Literature DB >> 8129865

Class III antiarrhythmics in overdose. Presenting features and management principles.

E W Leatham1, D W Holt, W J McKenna.   

Abstract

Class III (Vaughan-Williams classification) antiarrhythmic drugs prolong the cardiac action potential without affecting depolarisation. The 3 class III drugs currently in general use are amiodarone, sotalol and bretylium. The presenting features of acute toxicity are different for each agent and are, therefore, discussed separately. Several new class III antiarrhythmic agents are under development, including dofetilide and d-sotalol, but specific data on overdoses of these potent class III drugs are not yet available. Amiodarone toxicity following acute overdose is rare because poor bioavailability and a large volume of distribution limit the peak serum concentration. Toxicity is low even if high serum concentrations are reached. The major risks from acute overdose are hypotension (intravenous administration only) and arrhythmia if other factors, such as hypokalaemia or additional antiarrhythmic agents are present. Management is chiefly directed at reducing absorption with activated charcoal or cholestyramine, and monitoring for arrhythmia. Sotalol is a beta-blocker with additional class III activity. Oral bioavailability is high, and overdosed patients can present with bradycardia, hypotension and major haemodynamic collapse. The combination of bradycardia and prolongation of the QT interval is associated with malignant arrhythmias such as torsade de pointes. Management principles include observation and correction of bradycardia with endocardial pacing, intravenous adrenergic drugs and glucagon. The risk of arrhythmia can be substantially reduced by intravenous potassium and magnesium supplements. d-Sotalol is a potent class III drug devoid of beta-blocking activity and may be expected to share the proarrhythmic affects of the racemic mixture in overdose, without pronounced hypotension and bradycardia. Intravenous bretylium in overdose causes an initial hypertensive effect, followed by profound hypotension from systemic vasodilation. Management is directed at controlling hypotension with volume expansion and norepinephrine (noradrenaline).

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Year:  1993        PMID: 8129865     DOI: 10.2165/00002018-199309060-00008

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  52 in total

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Journal:  Br Med J (Clin Res Ed)       Date:  1984-10-20

2.  Satalol-induced torsade de pointes.

Authors:  A Kontopoulos; A Filindris; F Manoudis; P Metaxas
Journal:  Postgrad Med J       Date:  1981-05       Impact factor: 2.401

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Journal:  Gut       Date:  1993-04       Impact factor: 23.059

4.  Acceleration of digoxin clearance by activated charcoal.

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Journal:  Clin Pharmacol Ther       Date:  1985-04       Impact factor: 6.875

5.  Oral and intravenous bretylium disposition.

Authors:  J L Anderson; E Patterson; J G Wagner; J R Stewart; H L Behm; B R Lucchesi
Journal:  Clin Pharmacol Ther       Date:  1980-10       Impact factor: 6.875

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Journal:  Drug Intell Clin Pharm       Date:  1984-05

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Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1984-08

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Journal:  Br J Pharmacol       Date:  1970-08       Impact factor: 8.739

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Authors:  Y Bouffard; Y Berger; B Delafosse; J R Matteazzi; C Guillaume; P Tournadre; D Perrot; J Motin
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  3 in total

Review 1.  Therapeutic potential of antiarrhythmic peptides. Cellular coupling as a new antiarrhythmic target.

Authors:  S Dhein; T Tudyka
Journal:  Drugs       Date:  1995-06       Impact factor: 9.546

2.  Effects of class III antiarrhythmic drugs on the Na(+)-activated K+ channels in guinea-pig ventricular cells.

Authors:  K Mori; T Saito; Y Masuda; H Nakaya
Journal:  Br J Pharmacol       Date:  1996-09       Impact factor: 8.739

3.  Tolerance of High-Dose Oral Amiodarone for Cardioversion of Atrial Flutter.

Authors:  Vincent K Le; Katherine M Kavanagh; Satish R Raj; P Timothy Pollak
Journal:  CJC Open       Date:  2022-04-28
  3 in total

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