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Total Thrombus‐Formation Analysis System (T‐TAS) Can Predict Periprocedural Bleeding Events in Patients Undergoing Catheter Ablation for Atrial Fibrillation

BACKGROUND: Non–vitamin K antagonist oral anticoagulants are used to prevent thromboembolism in patients with atrial fibrillation. The T‐TAS “Total Thrombus‐formation Analysis System” (Fujimori Kogyo Co Ltd) was developed for quantitative analysis of thrombus formation using microchips with thrombog...

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Detalles Bibliográficos
Autores principales: Ito, Miwa, Kaikita, Koichi, Sueta, Daisuke, Ishii, Masanobu, Oimatsu, Yu, Arima, Yuichiro, Iwashita, Satomi, Takahashi, Aya, Hoshiyama, Tadashi, Kanazawa, Hisanori, Sakamoto, Kenji, Yamamoto, Eiichiro, Tsujita, Kenichi, Yamamuro, Megumi, Kojima, Sunao, Hokimoto, Seiji, Yamabe, Hiroshige, Ogawa, Hisao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859393/
https://www.ncbi.nlm.nih.gov/pubmed/26811167
http://dx.doi.org/10.1161/JAHA.115.002744
Descripción
Sumario:BACKGROUND: Non–vitamin K antagonist oral anticoagulants are used to prevent thromboembolism in patients with atrial fibrillation. The T‐TAS “Total Thrombus‐formation Analysis System” (Fujimori Kogyo Co Ltd) was developed for quantitative analysis of thrombus formation using microchips with thrombogenic surfaces (collagen, platelet chip [PL] ; collagen plus tissue factor, atheroma chip [AR]). We evaluated the utility of T‐TAS in predicting periprocedural bleeding in atrial fibrillation patients undergoing catheter ablation (CA). METHODS AND RESULTS: After exclusion of 20 from 148 consecutive patients undergoing CA, the remaining 128 patients were divided into 2 treatment groups: the warfarin group (n=30) and the non–vitamin K antagonist oral anticoagulants group (n=98). Blood samples obtained on the day of CA (anticoagulant‐free point) and at 3 and 30 days after CA were used in T‐TAS to compute the thrombus formation area under the curve (AUC; AUC for the first 10 minutes for PL tested at flow rate of 24 μL/min [PL (24)‐AUC (10)]; AUC for the first 30 minutes for AR tested at flow rate of 10 μL/min [AR (10)‐AUC (30)]). AR (10)‐AUC (30) and PL (24)‐AUC (10) levels were similar in the 2 groups on the day of CA. Levels of AR (10)‐AUC (30), but not PL (24)‐AUC (10), were significantly lower in the 2 groups at days 3 and 30 after CA. Multiple logistic regression analyses identified the AR (10)‐AUC (30) level on the day of CA as a significant predictor of periprocedural bleeding events (odds ratio 5.7; 95% CI 1.54–21.1; P=0.009). Receiver operating characteristic analysis showed that the AR (10)‐AUC (30) level on the day of CA significantly predicted periprocedural bleeding events (AUC 0.859, 95% CI 0.766–0.951; P<0.001). The cutoff AR (10)‐AUC (30) level was 1648 for identification of periprocedural bleeding events. CONCLUSIONS: These results suggested that the AR (10)‐AUC (30) level determined by T‐TAS is a potentially useful marker for prediction of bleeding events in atrial fibrillation patients undergoing CA.