Cigna Healthcare (Commercial) · percutaneous vertebral augmentation
✓ conditional · commercial
Criteria checklist
0 of 6 ticked- enumerated: yes
- covered:
- name: Painful vertebral compression fracture / lesion (T5-L5), imaging-concordant
- criteria:
- levels: T5-L5 only; <=2 levels per date of service
- etiologies:
- osteoporotic
- osteolytic
- osteonecrotic (Kummell)
- steroid-induced
- aggressive hemangioma / eosinophilic granuloma
- malignancy (osteolytic mets, myeloma, primary bone/marrow tumor)
- prophylactic to facilitate fusion
- imaging: concordant with symptoms/exam; functional impairment documented
- conservative pathway:
- acute: 0-6 weeks, pain preventing transfers/ambulation -> no conservative trial required
- subacute: >6 weeks -> requires 4 weeks Rx analgesics/NSAIDs AND 4 weeks provider-directed exercise
- osteoporotic fx: must be enrolled in an osteoporosis treatment/prevention program
- urgent emergent: pathologic fracture / incapacitating pain bypasses non-surgical management
- investigational:
- percutaneous SACROPLASTY and coccygeoplasty
- cervical and T1-T4 levels
- prophylaxis for osteoporosis or chronic LBP (>6 months, even with an old fracture)
- non-painful hemangioma; spinoplasty / OptiMesh; non-FDA-approved cement
- required: yes
- min duration months: not stated in the policy
- min duration weeks: 4
- satisfied by:
- acute (0-6 wk) disabling: none required
- subacute (>6 wk): 4 wk meds + 4 wk exercise
- urgent/emergent: bypass
- contraindicated
- modalities named:
- analgesics / NSAIDs / steroids
- provider-directed exercise
- osteoporosis program (osteoporotic fx)
- required: no
- min duration days: not stated in the policy
- success criteria: not stated in the policy
- threshold is binding: no
- required: no
- must clear: no
- note posture: not required
- applies: yes
- levels per dos: 2
- eligible levels: T5-L5
Cigna delegates vertebral augmentation to eviCore CMM-607. Covers painful VCF/lesion at T5-L5 (<=2 levels/DOS) with concordant imaging. Conservative pathway is acuity-tiered: acute (0-6 wk) disabling pain needs no trial; subacute (>6 wk) requires 4 weeks meds + 4 weeks exercise; osteoporotic fractures must be enrolled in an osteoporosis program. KEY divergences from Medicare: hard T5-L5 + <=2-level caps; osteoporosis-program enrollment; flatly excludes SACROPLASTY, coccygeoplasty, and cervical/T1-T4; does NOT mandate MR marrow edema. From the actual fetched eviCore PDF (criteria unchanged from V1.0.2024).
Ticks are a documentation aid — nothing is stored; they reset on reload.
Dot phrase
Self-contained narrative A&P attestation. `***` = fill-in. Maps to eviCore CMM-607 (Primary Vertebral Augmentation), UM delegated by Cigna. Hard caps: T5-L5 only, <=2 levels per date of service; the conservative requirement is ACUITY-TIERED — date the pain onset in the note.
.KYPHOCIGNA Assessment: *** — painful vertebral compression fracture or lesion at *** (T5-L5 only, <=2 levels this DOS), with imaging concordant with the symptoms and examination and functional impairment documented. Etiology: *** (osteoporotic / osteolytic / osteonecrotic [Kummell] / steroid-induced / aggressive hemangioma or eosinophilic granuloma / malignancy [osteolytic mets, myeloma, primary bone-marrow tumor] / prophylactic to facilitate fusion). Medical necessity per Cigna eviCore CMM-607: the conservative requirement is acuity-tiered, and this patient falls in the [acute, 0-6 wk] tier with pain preventing transfers and ambulation, which requires no conservative trial | the [subacute, >6 wk] tier, having completed 4 weeks of prescription analgesics/NSAIDs and 4 weeks of provider-directed exercise: *** | the [urgent/emergent] tier with a pathologic fracture or incapacitating pain, which bypasses non-surgical management — or conservative care was contraindicated. [If the fracture is osteoporotic:] the patient is enrolled in an osteoporosis treatment and prevention program: *** . The exclusions are absent: this is not sacroplasty or coccygeoplasty, not cervical or T1-T4, not prophylaxis for osteoporosis or chronic low back pain (>6 months, even with an old fracture), and not a non-painful hemangioma; no spinoplasty or OptiMesh is planned, and no non-FDA-approved cement will be used. Plan: Percutaneous *** (kyphoplasty 22513 thoracic / 22514 lumbar [+22515 each add'l]; or vertebroplasty 22510-22512) at level(s) *** within T5-L5 and <=2 this DOS, under imaging guidance. Risks, benefits, and alternatives discussed; consent obtained.
Where this payor diverges from the Medicare baseline
Cautions
Prior-auth pathway
- required: yes
- pathway: eviCore / Evernorth (CMM-600.1)
Provenance
- authority:
- type: commercial_policy
- id: Cigna eviCore CMM-607
- title: Primary Vertebral Augmentation (Percutaneous Vertebroplasty / Kyphoplasty) and Sacroplasty (CMM-607)
- delegated by: Cigna (authored by eviCore / Evernorth)
- applies because: Cigna delegates vertebral augmentation UM to eviCore CMM-607
- source: https://www.evicore.com/sites/default/files/clinical-guidelines/2026-02/Cigna_CMM-607%20Prim%20Vert%20Aug%20Per_Final_V1.1.2025_Eff02.25.2026_pub02.13.2026.pdf
- archived copy:
sources/evicore_cmm607-vert-aug_2026-02-25.pdf(sha256 2ac8c1e81a98… — kept in the content repo, not served here) - effective: 2026-02-25 · payor last reviewed: 2026-02-25 · we verified: 2026-07-24 · v1
Change history
- 2026-07-24commercial cells: re-verify 27 source PDFs by SHA-256 (Carelon/eviCore/UHC/Cigna) - all unchanged vs committed archive; last_verified -> 2026-07-24
3615c231f0 - 2026-06-30Archive commercial source PDFs into sources/ + wire source_file/source_hash
c5466694c8 - 2026-06-28Add commercial Vertebral Augmentation cells: Anthem, UHC, Cigna
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