STUDY DESIGN: Retrospective consecutive cohort study. OBJECTIVE: To study the effectiveness of β-tricalcium phosphate (β-TCP) granules as a packing material in the titanium cages for anterior cervical discectomy and fusion (ACDF), compared with the conventional hydroxyapatite (HA) granules. SUMMARY OF BACKGROUND DATA: ACDF using titanium cages is a standard procedure for the treatment of cervical spinal degenerative diseases. Synthetic bone substitutes are widely used to pack the titanium cage to augment intervertebral bony fusion, but the efficacy has not been confirmed. METHODS: Fusion condition was evaluated on lateral radiographs and computed tomography. Complete fusion of the treated segments was defined by three criteria: movement of the spinous process at flexion and extension positions of less than 3 mm, bony bridging between vertebral bodies, and absence of the halo around the titanium cage. The evaluation was performed at 6 months, 1 year, and 2 years after surgery. RESULTS: Intervertebral fusion was studied in patients who underwent ACDF using β-TCP (93 segments of 57 patients) or HA (72 segments of 48 patients) packing of cylindrical titanium cages. Complete fusion rate at 6 months and 1 year was significantly better in the β-TCP group (46% at 6 months and 69% at 1 year) than in the HA group (24% at 6 months and 49% at 1 year), but the rate was similar at 2 years in the β-TCP group (94%) and the HA group (90%). There were no material-related adverse effects. CONCLUSION: Satisfactory final fusion rates were obtained after ACDF using both β-TCP- and HA-packed titanium cages. β-TCP showed higher fusion rate in the early stage after surgery and can be recommended as a bone substitute for ACDF with titanium cages.
STUDY DESIGN: Retrospective consecutive cohort study. OBJECTIVE: To study the effectiveness of β-tricalcium phosphate (β-TCP) granules as a packing material in the titanium cages for anterior cervical discectomy and fusion (ACDF), compared with the conventional hydroxyapatite (HA) granules. SUMMARY OF BACKGROUND DATA: ACDF using titanium cages is a standard procedure for the treatment of cervical spinal degenerative diseases. Synthetic bone substitutes are widely used to pack the titanium cage to augment intervertebral bony fusion, but the efficacy has not been confirmed. METHODS: Fusion condition was evaluated on lateral radiographs and computed tomography. Complete fusion of the treated segments was defined by three criteria: movement of the spinous process at flexion and extension positions of less than 3 mm, bony bridging between vertebral bodies, and absence of the halo around the titanium cage. The evaluation was performed at 6 months, 1 year, and 2 years after surgery. RESULTS: Intervertebral fusion was studied in patients who underwent ACDF using β-TCP (93 segments of 57 patients) or HA (72 segments of 48 patients) packing of cylindrical titanium cages. Complete fusion rate at 6 months and 1 year was significantly better in the β-TCP group (46% at 6 months and 69% at 1 year) than in the HA group (24% at 6 months and 49% at 1 year), but the rate was similar at 2 years in the β-TCP group (94%) and the HA group (90%). There were no material-related adverse effects. CONCLUSION: Satisfactory final fusion rates were obtained after ACDF using both β-TCP- and HA-packed titanium cages. β-TCP showed higher fusion rate in the early stage after surgery and can be recommended as a bone substitute for ACDF with titanium cages.
Authors: Abhijeet Kadam; Paul W Millhouse; Christopher K Kepler; Kris E Radcliff; Michael G Fehlings; Michael E Janssen; Rick C Sasso; James J Benedict; Alexander R Vaccaro Journal: Int J Spine Surg Date: 2016-09-22
Authors: Jemin Yi; Gun Woo Lee; Woo Dong Nam; Kye Young Han; Myung-Ho Kim; Jong Won Kang; Jonghwa Won; Seong Wan Kim; Won Noh; Jin S Yeom Journal: Asian Spine J Date: 2015-02-13