Back to Search Start Over

Functional recovery after treatment of extra-articular distal radius fractures in the elderly using the IlluminOss® System (IO-Wrist); A multicenter prospective observational study

Authors :
Hagenaars, T. (Tjebbe)
Van Oijen, G.W. (Guido W.)
Roerdink, W.H. (Herbert)
Vegt, P.A. (Paul)
Vroemen, J.P.A.M. (Jos P.A.M.)
Verhofstad, M.H.J. (Michiel)
Lieshout, E.M.M. (Esther) van
Hagenaars, T. (Tjebbe)
Van Oijen, G.W. (Guido W.)
Roerdink, W.H. (Herbert)
Vegt, P.A. (Paul)
Vroemen, J.P.A.M. (Jos P.A.M.)
Verhofstad, M.H.J. (Michiel)
Lieshout, E.M.M. (Esther) van
Publication Year :
2016

Abstract

Background: Approximately 17 % of all fractures involve the distal radius. Two-thirds require reduction due to displacement. High redislocation rates and functional disability remain a significant problem after non-operative treatment, with up to 30 % of patients suffering long-term functional restrictions. Whether operative correction is superior to non-operative treatment with respect to functional outcome has not unequivocally been confirmed. The IlluminOss® System was introduced in 2009 as a novel, patient-specific, and minimally invasive intramedullary fracture fixation. This minimally invasive technique has a much lower risk of iatrogenic soft tissue complications. Because IlluminOss® allows for early mobilization, it may theoretically lead to earlier functional recovery and ADL independence than non-operative immobilization. The main aim of this study is to examine outcome in elderly patients who sustained a unilateral, displaced, extra-articular distal radius fracture that was treated with IlluminOss®. Methods/design: The design of the study will be a multicenter, prospective, observational study (case series). The study population comprises elderly (60 years or older; independent in activities of daily living) with a unilateral, displaced, extra-articular distal radius fracture (AO/OTA type 23-A2 and A3) that after successful closed reduction was fixed within 2 weeks after the injury with IlluminOss®. Critical elements of treatment will be registered, and outcome will be monitored until 1 year after surgery. The Disabilities of the Arm, Shoulder, and Hand score will serve as primary outcome measure. The Patient-Rated Wrist Evaluation score, level of pain, health-related quality of life (Short Form-36 and EuroQoL-5D), time to ADL independence, time to activities/work resumption, range of motion of the wrist, radiological outcome, and complications are secondary outcome measures. Health care consumption and lost productivity will be used for a cost analysis.

Details

Database :
OAIster
Notes :
application/pdf, BMC Musculoskeletal Disorders vol. 17 no. 1, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1019676882
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1186.s12891-016-1077-9