Parameter | Hypotension (nā=ā58) | No hypotension (nā=ā20) | P value |
---|---|---|---|
Age | 65 (57 ā 72) | 66 (54 ā 70) | 0.828 |
Gender, male | 40 (69.0) | 9 (45.0) | 0.056 |
Causes of septic shocka | Ā | Ā | 0.588 |
āPneumonia | 28 (48.3) | 11 (55.0) | Ā |
āIntraabdominal infection | 16 (27.6) | 8 (40.0) | Ā |
āUrogenital infection | 9 (15.5) | 5 (25.0) | Ā |
āCather related infection | 4 (6.9) | 1 (5.0) | Ā |
āEndocarditis | 2 (3.4) | 0 (0.0) | Ā |
āOthersb | 3 (5.2) | 0 (0.0) | Ā |
MAP before initial resuscitation, mmHg | 52 (43 ā 57) | 52 (50 ā 58) | 0.414 |
CVP before initial resuscitation, mmHg | 6 (4 ā 8) | 7 (5 ā 10) | 0.250 |
MAP at the time of vasopressor initiated, mmHg | 55 (51 ā 60) | 54 (50 ā 59) | 0.649 |
CVP at the time of vasopressor initiated, mmHg | 11 (9 -14) | 10 (8 ā 13) | 0.516 |
Total bilirubin, mg/dL | 1.15 (0.50 ā 2.70) | 0.90 (0.60 ā 1.83) | 0.406 |
Serum creatinine, mg/dL | 1.42 (0.95 ā 2.09) | 1.16 (0.76 ā 1.86) | 0.351 |
Lactic acid, mmol/L | 4.19 (2.64 ā 6.07) | 3.15 (2.36 ā 4.99) | 0.329 |
PCT, ng/mL | 11.81 (2.62 ā 34.12) | 15.36 (3.61 ā 54.96) | 0.417 |
CRP, mg/mL | 12.60 (5.83 ā 21.19) | 20.66 (11.97 ā 26.10) | 0.026 |
Maximum NE dose during study period, ug/kg/min | 0.70 (0.50 ā 1.31) | 0.40 (0.31 ā 1.12) | 0.020 |
SAPS3 | 73 (62 ā 74) | 79 (72 ā 90) | 0.297 |
SOFA score | 10 (8 ā 12) | 10 (8 ā 11) | 0.936 |
Clinical status on randomization | |||
āMAP, mmHg | 77 (71 ā 80) | 76 (68 ā 83) | 0.936 |
āCVP, mmHg | 10 (8 ā 14) | 10 (9 ā 13) | 0.606 |
āNeed for mechanical ventilation | 41 (70.7) | 13 (65.0) | 0.635 |
āNeed for renal replacement therapy | 18 (31.0) | 4 (20.0) | 0.344 |
āNeed for dobutamine | 4 (6.9) | 2 (10.0) | 0.643 |
āSOFA score | 12 (10 ā 15) | 12 (9 ā 15) | 0.704 |
āPF ratio | 164.9 (99.1 ā 267.9) | 164.5 (103.1ā 258.5) | 0.972 |
āTotal bilirubin, mg/dL | 1.40 (0.78 ā 3.70) | 1.25 (0.50 ā 3.73) | 0.453 |
āSerum creatinine, mg/dL | 1.26 (0.74 ā 2.10) | 1.01 (0.68 ā 1.26) | 0.093 |
āCorticosteroid treatment | 52 (94.5) | 20 (100.0) | 0.500 |
āCopeptin, pg/mL (nā=ā76) | 144 (105 ā 199) | 223 (109 ā 281) | 0.032 |
āTime to randomization, hours | 23.3 (12.1 ā 44.7) | 24.4 (14.8 ā 30.5) | 0.868 |
MAP at the evaluation of outcomes, mmHg | 62 (59 ā 63) | 72 (67 ā 77) | <ā0.001 |
CVP at the evaluation of outcomes, mmHg | 10 (7 ā 14) | 10 (8 ā 14) | 0.499 |
NE tapering at the evaluation of event outcomes | 46 (79.3) | 11 (55.0) | 0.035 |
AVP tapering at the evaluation of event outcomes | 12 (20.7) | 9 (45.0) | 0.035 |
Total vasopressor duration, hours | 57.8 (39.0 ā 110.6) | 30.8 (21.3 ā 36.7) | <ā0.001 |
Clinical outcomes | |||
āICU mortality | 18 (31.0) | 8 (40.0) | 0.463 |
āICU length of stay, days | 9 (4 ā 13) | 7 (3 ā 12) | 0.387 |
ā28-day mortality | 22 (38.6) | 7 (35.0) | 0.775 |
āHospital mortality | 26 (44.8) | 10 (50.0) | 0.689 |
āHospital length of stay, days | 23 (14 ā 37) | 19 (14 ā 42) | 0.936 |