Division of Cardiology, Nihon University Itabashi Hospital.
Department of Cardiology, Nihon University Hospital.
Circ J. 2020 Aug 25;84(9):1475-1482. doi: 10.1253/circj.CJ-20-0090. Epub 2020 Jul 22.
In the Japanese clinical setting, the prevalence, potential cofounders of gastrointestinal (GI) bleeding from anticoagulant therapy, including direct oral anticoagulants (DOACs) and warfarin, and prognosis after GI bleeding are unclear.
We examined about GI bleeding from anticoagulant therapy using data from the SAKURA AF Registry, a prospective multicenter registry in Japan. Among 3,237 enrollees, 48.8% (n=1,561) were warfarin users and 51.2% (n=1,676) DOAC users. GI bleeding was identified in 68 patients (2.1%). No incidental differences in GI bleeding were observed between the DOAC and warfarin users (32 [1.9%] patients [0.67 events per 100 person-years] vs. 36 [2.3%] patients [0.75 events per 100 person-years], respectively; P=0.43). Multivariate Cox proportional hazard model analysis revealed that creatinine (hazard ratio [HR] 1.379, 95% confidence interval [CI] 1.091-1.743 P=0.007) and hemoglobin (HR 0.814, 95% CI 0.705-0.941, P=0.005) remained independent determinants of GI bleeding. Patients experiencing GI bleeding events had a higher risk of all-cause death (18%) than those without GI bleeding (6%) (P=0.045).
GI bleeding was strongly associated with anemia and renal impairment. Patients experiencing GI bleeding had higher risk for all-cause death than those without GI bleeding.
在日本的临床环境中,抗凝治疗(包括直接口服抗凝剂 [DOAC] 和华法林)相关的胃肠道 [GI] 出血的流行情况、潜在混杂因素以及 GI 出血后的预后尚不清楚。
我们使用来自日本 SAKURA AF 注册研究(一项前瞻性多中心注册研究)的数据来检查抗凝治疗相关的 GI 出血情况。在 3237 名入组患者中,48.8%(n=1561)为华法林使用者,51.2%(n=1676)为 DOAC 使用者。共发现 68 例(2.1%)GI 出血患者。DOAC 使用者与华法林使用者之间在 GI 出血方面未观察到偶然差异(32 例[1.9%]患者 [每 100 人年 0.67 例] 与 36 例[2.3%]患者 [每 100 人年 0.75 例];P=0.43)。多变量 Cox 比例风险模型分析显示,肌酐(风险比 [HR] 1.379,95%置信区间 [CI] 1.091-1.743,P=0.007)和血红蛋白(HR 0.814,95% CI 0.705-0.941,P=0.005)是 GI 出血的独立决定因素。发生 GI 出血事件的患者全因死亡风险(18%)高于未发生 GI 出血的患者(6%)(P=0.045)。
GI 出血与贫血和肾功能损害密切相关。发生 GI 出血的患者全因死亡风险高于未发生 GI 出血的患者。