Variables | Hypotension on tapering of AVP (nā=ā12) | Hypotension on tapering of NE (nā=ā46) | P value |
---|---|---|---|
Age | 67 (59 ā 69) | 65 (56 ā 73) | 0.773 |
Gender, male | 10 (83.3) | 30 (65.2) | 0.307 |
Causes of septic shocka | Ā | Ā | 0.246 |
āPneumonia | 8 (66.7) | 20 (43.5) | Ā |
āIntraabdominal infection | 2 (16.7) | 14 (30.4) | Ā |
āUrogenital infection | 3 (25.0) | 6 (13.0) | Ā |
āCather related infection | 0 (0.0) | 4 (8.7) | Ā |
āEndocarditis | 0 (0.0) | 2 (4.3) | Ā |
āOthersb | 0 (0.0) | 3 (6.5) | Ā |
MAP before initial resuscitation, mmHg | 53 (47 ā 57) | 51 (42 ā 57) | 0.214 |
CVP before initial resuscitation, mmHg | 7 (3 ā 10) | 6 (6 ā 8) | 0.161 |
MAP at the time of vasopressor initiated, mmHg | 55 (47 ā 57) | 55 (52 ā 60) | 0.612 |
CVP at the time of vasopressor initiated, mmHg | 11 (10 ā 13) | 11 (8 ā 14) | 0.669 |
Total bilirubin, mg/dL | 0.90 (0.35 ā 3.05) | 1.20 (0.50 ā 2.70) | 0.382 |
Serum creatinine, mg/dL | 1.47 (0.71 ā 2.01) | 1.42 (0.97 ā 2.32) | 0.687 |
Lactic acid, mmol/L (nā=ā57) | 3.27 (1.91 ā 4.62) | 4.31 (2.67 ā 6.32) | 0.229 |
Procalcitonin, ng/mL (nā=ā53) | 13.09 (4.18 ā 81.53) | 11.01 (2.61 ā 30.97) | 0.602 |
C-reactive protein, mg/mL | 14.87 (8.51 ā 29.72) | 12.57 (5.59 ā 19.42) | 0.129 |
Maximum NE dose during study period, ug/kg/min | 0.74 (0.54 ā 1.56) | 0.70 (0.46 ā 1.20) | 0.448 |
SAPS3 | 74 (62 ā 86) | 73 (62 ā 84) | 0.931 |
SOFA | 9 (8 ā 13) | 10 (8 ā 12) | 0.601 |
Clinical status on randomization | |||
āMAP, mmHg | 72 (70 ā 78) | 77 (73 ā 81) | 0.138 |
āCVP, mmHg | 10 (8 ā 12) | 10 (8 ā 14) | 0.420 |
āNeed for mechanical ventilation | 10 (83.3) | 31 (67.4) | 0.478 |
āNeed for renal replacement therapy | 4 (33.3) | 14 (30.4) | 1.000 |
āNeed for dobutamine | 1 (8.3) | 3 (6.5) | 1.000 |
āSOFA | 13(11 ā 16) | 12 (9 ā 15) | 0.255 |
āPF ratio | 118.8 (81.9 ā 177.9) | 186.9 (105.4 ā 278.0) | 0.110 |
āTotal bilirubin, mg/dL | 1.35 (0.53 ā 3.68) | 1.40 (0.80 ā 3.88) | 0.744 |
āSerum creatinine, mg/dL | 1.25 (0.60 ā 1.99) | 1.26 (0.81 ā 2.21) | 0.508 |
āCorticosteroid treatment | 10 (90.9) | 42 (95.5) | 0.495 |
āCopeptin, pg/mL (nā=ā56) | 77 (67 ā 90) | 168 (131 ā 207) | <ā0.001 |
āTime to randomization, hours | 25.1 (14.1 ā 41.8) | 21.1 (11.8 ā 46.2) | 0.818 |
Time to discontinuation of vasopressors just before hypotension developed | 28.8 (18.5-44.3) | 22.0 (13.6-47.2) | 0.946 |
Time to hypotension after discontinuation of vasopressor, hours | 2.5 (1.1 ā 3.3) | 2.5 (1.9 ā 4.7) | 0.442 |
āMAP at the time of hypotension developed on tapering of vasopressor, mmHg | 61 (57 ā 63) | 62 (59 ā 63) | 0.214 |
āCVP at the time of hypotension developed on tapering of vasopressor, mmHg | 10 (6 ā 12) | 10 (7 ā 14) | 0.735 |
Total vasopressor duration, hours | 63.4 (38.9 ā 122.6) | 57.8 (38.9 ā 88.0) | 0.578 |
Clinical outcomes | |||
āICU mortality | 5 (41.7) | 13 (28.3) | 0.486 |
āICU length of stay, days | 12 (8 ā 22) | 8 (3 ā 12) | 0.108 |
ā28-day mortality | 5 (41.7) | 17 (37.8) | 1.000 |
āHospital mortality | 6 (50.0) | 20 (46.5) | 0.686 |
āHospital stay, days | 27 (19 ā 30) | 22 (14 ā 39) | 0.617 |