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NOACs new data in
cardiology, from trial
to real world
By
M.Wafaie aboleineen,MD,FACC
Sandeep P. Kishore et al. JACC 2018;71:564-574
CONCLUSIONS
Among patients who received 5 days of
rivaroxaban prophylaxis after total hip or total knee
arthroplasty, extended prophylaxis with aspirin was
not significantly different from rivaroxaban in the
prevention of symptomatic VTE
Results Six trials (14 580 with STEMI and 15 036
with NSTE-ACS). The primary efficacy end point risk
was significantly lower with DOAC ( P < .001) ,
pronounced in STEMI ( P < .001), no significant
with NSTE-ACS (P = .36).
DOACs associated with a higher risk of major
bleeding ( P < .001) .
Chiarito M, et al. , . JAMA Cardiol 2018;Feb 7
Conclusions and Relevance To their
knowledge, these findings are the first
evidence to support differential treatment
effects of DOAC in addition to APT in ACS .
with NSTEI, the risk-benefit profile of DOAC
appears unfavorable.
DOAC in addition to APT might represent an
attractive option for patients with STEMI
Specific antidotes to NOACs
Idarucizumab PER977
Andexanet
alpha
Structure
Humanized
Fab fragment
Synthetic small
molecule
Human
rXa variant
Target Dabigatran Universal FXa inhibitors
Binding
Non-competit.
High affinity
? Competitive
Clinical studies
Rapid complete
reversal
?
Rapid, near
complete
reversalLauw M, et al. Can J Cardiol 2014 (accepted).
Conclusions
NOACs minimize growing burden of
thromboembolism (especially AF) and bleeding
Specific antidotes will provide
reassurance to physicians .
Low doses are usefule for secondry
prevention ( in addition to DAPT)especially
after STEMI.
Noacs

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Noacs

  • 1. NOACs new data in cardiology, from trial to real world By M.Wafaie aboleineen,MD,FACC
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  • 3. Sandeep P. Kishore et al. JACC 2018;71:564-574
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  • 12. CONCLUSIONS Among patients who received 5 days of rivaroxaban prophylaxis after total hip or total knee arthroplasty, extended prophylaxis with aspirin was not significantly different from rivaroxaban in the prevention of symptomatic VTE
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  • 23. Results Six trials (14 580 with STEMI and 15 036 with NSTE-ACS). The primary efficacy end point risk was significantly lower with DOAC ( P < .001) , pronounced in STEMI ( P < .001), no significant with NSTE-ACS (P = .36). DOACs associated with a higher risk of major bleeding ( P < .001) .
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  • 28. Chiarito M, et al. , . JAMA Cardiol 2018;Feb 7 Conclusions and Relevance To their knowledge, these findings are the first evidence to support differential treatment effects of DOAC in addition to APT in ACS . with NSTEI, the risk-benefit profile of DOAC appears unfavorable. DOAC in addition to APT might represent an attractive option for patients with STEMI
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  • 30. Specific antidotes to NOACs Idarucizumab PER977 Andexanet alpha Structure Humanized Fab fragment Synthetic small molecule Human rXa variant Target Dabigatran Universal FXa inhibitors Binding Non-competit. High affinity ? Competitive Clinical studies Rapid complete reversal ? Rapid, near complete reversalLauw M, et al. Can J Cardiol 2014 (accepted).
  • 31. Conclusions NOACs minimize growing burden of thromboembolism (especially AF) and bleeding Specific antidotes will provide reassurance to physicians . Low doses are usefule for secondry prevention ( in addition to DAPT)especially after STEMI.