In their article, “Hypertensive Emergencies and Urgencies: Update on Management”
(CONSULTANT, March 2004, page 341), Drs Iris Reyes and Rex Mathew
write that labetalol(Drug information on labetalol) is specifically indicated for most hypertensive emergencies,
“especially stroke and acute cocaine intoxication.” In fact, labetalol is potentially
deadly and is contraindicated in acute hypertension and/or concomitant chest
pain related to cocaine intoxication. Labetalol and other β-blockers should be
avoided in this setting.
Cocaine is a powerful sympathomimetic agent that stimulates both α1- and
β1- and β2-receptors. α1-Stimulation causes marked vasoconstriction of peripheral
arteries, which results in hypertension; more importantly, it causes vasoconstriction
of the epicardial coronary arteries, which can lead to ischemic myocardial injury.
Fortunately, the potent α1-mediated vasoconstriction associated with cocaine
is limited by the coexisting vasodilatory effect mediated by the β2-receptors. If a patient
with hypertension caused by acute cocaine intoxication were given labetalol
(or any other β-blocker), the result would be complete β-blockade, which would
lead to relatively unopposed vasoconstriction mediated solely by α1-receptors. Labetalol,
which has both α- and β-adrenergic blocking activity, reverses the cocaine-induced increase in
systemic arterial pressure but exerts no demonstrable effect on cocaine-induced vasoconstriction of the
coronary arteries.
It is prudent to assume that there may likely be coronary vasoconstriction along with hypertension
even in young, otherwise healthy patients with no comorbid evidence of other atherosclerotic risk factors.
Cocaine-related hypertension can be reversed safely and effectively with nitroglycerin and calcium channel
blockers, such as verapamil. Cocaine-induced vasoconstriction of the coronary arteries can be reversed
with phentolamine(Drug information on phentolamine), an α1-receptor antagonist. The revised guidelines of the American Heart Association
(AHA) for emergency cardiovascular care recommend nitroglycerin, calcium channel blockers,
and benzodiazepines as first-line agents for patients with cocaine-related myocardial ischemia and
hypertension. Phentolamine is a second-line agent, and β-blockers are contraindicated in this setting.
—— Matthew Zaccheo, DO
St Luke’s Hospital
Bethlehem, Pa
Much debate surrounds the treatment of
hypertension associated with cocaine
toxicity. The advantage of labetalol over
pure β-blockers is the additional α-adrenergic
blockade that labetalol provides.
Treatment with pure β-adrenergic blockers, such as propranolol(Drug information on propranolol),
has been shown to enhance some of the cardiovascular
effects of cocaine. A controlled study by Sofuoglu
and colleagues1 demonstrated that labetalol reduces the
increases in systolic blood pressure and heart rate induced
by repeated doses of smoked cocaine. In another study,
labetalol failed to reverse the coronary vasoconstriction
induced by intranasal cocaine in subjects who underwent
cardiac catheterization, but it exerted no demonstrable
adverse effect on cocaine-induced vasoconstriction of the
coronary arteries.2 Numerous authors therefore recommend
the selective use of labetalol in patients with cocaine
toxicity—first intravenously in the acute setting and then
orally for long-term therapy. Intravenous nitroglycerin or verapamil(Drug information on verapamil) can also be used because they reverse both the
vasoconstriction and hypertension caused by acute cocaine
exposure.
Still, the use of β-blockers as a class in the setting of
cocaine toxicity remains controversial. The American
College of Cardiology/AHA guidelines recommend β-
blockers for select conditions caused by cocaine toxicity.3
However, it should be noted that this recommendation is
based only on expert consensus. The Advanced Cardiovascular
Life Support guideline revision of 2000 recommends
that nitrates be used as first-line therapy in patients
with a history of cocaine abuse and ventricular arrhythmias
or acute coronary syndromes.4 It also suggests that separate review of the literature surrounding this issue, Knuepfer5 justifiably
concludes that there are insufficient experimental and clinical data at this time
to determine whether labetalol may be beneficial in treating cocaine toxicity.
—— Rex Mathew, MD
Hospital of the University of Pennsylvania
Philadelphia
