Division of Cardiology, Osaka Police Hospital, Osaka, Japan.
Division of Cardiology, Osaka Police Hospital, Osaka, Japan.
Am J Cardiol. 2019 Oct 1;124(7):1044-1048. doi: 10.1016/j.amjcard.2019.07.005. Epub 2019 Jul 15.
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.
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。