In the clinical study, patients were allowed to travel and engage in light activity such as walking as soon as they felt they could. Please listen to your surgeon’s instructions on how much activity you can do after your surgery and for how long. During the clinical study, walking during the first six weeks following surgery was usually acceptable. The surgeon may also ask you to reduce your physical activities in the first six weeks after your operation. The surgeon may ask you to return for an examination about six weeks after surgery. How soon can I resume activities of daily living after coflex® surgery? Based on the clinical study results, 85 out of 100 coflex® patients had significant pain relief at six weeks compared to 68 out of 100 patients who had fusion surgery.1 Always be sure to follow the physician’s instructions on physical rehabilitation and activities following surgery.Īfter surgery, medication may be provided by the surgeon. When the surgeon says you can leave the hospital, the doctor may prescribe physical therapy. In some cases, the surgeon may elect to perform a decompression using the coflex® device at a surgery center, which means that some patients will not require a hospital stay.1 Three out of four coflex® patients in a clinical study left the hospital within 24–48 hours after surgery, compared to one out of three fusion patients.* For all coflex® patients in the clinical study, the hospital stay was less than a week. How long will I need to stay in the hospital or surgery center? How do patients with coflex® compare to patients with spinal fusion?Ī 2013 published study comparing the coflex® device with spinal fusion found 12 that the coflex® device had “advantages in perioperative outcomes,” and that “equivalent or superior 2-year clinical outcomes were seen with coflex®.” The 3 article concluded that “coflex® is a safe, efficacious, and viable alternative to spinal fusion in the treatment of spinal stenosis with low back pain.” The unique design of the coflex® implant maintains stability in the spine while preserving more natural movement at the affected area. The implant is then positioned onto the laminar bone, which is the strongest bone in the back of your spine. In 2012, the FDA approved the coflex® spinal implant, which is a small, U-shaped titanium device that provides spinal stability without the mobility loss associated with spinal fusion.Īfter the surgical decompression, which removes pressure on the impinged nerves, your surgeon will insert the coflex® implant through the same incision. For decades, LSS patients’ surgical options were limited to either decompression or decompression with spinal fusion.
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