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临床试验/NCT04586764
NCT04586764招募中不适用

ST Elevation Myocardial Infarction Hemodynamic OutComes: Role of Non-Invasive Cardiac System (SHOCk-NICaS) Study

University of Manitoba1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2019年10月9日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
500
试验地点
1
主要终点
Prolonged hospitalization due to heart failure (> 96 hours)

研究概览

简要总结

Proposed novel solution for high-risk heart disease Overall in-hospital mortality among ST elevation myocardial infarction (STEMI) patients is 3-4%, but >50% patients experiencing cardiogenic shock (CS) secondary to STEMI die in the hospital. Evidence suggests early diagnosis and treatment of CS results in improved outcomes, albeit, there is no tool to diagnose CS reliably in a timely fashion in STEMI patients through the continuous monitoring. We hypothesize that bioimpedance-derived hemodynamic measures obtained using the Non-Invasive Cardiac System (NICaS) can facilitate early detection of CS, predict outcomes, and revolutionize the STEMI patient management. The objectives of SHOCk-NICaS study in STEMI patients are to: a) identify the CS early, using NICaS derived cardiac index of ≤1.8L/min/m2 or ≤2.2L/min/m2 with the use of vasopressor and/or inotropes, and compare it with the incidence of CS based upon lactate level ≥2mmol/L, and systolic blood pressure <90mmHg; b): determine the impact of primary percutaneous coronary intervention (PPCI), using NICaS derived hemodynamic measures (stroke volume, cardiac index, cardiac power index, etc), by comparing pre- and post-angioplasty; and c) identify outcome-associated hemodynamic markers. A composite score of death during hospital stay, prolonged hospitalization due to heart failure (>72hrs), and use of inotropic or mechanical circulation support is a primary outcome.

Methodology This is a multi-center, double-blind, prospective cohort study enrolling STEMI patients aged ≥18years visiting at 4 cardiac centers (St Boniface, St. Michael's, McGill University Hospital). Using validated NICaS protocol, hemodynamic parameters will be recorded at baseline, during the PPCI procedure, and within 24-hour post PPCI without altering the standard care. Statistical analysis: Baseline data will be reported as mean±SD or median±interquartile range. The outcomes will be assessed using multivariable logistic regression. We will analyze the impact of age, sex, gender, and ethnicity on hemodynamic measures. The targeted 500 patients will ensure a margin of error of 5% at a 95% CI. So far recruited 76 STEMI patients mark the study feasibility.

Significance This novel study in high-risk STEMI patients will provide a promising cost-effective, rapid, and non-invasive tool to identify CS early; a prompt intervention may curtail the high morbidity and mortality. The meticulously designed pragmatic study outcomes may revolutionize STEMI patient management.

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

  • Patients aged ≥18 years, presenting with EKG confirmed diagnosis of STEMI
  • Able to understand, and consent to participate in the study

排除标准

  • Patients unwilling to participate in the study
  • Patients with any life-threatening medical condition with an expected life span of ≤1 year (e.g., metastatic cancer, terminal COPD)

结局指标

主要结局

Prolonged hospitalization due to heart failure (> 96 hours)

时间窗: At 7 days

Documented pulmonary edema on x-ray chest, elevated BNP or initiation of diuretic therapy lasting longer than 24 hours.

Use of inotropic - vasopressor therapy

时间窗: At 7 days

Use of norepinephrine, epinephrine, milrinone, dobutamine, or dopamine

Use of mechanical circulation support

时间窗: At 7 days

Intra aortic balloon pump, impella or extra-corporeal membrane oxygenation (ECMO) insertion

Death

时间窗: At 1 year

次要结局

  • Killip classification(At 24 hours)
  • Implantable Cardioverter Defibrillator (ICD) implantation(At 1 year)
  • New-onset atrial/ventricular arrhythmia(From 30 days to 1 year)
  • New diagnosis of heart failure(From 30 days to 1 year)
  • Cardiac Re-synchronization Therapy/Defibrillator (CRT-D) implantation(At 1 year)

研究者

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

Ashish H Shah

Assistant Professor

University of Manitoba

研究点 (1)

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