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Title: Volar plate fixation for the treatment of distal radius fractures: analysis of adverse events. Author: Tarallo L, Mugnai R, Zambianchi F, Adani R, Catani F. Journal: J Orthop Trauma; 2013 Dec; 27(12):740-5. PubMed ID: 23515129. Abstract: OBJECTIVES: Determining the rate of specific adverse events after volar plating performed for distal radius fractures. DESIGN: Retrospective. SETTING: University level I trauma center. PATIENTS: We searched the electronic database of all surgical procedures performed in our department using the following keywords: distal radius fracture, wrist fracture, and plate fixation. We identified 315 patients, 12 of whom were lost at follow-up. INTERVENTION: Volar plate fixation for the treatment of distal radius fractures. MAIN OUTCOME MEASUREMENTS: At an average follow-up of 5 years, 303 patients were evaluated through medical records and clinical and radiographic assessment for specific adverse events after volar plate fixation. RESULTS: Adverse events were observed in 18 patients (5.9%). Implant-related adverse events, including tendon impairments, intra-articular screws, and screw loosening, were observed in 15 patients (5.0%). Extensor tendon impairments were represented by 5 cases of extensor tenosynovitis and 3 cases of rupture of the extensor pollicis longus due to screws protruding dorsally. Flexor impairments were represented by 2 cases of tenosynovitis and 2 cases of flexor pollicis longus rupture. Screw penetration into the radioulnar joint was observed in 1 case. Loss of reduction was identified in 3 cases. One patient had a deep postoperative infection treated with operative debridement. One patient experienced injury to the median nerve during routine implant removal unrelated to tendon issues. CONCLUSIONS: The majority of adverse events after volar plate fixation were due to technical errors in implant placement. In our cohort, tendon impairments were the most frequently observed; among these, extensor tendon impairments were the most represented (50% of all adverse events). All 12 tendon-related adverse events were due to technical shortcomings with implant placement. LEVEL OF EVIDENCE: Therapeutic level IV.[Abstract] [Full Text] [Related] [New Search]