Impact of the Implementation of a Referral Veno-venous Extracorporeal Membrane Oxygenation Centre on Mortality
Completed
- Conditions
- Extracorporeal Membrane Oxygenation
- Interventions
- Other: Collection of medical data
- Registration Number
- NCT05154071
- Lead Sponsor
- Centre Hospitalier Universitaire Dijon
- Brief Summary
Current evidence suggest that regrouping patient supported by veno-venous ECMO in high-volume centre could improve outcome. A dedicated ECMO unit was implemented in Dijon.
The objective of the present study was to evaluate the implementation of this unit. The hypothesis was that patient taken care within this structured care system would have lower mortality.
This research comprises a retrospective observational study conducted in Dijon university hospital
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 172
Inclusion Criteria
- patient in an adult Dijon ICUs supported by veno-venous ECMO
- patient hospitalized between January the 1st 2011 and June the 30th 2021
Exclusion Criteria
- Refusal to participate,
- patient admitted to pediatric ICU
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description ECMO VV dedicated unit Collection of medical data Patient having benefited from an ECMO within the structured care unit ECMO VV without dedicated unit Collection of medical data Patient having benefited from an ECMO without the structured care unit
- Primary Outcome Measures
Name Time Method Mortality rate 90 days
- Secondary Outcome Measures
Name Time Method Rate of ECMO adverse events through study completion, an average of 3 years Hospital length of stay through study completion, an average of 3 years ICU length of stay through study completion, an average of 3 years
Trial Locations
- Locations (1)
Chu Dijon Bourogne
🇫🇷Dijon, France