N17
Conditions
Interventions
Group 1: All patients will be assessed for their medical history, postoperative renal function and implemented measures of care. All data will be extracted from the medical records.
Preoperative data
Sponsors
Department of Anesthesiology, Intensive Care and Pain Medicine, University Hospital Münster
Eligibility
Sex/Gender
All
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: 1. Adult patients undergoing cardiac surgery with CPB 2. Age between 18-90 years 3. Written informed consent
Exclusion criteria
Exclusion criteria: 1. Preexisting AKI (stage 1 and higher) 2. Patients with cardiac assist devices (ECMO, LVAD, RVAD, IABP) 3. Pregnancy, breastfeeding 4. Known (Glomerulo-) Nephritis, interstitial nephritis or vasculitis 5. Chronic kidney disease (CKD) with eGFR < 20 ml/min/1.73m2 6. Dialysis dependent CKD 7. Prior kidney transplant within the last 12 months 8. Persons held in an institution by legal or official order 9. Persons with any kind of dependency on the investigator or employees by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the adherence to the preventive care bundle according to the KDIGO guidelines in patients undergoing cardiac surgery with cardiopulmonary bypass | — |
Secondary
| Measure | Time frame |
|---|---|
| - occurrence of AKI within 72 hours after cardiac surgery - severity stage of AKI within 72 hours after cardiac surgery - use and duration of renal replacement therapy (RRT) - length of ICU stay - length of hospital stay - MAKE30 (combined endpoint consisting of persistent renal dysfunction (defined as serum creatinine = 1.5-times baseline), RRT and mortality) at day 30) | — |
Countries
Germany, Russia, Spain
Contacts
Public ContactChristina Massoth
Klinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie, Universitätsklinik Münster
Outcome results
None listed