J. Lodder et al., Diazepam treatment to increase the cerebral GABAergic activity in acute stroke: A feasibility study in 104 patients, CEREB DIS, 10(6), 2000, pp. 437-440
In preparation of a trial on the neuroprotective effect of GABAergic activa
tion by a benzodiazepine, we performed a feasibility study in 104 patients
with acute (less than 24 h) stroke. 5 mg diazepam twice daily for 5 days (n
= 44) was well tolerated, feasible, and appeared to be safe. Testing a dos
e of 10 mg twice daily for 5 days (n = 17) was stopped early because of dro
wsiness around day 5, interfering with regular patient care. A dose of 10 m
g twice daily for 3 days was well tolerated, despite reported drowsiness in
12 of 43 patients. First-dose application by rectiole was feasible in 97%
of the 104 patients. No blood pressure drop or respiratory arrest or insuff
iciency were detected, whereas the 2-week case fatality rate was similar to
that of controls matched for age, sex, and stroke severity. We conclude th
at testing the GABAergic activity during the acute phase of stroke by 10 mg
diazepam twice daily for 3 days is well tolerated and practically feasible
, and it does not subject patients to an increased risk of potential seriou
s adverse effects. Preparations for a large randomized trial are in a final
stage. Copyright (C) 2000 S. Karger AG. Basel.