跳至主要内容
临床试验/NCT02947360
NCT02947360已完成不适用

The FOVUS-ER Study: Focused Vascular Ultrasound to Risk Stratify Patients With Suspected Ischemic Chest Pain in the Emergency Department

Queen's University2 个研究点 分布在 1 个国家目标入组 326 人开始时间: 2016年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
326
试验地点
2
主要终点
Major adverse cardiac events

研究概览

简要总结

Broad Goal: To demonstrate that focused vascular ultrasound (FOVUS) can accurately risk stratify patients with chest pain in the emergency department (ED).

Background and Rationale: Traditional risk assessment focuses on characteristics of the pain, known Coronary Artery Disease (CAD), risk factors, electrocardiogram (ECG), and blood tests to identify active ischemia. Identifying clinically significant CAD remains one of the most challenging tasks in the ED. Current clinical decision rules err on the side of over investigation and admission. To address this limitation, the Investigators have developed a point-of-care carotid ultrasound test predictive of CAD. The Investigators have shown that carotid plaque is strongly associated with significant angiographic CAD in a population referred for angiogram.

Research Aims:

Primary - To determine the association between carotid plaque measured by a dedicated sonographer and 30-day major adverse cardiac events (MACE), including MI, reperfusion, or death in patients presenting to the ED with suspected cardiac ischemia.

Secondary - To determine the agreement sonographer and emergency physician FOVUS results.

Methodology: The Investigators propose a prospective cohort study to assess the prognostic value of a novel point-of-care carotid ultrasound plaque quantification protocol in the ED of Kingston General Hospital. We will enroll 500 consecutive patients presenting with a chief complaint of chest pain prompting at least one 12-lead ECG and troponin measurement. Patients will undergo carotid scan by a dedicated sonographer and emergency physician. Patients will be followed for MACE for 30 days. Those performing scans will be blinded to clinician's impression and care plans while clinicians will be blinded to FOVUS findings. The primary analysis will involve determination of the sensitivity, sensitivity, positive predictive value, negative predictive value and likelihood ratios associated with FOVUS for 30-day MACE.

Expected Outcomes: The study will provide evidence to determine whether FOVUS may be a useful prognostic tool for emergency physicians assessing patients with suspected ischemic chest pain. The secondary analysis will provide evidence to determine whether emergency physicians can be trained to measure carotid plaque height accurately when compared to the gold standard ultrasonographer measurement.

Significance: If FOVUS can reliably identify very low risk patients, implementation of this novel tool could reduce ED length of stay, monitoring, and overcrowding.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Men and women ≥25 years of age;
  • Chief complaint of chest pain possibly due to coronary ischemia and requiring cardiac investigations (e.g. ECG, troponin) in the opinion of the treating emergency physician;
  • Receiving at least one 12-lead ECG;
  • Receiving at least one serum troponin measurement;
  • Willing to provide informed consent.

排除标准

  • Acute ST-segment elevation on the initial ECG;
  • Hemodynamic instability;
  • High clinical suspicion of pulmonary edema;
  • History of recent cocaine or amphetamine use;
  • Inability to communicate in English;
  • A clear traumatic etiology;
  • Prior enrollment in the study within the past 6 months;
  • Terminal non-cardiac illness;
  • Previous carotid surgery (endarterectomy or stent);
  • Anatomic consideration rendering carotid artery inaccessible (tumor, abscess, scarring, mechanical device).

研究组 & 干预措施

FOVUS

Experimental

All eligible and consenting patients will receive a focused vascular ultrasound examination of the carotid arteries

干预措施: Focused vascular ultrasound of the carotid arteries (Other)

结局指标

主要结局

Major adverse cardiac events

时间窗: 30 days

Major adverse cardiac events will include acute myocardial infarction (MI),revascularization or mortality

次要结局

  • Plaque height measurement during FOVUS(At enrollment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Steven Brooks

Associate Professor, Principal Investigator

Queen's University

研究点 (2)

Loading locations...

相似试验