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ST 段抬高型心肌梗死合并心原性休克患者行直接经皮冠状动脉介入治疗的延误。

Delays in Primary Percutaneous Coronary Intervention in ST-Segment Elevation Myocardial Infarction Patients Presenting With Cardiogenic Shock.

机构信息

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

出版信息

JACC Cardiovasc Interv. 2018 Sep 24;11(18):1824-1833. doi: 10.1016/j.jcin.2018.06.030.

Abstract

OBJECTIVES

This study sought to examine whether quality improvement initiatives across multiple ST-segment elevation myocardial infarction (STEMI) systems translated to faster first medical contact (FMC)-to-device times for patients presenting with cardiogenic shock (CS).

BACKGROUND

There are limited data describing contemporary rates of achieving guideline-directed FMC-to-device times for STEMI patients with CS.

METHODS

From 2012 to 2014, the American Heart Association Mission: Lifeline STEMI Systems Accelerator project established a protocol-guided approach to STEMI reperfusion systems in 484 U.S. hospitals. The study was stratified by CS versus no CS at presentation and performed Cochrane-Armitage tests to evaluate trends of achieving FMC-to-device time targets. A multivariable logistic regression model assessed the association between achieving guideline-directed FMC-to-device times and mortality.

RESULTS

Among 23,785 STEMI patients, 1,993 (8.4%) experienced CS at presentation. For direct presenters, patients with CS were less likely to achieve the 90-min FMC-to-device time compared with no-CS patients (37% vs. 54%; p < 0.001). For transferred patients, CS patients were even less likely to reach the 120-min FMC-to-device time compared with no-CS patients (34% vs. 47%; p < 0.0001). The Accelerator intervention did not result in improvements in the FMC-to-device times for direct-presenting CS patients (p for trend = 0.53), although there was an improvement for transferred patients (p for trend = 0.04). Direct-presenting patients arriving within 90 min had lower mortality rates compared with patients who reached after 90 min (20.49% vs. 39.12%; p < 0.001).

CONCLUSIONS

Fewer than 40% of STEMI patients presenting with CS achieved guideline-directed FMC-to-device targets; delays in reperfusion for direct-presenting patients were associated with higher mortality.

摘要

目的

本研究旨在探讨在多个 ST 段抬高型心肌梗死(STEMI)系统中实施质量改进措施是否能缩短出现心源性休克(CS)的患者从首次医疗接触(FMC)到接受器械治疗的时间。

背景

目前,有关达到心源性休克的 STEMI 患者指南指导的 FMC 到器械时间的最新数据有限。

方法

2012 年至 2014 年,美国心脏协会使命:生命线 STEMI 系统加速器项目在美国 484 家医院建立了一种基于协议的 STEMI 再灌注系统方法。本研究根据患者就诊时是否出现 CS 进行分层,并进行 Cochrane-Armitage 检验以评估达到 FMC 到器械时间目标的趋势。多变量逻辑回归模型评估了达到指南指导的 FMC 到器械时间与死亡率之间的关联。

结果

在 23785 例 STEMI 患者中,有 1993 例(8.4%)就诊时出现 CS。对于直接就诊者,与无 CS 患者相比,CS 患者更不可能达到 90 分钟的 FMC 到器械时间(37%比 54%;p<0.001)。对于转院患者,与无 CS 患者相比,CS 患者甚至更不可能达到 120 分钟的 FMC 到器械时间(34%比 47%;p<0.0001)。尽管对于转院患者,加速器干预确实改善了 FMC 到器械时间(趋势检验 p 值=0.04),但对于直接就诊的 CS 患者,该干预并未改善 FMC 到器械时间(趋势检验 p 值=0.53)。在 90 分钟内到达的直接就诊患者的死亡率低于 90 分钟后到达的患者(20.49%比 39.12%;p<0.001)。

结论

不到 40%的出现 CS 的 STEMI 患者达到了指南指导的 FMC 到器械目标;直接就诊患者的再灌注延迟与更高的死亡率相关。

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