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World J Orthop. Apr 18, 2013; 4(2): 53-57
Published online Apr 18, 2013. doi: 10.5312/wjo.v4.i2.53
Bone morphogenetic protein in complex cervical spine surgery: A safe biologic adjunct?
Darren R Lebl
Darren R Lebl, Hospital for Special Surgery, New York, NY 10021, United States
Author contributions: Lebl DR solely contributed to this paper.
Correspondence to: Darren R Lebl, MD, Hospital for Special Surgery, 523 E 72nd Street, New York, NY 10021, United States. drlebl@alumni.stanford.org
Telephone: +1-212-6061052 Fax: +1-212-7747062
Received: November 12, 2012
Revised: November 17, 2012
Accepted: January 17, 2013
Published online: April 18, 2013
Processing time: 161 Days and 6.3 Hours
Abstract

The advent of recombinant DNA technology has substantially increased the intra-operative utilization of biologic augmentation in spine surgery over the past several years after the Food and Drug Administration approval of the bone morphogenetic protein (BMP) class of molecules for indications in the lumbar spine. Much less is known about the potential benefits and risks of the “off-label” use of BMP in the cervical spine. The history and relevant literature pertaining to the use of the “off-label” implantation of the BMP class of molecules in the anterior or posterior cervical spine are reviewed and discussed. Early prospective studies of BMP-2 implantation in anterior cervical spine constructs showed encouraging results. Later retrospective studies reported potentially “life threatening complications” resulting in a 2007 public health advisory by the FDA. Limited data regarding BMP-7 in anterior cervical surgery was available with one group reporting a 2.4% early (< 30 d) complication rate (brachialgia and dysphagia). BMP use in the decompressed posterior cervical spine may result in neurologic or wound compromise according to several retrospective reports, however, controlled use has been reported to increase fusion rates in select complex and pediatric patients. There were no cases of de novo neoplasia related to BMP implantation in the cervical spine. BMP-2 use in anterior cervical spine surgery has been associated with a high early complication rate. Definitive recommendations for BMP-7 use in anterior cervical spine surgery cannot be made with current clinical data. According to limited reports, select complex patients who are considered “high risk” for pseudoarthrosis undergoing posterior cervical or occipitocervical arthrodesis or children with congenital or traumatic conditions may be candidates for “off-label” use of BMP in the context of appropriate informed decision making. At the present time, there are no high-level clinical studies on the outcomes and complication rates of BMP implantation in the cervical spine.

Keywords: Cervical spine; Bone morphogenetic protein; Bone morphogenetic protein