Guideline-directed medical therapies for comorbidities among patients with atrial fibrillation: results from GARFIELD-AF.

Alan John Camm, Jan Steffel, Saverio Virdone, Jean-Pierre Bassand, Keith A A Fox, Samuel Z Goldhaber, Shinya Goto, Sylvia Haas, Alexander G G Turpie, Freek W A Verheugt, Frank Misselwitz, Ramón Corbalán Herreros, Gloria Kayani, Karen S Pieper, Ajay K Kakkar
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Abstract

Aims: This study aimed to identify relationships in recently diagnosed atrial fibrillation (AF) patients with respect to anticoagulation status, use of guideline-directed medical therapy (GDMT) for comorbid cardiovascular conditions (co-GDMT), and clinical outcomes. The Global Anticoagulant Registry in the FIELD (GARFIELD)-AF is a prospective, international registry of patients with recently diagnosed non-valvular AF at risk of stroke (NCT01090362).

Methods and results: Guideline-directed medical therapy was defined according to the European Society of Cardiology guidelines. This study explored co-GDMT use in patients enrolled in GARFIELD-AF (March 2013-August 2016) with CHA2DS2-VASc ≥ 2 (excluding sex) and ≥1 of five comorbidities-coronary artery disease, diabetes mellitus, heart failure, hypertension, and peripheral vascular disease (n = 23 165). Association between co-GDMT and outcome events was evaluated with Cox proportional hazards models, with stratification by all possible combinations of the five comorbidities. Most patients (73.8%) received oral anticoagulants (OACs) as recommended; 15.0% received no recommended co-GDMT, 40.4% received some, and 44.5% received all co-GDMT. At 2 years, comprehensive co-GDMT was associated with a lower risk of all-cause mortality [hazard ratio (HR) 0.89 (0.81-0.99)] and non-cardiovascular mortality [HR 0.85 (0.73-0.99)] compared with inadequate/no GDMT, but cardiovascular mortality was not significantly reduced. Treatment with OACs was beneficial for all-cause mortality and non-cardiovascular mortality, irrespective of co-GDMT use; only in patients receiving all co-GDMT was OAC associated with a lower risk of non-haemorrhagic stroke/systemic embolism.

Conclusion: In this large prospective, international registry on AF, comprehensive co-GDMT was associated with a lower risk of mortality in patients with AF and CHA2DS2-VASc ≥ 2 (excluding sex); OAC therapy was associated with reduced all-cause mortality and non-cardiovascular mortality, irrespective of co-GDMT use.

Clinical trial registration: Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362.

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房颤患者合并症的指导药物治疗:GARFIELD-AF结果
目的:本研究旨在确定最近诊断的房颤(AF)患者在抗凝状态、使用指南指导的药物治疗(GDMT)治疗合并症心血管疾病(co-GDMT)和临床结果方面的关系。全球房颤抗凝登记(GARFIELD)-AF是一项前瞻性的国际登记,登记了最近诊断的有卒中风险的非瓣膜性房颤患者(NCT01090362)。方法和结果:根据欧洲心脏病学会指南确定指导药物治疗。本研究探讨了GARFIELD-AF(2013年3月- 2016年8月)纳入的CHA2DS2-VASc≥2(不包括性别)且5种合并症(冠状动脉疾病、糖尿病、心力衰竭、高血压和周围血管疾病)≥1的患者(n = 23 165)的gdmt联合使用情况。采用Cox比例风险模型评估共gdmt与结局事件之间的关联,并根据五种合并症的所有可能组合进行分层。大多数患者(73.8%)按照推荐使用口服抗凝剂(OACs);15.0%未接受推荐的co-GDMT治疗,40.4%接受部分推荐的co-GDMT治疗,44.5%接受全部推荐的co-GDMT治疗。在2年时,与不充分/没有GDMT相比,全面的co-GDMT与全因死亡率[危险比(HR) 0.89(0.81-0.99)]和非心血管死亡率[HR 0.85(0.73-0.99)]相关,但心血管死亡率没有显著降低。无论是否联合使用gdmt, OACs治疗对全因死亡率和非心血管死亡率都有利;只有在接受所有联合gdmt的患者中,OAC与非出血性卒中/全身性栓塞的风险较低相关。结论:在这项关于房颤的大型前瞻性国际登记中,综合co-GDMT与房颤和CHA2DS2-VASc≥2(排除性别)患者的较低死亡风险相关;OAC治疗与降低全因死亡率和非心血管死亡率相关,与联合使用gdmt无关。临床试验注册:临床试验注册-网址:http://www.clinicaltrials.gov唯一标识符:NCT01090362。
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