跳至主要内容
临床试验/NCT03248557
NCT03248557已完成不适用

Early Prognostic Value of an Algorithm Based on Spectral Variables of Ventricular fibrillAtion From the EKG of Patients With suddEn Cardiac Death: a Multicenter Observational Trial

Hospital San Carlos, Madrid5 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2016年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
168
试验地点
5
主要终点
Favorable neurological performance (FNP) during hospitalization

研究概览

简要总结

Ventricular fibrillation (VF)-related sudden cardiac death (SCD) is a leading cause of mortality. Patients may survive with neurological damage despite state-of-the-art treatment. Current biological and imaging parameters show significant limitations on early predicting cerebral performance at hospital admission. A spectral-based model was recently suggested to correlate time-dependent VF spectral changes with acute cerebral injury in comatose survivors after cardiac arrest, which opens the possibility to implement early prognostic tools in clinical practice. The AWAKE trial is an investigator-initiated, multicenter, observational trial aiming to validate a spectral-based model to early predict cerebral performance and survival in resuscitated comatose survivors admitted to specialized intensive care units. The primary clinical outcome is favorable neurological performance (FNP) during hospitalization. Patients will be categorized into 4 subsets of NP according to the risk score obtained from the predictive model. The secondary clinical outcomes are survival to hospital discharge, and FNP and survival after 6 months of follow-up. Model-derived categorization will be compared with clinical outcomes to assess model sensitivity, specificity and accuracy. Eligible patients will be included prospectively and retrospectively, using an electronic Case Report Form to enter data from medical records and in-person interviews. Patients will be divided into: study group (predictive data required) including comatose (Glasgow Coma Scale -GCS- ≤8) survivors undergoing temperature control after return of spontaneous circulation (RoSC), and control group including patients who regain consciousness (GCS=15) after RoSC. VF tracings prior to the first DC shock will be digitized and analyzed to derive spectral data and risk scores.

详细描述

Trial design:

The AWAKE trial is an investigator-initiated, multicenter, observational trial currently underway in 4 centers in Spain (Hospital Clínico San Carlos, Hospital Universitario La Paz, Hospital General Universitario de Ciudad Real, and Hospital Universitario Gregorio Marañón), and open to more participant hospitals. Only tertiary care hospitals with extensive expertise in the management of SCD and post-resuscitation care will participate in the trial. All of them are required to have on-site 24 hours a day, 7 days a week availability for percutaneous coronary intervention, and critical care units staffed by cardiologists and/or critical care specialists. This selective center recruitment is supported by recent data suggesting that direct admission to invasive heart centers is associated with lower mortality in patients with out-of-hospital cardiac arrest (OHCA).

Consecutive patients admitted to the hospital after out or in-hospital cardiac arrest due to VF will be registered and screened for potential inclusion in the study. Patients will be classified into either of two groups:

  1. Study group: comatose survivors (GCS ≤8) after RoSC and, in whom neurological prognosis is unknown at the time of admission. This group is divided into a prospective cohort (new admissions), and a retrospective one, in which cases will be obtained from existing databases in the participating centers.
  2. Control group: patients who are conscious (GCS=15) and whose neurological status is known and good at admission. This will be the control group for the spectral-based predictive model, setting the gold standard for predicting FNP.

Ethics:

研究设计

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

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

  • In or out-of-hospital cardiac arrest with ventricular fibrillation (VF) as first documented rhythm.
  • A ≥3-second VF tracings before the first direct current (DC) shock.
  • Signed informed consent. Patients unable to consent, it will be requested to an authorized relative.
  • Study group: GCS ≤8 and subject to temperature management (hypothermia 32-34ºC or normothermia 36ºC).
  • Control group: GCS=15, thus no indication for temperature management.

排除标准

  • First documented rhythm other than VF (e.g. ventricular tachycardia, pulseless electrical activity, asystole)
  • Unavailable or suboptimal quality of the ECG tracing before the first DC shock.
  • Terminal disease or cognitive impairment before the SCD event.
  • Other possible causes of comatose status different from SCD (e.g. drugs, traumatic brain injury, hypoxia).
  • Aged under 18 .
  • Unwilling to provide the informed consent.
  • Comatose status (GCS≤8) and absence of temperature management or GCS ≥9 if temperature management was undertaken.
  • Hemodynamic instability leading to incomplete 24 h of temperature management
  • Early mortality and absence of subsequent withdrawal of sedation to assess cerebral performance.

结局指标

主要结局

Favorable neurological performance (FNP) during hospitalization

时间窗: Hospitalization, up to 2 months after admission

Patients will be assessed using the Pittsburgh Cerebral Performance Categories (CPC) outcome categorization of brain injury. They will be considered to have FNP if they score 1 or 2 in the CPC scale (good performance and moderate disability, respectively). CPCs 3, 4 and 5 (severe disability, vegetative state and brain death, respectively) will be considered as a non-FNP. In the prospective cohort, FNP will also be determined using the mini-mental state examination (cut-off value 24/30).

次要结局

  • Favorable neurological performance (FNP) at follow-up(6 months after discharge (prospective patients) or at patient enrollment (retrospective patients))
  • Survival to hospital discharge(Hospitalization, up to 2 months)
  • Survival at follow-up(6 months after discharge (prospective patients) or at patient enrollment (retrospective patients))

研究者

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

David Filgueiras-Rama

MD, PhD

Hospital San Carlos, Madrid

研究点 (5)

Loading locations...

相似试验

Prognostic Value of Ventricular Fibrillation... | 临床试验