observational
studies in the ICU
observational
studies in the ICU
connect with Sabrine Hemmes or Lorenzo Ball for general inquiries about the featured studies; each study includes a specific contact address for study–related questions
[1] PRoVENT
the ‘Epidemiological characteristics, practice of ventilation, and clinical outcomes in patients at risk of ARDS’ (PRoVENT) was an international multicenter observational prospective study undertaken at 119 ICUs in 16 countries worldwide
PRoVENT is registered at clinicaltrials (NCT01868321); the primary analysis was published in THE LANCET Respiratory Medicine (2016; 4:882)
the database of PRoVENT is harmonized with those from other observational studies, including PROVENT–iMiC, ERICC and LUNG SAFE in a pooled database
connect with Ary Serpa Neto or David van Meenen for secondary analyses of the PRoVENT database
[2] PRoVENT–iMiC
the ‘PRactice of VENTilation in Middle–income Countries’ (PRoVENT–iMiC) was an international multicenter observational study undertaken in approximately 60 ICUs in 11 Asian countries
PRoVENT–iMiC is registered at clinicaltrials (NCT03188770); the study protocol was published in British Medical Journal (2018; 8:e020841); the primary analysis was published in American Journal of Tropical Medicine & Hygiene (2021; 104:1022)
the database of PRoVENT–iMiC is harmonized with those from other observational studies, including PROVENT, the 'Clinical outcomes of patients requiring ventilatory support in Brazilian ICUs' (ERICC) and 'Large Observational Study to Understand the Global Impact of Severe Acute Respiratory Failure' (LUNG SAFE) into a pooled database named PRoPERLy
connect with Luigi Pisani or David van Meenen for secondary analyses of the PRoVENT–iMiC database
[3] LAMINAR
the ‘Local Assessment of Management of Burn Patients’ (LAMINAR) was an international multicenter observational study in burn patients
LAMINAR is registered at clinicaltrials (NCT02312869); the primary analysis was published in Burns & Trauma (2021; 9:34)
the database of LAMINAR is not harmonized with other observational studies, and not available for secondary analyses
[4] ENIO
PROVE Network supported the ‘Extubation Strategies in Neurocritical Care Patients’ (ENIO), an international multicenter observational study undertaken in 73 ICUs in 18 countries
ENIO is registered at clinicaltrials (NCT03400904); the study protocol was published in Annals of Translational Medicine (2020; 8:503); the primary analysis was published in Intensive Care Medicine (2022; 48:1539)
the database of ENIO is harmonized with those from PROVENT and PRoVENT–iMiC' into a pooled database named PRIME
the database of the soon to start ‘Extubation Strategies in Neurocritical Care Patients in Middle–income Countries’ (ENIO–iMiC) will be mergable with ENIO
connect with Raphael Cinotti and Chiara Robba for secondary analyses of the ENIO database
[5] VESPer
'Ventilatory Support in Pediatric Intensive Care Unit Patients' (VESPer) assessed ventilatory support settings in critically ill pediatric patients across European centers, and explored ventilatory support variables and parameters amongst various groups of critically ill patients receiving invasive or noninvasive ventilation
VESPer served as a pilot for PRoVENT–PED, an international multicenter prospective observational study (registered at clinicaltrials NCT06220825)
connect with Martin Kneyber or David van Meenen for secondary analyses of the VESPer database
[6] PRoVENT–PED
the ‘PRactice of VENTilation in PEDiatric patients’ (PRoVENT–PED) is an international multicenter prospective observational study, planned to capture data on epidemiology, ventilation characteristics, and outcomes in critically ill children
PRoVENT–PED is registered at clinicaltrials (NCT06220825); the study protocol will be made available soon (pending)
the study has started per March 1, 2024
PRoVENT–PED is designed so that its database can be harmonized and pooled with PRoVENT and PRoVENT 2+.
contact us in case you have questions
[7] REPOrt
the ‘REhabilitation and Physiotherapy in critically ill patients and association with Ventilator Free Days, Outcome, and Quality Of Life’ (REPOrt) is a new international multicenter observational study focusing on practice of physiotherapy and ventilation in critically ill ventilated patients
REPOrt will be registered at clinicaltrials (pending); the study protocol will be made available (pending)
the study protocol is currently under ethical consideration; more information can be found at the REPOrt website
REPOrt is designed so that its database can be harmonized and pooled with those from PRoVENT and PRoVENT 2+
contact us in case you have questions
[8] PRoVENT 2+
the ‘Update on the PRactice of mechanical VENTilation in non-ARDS patients’ (PRoVENT 2+) is a new international multicenter prospective observational study, planned to capture data on epidemiology, ventilation characteristics, and outcomes in critically ill patients
PRoVENT 2+ will be registered at clinicaltrials (pending); the study protocol will be made available (pending)
the study protocol is currently under ethical consideration
PRoVENT 2+ is the succesor of PRoVENT, and is designed so that their databases can be harmonized and pooled
contact us in case you have questions
connect with us if you want to join one of the running studies