RT info:eu-repo/semantics/article
T1 Clinical outcome after the use of a new craniocaudal expandable implant for vertebral compression fracture treatment: One year results from a prospective multicentric study
A1 Noriega González, David César
A1 Krüger, Antonio
A1 Ardura Aragón, Francísco
A1 Hansen-Algenstaedt, Nils
A1 Hassel, Frank
A1 Barreau, Xavier
A1 Beyerlein, Jörg
K1 Vertebral compression fracture
K1 Fractura vertebral por compresión
AB The purpose of this prospective multicentric observational study was to confirm the safety and clinical performance of a craniocaudal expandable implant used in combination with high viscosity PMMA bone cement for the treatment of vertebral compression fractures. Thirty-nine VCFs in 32 patients were treated using the SpineJack minimally invasive surgery protocol. Outcome was determined by using the Visual Analogue Scale for measuring pain, the Oswestry Disability Index for scoring functional capacity, and the self-reporting European Quality of Life scores for the quality of life. Safety was evaluated by reporting all adverse events. The occurrence of cement leakages was assessed by either radiographs or CT scan or both. Statistically significant improvements were found regarding pain, function, and quality of life. The global pain score reduction at 1 year was 80.9% compared to the preoperative situation and the result of the Oswestry Disability Index showed a decrease from 65.0% at baseline to 10.5% at 12 months postoperatively. The cement leakage rate was 30.8%. No device- or surgery-related complications were found. This observational study demonstrates promising and persistent results consisting of immediate and sustained pain relief and durable clinical improvement after the procedure and throughout the 1-year follow-up period.
PB Hindawi
SN 2314-6141
YR 2015
FD 2015
LK http://uvadoc.uva.es/handle/10324/44987
UL http://uvadoc.uva.es/handle/10324/44987
LA eng
NO BioMed Research International, 2015, vol. 2015. 7 p.
NO Producción Científica
DS UVaDOC
RD 25-abr-2024