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    v1.0.30
    OpenPayerPolicy UpdatesPain ManagementCigna Peripheral Nerve Destruction Coverage | Open…
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    ModifiedCignaPolicy 0525

    Peripheral Nerve Destruction for Pain Conditions

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    This policy governs coverage consideration for percutaneous cryoablation and other peripheral nerve ablation techniques used to manage pain conditions, including headache, occipital neuralgia, joint pain, and neuropathic or nerve entrapment syndromes. It applies to health benefit plans administered by Cigna Companies, subject to the applicable benefit plan and specific clinical circumstances.

    Policy Summary
    PayerCigna
    PolicyPeripheral Nerve Destruction for Pain Conditions
    Policy CodePolicy 0525
    Change TypeModified
    Effective DateNov 1, 2026
    Next Review DateFeb 15, 2027
    Key ActionPerform a diagnostic occipital nerve block before radiofrequency neurotomy and exclude alternative etiologies.
    SourceLink
    POLICY UPDATE CHANGES

    The policy statement for peripheral nerve destruction for trigeminal neuralgia was removed during the annual review dated 2/15/2026.

    The policy statement for percutaneous cryoablation was revised during the annual review dated 2/15/2026.

    A policy statement for pulsed radiofrequency ablation was added during the annual review dated 2/15/2026.

    Focused reviews dated 11/01/2026 and 9/15/2026 reported no policy statement changes.

    48Document pages
    5Ablation modalities
    9Not-covered pain regions or conditions
    3Material policy changes
    5Not-covered procedure codes

    Coverage Criteria

    Ablative treatments considered not medically necessary

    Considered not medically necessary when used for treatment of pain conditions:

    Specified ablative treatments: Percutaneous cryoablation or pulsed radiofrequency ablation of peripheral or truncal nerves

    Excluded pain conditions

    Not covered or reimbursable when used for treatment of any of the following pain conditions:

    Excluded conditions: Sacroiliac joint pain; knee pain; hip pain; shoulder pain; foot or heel pain; headache; occipital neuralgia; intercostal neuralgia; or extremity pain resulting from complex regional pain syndrome, peripheral nerve entrapment or compression, including carpal or tarsal tunnel syndrome or sciatica, or peripheral neuropathy

    Peripheral nerve destruction using cryoablation, laser, electrical, chemical, or radiofrequency ablation is excluded for these indications.

    Not Covered Diagnosis Indications

    Not covered or reimbursable when used for treatment of pain conditions associated with the listed diagnosis codes.

    Listed diagnosis indication: The pain condition is associated with one or more diagnosis codes identified in the Not Covered or Reimbursable section.

    Peripheral nerve destruction is not covered or reimbursable for these indications.

    Cervicogenic headache or occipital neuralgia

    Evidence is insufficient.

    Cervicogenic headache or occipital neuralgia: Peripheral nerve ablation using any method for cervicogenic headache and/or occipital neuralgia

    Published medical literature is insufficient to demonstrate safety and efficacy.

    Intercostal neuralgia

    Evidence is insufficient.

    Intercostal neuralgia: Peripheral nerve ablation using any method for intercostal neuralgia

    Published medical literature is insufficient to demonstrate safety and efficacy.

    Shoulder pain

    Evidence is insufficient.

    Shoulder pain: Peripheral nerve ablation for the treatment of shoulder pain

    Published medical literature is insufficient to demonstrate safety and efficacy.

    Sacroiliac and lumbar-related pain

    Evidence conclusion for sacroiliac and lumbar-related pain:

    Insufficient evidence: The clinical effectiveness and duration of sacroiliac joint nerve ablation have not been consistently demonstrated in well-designed studies.

    Evidence is insufficient to demonstrate safety and efficacy of sacroiliac joint radiofrequency ablation, lumbar or sacral dorsal rami ablation, and other ablative modalities such as laser, chemical, or electrical techniques for sacroiliac joint and similar lumbar-related pain.

    Hip pain

    Evidence conclusion for hip pain:

    Insufficient evidence: Published medical literature is insufficient to demonstrate the safety and effectiveness of peripheral nerve ablation, using any method, for treatment of hip pain.

    Although some professional guidance permits consideration after benefit from diagnostic nerve blocks, the policy evidence conclusion remains insufficient.

    Knee osteoarthritis

    Evidence conclusion for knee osteoarthritis:

    Routine use not supported: Current evidence does not support routine use of radiofrequency ablation or related minimally invasive interventions for knee osteoarthritis.

    The cited review recommends against routine use until more robust data are available.

    Peripheral neuroma

    Peripheral neuroma ablation is not supported as an established treatment.

    Peripheral neuroma: Evidence is insufficient to support the safety and efficacy of neuroablative treatment for a peripheral neuroma, such as Morton's neuroma; alcohol injections and radiofrequency ablation should be considered research treatments until further study clarifies efficacy.

    Foot pain

    Peripheral nerve ablation for foot pain is not supported.

    Foot pain: There is insufficient evidence in the published medical literature to demonstrate the safety and effectiveness of peripheral nerve ablation, using any method, for treatment of foot pain.

    Other pain conditions

    Peripheral nerve destruction is not supported for the listed other pain conditions.

    Other pain-related conditions: Evidence is insufficient to support the safety and efficacy of peripheral nerve destruction for chronic regional pain syndrome, chronic thoracic pain, craniofacial pain syndromes, pudendal neuralgia, peripheral nerve compression or entrapment conditions, peripheral neuropathic conditions, post-amputation pain, post-inguinal-herniorrhaphy pain, and oncologic pain.

    Other Pain Related Conditions

    Evidence is insufficient to support safety and efficacy.

    Other pain conditions: Peripheral nerve destruction is being considered for chronic regional pain syndrome, chronic thoracic pain, craniofacial pain syndromes, pudendal neuralgia, peripheral nerve compression or entrapment conditions, peripheral neuropathic conditions, post-amputation pain, post-inguinal-herniorrhaphy pain, or oncologic pain.

    The policy states that evidence is insufficient to support safety and efficacy for these conditions.

    Coverage consideration for peripheral nerve destruction depends on the specific ablative technique, the nerve or nerve branch treated, and the pain condition or diagnosis. The policy identifies percutaneous cryoablation and pulsed radiofrequency ablation as not medically necessary for pain treatment and excludes peripheral nerve destruction using cryoablation, laser, electrical, chemical, or radiofrequency ablation for specified pain conditions.

    Percutaneous cryoablation and pulsed radiofrequency ablation of peripheral or truncal nerves are considered not medically necessary when used to treat pain conditions.

    The policy lists ICD-10-CM diagnoses that are not covered or reimbursable when associated with pain treatment by peripheral nerve destruction. The exclusions include infectious and inflammatory arthropathies, rheumatoid and juvenile arthritis, traumatic and degenerative joint conditions, osteoarthritis, joint derangements, instability, shoulder conditions, spinal and musculoskeletal pain, regional soft-tissue disorders, headache, nerve-related conditions, injuries, sprains, strains, and prosthetic-joint diagnoses.

    Peripheral nerve destruction is not covered or reimbursable when used for a pain condition associated with any diagnosis code listed in the policy’s Not Covered or Reimbursable section. The applicable diagnosis lists include numerous ICD-10-CM codes spanning arthropathies, osteoarthritis, joint and spinal disorders, shoulder, hip, knee, ankle, foot, headache, neuropathic, injury, and prosthetic-joint conditions.

    The evidence is insufficient to demonstrate the safety and efficacy of sacroiliac joint radiofrequency ablation or ablation of the lumbar or sacral dorsal rami for sacroiliac joint and other lumbar-related pain. The clinical effectiveness and duration of benefit have not been consistently demonstrated in well-designed studies; evidence is also insufficient for laser, chemical, and electrical techniques in similar indications.

    Although limited professional guidance describes hip radiofrequency neurotomy after benefit from diagnostic nerve blocks, the policy concludes that published medical literature is insufficient to demonstrate the safety and effectiveness of peripheral nerve ablation, using any method, for hip pain.

    Published medical literature is insufficient to demonstrate the safety and effectiveness of peripheral nerve ablation, using any method, for foot pain. The policy also notes caution regarding cryoablation, radiofrequency ablation, and alcohol injections for peripheral neuromas and identifies further research needs.

    Evidence is insufficient to support the safety and efficacy of peripheral nerve destruction for chronic regional pain syndrome, chronic thoracic pain, craniofacial pain syndromes, pudendal neuralgia, peripheral nerve compression or entrapment, peripheral neuropathic conditions, post-amputation pain, post-inguinal-herniorrhaphy pain, and oncologic pain.

    Percutaneous cryoablation of peripheral or truncal nerves is considered not medically necessary for treatment of pain conditions.

    Pulsed radiofrequency ablation of peripheral or truncal nerves is considered not medically necessary for treatment of pain conditions.

    The published literature is insufficient to demonstrate the safety and efficacy of peripheral nerve ablation, using any method, for cervicogenic headache and/or occipital neuralgia. The cited headache guideline also found insufficient evidence to recommend for or against pulsed radiofrequency treatment of the upper cervical nerves for chronic migraine.

    The published literature is insufficient to demonstrate the safety and efficacy of peripheral nerve ablation, using any method, for intercostal neuralgia. Neuroablative procedures should generally be reserved for patients who have not obtained adequate relief from conservative or less invasive therapies.

    The published literature is insufficient to demonstrate the safety and efficacy of peripheral nerve ablation for shoulder pain. In the cited study, intra-articular corticosteroid injection produced greater pain reduction and range-of-motion improvement than pulsed radiofrequency ablation, although the evidence was limited by methodological and follow-up limitations.

    Coding and Code Sets

    Considered Not Medically Necessary CPT and HCPCS CodesmixedNot Covered
    64999Unlisted procedure, nervous system
    0440TAblation, percutaneous, cryoablation, includes imaging guidance; upper extremity distal/peripheral nerve
    0441TAblation, percutaneous, cryoablation, includes imaging guidance; lower extremity distal/peripheral nerve
    0442TAblation, percutaneous, cryoablation, includes imaging guidance; nerve plexus or other truncal nerve (eg, brachial plexus, pudendal nerve)
    C9808Nerve cryoablation probe (e.g., cryoICE, cryoSPHERE, cryoSPHERE MAX, cryoICE cryosphere, cryoICE cryo2), including probe and all disposable system components, non-opioid medical device (must be a qualifying Medicare non-opioid medical device for post-surgical pain relief in accordance with Section 4135 of the CAA, 2023)
    C9809Cryoablation needle (e.g., iovera system), including needle/tip and all disposable system components, non-opioid medical device (must be a qualifying Medicare non-opioid medical device for post-surgical pain relief in accordance with Section 4135 of the CAA, 2023)
    Not Covered or Reimbursable CPT CodesCPTNot Covered
    64620Destruction by neurolytic agent, intercostal nerve
    64624Destruction by neurolytic agent, genicular nerve branches including imaging guidance, when performed
    64632Destruction by neurolytic agent; plantar common digital nerve
    64640Destruction by neurolytic agent; other peripheral nerve or branch
    1096TInjection(s) of thermoregulated multiphase suspension to demyelinate nerves innervating the knee joint, including imaging guidance, when performed
    Not Covered or Reimbursable ICD-10-CM Diagnosis CodesICD-10Not Covered
    G43.001Migraine without aura, not intractable, with status migrainosus
    G43.009Migraine without aura, not intractable, without status migrainosus
    G43.011Migraine without aura, intractable, with status migrainosus
    G43.019Migraine without aura, intractable, without status migrainosus
    G43.101Migraine with aura, not intractable, with status migrainosus
    G43.109Migraine with aura, not intractable, without status migrainosus
    G43.111Migraine with aura, intractable, with status migrainosus
    G43.119Migraine with aura, intractable, without status migrainosus
    G43.401Hemiplegic migraine, not intractable, with status migrainosus
    G43.409Hemiplegic migraine, not intractable, without status migrainosus
    1–10 of 89
    1/9
    Not Covered or Reimbursable — infectious and reactive shoulder arthropathiesICD-10Not Covered
    M00.011Staphylococcal arthritis, right shoulder
    M00.012Staphylococcal arthritis, left shoulder
    M00.019Staphylococcal arthritis, unspecified shoulder
    M00.111Pneumococcal arthritis, right shoulder
    M00.112Pneumococcal arthritis, left shoulder
    M00.119Pneumococcal arthritis, unspecified shoulder
    M02.811Other reactive arthropathies, right shoulder
    M02.812Other reactive arthropathies, left shoulder
    M02.819Other reactive arthropathies, unspecified shoulder
    M05.111Rheumatoid lung disease with rheumatoid arthritis of right shoulder
    Not Covered or Reimbursable — rheumatoid arthritis with systemic manifestationsICD-10Not Covered
    M05.112Rheumatoid lung disease with rheumatoid arthritis of left shoulder
    M05.119Rheumatoid lung disease with rheumatoid arthritis of unspecified shoulder
    M05.151Rheumatoid lung disease with rheumatoid arthritis of right hip
    M05.152Rheumatoid lung disease with rheumatoid arthritis of left hip
    M05.159Rheumatoid lung disease with rheumatoid arthritis of unspecified hip
    M05.161Rheumatoid lung disease with rheumatoid arthritis of right knee
    M05.162Rheumatoid lung disease with rheumatoid arthritis of left knee
    M05.169Rheumatoid lung disease with rheumatoid arthritis of unspecified knee
    M05.171Rheumatoid lung disease with rheumatoid arthritis of right ankle and foot
    M05.172Rheumatoid lung disease with rheumatoid arthritis of left ankle and foot
    1–10 of 47
    1/5
    Not Covered or Reimbursable — rheumatoid arthritis and rheumatoid-factor diagnosesICD-10Not Covered
    M05.50-Rheumatoid polyneuropathy with rheumatoid arthritis
    M05.59Rheumatoid polyneuropathy with rheumatoid arthritis
    M05.611Rheumatoid arthritis of right shoulder with involvement of other organs and systems
    M05.612Rheumatoid arthritis of left shoulder with involvement of other organs and systems
    M05.619Rheumatoid arthritis of unspecified shoulder with involvement of other organs and systems
    M05.651Rheumatoid arthritis of right hip with involvement of other organs and systems
    M05.652Rheumatoid arthritis of left hip with involvement of other organs and systems
    M05.659Rheumatoid arthritis of unspecified hip with involvement of other organs and systems
    M05.661Rheumatoid arthritis of right knee with involvement of other organs and systems
    M05.662Rheumatoid arthritis of left knee with involvement of other organs and systems
    1–10 of 49
    1/5
    Not Covered or Reimbursable — juvenile, traumatic, specified, monoarticular, Charcot, and other arthropathiesICD-10Not Covered
    No codes listed
    Not Covered or Reimbursable — hip, knee, shoulder, and ankle/foot osteoarthritisICD-10Not Covered
    No codes listed
    Not Covered or Reimbursable — joint derangements, instability, and shoulder painICD-10Not Covered
    No codes listed
    Not Covered or Reimbursable Diagnosis Codes—musculoskeletal and spinal pain conditionsICD-10Not Covered
    No codes listed
    Not Covered or Reimbursable Diagnosis Codes—regional soft-tissue, shoulder, hip, knee, ankle, foot and headache conditionsICD-10Not Covered
    No codes listed
    Not Covered or Reimbursable Diagnosis Codes—headache, injury, sprain, strain and prosthetic-joint conditionsICD-10Not Covered
    R07.82Intercostal pain
    R51.0Headache with orthostatic component, not elsewhere classified
    R51.9Headache, unspecified
    S34.22XAInjury of nerve root of sacral spine, initial encounter
    S34.22XDInjury of nerve root of sacral spine, subsequent encounter
    S34.22XSInjury of nerve root of sacral spine, sequela
    S43.431ASuperior glenoid labrum lesion of right shoulder, initial encounter
    S43.432ASuperior glenoid labrum lesion of left shoulder, initial encounter
    S43.439ASuperior glenoid labrum lesion of unspecified shoulder, initial encounter
    S43.491AOther sprain of right shoulder joint, initial encounter
    1–10 of 19
    1/2
    FDA 510(k) device identifiersmixed
    K182565cryoICE cryoSPHERE cryoablation probe
    K250371cryoICE cryoXT cryoablation probe (cryoXT)
    K243677iovera° System
    K242057COOLIEF* Radiofrequency Generator
    K203066COOLIEF Cooled Radiofrequency Kit Advanced
    K251247GX1 Radiofrequency Generator Kit
    K231675OneRF Ablation System
    FDA product codesmixed
    GXHFDA product code
    GXDFDA product code
    GXIFDA product code
    Cervical RFA Diagnostic Threshold
    Diagnostic block response80% pain relief
    ProcedureCervical radiofrequency ablation
    Clinical contextThe diagnostic block is performed before cervical RFA for cervicogenic pain, including headaches.
    Sacroiliac Diagnostic Response
    Required response≥50% pain relief
    Diagnostic proceduresSacroiliac joint injection and lateral branch block
    Study populationIndividuals with injection-confirmed sacroiliac joint pain
    Sacroiliac Joint Pain Duration
    Minimum durationAt least 3 months
    ConditionChronic sacroiliac joint pain
    Evaluation contextEligibility also required at least one positive provocation test and no other major identifiable source of low back pain.
    Sacroiliac Baseline Pain
    Minimum average pain scoreNRS pain score ≥4
    Assessment periodOver the past 7 days
    ScaleNumeric Rating Scale (NRS)

    Provider Documentation and Action Items

    Documentation Required

    Diagnostic Occipital Nerve Block Required

    Before occipital radiofrequency neurotomy, perform a diagnostic block of the suspected occipital nerve and document the response. Alternative causes of the pain must be excluded.

    • Confirm the greater or lesser occipital nerve as the pain generator through diagnostic blockade.
    • Document exclusion of alternative etiologies before proceeding.
    Step Therapy

    Cervical RFA Requires 80% Diagnostic Relief

    Cervical radiofrequency ablation should be considered only after a diagnostic block produces 80% pain relief, consistent with guideline-supported patient selection.

    • Document the diagnostic block result and percentage of pain relief.
    • Record the cervical nerve or medial branch targeted.
    Step Therapy

    Document Failure of Conservative Therapy

    Reserve neuroablative procedures for patients who have not achieved adequate relief with conservative or less invasive therapies.

    • Document prior conservative treatment, such as physical therapy, medications, posture exercises, massage, or other appropriate measures.
    • Document failure, inadequate relief, or intolerance of less invasive interventions before neuroablation.
    Documentation Required

    Identify Procedure, Nerve, and Indication

    Clearly identify the procedure performed or requested, the specific nerve or nerve branch targeted, and the pain condition or indication in the clinical record and claim.

    • Specify the ablation or neurolytic technique.
    • Identify the treated nerve, branch, or nerve plexus.
    • Link the procedure to the documented indication.
    Documentation Required

    Document Headache or Occipital Neuralgia Diagnosis

    For headache or occipital neuralgia, document the clinical diagnosis using history, physical examination, and appropriate imaging when indicated. A positive diagnostic nerve block supports the diagnosis.

    • Describe the characteristic headache or occipital neuralgia pattern and relevant examination findings.
    • Document MRI or CT findings when clinically indicated.
    • Record diagnostic block response.
    Prior Authorization

    Diagnostic Blockade Before Occipital Neurotomy

    A diagnostic occipital nerve blockade should precede occipital neurotomy, with documentation that the greater or lesser occipital nerve is the confirmed pain generator.

    • Document the nerve blocked and the degree and duration of relief.
    • Do not proceed without evaluating alternative pain etiologies.
    Documentation Required

    Document SI Joint Pain Evaluation

    For sacroiliac joint pain, document chronicity, examination findings, injection or block response, pain severity, and the absence of another major identifiable source of low back pain.

    • Document at least three months of chronic SI joint pain.
    • Record at least one positive provocation test.
    • Document at least 50% relief from a diagnostic or therapeutic SI joint injection and lateral branch block.
    • Document average NRS pain of at least 4 and evaluation for competing causes of low back pain.
    Billing Rule

    Use Covered Diagnoses and Procedure Codes

    Submit services with the covered diagnosis and procedure codes applicable on the date of service. Claims lacking covered codes under the policy may be denied as not covered.

    • Use the most appropriate current codes as of the submission date.
    • Ensure the diagnosis and procedure code combination matches the policy indication.
    • Verify the applicable benefit plan document and any controlling mandate.
    Denial Risk

    Excluded Pain Conditions and Indications

    Peripheral nerve destruction using cryoablation, laser, electrical, chemical, or radiofrequency ablation is not covered or reimbursable for the listed pain conditions.

    • Sacroiliac joint pain, knee pain, hip pain, shoulder pain, and foot or heel pain.
    • Headache, occipital neuralgia, and intercostal neuralgia.
    • Extremity pain due to complex regional pain syndrome, peripheral nerve entrapment or compression, or peripheral neuropathy.
    Denial Risk

    Ablation Techniques Not Medically Necessary

    The following ablative techniques are considered not medically necessary for pain conditions under this policy.

    • Percutaneous cryoablation.
    • Pulsed radiofrequency ablation.
    • Peripheral nerve destruction using cryoablation, laser, electrical, chemical, or radiofrequency ablation for excluded indications.
    Billing Rule

    Verify Code Validity and Effective Dates

    Deleted codes and codes that are not effective on the date the service is rendered may not be eligible for reimbursement.

    • Confirm code validity and effective dates before claim submission.
    • Check AMA and CMS updates because code lists may change more frequently than the policy.
    Denial Risk

    Avoid Excluded Diagnosis Associations

    Do not associate peripheral nerve destruction claims with diagnosis codes listed as not covered or reimbursable for the policy’s pain indications.

    • Review the complete applicable ICD-10-CM exclusion list, including listed shoulder, ankle, foot, and joint conditions.
    • Ensure the diagnosis association reflects the actual covered indication, when applicable.
    Billing Rule

    Use Listed Diagnosis Indications

    Use peripheral nerve destruction only for diagnosis indications listed as covered under the applicable policy and benefit plan; listed conditions that are not covered or reimbursable will result in denial risk.

    • Confirm the diagnosis is an eligible policy indication before scheduling or billing.
    • Do not rely on a procedure code alone to establish coverage.
    Documentation Required

    Document Procedure-Related Risks

    Neuroablative procedures can cause clinically significant complications, and these risks should be considered and documented during informed consent and treatment planning.

    • Bleeding, infection, prolonged numbness or tingling, temporary increased pain, and injury to nearby tissue.
    • Cryoanalgesia may cause skin color changes or frostbite-type injury.
    • Chemical neurolysis may cause neuritis, neuraxial spread, or unintended tissue destruction.
    Denial Risk

    Headache or Occipital Neuralgia: Insufficient Evidence

    Evidence is insufficient to demonstrate the safety and efficacy of peripheral nerve ablation for cervicogenic headache or occipital neuralgia.

    • Coverage or reimbursement remains at risk despite reported short-term benefits.
    • Document clinical rationale, alternatives, and the limited and conflicting evidence when requesting the service.
    Denial Risk

    Intercostal Neuralgia: Insufficient Evidence

    Evidence is insufficient to demonstrate the safety and efficacy of peripheral nerve ablation for intercostal neuralgia.

    • Do not assume coverage based on guideline discussion or an individual diagnostic response.
    • Document alternatives and the rationale if the procedure is considered.
    Denial Risk

    Shoulder Pain: Insufficient Evidence

    Evidence is insufficient to demonstrate the safety and efficacy of peripheral nerve ablation for shoulder pain.

    • Shoulder pain is also identified as an excluded pain condition under the policy.
    • Expect coverage and reimbursement risk for ablation performed for this indication.
    Denial Risk

    SI and Lumbar-Related Pain: Insufficient Evidence

    Evidence is insufficient to establish the safety and efficacy of SI joint radiofrequency ablation, lumbar or sacral dorsal ramus ablation, or other ablative modalities for SI joint and related lumbar pain.

    • Applicable modalities include radiofrequency, laser, chemical, and electrical ablation.
    • A weak guideline recommendation does not establish sufficient evidence for coverage.
    Denial Risk

    Hip Pain: Insufficient Evidence

    Evidence is insufficient to demonstrate the safety and effectiveness of peripheral nerve ablation for hip pain, regardless of the ablation method.

    • Although diagnostic-block-selected hip RFN has been studied, evidence remains limited and substantial gaps persist.
    • Expect coverage and reimbursement risk for hip pain ablation.
    Denial Risk

    Knee Osteoarthritis: Limited Evidence

    Current evidence does not support routine use of radiofrequency ablation or related minimally invasive interventions for knee osteoarthritis.

    • Evidence is limited by small or methodologically constrained studies and short follow-up.
    • Knee pain is an excluded pain condition under the policy.
    Denial Risk

    Peripheral Neuroma Ablation Is Investigational

    Neuroablative treatment for peripheral neuroma, including Morton’s neuroma, lacks sufficient evidence and should be considered investigational or a research treatment until further study is available.

    • Alcohol injections and radiofrequency ablation have only shown promise in observational case series.
    • Document that evidence is insufficient to establish safety and efficacy.
    Denial Risk

    Foot Pain Ablation: Insufficient Evidence

    Evidence is insufficient to demonstrate the safety and effectiveness of peripheral nerve ablation for foot pain.

    • Ablation as primary treatment of Morton’s neuroma is not recommended in the cited guideline.
    • Foot and heel pain are excluded pain conditions under the policy.
    Denial Risk

    Other Pain Conditions: Insufficient Evidence

    The policy identifies insufficient evidence for peripheral nerve destruction in other pain conditions, including complex regional pain syndrome, chronic thoracic pain, craniofacial pain, pudendal neuralgia, nerve compression or entrapment, peripheral neuropathy, post-amputation pain, post-herniorrhaphy pain, and oncologic pain.

    • Do not represent these procedures as established effective treatment for these conditions.
    • Document the limited evidence and consider established alternatives.
    Denial Risk

    Insufficient Evidence for Other Pain Conditions

    There is a paucity of peer-reviewed evidence supporting the safety and efficacy of neuroablative procedures for pain conditions outside the specifically evaluated indications.

    • This includes chronic regional pain syndrome, chronic thoracic pain, craniofacial pain syndromes, pudendal neuralgia, peripheral nerve compression or entrapment, peripheral neuropathic conditions, post-amputation pain, post-inguinal herniorrhaphy pain, and oncologic pain.
    • Treat such uses as unsupported unless applicable plan terms or updated evidence establish coverage.

    Policy Background

    Peripheral nerve destruction is used in pain management to interrupt or alter pain signaling. The policy addresses cryoablation, conventional, cooled, and pulsed radiofrequency techniques, and chemical neurolysis, which may be performed alone or in combination for conditions such as headache, occipital neuralgia, joint pain, and neuropathic or nerve-entrapment syndromes. Neuroablative procedures should be considered only after conservative or less invasive therapies have not provided adequate relief.

    Definitions and Clinical Terms

    Cryoanalgesia
    TemperatureApproximately 70°C
    MechanismFreezes the nerve, creating a temporary axonal injury that blocks pain signals
    Tissue effectPreserves surrounding nerve structure and allows natural regeneration
    Radiofrequency Ablation
    Energy sourceElectromagnetic energy
    MechanismHeats neural tissue to induce focal neurodestruction
    Conventional thermal RFAApplies approximately 60–90°C for 90–120 seconds
    Pulsed Radiofrequency Ablation
    Energy deliveryBrief bursts of radiofrequency energy
    TemperatureMaintained below 42°C
    Tissue effectAlters nociceptive signaling without destroying tissue
    Chemical Neurolysis
    MethodInjection of neurolytic agents
    ExamplesPhenol or alcohol
    PurposeIntentionally destroys targeted nerve fibers
    Cervicogenic Headache
    OriginDisorders of the cervical spine, including bones, discs, or soft tissues
    Typical patternUnilateral head pain beginning in the neck and radiating toward the head
    Potential causesTrauma, such as whiplash injury, or arthritis
    Occipital Neuralgia
    CauseIrritation or entrapment of the greater occipital nerve as it passes through neck muscles
    Pain qualitySharp or shooting pain in the back of the head
    RadiationMay radiate to the scalp, forehead, or behind the eyes
    Cervicogenic Headache
    Anatomic originDisorders of the cervical spine, including bones, discs, or soft tissues
    Typical presentationTypically unilateral pain that begins in the neck
    RadiationMay radiate to the head
    Occipital Neuralgia
    Underlying conditionIrritation or entrapment of the greater occipital nerve through the neck muscles
    Pain descriptionSharp or shooting pain in the back of the head
    Possible spreadMay radiate to the scalp, forehead, or area behind the eyes
    Intercostal Neuralgia
    DefinitionNeuropathic pain in the distribution of one or more intercostal nerves
    Typical painSharp, aching, radiating, burning, or stabbing pain
    LocationAlong the ribs, chest, or upper abdominal wall
    Sacroiliac Joint Pain
    OriginThe sacroiliac joint or related muscles and ligaments
    Primary locationLower back
    Possible radiationMay radiate to one or both hips or legs
    Health Equity
    DefinitionThe highest level of health for all people
    Health inequityAn avoidable difference in health status or distribution of health resources
    Underlying conditionsSocial conditions in which people are born, grow, live, work, and age
    Social Determinants of Health
    DefinitionConditions in the environment that affect health, functioning, quality-of-life outcomes, and risks
    ExamplesHousing, transportation, neighborhoods, education, employment, income, and food access
    Additional factorsDiscrimination, physical activity opportunities, air and water quality, and language and literacy

    Conservative Treatment Requirements

    Conservative treatments should be ineffective before neuroablative procedures

    Before considering a neuroablative procedure:

    Conservative treatment: Other conservative treatments should have been ineffective.

    The policy does not specify a required duration or a fixed list of conservative modalities.

    Failure of conservative or less invasive treatment before neuroablative procedures

    Neuroablative procedures should be reserved for individuals who have not achieved adequate relief with conservative or less invasive therapies.

    Prior treatment response: The patient has not achieved adequate relief with conservative or less invasive treatment before the neuroablative procedure.

    Clinically appropriate conservative treatment trial before nerve ablation

    Before considering nerve ablation:

    Clinically appropriate conservative treatment: A trial of clinically appropriate conservative treatment has been completed, such as physical therapy, massage, cold compresses, posture exercises, transcutaneous electrical nerve stimulation, psychotherapy, or medications.

    Three months of conservative therapy before lumbar facet interventions

    Before considering lumbar facet interventions:

    Conservative therapy trial: The patient has completed a trial of conservative therapies, including medications, physical treatments, integrative approaches, and lifestyle modifications.3 months

    Adequate conservative therapy and positive diagnostic blockade before sacroiliac neuroablation

    Sacroiliac neuroablative procedures may be considered only when both requirements are met:

    ALL of the following

    • Conservative therapy: The patient has completed an adequate trial of conservative therapy.
    • Diagnostic blockade: The patient has demonstrated a positive response to diagnostic blockade.

    Failure of first- and second-line therapy before ablative treatment for intractable plantar fasciitis

    For intractable plantar fasciitis pain, ablative methods may be considered only after failure of first- and second-line therapies:

    ALL of the following

    • First-line therapy: First-line nonsurgical treatment has failed, including stretching exercises, ice, activity modification, weight loss when overweight, adaptive footwear, arch taping, nonsteroidal anti-inflammatory medication, shock-absorbing shoe inserts or orthoses, and iontophoresis.
    • Second-line therapy: Second-line treatment has failed, including night splints, steroidal anti-inflammatory injections, and/or a walking cast.
    • Duration: First- and second-line therapies have been tried before consideration of an ablative method for intractable pain.6–12 months

    Imaging and Diagnostic Evaluation

    Billing Rule

    Follow imaging requirements embedded in code descriptions

    Check the procedure code description for embedded imaging requirements. Listed percutaneous cryoablation codes and selected neurolytic nerve destruction codes include imaging guidance in the code description; the policy does not establish a separate general imaging requirement.

    Documentation Required

    Use appropriate diagnostic evaluation

    For evaluation of suspected cervicogenic headache or occipital neuralgia, use clinical criteria, history, and physical examination; MRI or CT may be used as part of the diagnostic evaluation, and relief after a diagnostic nerve block supports the diagnosis.

    Not Covered Services

    The policy identifies multiple categories of services as not covered or reimbursable, including percutaneous cryoablation and pulsed radiofrequency ablation, and peripheral nerve destruction using cryoablation, laser, electrical, chemical, or radiofrequency techniques for specified pain conditions. Excluded indications include sacroiliac, knee, hip, shoulder, foot or heel, headache, occipital, and intercostal pain; extremity pain related to complex regional pain syndrome, nerve entrapment or compression, or peripheral neuropathy; and other conditions for which published evidence is insufficient to establish safety and efficacy.

    Policy Summary
    PayerCigna
    PolicyPeripheral Nerve Destruction for Pain Conditions
    Policy CodePolicy 0525
    Change TypeModified
    Effective DateNov 1, 2026
    Next Review DateFeb 15, 2027
    Key ActionPerform a diagnostic occipital nerve block before radiofrequency neurotomy and exclude alternative etiologies.
    SourceLink
    On This Page
    Coverage CriteriaCoding and Code SetsProvider Documentation and Action ItemsPolicy BackgroundDefinitions and Clinical TermsConservative Treatment RequirementsImaging and Diagnostic EvaluationNot Covered Services

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