TY - JOUR
T1 - New oral anticoagulants and their reversal
AU - Pinto, Ian
AU - Giri, Anshu
AU - Arshad, Umbreen
AU - Gajra, Ajeet
N1 - Publisher Copyright:
© 2015 Bentham Science Publishers.
PY - 2015/10/1
Y1 - 2015/10/1
N2 - The advent of new oral anticoagulants (NOAC) has increased the armamentarium against thromboembolic diseases but has given rise to a conundrum on their reversal. NOAC’s have comparable efficacy to traditional vitamin K antagonists with similar rates of major bleeding. However there is no standardized method for reversal of these agents and no specific antidote. This is of concern not only in acute bleeding episodes but also in clinical scenarios where emergency surgery is required. Recent studies have investigated reversal of dabigatran, rivaroxaban, and apixaban using prothrombin complex concentrates (PCC), recombinant factor VIIa, and in the case of dabigatran, a monoclonal antibody. These studies have been encouraging in showing improvement of bleeding times and blood loss in most models, especially with the use of PCCs and the dabigatran antibody. Of note the majority of common currently used coagulation assays may not correlate with clinical reversal. The management of overt bleeding with NOACs is difficult due to the lack of clinical trials. Current animal trials, case reports and hemostatic testing on human blood have shown some promise; provide guidance but warrant further investigation.
AB - The advent of new oral anticoagulants (NOAC) has increased the armamentarium against thromboembolic diseases but has given rise to a conundrum on their reversal. NOAC’s have comparable efficacy to traditional vitamin K antagonists with similar rates of major bleeding. However there is no standardized method for reversal of these agents and no specific antidote. This is of concern not only in acute bleeding episodes but also in clinical scenarios where emergency surgery is required. Recent studies have investigated reversal of dabigatran, rivaroxaban, and apixaban using prothrombin complex concentrates (PCC), recombinant factor VIIa, and in the case of dabigatran, a monoclonal antibody. These studies have been encouraging in showing improvement of bleeding times and blood loss in most models, especially with the use of PCCs and the dabigatran antibody. Of note the majority of common currently used coagulation assays may not correlate with clinical reversal. The management of overt bleeding with NOACs is difficult due to the lack of clinical trials. Current animal trials, case reports and hemostatic testing on human blood have shown some promise; provide guidance but warrant further investigation.
KW - Administration, Oral
KW - Animals
KW - Anticoagulants/administration & dosage
KW - Antidotes/adverse effects
KW - Blood Coagulation Tests
KW - Blood Coagulation/drug effects
KW - Blood Loss, Surgical/prevention & control
KW - Elective Surgical Procedures
KW - Emergencies
KW - Hemorrhage/blood
KW - Humans
KW - Perioperative Care
KW - Predictive Value of Tests
KW - Risk Factors
KW - Treatment Outcome
UR - http://www.scopus.com/inward/record.url?scp=84947795797&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000218318100003&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.2174/1574886310666150416123530
DO - 10.2174/1574886310666150416123530
M3 - Article
C2 - 25877809
SN - 1574-8863
VL - 10
SP - 208
EP - 216
JO - Current Drug Safety
JF - Current Drug Safety
IS - 3
ER -