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POST-TRAUMATIC ANKLE COMPLICATIONS TREATED WITH POSTERIOR BLADE PLATE ANKLE ARTHRODESIS



Abstract

Purpose: To evaluate the appropriateness of posterior blade plate ankle arthrodesis as a salvage procedure, in a complex subgroup of ankle trauma patients.

Methods: We retrospectively identified all patients who underwent an ankle arthrodesis from our prospectively collected trauma database at Vancouver General hospital from 1997 to 2005. We then extracted those who had blade plate arthrodesis via the posterior approach for previous failed fracture fixation or failed previous fusion. Demographics, pre arthrodesis diagnosis, previous surgeries, deformity and complications were recorded. Clinical examination was based on outpatient evaluation and physical evaluation. This was supplemented with radiological follow up to confirm union and outcome scoring using the AOFAS and SF36 systems.

Results: Sixteen patients were identified from the trauma database who had undergone posterior blade plate ankle arthrodesis. Of these thirteen were available for follow up. There average age was 47 years (range 23–63 years). The male to female ratio was 3:1. Three cases were for failed previous ankle fusion by other means. Of the remaining ten patients with post traumatic osteoarthritis, seven had previous pilon fractures, two talar fractures and one fracture dislocated ankle. All cases went onto bony union. Patient satisfaction was good although functional outcome scoring was not normal

Conclusion: We have found this procedure to have several excellent benefits. It allows the surgeon to operate through virgin skin, reducing potential wound complications, and achieve good soft tissue coverage. The blade plate allows reconstitution of a normal plantar grade ankle and distal tibial orientation, when secured appropriately to bone. Excellent compression and union can be achieved with the AO compression device, but it’s important to have a second screw in the talus to prevent blade pull out. The procedure has good satisfaction among patients following previous failed surgery, as a salvage procedure.

Correspondence should be addressed to: EFORT Central Office, Technoparkstrasse 1, CH – 8005 Zürich, Switzerland. Email: office@efort.org