Souhrn:
The aim of this study was to evaluate the direct and late outcome after the
polypropylen-polyester Codubix® prosthesis implantation, and to compare the
results with patients who underwent the conventional osteoplastic craniotomy.
There were analysed 89 patients treated surgically at the Department of
Neurosurgery of Jagiellonian University in Cracow within 1995–2004. Thirty
nine patients had the Codubix® prosthesis implantated synchronically or after
a surgery which caused a cranial defect. Fifty patients underwent osteoplastic
craniotomy and had an uneventful clinical course. Directly after the surgery
good healing was observed in all patients. In the Codubix® group seven patients
(17.8 %) had temporarily elevated temperature, three had haematoma collection
in the subgaleal space, one (2.6 %) developed meningitis which was treated
successfully with antibiotics, one (2.6 %) suffered from temporary circulation
disturbances of the scalp. In the late evaluation 16 patients (53.4 %) found the
cosmetic effect as very good, 10 patients (33 %) as good, and 4 (13.3 %) as
unsatisfactory in the Codubix® group, comparing to 14 patients (35.9 %) with
very good, 21 (53.9 %) with good, and 4 (10.2 %) with unsatisfactory cosmetic
effects in the osteoplastic craniotomy group. The commonest reason for critical
note was the depression of the plate, which appeared at 3 patients, and the
depression of the bone flap in two cases. The others 3 patients complained of
inappropriate profile of the plate causing the cranial vault asymmetry. The
properly performed implantation of accurate bone prosthesis Codubix® is safe
and has usually good cosmetic effects.
Klíčová slova:
cranial defect, cranioplasty, Codubix® prosthesis
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