Background
There are an estimated 1.5 million vertebral compression fractures that occur every year in the United States. Kyphoplasty has been approved by the FDA for treatment of vertebral compression fractures since 1998. It was a progression on the procedure that had traditionally been used to manage vertebral compression fractures since 1987, vertebroplasty. There are an estimated 100,000 cases of vertebral augmentation (both kyphoplasty and vertebroplasty) performed in the United States each year.
What is a Kyhpoplasty?
Kyphoplasty is a minimally invasive procedure that is performed through a small skin puncture utilizing X ray guidance to treat a vertebral compression fracture. The procedure typically takes 60 to 90 minutes to complete. The goals of the procedure include restoring height to the vertebral body, stabilizing the fractured vertebra, and reducing back pain associated with the fracture.
The procedure is performed in a special fluoroscopy suite. An IV is placed beforehand for administration of antibiotics and sedation medications. The patient lays face down on a padded table and the back is thoroughly cleaned. Local anesthesia is used to provide patient comfort throughout the procedure. A small incision is made in the back (less than 1 cm) through which a needle will be placed. The needle is advanced through the soft tissue and eventually into bone. Once bone is encountered, the patient may experience a tapping sensation which is the advancement of the needle through the pedicle and into the vertebral body. A special balloon is then inserted through the needle and into the vertebral body. That balloon is slowly inflated in an attempt to restore as much height to the vertebra as possible and in turn creating a cavity in the bone. The balloon is then deflated and removed. An injection device is then inserted to deliver a cement-like material called polymethylmethacrylate (PMMA). Once the vertebral body has sufficiently been filled with PMMA, the needles are removed and the patient is kept on the table to allow the PMMA to harden within the bone.