Center ID
Item
ID of Center
text
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Patient ID
Item
ID of patient
text
C2348585 (UMLS CUI [1])
Critical ill patients with acute kidney injury
Item
1) Patients who are critical ill with acute kidney injury (KDIGO Stadium 3)
boolean
C0010340 (UMLS CUI [1,1])
C0022660 (UMLS CUI [1,2])
Clinical indication for Renal Replacement Therapy
Item
2) Clinical indication for Renal Replacement Therapy?
boolean
C0392360 (UMLS CUI [1,1])
C0206074 (UMLS CUI [1,2])
Informed Consent
Item
Written informed consent? (given by patient or authorized representative or relative or carers or confirmation of emergency situation)
boolean
C0021430 (UMLS CUI [1])
Cardiovascular score
Item
Cardiovascular score (please record point value)
float
C0007226 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
Item
Urine amount
text
C1822256 (UMLS CUI [1])
CL Item
Oliguria (Oliguria)
CL Item
Normuria (Normuria)
Item
Patient's gender
text
C0079399 (UMLS CUI [1])
Code List
Patient's gender
Intensive Care duration
Item
Unlimited intesive care is planned at least for 3 days?
boolean
C0085559 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Age
Item
Age: 18 - 90 years old?
boolean
C0001779 (UMLS CUI [1])
Item
I. Severe sepsis or septic shock?
text
C1719672 (UMLS CUI [1])
C0036983 (UMLS CUI [2])
Code List
I. Severe sepsis or septic shock?
CL Item
unknown (unknown)
Item
II. Higher usage of catecholamine therapy? (Norepinephrine or Epinephrin ≥ 0,1 μg/kg/min OR Norepinephrine ≥ 0,05 μg/kg/min + Dobutamine each dose OR Norepinephrine ≥ 0,05 μg/kg/min + Vasopressin each dose OR Norepinephrine ≥ 0,05 μg/kg/min + Epinephrine ≥ 0,05 μg/kg/min
text
C0007412 (UMLS CUI [1])
Code List
II. Higher usage of catecholamine therapy? (Norepinephrine or Epinephrin ≥ 0,1 μg/kg/min OR Norepinephrine ≥ 0,05 μg/kg/min + Dobutamine each dose OR Norepinephrine ≥ 0,05 μg/kg/min + Vasopressin each dose OR Norepinephrine ≥ 0,05 μg/kg/min + Epinephrine ≥ 0,05 μg/kg/min
CL Item
unknown) (unknown))
Item
III. Development or deterioration of lung oedema due to refractory fluid overload (PaO2/ FiO2 < 300 mmHg and/or fluid balance > 10% of starting body weight)
text
C0034063 (UMLS CUI [1])
Code List
III. Development or deterioration of lung oedema due to refractory fluid overload (PaO2/ FiO2 < 300 mmHg and/or fluid balance > 10% of starting body weight)
CL Item
unknown (unknown)
Exclusion Criteria at Randomization
Item
If there is any exclusion Criteria at Randomization fulfilled, exclude the patient and do not randomize him/her. Is any of the exclusion Criteria positive?
boolean
C0680251 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
Item
Result of Randomization:
text
C1274040 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
Code List
Result of Randomization:
CL Item
Regional citrate group (Regional citrate group)
CL Item
Systemic heparin group (Systemic heparin group)