Li Zhengwei, Fu Guosheng
Department of Cardiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Key Laboratory of Cardiovascular Intervention and Regenerative Medicine of Zhejiang Province, Hangzhou, China.
Front Physiol. 2022 Feb 10;13:831212. doi: 10.3389/fphys.2022.831212. eCollection 2022.
Despite coronary re-vascularization, the common complications of acute myocardial infarction (AMI), cardiac remodeling, and heart failure (HF), is increasing globally. Sacubitril valsartan (SV), an angiotensin receptor-neprilysin inhibitor (ARNI), has been previously demonstrated to improve HF. We further hypothesize that ultra-early SV treatment is also effective in preventing cardiac remodeling for patients with AMI following primary percutaneous coronary intervention (PCI).
The Assessment of ultra-early administration of Sacubitril Valsartan to improve cardiac remodeling in patients with Acute Myocardial Infarction following primary PCI (ASV-AMI) trial is a prospective, multicenter, randomized controlled trial in China planning to enroll at least 1,942 eligible patients from 10 centers. After successful primary PCI of culprit artery within 24 h, AMI patients are randomized to 2 h group or 3-7 days group with SV treatment. The major endpoints are echocardiographic measurement, cardiothoracic ratio, and N-Terminal pro-B-Type Natriuretic Peptide (NT pro-BNP) at baseline, 1, 3, 6, and 12 months. The secondary endpoints included MACE (cardiac arrest, cardiogenic death, myocardial infarction, and target vessel re-vascularization), in-/out-patient HF, EuroQol Five Dimensions Questionnaire (EQ-5D), and Kansas City Cardiomyopathy Questionnaire (KCCQ).
The ASV-AMI trial is the first clinical trial of ultra-early administration of SV in the treatment of post-PCI AMI, adding more clinical evidence. Early application of SV to prevent cardiac remodeling in AMI patient is a major focus of this trial.
Trial registration Chinese Clinical Trial Registry (http://www.chictr.org.cn; ChiCTR2100051979). Registered on 11 October 2021.
尽管进行了冠状动脉血运重建,但急性心肌梗死(AMI)的常见并发症,即心脏重塑和心力衰竭(HF),在全球范围内仍呈上升趋势。沙库巴曲缬沙坦(SV)是一种血管紧张素受体脑啡肽酶抑制剂(ARNI),此前已被证明可改善心力衰竭。我们进一步假设,超早期使用SV治疗对接受直接经皮冠状动脉介入治疗(PCI)后的AMI患者预防心脏重塑也有效。
评估超早期给予沙库巴曲缬沙坦以改善直接PCI后急性心肌梗死患者心脏重塑(ASV-AMI)试验是一项在中国进行的前瞻性、多中心、随机对照试验,计划从10个中心招募至少1942名符合条件的患者。在罪犯血管成功进行直接PCI后24小时内,将AMI患者随机分为2小时组或3 - 7天组接受SV治疗。主要终点是基线、1、3、6和12个月时的超声心动图测量、心胸比率和N末端B型利钠肽原(NT pro-BNP)。次要终点包括主要不良心血管事件(心脏骤停、心源性死亡、心肌梗死和靶血管血运重建)、门诊/住院心力衰竭、欧洲五维健康量表(EQ-5D)和堪萨斯城心肌病问卷(KCCQ)。
ASV-AMI试验是超早期使用SV治疗PCI后AMI的首个临床试验,增加了更多临床证据。早期应用SV预防AMI患者的心脏重塑是该试验的主要重点。
试验注册于中国临床试验注册中心(http://www.chictr.org.cn;ChiCTR2100051979)。于2021年10月11日注册。