Abstract

Cadaveric mechanical testing of a percutaneous osseointegration docking system (PODS) for osseointegration (OI) prosthetic limb attachment revealed that translation of the exact system from the humerus to the tibia may not be suitable. The PODS, designed specifically for the humerus achieved 1.4–4.8 times greater mechanical stability in the humerus than in the tibia despite morphology that indicated translational feasibility. To better understand this discrepancy, finite element analyses (FEAs) modeled the implantation of the PODS into the bones. Models from cadaveric humeri (n = 3) and tibia (n = 3) were constructed from CT scans, and virtual implantation preparation of an array of endoprosthesis sizes that made contact with the endosteal surface but did not penetrate the outer cortex was performed. Final impaction of the endoprosthesis was simulated using a displacement ramp function to press the endoprosthesis model into the bone. Impaction force and maximum first principal (circumferential) stress were recorded to estimate stability and assess fracture risk of the system. We hypothesized that the humerus and tibia would have different optimal PODS sizing criteria that maximized impaction force and minimized first principal stress. The optimal sizing for the humerus corresponded to implantation instructions, whereas for the tibia optimal sizing was three times larger than the guidelines indicated. This FEA examination of impaction force and stress distribution lead us to believe that the same endoprosthesis strategy for the humerus is not suitable for the tibia because of thin medial and lateral cortices that compromise implantation.

Highlights

  • Percutaneous osseointegration endoprosthetic systems are surgically implanted into the medullary canal of amputated bone, and are passed permanently through the skin and connected to distal exoprostheses

  • We hypothesized that the humerus and tibia would have a different percutaneous osseointegration docking system (PODS) sizing criterion that optimized maximum impaction force and minimum circumferential stress

  • Our primary objective was to determine the mechanism that causes a large discrepancy in mechanical failure data of the same endoprosthesis for the humerus and tibia

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Summary

Introduction

Percutaneous osseointegration endoprosthetic systems are surgically implanted into the medullary canal of amputated bone, and are passed permanently through the skin and connected to distal exoprostheses. This process bypasses socket suspension, returning limb loading to the bone and proximal joints. The Percutaneous Osseointegration Prosthesis (POP) (DJO Surgical, Austin, TX, United States), for example, was developed by the Salt Lake City VA and University of Utah for transfemoral amputees. The POP was clinically introduced to 10 patients (Early Feasibility Study, ClinicalTrials.gov NCT02720159) who had improved 1-year post-operative functional outcomes, such as increased bone mineral density and decreased don/doff time [6, 7]

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