Anterior Cervical Disc Replacement for Degenerative Disc Disease

Purpose. To review the outcomes of anterior cervical disc replacement using the Prestige LP system for degenerative disc disease. Methods. Medical records of 12 men and 23 women aged 26 to 66 (mean, 46) years who underwent 48 anterior cervical disc replacements using the Prestige LP system by a sing...

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Main Authors: Sudarshan Munigangaiah, John P McCabe
Format: Article
Language:English
Published: SAGE Publishing 2014-12-01
Series:Journal of Orthopaedic Surgery
Online Access:https://doi.org/10.1177/230949901402200320
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spelling doaj-dc8833347b994665b69b40f3c9ce4d6c2020-11-25T02:48:37ZengSAGE PublishingJournal of Orthopaedic Surgery2309-49902014-12-012210.1177/230949901402200320Anterior Cervical Disc Replacement for Degenerative Disc DiseaseSudarshan MunigangaiahJohn P McCabePurpose. To review the outcomes of anterior cervical disc replacement using the Prestige LP system for degenerative disc disease. Methods. Medical records of 12 men and 23 women aged 26 to 66 (mean, 46) years who underwent 48 anterior cervical disc replacements using the Prestige LP system by a single spine surgeon were reviewed. 22 patients underwent one-level disc replacement at C5-C6 (n=13) and C6-C7 (n=9), and 13 patients underwent 2-level disc replacement at C5-C6 and C6-C7 (n=11), C4-C5 and C5-C6 (n=1), and C6-C7 and C7-T1 (n=1). Neck Disability Index (NDI) score, visual analogue scale (VAS) for pain in the neck and arm, and physical and mental component scores of the Short Form 36 were evaluated at week 6 and months 6, 12, 24, 36, and 48. Results. The NDI score, VAS score for neck and arm pain, and physical and mental component scores of the Short Form 36 improved significantly after surgery (p<0.001). 80% of patients were satisfied with the treatment. One patient developed a neck haematoma on day 1 and underwent surgical evacuation. Another patient developed Horner's syndrome and achieved partial recovery at 6 weeks and complete recovery at 6 months. No patient had implant-related complications or reoperation. Conclusion. The Prestige LP cervical disc implant was safe for one- and 2-level cervical disc replacement.https://doi.org/10.1177/230949901402200320
collection DOAJ
language English
format Article
sources DOAJ
author Sudarshan Munigangaiah
John P McCabe
spellingShingle Sudarshan Munigangaiah
John P McCabe
Anterior Cervical Disc Replacement for Degenerative Disc Disease
Journal of Orthopaedic Surgery
author_facet Sudarshan Munigangaiah
John P McCabe
author_sort Sudarshan Munigangaiah
title Anterior Cervical Disc Replacement for Degenerative Disc Disease
title_short Anterior Cervical Disc Replacement for Degenerative Disc Disease
title_full Anterior Cervical Disc Replacement for Degenerative Disc Disease
title_fullStr Anterior Cervical Disc Replacement for Degenerative Disc Disease
title_full_unstemmed Anterior Cervical Disc Replacement for Degenerative Disc Disease
title_sort anterior cervical disc replacement for degenerative disc disease
publisher SAGE Publishing
series Journal of Orthopaedic Surgery
issn 2309-4990
publishDate 2014-12-01
description Purpose. To review the outcomes of anterior cervical disc replacement using the Prestige LP system for degenerative disc disease. Methods. Medical records of 12 men and 23 women aged 26 to 66 (mean, 46) years who underwent 48 anterior cervical disc replacements using the Prestige LP system by a single spine surgeon were reviewed. 22 patients underwent one-level disc replacement at C5-C6 (n=13) and C6-C7 (n=9), and 13 patients underwent 2-level disc replacement at C5-C6 and C6-C7 (n=11), C4-C5 and C5-C6 (n=1), and C6-C7 and C7-T1 (n=1). Neck Disability Index (NDI) score, visual analogue scale (VAS) for pain in the neck and arm, and physical and mental component scores of the Short Form 36 were evaluated at week 6 and months 6, 12, 24, 36, and 48. Results. The NDI score, VAS score for neck and arm pain, and physical and mental component scores of the Short Form 36 improved significantly after surgery (p<0.001). 80% of patients were satisfied with the treatment. One patient developed a neck haematoma on day 1 and underwent surgical evacuation. Another patient developed Horner's syndrome and achieved partial recovery at 6 weeks and complete recovery at 6 months. No patient had implant-related complications or reoperation. Conclusion. The Prestige LP cervical disc implant was safe for one- and 2-level cervical disc replacement.
url https://doi.org/10.1177/230949901402200320
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