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改善未经充分治疗的钙化性冠状动脉疾病女性患者斑块的公平性:EMPOWER CAD研究的设计与原理

Equity in Modifying Plaque of Women With Undertreated Calcified Coronary Artery Disease: Design and Rationale of EMPOWER CAD study.

作者信息

McEntegart Margaret, Gonzalo Nieves, Fendelander Lahn, West Nick E J, Lansky Alexandra J

机构信息

Center for Interventional Cardiovascular Care, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center, New York, New York.

Interventional Cardiology Department, Clinico San Carlos University Hospital, Madrid, Spain.

出版信息

J Soc Cardiovasc Angiogr Interv. 2024 Oct 28;3(11):102289. doi: 10.1016/j.jscai.2024.102289. eCollection 2024 Nov.

Abstract

BACKGROUND

Coronary artery disease (CAD) is the leading cause of death for women, yet they remain underrepresented in interventional CAD studies. Women have been shown to be at increased risk of mortality and major adverse events after percutaneous coronary intervention (PCI). The poorer outcomes are likely because women are typically diagnosed with CAD late, at an older age, with more comorbidities, and with more challenging anatomy including smaller vessels and higher prevalence of coronary artery calcification.

METHODS

The EMPOWER CAD study (NCT05755711) is a postmarket, prospective, multicenter, single-arm observational study of the Shockwave Coronary intravascular lithotripsy (IVL) system for the treatment of women with calcified coronary artery disease. The study will enroll 400 female patients referred for PCI with coronary IVL and stenting. The primary safety end point is target lesion failure (TLF) at 30 days, defined as a composite of cardiac death, target vessel myocardial infarction, or ischemia-driven target lesion revascularization. The primary effectiveness end point is procedural success, defined as stent delivery with a residual in-stent stenosis ≤30% in all target lesions and without in-hospital TLF as assessed by an independent core laboratory and clinical events committee. Patients will be followed up for 3 years.

CONCLUSIONS

The EMPOWER CAD study will enroll real-world female patients. Adjunctive use of IVL with other calcium modification technologies will be assessed, as well as a subcohort analysis of patients with optical coherence tomography imaging. The EMPOWER CAD study therefore directly addresses the underrepresentation of women in interventional cardiology clinical trials.

摘要

背景

冠状动脉疾病(CAD)是女性的主要死因,但在CAD介入研究中,女性的代表性仍然不足。经皮冠状动脉介入治疗(PCI)后,女性的死亡率和主要不良事件风险增加。预后较差可能是因为女性通常在较晚的年龄、患有更多合并症且解剖结构更具挑战性(包括血管较小和冠状动脉钙化患病率较高)的情况下被诊断出患有CAD。

方法

EMPOWER CAD研究(NCT05755711)是一项上市后、前瞻性、多中心、单臂观察性研究,旨在评估用于治疗钙化性冠状动脉疾病女性患者的冲击波冠状动脉血管内碎石术(IVL)系统。该研究将纳入400名因冠状动脉IVL和支架置入术而接受PCI的女性患者。主要安全终点是30天时的靶病变失败(TLF),定义为心源性死亡、靶血管心肌梗死或缺血驱动的靶病变血运重建的复合终点。主要有效性终点是手术成功,定义为在所有靶病变中支架置入后残余支架内狭窄≤30%,且独立核心实验室和临床事件委员会评估无院内TLF。患者将接受3年的随访。

结论

EMPOWER CAD研究将纳入真实世界的女性患者。将评估IVL与其他钙修饰技术的联合使用,以及光学相干断层扫描成像患者的亚组分析。因此,EMPOWER CAD研究直接解决了女性在介入心脏病学临床试验中代表性不足的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad63/11624350/e2b6dcec5f52/gr2.jpg

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