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



Bikdeli B1, 2, 3, 4 ; Zahedi Tajrishi F5 ; Sadeghipour P6, 7 ; Talasaz AH8, 9 ; Fanikos J10 ; Lippi G11 ; Siegal DM12 ; Eikelboom JW13 ; Monreal M14 ; Jimenez D15 ; Connors JM16 ; Ageno W17 ; Barnes GD18 ; Piazza G1, 2 Show All Authors
Authors
  1. Bikdeli B1, 2, 3, 4
  2. Zahedi Tajrishi F5
  3. Sadeghipour P6, 7
  4. Talasaz AH8, 9
  5. Fanikos J10
  6. Lippi G11
  7. Siegal DM12
  8. Eikelboom JW13
  9. Monreal M14
  10. Jimenez D15
  11. Connors JM16
  12. Ageno W17
  13. Barnes GD18
  14. Piazza G1, 2
  15. Angiolillo DJ19
  16. Parikh SA4, 20
  17. Kirtane AJ4, 20
  18. Lopes RD21, 22
  19. Bhatt DL1
  20. Weitz JI23, 24
  21. Mehran R25
  22. Krumholz HM3, 26, 27
  23. Goldhaber SZ1, 2
  24. Lip GYH28, 29

Source: JAMA Cardiology Published:2022


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. © 2022 American Medical Association. All rights reserved.
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