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直接口服抗凝剂在非瓣膜性心房颤动患者中应用的 ORBIT 出血评分和 HAS-BLED 评分的外部验证(DIRECT 注册研究的亚洲数据)。

External Validation of the ORBIT Bleeding Score and the HAS-BLED Score in Nonvalvular Atrial Fibrillation Patients Using Direct Oral Anticoagulants (Asian Data from the DIRECT Registry).

机构信息

Division of Cardiology, Osaka Police Hospital, Osaka, Japan.

Division of Cardiology, Osaka Police Hospital, Osaka, Japan.

出版信息

Am J Cardiol. 2019 Oct 1;124(7):1044-1048. doi: 10.1016/j.amjcard.2019.07.005. Epub 2019 Jul 15.

Abstract

For Asian patients with nonvalvular atrial fibrillation (NVAF) using direct oral anticoagulants (DOACs), performance of contemporary various bleeding risk scores in a real-world setting is unknown. The objective of this study was to externally validate the ORBIT bleeding score and the HAS-BLED score in a large pooled real-world Asian population with NVAF using DOACs. We conducted a single-center prospective observational registry of NVAF patients treated with DOACs: the DIRECT registry (UMIN000033283). We assessed predictive and discriminative performance of the ORBIT bleeding and the HAS-BLED scores for major bleeding in 2,216 patients with NVAF using DOACs (63.6% male, median age 73 years, median CHADS score 2). The overall incidence of major bleeding was 4.2% after a median follow-up of 315 days (interquartile range: 76 to 621). The ORBIT bleeding and the HAS-BLED scores both had modest discrimination ability to identify those who had bled versus who had not (C index = 0.64 [95% confidence interval {CI} 0.59, 0.70] and 0.62 [95% CI 0.57, 0.68], respectively). Calibration plots of the ORBIT bleeding score showed similar predictive performance compared with the HAS-BLED score (slope: 0.91 [95% CI 0.40, 1.43] vs 0.72 [95% CI 0.03, 1.40], intercept: 0.24 [95% CI -2.13, 2.61] vs 0.71 [95% CI -2.35, 3.76], respectively). In conclusion, the ORBIT bleeding score and the HAS-BLED score in a real-world of NVAF population with DOACs showed a modest discriminative performance and a similar predictive performance for major bleeding.

摘要

对于使用直接口服抗凝剂(DOAC)的亚洲非瓣膜性心房颤动(NVAF)患者,在真实环境中使用现代各种出血风险评分的表现尚不清楚。本研究的目的是在使用 DOAC 的大型亚洲 NVAF 真实人群中,对 ORBIT 出血评分和 HAS-BLED 评分进行外部验证。我们进行了一项使用 DOAC 治疗 NVAF 患者的单中心前瞻性观察性登记研究:DIRECT 登记研究(UMIN000033283)。我们使用 DOAC 治疗的 2216 例 NVAF 患者(63.6%为男性,中位年龄 73 岁,中位 CHADS2 评分为 2)评估了 ORBIT 出血和 HAS-BLED 评分对主要出血的预测和区分性能。在中位随访 315 天(四分位距:76 至 621)后,主要出血的总发生率为 4.2%。ORBIT 出血和 HAS-BLED 评分对识别出血患者和未出血患者均具有适度的区分能力(C 指数分别为 0.64(95%置信区间 0.59,0.70)和 0.62(95%置信区间 0.57,0.68))。ORBIT 出血评分的校准图显示与 HAS-BLED 评分具有相似的预测性能(斜率:0.91(95%置信区间 0.40,1.43)与 0.72(95%置信区间 0.03,1.40),截距:0.24(95%置信区间 -2.13,2.61)与 0.71(95%置信区间 -2.35,3.76))。总之,在使用 DOAC 的 NVAF 人群的真实世界中,ORBIT 出血评分和 HAS-BLED 评分对主要出血具有适度的区分性能和相似的预测性能。

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