医学
阿哌沙班
拜瑞妥
达比加群
依杜沙班
心房颤动
冲程(发动机)
内科学
随机对照试验
重症监护医学
华法林
机械工程
工程类
作者
Behnood Bikdeli,Farbod Zahedi Tajrishi,Parham Sadeghipour,Azita H. Talasaz,John Fanikos,Giuseppe Lippi,Deborah M. Siegal,John W. Eikelboom,Manuel Monréal,David Jiménez,Jean M. Connors,Walter Ageno,Geoffrey D. Barnes,Gregory Piazza,Dominick J. Angiolillo,Sahil A. Parikh,Ajay J. Kirtane,Renato D. Lópes,Deepak L. Bhatt,Jeffrey I. Weitz,Roxana Mehran,Harlan M. Krumholz,Samuel Z. Goldhaber,Gregory Y.H. Lip
出处
期刊:JAMA Cardiology
[American Medical Association]
日期:2022-06-01
卷期号:7 (7): 747-747
被引量:23
标识
DOI:10.1001/jamacardio.2022.1292
摘要
Importance
Dose-reduced regimens of direct oral anticoagulants (DOACs) may be used for 2 main purposes: dose-adjusted treatment intended as full-intensity anticoagulation (eg, for stroke prevention in atrial fibrillation [AF] in patients requiring dose reduction) or low-intensity treatment (eg, extended-duration treatment of venous thromboembolism [VTE]). We reviewed randomized clinical trials (RCTs) to understand the scenarios in which dose-adjusted or low-intensity DOACs were tested and reviewed the labeled indications by regulatory authorities, using data from large registries to assess whether the use of dose-reduced DOACs in routine practice aligned with the findings of RCTs. Observations
Among 4191 screened publications, 35 RCTs that used dose-adjusted DOACs were identified for dabigatran, apixaban, rivaroxaban, and edoxaban. Of these 35 RCTs, 29 were related to stroke prevention in AF. Efficacy and safety results for dose-adjusted DOACs in large RCTs of AF were similar to those found for full-dose DOACs. To our knowledge, dabigatran, apixaban, and rivaroxaban have not been studied as dose-adjusted therapy for acute VTE treatment. Low-intensity DOACs were identified in 37 RCTs. Low-intensity DOACs may be used for extended-duration treatment of VTE (apixaban and rivaroxaban), primary prevention in orthopedic surgeries (dabigatran, apixaban, and rivaroxaban), primary prevention in ambulatory high-risk cancer patients (apixaban and rivaroxaban) or (postdischarge) high-risk medical patients (rivaroxaban), in stable atherosclerotic vascular disease, or after a recent revascularization for peripheral artery disease in conjunction with aspirin (rivaroxaban). Minor variations exist between regulatory authorities in different regions regarding criteria for dose adjustment of DOACs. Data from large registries indicated that dose-reduced DOACs were used occasionally with doses or for clinical scenarios different from those studied in RCTs or recommended by regulatory authorities. Conclusions and Relevance
Dose adjustment and low-intensity treatment are 2 different forms of dose-reduced DOACs. Dose adjustment is mostly relevant for AF and should be done based on the approved criteria. Dose adjustment of DOACs should not be used for acute VTE treatment in most cases. In contrast, low-intensity DOACs may be used for primary or secondary VTE prevention for studied and approved indications. Attention should be given to routine practice patterns to align the daily clinical practice with existing evidence of safety and efficacy.