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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 />

38<br />

k i j k o o k o p w w w . c o n g r e s s c o m p a n y . c o m<br />

o f w w w . r a d i o l o g e n . n l

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