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<dc:title>Percutaneous dorsal instrumentation of vertebral burst fractures: Value of additional percutaneous intravertebral reposition-cadaver study</dc:title>
<dc:creator>Krüger, Antonio</dc:creator>
<dc:creator>Schmuck, Maya</dc:creator>
<dc:creator>Noriega González, David César</dc:creator>
<dc:creator>Ruchholtz, Steffen</dc:creator>
<dc:creator>Baroud, Gamal</dc:creator>
<dc:creator>Oberkircher, Ludwig</dc:creator>
<dcterms:abstract>Purpose. The treatment of vertebral burst fractures is still controversial. The aim of the study is to evaluate the purpose of&#xd;
additional percutaneous intravertebral reduction when combined with dorsal instrumentation. Methods. In this biomechanical&#xd;
cadaver study twenty-eight spine segments (T11-L3) were used (male donors, mean age 64.9 ± 6.5 years). Burst fractures of L1&#xd;
were generated using a standardised protocol. After fracture all spines were allocated to four similar groups and randomised&#xd;
according to surgical techniques (posterior instrumentation; posterior instrumentation + intravertebral reduction device + cement&#xd;
augmentation; posterior instrumentation + intravertebral reduction device without cement; and intravertebral reduction device +&#xd;
cement augmentation). After treatment, 100000 cycles (100–600 N, 3 Hz) were applied using a servohydraulic loading frame. Results.&#xd;
Overall anatomical restoration was better in all groups where the intravertebral reduction device was used (𝑝 &lt; 0.05). In particular,&#xd;
it was possible to restore central endplates (𝑝 > 0.05). All techniques decreased narrowing of the spinal canal. After loading,&#xd;
clearance could be maintained in all groups fitted with the intravertebral reduction device. Narrowing increased in the group treated&#xd;
with dorsal instrumentation. Conclusions. For height and anatomical restoration, the combination of an intravertebral reduction&#xd;
device with dorsal instrumentation showed significantly better results than sole dorsal instrumentation.</dcterms:abstract>
<dcterms:dateAccepted>2021-01-14T12:31:25Z</dcterms:dateAccepted>
<dcterms:available>2021-01-14T12:31:25Z</dcterms:available>
<dcterms:created>2021-01-14T12:31:25Z</dcterms:created>
<dcterms:issued>2015</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>BioMed Research International, 2015, vol. 2015. 10 p.</dc:identifier>
<dc:identifier>2314-6141</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/44991</dc:identifier>
<dc:identifier>10.1155/2015/434873</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://www.hindawi.com/journals/bmri/2015/434873/</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/</dc:rights>
<dc:rights>© 2015 Hindawi</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivs 3.0 Unported</dc:rights>
<dc:publisher>Hindawi</dc:publisher>
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