2013
DOI: 10.1093/eurheartj/eht310.p5444
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Periinterventional management of novel oral anticoagulants: results of the prospective Dresden NOAC registry

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Cited by 11 publications
(21 citation statements)
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“…The results from the prospective Dresden novel oral anticoagulant registry showed that HBT during peri-procedural management of transluminal cardiac, arterial, and venous interventions did not reduce cardiovascular events but was associated with a significant increase in the incidence of major bleeding (2.7% vs 0.5%, P = 0.01) compared with the absence of HBT. 12 In a sub-study of the RE-LY trial, HBT after the cessation of dabigatran also resulted in higher rates of major bleeding (6.5% vs 1.8%, P < 0.001) with no significant reduction in thromboembolism compared with non-HBT. 18 However, no reports have described colonic EMR in patients taking DOACs without HBT.…”
Section: Discussionmentioning
confidence: 93%
See 1 more Smart Citation
“…The results from the prospective Dresden novel oral anticoagulant registry showed that HBT during peri-procedural management of transluminal cardiac, arterial, and venous interventions did not reduce cardiovascular events but was associated with a significant increase in the incidence of major bleeding (2.7% vs 0.5%, P = 0.01) compared with the absence of HBT. 12 In a sub-study of the RE-LY trial, HBT after the cessation of dabigatran also resulted in higher rates of major bleeding (6.5% vs 1.8%, P < 0.001) with no significant reduction in thromboembolism compared with non-HBT. 18 However, no reports have described colonic EMR in patients taking DOACs without HBT.…”
Section: Discussionmentioning
confidence: 93%
“…5 The half-time metabolism of DOACs is 5 h to 17 h. 11 The short half-lives of these drugs reduce the interval of pre-procedural interruption to 1 or 2 days, and their fast onset of action achieves the rapid restitution of anticoagulant activity after the procedure. 12 In the patients taking DOACs the resection was performed on the next day of hospitalization regardless of their PT-INR. Oral administration of DOACs was omitted on the morning of the resection and restarted at the same dose later that day.…”
Section: Non-hbt Groupmentioning
confidence: 99%
“…However, a recent prospective registry of .2,100 patients on the DOACs provides additional evidence that bridging anticoagulation should only be used for patients with a high risk for thromboembolism. 12 Like the BRIDGE trial, they found that while heparin bridging of patients on DOACs did not decrease cardiovascular events, it did increase the risk of bleeding significantly (2.7%; 95% confidence interval [CI] 1.1-5.5) compared with no bridging (0.5%; 0.1-1.4; P ¼ 0.010). Consistent with this finding, the most recent European Heart Rhythm Guidelines recommend against bridging if the patient is on a DOAC.…”
Section: Direct Oral Anticoagulants (Doacs) Versus Warfarinmentioning
confidence: 98%
“…The American College of Chest Physicians (ACCP) recommends stopping vitamin K antagonists (VKAs) five days before surgery and advises that patients taking VKA who are at high risk of thromboembolism (mechanical heart valve, atrial fibrillation (AF), or VTE) be 'bridged' with LMWH. 19 On the other hand, for patients at low risk of thromboembolism no covering therapy is required when stopping anticoagulants electively. 20 In case of surgery or an invasive procedure, the degree of urgency should be assessed in order to decrease the bleeding risk: Non-VKA therapy must be discontinued, time of the last dose should be known and recorded, and where possible invasive procedures should be delayed until the effect of non-VKA medication is reduced.…”
Section: Patients On Long-term Anticoagulationmentioning
confidence: 99%
“…Although limited data are available, Beyer-Westendorf et al concluded that short-term interruption is safe for most invasive procedures and that bridging therapy may not be required in patients on NOACs preoperatively. 19 The British Society of Haematology recommends that postoperative bridging therapy should not be started until at least 48 hours after high-risk surgery. Patients with a bileaflet aortic mechanical heart valve (MHV) with no other risk factors do not require bridging therapy.…”
Section: Perioperative Anticoagulation and Bridgingmentioning
confidence: 99%