The Spine Journal
Volume 4, Issue 1 , Pages 99-105, 2 January 2004

Bone ingrowth characteristics of porous tantalum and carbon fiber interbody devices: an experimental study in pigs

  • Xuenong Zou, MD

      Affiliations

    • Orthopaedic Research Laboratory and Spine Section, Department of Orthopaedics, Nørrebrogade 44, Building 1A, DK-8000 Aarhus, Denmark
    • Department of Orthopaedics, The 5th Affiliated Hospital of Zhongshan (Sun Yat-Sen) University, Meihuadonglu 52, 519000 Zhuhai, Guangdong, P. R. China
    • Corresponding Author InformationCorresponding author. Orthopaedic Research Laboratory, Kommunehospitalet/Aarhus University Hospital, Nørrebrogade 44, Building 1A, DK-8000 Aarhus C, Denmark. Tel.: +45 89494136; fax: +45 89494150.
  • ,
  • Haisheng Li, MD

      Affiliations

    • Orthopaedic Research Laboratory and Spine Section, Department of Orthopaedics, Nørrebrogade 44, Building 1A, DK-8000 Aarhus, Denmark
  • ,
  • Mathias Bünger, MS

      Affiliations

    • Orthopaedic Research Laboratory and Spine Section, Department of Orthopaedics, Nørrebrogade 44, Building 1A, DK-8000 Aarhus, Denmark
  • ,
  • Niels Egund, MD, DMSc

      Affiliations

    • Department of Radiology, Aarhus University Hospital, Nørrebrogade 44, Building 6, DK-8000 Aarhus, Denmark
  • ,
  • Martin Lind, MD, PhD, DMSc

      Affiliations

    • Orthopaedic Research Laboratory and Spine Section, Department of Orthopaedics, Nørrebrogade 44, Building 1A, DK-8000 Aarhus, Denmark
  • ,
  • Cody Bünger, MD, DMSc

      Affiliations

    • Orthopaedic Research Laboratory and Spine Section, Department of Orthopaedics, Nørrebrogade 44, Building 1A, DK-8000 Aarhus, Denmark

Received 3 February 2003; accepted 6 July 2003.

Abstract 

Background context

In preclinical and clinical joint replacement applications, porous tantalum has been shown to be osteoconductive and effective for biological fixation. Relatively little research has been undertaken to investigate the porous tantalum implants for potential application in intervertebral spinal fusion.

Purpose

The current study was designed to assess the radiographic and histological performance of porous tantalum and carbon fiber devices in the porcine anterior lumbar interbody fusion (ALIF) model.

Study design

A total of 10 Danish Landrace pigs underwent a three-level anterior intervertebral lumbar arthrodeses at L2–L3, L4–L5 and L6–L7. Each level was randomly allocated to one of three implants: a solid piece of porous tantalum, a porous tantalum ring packed with autograft or a carbon fiber cage, likewise packed with autograft. Two staples for fixation were supplemented in front of implant.

Methods

Pigs were sacrificed 3 months after operation. Specimens were evaluated by plain radiography, conventional tomography and histology.

Results

Bone graft filled into the central hole of the porous tantalum ring was less than that of the carbon fiber cage (p<.001). Radiolucencies around the porous tantalum solid were significantly higher than the carbon fiber cage (p=.02) and were not different between the porous tantalum ring and the carbon fiber cage. The bone volume in the hole of implants, within the pores of the porous tantalum and in the implant interface did not differ between implants. Bone volume in the hole of the porous tantalum ring did not differ from that of the adjacent vertebral bone; however, it was significantly different in the carbon fiber cage and the adjacent vertebral bone (p=.005).

Conclusions

In this porcine ALIF model, the radiographic and histological appearances of the porous tantalum ring were equivalent to those of the carbon fiber cage. The high presence of radiolucencies and fibrous tissue layer at the vertebrae–implant interface suggests that an initial stabilizing biomechanical environment is important in order to achieve bone ingrowth in the interbody fusion devices in this ALIF model.

Keywords:  Porous tantalum, Carbon fiber cage, Anterior lumbar interbody fusion, Bone ingrowth, Radiology, Histology, Animal model

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 FDA device/drug status: investigational/not approved (Hedrocel Interbody Fusion Device)Support in whole or in part was received from Danish Rheumatism Foundation Grant 233-425.17.04.00, Implex Corporation Research Grant 416-386.20.10.00 and the Institute of Experimental Clinical Research, University of Aarhus, Denmark. Nothing of value from a commercial entity related to this research.

PII: S1529-9430(03)00407-8

doi:10.1016/S1529-9430(03)00407-8

The Spine Journal
Volume 4, Issue 1 , Pages 99-105, 2 January 2004