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. 2022 Jun 28;26:190. doi: 10.1186/s13054-022-04053-6

Table 1.

Clinical characteristics of study cohort

n Level Overall—n (%) Survivor—n (%) Non-survivor—n (%) p
673 (100) 211 (31.4) 462 (68.6)
(1) Demographics, Risk factors, comorbidities
Date of hospital admission 04/2020–06/2020 186 (27.6) 75 (35.5) 111 (24.0) 0.0019
07/2020–03/2021 487 (72.4) 136 (64.5) 351 (76.0)
Age [years] 19–40 50 (7.4) 29 (13.7) 21 (4.6)  < 0.0001
41–70 578 (85.9) 178 (84.4) 400 (86.6)
 > 70 42 (6.2) 4 (1.9) 38 (8.2)
Missing 3 (0.4) 0 (0.00) 3 (0.7)
Sex m 535 (79.5) 161 (76.3) 374 (81,095) 0.3661
w 131 (19.5) 48 (22.8) 83 (18.0)
Missing 7 (1.0) 2 (0.9) 5 (1.1)
BMI [kg/m2]  < 25 81 (12.0) 21 (10.0) 60 (13.0) 0.0414
25–30 263 (39.1) 83 (39.3) 180 (39.0)
30–35 147 (21.8) 43 (20.4) 104 (22.5)
 ≥ 35 157 (23.3) 61 (28.9) 96 (20.8)
Missing 25 (3.7) 3 (1.4) 22 (4.8)
Cardiovascular disease No 226 (33.6) 82 (38.9) 144 (31.2) 0.1323
Yes 416 (61.8) 119 (56.4) 297 (64.3)
Missing 31 (4.6) 10 (4.7) 21 (4.6)
Chronic pulmonary disease No 564 (83.8) 179 (84.8) 385 (83.3) 0.8043
Yes 103 (15.3) 31 (14.7) 72 (15.6)
Missing 6 (0.9) 1 (0.5) 5 (1.1)
Diabetes mellitus No 483 (71.8) 153 (72.5) 330 (71.4) 0.9401
Yes 186 (27.6) 57 (27.0) 129 (27.9)
Missing 4 (0.6) 1 (0.5) 3 (0.7)
Moderate to severe kidney disease No 619 (92.0) 192 (91.0) 427 (92.4) 0.6161
Yes 49 (7.3) 18 (8.5) 31 (6.7)
Missing 5 (0.7) 1 (0.5) 4 (0.9)
Immunosuppression within 6 months prior to admission No 523 (77.7) 158 (74.9) 365 (79.0) 0.0334
Yes 39 (5.8) 8 (3.8) 31 (6.7)
Unknown 111 (16.5) 45 (21.3) 66 (14.3)
(2) Severity of disease, laboratory parameters (day 1)
EOLIA criteria Met 284 (42.2) 108 (51.2) 176 (38.1) 0.0014
Not met 389 (57.8) 103 (48.8) 286 (61.9)
Indication of ECMO Hypoxemia 419 (62.3) 126 (59.7) 293 (63.4) 0.5229
Hypercapnia 141 (21.0) 43 (20.4) 98 (21.2)
Lung protective ventilation 48 (7.1) 16 (7.6) 32 (6.9)
Right heart failure 2 (0.3) 1 (0.5) 1 (0.2)
Left heart failure 4 (0.6) 1 (0.5) 3 (0.6)
Cardiopulmonary resuscitation 6 (0.9) 0 (0.0) 6 (1.3)
Pulmonary embolism 3 (0.4) 3 (1.4) 0 (0.0)
Other 9 (1.3) 5 (2.4) 4 (0.9)
Intubation prior to ECMO [days]  < 5 275 (40.9) 102 (48.3) 173 (37.4) 0.0004
5–7 102 (15.2) 20 (9.5) 82 (17.7)
 ≥ 8 179 (26.6) 44 (20.9) 135 (29.2)
No prior intubation 75 (11.1) 33 (15.6) 42 (9.1)
Missing 42 (6.2) 12 (5.7) 30 (6.5)
Creatinine [mg/dl]  ≤ 1.17 313 (46.5) 99 (46.9) 214 (46.3) 0.8757
 > 1.17 304 (45.2) 93 (44.1) 211 (45.7)
Missing 56 (8.3) 19 (9.00) 37 (8.0)
Mode of ventilation Spontaneous 18 (2.67) 9 (4.27) 9 (1.95) 0.3042
Assisted 71 (10.55) 19 (9.00) 52 (11.26)
Controlled 544 (80.83) 170 (80.57) 374 (80.95)
Missing 40 (5.94) 13 (6.16) 27 (5.84)
Lung compliance [ml/cm H2O] 25.5 [18.1, 34.2] 26.0 [17.6, 35.7] 25.4 [18.4, 33.9] 0.7168
(3) ECMO and adjunct therapy
Mode of ECMO VV 651 (96.7) 205 (97.2) 446 (96.5) 0.5104
VA 12 (1.8) 2 (0.9) 10 (2.2)
VVA 10 (1.5) 4 (1.9) 6 (1.3)
Cannula Single lumen 544 (80.8) 153 (72.5) 391 (84.6) 0.0028
Double lumen 52 (7.7) 22 (10.4) 30 (6.5)
Unknown 70 (10.4) 33 (15.6) 37 (8.0)
Missing 7 (1.0) 3 (1.4) 4 (0.9)
Case volume ECMO center [n/year] Low (< 20) 96 (14.3) 19 (9.0) 77 (16.7) 0.0024
Intermediate (20–49) 329 (48.9) 97 (46.0) 232 (50.2)
High (≥ 50) 248 (36.9) 95 (45.0) 153 (33.1)
Duration of ECMO support [h] 312.5 [144.0, 528.0] 336.0 [178.2, 560.8] 300.0 [120.0, 502.5] 0.0046
Prone positioning No 240 (35.7) 64 (30.3) 176 (38.1) 0.1314
Yes 333 (49.5) 111 (52.6) 222 (48.1)
Missing 100 (14.9) 36 (17.1) 64 (13.9)
Therapeutic Anticoagulation No 53 (7.9) 22 (10.4) 31 (6.7) 0.0968
Yes 620 (92.1) 189 (89.6) 431 (93.3)
(4) Complications during ECMO
Major bleeding or thromboembolic event No 231 (34.3) 97 (46.0) 134 (29.0)  < 0.0001
Yes 442 (65.7) 114 (54.0) 328 (71.0)
Secondary bacterial infection (respiratory tract or bloodstream) No 239 (35.5) 81 (38.4) 158 (34.2) 0.2921
Yes 434 (64.5) 130 (61.6) 304 (65.8)
Renal replacement therapy No 282 (41.9) 123 (58.3) 159 (34.4)  < 0.0001
Yes 391 (58.1) 88 (41.7) 303 (65.6)

Clinical characteristics of study cohort. Clinical characteristics in total population (n = 673) and survivor (n = 211) vs. non-survivor (n = 462). Parameters were slit up into blocks: (1) Demographics, Risk factors, Comorbidities; (2) Severity of Disease, Laboratory Parameters (day 1); (3) ECMO and adjunct therapy; (4) Complications during ECMO. Descriptive statistics are expressed as frequencies for categorical variables (including a category for missing data). Lung compliance is expressed as median (IQR) and data are missing for 34%, since the parameter was recorded in controlled ventilated patients only. Differences between groups were tested using the Mann–Whitney U test (continuous variables), χ2 test (categorical variables) or Fisher’s exact test (categorical variables with observed frequencies < 5), as appropriate