Stress response in the daily lives of simulation repeaters. A randomized controlled trial assessing stress evolution over one year of repetitive immersive simulations
- Others:
- Emergency Department [Paris] ; AP-HP - Hôpital Bichat - Claude Bernard [Paris] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Emergency Medical Service [Paris] ; AP-HP - Hôpital Bichat - Claude Bernard [Paris] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Laboratoire Universitaire Médical d'Enseignement basé sur les technologies Numériques et de Simulation (iLumens - site Paris 7) ; Université Paris Diderot - Paris 7 (UPD7)-Université Sorbonne Paris Cité (USPC)
- Laboratoire d'Anatomie, Biomécanique et Simulation (ABS Lab) ; Université de Poitiers - Faculté de Médecine et de Pharmacie ; Université de Poitiers-Université de Poitiers-Université de Poitiers - Faculté de Sciences fondamentales et appliquées ; Université de Poitiers
- Diagnosis and Therapeutic Center [Paris] ; Hôpital Hôtel-Dieu [Paris] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Service de cardiologie [CHU de Poitiers] ; Centre hospitalier universitaire de Poitiers (CHU Poitiers)
- Adult Psychiatric Unit [Poitiers] ; Centre hospitalier universitaire de Poitiers (CHU Poitiers)
- CIC - Poitiers ; Université de Poitiers-Centre hospitalier universitaire de Poitiers (CHU Poitiers)-Direction Générale de l'Organisation des Soins (DGOS)-Institut National de la Santé et de la Recherche Médicale (INSERM)
- Pediatric Emergency Department [Poitiers] ; Centre hospitalier universitaire de Poitiers (CHU Poitiers)
- DA Ghazali was the recipient of a grant from the French Emergency Medicine Society (SFMU). The commercial company Laerdal (Tanke Svilandsgt 30. Stavanger, 4002. Norway) provided the SFMU with the amount of the grant.
Description
BACKGROUND:Simulations in healthcare reproduce clinical situations in stressful conditions. Repeated stress exposure might influence the learning process in simulation as well as real-life.OBJECTIVES:1) To record heart rate and heart rate variability evolution during one-day simulation over one year; 2) To analyze the effect of repetitive high-fidelity simulations on the risk of post-traumatic stress disorder.STUDY DESIGN:Single-center, investigator-initiated RCT. 48 participants were randomized in 12 multidisciplinary teams of French Emergency Medical Services to manage infant shock in high-fidelity simulations. In the experimental group, 6 multidisciplinary teams were exposed to 9 different simulation sessions over 1 year. In the control group, 6 multidisciplinary teams participated in only 3 simulation sessions, in common with those of the experimental group (initial, intermediate after 6 months, and finally after 1 year). Heart rate (HR) and heart rate variability (HRV) were analyzed on a 24-hour Holter from the day prior to simulation until the end of simulation. Questionnaires of Impact of Event Scale-Revised at 7 days and Post-traumatic Check-List Scale at 1 month were used to detect possible post-traumatic stress disorder in participants. p<0.05 was considered significant.RESULTS:Stress increased during each simulation in the two groups. After analysis on the 24-hour period, there was no significant difference between the two groups during the initial simulation session in terms of heart rate and heart rate variability. In the 24-hour period of the intermediate and final simulation sessions, the level of stress was higher in the control group during the diurnal (p = 0.04) and nocturnal periods (p = 0.01). No participant developed post-traumatic stress disorder after the 72 simulation sessions.CONCLUSIONS:Despite the stress generated by simulation, the more the sessions were repeated, the less were their repercussions on the daily lives of participants, reflected by a lower sympathetic activity. Moreover, repetition of simulations did not lead to post-traumatic stress disorder.TRIAL REGISTRATION:ClinicalTrials.gov NCT02424890.
Abstract
International audience
Additional details
- URL
- https://www.hal.inserm.fr/inserm-02265044
- URN
- urn:oai:HAL:inserm-02265044v1
- Origin repository
- UNICA