Neurological deficit due to cement extravasation following a vertebral augmentation procedure. Review uri icon

Overview

abstract

  • The authors endeavor to highlight the surgical management of severe neurological deficit resulting from cement leakage after percutaneous vertebroplasty and to systematically review the literature on the management of this complication. A patient presented after a vertebroplasty procedure for traumatic injury. A CT scan showed polymethylmethacrylate leakage into the right foramina at T-11 and L-1 and associated central stenosis at L-1. He underwent decompression and fusion for removal of cement and stabilization of the fracture segment. In the authors' systematic review, they searched Medline, Scopus, and Cochrane databases to determine the overall number of reported cases of neurological deficit after cement leakage, and they collected data on symptom onset, clinical presentation, surgical management, and outcome. After surgery, despite neurological recovery postoperatively, the patient developed pneumonia and died 16 days after surgery. The literature review showed 21 cases of cement extravasation with neurological deficit. Ultimately, 15 patients had resolution of the postoperative deficit, 5 had limited change in neurological status, and 2 had no improvement. Cement augmentation procedures are relatively safe, but certain precautions should be taken to avoid such complications including high-resolution biplanar fluoroscopy, considering the use of a local anesthetic, and controlling the location of cement spread in relationship to the posterior vertebral body. Immediate surgical intervention with removal of cement provides good results with complete recovery in most cases.

publication date

  • May 3, 2013

Research

keywords

  • Extravasation of Diagnostic and Therapeutic Materials
  • Lumbar Vertebrae
  • Orthopedic Procedures
  • Polymethyl Methacrylate
  • Reoperation
  • Thoracic Vertebrae
  • Vertebroplasty

Identity

Scopus Document Identifier

  • 84880063308

Digital Object Identifier (DOI)

  • 10.3171/2013.4.SPINE12978

PubMed ID

  • 23641675

Additional Document Info

volume

  • 19

issue

  • 1