Over the last few years, many severe cardiac side effects of antimalarial d
rugs have been reported. Ventricular arrhythmias were the most frequent (ve
ntricular premature beats, ventricular tachycardia, and torsades de pointes
[polymorphic ventricular tachycardia]). These events occurred with most an
timalarial drugs belonging to the aryl-amino-alcohol family including quini
ne, mefloquine, and halofantrine. These agents have a biochemical structure
, tissue distribution, and mechanism of action similar to those of quinidin
e and Class I Vaughan-Williams antiarrythmic agents. All induced ECG QTc le
ngthening. These cardiac complications occurred more frequently in the case
of predisposing factors such as hypokalemia, bradycardia, and treatment wi
th drugs modifying the QT interval. Atrial flutter was reported with mefloq
uine and restrictive cardiomyopathy was described in long-course chloroquin
e treatment at a higher dosage. No cardiac adverse event has yet been repor
ted with such new antimalarial drugs as qinghaosu derivatives. Given this d
ata concerning cardiac side effects, the authors have written out recommend
ations for the prescription of antimalarial drugs. (C) 1999 Editions scient
ifiques et medicales Elsevier SAS.