Peri-interventional management of novel oral anticoagulants in daily care: Results from the prospective Dresden NOAC registry

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Jan Beyer-Westendorf - , Medizinische Klinik und Poliklinik III, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Vera Gelbricht - , Universitätsklinikum Carl Gustav Carus Dresden, Medizinische Klinik und Poliklinik 3 (Autor:in)
  • Kati Förster - , Universitätsklinikum Carl Gustav Carus Dresden, Medizinische Klinik und Poliklinik 3 (Autor:in)
  • Franziska Ebertz - , Universitätsklinikum Carl Gustav Carus Dresden, Medizinische Klinik und Poliklinik 3 (Autor:in)
  • Christina Köhler - , Universitätsklinikum Carl Gustav Carus Dresden, Medizinische Klinik und Poliklinik 3 (Autor:in)
  • Sebastian Werth - , Medizinische Klinik und Poliklinik III, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Eberhard Kuhlisch - , Institut für Medizinische Informatik und Biometrie (Autor:in)
  • Thoralf Stange - , Institut für Medizinische Informatik und Biometrie (Autor:in)
  • Christoph Thieme - , Universitätsklinikum Carl Gustav Carus Dresden, Medizinische Klinik und Poliklinik 3 (Autor:in)
  • Katharina Daschkow - , Universitätsklinikum Carl Gustav Carus Dresden, Medizinische Klinik und Poliklinik 3 (Autor:in)
  • Norbert Weiss - , Medizinische Klinik und Poliklinik III, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)

Abstract

Aims Patients receiving novel oral anticoagulants (NOACs) frequently undergo interventional procedures. Short half-lives and rapid onset of action allow for short periods of NOAC interruption without heparin bridging. However, outcome data for this approach are lacking. We evaluated the peri-interventional NOAC management in unselected patients from daily care. Methods and results Effectiveness and safety data were collected from an ongoing, prospective, non-interventional registry of >2100 NOAC patients. Outcome events were adjudicated using standard event definitions. Of 2179 registered patients, 595 (27.3%) underwent 863 procedures (15.6% minimal, 74.3% minor, and 10.1% major procedures). Until Day 30 ± 5 post-procedure, major cardiovascular events occurred in 1.0% of patients [95% confidence interval (95% CI) 0.5-2.0] and major bleeding complications in 1.2% (95% CI 0.6-2.1). Cardiovascular and major bleeding complications were highest after major procedures (4.6 and 8.0%, respectively). Heparin bridging did not reduce cardiovascular events, but led to significantly higher rates of major bleeding complications (2.7%; 95% CI 1.1-5.5) compared with no bridging (0.5%; 0.1-1.4; P = 0.010). Multivariate analysis demonstrated diabetes [odds ratio (OR) 13.2] and major procedures (OR 7.3) as independent risk factors for cardiovascular events. Major procedures (OR 16.8) were an independent risk factor for major bleeding complications. However, if major and non-major procedures were separately assessed, heparin bridging was not an independent risk factor for major bleeding. Conclusion Continuation or short-term interruption of NOAC is safe strategies for most invasive procedures. Patients at cardiovascular risk undergoing major procedures may benefit from heparin bridging, but bleeding risks need to be considered.

Details

OriginalspracheEnglisch
Seiten (von - bis)1888-1896
Seitenumfang9
FachzeitschriftEuropean heart journal
Jahrgang35
Ausgabenummer28
PublikationsstatusVeröffentlicht - 21 Juli 2014
Peer-Review-StatusJa

Externe IDs

PubMed 24394381

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Apixaban, Bridging, Dabigatran, Invasive procedures, Oral anticoagulants, Rivaroxaban