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使用Saranas早期出血监测系统(SAFE-MCS)对机械循环支持下的经皮冠状动脉介入治疗进行安全监测的研究设计与原理

Design and Rationale of the Safe Surveillance of PCI Under Mechanical Circulatory Support With the Saranas Early Bird Bleed Monitoring System (SAFE-MCS) Study.

作者信息

Généreux Philippe, Kaki Amir, Naguib Mostafa, Fuller Brittany, Naik Hursh, Kim Michael, Masoumi Amirali, Waggoner Thomas, Syed Zaffer, Walsh Julia, Karmpaliotis Dimitri, Basir Mir Babar

机构信息

Gagnon Cardiovascular Institute, Morristown Medical Center, Morristown, New Jersey.

Ascension St. John Hospital, Detroit, Michigan.

出版信息

J Soc Cardiovasc Angiogr Interv. 2023 Jul 5;2(5):101049. doi: 10.1016/j.jscai.2023.101049. eCollection 2023 Sep-Oct.

Abstract

BACKGROUND

High-risk percutaneous coronary intervention (PCI) with mechanical circulatory support (MCS) has been associated with varying rates of bleeding due to variable bleeding definitions, incomplete data relative to site-specific bleeding, and inclusion of variable patient populations.

STUDY DESIGN AND OBJECTIVES

SAFE-MCS (NCT05077657) is a multicenter, single-arm, open-label study designed to evaluate the safety of complex high-risk PCI using Impella and surveillance with the Saranas Early Bird Bleed Monitoring System (EBBMS). The study aims to enroll 184 evaluable subjects at up to 15 US centers. The primary clinical end point is the incidence of access-site related BARC type III or V bleeding. Secondary clinical end points include the incidence of each of the Saranas EBBMS level 1, 2, and 3 indicators and the incidence of all BARC type III or V bleeding. Enrollment is anticipated to complete in September 2023 with no longitudinal follow-up.

CONCLUSIONS

SAFE-MCS is the first study to exclusively assess bleeding complications in patients undergoing PCI with Impella with independent adjudication via a clinical end point committee and will gather meaningful real-world data using contemporary practice.

摘要

背景

由于出血定义不同、特定部位出血相关数据不完整以及纳入的患者群体各异,采用机械循环支持(MCS)的高风险经皮冠状动脉介入治疗(PCI)出血发生率有所不同。

研究设计与目标

SAFE-MCS(NCT05077657)是一项多中心、单臂、开放标签研究,旨在评估使用Impella进行复杂高风险PCI的安全性以及通过Saranas早期出血监测系统(EBBMS)进行监测的情况。该研究旨在在美国多达15个中心招募184名可评估受试者。主要临床终点是与穿刺部位相关的BARC III型或V型出血的发生率。次要临床终点包括Saranas EBBMS 1级、2级和3级指标各自的发生率以及所有BARC III型或V型出血的发生率。预计2023年9月完成入组,无长期随访。

结论

SAFE-MCS是第一项专门评估使用Impella进行PCI的患者出血并发症的研究,通过临床终点委员会进行独立判定,并将采用当代实践收集有意义的真实世界数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a217/11308036/18966eb2a0fd/fx1.jpg

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