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We merged the dataset of three large observational studies of invasive ventilation in critically ill patients.
PRIME contains the individual patient data of 3 large observational studies of ventilation, 'PRactice of VENTilation in critically ill patients without ARDS' (PRoVENT), 'PRactice of VENTilation in critically ill patients in Middle-income Countries' (PRoVENT-iMiC) and 'Extubation strategies and in neuro-intensive care unit patients and associations with outcomes' (ENIO).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients receiving invasive ventilation | Patients receiving invasive ventilation, included in PRoVENT, PRoVENT-iMiC, and ENIO |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Invasive ventilation | Other | Invasive ventilation and respiratory support |
|
| Measure | Description | Time Frame |
|---|---|---|
| ICU morality | any mortality occurred during ICU stay | ICU stay, anticipated average 15 days |
| Measure | Description | Time Frame |
|---|---|---|
| Mechanical Power | All variables or parameters recorded from the ventilator, when the patient is under mechanical ventilation, to calculate the mechanical power (calculated in Joule/minute) | During the first 7 days of invasive ventilation |
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All patients in the PRIME database are eligible for participation in the initial analysis presented here. We will exclude patients receiving ventilation fir another reason than acute brain injury.
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PROVENT, PROVENT-iMiC and ENIO included various types of patients, receiving ventilation for different reasons. For this first analysis we will select patients receiving invasive ventilation for acute brain injury.
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| Name | Affiliation | Role |
|---|---|---|
| Marcus J Schultz, Prof | Amsterdam UMC | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) | Amsterdam | Netherlands |
Notably, after this initial analysis of PRIME, the database is available for post-hoc analysis.
After our first pubblication (next six months) and they will remain available for ever
For this, interested investigators will have to provide a detailed analysis plan, containing a testable hypothesis, clearly described endpoints and an analysis plan. After approval, investigators will be provided with a mock database that will allow them to write an analysis script in R. PROVE network investigators will then run the script on the PRIME database and provide the investigators with the results. Any publication from an additional analysis must follow the rules for publication denoted by the PROVE network
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| ID | Term |
|---|---|
| D063087 | Noninvasive Ventilation |
| ID | Term |
|---|---|
| D012121 | Respiration, Artificial |
| D058109 | Airway Management |
| D013812 | Therapeutics |
| D012138 | Respiratory Therapy |
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