亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

An estimation of the consequences of reinforcing the 2016 and 2019 European Society of Cardiology/European Atherosclerosis Society guidelines on current lipid-lowering treatment in patients with type 2 diabetes in tertiary care—a SwissDiab study

医学 以兹提米比 狼牙棒 人口 2型糖尿病 他汀类 内科学 指南 糖尿病 观察研究 2型糖尿病 重症监护医学 心脏病学 内分泌学 环境卫生 病理 心肌梗塞 传统PCI
作者
Hélène Singeisen,Frida Renström,Markus Laimer,Roger Lehmann,Stefan Bilz,Michael Brändle
出处
期刊:European Journal of Preventive Cardiology [Oxford University Press]
卷期号:30 (14): 1473-1481 被引量:4
标识
DOI:10.1093/eurjpc/zwad178
摘要

In 2019, the European Society of Cardiology/European Atherosclerosis Society updated the 2016 guidelines for the management of dyslipidaemias recommending more stringent low-density lipoprotein cholesterol (LDL-C) targets in diabetes mellitus type 2 (DM2). Based on a real-world patient population, this study aimed to determine the feasibility and cost of attaining guideline-recommended LDL-C targets, and assess cardiovascular benefit.The Swiss Diabetes Registry is a multicentre longitudinal observational study of outpatients in tertiary diabetes care. Patients with DM2 and a visit between 1 January 2018 and 31 August 2019 that failed the 2016 LDL-C target were identified. The theoretical intensification of current lipid-lowering medication needed to reach the 2016 and 2019 LDL-C target was determined and the cost thereof extrapolated. The expected number of major adverse cardiovascular events (MACE) prevented by treatment intensification was estimated. Two hundred and ninety-four patients (74.8%) failed the 2016 LDL-C target. The percentage of patients that theoretically achieved the 2016 and 2019 target with the indicated treatment modifications were high-intensity statin, 21.4% and 13.3%; ezetimibe, 46.6% and 27.9%; proprotein convertase subtilisin/kexin type 9 inhibitor (PCSK9i), 30.6% and 53.7%; ezetimibe and PCSK9i, 1.0% and 3.1%; whereas one (0.3%) and five patients (1.7%) failed to reach target, respectively. Achieving the 2016 vs. 2019 target would reduce the estimated 4-year MACE from 24.9 to 18.6 vs. 17.4 events, at an additional annual cost of medication of 2140 Swiss francs (CHF) vs. 3681 CHF per patient, respectively.For 68% of the patients, intensifying statin treatment and/or adding ezetimibe would be sufficient to reach the 2016 target, whereas 57% would require cost-intensive PCSK9i therapy to reach the 2019 target, with limited additional medium-term cardiovascular benefit.Based on 294 patients with type 2 diabetes and elevated low-density lipoprotein (LDL) cholesterol, this study looked at how much patients’ lipid-lowering medication would need to be intensified for them to be able to reach the old and the new, lower treatment target for LDL-cholesterol that was introduced in 2019, along with the cost and feasibility, and estimated cardiovascular benefits of doing so. The majority of patients would reach the old LDL-cholesterol target by optimizing therapy with statin and ezetimibe, with a clear expected cardiovascular benefit. It would however be difficult for the majority of patients to reach the new, lower LDL-cholesterol target, as this would require treatment with a proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. This expensive treatment would not be reimbursed for the majority of patients that would need them. The additional expected cardiovascular benefit was also less clear. Tools that help physicians to weigh the additional reduction in cardiovascular risk that the patient might benefit from by reaching the new rather than the old LDL-cholesterol target against known benefits of targeting other important risk factors (e.g. smoking, physical inactivity, overweight, and obesity) would help guide efficient cardiovascular risk management, and identify patients that would most benefit from PCSK9 inhibitor therapy.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
虚幻心锁发布了新的文献求助10
4秒前
TXZ06发布了新的文献求助30
28秒前
48秒前
沉静盼易发布了新的文献求助10
1分钟前
1分钟前
wesz9887完成签到,获得积分10
3分钟前
zsmj23完成签到 ,获得积分0
3分钟前
无限的可乐完成签到,获得积分10
4分钟前
不想看文献完成签到 ,获得积分10
4分钟前
5分钟前
starbinbin发布了新的文献求助30
5分钟前
科研通AI2S应助科研通管家采纳,获得10
6分钟前
充电宝应助科研通管家采纳,获得10
6分钟前
6分钟前
8分钟前
优雅听枫应助科研通管家采纳,获得10
8分钟前
MchemG应助科研通管家采纳,获得10
8分钟前
Chen完成签到 ,获得积分10
9分钟前
9分钟前
XXXXX完成签到 ,获得积分10
9分钟前
貔貅完成签到 ,获得积分10
9分钟前
TXZ06完成签到,获得积分10
9分钟前
JamesPei应助沉静盼易采纳,获得10
9分钟前
沉静盼易完成签到,获得积分10
9分钟前
老迟到的梦旋完成签到 ,获得积分10
10分钟前
一只小锦鲤完成签到 ,获得积分10
10分钟前
dd发布了新的文献求助10
11分钟前
dd完成签到,获得积分10
12分钟前
12分钟前
12分钟前
噔噔蹬发布了新的文献求助10
12分钟前
Ava应助科研通管家采纳,获得10
12分钟前
MchemG应助科研通管家采纳,获得10
12分钟前
12分钟前
非洲大象完成签到,获得积分10
13分钟前
13分钟前
机智的孤兰完成签到 ,获得积分10
14分钟前
小马甲应助药石无医采纳,获得10
14分钟前
药石无医发布了新的文献求助10
14分钟前
14分钟前
高分求助中
(应助此贴封号)【重要!!请各位详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane: Insecta, Polyneoptera [The Mantids of French Guiana] 3000
F-35B V2.0 How to build Kitty Hawk's F-35B Version 2.0 Model 2500
줄기세포 생물학 1000
The Netter Collection of Medical Illustrations: Digestive System, Volume 9, Part III - Liver, Biliary Tract, and Pancreas (3rd Edition) 600
INQUIRY-BASED PEDAGOGY TO SUPPORT STEM LEARNING AND 21ST CENTURY SKILLS: PREPARING NEW TEACHERS TO IMPLEMENT PROJECT AND PROBLEM-BASED LEARNING 500
2025-2031全球及中国蛋黄lgY抗体行业研究及十五五规划分析报告(2025-2031 Global and China Chicken lgY Antibody Industry Research and 15th Five Year Plan Analysis Report) 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 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 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4498758
求助须知:如何正确求助?哪些是违规求助? 3949769
关于积分的说明 12244804
捐赠科研通 3608227
什么是DOI,文献DOI怎么找? 1984839
邀请新用户注册赠送积分活动 1021239
科研通“疑难数据库(出版商)”最低求助积分说明 913670