2016
DOI: 10.1097/bsd.0b013e3182956ec5
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Effect of an Annular Closure Device (Barricaid) on Same-Level Recurrent Disk Herniation and Disk Height Loss After Primary Lumbar Discectomy

Abstract: Implantation of a novel annular repair device was associated with greater maintenance of disk height and improved 1-year leg pain, back pain, and low-back disability. Recurrent disk herniation did not occur in any patient after annular repair. Closure of annular defect after lumbar discectomy may help preserve the physiological disk function and prevent long-term disk height loss and associated back and leg pain.

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Cited by 90 publications
(108 citation statements)
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References 30 publications
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“…Wilke et al 45 studied this device in a human cadaveric disc model and the implant effectively prevented re-herniation without migration. Parker et al, 46 in a prospective 2-year trial, demonstrated a 0% re-herniation rate (vs. 6.5% for the control cohort), no complications, and a trend toward less disc height loss with the utilization of the Barricaid™. Another closure device, Xclose Tissue Repair System™ (Anulex Technologies, Minnetonka, MN), uses suture/ anchor combination to directly repair the annular defect.…”
Section: Annular Repairmentioning
confidence: 94%
“…Wilke et al 45 studied this device in a human cadaveric disc model and the implant effectively prevented re-herniation without migration. Parker et al, 46 in a prospective 2-year trial, demonstrated a 0% re-herniation rate (vs. 6.5% for the control cohort), no complications, and a trend toward less disc height loss with the utilization of the Barricaid™. Another closure device, Xclose Tissue Repair System™ (Anulex Technologies, Minnetonka, MN), uses suture/ anchor combination to directly repair the annular defect.…”
Section: Annular Repairmentioning
confidence: 94%
“…Besides contributing to reherniation risk, defects in the annulus result in altered biomechanical response (30–32), decreased cellularity (33), accelerated degeneration (34) and decreased IVD height (25). The Barricaid (Intrinsic Therapeutics, Inc., Woburn, Massachusetts), a shield within the annulus fibrosus secured to the inferior vertebral body (35) prevents reherniation (36) and protects the facet joint (37), but does not seal AF defects. Developing biomaterials that can seal AF defects is an area of active research (38).…”
Section: Introductionmentioning
confidence: 99%
“…Some annular closure devices and NP replacement devices have been introduced clinically, including Barricaid (Intrinsic Therapeutics, Woburn, MA, USA), Xclose Tissue Repair System (Anulex Technologies, Minnetonka, MN), Inclose Surgical Mesh System (Anulex Technologies, Inc., Minnetonka, MN), NuCore® Injectable Nucleus hydrogel (Spine Wave, Inc., Shelton, CT, USA), NeuDIsc (Replication Medical, Inc., Cranberry, NJ), DiscCell (Gentis, Wayne, Pennsylvania), DASCOR Disc Arthroplasty System (Disc Dynamics, Inc., Eden Prairie, Minnesota), BioDisc (CryoLife, Atlanta, Georgia), and NucleoFix (Replication Medical, Inc., Cranberry, NJ) . The Barricaid AF closure device showed midterm clinical feasibility, efficacy, and safety . Although an FDA panel confirmed its efficacy in preventing reherniations following discectomy, the presence of lytic endplate lesions and device subsidence raised safety concerns .…”
Section: Available Clinical Treatments For Discogenic Painmentioning
confidence: 99%