LANX ASPEN SURGICAL TECHNIQUE PDF

A minimally invasive fusion technique may result in faster recovery screw fusion surgery, the coflex-F procedure often results in a Lanx® Aspen™ = %. Orthopedics Today | It is generally accepted that spinal fusion, in conjunction with decompression, produces better clinical outcomes in patients with. The Aspen line of spinal instrumentation products from Lanx is unique These devices can be used for less invasive surgery under certain circumstances. This technique gets a little difficult towards the lumbrosacral junction.

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The Posterior Fusion System is a titanium implant that has an adjustable, fenestrated core and adjustable-length plates which allows for expansion and compression. To define the appropriate implant size, trials are utilized. The two wings are approximated towards the midline and the screw is secured. The purpose of this paper is to provide a comprehensive overview on interspinous implants, their mechanisms of action, safety, cost, and effectiveness in the treatment of lumbar stenosis and degenerative disc diseases.

Aspen MIS Fusion System | Aspen MIS Fusion System by Zimmer Biomet

The X-Stop device Medtronic, Tolochenaz, Switzerland was approved by the US Food and Drug Administration in for the treatment of neurogenic intermittent claudication secondary to lumbar stenosis [ 38 ]. Food and Drug Administration approval of X-Stop surgjcal decompression system was based on laboratory, mechanical, and cadaver studies and also a multicenter, prospective randomized controlled clinical study [ 38 ].

In a reported prospective trial, the application of the first generation Wallis device improved outcome in patients who underwent a second discectomy.

Currently, there are no long-term clinical trials for IPD: The oval spacer distributes the load along the concave shape of the spinous processes. Never reuse any implant even if it appears unmarked or undamaged. There are three different implant designs and a wide range of sizes for an optimum anatomical fit. The appropriate sized interspinous device is chosen and placed between the spinous processes and squeezed together, and the device is compressed or distract with an appropriate device.

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The BacJac interspinous device implanted in a lumbar spinal model. In this paper we provide an overview of the current notions of the biomechanical principles of the interspinous process devices, as well as in experimental and clinical studies.

The first interspinous implant for the lumbar spine was developed in the s by Knowles. By turning the actuating handle of the inserter, a compressive force is created, retracting the outer shell and deploying the wings, which expand on each side of the spinous process, stabilizing the interspinous implant on the midline Figures 101112and After a solid fusion occurs, the system serves no functional purpose and should be removed.

It is composed of a self-distracting helical tip Figure The Aspen system can be used in single- or multi-level constructs.

They found that they all had similar effect on the flexibility, reducing the intradiscal pressure in extension, but having no effect in flexion, lateral bending, and axial rotation. Standard Implant For Aspen Standard, the implant barrel is 21mm long and may be best suited for a thick spinous process Medium Implant With a medial-lateral dimension that is 3mm shorter in the barrel, the Aspen Medium implant may be preferred. Warnings A successful result is not always achieved in every surgical case.

The exhaustive mechanism of the intradiscal pressure interaction with the neural structures is today not clarified. The spacer has a distal and proximal 10 degrees inclined groove to better wurgical the spinous processes and adapt to the anatomy of the spinous processes.

Table of Contents Alerts. The wings of the device are folded as the inserter flanges are compressed, thus the DIAM is driven as far anterior as possible using the impactor. Surgeons should be aware that the insertion of an interspinous device requires personalized forces and caution, but osteopenia is not an absolute contraindication for the operation. Type of Implants Contemporary models of fusion interspinous devices have evolved from spinous process wiring with bone blocks and early device designs as the Wilson surical The Helifix Interspinous Surgiical System is a percutaneous self-distracting implant manufactured from PEEK polyetheretherketone material and tantalum radiographic markers.

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The implant core is made of titanium TiAl6V4 alloy, whereas the external shell tfchnique composed of commercially pure titanium. To receive news and publication updates for BioMed Research International, enter your email address in the box below.

It is recommended that regular postoperative follow-up is undertaken to detect early signs of failure of the implants and to consider the action to be taken.

BioMed Research International

The typical findings are radial fissures, prolapses, endplate damage, annular protrusion, internal disc disruption, disc space techinque, hypertrophic ligaments, hypertrophic facet joints, and osteophytes [ 1 — 4 ]. The device consists of an interspinous spacer made of polyetheretherketone PEEKwhich limits extension, and two woven dacron bands that secure the implant and limit flexion Figure 4. Any neuromuscular deficit which places an unusually heavy load on the device during the healing period.

The inferior aspect of the spinous processes must be trimmed, if necessary, to facilitate insertion of the interspinous spacer. X-Stop is the only IDP device with class I data and a prospective randomized control trial supporting its safety and efficacy compared to the nonoperative treatment. The images are subsequently evaluated to identify load-induced durgical. It is a titanium device with a U-shaped body and two wings on each side Figure 3. This material is intended for health care professionals.

The spacers have all the same width but the heights increases from 8, 10, 12, and 14 to View at Google Scholar U. Outside the United States The Aspen system is a spinous process fixation device intended to provide stabilisation in the thoracic, lumbar and sacral spine T1-S1.

The flat polyester bands have an increased surface contact with the spinous processes, minimizing local concentration of contact stresses on the bone during flexion movements. The cost difference was secondary to the fact that laminectomy was performed as an inpatient surgery, whereas X-Stop was performed as an ambulatory setting.