评估diltiazem或维拉帕米尔与直接口服抗凝剂的同时使用:元分析
Kazuhiko Kido1, Mikiko Shimizu2, Tsuyoshi Shiga3
1Department of Clinical Pharmacy, School of Pharmacy, West Virginia University, Morgantown, WV, USA.
The Annals of pharmacotherapy
|May 6, 2025
概括
将直接口服抗凝剂 (DOAC) 与迪尔提亚或维拉帕米尔结合使用显著增加出血风险. 这种疗法也降低了中风风险,但整体出血问题对患者安全至关重要.
科学领域:
- 药理学和心脏病学 药理学和心脏病学
- 药物相互作用 药物相互作用
- 临床风险评估临床风险评估
背景情况:
- 迪尔提亚和维拉帕米尔是中度CYP3A4和P-葡萄糖蛋白抑制剂.
- 这些药物可以显著增加直接口服抗凝剂 (DOAC) 度.
- 同时使用可能会增加出血风险,之前的研究显示了相互矛盾的结果.
研究的目的:
- 为了评估与联合迪尔提亚泽姆/维拉帕米尔和DOAC治疗相比DOAC单独治疗相关的出血和中风风险.
- 综合现实研究的证据,以澄清这种药物组合的安全性.
主要方法:
- 一项对研究进行的元分析,比较了同时使用diltiazem/verapamil和DOAC治疗与DOAC单一治疗.
- 在MEDLINE和谷歌学者中进行的搜索截至2024年11月16日.
- 主要结局:严重出血;次要结局:中风/全身血栓塞,胃肠道出血.
主要成果:
- 分析包括6项研究.
- 同时治疗显著增加大出血 (OR=1.38) 和胃肠道出血 (OR=1.19) 的风险.
- 观察到,中风或全身血栓塞的风险明显降低 (OR=0.83).
结论:
- 同时使用DOAC与diltiazem/verapamil,与DOAC单独治疗相比,会增加出血风险.
- 虽然中风风险可能会降低,但增加的出血风险需要在临床实践中仔细考虑.
相关概念视频
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
671
Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
671
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
986
Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
986
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
384
Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
384
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
1.0K
Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
1.0K
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
805
Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of...
805
Anticoagulant Drugs: Low-Molecular-Weight Heparins
532
Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
532


