Congenital Stenosis and Adjacent Segment Disease in the Cervical Spine

• DOI: 10.3928/01477447-20130920-15
• Publication Date: 2014-08-19T21:03:18Z
• Authors: Jason David Eubanks; Jon Belding; Erik Schnaser; Andrew Rowan; Gable Moffitt; John Weaver; Michael S. Reich; Chris Bechtel; Ke Xie; Abhiram Gande; Justin Hohl; Brett Braly; Alan Hilibrand; James D. Kang
• Keywords: Adult; Aged, 80 and over; Male; Adolescent; Incidence; Middle Aged; United States; 3. Good health; Young Adult; 03 medical and health sciences; Postoperative Complications; Spinal Fusion; Spinal Stenosis; 0302 clinical medicine; Cervical Vertebrae; Humans; Female; Aged; Retrospective Studies

Symptomatic adjacent segment disease (ASD) after anterior cervical fusion (ACF) is reported in 25% of patients at 10 years postoperatively. Debate continues as to whether this degeneration is due to the natural history of the disk or the changed biomechanics after ACF. This study explored whether congenital stenosis predisposes patients to an increased incidence of ASD after ACF. A retrospective review of 635 patients with myelopathy or radiculopathy was performed; 364 patients had complete records for review. Patients underwent 1- to 5-level ACF (94 one-level, 145 two-level, 79 three-level, 45 four-level, and 1 five-level). Radiographs were evaluated for bony congenital stenosis using validated parameters, and ASD was measured according to Hilibrand’s criteria and correlated with symptomatic ASD. Congenital stenosis was found in 21.7% of patients and radiographic ASD in 33.5%, with a significant association between these parameters. However, symptomatic ASD occurred in 11.8% of patients; no association between congenital stenosis and symptomatic ASD or myelopathy and ASD was found. Clinical results demonstrated excellent or good Robinson scores in 86.2% of patients and Odom scores in 87% of patients. Despite mostly excellent to good outcomes, symptomatic ASD is common after ACF. Although congenital stenosis appears to increase the incidence of radiographic ASD, it does not appear to predict symptomatic ASD.