All patients | Survivors | Non-Survivors | p | |
---|---|---|---|---|
n | 55 | 25 (45%) | 30 (55%) | |
Male | 43 (78%) | 17 (68%) | 26 (87%) | 0.090 |
Age [years] | 65 (58; 69) | 63 (57; 68) | 68 (61; 71) | < 0.05 |
Body-Mass-Index [kg/m2] | 28 (25; 36) | 31 (25; 36) | 28 (25; 31) | 0.723 |
Time from first symptom to hospital admission [days] | 6 (4; 10) | 6 (4; 8) | 7 (4; 10) | 0.416 |
Time from first symptom to ICU admission [days] | 10 (6; 14) | 10 (6; 15) | 9 (6; 14) | 0.442 |
Time from first symptom to invasive ventilation [days] | 10 (6; 15) | 10 (6; 17) | 11 (7; 14) | 0.629 |
Time from first symptom to ECMO therapy [days] | 17 (13; 23) | 19 (11; 23) | 16 (14; 21) | 0.769 |
Time from first symptom to admission to our ICU [days] | 12 (7; 17) | 13 (8; 18) | 12 (7; 16) | 0.741 |
Nosocomial infection | 8 (15%) | 3 (12%) | 5 (17%) | 0.841 |
UFH dose [IE/h] * | 1500 (1100; 1900) | 1600 (1100; 1900) | 1450 (1050; 1750) | 0.327 |
UFH dose [IE/kg/h] * | 17 (11; 20) | 18 (14; 21) | 15 (9; 20) | 0.203 |
LMWH dose [mg/d] * | 120 (100; 180) | 120 (80; 120) | 130 (120; 180) | 0.329 |
LMWH dose [mg/kg/d] * | 1.5 (1.1; 2) | 1.2 (1.1; 1.2) | 1.6 (1.5; 2.0) | 0.429 |
Prophylactic ACT * | 12 (22%) | 5 (20%) | 7 (23%) | 0.514 |
Intermediate ACT * | 26 (47%) | 14 (56%) | 12 (40%) | 0.181 |
Therapeutic ACT * | 17 (30%) | 6 (24%) | 11 (37%) | 0.237 |
VV-ECMO therapy | 22 (40%) | 12 (48%) | 10 (33%) | 0.269 |
Direct transfer to our ICU from other hospital | 34 (62%) | 17 (68%) | 17 (57%) | 0.389 |
Invasive mechanical ventilation before admission to our ICU | 13 (24%) | 13 (52%) | 0 | < 0.05 |
SOFA score [points] * | 11 (10; 13) | 10 (9; 11) | 12 (11; 14) | < 0.05 |
Horovitz – Index at admission to our ICU without patients under ECMO therapy [mmHg] | 146 (114; 219) | 204 (138; 220) | 129 (111; 179) | 0.118 |
ARDS level mild * | 11 (20%) | 7 (28%) | 4 (13%) | 0.176 |
ARDS level moderate * | 19 (35%) | 5 (20%) | 14 (47%) | < 0.05 |
ARDS level severe * | 25 (45%) | 13 (52%) | 12 (40%) | 0.373 |
Norepinephrine [mg/h] * | 0.5 (0.3; 1.1) | 0.4 (0.15; 0.7) | 0.8 (0.4; 1.4) | < 0.05 |
Norepinephrine [µg/kg/min] * | 0.09 (0.05; 0.24) | 0.07 (0.02; 0.12) | 0.14 (0.07; 0.31) | < 0.05 |
Charlson comorbidity index [points] | 3 (2; 5) | 3 (2; 5) | 3 (2; 6) | 0.148 |
Terminal renal insufficiency with need of Renal Replacement Therapy | 3 (6%) | 0 | 3 (10%) | 0.147 |
Systemic thrombolysis before admission to our ICU | 3 (6%) | 1 (4%) | 2 (7%) | 0.569 |
Oral anticoagulation before hospital admission | 5 (9%) | 4 (17%) | 1 (3%) | 0.122 |
Single platelet inhibition before hospital admission | 10 (18%) | 5 (20%) | 5 (17%) | 0.510 |
Dual platelet inhibition before hospital admission | 1 (2%) | 0 | 1 (3%) | 0.545 |
All Patients with complications related to coagulopathy* | 31 (56%) | 15 (60%) | 16 (53%) | 0.412 |
All patients with bleeding complications | 10 (18%) | 5 (20%) | 5 (17%) | 0.510 |
BARC-classification II | 4 (7%) | 2 (8%) | 2 (7%) | 0.622 |
BARC-classification III-V | 8 (15%) | 4 (16%) | 4 (13%) | 0.573 |
All ATE/VTE during hospital stay | 27 (49%) | 14 (56%) | 13 (43%) | 0.620 |
ATE/VTE diagnosed before admission to our ICU | 22 (40%) | 11 (44%) | 11 (37%) | 0.391 |
New ATE/VTE diagnosed during stay on our ICU | 5 (9%) | 3 (12%) | 2 (7%) | 0.412 |