TY - JOUR
T1 - Difference in occurrence of heterotopic ossification according to prosthesis type in the cervical artificial disc replacement
AU - Yi, Seong
AU - Kim, Keung Nyun
AU - Yang, Moon Sul
AU - Yang, Joong Won
AU - Kim, Hoon
AU - Ha, Yoon
AU - Yoon, Do Heum
AU - Shin, Hyun Chul
PY - 2010/7/15
Y1 - 2010/7/15
N2 - Study Design: Retrospective study of the difference of heterotopic ossification (HO) occurrence according to 3 different types of prosthesis. Objective: This study was designed to investigate the difference of HO occurrence according to different type of prosthesis. Summary of Background Data: HO is defined as formation of the bone outside the skeletal system. Reported HO occurrence rate in cervical artificial disc replacement (ADR) was unexpectedly high and varied. But the influencing factors of HO in cervical ADR have not been elucidated well. The prosthesis-related factors for making difference of HO occurrence were investigated in this study. Methods: A total of 170 patients undergoing cervical arthroplasty with the Bryan cervical disc prosthesis (Medtroic Sofamor Danek, Memphis, TN), Mobi-C disc prosthesis (LDR Medical, Troyes, France), and ProDisc-C (Synthes, Inc., West Chester, PA) were included. Cervical lateral radiographs obtained before and after surgery were used to identify HO. Occurrence rate, occurrence-free period, location, and grade of HOs were investigated according to the different prosthesis. Results: Each prosthesis group included patients as follows: Bryan disc, 81 patients; Mobi-C, 61 patients; and ProDisc-C, 28 patients. Overall HO rate was 40.6% (69 of 170 patients). Each HO occurrence rate by prosthesis was as follows: the Bryan disc group, 21.0%; Mobi-C group, 52.5%; and the ProDisc-C group, 71.4%. In the survival analysis, all patients showed 27.1 ± 3.7 months as the median survival. The Bryan disc group showed statistically longer survival (48.4 ± 7.4 months) than the other groups. Conclusion: Occurrence of HO is an inevitable postoperative complication after cervical ADR. The occurrence rate of HO was higher than our expectation. Moreover, definite differences in occurrence rate according to the prosthe is type were identified by this study.
AB - Study Design: Retrospective study of the difference of heterotopic ossification (HO) occurrence according to 3 different types of prosthesis. Objective: This study was designed to investigate the difference of HO occurrence according to different type of prosthesis. Summary of Background Data: HO is defined as formation of the bone outside the skeletal system. Reported HO occurrence rate in cervical artificial disc replacement (ADR) was unexpectedly high and varied. But the influencing factors of HO in cervical ADR have not been elucidated well. The prosthesis-related factors for making difference of HO occurrence were investigated in this study. Methods: A total of 170 patients undergoing cervical arthroplasty with the Bryan cervical disc prosthesis (Medtroic Sofamor Danek, Memphis, TN), Mobi-C disc prosthesis (LDR Medical, Troyes, France), and ProDisc-C (Synthes, Inc., West Chester, PA) were included. Cervical lateral radiographs obtained before and after surgery were used to identify HO. Occurrence rate, occurrence-free period, location, and grade of HOs were investigated according to the different prosthesis. Results: Each prosthesis group included patients as follows: Bryan disc, 81 patients; Mobi-C, 61 patients; and ProDisc-C, 28 patients. Overall HO rate was 40.6% (69 of 170 patients). Each HO occurrence rate by prosthesis was as follows: the Bryan disc group, 21.0%; Mobi-C group, 52.5%; and the ProDisc-C group, 71.4%. In the survival analysis, all patients showed 27.1 ± 3.7 months as the median survival. The Bryan disc group showed statistically longer survival (48.4 ± 7.4 months) than the other groups. Conclusion: Occurrence of HO is an inevitable postoperative complication after cervical ADR. The occurrence rate of HO was higher than our expectation. Moreover, definite differences in occurrence rate according to the prosthe is type were identified by this study.
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U2 - 10.1097/BRS.0b013e3181c6526b
DO - 10.1097/BRS.0b013e3181c6526b
M3 - Article
C2 - 20581764
AN - SCOPUS:77955012641
SN - 0362-2436
VL - 35
SP - 1556
EP - 1561
JO - Spine
JF - Spine
IS - 16
ER -