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Bone tumor ablation

Stryker provides a single-source solution for treating bone tumors

Bone tumor ablation (BTA) is a minimally invasive procedure for treating painful bone tumors. As Stryker's first Interventional Oncology technology, OptaBlate is designed to help optimize aspects of the procedure—from set-up to ablation.

Features:

  • Treatment of two vertebral body levels at once using a bipedicular or unipedicular curved approach
  • Microinfusion technology, which is designed to keep the zone hydrated and is designed to reduce impedance errors and prevent charring1

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Up to 26% of BTA-eligible patients* do not experience pain relief after radiation therapy.1 This can leave patients* feeling like they are out of options. Bone tumor ablation may provide those living with painful and often debilitating bone tumors much-needed relief.

Procedure

Straight approach

1


Under x-ray guidance, insert access cannulas and advance to the posterior 1/3 of the vertebral body.

2


Insert hand drill into the anterior third of the vertebral body to create a pathway. The color bands on the hand drill will help you determine which probe size is appropriate for the ablation. Teal indicates a 15mm probe, orange indicates a 20mm probe and purple indicates a 10mm probe.

3


Insert OptaBlate probes and connect microinfuser to begin the flow of sterile saline to the lesion site.

4


Ablate surrounding tissue using radiofrequency energy.


If performing vertebral augmentation, refer to the Instructions for Use (IFU) for the selected device.

Curve approach

1


Under x-ray guidance, insert access cannula and advance to the posterior one third of the vertebral body.

2


Insert introducer with sheath, then squeeze the gray introducer lever. Advance introducer using a mallet.

3


Release the lever, then remove the introducer handpiece, leaving the sheath in place.

4


Insert probe and adjust placement of spacer, then pull back the working conduit and start flow of sterile saline to the probe.

5


Start ablation.


If performing vertebral augmentation, refer to the Instructions for Use (IFU)* for the selected device.