programma & abstracts - Nederlandse Vereniging voor Radiologie
programma & abstracts - Nederlandse Vereniging voor Radiologie
programma & abstracts - Nederlandse Vereniging voor Radiologie
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5<br />
<strong>programma</strong> <strong>abstracts</strong> & <strong>abstracts</strong><br />
O5.2<br />
CLINICAL PERFORMANCE OF A NOVEL<br />
BIOACTIVE COMPOSITE IN THE TREATMENT<br />
OF VERTEBRAL COMPRESSION FRACTURES<br />
R. Schepers-Bok 1 , M. Geerdes 1 , M.E. Havinga 1 , R. Aquarius 2 ,<br />
P.J.W. Wensing 1<br />
1<br />
Ziekenhuisgroep Twente, Hengelo<br />
2<br />
Radboud University Nijmegen Medical Centre, Nijmegen<br />
Objective: To analyse the outcome of percutaneous vertebroplasty<br />
with CortossTM in patients with vertebral compression<br />
fractures.<br />
Methods: Between 2005 and 2010, 221 vertebral compression<br />
fractures were treated with percutaneous vertebroplasty<br />
in 132 patients. Inclusion criteria were: compression fractures<br />
due to osteoporosis, trauma or malignancy, invalidating<br />
back pain due to compression fracture, no improvement<br />
to standard conservative therapy for minimal 6 weeks,<br />
Numerical Rating Scale (NRS) score of at least 7 and bone<br />
marrow edema on MRI scan.<br />
NRS score was obtained before, and two and six weeks<br />
after vertebroplasty. Primary outcome was pain reduction<br />
measured by NRS score. Clinically significant pain relief<br />
was defined as a decrease in NRS score of at least 3 points.<br />
Secondary outcome were new vertebral fractures, injected<br />
volume and complications.<br />
Results: Two weeks after vertebroplasty, 84,7% of the<br />
patients showed a decrease of at least three points on NRS<br />
score. This increased to 86,8% after six weeks. 34 new fractures<br />
occurred in 22 patients (17,4%).No embolisms occurred.<br />
Mean injected volume of Cortoss was 1,54 mL.<br />
Conclusion: In a group of patients with vertebral compression<br />
fractures percutaneous vertebroplasty with Cortoss is<br />
an effective and safe treatment option. PVP leads to a significant,<br />
rapid decrease in pain. Our results are comparable<br />
to results of other studies which used PMMA. These good<br />
clinical results, together with advantages of Cortoss, such<br />
as the low cement volume needed, and the mix-on-demand<br />
delivery system, make it a strong candidate to be a standard<br />
material in vertebral augmentation.<br />
Figure 1: Distribution of Cortoss: trabecular pattern.<br />
Table 1: Patient characteristics.<br />
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