临床试验的启示:新证据支持手术干预而非药物疗法治疗心房颤动

Akshat D. Modi , Akriti Sharma , Dharmeshkumar M. Modi
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引用次数: 0

摘要

心房颤动(房颤)是世界上最常见的心律失常之一。心房颤动是导致心血管疾病死亡的最主要原因之一,给患者、医生和全球医疗保健系统带来了沉重负担。多年来,研究人员一直在进行临床试验,研究心房颤动患者治疗的有效性、成本和实用性。房颤(急性、慢性、持续性、阵发性、非瓣膜性、非风湿性和快速性)的主要治疗策略包括使用抗心律失常药物(AAD)和抗凝药物(ACD)来控制心率和心律,以及预防中风。本综述旨在讨论比较 AADs(Ia 类:奎尼丁;Ic 类:非卡内酯、普罗帕酮;III 类:索他洛尔、胺碘酮)和 ACDs(维生素 K 拮抗剂:华法林;Xa 因子抑制剂:阿哌沙班、利伐沙班;凝血酶抑制剂:达比加群)与心血管外科干预(即:导管消融、冷冻治疗)的临床试验、导管消融、冷冻球囊消融、消融和 DDDR 起搏器、心脏电复律、左心房阑尾封堵术)治疗各种类型房颤的临床试验。本研究对有关这一主题的临床试验进行了回顾,使医护人员能够确定最适合患者的治疗方法。
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Insights from clinical trials: New evidence supports surgical interventions over drug therapies for atrial fibrillation

Atrial fibrillation (AF) is one of the world’s most prevalent cardiac arrhythmias. It poses a heavy burden on patients, physicians and the global healthcare system as it is one of the top leading causes of cardiovascular death. Researchers have spent numerous years conducting clinical trials to investigate the effectiveness, cost and practicality of treatment for patients suffering from AF. The primary treatment strategy for AF (acute, chronic, persistent, paroxysmal, non-valvular, nonrheumatic, and rapid) involves the use of antiarrhythmic drugs (AAD) and anticoagulant drugs (ACD) to manage heart rate and rhythm, as well as to prevent strokes. This review aims to discuss clinical trials that compared AADs (class Ia: quinidine; class Ic: flecainide, propafenone; class III: sotalol, amiodarone) and ACDs (vitamin K antagonist: warfarin; factor Xa inhibitor: apixaban, rivaroxaban; thrombin inhibitor: dabigatran) with cardiovascular surgical interventions (i.e., catheter ablation, cryoballoon ablation, ablation and DDDR pacemaker, electrical cardioversion, and left atrial appendage occlusion) to treat various types of AF in patients with a diverse history of cardiovascular diseases and medical history. This study provides a review of clinical trials on this topic and enables healthcare professionals to determine the best-suited treatment for their patients.

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来源期刊
Medicine in Drug Discovery
Medicine in Drug Discovery Medicine-Pharmacology (medical)
CiteScore
8.30
自引率
0.00%
发文量
30
审稿时长
21 days
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