Department of Cardiovascular Diseases, University of Cincinnati, Cincinnati, OH, USA.
Cardiovasc Ther. 2014 Feb;32(1):19-25. doi: 10.1111/1755-5922.12054.
This review aims to clarify the underlying risk of arrhythmia associated with the use of macrolides and fluoroquinolones antibiotics. Torsades de pointes (TdP) is a rare potential side effect of fluoroquinolones and macrolide antibiotics. However, the widespread use of these antibiotics compounds the problem. These antibiotics prolong the phase 3 of the action potential and cause early after depolarization and dispersion of repolarization that precipitate TdP. The potency of these drugs, as potassium channel blockers, is very low, and differences between them are minimal. Underlying impaired cardiac repolarization is a prerequisite for arrhythmia induction. Impaired cardiac repolarization can be congenital in the young or acquired in adults. The most important risk factors are a prolonged baseline QTc interval or a combination with class III antiarrhythmic drugs. Modifiable risk factors, including hypokalemia, hypomagnesemia, drug interactions, and bradycardia, should be corrected. In the absence of a major risk factor, the incidence of TdP is very low. The use of these drugs in the appropriate settings of infection should not be altered because of the rare risk of TdP, except among cases with high-risk factors.
这篇综述旨在阐明与大环内酯类和氟喹诺酮类抗生素使用相关的心律失常潜在风险。尖端扭转型室性心动过速(TdP)是氟喹诺酮类和大环内酯类抗生素的一种罕见潜在副作用。然而,这些抗生素的广泛使用使问题更加复杂。这些抗生素延长动作电位的第 3 相,并导致早期后除极和复极离散,从而引发 TdP。这些药物作为钾通道阻滞剂的效力非常低,它们之间的差异很小。潜在的心脏复极受损是心律失常诱导的前提。心脏复极受损在年轻人中可能是先天性的,在成年人中可能是获得性的。最重要的危险因素是基线 QTc 间期延长或与 III 类抗心律失常药物联合使用。可改变的危险因素包括低钾血症、低镁血症、药物相互作用和心动过缓,应予以纠正。在没有重大危险因素的情况下,TdP 的发生率非常低。除非存在高风险因素,否则不应因 TdP 的罕见风险而改变这些药物在感染适当情况下的使用。