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Cardiopulmonary Resuscitation Performance of Professional Rescuers With a New Defibrillation Algorithm

Professional Rescuers Cardiopulmonary Resuscitation Performance After Implementation of a Defibrillation Algorithm for Early Treatment of Refibrillation, an Observational Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04691089
Acronym
DEFI-2022
Enrollment
285
Registered
2020-12-31
Start date
2021-01-18
Completion date
2022-04-02
Last updated
2024-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest, Sudden, Sudden Cardiac Death, Ventricular Fibrillation, Ventricular Tachycardia

Keywords

Cardiac Arrest, Automatic External Defibrillator, Chest Compression Fraction, Electrical Cardiac Analysis under Chest Compressions

Brief summary

In the Paris (France) Medical Emergency system, in the early phase of Out-of-hospital Cardiac Arrest (OHCA), the treatment of a Ventricular Fibrillation (VF) consists of delivering an External Electric Shock (EES) by a rescuer with the use of an Automated External Defibrillator (AED). This latter realizes a cardiac rhythm analysis every two minutes. This analysis requires that chest compressions (CC) be interrupted for a while. However, CC interruptions are potentially harmful due to the brain, and heart perfusions decrease. On the other hand, the recurrence of VF occurs mostly during the first minute after the shock, whereas the delay between 2 rhythm analysis is 2 minutes. The consequence is excessive time spent in VF, which is deleterious in terms of coronary and cerebral perfusion. The investigator implements a new AED algorithm whose operating principle is as follows. One minute after an EES administration, the AED realizes a cardiac rhythm analysis during which the rescuers do not need to interrupt the chest compressions (CC): this is called the rhythm analysis in presence of CC The detection of a VF in presence of CC needs to be confirmed, in absence of CC The CC's are therefore interrupted for new rhythm analysis. Once the presence of VF is approved, the AED proposes a shock to be administred The aim of the study Study Design: This is a prospective observational study. The eligibility criteria are as follows: * Patients in Out-Of-Hospital Cardiac Arrest. * Basic Life support care with an AED. The primary endpoint is the chest-compression fraction (CCF) that represents the CPR-time performance during the ten first minutes of BLS care ( or \< 10 min in case of Return Of Spontaneus Circulation (ROSC))

Detailed description

BACKGROUND For Out-Of-Hospital Cardiac Arrest (OHCA) patients suffering from ventricular fibrillation (VF) or ventricular tachycardia (VT), BLS care consists of administering external electric shocks (EES) and cardiopulmonary resuscitation (CPR). However, despite successful defibrillation, VF recurs in 50% of cases. Rescuers are forced to repeat EES as often as needed, without the recommendations specifying a maximum number. International guidelines recommend a 2-min CPR time between 2 rhythm analysis, that means one shock every 2 min. Since refibrillation occurs mostly during the first-minute post-shock, the patient will have to wait until the end of the 2 minutes before receiving the next EES. During that time, the chest compressions (CC) provide a reduced fraction of physiologic blood flow. The new AED algorithm provides the following changes : * After a 60-second post-shock CPR-period, the AED performs an analysis in presence of CC i.e., without CC interruption is performed. * Each time the AED detects a VF in presence of CC the algorithm requires the CC to be interrupted to perform an analysis in absence of CC to confirm the rhythm shockability. * Analyses in presence of CC are triggered every minute, possibly followed or not by an analysis in absence of CC * at least, the algorithm performs an analysis in absence of CC systematically every 2 minutes. This new algorithm fits in between two historical CPR algorithms used in western medical systems - the one-minute and the two-minute CPR cycle- depending on the rhythm shockability detected in presence of CC OBJECTIVES The main objective is to measure the CC fraction during the ten first minutes of Fire Fighter BLS care in OHCA. The secondary objectives : 1. Report on the available CPR quality parameters (CC frequency, hands-off maximum). 2. Report on the AED's diagnostic performance when analyzing the rhythm in presence of CC 3. Report on the AED's diagnostic performance when analyzing the rhythm in absence of CC 4. Report on the overall AED's diagnostic performance that results from the combination of two consecutive analyses in presence of CC and in absence of CC 5. Report on post-shock rhythms and their incidence 6. Report on the number of EES per patient 7. Report on the time distribution for the shocks administered per-patient to describe the rhythmic storm. 8. Report on the incidence of Return Of Spontaneous Circulation (ROSC), survival at hospital admission, and survival at hospital discharge. 9. Compare these reports to a historical cohort (2017). METHOD This is a prospective observational study. * The observation window is limited to CPR cycles within the first 10 minutes of BLS care, or less if ROSC is presumed. * The choice of 10 minutes is intended to observe the BLS team's action, without interfering with the ALS team that arrives later. * The three following criteria define a presumptive ROSC: * 1\. presence of QRS complexes of broadly similar morphology * 2\. synchronous impedance curve variation with the QRS complexes (indicating intrathoracic movement, in that case, cardiac mechanical activity) * 3\. no on-going CC * A CPR cycle is defined by the delay between two in absence of CC analyses. The study does not imply any change in current practice. There is no planned interim analysis. All consecutive participants with inclusion criteria and no exclusion criteria will be analyzed. STUDY SIZE The sample size was calculated to perform a non-inferiority analysis first, followed by a superiority test if non-inferiority was demonstrated. Non-inferiority test. The formula for calculating the required sample size in each group is based on a well-established statistical methodology designed for comparing two means in the context of a non-inferiority test. n = ((Z α/2 + Z β)2 X (σ12 + σ22)) / (μ1- μ2 - δ)2 With: * Sample size (n): the number of subjects required in each group. * α risk: Initially set at 0.025, this value is adjusted to account for multiple hypothesis testing by applying the Bonferroni correction. * Power 1- β: Established at 90% * Expected mean difference: This value is set to zero for this study. * σ (Standard Deviation): The value for each group has been set to 17. * δ (Non-Inferiority Margin): This margin is set at 5, an arbitrary value considered the maximal loss of effect (inferiority) that would be clinically acceptable when comparing CCF 2021 with CCF 2017 After the calculations, the required sample size was 208 subjects for each group involved in the non-inferiority testing. Superiority test. Should the non-inferiority hypothesis not be rejected, the study design allows for a subsequent superiority test to be conducted. For superiority, the investigators use the formula : n = ((Z α/2 + Z β)2 X (σ12 + σ22)) / (μ1- μ2)2 With: * Z α/2 : the Z value for an alpha/2 significance level * Z β : the Z value for a 1-beta power * σ12 and σ22 : the variances of the two groups * μ1 and μ2 : the means of the two groups. For α risk = 0.025 (Bonferroni correction), a power established at 90%, a standard deviation of 17, and a detectable difference between the two groups of 5%, the required sample size was 256 subjects for each group involved in the superiority testing. (STATA : sampsi 65 70 ,SD(17) alpha(0.025)) To account for a 10% loss of subjects, the number of patients was increased to 282, rounded up to 285 per group, i.e., a total of 570 patients. To observe 285 shockable patients, the investigators estimate the observation time required to be one year. Note that this same number of patients will be sufficient to detect an absolute 10% difference with an alpha risk of 5% and a power of 90%, between patients in the 2017 group and patients in the 2020 group with regard to the secondary endpoint Survival at hospital admission INTERRUPTION OR STOPPING OF THE STUDY The sponsor has the responsibility to report, to the national health authority, any serious and unexpected adverse events attributable to the new AED algorithm. RISKS A full report on the risks, the description of incidents, accidents and adverse events will be the subject of a chapter in the results section and also in the discussion. FINANCING Funding for the study is provided by the Paris Fire Brigade (promoter, following acceptance of the survey under French policy for clinical research projects) DISCUSSION The study will report on the CC fraction of an AED algorithm designed to analyze under CC.

Interventions

None listed

Sponsors

French Defence Health Service
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

Inclusion criteria

-Non-traumatic OHCA in adults, treated by a BLS team and connected to an AED equipped either with the 2017 or with the 2020 algorithm.

Exclusion criteria

* Use of AED in a pediatric mode * CPR administered in 15:2 mode * Patient already connected to another defibrillator at the arrival of the BLS Team * No shock advised by defibrillator at first analysis * Patient with a pacemaker Secondary

Design outcomes

Primary

MeasureTime frameDescription
Report on Chest Compression Fraction (CCf)10 minutesCCf is the length of time the patient receives chest compression/management time (describe as a %)

Secondary

MeasureTime frameDescription
Report on Cardiopulmonary Resuscitation (CPR) parameters :Prompt CPR fraction10 minutesPrompt CPR fraction (duration between the two AED announcements resume massage and interrupt massage/ total management time; describe as a %)
Report on Cardiopulmonary Resuscitation (CPR) parameters:Maximal Hands-Off time10 minutesMaximal Hands-Off time (longest time frame without any CC; describe in seconds)
Report on Cardiopulmonary Resuscitation (CPR) parameters:Chest Compression Frequency10 minutesChest Compression Frequency (i.e., measurement of the mobile frequency over 3 to 5 compressions; describe as number of chest compressions by minute)
Report on the diagnostic performance of the AED algorithms during CC and in absence of CC10 minutesCalculate Sensibility and Specificity
Report on the overall diagnostic performance resulting from the combination of the consecutive analyses in presence of CC and in absence of CC10 minutesCalculate Sensibility and Specificity
Report on five-second-post-shock rhythms and their incidence10 minutesasystole, pulseless electrical activity, ventricular tachycardia, ventricular fibrillation for in absence of CC analysis, at 5 seconds
Report on 60-second-post-shock rhythms and their incidence10 minutesasystole, pulseless electrical activity, ventricular tachycardia, ventricular fibrillation for in absence of CC analysis, at 60 seconds
Report on 120 second-post-shock rhythms and their incidence10 minutesasystole, pulseless electrical activity, ventricular tachycardia, ventricular fibrillation for in absence of CC analysis, at 120 seconds
Report on 15-second-post-shock rhythms and their incidence10 minutesasystole, pulseless electrical activity, ventricular tachycardia, ventricular fibrillation for in absence of CC analysis, at 15 seconds
Report on 30-second-post-shock rhythms and their incidence10 minutesasystole, pulseless electrical activity, ventricular tachycardia, ventricular fibrillation for in absence of CC analysis, at 30 seconds
Report on the number of electrical shocks (EES) delivered and the duration of the rhythmic storm1 hourTotal number of EES delivered (describe as a number)
Report on the number of electrical shocks (EES) intended and the duration of the rhythmic storm1 hourRatio number of EES intended / number of EES delivered (describe as a ratio %)
Report on the temporal distribution of electrical shocks (EES) and the duration of the rhythmic storm1 hourEES temporal distribution per patient
Report on the delay from start to end of cumulative VF episodes1 hourThe time period from the start of the first occurence of VF to to the ending of the last episode of ventricular fibrillation (VF) ( seconds)
Report on Cardiopulmonary Resuscitation (CPR) parameters : CPR ratio10 minutesCPR ratio (time during which the patient receives chest compression and bag ventilation / total management time; describe as a %)
The distribution over time of EES.1 hourThe distribution over time of EES.
Outcomes - ROSC2 hoursReturn Of Spontaneous Circulation (ROSC) (describe as a ratio of patients with ROSC / patients included)
Outcomes - admitted alive at hospital2 hoursSurvival to hospital admission (describe as a ratio of patients admitted beating heart to hospital / patients included)
Outcomes - discharged from hospital1 monthSurvival at hospital discharge (describe as a ratio of patients discharged alive from hospital / patients included)
Compare Chest Compression Fraction (CCf) to Paris Fire Brigade 2017 historical data10 minutesCCf is the length of time the patient receives chest compression/management time (describe as a %)
Prompt CPR fraction (duration between the two AED announcements resume massage and interrupt massage/ total management time; describe as a %)10 minutesPrompt CPR fraction (duration between the two AED announcements resume massage and interrupt massage/ total management time; describe as a %)
CPR ratio (time during which the patient receives chest compression and bag ventilation / total management time; describe as a %)10 minutesCPR ratio (time during which the patient receives chest compression and bag ventilation / total management time; describe as a %)
Maximal Hands-Off time (longest time frame without any CC; describe in seconds)10 minutesMaximal Hands-Off time (longest time frame without any CC; describe in seconds)
Chest Compression Frequency (i.e., measurement of the mobile frequency over 3 to 5 compressions; describe as number of chest compressions by minute)10 minutesChest Compression Frequency (i.e., measurement of the mobile frequency over 3 to 5 compressions; describe as number of chest compressions by minute)
Compare Sensibility and Specificity of AED algorithm during CC and in absence of CC to 2017 algorithm Sensibility and Specificity10 minutesCompare Sensibility and Specificity of AED algorithm during CC and in absence of CC to 2017 algorithm Sensibility and Specificity
Compare the overall diagnostic performance resulting from the combination of the consecutive analyses in presence of CC and in absence of CC to Paris Fire Brigade 2017 historical data10 minutesCompare the overall diagnostic performance resulting from the combination of the consecutive analyses in presence of CC and in absence of CC to Paris Fire Brigade 2017 algorithm Sensibility and Specificity
Compare post-shock rhythms and their incidence to Paris Fire Brigade 2017 historical data10 minutesCompare asystole, pulseless electrical activity, ventricular tachycardia, ventricular fibrillation incidence for in presence of CC analysis, at 5 seconds to Paris Fire Brigade 2017 differents rhythms incidences.
Compare number of electrical shocks (EES) and the duration of the rhythmic storm to Paris Fire Brigade 2017 historical data10 minutesTotal number of EES delivered (describe as a number) compare to Paris Fire Brigade 2017 historical data
Outcomes - hospital discharge1 monthCompare survival at hospital discharge to Paris Fire Brigade 2017 historical data (describe as a ratio of patients discharged alive from hospital / patients included)
The time period from the AED-switch-on and the first EES (describe in seconds)1 hourThe time period from the AED-switch-on and the first EES (describe in seconds)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026