Early clinical experience with the mobi-C disc prosthesis

Yonsei Med J. 2007 Jun 30;48(3):457-64. doi: 10.3349/ymj.2007.48.3.457.

Abstract

Purpose: We have experienced 23 patients who had underwent cervical disc replacement with Mobi-C disc prosthesis and analyzed their radiological results to evaluate its efficacy.

Patients and methods: This study was performed on 23 patients with degenerative cervical disc disease who underwent CDR with Mobi-C disc prosthesis from March 2006 to June 2006.

Results: The age of the study population ranged from 31 to 62 years with mean of 43 years, and 16 male and 7 female cases. Regarding axial pain, the average preoperative VAS score was 6.47 +/- 1.4, while at final follow-up it was 1.4 +/- 0.7 (p < 0.001). The preoperatively VAS score for radiculopathy was 6.7 +/- 0.7 compared with an average score of 0 +/- 0 at the final follow-up (p < 0.001). At postoperative 6th month, Odom's criteria were excellent, good, or fair for all 23 patients (100%). 7 patients (30.4%) were classified as excellent, 15 patients (65.2%) as good, and 1 patients (4.4%) as fair. Prolo economic and functional rating scale was average 8.9 +/- 0.7 at postoperative 6th month. ROM in C2-7, ROM of FSU, and ROM in upper adjacent level were well preserved after CDR.

Conclusion: This report would be the first document about the CDR with Mobi-C disc prosthesis in the treatment of degenerative cervical disc disease. CDR with Mobi-C disc prosthesis provided a favorable clinical and radiological outcome in this study. However, Long-term follow-up studies are required to prove its efficacy and ability to prevent adjacent segment disease.

MeSH terms

  • Adult
  • Cervical Vertebrae / physiopathology
  • Cervical Vertebrae / surgery*
  • Diskectomy / adverse effects
  • Diskectomy / instrumentation
  • Diskectomy / methods*
  • Female
  • Humans
  • Joint Prosthesis / adverse effects
  • Male
  • Middle Aged
  • Postoperative Complications / prevention & control
  • Range of Motion, Articular
  • Time Factors
  • Treatment Outcome