BackgroundTh e DASCOR device has recently been introduced as an innovative nucleus replacement alternative for the treatment of low-back pain caused by degenerative intervertebral disc disease. Th e purpose of this study was to characterize, through a series of preclinical mechanical bench and biomechanical tests, the eff ectiveness of this device.
MethodsA number of samples were created using similar preparation methods in order to characterize the nucleus replacement device in multiple mechanical bench tests, using ASTM-guided protocols, where appropriate. Mechanical bench testing included static testing to characterize the device's compressive, shear properties, and fatigue testing to determine the device's compressive fatigue strength, wear, and durability. Biomechanical testing, using human cadaveric lumbar spines, was also conducted to determine the ability of the device to restore multidirectional segmental fl exibility and to determine its resulting endplate contact stress.
ResultsTh e static compressive and shear moduli of the nucleus replacement device were determined to be between 4.2-5.6 MPa and 1.4-1.9 MPa, respectively. Similarly, the ultimate compressive and shear strength were 12,400 N and 6,993 N, respectively. Th e maximum axial compressive fatigue strength of the tested device that was able to withstand a runout without failure was determined to be approximately 3 MPa. Th e wear assessment determined that the device is durable and yielded minimal wear rates of 0.29mg/Mc. Finally, the biomechanical testing demonstrated that the device can restore the multidirectional segmental fl exibility to a level seen in the intact condition while concurrently producing a uniform endplate contact stress.
ConclusionsTh e results of the present study provided a mechanical justifi cation supporting the clinical use of the nucleus replacement device and also help explain and support the positive clinical results obtained from two European studies and one US pilot study.
Clinical RelevanceNucleus replacement devices are rapidly emerging to address specifi c conditions of degenerative disc disease. Preclinical testing of such devices is paramount in order to potentially ensure successful clinical outcomes post implantation