Vascularized Bone Grafts for Spinal Fusion-Part 1: The Iliac Crest.

Autograft Iliac crest Pseudoarthrosis Spinal fusion Spinoplastic reconstruction Vascularized bone graft

Journal

Operative neurosurgery (Hagerstown, Md.)
ISSN: 2332-4260
Titre abrégé: Oper Neurosurg (Hagerstown)
Pays: United States
ID NLM: 101635417

Informations de publication

Date de publication:
15 04 2021
Historique:
received: 15 08 2020
accepted: 25 12 2020
pubmed: 23 2 2021
medline: 22 6 2021
entrez: 22 2 2021
Statut: ppublish

Résumé

Iliac crest autograft has been the gold standard for harvest of fusion materials in spine surgery. The benefits of a vascularized version of this bone graft-including delivery of stem cells, ability to deliver antibiotics to the fusion bed, and relative ease of harvest-make this technique superior to free bone transfer in the achievement of augmented spinal fusion. To present a brief summary of similar existing concepts before describing the novel technique of this vascularized posterior iliac crest bone graft. Vascularized posterior iliac crest bone graft can be harvested from the same midline lumbar incision used for thoracolumbar spinal fusion, through lateral dissection around the paraspinals to the iliac crest. Recipient sites in the posterolateral bony spinal gutters may be as rostral as T12 and caudal as the sacrum. The ability to cover multiple lumbar levels can be achieved with desired lengths of the donor iliac crest. Over 14 vascularized iliac crest bone grafts have been performed to augment lumbar fusion for salvage after pseudoarthrosis. Operative time and bleeding are reduced compared to free flap procedures, and no patients have experienced any complications related to these grafts. Indocyanine green (ICG) angiography has been utilized in a novel way to ensure the vascularity of the bone graft prior to arthrodesis. While long-term follow-up will be required to fully characterize fusion rates and patient morbidity, this innovative surgical option augments spinal fusion in patients with, or at increased risk for, pseudoarthrosis.

Sections du résumé

BACKGROUND
Iliac crest autograft has been the gold standard for harvest of fusion materials in spine surgery. The benefits of a vascularized version of this bone graft-including delivery of stem cells, ability to deliver antibiotics to the fusion bed, and relative ease of harvest-make this technique superior to free bone transfer in the achievement of augmented spinal fusion.
OBJECTIVE
To present a brief summary of similar existing concepts before describing the novel technique of this vascularized posterior iliac crest bone graft.
METHODS
Vascularized posterior iliac crest bone graft can be harvested from the same midline lumbar incision used for thoracolumbar spinal fusion, through lateral dissection around the paraspinals to the iliac crest. Recipient sites in the posterolateral bony spinal gutters may be as rostral as T12 and caudal as the sacrum. The ability to cover multiple lumbar levels can be achieved with desired lengths of the donor iliac crest.
RESULTS
Over 14 vascularized iliac crest bone grafts have been performed to augment lumbar fusion for salvage after pseudoarthrosis. Operative time and bleeding are reduced compared to free flap procedures, and no patients have experienced any complications related to these grafts. Indocyanine green (ICG) angiography has been utilized in a novel way to ensure the vascularity of the bone graft prior to arthrodesis.
CONCLUSION
While long-term follow-up will be required to fully characterize fusion rates and patient morbidity, this innovative surgical option augments spinal fusion in patients with, or at increased risk for, pseudoarthrosis.

Identifiants

pubmed: 33616183
pii: 6146305
doi: 10.1093/ons/opab037
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

493-496

Informations de copyright

© Congress of Neurological Surgeons 2021.

Auteurs

Edward M Reece (EM)

Division of Plastic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Division of Plastic Surgery, Department of Surgery, Texas Children's Hospital, Houston, Texas, USA.

Matthew J Davis (MJ)

Division of Plastic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Division of Plastic Surgery, Department of Surgery, Texas Children's Hospital, Houston, Texas, USA.

Ryan D Wagner (RD)

Division of Plastic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Division of Plastic Surgery, Department of Surgery, Texas Children's Hospital, Houston, Texas, USA.

Amjed Abu-Ghname (A)

Division of Plastic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Division of Plastic Surgery, Department of Surgery, Texas Children's Hospital, Houston, Texas, USA.

Alex Cruz (A)

Department of Orthopedic Surgery, Baylor College of Medicine, Houston, Texas, USA.

Geoffrey Kaung (G)

Department of Orthopedic Surgery, Baylor College of Medicine, Houston, Texas, USA.

Terence Verla (T)

Department of Neurosurgery, Baylor College of Medicine, Houston, Texas, USA.

Sebastian Winocour (S)

Division of Plastic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.

Alexander E Ropper (AE)

Department of Neurosurgery, Baylor College of Medicine, Houston, Texas, USA.

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