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Facet Joint Injections/ Medial Branch Blocks - (Effective Date - 2026-10-15) 7.01.116
Excellus BlueCross BlueShield·Orthopedics, Pain Management, Neurosurgery·Bone & Joints (Orthopedic)
Effective date
Oct 15, 2026
We identified it
Jul 16, 2026
Summary
Excellus BlueCross BlueShield released a comprehensive new policy (7.01.116) effective October 15, 2026, establishing strict medical necessity criteria for facet joint injections and medial branch blocks. The policy requires documented conservative treatment failure, imaging correlation, fluoroscopic/CT guidance, limits procedures to 3 contiguous levels, restricts diagnostic injections to 2 per level, and requires positive response confirmation before therapeutic treatment. Billing teams must immediately implement prior authorization workflows to enforce these requirements.
Action Required
By September 15, 2026 (30 days before effective date): Billing team must implement prior authorization requirements for all facet joint injections and medial branch blocks. REQUIREMENTS: (1) Update billing system to require prior authorization for all requests, flagging any claims without documentation of: conservative treatment for ≥4 weeks in past 3 months, axial pain persistence ≥3 months, imaging studies confirming no other etiology, and fluoroscopic or CT guidance; (2) Implement denial logic to reject claims missing required documentation elements per criteria sections I-VI; (3) Configure system to deny claims for: procedures without fluoroscopic/CT guidance, same-day billing with other invasive procedures (except TFESI with synovial cyst aspiration), more than 3 contiguous levels, levels above C2-C3 or below L5-S1, non-anesthetic/corticosteroid/contrast injectates, ultrasound-guided procedures, or procedures scheduled as 'series' without prior response evaluation; (4) Add validation rules to prevent billing >2 diagnostic injections at same level(s); (5) Require documentation of 80% pain relief response for second diagnostic injection and 50% pain relief for subsequent therapeutic injections; (6) For therapeutic injections (alternative to RF ablation), verify documentation of contraindication (pseudoarthrosis or implanted electrical device) and confirm 6-month minimum interval since prior injection; (7) Train billing staff, coders, and providers on new documentation requirements. Consequences: Claims submitted without compliance will be denied; retrospective denials will impact revenue.