In this review, we summarise Vaughan Williams' classification of antiarrhyt
hmic agents and the trials that have explored their efficacy in reducing mo
rtality after myocardial infarction (MI). After analysing the data, it is c
lear that there is no role for class I antiarrhythmic agents as prophylaxis
after MI since their use has been associated with increased mortality. Cla
ss II agents, i.e. beta-blockers, have demonstrated a reduction in mortalit
y in combined and individual trials which extended for up to 6 years after
the initial event. The class III drug, d,l-sotalol has been shown to have p
ossible benefit, whereas its isomer without any beta-blocking properties, d
exsotalol, has been shown to increase the incidence of arrhythmias. Amiodar
one appears to reduce the incidence of deaths due to arrhythmia and sudden
deaths without changing overall mortality. As a group, the calcium antagoni
sts, class IV agents, have not been shown to reduce mortality and, in the c
ase of nifedipine, may even increase it. Verapamil has been shown to be ben
eficial in one large study and may have a role in those patients in whom th
e use of beta-blockers is contraindicated. At this time, we recommend early
implementation of beta-blockers for all patients without contraindications
after MI. Further studies evaluating implantable defibrillators as primary
and secondary prevention have provided significant risk reductions in cert
ain high risk patient subsets. Future efforts will need to focus on more ac
curate risk stratification of post-MI patients and the role of both defibri
llators and, possibly, amiodarone in improving survival.
Multiple arrhythmias can accompany acute myocardial infarction (MI). These
include tachyarrhythmias - both supraventricular and ventricular sinus brad
ycardia, accelerated idioventricular rhythms and varying degrees of heart b
lock. Each requires appropriate management for an individual patient. Follo
wing the acute event, the greatest management dilemmas have surrounded thos
e patients with persistent frequent premature ventricular contractions and
nonsustained ventricular tachyarrhythmias. Ventricular arrhythmias followin
g acute MI were first noted to be associated with increased post MI mortali
ty in the 1960s.([1,2]) Following this, several observational studies were
performed confirming that those patients with complex ventricular premature
beats (VPBs) on I hour ECG and 6- and 24-hour holter monitors had a higher
mortality rate than those with only simple VPBs or none at all.([3-5]) Sev
eral of these studies also demonstrated an increased risk of sudden death i
n these patients, suggesting that mortality after acute MI would be reduced
if these arrhythmias could be suppressed. This review focuses on the trial
s of aritiarrhythmic therapy in patients with MI with emphasis on trials wh
ich attempted to determine if control of ventricular arrhythmias is associa
ted with improved survival.