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Global Spine J. 2012 Dec;2(4):239-48. doi: 10.1055/s-0032-1315454. Epub 2012 Oct 9.

Improving the clinical evidence of bone graft substitute technology in lumbar spine surgery.

Author information

  • 1Department of Orthopaedic Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • 2Department of Orthopaedic Surgery, UCLA Comprehensive Spine Center, Santa Monica, California.
  • 3University of Connecticut Medical Center, Farmington, Connecticut.
  • 4Rush University Medical Center, Chicago, Illinois.
  • 5Emory Spine Center, Atlanta, Georgia.
  • 6Durango Orthopedic Associates, PC/Spine Colorado.
  • 7University of Utah, Salt Lake City, Utah.
  • 8Resources for Medical Education and Collaboration, Durango, Colorado.

Abstract

Bone graft substitutes have been used routinely for spine fusion for decades, yet clinical evidence establishing comparative data remains sparse. With recent scrutiny paid to the outcomes, complications, and costs associated with osteobiologics, a need to improve available data guiding efficacious use exists. We review the currently available clinical literature, studying the outcomes of various biologics in posterolateral lumbar spine fusion, and establish the need for a multicenter, independent osteobiologics registry.

KEYWORDS:

autograft; biologics; bone graft substitute; bone morphogenetic protein; ceramics; demineralized bone matrix; osteobiologics; spine fusion

PMID:
24353975
[PubMed]
PMCID:
PMC3864464
Free PMC Article

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