Sisáková M, Toman O, Floriánová A, Kadlecová J, Chroust K, Papousek I, Spinar J
Interní kardiologická klinika Lékarské fakulty MU a FN Brno, pracoviste Bohunice.
Vnitr Lek. 2006 Mar;52(3):271-3.
Many non-cardiovascular drugs have a potential for QT interval prolongation. This phenomenon can be related to occurence of ventricular tachycardia torsades de pointes, syncopi and even sudden death.
A female patient treated with antracycline cytostatics developed a depression of left ventricle ejection fraction. At the same time she was administered 2 common drugs with proarrhythmic potential--terfenadine and itraconazole. In this patient hypokalemia also occured. Combination of the above mentioned risk factors led to QT interval prolongation and frequent ventricular tachycardias torsades de pointes degenerating in ventricular fibrillations with need of repeated defibrillations. Both drugs were withdrawn and dysiontaemia corrected. Then arrhythmias disappeared and QT interval completely normalized. In this patient the congenital long QT syndrome was not proved.
In proarrhythmic effect of non-cardiovascular drugs the following factors play role: predisposition of a particular individual, "repolarization reserve", interindividual differences in drug metabolism. The risk factors are age, sex, dysiontaemia, heart disease and drug interactions. By different choice of medication and attention to risk factors teh life threat to the described patient could have been avoided.
许多非心血管药物具有延长QT间期的潜在风险。这种现象可能与尖端扭转型室性心动过速、晕厥甚至猝死的发生有关。
一名接受蒽环类细胞毒性药物治疗的女性患者出现左心室射血分数降低。与此同时,她还服用了两种具有促心律失常潜力的常用药物——特非那定和伊曲康唑。该患者还出现了低钾血症。上述危险因素共同作用导致QT间期延长,并频繁发生尖端扭转型室性心动过速,进而恶化为心室颤动,需要反复进行除颤。停用了这两种药物并纠正了电解质紊乱。随后心律失常消失,QT间期完全恢复正常。该患者未证实存在先天性长QT综合征。
在非心血管药物的促心律失常作用中,以下因素发挥作用:特定个体的易感性、“复极储备”、药物代谢的个体差异。危险因素包括年龄、性别、电解质紊乱、心脏病和药物相互作用。通过不同的药物选择并关注危险因素,本病例患者面临的生命威胁本可避免。