Chu Dijon Bourogne
Dijon, 21000, France
NCT Number: NCT05154071
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
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Notify Me18 year and older
All sexes
Observational
Dijon, 21000, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Collection of adverse events, of mortality, length of hospitalization
Time frame: 90 days
Time frame: through study completion, an average of 3 years
Time frame: through study completion, an average of 3 years
Time frame: through study completion, an average of 3 years
Centre Hospitalier Universitaire Dijon
Other
Acronym: ECMO UNIT
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