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临床试验/NCT03658577
NCT03658577Unknown不适用

Association of Beta-Blocker Therapy at Discharge With Clinical Outcomes in Patients With Actue Coronary Syndrome Undergoing Percutaneous Coronary Intervention

Shenzhen People's Hospital1 个研究点 分布在 1 个国家目标入组 582 人开始时间: 2018年3月2日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
582
试验地点
1
主要终点
all-cause death

研究概览

简要总结

Limited data are available on the efficacy of beta-blocker therapy for secondary prevention in Actue Coronary Syndrome(ACS) patients. This study sought to investigate the association of beta-blocker therapy at discharge with clinical outcomes in patients with ACS after percutaneous coronary intervention (PCI).

详细描述

The American College of Cardiology (ACC)/American Heart Association (AHA) guidelines recommend beta-blockers for secondary prevention in patients with ACS without regard to reperfusion therapy. However, evidence supporting this recommendation originated from studies conducted before the introduction of reperfusion therapy or studies in patients treated with fibrinolysis. In the present era of PCI, there are no prospective randomized studies looking at the effects of long-term beta-blocker therapy on clinical outcomes in ACS patients. Moreover, results from registry data and post-hoc analysis on beta-blocker therapy in patients undergoing PCI are inconsistent.

In particular, the beneficial effect of long-term beta-blocker therapy has not been well established in patients with relatively low risk, such as preserved left ventricular systolic function or single-vessel disease. Therefore, we investigated the association of beta-blocker therapy at discharge with clinical outcomes in ACS patients after PCI.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • consecutive patients 18 years of age or older;
  • patients diagnosed as ACS(including STEMI、NSTEMI and UA) by doctor at discharge;
  • patients undergoing primary PCI.

排除标准

  • missing beta-blocker information.

结局指标

主要结局

all-cause death

时间窗: 3 years

The primary outcome was all-cause death during follow up.

次要结局

  • MACE(3 year)

研究者

发起方
Shenzhen People's Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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