Silent myocardial ischemia, whether it occurs at rest or during exerci
se, is associated with an unfavorable prognosis and may lead to sudden
cardiac death. Agents used to treat silent myocardial ischemia have i
ncluded nitrates, beta-blockers, and calcium antagonists (CAs). Despit
e treatment with traditional anti-ischemic agents, studies have shown
that up to 40% of patients who receive what is considered to be clinic
ally optimal antianginal therapy continue to have daily episodes of si
lent myocardial ischemia. The use of nitrates and beta-blockers is som
etimes confounded by issues of tolerance and tolerability. Although th
e CAs have been found to be effective in decreasing the duration and f
requency of episodes of silent ischemia, in general beta-blockers prod
uce a greater reduction in these variables. Thus a need for effective
and tolerable antiischemic agents persists. A new class of CAs, the te
tralol derivatives, may show promise in this regard. The first of this
new class, mibefradil, is characterized by selective blockade of T-ty
pe calcium-ion channels and has been shown in a few studies to reduce
the frequency and duration of asymptomatic ischemic episodes in patien
ts with stable exertional angina pectoris. Large-scale clinical trials
are necessary before the efficacy and tolerability of this new CA can
be compared fully with those of the beta-blockers and currently avail
able CAs.