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.
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.
Coverage Criteria
Ablative treatments considered not medically necessary
Considered not medically necessary when used for treatment of pain conditions:
Excluded pain conditions
Not covered or reimbursable when used for treatment of any of the following pain conditions:
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.
Peripheral nerve destruction is not covered or reimbursable for these indications.
Cervicogenic headache or occipital neuralgia
Evidence is insufficient.
Published medical literature is insufficient to demonstrate safety and efficacy.
Intercostal neuralgia
Evidence is insufficient.
Published medical literature is insufficient to demonstrate safety and efficacy.
Shoulder pain
Evidence is insufficient.
Published medical literature is insufficient to demonstrate safety and efficacy.
Sacroiliac and lumbar-related pain
Evidence conclusion for sacroiliac and lumbar-related pain:
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:
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:
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.
Foot pain
Peripheral nerve ablation for foot pain is not supported.
Other pain conditions
Peripheral nerve destruction is not supported for the listed other pain conditions.
Other Pain Related Conditions
Evidence is insufficient to support safety and efficacy.
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
| 64999 | Unlisted procedure, nervous system |
| 0440T | Ablation, percutaneous, cryoablation, includes imaging guidance; upper extremity distal/peripheral nerve |
| 0441T | Ablation, percutaneous, cryoablation, includes imaging guidance; lower extremity distal/peripheral nerve |
| 0442T | Ablation, percutaneous, cryoablation, includes imaging guidance; nerve plexus or other truncal nerve (eg, brachial plexus, pudendal nerve) |
| C9808 | Nerve 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) |
| C9809 | Cryoablation 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) |
| 64620 | Destruction by neurolytic agent, intercostal nerve |
| 64624 | Destruction by neurolytic agent, genicular nerve branches including imaging guidance, when performed |
| 64632 | Destruction by neurolytic agent; plantar common digital nerve |
| 64640 | Destruction by neurolytic agent; other peripheral nerve or branch |
| 1096T | Injection(s) of thermoregulated multiphase suspension to demyelinate nerves innervating the knee joint, including imaging guidance, when performed |
| G43.001 | Migraine without aura, not intractable, with status migrainosus |
| G43.009 | Migraine without aura, not intractable, without status migrainosus |
| G43.011 | Migraine without aura, intractable, with status migrainosus |
| G43.019 | Migraine without aura, intractable, without status migrainosus |
| G43.101 | Migraine with aura, not intractable, with status migrainosus |
| G43.109 | Migraine with aura, not intractable, without status migrainosus |
| G43.111 | Migraine with aura, intractable, with status migrainosus |
| G43.119 | Migraine with aura, intractable, without status migrainosus |
| G43.401 | Hemiplegic migraine, not intractable, with status migrainosus |
| G43.409 | Hemiplegic migraine, not intractable, without status migrainosus |
| M00.011 | Staphylococcal arthritis, right shoulder |
| M00.012 | Staphylococcal arthritis, left shoulder |
| M00.019 | Staphylococcal arthritis, unspecified shoulder |
| M00.111 | Pneumococcal arthritis, right shoulder |
| M00.112 | Pneumococcal arthritis, left shoulder |
| M00.119 | Pneumococcal arthritis, unspecified shoulder |
| M02.811 | Other reactive arthropathies, right shoulder |
| M02.812 | Other reactive arthropathies, left shoulder |
| M02.819 | Other reactive arthropathies, unspecified shoulder |
| M05.111 | Rheumatoid lung disease with rheumatoid arthritis of right shoulder |
| M05.112 | Rheumatoid lung disease with rheumatoid arthritis of left shoulder |
| M05.119 | Rheumatoid lung disease with rheumatoid arthritis of unspecified shoulder |
| M05.151 | Rheumatoid lung disease with rheumatoid arthritis of right hip |
| M05.152 | Rheumatoid lung disease with rheumatoid arthritis of left hip |
| M05.159 | Rheumatoid lung disease with rheumatoid arthritis of unspecified hip |
| M05.161 | Rheumatoid lung disease with rheumatoid arthritis of right knee |
| M05.162 | Rheumatoid lung disease with rheumatoid arthritis of left knee |
| M05.169 | Rheumatoid lung disease with rheumatoid arthritis of unspecified knee |
| M05.171 | Rheumatoid lung disease with rheumatoid arthritis of right ankle and foot |
| M05.172 | Rheumatoid lung disease with rheumatoid arthritis of left ankle and foot |
| M05.50- | Rheumatoid polyneuropathy with rheumatoid arthritis |
| M05.59 | Rheumatoid polyneuropathy with rheumatoid arthritis |
| M05.611 | Rheumatoid arthritis of right shoulder with involvement of other organs and systems |
| M05.612 | Rheumatoid arthritis of left shoulder with involvement of other organs and systems |
| M05.619 | Rheumatoid arthritis of unspecified shoulder with involvement of other organs and systems |
| M05.651 | Rheumatoid arthritis of right hip with involvement of other organs and systems |
| M05.652 | Rheumatoid arthritis of left hip with involvement of other organs and systems |
| M05.659 | Rheumatoid arthritis of unspecified hip with involvement of other organs and systems |
| M05.661 | Rheumatoid arthritis of right knee with involvement of other organs and systems |
| M05.662 | Rheumatoid arthritis of left knee with involvement of other organs and systems |
| No codes listed |
| No codes listed |
| No codes listed |
| No codes listed |
| No codes listed |
| R07.82 | Intercostal pain |
| R51.0 | Headache with orthostatic component, not elsewhere classified |
| R51.9 | Headache, unspecified |
| S34.22XA | Injury of nerve root of sacral spine, initial encounter |
| S34.22XD | Injury of nerve root of sacral spine, subsequent encounter |
| S34.22XS | Injury of nerve root of sacral spine, sequela |
| S43.431A | Superior glenoid labrum lesion of right shoulder, initial encounter |
| S43.432A | Superior glenoid labrum lesion of left shoulder, initial encounter |
| S43.439A | Superior glenoid labrum lesion of unspecified shoulder, initial encounter |
| S43.491A | Other sprain of right shoulder joint, initial encounter |
| K182565 | cryoICE cryoSPHERE cryoablation probe |
| K250371 | cryoICE cryoXT cryoablation probe (cryoXT) |
| K243677 | iovera° System |
| K242057 | COOLIEF* Radiofrequency Generator |
| K203066 | COOLIEF Cooled Radiofrequency Kit Advanced |
| K251247 | GX1 Radiofrequency Generator Kit |
| K231675 | OneRF Ablation System |
| GXH | FDA product code |
| GXD | FDA product code |
| GXI | FDA product code |
Provider Documentation and Action Items
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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
Conservative Treatment Requirements
Conservative treatments should be ineffective before neuroablative procedures
Before considering a neuroablative procedure:
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.
Clinically appropriate conservative treatment trial before nerve ablation
Before considering nerve ablation:
Three months of conservative therapy before lumbar facet interventions
Before considering lumbar facet interventions:
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
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.
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.
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