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接受阿司匹林联合抗凝治疗的真性红细胞增多症患者的出血情况:一项前瞻性观察性研究。

Hemorrhage in patients with polycythemia vera receiving aspirin with an anticoagulant: a prospective, observational study.

机构信息

Beth Israel Deaconess Medical Center, Division of Hematology, Harvard Medical School, Boston, MA.

Incyte Corporation, Wilmington, DE.

出版信息

Haematologica. 2022 May 1;107(5):1106-1110. doi: 10.3324/haematol.2021.279032.

Abstract

Polycythemia vera (PV) is associated with increased risk of thrombosis and hemorrhage. Aspirin, recommended for primary thromboprophylaxis, is often combined with anticoagulants during management of acute thrombotic events. The safety of dual antiplatelet and anticoagulant therapy is not established in PV. In a prospective, observational study, 2,510 patients with PV were enrolled at 227 sites in the United States. Patients were monitored for the development of hemorrhage and thrombosis after enrollment. A total of 1,602 patients with PV received aspirin with median follow-up of 2.4 years (range, 0-3.6 years). The exposure-adjusted rate of all hemorrhages in patients receiving aspirin alone was 1.40 per 100 patient-years (95% confidence interval [CI]: 0.99-1.82). The combination of aspirin plus anticoagulant was associated with an incidence of hemorrhage of 6.75 per 100 patient-years (95% CI: 3.04-10.46). The risk of hemorrhage was significantly greater in patients receiving the combination of aspirin and anticoagulant compared with aspirin alone (total hemorrhages, hazard ratio [HR]: 5.83; 95% CI: 3.36-10.11; P<0.001; severe hemorrhage, HR: 7.49; 95% CI: 3.02-18.62; P<0.001). Periods of thrombocytosis (>600×109/L) were associated with an increased risk of hemorrhage (HR: 2.25; 95% CI: 1.16- 4.38; P=0.02). Rates of hemorrhage were similar for aspirin in combination with warfarin or direct-acting oral anticoagulants. We conclude that the combination of aspirin and anticoagulants is associated with significantly increased risk of hemorrhage in patients with PV (clinicaltrials gov. Identifier: NCT02252159).

摘要

原发性血小板增多症(PV)与血栓形成和出血风险增加有关。阿司匹林被推荐用于一级血栓预防,在急性血栓事件的管理中,常与抗凝剂联合使用。在 PV 中,双联抗血小板和抗凝治疗的安全性尚未确定。在一项前瞻性、观察性研究中,在美国 227 个地点共招募了 2510 例 PV 患者。患者在入组后接受出血和血栓形成的监测。共有 1602 例 PV 患者接受了阿司匹林治疗,中位随访时间为 2.4 年(范围 0-3.6 年)。单独使用阿司匹林的患者中所有出血的暴露调整发生率为 1.40/100 患者年(95%置信区间:0.99-1.82)。阿司匹林联合抗凝剂的组合与出血发生率为 6.75/100 患者年(95%置信区间:3.04-10.46)。与单独使用阿司匹林相比,接受阿司匹林联合抗凝剂的患者出血风险显著增加(总出血,风险比[HR]:5.83;95%置信区间:3.36-10.11;P<0.001;严重出血,HR:7.49;95%置信区间:3.02-18.62;P<0.001)。血小板增多期(>600×109/L)与出血风险增加相关(HR:2.25;95%置信区间:1.16-4.38;P=0.02)。阿司匹林联合华法林或直接口服抗凝剂的出血发生率相似。我们得出结论,阿司匹林和抗凝剂的联合使用与 PV 患者出血风险显著增加相关(临床试验.gov 标识符:NCT02252159)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68bc/9052904/62c6132d7353/1071106.fig1.jpg

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