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    v1.0.30
    OpenPayerPolicy UpdatesSleep MedicineArizona Complete Health PSG Policy Update Prior Au…
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    ModifiedArizona Complete HealthPolicy CP.MP.248

    Facility-based Sleep Studies for Obstructive Sleep Apnea

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    Medical necessity criteria for facility-based polysomnography (PSG), split-night studies, and facility-based CPAP/BiPAP titration (including hypoglossal nerve stimulation titration) for adult members/enrollees, applicable to non-Medicare Arizona Complete Health plans.

    Policy Summary
    PayerArizona Complete Health
    PolicyFacility-based Sleep Studies for Obstructive Sleep Apnea
    Policy CodePolicy CP.MP.248
    Change TypeCriteria additions and clarifications (HNS titration addedHSAT exceptions expandedactigraphy excluded)
    Effective Date
    Last ReviewOct 25, 2025
    Next Review Date
    Key ActionObtain prior authorization for facility-based PSG/titration (CPT 95807–95811) and document why HSAT is inappropriate when applicable.
    SourceLink
    POLICY UPDATE CHANGES

    Added criteria section IV for titration PSG for hypoglossal nerve stimulation (HNS).

    Expanded scope to explicitly include split-night studies and clarified facility-based titration criteria.

    Added specific situations where HSAT is not appropriate (e.g., chronic opioid use, mission-critical workers, BMI ≥50, moderate-severe chronic pulmonary disease, NYHA class III/IV).

    Specified that actigraphy testing alone is insufficient to diagnose OSA.

    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.

    ≥18age threshold for adult criteria
    ≥50BMI threshold
    3-6 moHNS titration timing
    ≤2max studies/yr
    95807-95811covered CPTs
    95803not covered code

    Coverage and Medical Necessity Criteria

    Initial Therapy

    Covered when ALL of the following are met:

    Initial PSG or split-night study (age): Member/enrollee is ≥ 18 years of age
    Suspected condition: Member/enrollee has suspected obstructive sleep apnea (OSA)

    HSAT not appropriate — any one qualifies

    • Availability/ability: Portable/HSAT services not available OR member unable to properly operate/tolerate home study equipment and no assistant available
    • Prior HSAT: Previous HSAT results are negative or inadequate for diagnosis OR inadequate for autotitration of APAP
    • Clinical risk factors: Chronic opioid use; low pretest probability (e.g., BMI <30, Mallampati 1–2, no snoring, normal neck circumference); mission-critical worker; BMI ≥50 kg/m2; documentation of moderate–severe chronic pulmonary disease; congestive heart failure NYHA class III/IV; history of ventricular fibrillation or sustained ventricular tachycardia; significant neurologic/neuromuscular disease; concern for non-respiratory sleep disorder(s) that interfere with HSAT; hypoventilation syndrome

    Repeat Therapy

    Covered when ALL of the following are met:

    Repeat study prerequisites: All criteria in section I.B are met
    Frequency limit: The requested study and any previous studies amount to two or less per rolling year≤2 per rolling year

    Acceptable reasons for repeat

    • Oral appliance has been adjusted for fit and requires assessment of efficacy
    • Change of device due to intolerance of current device
    • Assessment of whether PAP settings need change (including continued symptoms despite adherent use: ≥4 hours/night for 70% of nights over a 30-day period)

    Titration PSG

    Facility-based titration is medically necessary when one of the following is met:

    Titration option A: Meets criteria in section I for facility-based sleep study and has not attempted a home-based study for titration of APAP
    Titration option B: Diagnosed with OSA during HSAT and there is evidence or documentation of failure of an APAP trial (e.g., downloaded compliance data)

    HNS Titration

    Covered when the following is met:

    HNS titration timing: Facility-based titration PSG for hypoglossal nerve stimulation is conducted three to six months after device implantation3-6 months

    Used to calibrate stimulation strength for efficacy and comfort.

    Unsupported Tests

    Actigraphy: Insufficient evidence to support the use of actigraphy testing alone for diagnosis of OSA

    CPT 95803 listed as not supporting coverage.

    Criteria revisions and additions

    Policy criteria were revised in multiple subitems (I.B. series) and new items added; titration PSG for HNS added to Criteria IV.

    Revisions and additions: Multiple criteria items were updated or added: I.B.8.a.vi (Hypoventilation syndrome) added; I.B.8.a.v wording expanded to include disorders that interfere with HSAT (e.g., parasomnias); I.B.8.b revisions (removal of Epworth Sleepiness Scale criteria and addition of habitual loud snoring and diagnosis of hypertension); Criteria II and III added/clarified for repeat studies and titration; Criteria IV added to include titration PSG for HNS; 'non-Medicare' verbiage added in Criteria V for clarification.

    Full logical criteria details and minor wording changes summarized from revisions noted in the policy history.

    The policy specifies that actigraphy testing alone (CPT 95803) is not supported for the diagnosis of obstructive sleep apnea. The document states there is insufficient evidence to support actigraphy as a standalone diagnostic modality for OSA because its effectiveness has not been established and the measure does not replace facility-based polysomnography or validated HSAT modalities.

    The policy notes that there are CPT codes that do not support coverage and excludes those procedures from payment; specific codes referenced in the full policy are documented elsewhere in the coding section. Providers should consult the coding table in this policy for the exact list of excluded CPT codes when preparing prior authorization requests.

    Facility-based polysomnography may be considered not medically necessary when a validated home sleep apnea test (HSAT) is appropriate and available. HSAT is an alternative for adult patients with a high pretest probability of uncomplicated moderate-to-severe OSA and no significant comorbid cardiorespiratory disease or suspected non‑respiratory sleep disorders (for example, no concern for narcolepsy, significant pulmonary disease, or complex sleep disorders). In such situations, HSAT is an accepted diagnostic option and facility PSG may be denied if HSAT would adequately address the clinical question.

    The policy indicates that certain procedures/CPT codes are designated as not medically necessary (NMN) and therefore do not support coverage under the policy. Specific NMN conditions and the exact codes referenced are provided in the policy's coding and exclusions sections and should be reviewed when determining coverage and submitting authorizations.

    Relevant CPT Codes and Limits

    Covered CPT CodesCPTCovered
    95807Sleep study, simultaneous recording of ventilation, respiratory effort, ECG or heart rate, and oxygen saturation, attended by a technologist.
    95808Polysomnography; any age, sleep staging with 1-3 additional parameters of sleep, attended by a technologist.
    95810Polysomnography; age 6 years or older, sleep staging with 4 or more additional parameters of sleep, attended by a technologist.
    95811Polysomnography; age 6 years or older, sleep staging with 4 or more additional parameters of sleep, with initiation of continuous positive airway pressure therapy or bilevel ventilation, attended by a technologist.
    CPT codes that do not support coverageCPTNot Covered
    95803Actigraphy testing, recording, analysis, interpretation, and report (minimum of 72 hours to 14 consecutive days of recording).
    CPT codes referencedmixed
    CPT codes that do not support coverageDocument notes existence of CPT codes that do not support coverage (specific codes not listed in provided chunks).
    affected codesPlaceholder reference to codes affected by inclusion of titration PSG for HNS.
    Titration PSG for HNS (referenced)mixed
    affected codesCodes referenced in association with inclusion of titration polysomnography for hypoglossal nerve stimulation (HNS); specific CPT codes not enumerated in these chunks.
    Maximum facility-based studies per rolling year (repeat studies)
    Maximum facility-based studies per rolling yearThe requested study and any previous studies must amount to two or less per rolling year (≤ 2)
    Repeat study prerequisitesAll criteria in section I.B (initial PSG criteria) must be met before a repeat study is considered
    Acceptable reasons for repeatExamples include oral appliance adjustment, device change for intolerance, reassessment of PAP settings despite adherence, significant weight change (≥10%), postoperative assessment after airway surgery, re-establishing diagnosis if remote history, or new/worsening symptoms after prior negative study
    BMI threshold indicating facility testing
    BMI threshold indicating facility testingMember/enrollee has a BMI of ≥ 50 kg/m2

    Prior Authorization, Documentation, and Denial Risks

    Prior Authorization

    Prior authorization required for facility-based PSG and titration

    Facility-based initial PSG, split-night, and titration studies (CPT 95807, 95808, 95810, 95811) require prior authorization and must meet the policy's medical necessity criteria (suspected OSA and reasons HSAT is not appropriate or other listed indications).

    • Applicable procedure codes: 95807, 95808, 95810, 95811
    Prior Authorization

    Include HNS titration PSG in prior authorization requests

    Titration polysomnography (PSG) for hypoglossal nerve stimulation (HNS) is included in the policy and is subject to the same prior authorization expectations as other facility-based titration PSGs.

    • HNS titration must be requested and authorized as a facility-based titration PSG (see Criteria IV).

    Clinical Background

    Obstructive sleep apnea (OSA) is characterized by repeated upper airway collapse during sleep that leads to intermittent hypoxemia, sleep fragmentation and resultant daytime sleepiness as well as a range of cardiopulmonary consequences. Polysomnography (PSG) is the diagnostic gold standard because it continuously measures multiple physiologic variables (including respiratory flow, respiratory effort, oximetry and ventilation) to establish diagnosis and guide therapy, including positive airway pressure titration. Home sleep apnea testing (HSAT) can be an appropriate alternative in selected high–pretest‑probability adults without significant comorbidities, but HSAT measures fewer variables and may miss mild or complex sleep disorders.

    Key Definitions

    PSG — Polysomnography definition
    DefinitionPolysomnography (PSG) is the continuous and concurrent monitoring and recording of various physiological and pathophysiological parameters of sleep that includes physician evaluation, interpretation and dissemination
    PurposePerformed to diagnose sleep disorders and evaluate response to treatments such as CPAP; used for diagnosis, PAP titration, and assessment of other sleep disorders
    FormatsConducted as full-night or split-night studies; split-night allows diagnosis and immediate PAP titration the same night
    HSAT — Home sleep apnea testing (type 3/4 devices)
    DefinitionHome sleep apnea testing (HSAT) refers to portable sleep monitoring devices used at home, commonly classified as type 3 or type 4 devices
    Device preference

    Policy Updates and Review Cycle

    01/24revision

    Multiple criteria updates including adding 'Hypoventilation syndrome' (I.B.8.a.vi), wording changes to I.B.8.b.ii and other clarifications; references reviewed and updated; annual review.

    10/24revision

    Minor rewording and addition of hypertension diagnosis to I.B.8.b.ii.c; annual review and description updated to include titration polysomnography (PSG) for hypoglossal nerve stimulation (HNS).

    10/25revision
    Policy Summary
    PayerArizona Complete Health
    PolicyFacility-based Sleep Studies for Obstructive Sleep Apnea
    Policy CodePolicy CP.MP.248
    Change TypeCriteria additions and clarifications (HNS titration addedHSAT exceptions expandedactigraphy excluded)
    Effective Date
    Last ReviewOct 25, 2025
    Next Review Date
    Key ActionObtain prior authorization for facility-based PSG/titration (CPT 95807–95811) and document why HSAT is inappropriate when applicable.
    SourceLink
    On This Page
    Coverage and Medical Necessity CriteriaRelevant CPT Codes and LimitsPrior Authorization, Documentation, and Denial RisksClinical BackgroundKey DefinitionsPolicy Updates and Review Cycle
  1. Significant weight loss (≥10%) in a member using PAP to determine if it can be discontinued
  2. Significant weight gain (≥10%) or recurrent symptoms to inform whether PAP should be reinstituted
  3. Postoperative assessment of efficacy after upper airway surgery for OSA
  4. Remote history of OSA not on PAP needing re-establishment of diagnosis and/or initiation of CPAP
  5. New signs or symptoms after prior negative study suggesting OSA (e.g., weight gain with symptoms, new nocturia)
  6. Signs, symptoms and strong clinical suspicion of OSA with a negative study at least six months prior
  7. Use in triageBMI ≥50 is listed as one of the indications making HSAT not appropriate and supporting facility-based PSG
    Applies to initial studiesIncluded among criteria for initial facility-based PSG or split-night study for adults ≥18 years
    Step Therapy

    Require documentation of failed APAP trial for titration after HSAT

    When OSA is diagnosed by HSAT, facility-based titration is medically necessary only if there is documentation of failure of an APAP trial (for example, downloaded compliance data), or if the member meets criteria for a facility-based study and has not attempted a home-based titration.

    • Acceptable justification: evidence/documentation of failed APAP trial (e.g., downloaded compliance data).
    • Alternative pathway: no prior home-based APAP titration attempted and meets facility-based PSG criteria.
    Note

    Operational detail: specify study type and indication on requests

    Ensure prior authorization requests clearly state the specific CPT code and indication (initial PSG, split-night, titration, or HNS titration) and reference the member’s age and suspected OSA status to expedite review.

    • State whether HSAT was attempted and results (if applicable).
    • Include which type of facility study is requested (initial, split-night, titration, HNS titration).
    Documentation Required

    Required documentation to support facility-based PSG requests

    Document suspected OSA and one or more reasons why HSAT is not appropriate (examples include HSAT services unavailable; inability to operate/tolerate equipment; prior HSAT negative or inadequate; chronic opioid use; mission-critical worker; BMI ≥ 50 kg/m2; listed comorbid risks). For repeat studies, document that the requested study plus any prior studies total two or fewer per rolling year and include the specific repeat-study justification (e.g., device adjustment, device change for intolerance, failed APAP trial, significant weight change, postoperative assessment).

    • List the specific HSAT-inappropriateness reason(s) from policy I.B.1–9.
    • For repeats, confirm total studies ≤ 2 per rolling year and cite the repeat criterion met (see II.C.1–9).
    Documentation Required

    Incorporate new documentation items from recent criteria revisions

    Policy revisions added explicit documentation expectations in I.B.8.a (including documentation for conditions such as hypoventilation syndrome) and other clarifying language; include any newly added supporting documentation (e.g., for hypoventilation syndrome) when applicable to the request.

    • If relying on newly added indications (e.g., hypoventilation syndrome), include supporting clinical documentation as described in the updated criteria.
    Denial Risk

    Denial risk: HSAT appropriateness and repeat-study frequency limits

    Requests may be denied if HSAT is appropriate and available for the member, or if the requested repeat studies exceed two per rolling year without meeting the policy’s repeat-study criteria.

    • Confirm HSAT is inappropriate per I.B. reasons before requesting facility PSG.
    • For repeat requests, demonstrate the requested study plus prior studies are ≤ 2 per rolling year and that one of II.C.1–9 applies.
    Billing Rule

    Provider alert: CPT codes that do not support coverage (actigraphy)

    Actigraphy (CPT 95803) is listed as not supporting coverage; include supported CPT codes (95807, 95808, 95810, 95811) in requests and avoid using CPT 95803 as the diagnostic basis for OSA.

    • Do not submit actigraphy (CPT 95803) alone to support diagnosis of OSA.
    • Use supported facility PSG codes (95807–95811) when requesting facility-based studies.
    Type 3 devices are preferred over type 4 because they measure more variables (four to seven vs. one to three)
    Appropriate useHSAT may be appropriate for select patients with high pretest probability of uncomplicated moderate-to-severe OSA and no significant comorbidities or suspected non‑respiratory sleep disorders
    Hypoventilation syndrome — referenced indication
    Reference in criteriaHypoventilation syndrome was added as an indication in the policy (I.B.8.a.vi) as a reason HSAT may be inappropriate
    ContextListed among clinical risk factors and conditions that support facility-based PSG rather than HSAT
    Implication for testingPresence of hypoventilation syndrome supports using facility-based PSG for comprehensive monitoring
    Titration PSG for HNS — description
    Definition/descriptionTitration PSG for hypoglossal nerve stimulation (HNS) is a facility-based polysomnography performed to calibrate HNS device stimulation strength for efficacy and comfort
    TimingPolicy specifies HNS titration PSG is conducted three to six months after device implantation
    Policy inclusionTitration PSG for HNS has been added to policy Criteria IV and is part of the medical necessity requirements for facility-based PSG/titration
    Latest

    Added Criteria IV to include titration PSG for HNS, added 'non‑Medicare' clarification in Criteria V, updated background and coding descriptions; annual review and approval.