Nerve Autografts, Allografts, Conduits, Wraps, and Glue. What Should I Do?

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Nerve Autografts, Allografts, Conduits, Wraps, and Glue. What Should I Do? David Kahan, MD Fellow, Hand & Upper Extremity Surgery Rothman Institute at Thomas Jefferson University

Outline Wallerian Degeneration Regeneration Direct Repair Gap Repair Conduits Allografts Autografts Wraps Algorithm

Wallerian Degeneration In 1849 Augustus Waller Distal portion of nerve undergoes progressive degeneration WD begins with axon degeneration. Blood-tissue barrier permeability increases Myelin sheath breaks down Influx of macrophages occurs, Myelin debris contains several inhibitors of axon regeneration Clearance mediated first by Schwann cells and later by hematogenous phagocytes

Wallerian Degeneration Acute axonal degeneration (AAD) 30 min post injury, axon segments at both the proximal and distal ends degenerate hundreds of micrometers Granular disintegration of the axonal cytoskeleton (GDC) Breakdown of neurofilaments and microtubules Committed step in Wallerian degeneration. After onset axons disintegrate within an hour in an all-or-none fashion Time lag of 1 2 days in the rodent and up to 7 days in humans exists between injury and GDC Depends on the species, the distance of injury from cell body, and the diameter of the axon

Axonal Regeneration Following axon degeneration, SC proliferation is a key event in promoting axon regeneration Provide structural guidance and growthpromoting substrates to regenerating axons. Grow in close association with SCs along the basal laminar tubes (endoneurium) and are thus able to retrace their former pathways

Axonal Regeneration 1-2mm/day Same velocity of slow anterograde axoplasmic transport Facial nerve grafting with sural Timing determined by tinels Braam-Microsurgery-1993

Axonal Regeneration Motor axons must reach the target muscle in a critical time window (12 18 months). In the case of neurotmesis (Sunderland Type V), it is estimated that there is a 50% loss of axons across each coaptation site. Axonal Escape Neurofibrosis Furthermore, of the small percentage of axons that do reach their target muscle, it is estimated that even a smaller percentage are able to remake functional connections. Nevertheless, our best option remains guiding axonal growth

Guided Growth: Must be out of Zone of Injury Berrocal-J Neurosurg-2013

Guided Growth: Tension-free Repair 12% Strain Non-Reversible Ischemia

Guided Growth: Tension-free Repair Cyclic Sub-Threshold Strain Non-Reversible Ischemia

Direct Repair Suture vs. Glue Rat Model 8wks post repair Crush Glue Histologic & Functional Outcomes: Crush>Suture=Glue Suture Felix-Microsurgery-2013

Direct Repair Suture vs. Glue Human Cadaveric Model: Tibial nerve Resistance to Gapping: All glues > No glue 2 sutures +/- various fibrin glues Isaacs-JHS-2008 Load to Failure: No difference

Direct Repair Often Not Possible AAD Innate neural tension/retraction Zone of Injury Often Faced with a Gap

Gap Repair Options

Advantages Combat Axonal Escape Can Aid in Repair Technique Conduits Can be Filled with Pro-Regeneration substrates (SCs, ADSCs) [Animal Studies Only] Conduit Assisted Repairs: Inexperienced = Experienced Suture Only: Experienced > Inexperienced Isaacs-JHS-2016

Disadvantages Lack Endoneurial Architecture Lack Support Cells Relies on Fibrin Matrix as Scaffold Conduits Limited Length-Stability: Don t yet know limits Diameter Mismatch 14mm Gap 28mm Gap 6wks Rat Sciatic Model 12wks Whitlock-Muscle Nerve-2009

Acellular Allograft Advantages Endoneurial Architecture Varying Diameters No Donor Morbidity No WD debris mediated regeneration inhibition

Acellular Allograft Animal Data: Superiority to Cabled Autograft Force Transduction: Reversed Autograft > Allograft > Cabled Autograft Tang-Microsurgery-2013

Acellular Allograft Tang-Microsurgery-2013 Mid-Graft Nerve Fiber Count (6 & 12 wks): Reversed Autograft > Allograft > Cabled Autograft

Acellular Allograft Level III Evidence Demonstrating Promising Clinical Results Cho-JHS-2012

Acellular Allograft Disadvantages No Support Cells Cost Limited Clinical Data Length limited to 7cm

Advantages Autograft Gold-standard since 1920 s with extensive evidence Frykman & Gramyk 80% median n recovery 60% ulnar n recovery Support Cells (Survive Devascularization) Graft SCs labeled: 1 day 14 days Trumble-JHS-1994

Autograft Advantages Endoneurial Architecture Non-immunogenic Segments > 7cm

Autograft Disadvantages Donor Morbidity Functional loss Neuroma formation WD debris Diameter Mismatch Cabled grafts < Single Animal Data Source of graft matters Motor Donor Sensory Donor Distal to Graft Nerve Fibers: Motor > Sensory Brenner-Laryngoscopy-2006

Wraps Advantages Custom-sized conduit Vein wraps, Synthetic wraps Animal Data XU-JHS-2000 Reduces adhesion/fibrosis formation Improved functional and histologic outcomes Disadvantages Possible to overtighten leading to compression Some wraps limit neovascularization and diffusion Limited Data

Algorithim Ducic-Annals Plastic Surg-2012

Conduit A, Traumatic injury to the radial sensory digital nerve in 65 year-old patient, resulting in pain at the injury site and finger numbness. B, Excision of pain-generating neuroma. C, Resulting 5 mm gap reconstructed with nerve conduit.

Allograft A, Knife injury to hand in a 37 year-old patient, resulting in irregular scar, pain and finger numbness. B, Excision of neuroma-in-continuity of the index finger digital nerve. C, Reconstruction of 20 mm nerve defect to restore finger sensibility with nerve allograft and anastomotic nerve connector.

Allograft A, Peripheral nerve tumor requiring excision of associated fascicle. B, Reconstruction of 40 mm nerve fascicle defect with nerve allograft and anastomotic nerve connector.

Autograft A, Traumatic injury to a major peripheral nerve in a 25 year-old patient. B, Final defect size after stump debridement to healthy fascicular tissue. C, Reconstruction of 50 mm nerve defect with sural nerve autograft. (Donor medial and lateral sural nerve defect reconstructed with 50 mm nerve allograft and anastomotic nerve connector.)

David Kahan, MD Fellow, Hand & Upper Extremity Surgery Rothman Institute at Thomas Jefferson University Thank You!