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Table 1 Clinical characteristics of study cohort

From: Key characteristics impacting survival of COVID-19 extracorporeal membrane oxygenation

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)

 
  1. 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