G. Bogliun et al., Anticonvulsants and peripheral nerve function - Results of prospective monitoring in patients with newly diagnosed epilepsy, CLIN DRUG I, 20(3), 2000, pp. 173-180
Background: Retrospective studies report that long-term use of anticonvulsa
nts correlates with peripheral nerve dysfunction. However, these results ar
e biased by different drug combinations, the use of toxic dosages, and the
presence of other causes of polyneuropathy.
Objective: To assess the risk of peripheral nerve impairment in patients kn
own to be free from polyneuropathy who received anticonvulsants as monother
apy at standard daily dosages.
Design and Setting: This was a prospective observational study of outpatien
ts seen at two hospital centres in Italy.
Patients and Participants: 39 men and 42 women aged 13 to 67 years (mean 30
.5 years) with previously untreated epilepsy.
Methods: Patients were given monotherapy with valproic acid (sodium valproa
te) [n = 44] or carbamazepine (n = 37) at standard daily dosages to achieve
normal plasma concentrations. Each patient was screened for existing polyn
europathy or risk factors for polyneuropathy before inclusion; they were th
en assessed for clinical and electrophysiological findings of polyneuropath
y at entry and at 6, 12 and 24 months.
Results: After 24 months of treatment only one patient had clinical signs o
f polyneuropathy, and six patients had symptoms of polyneuropathy. The elec
trophysiological values did not show significant changes or trends. Only on
e patient had abnormal electrophysiological findings, which were only subcl
inical, in all the follow-up examinations, and eight patients had abnormal
values at two subsequent visits. No consistent patterns were found, and dat
a were unaffected when the drugs were examined separately or when patients
were grouped according to whether or not they had symptoms of polyneuropath
y.
Conclusions: Previously untreated young to middle-aged patients receiving m
onotherapy with standard daily dosages of valproic acid or carbamazepine ar
e not at risk of developing polyneuropathy within 24 months.