To perform an evidence synthesis of the literature assessing the efficacy of arthroplasty, oblique corpectomy without fusion, and skip laminectomy to treat symptomatic cervical spondylotic myelopathy (CSM).
Traditionally, patients with symptomatic cervical spinal cord compression due to degenerative disease have been treated with anterior or posterior approaches or both. Recent reports suggest that there are several nontraditional management strategies that merit attention. The anterior procedures include decompression and anterior reconstruction with an artificial disc and oblique corpectomy without fusion. A posterior option is decompression, using the skip laminectomy technique.
We conducted a systematic search in MEDLINE and the Cochrane Collaboration Library for literature published through October 15, 2012, on human studies published in the English language containing abstracts to answer the following key questions: (1) Is there evidence that artificial disc replacement after neural decompression results in equal or improved outcomes compared with anterior cervical decompression and fusion for CSM? (2) Describe the outcomes of oblique corpectomy without fusion for CSM? (3) Is there evidence that skip laminectomy results in equal or improved outcomes compared with laminoplasty for CSM?
The initial literature search yielded 141 unique, potentially relevant citations, which were evaluated against the inclusion/exclusion criteria set a priori. A total of 10 studies were selected for inclusion. For question 1, 2 studies suggested that neurological outcomes favored artificial disc replacement compared with anterior cervical decompression and fusion, whereas functional and pain outcomes were inconsistently reported. For question 2, 5 reported case series suggested favorable neurological, functional, and pain outcomes associated with oblique corpectomy in subjects with CSM, compared with the pretreatment condition. For question 3, 3 studies comparing laminoplasty with skip laminectomy suggested similar neurological outcomes between treatment groups, although functional and pain outcomes were inconsistently reported.
A paucity of high-quality literature exists regarding treatment outcomes associated with arthroplasty, oblique corpectomy without fusion, and skip laminectomy for symptomatic CSM. Comparative prospective studies with long-term follow-up and standardized outcome measures are needed to assess treatment outcomes associated with these alternative techniques appropriately.
Evidence-Based Clinical Recommendations.
Recommendation 1. No recommendation can be made from comparative literature regarding treatment outcomes comparing ADR with ACDF for CSM.
Overall Strength of Evidence. Insufficient
Strength of Recommendation. Strong
Recommendation 2. No recommendation can be made from comparative literature regarding treatment outcomes comparing laminoplasty with skip laminectomy for CSM.
Overall Strength of Evidence. Low
Strength of Recommendation. Strong
Summary Statements. Oblique corpectomy is an option in selected cases of CSM. It should not be considered a first-line treatment strategy because of the relatively high morbidity associated with this procedure.
Supplemental Digital Content is Available in the Text.A systematic review of the literature was performed to assess the efficacy of arthroplasty, oblique corpectomy without fusion, and skip laminectomy for cervical spondylotic myelopathy. The authors found a relative lack of high-quality data comparing these so-called “alternative” techniques with standard surgical decompression with or without fusion.
*Rush University Medical Center, Chicago, IL
†University of Kansas, Kansas City, KS
‡Division of Neurosurgery, University of Saskatchewan, Saskatoon, Saskatchewan, Canada
§Department of Orthopaedics and Sports Medicine, Harborview Medical Center, University of Washington, Seattle, WA; and
¶Spectrum Research, Inc., Tacoma, WA.
Address correspondence and reprint requests to Vincent C. Traynelis, MD, Rush University Medical Center, 1653 W. Congress Parkway, Chicago, IL 60612; E-mail: firstname.lastname@example.org
Acknowledgment date: March 5, 2013. First revision date: May 22, 2013. Acceptance date: July 12, 2013.
The device(s)/drug(s) is/are FDA approved or approved by corresponding national agency for this indication.
Supported by AOSpine North America, Inc. Analytic support for this work was provided by Spectrum Research, Inc., with funding from the AOSpine North America.
Relevant financial activities outside the submitted work: consultancy, support for travel, fees for participation in review activities, payment for writing or reviewing the manuscript, payment for lectures, grant, consulting fee or honorarium, grants/grants pending, honorarium for teaching activities, patents and royalties.