Status epilepticus Nervous System Diseases
Conditions
Interventions
All participating physicians will receive a standardized introduction of the technicalities of the simulator and the simulator room. Participating physicians will be asked if they would like to volunt
Sponsors
University Hospital Basel
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Volunteering medical doctors working as resident physicians in different medical fields, including intensive care medicine, emergency medicine, internal medicine, and neurology
Exclusion criteria
Exclusion criteria: Physicians already having participated in the same simulated clinical scenario
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Time to airway protection 2. Time to administration of supplementary oxygen 3. Time to administration of first- and second-line antiseizure drugs All times are measured during simulation (i.e. time from start of simulated scenario to action/treatment). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Assessment of vital signs and neurologic status 2. Ascertainment of medical history and laboratory results 3. Performance of and time to assessment of treatment responsiveness 4. Correct aftermath reporting of clinical characteristics, management aspects, diagnosis and etiology 5. Subjective self-evaluation, including subjective stress level, quality of their performance, the performance of the nurse and certainty of diagnosis, assessed using a questionnaire Secondary outcomes 1-4 are assessed by analyses of the audio-video recordings by two independent investigators. In cases of disagreement or discrepancies, re-analysis of the recordings are performed to reach consensus. | — |
Countries
Switzerland
Outcome results
None listed