Clinical results and development of heterotopic ossification in total cervical disc replacement during a 4-year follow-up
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20035357
PubMed Central
PMC2899807
DOI
10.1007/s00586-009-1259-3
Knihovny.cz E-resources
- MeSH
- Ankylosis etiology pathology physiopathology MeSH
- Neck Pain etiology pathology physiopathology MeSH
- Time MeSH
- Time Factors MeSH
- Diskectomy adverse effects MeSH
- Adult MeSH
- Spinal Fusion adverse effects MeSH
- Ossification, Heterotopic etiology pathology physiopathology MeSH
- Head Movements physiology MeSH
- Internal Fixators adverse effects MeSH
- Cervical Vertebrae pathology surgery MeSH
- Middle Aged MeSH
- Humans MeSH
- Stress, Mechanical MeSH
- Pain Measurement MeSH
- Follow-Up Studies MeSH
- Postoperative Complications etiology pathology physiopathology MeSH
- Disability Evaluation MeSH
- Recurrence MeSH
- Range of Motion, Articular physiology MeSH
- Intervertebral Disc Displacement complications pathology surgery MeSH
- Weight-Bearing physiology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Cervical total disc replacement (CTDR) aims to decrease the incidence of adjacent segment disease through motion preservation in the operated disc space. Ongoing data collection and increasing number of studies describing heterotopic ossification (HO) resulting in decreased mobility of implants, forced us to carefully evaluate our long-term clinical and morphological results of patients with CTDR. We present the first 54 consecutive patients treated with 65 ProdiscC prostheses during a 12-month period (2/2004-3/2005). All patients signed an informed consent and were included in prospective long-term study approved by hospital ethical committee. The 1- and 2-year follow-up analysis were available for all patients included and 4-year results for 50 patients (60 implants). Clinical (neck disability index-NDI, visual analog scale-VAS) and radiological follow-up was conducted at 1-, 2- and 4-years after the procedure. The Mehren/Suchomel modification of McAfee scale was used to classify the appearance of HO. Mean preoperative NDI was 34.5%, VAS for neck pain intensity 4.6 and VAS for arm pain intensity 5.0. At 1-, 2- and 4-year follow-up, the mean NDI was 30.7, 27.2, and 30.4, mean VAS for neck pain intensity 2.5, 2.1 and 2.9 and mean VAS for arm pain intensity pain 2.2, 1.9 and 2.3, respectively. Significant HO (grade III) was present in 45% of implants and segmental ankylosis (grade IV) in another 18% 4 years after intervention. This finding had no clinical consequences and 92% of patients would undergo the same surgery again. Our clinical results (NDI, VAS) are comparable with fusion techniques. Although, advanced non-fusion technology is used, a significant frequency of HO formation and spontaneous fusion in cervical disc replacement surgery must be anticipated during long-term follow-up.
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