those specified clinical concerns.

    Comprehensive otoacoustic emissions testing (CPT 92588) is considered experimental and investigational and not medically necessary when used for initial hearing screening because available evidence does not demonstrate added value of comprehensive testing over limited/ screening OAE for that indication.

    Auditory screening or diagnostic testing using otoacoustic emissions (OAEs) is considered unproven and not medically necessary for populations and clinical conditions that are not explicitly listed as covered indications in this policy. The policy notes inadequate evidence that OAE screening or diagnostic OAE testing improves health outcomes compared with standard screening audiometry for groups not specified as medically necessary.

    No explicit exclusions beyond the listed limitations are stated in the portions of the policy that enumerate applicable diagnosis codes and related code lists. Providers should use the diagnosis codes shown in the policy to support medical‑necessity determinations where applicable.

    This section of the document does not list any additional explicit exclusions beyond those identified under Limitations/Exclusions; absence of further exclusions in this portion does not alter the coverage limitations stated elsewhere in the policy.

    Specifically, routine evoked OAE screening (CPT 92558) at well‑child visits for children aged 3 years or younger who have passed the newborn screen is designated not medically necessary unless one of the policy’s exceptions is present (risk factor for hearing loss, speech/auditory impairment, or abnormal middle ear status). When such exceptions exist, screening may be appropriate and should be documented.

    Comprehensive OAE testing (CPT 92588) is explicitly identified as experimental/investigational and not medically necessary when used for initial screening, given lack of evidence demonstrating benefit beyond limited or screening OAE approaches for that purpose.

    Some document sections that list applicable ICD‑10 diagnosis codes do not include additional explicit 'not medically necessary' statements; those lists are intended to provide diagnosis coding that may support medical‑necessity determinations when the policy criteria are met.

    Procedure and Diagnosis Codes

    Applicable Procedure CodesCPT
    92558Evoked otoacoustic emissions, screening (qualitative measurement of distortion product or transient evoked otoacoustic emissions), automated analysis.
    92587Distortion product evoked otoacoustic emissions; limited evaluation (to confirm the presence or absence of hearing disorder, 3-6 frequencies) or transient evoked otoacoustic emissions, with interpretation and report.
    92588Distortion product evoked otoacoustic emissions; comprehensive diagnostic evaluation (quantitative analysis of outer hair cell function by cochlear mapping, minimum of 12 frequencies), with interpretation and report.
    Applicable ICD-10 Diagnosis Codes (partial list)ICD-10
    A17.0Tuberculous meningitis
    A39.0Meningococcal meningitis
    A52.13Late syphilitic meningitis
    A80.0Acute paralytic poliomyelitis, vaccine-associated
    A80.1Acute paralytic poliomyelitis, wild virus, imported
    A80.2Acute paralytic poliomyelitis, wild virus, indigenous
    A80.30Acute paralytic poliomyelitis, unspecified
    A80.39Other acute paralytic poliomyelitis
    A80.9Acute poliomyelitis, unspecified
    A87.0Enteroviral meningitis
    1–10 of 147
    1/15
    Applicable ICD-10 Hearing Loss/Ototoxicity/Sudden Hearing Loss CodesICD-10
    H90.8Mixed conductive and sensorineural hearing loss, unspecified
    H90.A11Conductive hearing loss, unilateral, right ear with restricted hearing on the contralateral side
    H90.A12Conductive hearing loss, unilateral, left ear with restricted hearing on the contralateral side
    H90.A21Sensorineural hearing loss, unilateral, right ear, with restricted hearing on the contralateral side
    H90.A22Sensorineural hearing loss, unilateral, left ear, with restricted hearing on the contralateral side
    H90.A31Mixed conductive and sensorineural hearing loss, unilateral, right ear with restricted hearing on the contralateral side
    H90.A32Mixed conductive and sensorineural hearing loss, unilateral, left ear with restricted hearing on the contralateral side
    H91.01Ototoxic hearing loss, right ear
    H91.02Ototoxic hearing loss, left ear
    H91.03Ototoxic hearing loss, bilateral
    1–10 of 15
    1/2
    Applicable ICD-10 Tinnitus/Other Auditory Perception CodesICD-10
    H91.8X1Other specified hearing loss, right ear
    H91.8X2Other specified hearing loss, left ear
    H91.8X3Other specified hearing loss, bilateral
    H91.8X9Other specified hearing loss, unspecified ear
    H93.011Transient ischemic deafness, right ear
    H93.012Transient ischemic deafness, left ear
    H93.013Transient ischemic deafness, bilateral
    H93.019Transient ischemic deafness, unspecified ear
    H93.11Tinnitus, right ear
    H93.12Tinnitus, left ear
    1–10 of 12
    1/2
    Applicable ICD-10 Auditory Perception/Hyperacusis/Diplacusis CodesICD-10
    H93.211Auditory recruitment, right ear
    H93.212Auditory recruitment, left ear
    H93.213Auditory recruitment, bilateral
    H93.219Auditory recruitment, unspecified ear
    H93.221Diplacusis, right ear
    H93.222Diplacusis, left ear
    H93.223Diplacusis, bilateral
    H93.229Diplacusis, unspecified ear
    H93.231Hyperacusis, right ear
    H93.232Hyperacusis, left ear
    1–10 of 12
    1/2
    Additional Auditory Disorder CodesICD-10
    H93.241Temporary auditory threshold shift, right ear
    H93.242Temporary auditory threshold shift, left ear
    H93.243Temporary auditory threshold shift, bilateral
    H93.249Temporary auditory threshold shift, unspecified ear
    H93.25Central auditory processing disorder
    H93.291Other abnormal auditory perceptions, right ear
    H93.292Other abnormal auditory perceptions, left ear
    H93.293Other abnormal auditory perceptions, bilateral
    H93.299Other abnormal auditory perceptions, unspecified ear
    H93.A1Pulsatile tinnitus, right ear
    1–10 of 13
    1/2
    Cerebrovascular Codes Related to Auditory/Neurologic SequelaeICD-10
    I67.2Cerebral atherosclerosis
    I67.81Acute cerebrovascular insufficiency
    I67.82Cerebral ischemia
    I67.850Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
    I67.89Other cerebrovascular disease
    I68.0Cerebral amyloid angiopathy
    Sequelae of Cerebrovascular Disease CodesICD-10
    I69.00Unspecified sequelae of nontraumatic subarachnoid hemorrhage
    I69.010Attention and concentration deficit following nontraumatic subarachnoid hemorrhage
    I69.011Memory deficit following nontraumatic subarachnoid hemorrhage
    I69.012Visuospatial deficit and spatial neglect following nontraumatic subarachnoid hemorrhage
    Screening and Encounter Z-codesICD-10
    Z01.110Encounter for hearing examination following failed hearing screening
    Z01.118Encounter for examination of ears and hearing with other abnormal findings
    Z13.40Encounter for screening for unspecified developmental delays
    Z13.41Encounter for autism screening
    Z13.42Encounter for screening for global developmental delays (milestones)
    Z13.49Encounter for screening for other developmental delays
    Z13.5Encounter for screening for eye and ear disorders
    Trauma to Ear Drum CodesICD-10
    S09.20XATraumatic rupture of unspecified ear drum, initial encounter
    S09.21XATraumatic rupture of right ear drum, initial encounter
    S09.22XATraumatic rupture of left ear drum, initial encounter
    Neonatal, Genetic, Symptom, Toxicity and Other Relevant CodesICD-10
    P11.1Other specified brain damage due to birth injury
    P11.2Unspecified brain damage due to birth injury
    Q90.0Trisomy 21, nonmosaicism (meiotic nondisjunction)
    Q90.1Trisomy 21, mosaicism (mitotic nondisjunction)
    Q90.2Trisomy 21, translocation
    Q90.9Down syndrome, unspecified
    R42Dizziness and giddiness
    R94.120Abnormal auditory function study
    T36.5X1APoisoning by aminoglycosides, accidental (unintentional), initial encounter
    T36.5X5AAdverse effect of aminoglycosides, initial encounter
    1–10 of 11
    1/2
    Medication-related Toxicity and History CodesICD-10
    T36.8X1APoisoning by other systemic antibiotics, accidental, initial encounter
    T45.1X1APoisoning by antineoplastic and immunosuppressive drugs, accidental, initial encounter
    Z92.21Personal history of antineoplastic chemotherapy
    Applicable ICD-10 Diagnosis CodesICD-10
    T36.5X3APoisoning by aminoglycosides, assault, initial encounter
    T36.5X3DPoisoning by aminoglycosides, assault, subsequent encounter
    T36.5X3SPoisoning by aminoglycosides, assault, sequela
    T36.5X4APoisoning by aminoglycosides, undetermined, initial encounter
    T36.5X4DPoisoning by aminoglycosides, undetermined, subsequent encounter
    T36.5X4SPoisoning by aminoglycosides, undetermined, sequela
    T36.5X5AAdverse effect of aminoglycosides, initial encounter
    T36.5X5DAdverse effect of aminoglycosides, subsequent encounter
    T36.5X5SAdverse effect of aminoglycosides, sequela
    T36.6X1APoisoning by rifampicins, accidental, initial encounter
    1–10 of 40
    1/4

    Provider Requirements and Prior Authorization

    Prior Authorization

    Authorization requirement — submit clinical documentation

    Providers must submit clinical documentation that the member meets the policy criteria when requesting authorization for CPT codes 92558 (screening), 92587 (limited diagnostic), and 92588 (comprehensive diagnostic).

    • Applicable CPT codes: 92558, 92587, 92588
    Prior Authorization

    Prior authorization — include an applicable ICD-10 diagnosis code

    The policy lists applicable ICD-10 diagnosis codes that may support coverage determinations for OAE services; include one of the listed ICD-10 codes on authorization requests and claims as applicable.

    • See ICD-10 lists in the policy (e.g., H90.8, H91.01–H91.03, H93.11, Z01.110, Z01.118, T36.x/T45.x series).
    Prior Authorization

    Background and Scope

    Otoacoustic emissions (OAEs) are low‑amplitude sounds generated by healthy cochlear outer hair cells in response to acoustic stimulation. OAEs are recorded with a lightweight ear‑canal probe that presents stimuli (clicks for transient‑evoked OAEs; tones for distortion‑product OAEs) and uses a microphone to average multiple responses into a repeatable waveform. OAEs assess cochlear (outer hair cell) function and are used for newborn and early‑childhood screening, for patients unable to cooperate with behavioral audiometry, for tinnitus evaluation, suspected malingering, and for monitoring cochlear damage from ototoxic medications. OAEs do not assess neural transmission and may miss auditory neuropathy; auditory brainstem response (ABR) testing may be required for definitive evaluation in some clinical contexts.

    Definitions and Test Types

    Transient evoked otoacoustic emissions (TEOAE) — definition and use in screening
    DefinitionTransient evoked otoacoustic emissions (TEOAE): OAEs generated in response to wide-band clicks recorded via an ear‑canal probe to assess cochlear (outer hair cell) function.
    Primary useUsed as a screening tool for newborns and young children and for patients unable to complete behavioral audiometry.
    Test methodA light‑weight ear canal probe presents click stimuli and a microphone records averaged responses to produce repeatable waveforms.
    Clinical contextsEmployed for newborn/early‑childhood hearing screening, evaluation of tinnitus, suspected malingering, and monitoring cochlear damage from ototoxic drugs.
    LimitationsTEOAEs assess cochlear function but do not evaluate neural transmission and can miss auditory neuropathy; ABR may be required for definitive testing.
    Policy Summary
    PayerEmblemHealth
    PolicyOtoacoustic Emissions Testing
    Policy CodePolicy MG.MM.ME.33bC2
    Change TypeNo material changes
    Effective Date
    Last ReviewApr 11, 2025
    Next Review DateApr 11, 2025
    Key ActionProviders must submit clinical documentation that the member meets the policy criteria when requesting authorization for CPT codes 92558, 92587, and 92588.
    SourceLink
    On This Page
    Coverage Criteria for OAE Screening and Diagnostic TestingProcedure and Diagnosis CodesProvider Requirements and Prior AuthorizationBackground and ScopeDefinitions and Test Types
    Diagnostic indications (CPT 92587, 92588): Individuals with auditory neuropathy spectrum disorder (ANSD) or auditory processing disorder (APD).

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Individuals with known or suspected sensorineural hearing loss.

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Individuals with abnormal auditory function studies or a failed hearing exam.

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Individuals suspected of feigning hearing loss.

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Diagnostic indications (CPT 92587, 92588): Monitoring of ototoxicity before, during, and after administration of agents known to be ototoxic (for example, aminoglycosides or chemotherapy agents).

    Use CPT 92587 for limited evaluation and CPT 92588 for comprehensive diagnostic evaluation

    Use an appropriate listed ICD-10 diagnosis code

    When prior authorization is required, use an appropriate ICD-10 diagnosis code from the policy’s listed codes to support medical necessity for the requested OAE testing.

    • Examples include hearing loss/ototoxicity codes (H91.x), screening/follow-up Z-codes (Z01.110, Z01.118), and toxicity/history codes (T36.5X5A, Z92.21).
    Step Therapy

    Screening protocol note — OAE then ABR for failures

    Newborn hearing screening programs commonly use a one-step or two-step validated protocol, frequently involving OAE followed by ABR for those who fail the first test.

    • Ensure protocols for follow-up evaluation and screening before one month of age; infants who fail should have audiologic and medical evaluation before 3 months of age.
    Note

    No additional provider actions specified in these sections

    No specific provider action is labeled in this portion of the policy beyond the requirements to submit documentation and appropriate diagnosis codes; include encounter and diagnosis codes as applicable on requests and claims.

    • If no prior authorization text applies, rely on listed ICD-10 codes to document medical necessity.
    Note

    No further provider actions specified here

    No additional specific provider actions were specified in these chunks; follow the authorization and documentation requirements already stated in the policy when submitting requests.

    • Include relevant diagnosis and history codes from the lists when applicable.
    Documentation Required

    Submit clinical evidence from treating physician or PCP

    The treating physician or primary care provider must submit clinical evidence demonstrating the member meets the policy criteria for the requested OAE service to enable preauthorization or post-payment review.

    • Clinical evidence should document the indication (e.g., failed newborn screen, developmental concerns, ototoxic exposure) that meets the policy criteria.
    Documentation Required

    Encounter and screening diagnosis codes — listed for support

    Encounter and screening diagnosis codes that would support documentation for screening and follow-up are listed in the policy but specific encounter-only requirements are not otherwise specified in these chunks.

    • Relevant Z-codes include Z01.110 (hearing exam following failed screening), Z01.118 (exam of ears/hearing with abnormal findings), Z13.4x/Z13.5 series.
    Documentation Required

    Include encounter and history diagnosis codes (Z-codes)

    Include relevant encounter and history diagnosis codes on authorization requests and claims where applicable, for example Z01.110, Z01.118, and Z92.21 to support the clinical context.

    • Z01.110 — Encounter for hearing exam following failed screening
    • Z01.118 — Encounter for exam of ears/hearing with other abnormal findings
    • Z92.21 — Personal history of antineoplastic chemotherapy
    Denial Risk

    Documentation requirement — submit required clinical evidence

    Failure to submit the clinical evidence that the member meets the policy criteria will prevent EmblemHealth from properly reviewing the preauthorization or post-payment request.

    • Ensure documentation clearly demonstrates the covered indication per the policy (e.g., neonatal screen failure, ototoxicity monitoring).
    Denial Risk

    No additional denial triggers specified here

    No specific denial triggers beyond documentation and coding requirements are specified in these chunks; denial triggers are not present in this document portion.

    • Continue to follow the policy documentation and coding guidance to avoid denial risk.
    Denial Risk

    Diagnosis code documentation risk — include a listed ICD-10 code

    Claims or authorization requests that lack an applicable ICD-10 diagnosis code from the policy’s listed codes (for example, hearing screening follow-up, ototoxicity, or exposure/toxicity codes) may be at risk for denial if documentation does not support medical necessity.

    • Verify that the claim/authorization includes a diagnosis from the policy lists (e.g., H91.x series, H90.A21–A22, T36.5X5A, Z01.110).
    Distortion product otoacoustic emissions (DPOAE) — definition and use for diagnostic evaluation
    DefinitionDistortion product otoacoustic emissions (DPOAE): OAEs produced in response to tones (two simultaneous pure‑tone stimuli) recorded via an ear‑canal probe to evaluate cochlear (outer hair cell) function.
    Primary useUsed for diagnostic evaluation of cochlear function, including limited (92587) and comprehensive (92588) otoacoustic emission testing.
    Test methodTone‑pair stimuli are presented through a probe and resulting emissions are recorded and averaged to generate frequency‑specific responses.
    Clinical contextsApplied when more frequency‑specific diagnostic information is needed (e.g., suspected sensorineural loss, ototoxicity monitoring, cases where audiometry is not feasible).
    LimitationsLike other OAEs, DPOAEs do not assess neural pathways and may miss neural auditory disorders; ABR may be necessary for comprehensive evaluation.
    Hearing loss and related auditory disorder diagnosis codes (examples)
    Examples (mixed and conductive/sensorineural)H90.8 — Mixed conductive and sensorineural hearing loss, unspecified.
    Conductive and sensorineural subtypesH90.A11, H90.A12, H90.A21, H90.A22, H90.A31, H90.A32 — Unilateral and mixed hearing loss subcategories.
    Ototoxic and sudden lossH91.01–H91.03, H91.09, H91.20–H91.23 — Ototoxic hearing loss and sudden idiopathic hearing loss codes.
    Other specified hearing lossH91.8X1–H91.8X9 — Other specified hearing loss (right, left, bilateral, unspecified).
    Auditory/vestibular perceptionsH93.011–H93.019, H93.11–H93.19 — Transient ischemic deafness and tinnitus codes.
    Screening/encounter and history codes relevant to hearing screening and follow-up
    Encounter for failed screeningZ01.110 — Encounter for hearing examination following failed hearing screening.
    Encounter with abnormal findingsZ01.118 — Encounter for examination of ears and hearing with other abnormal findings.
    Developmental screening seriesZ13.40–Z13.49 — Encounters for screening for developmental delays (unspecified, autism, global, other).
    Screening for eye/ear disordersZ13.5 — Encounter for screening for eye and ear disorders.
    History of chemotherapyZ92.21 — Personal history of antineoplastic chemotherapy (relevant for ototoxicity monitoring).
    Ototoxicity monitoring — definition describing systematic audiologic surveillance for patients exposed to ototoxic medications
    DefinitionOtotoxicity monitoring: systematic audiologic surveillance of patients exposed to ototoxic medications to detect early cochlear dysfunction.
    PurposeDetect early changes in cochlear (outer hair cell) function to allow intervention (medication adjustment or alternative therapies) to limit permanent hearing loss.
    Methods usedMonitoring commonly uses OAEs (DPOAE/TEOAE) and/or audiometry; OAEs are useful when behavioral audiometry is not feasible.
    Relevant guidanceProfessional guidance on ototoxicity monitoring is provided by the American Academy of Audiology (Ototoxicity Monitoring, 2009).
    Clinical applicationApplicable for patients receiving known ototoxic agents (e.g., aminoglycosides, antineoplastic drugs) and documented using appropriate ICD‑10 toxicity/history codes.