Continued Versus Interrupted Oral Anticoagulation During Transcatheter Aortic Valve Replacement in Patients With Atrial Fibrillation: A Meta-Analysis

Author:

Jain Hritvik1,Patel Nandan1,Daoud Tariq Muhammad2,Al-Shammari Ali Saad3,Khan Rozi4,Jain Jyoti1,Patel Rahul5,Ahmed Faizan6,Ahmed Raheel7,Alexander Thomas8

Affiliation:

1. Department of Cardiology, All India Institute of Medical Sciences (AIIMS), Jodhpur, India;

2. Department of Internal Medicine, Foundation University Medical College, Islamabad, Pakistan;

3. Department of Medicine, College of Medicine, University of Baghdad, Baghdad, Iraq;

4. Department of Internal Medicine, University of Pittsburgh Medical Center, Harrisburg, PA;

5. Department of Internal Medicine, University of North Carolina Health Blue Ridge, Morganton, NC;

6. Department of Cardiology, Duke University Hospital, Durham, NC;

7. Department of Cardiology, National Heart and Lung Institute, Imperial College London, London, United Kingdom; and

8. Department of Cardiology, Corpus Christi Medical Center, Corpus Christi, TX.

Abstract

Introduction: A substantial number of patients undergoing transcatheter aortic valve replacement (TAVR) require long-term oral anticoagulants (OAC) owing to comorbidities. This study examined whether continuing oral anticoagulation periprocedurally during TAVR is as safe and effective as interrupting it. Methods: A systematic search of the major databases was performed to identify relevant studies. Effect estimates were calculated using risk ratios (RR) and 95% CIs by pooling the data using the inverse-variance random effects model. Statistical significance was set at P < 0.05. Results: Four studies were included, with 2962 patients undergoing TAVR with continued OAC (n = 1318) and interrupted OAC (n = 1644). The pooled analysis demonstrated that TAVR with continued OAC had comparable risks for all-cause mortality (RR: 0.91; 95% CI, 0.62–1.34; P = 0.64), cardiovascular mortality (RR: 0.89; 95% CI, 0.43–1.84; P = 0.76), stroke (RR: 0.67; 95% CI, 0.42–1.08; P = 0.09), closure device failure (RR: 0.86; 95% CI, 0.47–1.59; P = 0.64), major/life-threatening bleeding (RR: 0.93; 95% CI, 0.74–1.15; P = 0.49), and major vascular complications (RR: 0.97; 95% CI, 0.79–1.20; P = 0.80) compared with TAVR with interrupted OAC. Conclusions: In patients undergoing TAVR, continued OAC showed comparable safety and efficacy with interrupted OAC. These findings demonstrate that continuing OAC in the periprocedural period may be a viable option in patients with atrial fibrillation because of comorbidities requiring anticoagulants.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference39 articles.

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