Khan Shenel A, Emmanuel Soniya, Shantha Kumar Vivig, Nerella Resheek, Shaman Ameen Basim, Patel Dev, David John Jabez, Bodepudi Ranita, Seher Saniya, Penumetcha Sai Sri
General Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Cureus. 2024 Jul 31;16(7):e65857. doi: 10.7759/cureus.65857. eCollection 2024 Jul.
Long QT syndrome (LQTS) is a severe cardiac disorder characterized by an abnormally prolonged QTc interval on an electrocardiogram (ECG), which can result in life-threatening irregular heart rhythms. The use of certain medications, particularly anti-arrhythmic drugs such as quinidine, sotalol, and amiodarone, can lead to acquired LQTS by prolonging the QT interval through the inhibition of specific ion channels responsible for heart repolarization, which may present symptoms like fainting, seizures, and sudden cardiac arrest. This systematic review, conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines, focused on analyzing the association between Long QT syndrome and drugs utilized for managing arrhythmias, involving a thorough examination of six selected studies from an initial pool of 68 articles. It was found that antiarrhythmic drugs such as amiodarone, sotalol, dofetilide, procainamide, quinidine, and flecainide have the potential to cause QT prolongation as a side effect, which is often influenced by factors including dosage, coexisting medical conditions, electrolyte imbalances, and other risk factors. Prolonged QT interval significantly elevates the risk of a life-threatening arrhythmia called torsade de pointes. The management of this side effect typically involves reducing the medication dosage or discontinuing it altogether and, in some cases, employing selective beta blockers. However, further research is essential to improve the understanding and implementation of strategies to prevent and manage QT prolongation caused by antiarrhythmic drugs. Additional clinical studies are warranted to enhance knowledge and provide comprehensive guidelines to healthcare practitioners regarding the appropriate use of these medications. Close monitoring of the QT interval is recommended for patients receiving anti-arrhythmic therapy, and consideration should be given to patient-specific risk factors for LQTS, including age, sex, and electrolyte imbalances.
长QT综合征(LQTS)是一种严重的心脏疾病,其特征是心电图(ECG)上QTc间期异常延长,这可能导致危及生命的心律失常。使用某些药物,特别是抗心律失常药物,如奎尼丁、索他洛尔和胺碘酮,可通过抑制负责心脏复极的特定离子通道来延长QT间期,从而导致获得性LQTS,可能出现昏厥、癫痫发作和心脏骤停等症状。本系统评价遵循《系统评价和Meta分析的首选报告项目》(PRISMA)2020指南进行,重点分析长QT综合征与用于治疗心律失常的药物之间的关联,对从68篇文章的初始库中筛选出的6项研究进行了全面审查。结果发现,胺碘酮、索他洛尔、多非利特、普鲁卡因胺、奎尼丁和氟卡尼等抗心律失常药物有可能导致QT延长作为副作用,这通常受剂量、并存疾病、电解质失衡和其他风险因素等影响。QT间期延长显著增加了一种称为尖端扭转型室速的危及生命的心律失常的风险。这种副作用的管理通常包括减少药物剂量或完全停药,在某些情况下,使用选择性β受体阻滞剂。然而,进一步的研究对于提高对抗心律失常药物引起的QT延长的预防和管理策略的理解和实施至关重要。有必要进行更多的临床研究,以增强知识并为医疗保健从业者提供关于这些药物适当使用的全面指南。建议对接受抗心律失常治疗的患者密切监测QT间期,并应考虑患者特定的LQTS风险因素,包括年龄、性别和电解质失衡。