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Acta Neurochir. Suppl. · Jan 2005
Clinical TrialOzone chemonucleolysis in non-contained lumbar disc herniations: a pilot study with 12 months follow-up.
- J Buric and R Molino Lova.
- Unità Funzionale di Chirurgia Spinale c.d.c. Villanova, Florence, Italy. joburic@tin.it
- Acta Neurochir. Suppl. 2005 Jan 1;92:93-7.
Study DesignProspective case series with six and twelve months follow up.ObjectiveTo observe clinical and morphological results of the intradiscal ozone chemionucleolysis in patients affected by non-contained lumbar disc herniations.Methods30 patients were included in the study on the base of precise inclusion and exclusion criteria. The patients were followed on 6 and 12 months period by Visual Analogic Scale (VAS), Roland Morris Disability Questionnaire (RMDQ) and Overall Patient Rating Scale (OPRS). Disc herniation volume morphology was evaluated at 5 months by control MRI scanning.ResultsTwenty-seven patients (90%) showed a statistically significant improvement in pain (P < 0.001, Wilcoxon test) and function (P < 0.001, Wilcoxon test), on VAS and RMDQ evaluation, respectively. The mean satisfaction with the treatment on OPSR was 79.3%, with 24 patients referring satisfaction equal or greater than 80%. There were no major complications related to the procedure.ConclusionsThe results of this study indicate the ozone chemonucleolysis as a possibly effective modality of treatment in patients affected by signs and symptoms of non-contained lumbar disc herniations that have overpassed conservative measures and have not yet fulfilled the indications for open surgical treatment.
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