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抗血小板药物与原发性脑肿瘤患者的颅内出血。

Antiplatelet medications and intracranial hemorrhage in patients with primary brain tumors.

机构信息

Department of Internal Medicine, Beth Israel Deaconess Medical Center, Boston, MA. Electronic address: https://twitter.com/SiruiMaMD.

Division of Hematology and Hematologic Malignancies, Beth Israel Deaconess Medical Center, Boston, MA. Electronic address: https://twitter.com/rushadpatell.

出版信息

J Thromb Haemost. 2023 May;21(5):1148-1155. doi: 10.1016/j.jtha.2023.01.031. Epub 2023 Feb 3.

Abstract

BACKGROUND

Spontaneous intracranial hemorrhage (ICH) is a frequent and severe consequence of primary brain tumors. The safety of antiplatelet medications in this patient population is undefined.

OBJECTIVE

The primary objective was to determine whether antiplatelet medications are associated with an increased risk of ICH in patients with primary brain tumors.

PATIENTS/METHODS: We performed a matched, retrospective cohort study of patients with the diagnosis of primary brain tumor treated at our institution between 2010 and 2021. Radiographic images of all potential ICH events underwent blinded review. The primary end point of the study was the cumulative incidence of ICH at 1 year after tumor diagnosis.

RESULTS AND CONCLUSIONS

A total of 387 patients with primary brain tumors were included in the study population (130 exposed to antiplatelet agents, 257 not exposed). The most common malignancy was glioblastoma (n = 256, 66.1%). Among the intervention cohort, 119 patients received aspirin monotherapy. The cumulative incidence of any ICH at 1 year was 11.0% (95% CI, 5.3-16.6) in those receiving antiplatelet medications and 13.0% (95% CI, 8.5-17.6) in those not receiving antiplatelet medications (Gray test, p = 0.6). The cumulative incidence of major ICH was similar between the cohorts (3.3% in antiplatelet cohort vs 2.9% in control cohort, p = 1.0). This study did not identify an increased incidence of ICH in patients with primary brain tumors exposed to antiplatelet medications.

摘要

背景

自发性脑出血(ICH)是原发性脑肿瘤的常见且严重的后果。抗血小板药物在该患者人群中的安全性尚未确定。

目的

主要目的是确定抗血小板药物是否会增加原发性脑肿瘤患者发生 ICH 的风险。

患者/方法:我们对 2010 年至 2021 年在我院治疗的原发性脑肿瘤患者进行了匹配、回顾性队列研究。对所有潜在 ICH 事件的影像学图像进行了盲法审查。该研究的主要终点是肿瘤诊断后 1 年内 ICH 的累积发生率。

结果与结论

共纳入 387 例原发性脑肿瘤患者(130 例暴露于抗血小板药物,257 例未暴露)。最常见的恶性肿瘤是胶质母细胞瘤(n=256,66.1%)。在干预组中,119 例患者接受了阿司匹林单药治疗。接受抗血小板药物治疗的患者在 1 年内任何 ICH 的累积发生率为 11.0%(95%CI,5.3-16.6),未接受抗血小板药物治疗的患者为 13.0%(95%CI,8.5-17.6)(Gray 检验,p=0.6)。两个队列之间主要 ICH 的累积发生率相似(抗血小板组为 3.3%,对照组为 2.9%,p=1.0)。本研究未发现原发性脑肿瘤患者暴露于抗血小板药物会增加 ICH 的发生率。

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