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Table 1 Demographic and clinical characteristics at initiation of awake ECMO support

From: Extracorporeal membrane oxygenation in non-intubated immunocompromised patients

Characteristic at inclusion

Median (IQR)/no (%)

Number of patients

18

Age—years

54 (36–60)

Sex—no (%)

 

 Male

11 (61.1)

 Female

7 (38.9)

BMI—kg/m2

24.5 (21.3–27.1)

Adipositas (BMI > 30 kg/m2)—no (%)

2 (11.1)

Cause of immunosupression—no (%)

 

 Solid organ transplant

7 (38.9)

 HSCT

6 (33.3)

 AIDS

2 (11.1)

 Rheumatological disease

3 (16.7)

Pathogen—no (%)

 

 Gram + 

2 (11.1)

 Gram−

3 (16.7)

 CMV

1 (5.6)

 Fungal

2 (11.1)

 PcP

8 (44.4)

 Non-identified

5 (27.8)

Comorbidities—no (%)

 

 COPD

3 (16.7)

 Cystic fibrosis

1 (5.6)

 Pulmonary fibrosis

6 (33.3)

 Pulmonary hypertension

1 (5.6)

 Arterial hypertension

5 (27.8)

 Congestive heart failure

1 (5.6)

 Diabetes mellitus

3 (16.7)

 Chronic kidney disease

5 (27.8)

Ventilation support—no (%)

 

 HFNC

1 (5.6)

 NIV

17 (94.4)

Respiratory parameters

 

 FiO2

1 (1–1)

 PEEP—cmH2O

7 (5–8)

 Breaths per minute

32 (29–38)

 Tidal volume—ml

593 (476–786)

 Minute ventilation—l/min

21.3 (13.8–24.4)

 Peak—cmH2O

17 (14–19)

 PaO2—mmHg

65 (58–82)

 PaO2/FiO2—mmHg

72 (65–82)

 PaCO2—mmHg

40 (35–59)

 pH

7.36 (7.3–7.44)

 Lactate—mmol/l

1.5 (1.2–1.9)

 Vasopressor—no (%)

5 (27.8)

 Norepinephrine dose—μg/kg/min

0 (0–0.068)

 Inotropic—no (%)

0 (0)

 Renal replacement therapy—no (%)

1 (5.6)

 SOFA-score (points)

7 (4–8)

Organ dysfunction—no (%)

 

 Respiratory (PaO2/FiO2 < 300)

18 (100)

 Coagulation (thrombocytes < 100)

5 (27.8)

 Liver (bilirubin > 33 μmol/l)

2 (11.1)

 Cardiovascular (dobutamine or noradrenaline)

5 (27.8)

 Neurological (GCS < 13)

0 (0)

 Renal (creatinine > 170 μmol/l)

3 (16.7)

Multi-organ dysfunction—no (%)

 

 Two

11 (61.1)

 Three

1 (5.6)

 Four

1 (5.6)

 Five

0 (0)

 Six

0 (0)

CRP—mg/l

173 (78–226)

PCT—μg/l

0.8 (0.3–1.5)

Creatinine—μmol/l

69 (53–107)

24 h diuresis—ml

1230 (360–2165)

ECMO settings (directly after cannulation)

 

 Veno-venous

18 (100)

Cannulation (inflow–outflow)

 

 Femoral-jugular

16 (88.8)

 Femoral–femoral

1 (5.6)

 Femoral-subclavia

1 (5.6)

Pump speed—rpm

3410 (3030–3671)

Blood flow—l/min

3.6 (3.3–4)

FiO2

100 (100–100)

Sweep gas flow—l/min

3.5 (2–4.1)

  1. Description of the patient cohort (n = 18) that received awake ECMO support. All immunocompromised patients with severe ARDS were non-systematically screened by two ECMO experienced ICU attending intensivists for the possibility of an awake ECMO strategy following inclusion and exclusion criteria that have been previously defined by our group as part of the study describing first use of awake ECMO in ARDS patients (4) (NCT01669863). In general, the exclusion criteria stressed the absence of septic or cardiogenic shock and multi-organ failure
  2. Given are demographic and clinical characteristics at the time of ECMO initiation. Values are presented as median (25–75% interquartile range) or if categorical as numbers and percentage
  3. BMI, Body Mass Index; HSCT, Hematopoietic Stem Cell Transplantation; AIDS, Acquired Immuno Deficiency Syndrome; CMV, Cytomegalovirus; PcP, Pneumocystis carinii Pneumonia; COPD, Chronic Obstructive Pulmonary Disease; HFNC, High Flow Nasula Cannula; NIV, Non Invasive Ventilation; FiO2, Fraction on inspired oxygen; PEEP, Positive End Expiratory Pressure; rpm, rounds per minute; Ppeak, Peak Pressure; SOFA, Sequential Organ Failure Assessment Score; GCS, Glasgow Coma Score; CRP, C Reactive Protein; PCT, Procalcitonin