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The primary aim this prospective longitudinal observational outcomes study is to compare 18 month functional outcomes and health related quality of life (HRQoL) of patients undergoing salvage versus amputation following severe distal tibia, ankle and/or foot fractures with major soft tissue, bone and/or ankle articular surface loss. Functional outcomes and HRQoL will be measured using well established self reported measures, including the Veterans Rand Health Survey (VR-12) and the Short Musculoskeletal Functional Assessment (SMFA).
Hypothesis 1: As a group, salvage patients with severe distal tibia, ankle and/or foot injuries with major soft tissue, bone and/or ankle articular surface loss will have similar functional outcomes and HRQoL had they undergone a transtibial amputation (within 6 weeks of injury).
Hypothesis 2: The subgroup of salvage patients who have either (1) a soft tissue injury that requires tissue transfer; (2) articular damage requiring arthrodesis of the ankle joint; or (3) bone loss at the distal tibia or ankle will have better functional outcomes and HRQoL had they undergone a transtibial amputation (within 6 weeks of injury).
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Inclusion criteria
Patients with an injury that meets at least one of the following:
Ages 18-60 inclusive.
Admitted to the hospital prior to definitive wound closure.
Inclusion notes:
Patients may have other injuries except as noted below under exclusion criteria.
Foot crush and blast injuries are eligible if they are considered to be at significant risk for impaired outcome with moderate to severe disability and typically include one of the following associated injuries:
These injuries may include "toe-pan" injuries from motor vehicle accidents and crush-like injuries from motorcycle accidents, and traumatic amputations.
Exclusion criteria
Patient has a Glasgow Coma Scale motor score of 0-4 or a Glasgow Coma Scale motor score of 5 with a significant traumatic brain injury (defined as an AIS code of 5 or 6) at time of consent
Patient has third degree burns on >10% total surface area affecting the study limb
Patient has a previous leg or foot amputation of either limb
Patient is non-ambulatory due to an associated complete spinal cord injury
Patient non-ambulatory pre-injury
Patient speaks neither English nor Spanish
Patient likely to have severe problems with maintaining follow- up due to at least one of the following:
664 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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