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August 4, 1988New England Journal of Medicine145 citations

Clinical Characteristics of Patients with Ventricular Fibrillation during Antiarrhythmic Drug Therapy

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JMJoseph D. MinardoJHJames J. HegerWMWilliam M. Miles

Key Result

Left ventricular dysfunction was significantly associated with ventricular fibrillation during antiarrhythmic therapy, with lower ejection fractions in cases than controls (0.29 vs. 0.43; P<0.0001).

Study Design

Type

Case-Control (n=88)

Structured PICO

What clinical characteristics predispose patients to newly occurring ventricular fibrillation during antiarrhythmic drug therapy?

P
Population
90 patients treated for ventricular arrhythmias, including 28 patients with newly occurring ventricular fibrillation during antiarrhythmic drug therapy and 62 control patients.
I
Intervention
Single-drug antiarrhythmic therapy (quinidine, procainamide, or disopyramide) in patients who developed ventricular fibrillation (n=26 analyzed).
C
Comparator
Control group of 62 patients treated similarly for ventricular arrhythmias who did not develop ventricular fibrillation during treatment.
O
Outcome
Clinical characteristics predisposing to ventricular fibrillation (including left ventricular ejection fraction, baseline QT interval, and concomitant medications).safety

Left ventricular dysfunction, prolonged baseline QTc, and concomitant use of digitalis and diuretics predispose patients to early drug-associated ventricular fibrillation during antiarrhythmic therapy.

Main Result

Absolute Event Rate: 0.29% vs 0.43%

p-value: p=<0.0001

Abstract

We retrospectively studied 28 patients with 38 episodes of newly occurring ventricular fibrillation during antiarrhythmic drug therapy. Twenty-six of these patients, who had ventricular fibrillation during single-drug therapy with quinidine, procainamide, or disopyramide, were compared with a control group of 62 patients who had been treated similarly for ventricular arrhythmias but did not have ventricular fibrillation during treatment. The median duration of therapy before ventricular fibrillation was three days. The left ventricular ejection fraction of the study group was lower than that of the control group (0.29 vs. 0.43; P less than 0.0001), and concomitant treatment with digitalis and diuretic agents was more common in the study group. The base-line QT interval (corrected for heart rate) was slightly longer in the study group than in the controls (0.47 vs. 0.44; P less than 0.005), although both groups had similar degrees of QT prolongation during drug therapy. Four of 13 patients (31 percent) who underwent multiple trials of antiarrhythmic drugs had recurrent episodes of ventricular fibrillation. Six patients died suddenly after a mean follow-up of 18 months--four who were receiving antiarrhythmic therapy and two who were not. We conclude that drug-associated ventricular fibrillation is an early event, that there may be an increased risk of its recurrence with subsequent trials of antiarrhythmic drugs, and that left ventricular dysfunction and concomitant therapy with digitalis and diuretic agents may predispose patients to this complication.

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Cite This Study

Minardo et al. (1988) conducted a case-control in Ventricular fibrillation during antiarrhythmic drug therapy (n=88). Antiarrhythmic drug therapy (quinidine, procainamide, or disopyramide) vs. Patients treated similarly for ventricular arrhythmias without ventricular fibrillation was evaluated on Left ventricular ejection fraction (p=<0.0001). Left ventricular dysfunction was significantly associated with ventricular fibrillation during antiarrhythmic therapy, with lower ejection fractions in cases than controls (0.29 vs. 0.43; P<0.0001).

synapsesocial.com/papers/6a0f411f04e2b0ba896cbf8fhttps://doi.org/10.1056/nejm198808043190501
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