Literature DB >> 20844627

Syncope, widened QRS interval, and left ventricular systolic depression: coincident with propafenone therapy for atrial fibrillation.

Rodney A Samaan1, Hezekiah O Sobamowo, Frank Tamburrino, Richard Grodman, Nidal Isber.   

Abstract

We report the case of a 46-year-old man who developed syncope, a widened QRS interval, and depressed left ventricular systolic function during propafenone therapy for atrial fibrillation. These acute findings may have been consequent to an increased dosage of propafenone combined with heavy alcohol consumption that led to decreased metabolism of propafenone. In addition, propafenone is known to interfere with liver function, although this patient's test results showed scant evidence of liver abnormalities. Yet another possible factor is the genetic spectrum in the metabolism of propafenone and other class I antiarrhythmic agents. When propafenone is prescribed, we recommend advising patients that alcohol consumption and interactions with other drugs can lead to increased levels of the antiarrhythmic agent, with resultant toxicity that can lead to adverse cardiovascular effects. Patients taking propafenone should also undergo periodic liver function testing. Finally, attention should be paid to voluntary or official recalls of specific antiarrhythmic medications that are of unreliable quality or potency.

Entities:  

Keywords:  Anti-arrhythmia agents/administration & dosage/adverse effects; atrial fibrillation/diagnosis/drug therapy/etiology/prevention & control; cytochrome P-450 CYP2D6/genetics; dose-response relationship, drug; heart/drug effects; liver/enzymology/metabolism; propafenone/administration & dosage/adverse effects/therapeutic use

Mesh:

Substances:

Year:  2010        PMID: 20844627      PMCID: PMC2929852     

Source DB:  PubMed          Journal:  Tex Heart Inst J        ISSN: 0730-2347


  7 in total

1.  Effect of propafenone on left ventricular ejection fraction.

Authors:  B J Baker; H Dinh; D Kroskey; N D de Soyza; M L Murphy; J A Franciosa
Journal:  Am J Cardiol       Date:  1984-11-14       Impact factor: 2.778

2.  Effect of CYP2D6*10 genotype on propafenone pharmacodynamics in Chinese patients with ventricular arrhythmia.

Authors:  Wei-Min Cai; Jun Xu; Bing Chen; Fu-Min Zhang; Yuan-Zhu Huang; Yin-Di Zhang
Journal:  Acta Pharmacol Sin       Date:  2002-11       Impact factor: 6.150

3.  Safety and tolerability of long-term propafenone therapy for supraventricular tachyarrhythmias. The Propafenone Multicenter Study Group.

Authors:  P J Podrid; J L Anderson
Journal:  Am J Cardiol       Date:  1996-08-15       Impact factor: 2.778

4.  A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agents.

Authors:  Mossaab Shuraih; Tomohiko Ai; Matteo Vatta; Yoshiro Sohma; Eileen M Merkle; Erica Taylor; Zhaohui Li; Yutao Xi; Mehdi Razavi; Jeffrey A Towbin; Jie Cheng
Journal:  J Cardiovasc Electrophysiol       Date:  2007-01-10

5.  Propafenone hepatotoxicity: report of two new cases.

Authors:  Daniel Cocozzella; José Curciarello; Osvaldo Corallini; Adriana Olivera; María Malca Alburquerque; Emilio Fraquelli; Liliana Zamagna; Alejandro Olenchuck; Alberto Cremona
Journal:  Dig Dis Sci       Date:  2003-02       Impact factor: 3.199

6.  [Hepatic toxicity of propafenone: a case description].

Authors:  Antonello La Brocca
Journal:  Ann Ital Med Int       Date:  2002 Oct-Dec

7.  Cardiac memory induced by QRS widening due to propafenone toxicity.

Authors:  John V Wylie; Peter Zimetbaum; Mark E Josephson; Alexei Shvilkin
Journal:  Pacing Clin Electrophysiol       Date:  2007-09       Impact factor: 1.976

  7 in total

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