Department of Vascular Neurology, University Medical Centre Ljubljana, Zaloška 2, 1000, Ljubljana, Slovenia.
Neurology Department, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Clin Drug Investig. 2020 Nov;40(11):1053-1061. doi: 10.1007/s40261-020-00967-7.
The results of randomised clinical trials (RCTs) on direct oral anticoagulants (DOACs) for stroke prevention in patients with nonvalvular atrial fibrillation (NVAF) can mostly be applied to primary prevention in relatively young patients, since only a minority of patients included in these trials were receiving DOACs for secondary prevention. The real-life secondary prevention subgroup, comprising mostly elderly and high-risk patients, remains a point of interest where further exploration is needed. Our objective was to explore the effectiveness and safety of DOACs for secondary prevention in the real-life conditions.
In a six-year (2012-2018) period all consecutive patients with a history of transient ischaemic attack (TIA) or stroke, recorded NVAF and prescription of DOAC, were included in this single-centre registry. Choice of the DOAC and dose was based on the discretion of the attending clinician. Data regarding recurrent stroke/TIA or other embolic events, intracranial haemorrhage, other major bleeding, adherence and potential changes of therapy were collected and analysed.
During the study period, 566 patients were prescribed a DOAC for secondary stroke prevention, and follow-up data were available for 510 patients, with an average observational time of 2.6 years. The mean age of patients was 77.9 ± 8.7 years. The mean CHADS-VASc and HAS-BLED scores were 5.1 ± 1.2 and 2.4 ± 0.6, respectively. Dabigatran was prescribed in 66%, apixaban in 21% and rivaroxaban in 13% of patients; 58% of patients were prescribed the reduced dose of DOAC. The overall yearly incidence of recurrent stroke, major bleeding and intracranial bleeding was 1.7%, 1.6% and 0.2%, respectively. Thus, we found similar effectiveness and safety of both standard and reduced dose of DOACs for secondary stroke prevention, compared to the RCT and large registries.
Our real-life data study suggests that secondary stroke prevention with DOACs is as effective and safe as primary prevention, both in standard and reduced doses, in a typical group of patients who are older than patients included in RCTs.
随机临床试验(RCT)中关于非瓣膜性心房颤动(NVAF)患者卒中预防的直接口服抗凝剂(DOAC)的结果主要适用于相对年轻的患者的一级预防,因为这些试验中只有少数患者接受 DOAC 进行二级预防。真正的二级预防亚组主要由老年和高危患者组成,这仍然是一个需要进一步探索的关注点。我们的目的是探讨 DOAC 在真实情况下用于二级预防的有效性和安全性。
在六年(2012-2018 年)期间,所有连续记录有短暂性脑缺血发作(TIA)或卒中史、NVAF 和 DOAC 处方的患者均被纳入该单中心登记处。DOAC 的选择和剂量是基于主治医生的判断。收集并分析了关于复发性卒中/TIA 或其他栓塞事件、颅内出血、其他大出血、依从性和潜在治疗改变的数据。
在研究期间,566 名患者被处方 DOAC 进行二级卒中预防,510 名患者可获得随访数据,平均观察时间为 2.6 年。患者的平均年龄为 77.9±8.7 岁。平均 CHADS-VASc 和 HAS-BLED 评分分别为 5.1±1.2 和 2.4±0.6。达比加群在 66%的患者中被处方,阿哌沙班在 21%的患者中被处方,利伐沙班在 13%的患者中被处方;58%的患者被处方 DOAC 的低剂量。总的年复发性卒中、大出血和颅内出血发生率分别为 1.7%、1.6%和 0.2%。因此,与 RCT 和大型登记处相比,我们发现标准和低剂量 DOAC 用于二级卒中预防的有效性和安全性相似。
我们的真实数据研究表明,与一级预防相比,DOAC 用于二级卒中预防在标准和低剂量下同样有效和安全,适用于 RCT 中包含的患者年龄更大的典型患者群体。