Percutaneous vertebroplasty (PVP/VP) is an image-guided, percutaneous injection of an acrylic polymer (commonly polymethylmethacrylate, PMMA) into a fractured vertebral body to provide pain relief and mechanical stabilization for osteoporotic or osteolytic lesions that have not responded to conservative care. Kyphoplasty (also called balloon kyphoplasty or BKP/PKP) is a variation in which an inflatable bone tamp (balloon) is used to create or restore vertebral height prior to cement injection; this step is intended to reduce kyphotic deformity and may decrease cement extrusion compared with PVP. (Description: PVP/VP and KP/PKP).
Both procedures are performed with fluoroscopic or CT guidance and are intended to: relieve pain, improve function and quality of life, and provide vertebral body stabilization to prevent further collapse in selected patients. Indications most commonly supported by the literature and professional society guidance include painful osteoporotic vertebral compression fractures and selected pathologic (neoplastic) fractures; kyphoplasty may offer greater radiographic height restoration and lower rates of cement leakage but at higher resource use. (Intended benefits: pain relief, function, stability; KP vs PVP comparative outcomes).
The evidence base shows clinically relevant benefit for carefully selected patients but is heterogeneous. For acute/subacute osteoporotic vertebral compression fractures, many trials and meta-analyses report greater early pain relief with vertebral augmentation versus conservative management and durable improvement in some analyses up to one year, while sham-controlled trials of vertebroplasty introduce uncertainty about efficacy for some patients. For malignant or metastatic VCFs and multiple myeloma, consistent series and systematic reviews report meaningful palliative reductions in pain and improved function with low rates of major complications. For osteonecrosis-related unstable fractures (Kümmell's disease), kyphoplasty often achieves better height restoration and less cement leakage than vertebroplasty, with similar symptom improvement across techniques. Overall, use should be limited to patients meeting specific clinical and imaging criteria and after failure of Optimal Medical Therapy. (Evidence nuance: supportive in selected patients; limited/inconclusive for other indications).
UnitedHealthcare created this Idaho‑specific policy effective 06/01/2025 to define covered indications, required imaging and exclusions, and to emphasize documentation of failure of conservative therapy and imaging correlation of pain to the treated level before vertebral augmentation is authorized. Providers should follow the policy’s listed indications, exclusions (for example, significant vertebral collapse—vertebra reduced to less than one‑third of original height, spinal cord compression, healed or asymptomatic fractures, and sacrococcygeal lesions), and prior authorization requirements where applicable. (Policy scope, exclusions, and effective date).