Aspirin Versus Clopidogrel as Single Antithrombotic Therapy After Transcatheter Aortic Valve Replacement: Insight From the OCEAN-TAVI Registry.


Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
05 2021
Historique:
entrez: 18 5 2021
pubmed: 19 5 2021
medline: 16 10 2021
Statut: ppublish

Résumé

Current guidelines recommend dual antiplatelet therapy for the first 1 to 6 months after transcatheter aortic valve replacement (TAVR); however, recent studies have reported better outcomes with single antiplatelet therapy than with dual antiplatelet therapy in the occurrence of bleeding events, while not increasing thrombotic events. However, no data exist about optimal single antiplatelet therapy following TAVR. Patients who underwent TAVR between October 2013 and May 2017 were enrolled from the OCEAN-TAVI Japanese multicenter registry (Optimized Transcatheter Valvular Intervention). After excluding 1759 patients, 829 who received aspirin (100 mg/d) or clopidogrel (75 mg/d) after TAVR were identified and stratified according to the presence or absence of anticoagulation. Propensity score matching was performed to adjust the baseline characteristics between the aspirin and clopidogrel groups. Outcomes of interest were all-cause and cardiovascular deaths, stroke, and life-threatening or major bleeding within 2 years following TAVR. After propensity score matching, 98 and 157 pairs of patients without and with anticoagulation, respectively, were identified. Falsification end points of pneumonia, urinary tract infection, and hip fracture were evaluated, and their rates were not different between groups. All-cause deaths were not statistically different between the groups in patients with (aspirin, 17.5%; clopidogrel, 11.1%; log-rank P=0.07) and without (aspirin, 29.6%; clopidogrel, 20.1%; log-rank P=0.15) anticoagulation at 2 years post-TAVR, whereas clopidogrel was associated with a lower cardiovascular mortality at 2 years in patients with (aspirin, 8.5%; clopidogrel, 2.7%; log-rank P=0.03) and without (aspirin, 18.0%; clopidogrel, 5.2%; log-rank P=0.02) anticoagulation. We demonstrated that clopidogrel monotherapy was associated with a lower incidence of cardiovascular death compared with aspirin monotherapy during the 2-year follow-up after TAVR regardless of anticoagulation use. URL: https://upload.umin.ac.jp; Unique identifier: UMIN000020423.

Sections du résumé

BACKGROUND
Current guidelines recommend dual antiplatelet therapy for the first 1 to 6 months after transcatheter aortic valve replacement (TAVR); however, recent studies have reported better outcomes with single antiplatelet therapy than with dual antiplatelet therapy in the occurrence of bleeding events, while not increasing thrombotic events. However, no data exist about optimal single antiplatelet therapy following TAVR.
METHODS
Patients who underwent TAVR between October 2013 and May 2017 were enrolled from the OCEAN-TAVI Japanese multicenter registry (Optimized Transcatheter Valvular Intervention). After excluding 1759 patients, 829 who received aspirin (100 mg/d) or clopidogrel (75 mg/d) after TAVR were identified and stratified according to the presence or absence of anticoagulation. Propensity score matching was performed to adjust the baseline characteristics between the aspirin and clopidogrel groups. Outcomes of interest were all-cause and cardiovascular deaths, stroke, and life-threatening or major bleeding within 2 years following TAVR.
RESULTS
After propensity score matching, 98 and 157 pairs of patients without and with anticoagulation, respectively, were identified. Falsification end points of pneumonia, urinary tract infection, and hip fracture were evaluated, and their rates were not different between groups. All-cause deaths were not statistically different between the groups in patients with (aspirin, 17.5%; clopidogrel, 11.1%; log-rank P=0.07) and without (aspirin, 29.6%; clopidogrel, 20.1%; log-rank P=0.15) anticoagulation at 2 years post-TAVR, whereas clopidogrel was associated with a lower cardiovascular mortality at 2 years in patients with (aspirin, 8.5%; clopidogrel, 2.7%; log-rank P=0.03) and without (aspirin, 18.0%; clopidogrel, 5.2%; log-rank P=0.02) anticoagulation.
CONCLUSIONS
We demonstrated that clopidogrel monotherapy was associated with a lower incidence of cardiovascular death compared with aspirin monotherapy during the 2-year follow-up after TAVR regardless of anticoagulation use.
REGISTRATION
URL: https://upload.umin.ac.jp; Unique identifier: UMIN000020423.

Identifiants

pubmed: 34003663
doi: 10.1161/CIRCINTERVENTIONS.120.010097
doi:

Substances chimiques

Fibrinolytic Agents 0
Platelet Aggregation Inhibitors 0
Clopidogrel A74586SNO7
Aspirin R16CO5Y76E

Banques de données

UMIN-CTR
['UMIN000020423']

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e010097

Auteurs

Yusuke Kobari (Y)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Taku Inohara (T)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Tetsuya Saito (T)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Nobuhiro Yoshijima (N)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Makoto Tanaka (M)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).
Japanese Red Cross Ashikaga Hospital, Tochigi, Japan (M. Tanaka).

Hikaru Tsuruta (H)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Fumiaki Yashima (F)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).
Saiseikai Utsunomiya Hospital, Tochigi, Japan (F. Yashima).

Hideyuki Shimizu (H)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Keiichi Fukuda (K)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

Toru Naganuma (T)

New Tokyo Hospital, Matsudo, Japan (T.N.).

Kazuki Mizutani (K)

Osaka City General Hospital, Japan (K.M.).

Masahiro Yamawaki (M)

Saiseikai Yokohama-City Eastern Hospital, Japan (M. Yamawaki).

Norio Tada (N)

Sendai Kousei Hospital, Japan (N.T.).

Futoshi Yamanaka (F)

Shonan Kamakura General Hospital, Japan (F. Yamanaka).

Shinichi Shirai (S)

Kokura Memorial Hospital, Japan (S.S.).

Minoru Tabata (M)

Tokyo Bay Urayasu-Ichikawa Medical Center, Chiba, Japan (M. Tabata).

Hiroshi Ueno (H)

Toyama University Hospital, Japan (H.U.).

Kensuke Takagi (K)

Ogaki Municipal Hospital, Gifu, Japan (K.T.).

Yusuke Watanabe (Y)

Teikyo University School of Medicine, Tokyo, Japan (Y.W.).

Masanori Yamamoto (M)

Toyohashi Heart Center, Japan (M. Yamamoto).
Nagoya Heart Center, Japan (M. Yamamoto).

Kentaro Hayashida (K)

Keio University School of Medicine, Tokyo, Japan (Y.K., T.I., T.S., N.Y., M. Tanaka, H.T., F. Yashima, H.S., K.F., K.H.).

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