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. 2018 Feb 27;8:31. doi: 10.1186/s13613-018-0375-9

Table 1.

Baseline patient characteristics

Pre-ECMO team period (n = 70) Post-ECMO team period (n = 46) P value
Age (years) 61 (52–69) 60 (52–64) 0.672
Male 52 (74.3) 34 (73.9) 0.964
Body mass index (kg/m2) 23.1 (20.7–24.8) 23.8 (20.6–25.8) 0.163
Comorbidity
 Cardiovascular disease 7 (10.0) 5 (10.9) >0.999
 Chronic renal failure 6 (8.6) 3 (6.5) >0.999
 Asthma/COPD 12 (17.1) 2 (4.4) 0.039
 Liver cirrhosis 3 (4.3) 3 (6.5) 0.680
 Malignancy 0.052
  Solid tumor 18 (25.7)a 6 (13.0)b
  Hematologic malignancy 11 (15.7)c 5 (10.9)d
 Immunocompromised state 23 (32.9) 17 (37.0) 0.650
 Cardiac arrest before ECMO 8 (11.4) 10 (21.7) 0.134
Primary diagnosis
 Bacterial pneumonia 32 (45.7) 12 (26.1) 0.033
 Viral pneumonia 2 (2.9) 8 (17.4) 0.014
 Interstitial lung disease 15 (21.4) 5 (10.9) 0.141
 Trauma/burn 2 (2.9) 4 (8.7) 0.212
 Asphyxia 1 (1.4) 1 (2.2) >0.999
 Othere 18 (25.7) 16 (34.8) 0.294
Severity score on the first day in the ICU
 APACHE II 18 (15–25) 25 (21–32) <0.001
 SOFA 6 (4–9) 8 (6–14) 0.003
 RESP score 1 (−1 to 2) 0 (−2 to 2) 0.171
 PRESERVE score 5 (4–7) 6 (4–7) 0.664

Values are given as the median (interquartile range) or n (%)

APACHE II acute physiology and chronic health evaluation II, COPD chronic obstructive pulmonary disease, ECMO extracorporeal membrane oxygenation, ICU intensive care unit, PRESERVE predicting death for severe ARDS on VV-ECMO, RESP respiratory extracorporeal membrane oxygenation survival prediction, SOFA sequential organ failure assessment

aMeningioma (n = 1), malignant mesothelioma (n = 1), lung (n = 10), esophageal (n = 2), liver (n = 2), and colon cancer (n = 2)

bAcute myeloid leukemia (n = 3), acute lymphocytic leukemia (n = 1), chronic lymphocytic leukemia (n = 1), myelodysplastic syndrome (n = 4), and multiple myeloma (n = 2)

cGlioma (n = 1), lung cancer (n = 2), colon cancer (n = 2), and non-seminomatous germ cell tumor (n = 1)

dAcute myeloid leukemia (n = 1), multiple myeloma (n = 1), and lymphoma (n = 3)

eOther includes radiation therapy-induced pneumonitis, pulmonary tuberculosis, diffuse alveolar hemorrhage, pulmonary alveolar proteinosis, and airway occlusion by tumor mass or blood clot