4-Aminopyridine in the Treatment of Patients With Multiple Sclerosis
- 1 March 1994
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 51 (3) , 292-296
- https://doi.org/10.1001/archneur.1994.00540150090022
Abstract
Objective: To study the long-term efficacy and safety of 4-aminopyridine in patients with multiple sclerosis. Design: Case series, follow-up varying from 6 to 32 months. Setting: University referral center. Patients: Thirty-one patients with definite MS, 23 of them being exposed to long-term administration (6 to 32 months) of 4-aminopyridine, since they showed a favorable initial response to the drug. Interventions: Long-term oral treatment with 4-aminopyridine in daily doses of up to 0.5 mg/kg of body weight. Main Outcome Measures: Neurologic functions and symptoms as reported by the patients; side effects. Results: Twenty of 23 patients who showed a favorable initial response benefited from long-term administration. Ambulation and fatigue (each in 13 patients) and visual function (in five patients) were most frequently reported to be improved. Three major side effects did occur during a follow-up of 406 patient months: a generalized epileptic seizure in two patients and hepatitis in one. Conclusions: Although a substantial proportion of patients with multiple sclerosis seem to benefit from long-term administration of 4-aminopyridine, additional studies are needed to clarify the exact value of the drug.Keywords
This publication has 6 references indexed in Scilit:
- 4‐Aminopyridine in multiple sclerosisNeurology, 1991
- Orally administered 4‐aminopyridine improves clinical signs in multiple sclerosisAnnals of Neurology, 1990
- 4‐Aminopyridine improves clinical signs in multiple sclerosisAnnals of Neurology, 1987
- 4-aminopyridine leads to restoration of conduction in demyelinated rat sciatic nerveBrain Research, 1985
- Rating neurologic impairment in multiple sclerosisNeurology, 1983
- Effects of 4-aminopyridine in patients with multiple sclerosisJournal of the Neurological Sciences, 1983