Tittl Luise, Marten Sandra, Naue Christiane, Beyer-Westendorf Jan
Department of Medicine I, Division of Hemostaseology, University Hospital "Carl Gustav Carus" Dresden, Technical University, Fetscherstrasse 74, D-01307 Dresden, Germany.
Department of Medicine I, Division of Hemostaseology, University Hospital "Carl Gustav Carus" Dresden, Technical University, Fetscherstrasse 74, D-01307 Dresden, Germany.
Thromb Res. 2024 Apr;236:61-67. doi: 10.1016/j.thromres.2024.02.014. Epub 2024 Feb 19.
Data on long-term effectiveness and safety of rivaroxaban for stroke prevention in atrial fibrillation (SPAF) are scarce and not available from randomized clinical trials.
We used data from the prospective, non-interventional DRESDEN NOAC REGISTRY to evaluate rates of stroke/transient ischaemic attack (TIA)/systemic embolism (SE) and ISTH major bleeding, in general and changes of event patterns over time.
Between 1st October 2011 and 31st December 2022, 1204 SPAF patients receiving rivaroxaban were followed for 6.7 ± 3.4 years with a mean rivaroxaban exposure of 4.9 ± 3.5 years. During follow up, intention-to treat rates of stroke/TIA/SE were 3.5/100 pt. years (95 % CI 2.5-4.7) in the first year and fell to 1.6/100 pt. years (95 % CI 1.2-2.0) in years 2-5 and 2.1/100 pt. years (95 % CI 1.6-2.7) after 5 years. Similarly, on-treatment event rates fell from 2.4/100 pt. years (95 % CI 1.5-3.5) to 1.1 (95 % CI 0.7-1.5) and 1.6 (95 % CI 1.0-2.3), respectively. Major bleeding rates on treatment were 3.5/100 pt. years in the first treatment year (95 % CI 2.5-4.8) and 2.7 (95 % CI 2.2-3.4) and 3.5 (95 % CI 2.7-4.6) in the periods 2-5 and > 5 years, respectively. Of note, rates of fatal bleeding were low throughout follow-up (0.2 vs. 0.2 vs. 0.1/100 pt. years).
Our results demonstrate the long-term effectiveness and safety of rivaroxaban therapy in unselected SPAF patients in daily care. Our data indicate that patterns of cardiovascular events remain constant over many years. In contrast, bleeding patterns change over time, possibly due to effects of co-morbidities in an ageing population.
关于利伐沙班用于心房颤动患者预防卒中(SPAF)的长期有效性和安全性的数据稀缺,且随机临床试验中未提供此类数据。
我们使用了前瞻性、非干预性的德累斯顿新型口服抗凝药注册研究的数据,以评估卒中/短暂性脑缺血发作(TIA)/全身性栓塞(SE)以及国际血栓与止血学会(ISTH)定义的大出血的发生率,以及总体事件模式随时间的变化。
在2011年10月1日至2022年12月31日期间,1204例接受利伐沙班治疗的SPAF患者接受了6.7±3.4年的随访,利伐沙班的平均暴露时间为4.9±3.5年。在随访期间,卒中/TIA/SE的意向性治疗发生率在第一年为3.5/100患者年(95%CI 2.5 - 4.7),在第2 - 5年降至1.6/100患者年(95%CI 1.2 - 2.0),5年后为2.1/100患者年(95%CI 1.6 - 2.7)。同样,治疗期间的事件发生率分别从2.4/100患者年(95%CI 1.5 - 3.5)降至1.1(95%CI 0.7 - 1.5)和1.6(95%CI 1.0 - 2.3)。治疗期间的大出血发生率在第一个治疗年为3.5/100患者年(95%CI 2.5 - 4.8),在第2 - 5年期间为2.7(95%CI 2.2 - 3.4),在5年以上期间为3.5(95%CI 2.7 - 4.6)。值得注意的是,在整个随访期间,致命性出血的发生率较低(分别为0.2 vs. 0.2 vs. 0.1/100患者年)。
我们的结果证明了利伐沙班治疗在日常护理中未选择的SPAF患者中的长期有效性和安全性。我们的数据表明,心血管事件模式在许多年内保持不变。相比之下,出血模式随时间变化,可能是由于老年人群中合并症的影响。