清晨好,您是今天最早来到科研通的研友!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您科研之路漫漫前行!

Evolocumab for Early Reduction of LDL Cholesterol Levels in Patients With Acute Coronary Syndromes (EVOPACS)

Evolocumab公司 医学 安慰剂 他汀类 内科学 阿托伐他汀 阿利罗库单抗 临床终点 胃肠病学 急性冠脉综合征 置信区间 PCSK9 胆固醇 随机对照试验 脂蛋白 心肌梗塞 替代医学 载脂蛋白A1 病理 低密度脂蛋白受体
作者
Konstantinos C. Koskinas,Stephan Windecker,Giovanni Pedrazzini,Christian Mueller,Stéphane Cook,Christian M. Matter,Olivier Müller,Jonas Häner,Bariş Gencer,Carmela Crljenica,Poorya Amini,Olga Deckarm,Juan F. Iglesias,Lorenz Räber,Dik Heg,François Mach
出处
期刊:Journal of the American College of Cardiology [Elsevier]
卷期号:74 (20): 2452-2462 被引量:173
标识
DOI:10.1016/j.jacc.2019.08.010
摘要

Although guidelines recommend in-hospital initiation of high-intensity statin therapy in patients with acute coronary syndromes (ACS), low-density lipoprotein cholesterol (LDL-C) target levels are frequently not attained. Evolocumab, a rapidly acting, potent LDL-C-lowering drug, has not been studied in the acute phase of ACS.The purpose of this study was to assess the feasibility, safety, and LDL-C-lowering efficacy of evolocumab initiated during the in-hospital phase of ACS.The authors conducted an investigator-initiated, randomized, double-blind, placebo-controlled trial involving 308 patients hospitalized for ACS with elevated LDL-C levels (≥1.8 mmol/l on high-intensity statin for at least 4 weeks; ≥2.3 mmol/l on low- or moderate-intensity statin; or ≥3.2 mmol/l on no stable dose of statin). Patients were randomly assigned 1:1 to receive subcutaneous evolocumab 420 mg or matching placebo, administered in-hospital and after 4 weeks, on top of atorvastatin 40 mg. The primary endpoint was percentage change in calculated LDL-C from baseline to 8 weeks.Most patients (78.2%) had not been on previous statin treatment. Mean LDL-C levels decreased from 3.61 to 0.79 mmol/l at week 8 in the evolocumab group, and from 3.42 to 2.06 mmol/l in the placebo group; the difference in mean percentage change from baseline was -40.7% (95% confidence interval: -45.2 to -36.2; p < 0.001). LDL-C levels <1.8 mmol/l were achieved at week 8 by 95.7% of patients in the evolocumab group versus 37.6% in the placebo group. Adverse events and centrally adjudicated cardiovascular events were similar in both groups.In this first randomized trial assessing a PCSK9 antibody in the very high-risk setting of ACS, evolocumab added to high-intensity statin therapy was well tolerated and resulted in substantial reduction in LDL-C levels, rendering >95% of patients within currently recommended target levels. (EVOlocumab for Early Reduction of LDL-cholesterol Levels in Patients With Acute Coronary Syndromes [EVOPACS]; NCT03287609).
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
16秒前
Amadeus发布了新的文献求助10
19秒前
Amadeus完成签到,获得积分10
25秒前
实力不允许完成签到 ,获得积分10
32秒前
1分钟前
ww完成签到,获得积分10
1分钟前
波里舞完成签到 ,获得积分10
2分钟前
2分钟前
郑先生完成签到 ,获得积分10
2分钟前
科研通AI2S应助lilili采纳,获得10
2分钟前
刘刘完成签到 ,获得积分10
2分钟前
lilili发布了新的文献求助10
3分钟前
3分钟前
今天又来搬砖啦完成签到,获得积分10
5分钟前
川藏客完成签到 ,获得积分10
5分钟前
5分钟前
5分钟前
蔡俊辉发布了新的文献求助10
5分钟前
6分钟前
Eri_SCI完成签到 ,获得积分10
6分钟前
6分钟前
8R60d8应助付怀松采纳,获得10
6分钟前
mzhang2完成签到 ,获得积分10
7分钟前
zai完成签到 ,获得积分10
8分钟前
8分钟前
hugeyoung发布了新的文献求助10
8分钟前
hugeyoung完成签到,获得积分10
9分钟前
红箭烟雨完成签到,获得积分10
9分钟前
9分钟前
wy发布了新的文献求助10
9分钟前
脑洞疼应助qdlsc采纳,获得10
9分钟前
10分钟前
wy完成签到,获得积分10
10分钟前
qdlsc发布了新的文献求助10
10分钟前
小白完成签到 ,获得积分10
10分钟前
11分钟前
沙海沉戈完成签到,获得积分0
12分钟前
12分钟前
Kumquat发布了新的文献求助10
13分钟前
淡然平蓝完成签到,获得积分10
15分钟前
高分求助中
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Chen Hansheng: China’s Last Romantic Revolutionary 500
宽禁带半导体紫外光电探测器 388
Case Research: The Case Writing Process 300
Global Geological Record of Lake Basins 300
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3142805
求助须知:如何正确求助?哪些是违规求助? 2793651
关于积分的说明 7807147
捐赠科研通 2449931
什么是DOI,文献DOI怎么找? 1303553
科研通“疑难数据库(出版商)”最低求助积分说明 627016
版权声明 601350