Efficacy and safety of antithrombotic therapy with non-vitamin K antagonist oral anticoagulants after transcatheter aortic valve replacement: a systematic review and meta-analysis

Objective: A meta-analysis was performed to compare the efficacy and safety of antithrombotic therapy with non-vitamin K antagonist oral anticoagulants (NOACs) versus standard care in patients after successful transcatheter aortic valve replacement (TAVR). Methods: A systematic search of PubMed, Coc...

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Main Authors: Qing An (Author), Shuwen Su (Author), Yan Tu (Author), Lingfeng Gao (Author), Gaopeng Xian (Author), Yujia Bai (Author), Qiong Zhan (Author), Xingbo Xu (Author), Dingli Xu (Author), Qingchun Zeng (Author)
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Published: SAGE Publishing, 2021-11-01T00:00:00Z.
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100 1 0 |a Qing An  |e author 
700 1 0 |a Shuwen Su  |e author 
700 1 0 |a Yan Tu  |e author 
700 1 0 |a Lingfeng Gao  |e author 
700 1 0 |a Gaopeng Xian  |e author 
700 1 0 |a Yujia Bai  |e author 
700 1 0 |a Qiong Zhan  |e author 
700 1 0 |a Xingbo Xu  |e author 
700 1 0 |a Dingli Xu  |e author 
700 1 0 |a Qingchun Zeng  |e author 
245 0 0 |a Efficacy and safety of antithrombotic therapy with non-vitamin K antagonist oral anticoagulants after transcatheter aortic valve replacement: a systematic review and meta-analysis 
260 |b SAGE Publishing,   |c 2021-11-01T00:00:00Z. 
500 |a 2040-6231 
500 |a 10.1177/20406223211056730 
520 |a Objective: A meta-analysis was performed to compare the efficacy and safety of antithrombotic therapy with non-vitamin K antagonist oral anticoagulants (NOACs) versus standard care in patients after successful transcatheter aortic valve replacement (TAVR). Methods: A systematic search of PubMed, Cochrane Central Register of Controlled Trials, and EMBASE databases and ClinicalTrials.gov website (through 21 October 2020) was performed. Risk ratios (RRs) with 95% confidence intervals (CIs) for all outcomes were calculated using random-effects models. Results: Twelve studies (two studies were randomized controlled trials) comprising 6943 patients were included (5299 had indications for oral anticoagulation (OAC) and 1644 had none). No significant differences were found between NOACs and the standard care in the incidences of all stroke, a composite endpoint, and major/life-threatening bleeding. NOACs were associated with lower all-cause mortality than vitamin K antagonists (VKAs) in post-TAVR patients with indications for OAC after more than 1 year of follow-up [RR = 0.64; 95% CI, (0.42, 0.96); p  = 0.03], whereas NOACs exhibited poor outcomes than antiplatelet therapy (APT) in patients without indications for OAC [RR = 1.66; 95% CI, (1.12, 2.45); p  = 0.01]. In the prevention of valve thrombosis, NOACs and VKAs were not significantly different in patients with indications for OAC [RR = 0.66; 95% CI, (0.24, 1.84); p  = 0.43], whereas NOACs were better than APT in patients without indications for OAC [RR = 0.19; 95% CI, (0.04, 0.83); p = 0.03]. Conclusions: In patients with indications for OAC, post-TAVR antithrombotic therapy with NOACs was more favorable due to its lower all-cause mortality after more than 1 year of follow-up. In those without indications for OAC, NOACs presented poorer outcomes due to its higher all-cause mortality. 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Therapeutic Advances in Chronic Disease, Vol 12 (2021) 
787 0 |n https://doi.org/10.1177/20406223211056730 
787 0 |n https://doaj.org/toc/2040-6231 
856 4 1 |u https://doaj.org/article/6e65f45b552740a29ff89a75f7a1c335  |z Connect to this object online.