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. 2016 Jul 21;11(7):e0159761.
doi: 10.1371/journal.pone.0159761. eCollection 2016.

Comparison of 2 Zero-Profile Implants in the Treatment of Single-Level Cervical Spondylotic Myelopathy: A Preliminary Clinical Study of Cervical Disc Arthroplasty versus Fusion

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Comparison of 2 Zero-Profile Implants in the Treatment of Single-Level Cervical Spondylotic Myelopathy: A Preliminary Clinical Study of Cervical Disc Arthroplasty versus Fusion

Sheng Shi et al. PLoS One. .

Abstract

Objectives: Cervical disc arthroplasty (CDA) with Discover prosthesis or anterior cervical discectomy and fusion (ACDF) with Zero-P cage has been widely used in the treatment of cervical spondylotic myelopathy (CSM). However, little is known about the comparison of the 2 zero-profile implants in the treatment of single-level CSM. The aim was to compare the clinical outcomes and radiographic parameters of CDA with Discover prosthesis and ACDF with Zero-P cage for the treatment of single-level CSM.

Methods: A total of 128 consecutive patients who underwent 1-level CDA with Discover prosthesis or ACDF with Zero-P cage for single-level CSM between September 2009 and December 2012 were included in this study. Clinical outcomes were evaluated using the Japanese Orthopaedic Association (JOA) score and Neck Disability Index (NDI). For radiographic assessment, the overall sagittal alignment (OSA), functional spinal unit (FSU) angle, and range of motion (ROM) at the index and adjacent levels were measured before and after surgery. Additionally, the complications were also recorded.

Results: Both treatments significantly improved all clinical parameters (P < 0.05), without statistically relevant differences between the 2 groups. The OSA and FSU angle increased significantly in both groups (P <0.05). Compared with Zero-P group, ROMs at the index levels were well maintained in the Discover group (P < 0.05). However, there were no statistical differences in the ROMs of adjacent levels between the 2 groups (P > 0.05). Besides, no significant differences existed in dysphagia, subsidence, or adjacent disc degeneration between the 2 groups (P > 0.05). However, significant differences occurred in prosthesis migration in CDA group.

Conclusions: The results of this study showed that clinical outcomes and radiographic parameters were satisfactory and comparable with the 2 techniques. However, more attention to prosthesis migration of artificial cervical disc should be paid in the postoperative early-term follow-up.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. The methods about measurements of radiographic parameters.
The range of motion (ROM) at the adjacent levels by disc space angle in the Discover group (a). The overall alignment of C2-C7 (α,OSA) and functional spinal unit (β,FSU) angle in the Discover group (b). The range of motion (ROM) at the adjacent levels by disc space angle in the Zero-P group (c). The overall alignment of C2-C7 (α,OSA) and functional spinal unit (β,FSU) angle in the Zero-P group (d).
Fig 2
Fig 2. The representive case who suffered migration of Discover prothesis postoperatively.
Postoperative 2-day (a), and final follow-up (b) lateral radiographs showing anterior migration of the superior endplate of Discover prosthesis (White arrows).
Fig 3
Fig 3. The representive case who suffered prosthesis subsidence and adjacent disc degeneration postoperatively.
Postoperative 2-day (a), and final follow-up (b) lateral radiographs showing the superior endplate of Discover prosthesis subsiding into the cephalad vertebra and new anterior osteophyte formation in the patient after cervical disc arthroplasty with Discover prothesis. The white arrows indicate the subsidence of the prosthesis. The black arrows indicate the new anterior osteophyte formation.
Fig 4
Fig 4. The representive case who suffered heterotopic ossification of Discover prosthesis postoperatively.
Dynamic flexion-extension lateral radiographs at the final follow-up showing heterotopic ossification (Grade III) at the index level with significant restriction in the range of motion of Discover prothesis.

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