High-Dose Praziquantel for Neurocysticercosis: Efficacy and Tolerability

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Abstract
Standard therapeutic regimens of praziquantel for neurocysticercosis use daily doses of 50 mg/kg for 15–21 days, with prolonged remission being achieved in 60–80% patients. In this prospective study, 100 mg/kg daily was used for 10 days in 13 patients aged 32 ± 15 years (mean ± SD) with severe intra-, extraparenchymal or mixed forms of neurocysticercosis. Patients were monitored with computerized tomography and cerebrospinal fluid (CSF) examination on days 1, 5 and 10. Full blood count, sedimentation rate, blood sugar, urea, creatinine, bilirubin, liver transaminases, alkaline phosphatase, urine analysis and electrocardiogram were carried out before and after treatment. Doses of dexamethazone and of other drugs used concomitantly were controlled. There was no toxicity, clinical or detected by the methods employed in the study. After 22 ± 5 (mean ± SD) months follow-up, 6 patients needed ventriculoperitoneal shunting, 2 had died, 7 were improved and led useful lives and 4 were in prolonged remission. There was no correlation between serum or CSF praziquantel correlation and outcome of treatment. The proposed regimen is well tolerated, may be as efficient as previously advocated regimens, requires less hospitalization time and may be adopted routinely for therapy of neurocysticercosis.