A systematic review of cervical artificial disc replacement wear characteristics and durability
ABSTRACT Study design: Systematic review. Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding...
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Published in | Evidence-based spine-care journal Vol. 3; no. S 01; pp. 31 - 38 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Stettbachstrasse 6 8600 Dübendorf, Switzerland
AOSpine International
01.02.2012
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Subjects | |
Online Access | Get full text |
ISSN | 1663-7976 1869-4136 |
DOI | 10.1055/s-0031-1298606 |
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Abstract | ABSTRACT
Study design:
Systematic review.
Clinical questions:
(1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding the durability of C-ADR beyond 5 years?
Methods:
We searched electronic databases to identify published reports of explanted cervical artificial discs and biomechanical simulations of disc wear.
Results:
Nine articles were identified describing 17 devices explanted from human patients and four articles describing 23 devices explanted from non-human subjects. Wear properties were not consistently reported across studies, so summaries for specific variables are based on few cases. No device had been implanted longer than 4 years. In both human and non-human subjects, devices showed evidence of metallic and polymeric (for discs with polymer components) debris. Inflammatory cells were frequently present in surrounding soft tissues. Signs of infection were uncommon.
Four patients had reactions interpreted as hypersensitivity to metal. We identified three articles on biomechanical wear simulations. Devices were tested between 10 and 20 million cycles in axial loading, flexion/extension, and lateral bending. No device failures were reported. One study suggests such simulations may represent 50 or more years of wear in actual patients.
Conclusion:
Cervical disc implants consistently produced polymeric and metallic debris, which was typically accompanied by inflammation. Hypersensitivity to metal may increase risk for device failure. Biomechanical simulations indicate that cervical disc implants may be durable beyond the currently reported length of clinical follow-up. |
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AbstractList | Systematic review.Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding the durability of C-ADR beyond 5 years?
We searched electronic databases to identify published reports of explanted cervical artificial discs and biomechanical simulations of disc wear.
Nine articles were identified describing 17 devices explanted from human patients and four articles describing 23 devices explanted from non-human subjects. Wear properties were not consistently reported across studies, so summaries for specific variables are based on few cases. No device had been implanted longer than 4 years. In both human and non-human subjects, devices showed evidence of metallic and polymeric (for discs with polymer components) debris. Inflammatory cells were frequently present in surrounding soft tissues. Signs of infection were uncommon.Four patients had reactions interpreted as hypersensitivity to metal. We identified three articles on biomechanical wear simulations. Devices were tested between 10 and 20 million cycles in axial loading, flexion/extension, and lateral bending. No device failures were reported. One study suggests such simulations may represent 50 or more years of wear in actual patients.
Cervical disc implants consistently produced polymeric and metallic debris, which was typically accompanied by inflammation. Hypersensitivity to metal may increase risk for device failure. Biomechanical simulations indicate that cervical disc implants may be durable beyond the currently reported length of clinical follow-up. Study design: Systematic review. Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding the durability of C-ADR beyond 5 years? Methods: We searched electronic databases to identify published reports of explanted cervical artificial discs and biomechanical simulations of disc wear. Results: Nine articles were identified describing 17 devices explanted from human patients and four articles describing 23 devices explanted from non-human subjects. Wear properties were not consistently reported across studies, so summaries for specific variables are based on few cases. No device had been implanted longer than 4 years. In both human and non-human subjects, devices showed evidence of metallic and polymeric (for discs with polymer components) debris. Inflammatory cells were frequently present in surrounding soft tissues. Signs of infection were uncommon. Four patients had reactions interpreted as hypersensitivity to metal. We identified three articles on biomechanical wear simulations. Devices were tested between 10 and 20 million cycles in axial loading, flexion/extension, and lateral bending. No device failures were reported. One study suggests such simulations may represent 50 or more years of wear in actual patients. Conclusion: Cervical disc implants consistently produced polymeric and metallic debris, which was typically accompanied by inflammation. Hypersensitivity to metal may increase risk for device failure. Biomechanical simulations indicate that cervical disc implants may be durable beyond the currently reported length of clinical follow-up. Systematic review.Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding the durability of C-ADR beyond 5 years?STUDY DESIGN Systematic review.Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding the durability of C-ADR beyond 5 years? We searched electronic databases to identify published reports of explanted cervical artificial discs and biomechanical simulations of disc wear.METHODS We searched electronic databases to identify published reports of explanted cervical artificial discs and biomechanical simulations of disc wear. Nine articles were identified describing 17 devices explanted from human patients and four articles describing 23 devices explanted from non-human subjects. Wear properties were not consistently reported across studies, so summaries for specific variables are based on few cases. No device had been implanted longer than 4 years. In both human and non-human subjects, devices showed evidence of metallic and polymeric (for discs with polymer components) debris. Inflammatory cells were frequently present in surrounding soft tissues. Signs of infection were uncommon.Four patients had reactions interpreted as hypersensitivity to metal. We identified three articles on biomechanical wear simulations. Devices were tested between 10 and 20 million cycles in axial loading, flexion/extension, and lateral bending. No device failures were reported. One study suggests such simulations may represent 50 or more years of wear in actual patients.RESULTS Nine articles were identified describing 17 devices explanted from human patients and four articles describing 23 devices explanted from non-human subjects. Wear properties were not consistently reported across studies, so summaries for specific variables are based on few cases. No device had been implanted longer than 4 years. In both human and non-human subjects, devices showed evidence of metallic and polymeric (for discs with polymer components) debris. Inflammatory cells were frequently present in surrounding soft tissues. Signs of infection were uncommon.Four patients had reactions interpreted as hypersensitivity to metal. We identified three articles on biomechanical wear simulations. Devices were tested between 10 and 20 million cycles in axial loading, flexion/extension, and lateral bending. No device failures were reported. One study suggests such simulations may represent 50 or more years of wear in actual patients. Cervical disc implants consistently produced polymeric and metallic debris, which was typically accompanied by inflammation. Hypersensitivity to metal may increase risk for device failure. Biomechanical simulations indicate that cervical disc implants may be durable beyond the currently reported length of clinical follow-up.CONCLUSION Cervical disc implants consistently produced polymeric and metallic debris, which was typically accompanied by inflammation. Hypersensitivity to metal may increase risk for device failure. Biomechanical simulations indicate that cervical disc implants may be durable beyond the currently reported length of clinical follow-up. ABSTRACT Study design: Systematic review. Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding durability, wear, and reasons for failure of C-ADR? (2) What evidence is available from experimental models regarding the durability of C-ADR beyond 5 years? Methods: We searched electronic databases to identify published reports of explanted cervical artificial discs and biomechanical simulations of disc wear. Results: Nine articles were identified describing 17 devices explanted from human patients and four articles describing 23 devices explanted from non-human subjects. Wear properties were not consistently reported across studies, so summaries for specific variables are based on few cases. No device had been implanted longer than 4 years. In both human and non-human subjects, devices showed evidence of metallic and polymeric (for discs with polymer components) debris. Inflammatory cells were frequently present in surrounding soft tissues. Signs of infection were uncommon. Four patients had reactions interpreted as hypersensitivity to metal. We identified three articles on biomechanical wear simulations. Devices were tested between 10 and 20 million cycles in axial loading, flexion/extension, and lateral bending. No device failures were reported. One study suggests such simulations may represent 50 or more years of wear in actual patients. Conclusion: Cervical disc implants consistently produced polymeric and metallic debris, which was typically accompanied by inflammation. Hypersensitivity to metal may increase risk for device failure. Biomechanical simulations indicate that cervical disc implants may be durable beyond the currently reported length of clinical follow-up. |
Author | Skelly, Andrea C Anderson, Paul A Brewer, Devon D Bevevino, Adam J Lehman, Ronald |
AuthorAffiliation | 3 Spectrum Research Inc, Tacoma, WA, USA 2 Spectrum Research Inc, Tacoma, WA, USA. Interdisciplinary Scientific Research, Seattle WA, USA 4 Department of Orthopedics & Rehabilitation, University of Wisconsin, Madison, WI, USA 1 Walter Reed National Military Medical Center, Bethesda, MD, USA |
AuthorAffiliation_xml | – name: 3 Spectrum Research Inc, Tacoma, WA, USA – name: 4 Department of Orthopedics & Rehabilitation, University of Wisconsin, Madison, WI, USA – name: 2 Spectrum Research Inc, Tacoma, WA, USA. Interdisciplinary Scientific Research, Seattle WA, USA – name: 1 Walter Reed National Military Medical Center, Bethesda, MD, USA |
Author_xml | – sequence: 1 givenname: Ronald surname: Lehman fullname: Lehman, Ronald organization: Walter Reed National Military Medical Center, Bethesda, MD, USA – sequence: 2 givenname: Adam J surname: Bevevino fullname: Bevevino, Adam J organization: Walter Reed National Military Medical Center, Bethesda, MD, USA – sequence: 3 givenname: Devon D surname: Brewer fullname: Brewer, Devon D organization: Spectrum Research Inc, Tacoma, WA, USA. Interdisciplinary Scientific Research, Seattle WA, USA – sequence: 4 givenname: Andrea C surname: Skelly fullname: Skelly, Andrea C organization: Spectrum Research Inc, Tacoma, WA, USA – sequence: 5 givenname: Paul A surname: Anderson fullname: Anderson, Paul A organization: Department of Orthopedics & Rehabilitation, University of Wisconsin, Madison, WI, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23236311$$D View this record in MEDLINE/PubMed |
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References_xml | – reference: 16816760 - Spine (Phila Pa 1976). 2006 Jul 1;31(15):1666-73 – reference: 17242873 - Eur Spine J. 2007 Jul;16(7):1015-20 – reference: 16284586 - Spine (Phila Pa 1976). 2005 Nov 15;30(22):2497-502 – reference: 14560190 - Spine (Phila Pa 1976). 2003 Oct 15;28(20):S186-94 – reference: 21252827 - Spine (Phila Pa 1976). 2011 Apr 1;36(7):E492-7 – reference: 12435973 - Spine (Phila Pa 1976). 2002 Nov 15;27(22):2446-52 – reference: 19333091 - Spine (Phila Pa 1976). 2009 Apr 1;34(7):E262-5 – reference: 19815271 - Biomaterials. 2010 Jan;31(3):523-31 – reference: 9609285 - J Neurosurg. 1998 Jun;88(6):943-8 – reference: 15347007 - J Neurosurg Spine. 2004 Sep;1(2):202-10 – reference: 21289567 - Spine (Phila Pa 1976). 2011 Jun 15;36(14):E973-8 – reference: 21699471 - J Neurosurg Spine. 2011 Oct;15(4):348-58 |
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Snippet | ABSTRACT
Study design:
Systematic review.
Clinical questions:
(1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure... Systematic review.Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and retrieval regarding... Study design: Systematic review. Clinical questions: (1) What evidence is available from studies of cervical total disc arthroplasty (C-ADR) failure and... |
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Title | A systematic review of cervical artificial disc replacement wear characteristics and durability |
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