Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

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

9 janvier 2014 mis à jour par: 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.

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Observationnel

Inscription (Anticipé)

400

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

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

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 90 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

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

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Modèles d'observation: Cohorte
  • Perspectives temporelles: Rétrospective

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
Shockable arrest
Initial arrest rhythm shockable. This is either pulseless ventricular tachycardia (pulseless VT) or ventricular fibrillation (VF).
No therapeutic hypothermia was induced.
Autres noms:
  • No therapeutic hypothermia.
  • Contrôle.
Hypothermia was induced after successful resuscitation from cardiac arrest.
Autres noms:
  • Hypothermie
  • Induced hypothermia
  • Mild therapeutic hypothermia
  • Refroidissement
  • Targeted temperature management
Pulseless electrical activity
Initial arrest rhythm is pulseless electrical activity.
No therapeutic hypothermia was induced.
Autres noms:
  • No therapeutic hypothermia.
  • Contrôle.
Hypothermia was induced after successful resuscitation from cardiac arrest.
Autres noms:
  • Hypothermie
  • Induced hypothermia
  • Mild therapeutic hypothermia
  • Refroidissement
  • Targeted temperature management
Asystole
Initial arrest rhythm is asystole.
No therapeutic hypothermia was induced.
Autres noms:
  • No therapeutic hypothermia.
  • Contrôle.
Hypothermia was induced after successful resuscitation from cardiac arrest.
Autres noms:
  • Hypothermie
  • Induced hypothermia
  • Mild therapeutic hypothermia
  • Refroidissement
  • Targeted temperature management

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Cerebral performance category score on hospital discharge
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Hospital length of stay postcardiac arrest
Délai: 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
Délai: 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
Délai: 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

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Time to obeying commands
Délai: 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
Délai: 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)
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Eyad Althenayan, MD, Western University, Canada
  • Directeur d'études: Philip Jones, MD, FRCPC, Western University, Canada
  • Chaise d'étude: Bryan Young, MD, FRCPC, Western University, Canada
  • Directeur d'études: Ahmed F Hegazy, MD, FRCPC, Western University, Canada
  • Directeur d'études: Ana Igric, MD, FRCSC, Western University, Canada
  • Directeur d'études: Carolyn Benson, MD, Western University, Canada

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 janvier 2014

Achèvement primaire (Anticipé)

1 décembre 2014

Achèvement de l'étude (Anticipé)

1 février 2015

Dates d'inscription aux études

Première soumission

4 janvier 2014

Première soumission répondant aux critères de contrôle qualité

9 janvier 2014

Première publication (Estimation)

13 janvier 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

13 janvier 2014

Dernière mise à jour soumise répondant aux critères de contrôle qualité

9 janvier 2014

Dernière vérification

1 janvier 2014

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner