Use of Chronic Oral Anticoagulation and Associated Outcomes Among Patients Undergoing Percutaneous Coronary Intervention

Author:

Secemsky Eric A.123,Butala Neel M.24,Kartoun Uri52,Mahmood Sadiqa6,Wasfy Jason H.12,Kennedy Kevin F.7,Shaw Stanley Y.152,Yeh Robert W.23

Affiliation:

1. Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA

2. Harvard Medical School, Boston, MA

3. Smith Center for Outcomes Research in Cardiology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA

4. Department of Medicine, Massachusetts General Hospital, Boston, MA

5. Center for Systems Biology and Center for Assessment Technology & Continuous Health (CATCH), Massachusetts General Hospital, Boston, MA

6. Department of Quality, Safety and Value, Partners HealthCare, Boston, MA

7. Saint Luke's Mid‐America Heart Institute, Kansas City, MO

Abstract

Background Contemporary rates of oral anticoagulant ( OAC ) therapy and associated outcomes among patients undergoing percutaneous coronary intervention ( PCI ) have been poorly described. Methods and Results Using data from an integrated health care system from 2009 to 2014, we identified patients on OAC s within 30 days of PCI . Outcomes included in‐hospital bleeding and mortality. Of 9566 PCI s, 837 patients (8.8%) were on OAC s, and of these, 7.9% used non–vitamin K antagonist agents. OAC use remained stable during the study (8.1% in 2009, 9.0% in 2014; P =0.11), whereas use of non–vitamin K antagonist agents in those on OAC s increased (0% in 2009, 16% in 2014; P <0.01). Following PCI , OAC ‐treated patients had higher crude rates of major bleeding (11% versus 6.5%; P <0.01), access‐site bleeding (2.3% versus 1.3%; P =0.017), and non–access‐site bleeding (8.2% versus 5.2%; P <0.01) but similar crude rates of in‐hospital stent thrombosis (0.4% versus 0.3%; P =0.85), myocardial infarction (2.5% versus 3.0%; P =0.40), and stroke (0.48% versus 0.52%; P =0.88). In addition, prior to adjustment, OAC ‐treated patients had longer hospitalizations (3.9±5.5 versus 2.8±4.6 days; P <0.01), more transfusions (7.2% versus 4.2%; P <0.01), and higher 90‐day readmission rates (22.1% versus 13.1%; P <0.01). In adjusted models, OAC use was associated with increased risks of in‐hospital bleeding (odds ratio 1.50; P <0.01), 90‐day readmission (odds ratio 1.40; P <0.01), and long‐term mortality (hazard ratio 1.36; P <0.01). Conclusions Chronic OAC therapy is frequent among contemporary patients undergoing PCI . After adjustment for potential confounders, OAC ‐treated patients experienced greater in‐hospital bleeding, more readmissions, and decreased long‐term survival following PCI . Efforts are needed to reduce the occurrence of adverse events in this population.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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