ITMO public health
Last update : 08/17/2016 | Version : 1 | ID : 73199
| General | |
| Identification | |
| Detailed name | Electronic Registry of Cardiac Arrests |
| Sign or acronym | RéAC |
| CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | CNIL 910946 |
| General Aspects | |
| Medical area |
Anesthesiology – Intensive care Emergency medicine |
| Pathology (details) | Cardiac arrests |
| Keywords | cardiac arrest, SAMU/SMUR, registry, treatment |
| Scientific investigator(s) (Contact) | |
| Name of the director | Hubert |
| Surname | Hervé |
| Phone | +33 (0)7 81 97 89 95 |
| herve.hubert@univ-lille2.fr herve.hubert@registreac.org | |
| Unit | Lille Public Health Laboratory (EA2694) |
| Organization | Lille University |
| Name of the director | Gueugniaud |
| Surname | Pierre-Yves |
| Address |
Pôle « URMARS » Urgences – Réanimation Médicale – Anesthésie-Réanimation – SAMU Edouard Herriot Hospital Group Place d’Arsonval 69437 Lyon Cedex 03 |
| pierre-yves.gueugniaud@chu-lyon.fr | |
| Organization | Edouard Herriot Hospital Group |
| Collaborations | |
| Participation in projects, networks and consortia |
Yes |
| Details | EuReCA—European Registry of Cardiac Arrest |
| Funding | |
| Funding status |
Mixed |
| Details | French Society of Emergency Medicine — French Society of Anaesthesia and Critical Care Medicine (SFAR); patient foundation — French Cardiology Federation, two research support foundations — Heart and Artery Foundation and CNP Foundation; Lyon University Hospital; University Lille 2; Northern Region and European Community through FEDER funds |
| Governance of the database | |
| Sponsor(s) or organisation(s) responsible | RéAC |
| Organisation status |
Private |
| Presence of scientific or steering committees |
Yes |
| Additional contact | |
| Main features | |
| Type of database | |
| Type of database |
Morbidity registers |
| Database objective | |
| Main objective | The main aim of RéAC is to improve the treatment conditions for cardiac arrest victims, as well as improve the chances of survival for patients. |
| Inclusion criteria | Patients who were victims of out-of-hospital (registry created in July 2011) and in-hospital cardiac arrests (currently in testing phase within volunteer establishments). |
| Population type | |
| Age |
Newborns (birth to 28 days) Infant (28 days to 2 years) Early childhood (2 to 5 years) Childhood (6 to 13 years) Adolescence (13 to 18 years) Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
| Population covered |
Sick population |
| Gender |
Male Woman |
| Geography area |
National |
| Detail of the geography area | France |
| Data collection | |
| Dates | |
| Date of first collection (YYYY or MM/YYYY) | 2011 |
| Size of the database | |
| Size of the database (number of individuals) |
Greater than 20 000 individuals |
| Details of the number of individuals | 45,000 (June 2015) |
| Data | |
| Database activity |
Current data collection |
| Type of data collected |
Clinical data |
| Clinical data (detail) |
Direct physical measures Medical registration |
| Details of collected clinical data | Sociodemographic data; time periods and schedules; history of cardiac arrest; description of accompanying party; immediate outcome for patients. Cardiopulmonary resuscitation. |
| Presence of a biobank |
No |
| Health parameters studied |
Health event/morbidity Health event/mortality Health care consumption and services Quality of life/health perception |
| Procedures | |
| Data collection method | Cardiac arrest intervention sheet completed during procedure by Mobile Emergency and Resuscitation Service (SMUR) teams. |
| Quality procedure(s) used | Monitoring, SDV |
| Participant monitoring |
Yes |
| Details on monitoring of participants | 30-day follow-up for living patients on hospital admission. |
| Links to administrative sources |
No |
| Promotion and access | |
| Promotion | |
| Link to the document | http://registreac.org/?cat=41 |
| Access | |
| Presence of document that lists variables and coding procedures |
Yes |
| Terms of data access (charter for data provision, format of data, availability delay) |
Several access levels are in place:
—Principal data (statistics) at national level are freely available (website); —National data per centre are available to every registered investigator/user; —Database (anonymised) from the centre is available to all centre users (by SMUR, SAMU, entry network); —Full database (anonymised) is available to investigators or external parties by reasoned request (research project, thesis, etc.) to the registry scientific committee. |
| Access to aggregated data |
Free access |
| Access to individual data |
Access on specific project only |
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