Lanman Spinal Neurosurgery is one of the nations top leading innovators in the artificial disc replacement realm of spinal medicine, breaking down the different types of artificial disc replacements further defining common questions asked such as “what is artificial disc replacement?”. Artificial disc replacement prosthesis come in many different shapes and sizes, but current designs fall into one of four types: hydraulic, elastic, and mechanical discs.1
The BRYAN® Cervical Disc – The placement of the BRYAN® Cervical Disc was first reported in 2002.4 The placement of the BRYAN® Cervical Disc consists of a polycarbonate urethane nucleus that rests between two titanium alloy “shells.” Saline inside the nucleus adds compression to the disc. The metal parts of the BRYAN® device that interface with bone are porous to help integration. Because of its design, the BRYAN® Cervical Disc requires placement of the prosthesis precisely in its proper position. While the design is intriguing, the BRYAN® Cervical Disc is now obsolete.
The BRYAN® Cervical Disc
PRESTIGE® Cervical Disc – The PRESTIGE® Cervical Disc is made of a titanium ceramic composite and titanium carbide. The PRESTIGE® Cervical Disc has a “ball and trough” design, which means the upper part of the device has a rounded edge that moves in a divot in the bottom section of the artificial disc. This design and composition make the PRESTIGE® Cervical Disc highly durable and give the spine outstanding motion at one- and two-disc levels in the cervical spine. The endplates each have two low profile keels to help secure it to bone. Once placed, the artificial disc permits the spine to flex, extend, side bend, and rotate while maintaining alignment, height, and curvature of the natural spine. Of note, an earlier design called the PRESTIGE ST is now obsolete and has been replaced with the PRESTIGE LP. Patients continue to experience excellent results at least 10 years after artificial disc replacement surgery with the PRESTIGE® LP Cervical Disc.5
PRESTIGE® Cervical Disc
Mobi-C® Cervical Disc – The upper and lower bone-facing endplates of the Mobi-C® Cervical Disc are made of a cobalt chromium molybdenum alloy. The endplates are coated with a fine layer of titanium and hydroxyapatite to promote integration with bone. A mobile, polyethylene bearing rests between the two endplates to give the device and the spine good range of motion.
Mobi-C® Cervical Disc
SECURE-C® Cervical Disc – The SECURE-C® Cervical Disc is three separate pieces: a polyethylene inner core that is inserted between two cobalt chromium molybdenum alloy (metal) endplates. The specifications of the SECURE-C® Cervical Disc suggest that it permits up to ±15º motion in flexion-extension (nodding up and down) and up to ±10º motion in lateral bending (tilting the head from side to side).
SECURE-C® Cervical Disc
PCM® Cervical Disc – The PCM® Cervical Disc is two pieces: the upper portion is a cobalt chromium alloy (metal) endplate, while the lower metal endplate contains an integrated polyethylene spacer. The device has a titanium calcium phosphate coating to promote integration to bone. The PCM® Cervical Disc received premarket approval from the FDA in 2012, and like other cervical artificial discs, showed superior performance to spinal fusion surgery.6 It was FDA approved to be implanted adjacent to a fusion. It has since been removed from the market.
PCM® Cervical Disc
Prodisc-C® Cervical Disc – The Prodisc-C® Cervical Total Disc Replacement consists of two cobalt chromium molybdenum endplates and one ultra-high molecular weight polyethylene inlay. The inlay is technically separate from the endplate, but it locks into the lower metal such that they function as a single piece after installation. The upper endplate has a highly polished divot into which the plastic dome fits and moves. The metal surfaces are coated with a titanium plasma spray to help hold the artificial disc in place and promote bony growth.
Prodisc-C® Cervical Disc
The M6-C artificial cervical disc has 4 components: Titanium endplates, a viscoelastic polymer nucleus, an ultra-high molecular polyethylene annulus, and sheath. The two outer titanium plates have fixation keels that anchor the artificial disc into the vertebral bone and are coated with a titanium plasma spray to help promote integration with bone. The sheath surrounds the artificial nucleus and artificial annulus, presumably to keep out bone and other debris. Like other artificial discs, the artificial nucleus and artificial annulus allow for good range of motion in the treated spine.
M6-C Artificial Cervical Disc
CHARITÉ® Artificial Disc – The CHARITÉ® Artificial Disc was the first total disc replacement device to be developed and tested. The Type III version CHARITÉ® Artificial Disc has two highly polished metal endplates on either side of an ultra-high molecular weight polyethylene core.3 The endplates are porous so that bone can grow into and bond with the artificial disc. It was primarily used as a lumbar disc replacement and has since been removed from the market.
CHARITÉ® Artificial Disc
Prodisc-L® Lumbar Disc – The Prodisc-L® Total Lumbar Disc Replacement consists of two cobalt chrome alloy (metal) endplates and one ultra-high molecular weight polyethylene inlay. Each endplate has a single keel and has been plasma-sprayed with titanium to help promote bone integration. While tens of thousands of patients have received Prodisc-L® artificial discs at one vertebral disc level since its approval in 2005, the FDA approved the device to treat two-level disease in Spring 2020.
Prodisc-L® Lumbar Disc
ACTIV-L – The activL Artificial Disc has two titanium-coated cobalt-chromium metal alloy endplates with a mobile ultra-high molecular weight polyethylene core. The plastic core is flat on the bottom and round on top, providing both structural support and range of motion. Relative to other artificial lumbar disc designs, the activL Artificial Disc has the lowest height and the endplates come in a variety of sizes to fit individual patient anatomy. The activL Artificial Disc can be used in patients who have one level of degenerative disc disease at either L4/L5 or L5/S1.7