• Spine · Aug 2023

    Autograft: Cellular Contribution to Spinal Fusion and Effects of Intraoperative Storage Conditions.

    • Jeremy A Lombardo, Nick Russell, Jiawei He, Michael J Larson, William R Walsh, Gregory M Mundis, and Frank Vizesi.
    • SeaSpine Inc., Carlsbad, CA.
    • Spine. 2023 Aug 15; 48 (16): 118111891181-1189.

    Study DesignControlled animal study.ObjectiveTo assess the cellular contribution of autograft to spinal fusion and determine the effects of intraoperative storage conditions on fusion.Summary Of Background DataAutograft is considered the gold standard graft material in spinal fusion, purportedly due to its osteogenic properties. Autograft consists of adherent and non-adherent cellular components within a cancellous bone scaffold. However, neither the contribution of each component to bone healing is well understood nor are the effects of intraoperative storage of autograft.Materials And MethodsPosterolateral spinal fusion was performed in 48 rabbits. Autograft groups evaluated included: (1) Viable, (2) partially devitalized, (3) devitalized, (4) dried, and (5) hydrated iliac crest. Partially devitalized and devitalized grafts were rinsed with saline, removing nonadherent cells. Devitalized graft was, in addition, freeze/thawed, lysing adherent cells. For 90 minutes before implantation, air dried iliac crest was left on the back table whereas the hydrated iliac crest was immersed in saline. At 8 weeks, fusion was assessed through manual palpation, radiography, and microcomputed tomography. In addition, the cellular viability of cancellous bone was assayed over 4 hours.ResultsSpinal fusion rates by manual palpation were not statistically different between viable (58%) and partially devitalized (86%) autografts ( P = 0.19). Both rates were significantly higher than devitalized and dried autograft (both 0%, P < 0.001). In vitro bone cell viability was reduced by 37% after 1 hour and by 63% after 4 hours when the bone was left dry ( P < 0.001). Bone cell viability and fusion performance (88%, P < 0.001 vs . dried autograft) were maintained when the graft was stored in saline.ConclusionsThe cellular component of autograft is important for spinal fusion. Adherent graft cells seem to be the more important cellular component in the rabbit model. Autograft left dry on the back table showed a rapid decline in cell viability and fusion but was maintained with storage in saline.Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc.

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