Mocini David, Di Fusco Stefania Angela, De Luca Leonardo, Caldarola Pasquale, Cipriani Manlio, Corda Marco, Di Lenarda Andrea, De Nardo Alfredo, Francese Giuseppina Maura, Napoletano Cosimo, Navazio Alessandro, Riccio Carmine, Roncon Loris, Tizzani Emanuele, Nardi Federico, Urbinati Stefano, Valente Serafina, Gulizia Michele Massimo, Gabrielli Domenico, Oliva Fabrizio, Colivicchi Furio
Division of Clinical and Rehabilitation Cardiology, Emergency Department, P.O. San Filippo Neri - ASL Roma 1, Via G. Martinotti, 20, 00135, Roma, RM, Italy.
Cardiology, Department of Cardio-Thoraco-Vascular, Ospedale San Camillo, Circonvallazione Gianicolense, 87, 00152, Roma, RM, Italy.
Eur Heart J Suppl. 2022 May 18;24(Suppl C):C278-C288. doi: 10.1093/eurheartj/suac015. eCollection 2022 May.
The appropriateness of prescribing direct oral anticoagulants [dabigatran, rivaroxaban, apixaban, and edoxaban (DOACs)] is regulated on the criteria established in Phase III trials. These criteria are reported in the summary of the product characteristics of the four DOACs. In clinical practice, prescriptions are not always in compliance with established indications. In particular, the use of lower doses than those recommended in drug data sheets is not uncommon. Literature data show that the inappropriate prescription of reduced doses causes drug underexposure and up to a three-fold increase in the risk of stroke/ischaemic transient attack, systemic thromboembolism, and hospitalization. Possible causes of the deviation between the dose that should be prescribed and that prescribed in the real world include erroneous prescription, an overstated haemorrhagic risk perception, and the presence of frail and complex patients in clinical practice who were not included in pivotal trials, which makes it difficult to apply study results to the real world. For these reasons, we summarize DOAC indications and contraindications. We also suggest the appropriate use of DOACs in common clinical scenarios, in accordance with what international guidelines and national and international health regulatory bodies recommend.
直接口服抗凝剂(达比加群、利伐沙班、阿哌沙班和依度沙班)的处方适宜性是根据III期试验确立的标准进行规范的。这些标准在四种直接口服抗凝剂的产品特性摘要中有所报告。在临床实践中,处方并不总是符合既定的适应症。特别是,使用低于药品说明书中推荐剂量的情况并不少见。文献数据表明,不适当的低剂量处方会导致药物暴露不足,并使中风/缺血性短暂性脑缺血发作、全身性血栓栓塞和住院风险增加两倍。实际应处方剂量与实际处方剂量之间出现偏差的可能原因包括处方错误、对出血风险的过度认知,以及临床实践中存在未纳入关键试验的体弱和复杂患者,这使得难以将研究结果应用于现实世界。出于这些原因,我们总结了直接口服抗凝剂的适应症和禁忌症。我们还根据国际指南以及国家和国际卫生监管机构的建议,提出了在常见临床场景中合理使用直接口服抗凝剂的方法。