This study aims to investigate the quality of life and the outcome after veno-venous extracoporeal membrane oxygenation (ECMO) support fir severe acute respiratory syndrome (ARDS) in COVID-19 patients.
The investigators follow our COVID-19 patients supported by ECMO, we make phone calls or real-life visits to pthe patients to score the quality of life, by using the SF-36. The SF-36 measures eight scales: physical functioning, role physical, bodily pain, general health, vitality , social functioning , role emotional , and mental health. The participants are contacted 3 months, 6months, 1year and 2 years after the ECMO support started for evaluation of the SF-36.
Study Type
OBSERVATIONAL
Enrollment
28
veno-venous extracorporeal membrane oxygenation
Ghent university hospital
Ghent, Belgium
in-hospital mortality
Time frame: mortality during hospitalisation, up to two years
Quality of life 1y after ECMO insertion
Result of SF-36 1 year after VV-ECMO insertion
Time frame: 1 year
Quality of life 2y after ECMO insertion
Result of SF-36 2 years after VV-ECMO insertion
Time frame: 2 years
Lung complications requiring surgical treatment
Hemothorax or lung abcedation
Time frame: From the start of VV-ECMO support until weaning of VV-ECMO, up to two years
Duration of mechanical ventilation
Time frame: 2 years
LOS ICU
length of stay at the intensive care unit
Time frame: from the day of intensive care unit admission until the day of transfer to the ward, up to two years
LOS hospital
length of stay at the hospital
Time frame: from the day of hospital admission until the day that the participant is transferred to home, up to two years
death after hospital discharge
all-cause death
Time frame: after discharge from the hospital upon 2 years after
Incidence of acute kidney injury
Time frame: from the day of hospital admission until the day that the participant is transferred to home, up to two years
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