A cross-sectional study.
To assess using postoperative magnetic resonance imaging whether the posterior longitudinal ligament (PLL) caused residual cord compression after anterior cervical decompression and fusion (ACDF) in a series of patients in whom the PLL was retained.
There is a lack of data evaluating the postoperative compressive effects of the PLL in patients undergoing ACDF providing guidance as to whether to remove or retain the PLL during discectomy to facilitate adequate decompression.
Postoperative gadolinium enhanced magnetic resonance images were reviewed in a series of 33 patients who underwent ACDF for cervical radiculomyelopathy and who had persistent or recurrent postoperative symptoms. Patients with ossification of the posterior longitudinal ligament or with a herniated disc behind the PLL were excluded from this study.
There were no cases of discernible compression by the retained PLL identified on the magnetic resonance image (P < 0.001) as assessed by 2 independent reviewers. Four patients underwent subsequent revision surgery unrelated to the PLL.
We were unable to demonstrate magnetic resonance imaging evidence to suggest that the retained PLL caused compression after ACDF in this patient cohort. Therefore we suggest that removing the PLL should be considered for reasons other than concern about residual compression.
We assessed, using postoperative magnetic resonance imaging (MRI), whether the posterior longitudinal ligament (PLL) caused residual cord compression after anterior cervical decompression and fusion. We identified no cases of discernible compression by the retained PLL on the magnetic resonance image. We suggest that removing the PLL be considered for reasons other than concern about residual compression.
*Institute for Modern & Innovative Surgery (iMIS), Fort Lauderdale, FL
†Denver Spine, Greenwood Village, CO
‡Less Exposure Surgery (LES) Society, Fort Lauderdale, FL
§University Hospitals Case Medical Center, Cleveland, OH
¶Oregon Health & Science University, Portland, OR; and
‖Department of Orthopaedics, West Virginia University, Morgantown, WV.
Address correspondence and reprint requests to Kingsley R. Chin, MD, iMIS Surgery, 1100 W. Oakland Park Blvd. Ste 3, Fort Lauderdale, FL 33311; E-mail: Kingsleychin@gmail.com
Acknowledgment date: June 7, 2012. Revision date: June 26, 2012. Acceptance date: July 2, 2012.
The device(s)/drug(s) is/are FDA-approved or approved by corresponding national agency for this indication.
No funds were received in support of this work.
One or more of the author(s) has/have received or will receive benefits for personal or professional use from a commercial party related directly or indirectly to the subject of this manuscript: e.g., honoraria, gifts, consultancies, royalties, stocks, stock options, decision making position.