Method and Apparatus for Intervertebral Disc Expansion
An intervertebral disc is expanded and injected by forming and dilating an opening in the disc annulus and introducing an inflatable member into the disc nucleus pulposus. The inflatable member location within the nucleus pulposus is verified and the inflatable member is gradually inflated for augmenting a space in the nucleus pulposus. The internal pressure and expansion of the inflatable member are monitored. The inflatable member is subsequently deflated and a biomaterial is injected into the augmented space.
1 . A method of treating an intervertebral disc of a patient, the method comprising the steps of:
inserting a balloon into a nucleus pulposus without removing material from the nucleus pulposus, the balloon being connected to a catheter;
inflating the balloon with a biomaterial; and
removing the catheter from the patient while leaving the inflated balloon in the patient.
2 . The method of claim 1 , wherein inflating the balloon comprises introducing the biomaterial through the catheter.
3 . The method of claim 1 , further comprising:
providing the biomaterial as a formulation that includes one or more types of cells effective to promote healing, repair, regeneration and/or restoration of the intervertebral disc.
4 . The method of claim 1 , further comprising:
verifying the location of the balloon within the nucleus pulposus.
5 . The method of claim 4 , wherein the location of the balloon is verified by fluoroscopy.
6 . The method of claim 5 , wherein the inflation of the balloon is monitored by fluoroscopy.
7 . The method of claim 6 , wherein the biomaterial is at least partially radiopaque.
8 . A method of augmenting an intervertebral space, the method comprising the steps of:
inserting a balloon into a nucleus pulposus without removing material from nucleus pulposus, the balloon being connected to a catheter;
inflating the balloon with a first material;
allowing the balloon to remain inflated for a period of time;
removing the first material from the balloon;
injecting into the balloon a second material, the second material comprising a biomaterial; and
removing the catheter from the patient while leaving the balloon injected with the second material in the patient.
9 . The method of claim 8 , wherein inflating the balloon comprises introducing the first material through the catheter.
10 . The method of claim 9 , wherein removing the first material comprises extracting the first material through the catheter and wherein injecting the second material comprises introducing the second material through the catheter.
11 . The method of claim 10 , wherein removing the first material and injecting the second material are performed simultaneously.
12 . The method of claim 11 , wherein the catheter comprises a dual-lumen catheter and the first material is removed through a first lumen of the catheter and the second material is injected through a second lumen of the catheter.
13 . The method of claim 12 , wherein the balloon has an inflated volume from about 0.1 cc to about 8.0 cc.
14 . The method of claim 13 , wherein the balloon has an inflated volume sized to at least partially distract the vertebrae adjacent to the nucleus pulposus.
15 . A method of treating a patient, comprising the steps of:
inserting a balloon into a nucleus pulposus of an intervertebral disc without removing material from nucleus pulposus, the balloon being connected to a catheter;
inflating the balloon with a first material through the catheter;
allowing the balloon to remain inflated within the nucleus pulposus for a period of time;
removing the first material from the balloon leaving a prepared space within the nucleus pulposus;
removing the balloon from the patient; and
injecting a biomaterial into the prepared space of the nucleus pulposus.
16 . The method of claim 15 , wherein the biomaterial is selected from the group consisting of collagen, fibrin, albumin, silk, elastin, keratin, and other proteoglycans.
17 . The method of claim 16 , wherein the biomaterial further comprises a polysaccharide selected from the group consisting of hyaluronic acid, chitosan, cellulose, and agar.
18 . The method of claim 15 , wherein the biomaterial includes a synthetic material.
19 . The method of claim 18 , wherein the synthetic material includes an elastomeric material from a group consisting of silicone, polyurethane, silicone-polyurethane copolymers, polyolefin, and combinations thereof.
20 . The method of claim 19 , wherein the synthetic material includes a hydrogel material from a group consisting of polyester, polyacrylamide, polyacrylic acid, polyvinyl alcohol, polyethylene oxide, polyethylene glycol, and combinations thereof.
21 . The method of claim 19 , wherein the synthetic material includes a resorbable polymer material from a group consisting of polylactide, polyglycolide, poly(lactide-co-glycolide), poly(dioxanone), poly(ε-caprolactone), poly(hydroxylbutyrate), poly(hydroxylvalerate), tyrosine-based polycarbonate, polypropylene fumarate, and combinations thereof.
22 . A method treating an intervertebral disc of a patient, the method comprising:
forming and dilating an opening in a disc annulus without removing any of the disc annulus;
introducing an inflatable member through the dilated opening in the disc annulus and into a nucleus pulposus of the disc without removing any of the nucleus pulposus;
inflating the inflatable member with a first material to augment a space in the nucleus pulposus;
monitoring the internal pressure and expansion of the inflatable member;
extracting the first material from the inflatable member; and
injecting a biomaterial into the inflatable member.
23 . The method of claim 22 , wherein injecting the biomaterial comprises injecting the biomaterial through a passage in the inflatable member simultaneously with the extraction of the first material.
24 . The method of claim 23 , wherein the first material is extracted through a first lumen of a dual-lumen catheter and the biomaterial is injected through a second lumen of the dual-lumen catheter.