Danilo Menichelli, Francesco Del Sole, Arianna Di Rocco, Alessio Farcomeni, Annarita Vestri, Francesco Violi, Pasquale Pignatelli, Gregory Y H Lip, Daniele Pastori
{"title":"直接口服抗凝剂治疗房颤的安全性和有效性:605771例患者的系统回顾和荟萃分析","authors":"Danilo Menichelli, Francesco Del Sole, Arianna Di Rocco, Alessio Farcomeni, Annarita Vestri, Francesco Violi, Pasquale Pignatelli, Gregory Y H Lip, Daniele Pastori","doi":"10.1093/ehjcvp/pvab002","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>To analyse the safety and efficacy of direct oral anticoagulants (DOACs) in real-world studies including atrial fibrillation (AF) patients.</p><p><strong>Methods and results: </strong>Systematic review and meta-analysis of observational studies including AF patients on DOACs. Primary endpoints: any, major, gastrointestinal (GI), intracranial haemorrhage (ICH), and haemorrhagic stroke (HS). Secondary endpoints: ischaemic stroke (IS), systemic embolism (SE), myocardial infarction (MI), and all-cause of death. A set of pair-wise meta-analyses using a random effect model and a random effect network meta-analysis under a Bayesian framework were performed. Prospero registration number: CRD42019137111. We included 21 studies with 605 771 AF patients. Apixaban was associated with lower major and GI bleeding compared with Rivaroxaban [hazard ratio (HR) 2.0, 95% confidence interval (CI) 1.6-2.5] and Dabigatran (HR 1.6, 95% CI 1.3-2.1). The latter drug performed better than Rivaroxaban (HR 1.2, 95% CI 1.0-1.5). Dabigatran and Apixaban had a similar association with HS, but Apixaban performed better than Rivaroxaban (HR 1.8, 95% CI 1.1-3.0). Apixaban had a similar association with Rivaroxaban and Dabigatran for ICH, the latter drug performing better than Rivaroxaban (HR 1.3, 95% CI 1.0-1.7). Rankograms showed that Apixaban was likely to be the first-choice treatment in relation to any (65%) major (100%) and GI bleeding (100%) followed by Dabigatran (46%, 100%, 99%, respectively). Dabigatran and Apixaban had similar rank as first choice for ICH (44% and 55%) and HS (52% and 48%). DOACs showed similar association with IS/SE, MI, all-cause of death.</p><p><strong>Conclusions: </strong>Analysis of real-world studies shows significant differences for safety among DOACs.</p>","PeriodicalId":11995,"journal":{"name":"European Heart Journal — Cardiovascular Pharmacotherapy","volume":" ","pages":"f11-f19"},"PeriodicalIF":0.0000,"publicationDate":"2021-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Real-world safety and efficacy of direct oral anticoagulants in atrial fibrillation: a systematic review and meta-analysis of 605 771 patients.\",\"authors\":\"Danilo Menichelli, Francesco Del Sole, Arianna Di Rocco, Alessio Farcomeni, Annarita Vestri, Francesco Violi, Pasquale Pignatelli, Gregory Y H Lip, Daniele Pastori\",\"doi\":\"10.1093/ehjcvp/pvab002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aims: </strong>To analyse the safety and efficacy of direct oral anticoagulants (DOACs) in real-world studies including atrial fibrillation (AF) patients.</p><p><strong>Methods and results: </strong>Systematic review and meta-analysis of observational studies including AF patients on DOACs. Primary endpoints: any, major, gastrointestinal (GI), intracranial haemorrhage (ICH), and haemorrhagic stroke (HS). Secondary endpoints: ischaemic stroke (IS), systemic embolism (SE), myocardial infarction (MI), and all-cause of death. A set of pair-wise meta-analyses using a random effect model and a random effect network meta-analysis under a Bayesian framework were performed. Prospero registration number: CRD42019137111. We included 21 studies with 605 771 AF patients. Apixaban was associated with lower major and GI bleeding compared with Rivaroxaban [hazard ratio (HR) 2.0, 95% confidence interval (CI) 1.6-2.5] and Dabigatran (HR 1.6, 95% CI 1.3-2.1). The latter drug performed better than Rivaroxaban (HR 1.2, 95% CI 1.0-1.5). Dabigatran and Apixaban had a similar association with HS, but Apixaban performed better than Rivaroxaban (HR 1.8, 95% CI 1.1-3.0). Apixaban had a similar association with Rivaroxaban and Dabigatran for ICH, the latter drug performing better than Rivaroxaban (HR 1.3, 95% CI 1.0-1.7). Rankograms showed that Apixaban was likely to be the first-choice treatment in relation to any (65%) major (100%) and GI bleeding (100%) followed by Dabigatran (46%, 100%, 99%, respectively). Dabigatran and Apixaban had similar rank as first choice for ICH (44% and 55%) and HS (52% and 48%). 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引用次数: 0
摘要
目的:分析直接口服抗凝剂(DOACs)在包括心房颤动(AF)患者在内的现实世界研究中的安全性和有效性。方法和结果:系统回顾和荟萃分析包括房颤患者DOACs的观察性研究。主要终点:任何,主要,胃肠道(GI),颅内出血(ICH)和出血性脑卒中(HS)。次要终点:缺血性卒中(IS)、全身性栓塞(SE)、心肌梗死(MI)和全因死亡。使用随机效应模型和贝叶斯框架下的随机效应网络进行了一组成对元分析。普洛斯彼罗注册号:CRD42019137111。我们纳入了21项研究,共605771例房颤患者。与利伐沙班和达比加群相比,阿哌沙班与较低的大出血和胃肠道出血相关[风险比(HR) 2.0, 95%可信区间(CI) 1.6-2.5] (HR 1.6, 95% CI 1.3-2.1)。后一种药物的疗效优于利伐沙班(HR 1.2, 95% CI 1.0-1.5)。达比加群和阿哌沙班与HS有相似的相关性,但阿哌沙班优于利伐沙班(HR 1.8, 95% CI 1.1-3.0)。阿哌沙班与利伐沙班和达比加群对脑出血有相似的相关性,后者的表现优于利伐沙班(HR 1.3, 95% CI 1.0-1.7)。秩图显示阿哌沙班可能是任何(65%)严重出血(100%)和胃肠道出血(100%)的首选治疗方法,其次是达比加群(分别为46%、100%和99%)。达比加群和阿哌沙班作为ICH(44%和55%)和HS(52%和48%)的首选排名相似。DOACs与IS/SE、MI、全死因均有相似的相关性。结论:现实世界的研究分析显示,doac之间的安全性存在显著差异。
Real-world safety and efficacy of direct oral anticoagulants in atrial fibrillation: a systematic review and meta-analysis of 605 771 patients.
Aims: To analyse the safety and efficacy of direct oral anticoagulants (DOACs) in real-world studies including atrial fibrillation (AF) patients.
Methods and results: Systematic review and meta-analysis of observational studies including AF patients on DOACs. Primary endpoints: any, major, gastrointestinal (GI), intracranial haemorrhage (ICH), and haemorrhagic stroke (HS). Secondary endpoints: ischaemic stroke (IS), systemic embolism (SE), myocardial infarction (MI), and all-cause of death. A set of pair-wise meta-analyses using a random effect model and a random effect network meta-analysis under a Bayesian framework were performed. Prospero registration number: CRD42019137111. We included 21 studies with 605 771 AF patients. Apixaban was associated with lower major and GI bleeding compared with Rivaroxaban [hazard ratio (HR) 2.0, 95% confidence interval (CI) 1.6-2.5] and Dabigatran (HR 1.6, 95% CI 1.3-2.1). The latter drug performed better than Rivaroxaban (HR 1.2, 95% CI 1.0-1.5). Dabigatran and Apixaban had a similar association with HS, but Apixaban performed better than Rivaroxaban (HR 1.8, 95% CI 1.1-3.0). Apixaban had a similar association with Rivaroxaban and Dabigatran for ICH, the latter drug performing better than Rivaroxaban (HR 1.3, 95% CI 1.0-1.7). Rankograms showed that Apixaban was likely to be the first-choice treatment in relation to any (65%) major (100%) and GI bleeding (100%) followed by Dabigatran (46%, 100%, 99%, respectively). Dabigatran and Apixaban had similar rank as first choice for ICH (44% and 55%) and HS (52% and 48%). DOACs showed similar association with IS/SE, MI, all-cause of death.
Conclusions: Analysis of real-world studies shows significant differences for safety among DOACs.