We challenged five patients suffering from tardive akathisia (TA) with
intravenous benztropine (2 mg), propranolol (1 mg) and placebo (salin
e) using a random, double-blind cross-over design to examine the effec
ts of the drugs on the subjective, objective and global manifestations
of neuroleptic-induced akathisia. Benztropine produced a marginally s
ignificant, and propranolol a significant improvement in the overall m
anifestations of the disorder. The patients demonstrated a considerabl
e placebo effect and marked variation in their responses to the drugs.
The implications of these findings for the pathophysiology of TA in r
elation to acute akathisia and tardive dyskinesia are discussed.