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Review
June 1, 2022

Efficacy and Safety Considerations With Dose-Reduced Direct Oral Anticoagulants: A Review

Author Affiliations
  • 1Cardiovascular Medicine Division, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts
  • 2Thrombosis Research Group, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts
  • 3Yale New Haven Hospital/Yale Center for Outcomes Research and Evaluation, New Haven, Connecticut
  • 4Cardiovascular Research Foundation, New York, New York
  • 5Cardiac Primary Prevention Research Center, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran
  • 6Cardiovascular Intervention Research Center, Rajaie Cardiovascular, Medical, and Research Center, Iran University of Medical Sciences, Tehran, Iran
  • 7Clinical Trial Center, Rajaie Cardiovascular, Medical, and Research Center, Iran University of Medical Sciences, Tehran, Iran
  • 8Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran
  • 9Virginia Commonwealth University, Richmond
  • 10Department of Pharmacy, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts
  • 11Section of Clinical Biochemistry, University of Verona, Verona, Italy
  • 12Division of Hematology, Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada
  • 13Population Health Research Institute, Hamilton Health Sciences, McMaster University, Hamilton, Ontario, Canada
  • 14Department of Internal Medicine, Hospital Universitari Germans Trials i Pujol, Universidad Católica San Antonio de Murcia, Barcelona, Spain
  • 15Respiratory Department, Hospital Ramón y Cajal and Medicine Department, Universidad de Alcalá (Instituto de Ramón y Cajal de Investigación Sanitaria), Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, Madrid, Spain
  • 16Hematology Division, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts
  • 17Department of Medicine and Surgery, University of Insubria, Varese, Italy
  • 18Frankel Cardiovascular Center, Department of Internal Medicine, University of Michigan, Ann Arbor
  • 19Division of Cardiology, University of Florida College of Medicine, Jacksonville, Florida
  • 20Division of Cardiology, New York-Presbyterian Hospital/Columbia University Irving Medical Center, New York
  • 21Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina
  • 22Brazilian Clinical Research Institute, São Paulo, Brazil
  • 23McMaster University, Hamilton, Ontario, Canada
  • 24Thrombosis and Atherosclerosis Research Institute, Hamilton, Ontario, Canada
  • 25Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York
  • 26Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut
  • 27Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut
  • 28Liverpool Centre for Cardiovascular Science, Liverpool Heart and Chest Hospital, University of Liverpool, Liverpool, United Kingdom
  • 29Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
JAMA Cardiol. 2022;7(7):747-759. doi:10.1001/jamacardio.2022.1292
Abstract

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.

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