To Survive After ICU Discharge
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|ClinicalTrials.gov Identifier: NCT02599636|
Recruitment Status : Unknown
Verified July 2016 by Silvia Cano Hernández, Althaia Xarxa Assistencial Universitària de Manresa.
Recruitment status was: Active, not recruiting
First Posted : November 6, 2015
Last Update Posted : July 14, 2016
Many factors before and after ICU stay determine the outcome of patients at ICU discharge, the type of illness, physical dependence and other sequelae can be a trigger for complications in hospital ward which can induce ICU readmission and worse outcome. The quality of medical assistance during all the hospitalisation should be guaranteed and many complications or fatal events could be avoidable.
The objective of the present study is to demonstrate that collaboration between the intensivist and other medical teams in ward can reduce ICU readmission and hospital mortality after ICU discharge.
|Condition or disease||Intervention/treatment|
|In-Hospital Mortality Number of ICU Readmission Number of Warnings On-duty||Other: None intervention|
Material and Methods This observational multicenter study will be done in 21 medical-surgical ICUs. We will use Sabadell Score like prognostic scale at ICU discharge and the intensivist will collaborate with the medical team in medical assistance of patients at risk (Sabadell Score 1 and 2). Investigators will compare the hospital mortality and the readmission rate with a previous period when this collaboration didn't exist.
Anticipate results The collaboration of attending intensivist might reduce ward mortality after ICU discharge by 3%.
|Study Type :||Observational|
|Estimated Enrollment :||1200 participants|
|Official Title:||Multicenter Prospective Study: To Survive After ICU Discharge|
|Study Start Date :||October 2015|
|Estimated Primary Completion Date :||September 2016|
|Estimated Study Completion Date :||September 2016|
- Other: None intervention
Investigators will study the usual medical assistance
- The decline in hospital mortality [ Time Frame: 3 months ]
- The decline in number of warnings on-duty [ Time Frame: 3 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02599636
|Althaia Xarxa Assistencial Universitaria de Manresa|
|Manresa, Barcelona, Spain, 08243|
|Principal Investigator:||Silvia Cano Hernández, Physician||Althaia Xarxa Assistencial Universitaria de Manresa|