Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Cardiac Arrest
  • Sudden Death
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 65 years
Gender
Both males and females

Description

1 STATUS OF THE QUESTION 2.1 Circumstances surrounding the problem: 2.1.1 The limits of conventional resuscitation in cardiac arrests. Sudden adult death, unexpected cardiac arrest (CA) most often related to cardiovascular causes, affects more than 40,000 people in France every year. The prognosis o...

1 STATUS OF THE QUESTION 2.1 Circumstances surrounding the problem: 2.1.1 The limits of conventional resuscitation in cardiac arrests. Sudden adult death, unexpected cardiac arrest (CA) most often related to cardiovascular causes, affects more than 40,000 people in France every year. The prognosis of out-of-hospital sudden death is particularly sombre. Only 5 to 20% of the patients survive without neurological sequel. This prognosis can be partially improved by an efficient organization of management that implements the concept of the "survival chain". An early alert by witnesses of the CA, carrying out the first interventions, cardiopulmonary resuscitation (CPR), defibrillation by the public or persons qualified in first-aid, followed by specialized resuscitation by a medical team (such as the ambulance service) increase the amount of survivors. The reduction in the time that passes before the first interventions (called the no-flow period) and the duration of resuscitation before return of spontaneous circulation (ROSC) called low-flow, are considered to be the primary predictive factors of survival in CA. Just recently, better knowledge of post-cardiac arrest syndrome also contributed to an improvement in the prognosis and the quality of survival. The introduction of early angioplasty and the generalisation of therapeutic hypothermia now complete management for which coding is steadily improving through international and national recommendations that are updated every 5 years. However, in order to show what it is capable of, this conventional management of CA requires spontaneous cardiac activity to be re-established as quickly as possible. Therefore, a return of spontaneous circulation (ROSC) must be obtained in the field in out-of-hospital sudden deaths. Classically, in the absence of ROSC after 30 minutes of correctly administered resuscitation, the CA is considered to be refractory and the treatment options are limited. Just recently, it was shown that the chances of survival are non-existent after 16 minutes of resuscitation. In most cases, resuscitation is discontinued and the patient is declared dead on the spot. The regulatory inclusion of a physician on ambulance service teams relieves the difficulty of this decision. It is often simple to make and is medically indisputable when it is obvious that the prognostic factors are very unfavorable (notably, an extended no-flow period) and/or the conditions (advanced age, severe chronic disease, etc...) are not compatible with prolonged resuscitation. This decision is much more difficult when the prognostic factors are favorable and prolonged resuscitation efficiently provides spontaneous circulation (signs of the patient awaking during CPR). Under these circumstances, in France and several other European countries, the decision can be made to continue extracorporeal membrane oxygenation (ECMO) and transport the refractory CA victim. It was made possible by the development of mechanical external cardiac massage devices such as Autopulse ® and Lucas® which enable prolonged cardiac compression during transport by the emergency service. However, this continuation of resuscitation can only be considered if it enables another subsequent treatment for the patient. Two options are possible. The patient can be declared dead and become a potential organ donor in the framework of an organ harvesting procedure in a patient after "cardiac death". This harvesting, which is highly organized according to regulations, can only be done in certain hospitals authorized by the French Biomedicine Agency. Or, resuscitation can be prolonged by the use of extracorporeal circulatory support. 2.1.2. The progress of extracorporeal circulatory support and cardiac arrest Circulatory support is a technique that has been in common use for many years now perioperatively in cardiac surgery. One of its simplest forms, extracorporeal membrane oxygenation (ECMO) is being used more and more often outside of this field, notably in paediatrics and in the care of Acute Respiratory Distress Syndrome (ARDS) or refractory shock in adults. This technique has notably been widely introduced in general intensive care in the treatment of malignant influenzas that affect young subjects (H1N1 virus). In parallel with this extension of the indications for ECMO, the technical development of equipment was a major factor. ECMO devices, which are particularly easy to use, miniaturized and energy autonomous, are available. They make it possible to use ECMO during inter-hospital transport by ambulance or helicopter. In France, several teaching hospitals have therefore developed mobile teams called mobile circulatory support unit (UMAC) that enable the implementation of ECMO in intensive care units where there was none, and the transport of patients on circulatory and respiratory support to a reference center. 2.1.3. The implementation of extracorporeal membrane oxygenation (ECMO) in Cardiac Arrest (CA) It quickly became evident that the possibility of having artificial circulatory activity that enables efficient perfusion by oxygenated blood was important for CA victims whose heart had stopped beating. The first research, conducted primarily during refractory CAs that occurred in the hospital setting, demonstrated the unexpected possibility for survival in patients who, without this option would be dead, and for whom resuscitation would have been stopped. In 2003 in Taiwan, Chen et al. noted a survival rate of almost 30% in a series of CAs that occurred in the hospital setting. In Caen, France, the same phenomenon was noted: the survival of 8 out of 40 patients who benefited from ECMO following refractory CA. This technique proved to be highly adapted when the cause of the CA was potentially reversible. Mégarbane et al. noted the survival of 3 out of 12 victims of CA following acute intoxication with cardiotoxic drugs. In international recommendations, circulatory support is still only recommended in paediatrics. However, these indisputable successes in adults led to an attempt to rationalise the use of therapeutic ECMO in France. The indications considered as possible include the existence of hypothermia, intoxication, signs of life during Cardio-Pulmonary Ressucitation (CPR), and CPR (low-flow) of less than 100 minutes. The development of ECMO programmes for the treatment of refractory CA demonstrated a difference in prognosis between in-hospital and out-of-hospital CAs. In-hospital CAs quickly benefit from the implementation of ECMO. Out-of-hospital CA victims have late access to this possibility of resuscitation. In fact they require resuscitation of at least 30 minutes in the field to be considered as refractory, followed by transport under mechanical massage until arrival at a center with ECMO. Le Guen et al. noted that in a series of patients who were victims of sudden death in Paris in out-of-hospital settings, only 2 out of 51 patients survived in good neurological condition. Most of these patients had extended low-flow periods before the implementation of ECMO. A negative correlation between the duration of resuscitation before ECMO and survival explains this poor prognostic result. In addition, resuscitation prolonged by mechanical massage is burdened by its own morbidity as Agostinucci et al. emphasized. This negative influence before access to ECMO is also noted by Chen et al. in the hospital setting. The prognosis rapidly decreases when resuscitation is prolonged: more than 40% survival if resuscitation lasts less than 30 minutes; 17% when it surpasses 60 minutes. This difference in survival between in-hospital and out-of-hospital CA is also noted in another series of French studies (Gay, AFAR abstract). The prognosis for out-of-hospital CA is even worse when it is accompanied by prolonged CPR. Morbidity is also higher among these patients. Cadarelli et al. included all the research and case histories published up until 2008 in a meta-analysis and demonstrated the harmful effect of prolonged CPR. In this analysis, the speed at which ECMO is implemented appears to be a prognostic factor similar to patients' age and the total duration of circulatory support. Therefore, ECMO that is started after more than 30 minutes of CPR results in a decrease in survival. Kilbaught et al. emphasize that it is actually the time factor that makes the difference between in-hospital and out-of-hospital CAs. In their pre-hospital emergency system, very rapid transport of patients during CPR to start ECMO upon arrival in the emergency service is possible. With this strategy, they demonstrate that the difference in prognosis between in-hospital and out-of-hospital CAs is eliminated when the time for implementation of ECMO is comparable. As a result, ECMO is used earlier and earlier in hospitals in Japan with results currently being published that appear to be very positive for survival. 2.1.4 The concepts of pre-hospital extracorporeal membrane oxygenation (ECMO) The analysis of the international literature shows that ECMO might be a management method that improves the survival of CA victims. However, in the context of out-of-hospital sudden death in a medicalised emergency system and in the framework of French regulations, there are two limiting factors: the obligation for resuscitation for 30 minutes before categorically announcing that the CA is refractory and whether or not to choose another treatment option. the possibility to have access to ECMO within the closest time period to the 30 minutes of Cardio-Pulmonary Ressucitation (CPR), which appears to be an important threshold in determining the prognosis. Pre-hospital ECMO, which is the basis of the research concept being proposed, includes arterio-venous cannulation and the implementation of the extracorporeal system (pump, oxygenator) in a non-healthcare setting. It is therefore different from the in-hospital transport of patients on ECMO since the preceding steps take place in a hospital. The implementation of ECMO in hospital studies can be rapid, approximately 20 minutes in the Japanese study series and according to our experience. ECMO for out-of-hospital refractory CAs was the subject of a few clinical cases, in children and in sports events . Its feasibility by the ambulance service pre-hospital teams was confirmed in our last studies. The improvement in survival with early ECMO, close to a 30-minute period of CPR should also be demonstrated. It is only based on the extrapolation of the results of very fast transport and almost without specialised resuscitation of victims of sudden death close to a hospital with ECMO. Confirmation of this concept is therefore of particular importance and in fact: it would provide the prospect of a new treatment possibility for patients whose chances for survival are extremely slim, because prolonged CPR is required to have access to a hospital ECMO. It is an essential step before conducting a multi-centre randomised study to demonstrate the beneficial effect on survival. it would make it possible to stress the pertinence of the French teams' approach in this field, notably in comparison to European countries (Germany, Spain, etc...) that already have a medicalised pre-hospital emergency system, or that are currently developing it, like Japan. finally, it might also result in a better determination of the place of therapeutic ECMO and as a result, clarify the indications for organ harvesting after "cardiac death" in victims of pre-hospital sudden death. In brief, the objective of this project is to evaluate the advantage of pre-hospital ECMO in improving patient survival.

Tracking Information

NCT #
NCT02527031
Collaborators
Maquet Cardiovascular
Investigators
Principal Investigator: Lionel Lamhaut, MD Assistance Publique - Hôpitaux de Paris