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Study of Survivors of Different Types of Cardiac Arrest and Their Neurological Recovery

2014年1月9日 更新者:Eyad AlThenayan、Lawson Health Research Institute

Neurological Outcomes After Cardiac Arrest in Pulseless Electrical Activity in Comparison to Asystole. Are All Non-shockable Rhythms the Same?

After successful resuscitation from certain types of cardiac arrest, total body cooling is now a well established treatment that improves the chances of the brain recovering. This however, has only been definitively proven after a certain type of cardiac arrest that is "ventricular fibrillation / ventricular tachycardia". The purpose of this study is to explore if total body cooling is beneficial for patients recovering from another type of cardiac arrest that is "pulseless electrical activity".

HYPOTHESIS:

Patients undergoing post-cardiac arrest therapeutic hypothermia have better neurological outcomes if their initial arrest rhythm is pulseless electrical activity (PEA) in comparison to asystole.

研究概览

详细说明

STUDY RATIONALE AND BACKGROUND INFORMATION:

After successful resuscitation from cardiac arrest the body experiences a period of global reperfusion. During this period, patients may show signs of myocardial stunning, lactic acidosis, neurological injury and reperfusion syndrome. This constellation of findings constitutes what is known as post-cardiac arrest syndrome. The brain appears to be one of the most vulnerable organs to injury during this reperfusion phase and varying degrees of cognitive impairment may be the end result. Inducing mild therapeutic hypothermia has been shown to be protective for the brain in this setting and has been demonstrated to improve neurological recovery. The evidence for this however, is only conclusive in cases where the arrest is in a shockable rhythm i.e. pulseless ventricular tachycardia and ventricular fibrillation.

In 2002, two randomized controlled trials were published showing an improvement in neurological outcomes in patients treated with mild therapeutic hypothermia post resuscitation from shockable cardiac arrest. Therapeutic hypothermia has since been widely adopted by most authorities as part of the comprehensive treatment bundle for post cardiac arrest syndrome. Whether there is any benefit for patients arrested in non-shockable rhythms however, is a matter of controversy. Some have reported improved mortality and better neurological outcomes with therapeutic hypothermia in this patient population. Others have reported no benefit or even a trend towards harm. And although the matter remains controversial, the recommendation still stands for therapeutic hypothermia to be offered for all comatose survivors of cardiac arrest whatever the arrest rhythm.

Most previous reports have examined the differences between shockable and non-shockable rhythms in terms of neurological outcome and mortality rates after therapeutic hypothermia. To our knowledge, no study has examined the differences in outcome between the two types of non-shockable rhythms, that is pulseless electrical activity (PEA) and asystole. We hypothesize that during PEA arrests, patients may retain some degree of cerebral perfusion and hence have better neurological outcomes post-resuscitation. That is in contrast to asystole where patients are likely to have no cerebral perfusion. In this study we attempt to detect any possible differences in neurological recovery (as indicated by the Cerebral Performance Category scale on hospital discharge) after therapeutic hypothermia, between patients arrested in PEA arrest and those arrested in asystole.

研究类型

观察性的

注册 (预期的)

400

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Ontario
      • London、Ontario、加拿大、N6A 5A5
        • University Hospital, London Health Sciences Centre, University of Western Ontario
      • London、Ontario、加拿大、N6A 5W9
        • Victoria Hospital, London Health Sciences Centre, University of Western Ontario

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 90年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

非概率样本

研究人群

All patients admitted to the intensive care unit (ICU) with a diagnosis of postcardiac arrest between Jan 2008 and Dec 2012 will be examined.

描述

Inclusion Criteria:

  • Admission to adult ICU (age ≥18 years) at London Health Sciences Centre
  • Primary reason for ICU admission: postcardiac arrest
  • Both in-hospital and out-of-hospital cardiac arrest will be included
  • ICU admission between Jan 2008 and Dec 2012.

Exclusion Criteria:

- ICU admissions primarily for reasons other than cardiac arrest.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:队列
  • 时间观点:追溯

队列和干预

团体/队列
干预/治疗
Shockable arrest
Initial arrest rhythm shockable. This is either pulseless ventricular tachycardia (pulseless VT) or ventricular fibrillation (VF).
No therapeutic hypothermia was induced.
其他名称:
  • No therapeutic hypothermia.
  • 控制。
Hypothermia was induced after successful resuscitation from cardiac arrest.
其他名称:
  • 低温
  • Induced hypothermia
  • Mild therapeutic hypothermia
  • 冷却
  • Targeted temperature management
Pulseless electrical activity
Initial arrest rhythm is pulseless electrical activity.
No therapeutic hypothermia was induced.
其他名称:
  • No therapeutic hypothermia.
  • 控制。
Hypothermia was induced after successful resuscitation from cardiac arrest.
其他名称:
  • 低温
  • Induced hypothermia
  • Mild therapeutic hypothermia
  • 冷却
  • Targeted temperature management
Asystole
Initial arrest rhythm is asystole.
No therapeutic hypothermia was induced.
其他名称:
  • No therapeutic hypothermia.
  • 控制。
Hypothermia was induced after successful resuscitation from cardiac arrest.
其他名称:
  • 低温
  • Induced hypothermia
  • Mild therapeutic hypothermia
  • 冷却
  • Targeted temperature management

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Cerebral performance category score on hospital discharge
大体时间:Upon discharge from hospital, assessed up to 36 months postcardiac arrest

Neurological outcome on discharge from hospital as defined by the cerebral performance category (CPC) scale. The CPC scale is a 5 point scale. The outcome measure will be dichotomized into good or bad. Good outcome will be equivalent to CPC scores of 1 & 2 (where the patient is independent), and bad outcome will be equivalent to CPC scores of 3, 4 & 5 (where the patient is either dependent or dead).

CPC Scale:

  1. Functioning normally and independent, possibly with a minor disability.
  2. Moderately disabled, still independent.
  3. Conscious but with a severe disability, dependent.
  4. Unconscious (comatose or in a persistent vegetative state).
  5. Brain dead or dead by traditional criteria.
Upon discharge from hospital, assessed up to 36 months postcardiac arrest

次要结果测量

结果测量
措施说明
大体时间
Hospital length of stay postcardiac arrest
大体时间:Days spent in hospital after successful resuscitation from cardiac arrest, assessed up to 36 months from the date of cardiac arrest
Hospital length of stay (LOS) post-cardiac arrest will be calculated from the day of the cardiac arrest to the day of hospital discharge. If prior to the arrest the patient was an inpatient, we will only count the days from the arrest to discharge. Days spent in hospital prior to the arrest will not be included.
Days spent in hospital after successful resuscitation from cardiac arrest, assessed up to 36 months from the date of cardiac arrest
Intensive care unit length of stay postcardiac arrest
大体时间:Days spent in the intensive care unit after successful resuscitation from cardiac arrest, assessed up to 36 months from the date of cardiac arrest
The length of stay (LOS) in the intensive care unit (ICU) in days, after successful resuscitation from cardiac arrest.
Days spent in the intensive care unit after successful resuscitation from cardiac arrest, assessed up to 36 months from the date of cardiac arrest
Neurological status after hospital discharge
大体时间:Assessed up to 12 months from hospital discharge
Neurological status as documented on the patient's first outpatient clinic visit, assessed up to 12 months from hospital discharge. This will be analyzed as a secondary outcome only if enough data is generated on chart review.
Assessed up to 12 months from hospital discharge

其他结果措施

结果测量
措施说明
大体时间
Time to obeying commands
大体时间:Assessed up to 21 days postcardiac arrest
Total time in days from the cardiac arrest until the patient is able to obey commands, as documented in the patient's chart.
Assessed up to 21 days postcardiac arrest
Documented negative neurological prognosticators
大体时间:Upon withdrawal of life support, assessed up to 3 months postcardiac arrest

For patient's in which the reason for withdrawal of life support is poor neurological outcome, the number of negative neurological prognosticators recorded in the chart will be examined.

Examples of negative prognosticators include: negative somatosensory evoked potentials on post arrest day 3, post arrest status epilepticus, absent brain stem reflexes beyond post arrest day 2... etc.

Upon withdrawal of life support, assessed up to 3 months postcardiac arrest
Post arrest neurological investigations (including imaging studies)
大体时间:Performed within 21 days from cardiac arrest
All neurological investigations done within 21 days from cardiac arrest will be examined including electroencephalograms, somatosensory evoked potentials, brain magnetic resonance imaging, brain computerized tomography (CT) scans... etc.
Performed within 21 days from cardiac arrest

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Eyad Althenayan, MD、Western University, Canada
  • 研究主任:Philip Jones, MD, FRCPC、Western University, Canada
  • 学习椅:Bryan Young, MD, FRCPC、Western University, Canada
  • 研究主任:Ahmed F Hegazy, MD, FRCPC、Western University, Canada
  • 研究主任:Ana Igric, MD, FRCSC、Western University, Canada
  • 研究主任:Carolyn Benson, MD、Western University, Canada

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2014年1月1日

初级完成 (预期的)

2014年12月1日

研究完成 (预期的)

2015年2月1日

研究注册日期

首次提交

2014年1月4日

首先提交符合 QC 标准的

2014年1月9日

首次发布 (估计)

2014年1月13日

研究记录更新

最后更新发布 (估计)

2014年1月13日

上次提交的符合 QC 标准的更新

2014年1月9日

最后验证

2014年1月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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