Postoperative risk factors | Patients without delirium (n = 443) | Patients with delirium (n = 488) | p-value |
---|---|---|---|
Clinical characteristics | |||
 The presence of atrial fibrillation (AF) rhythm, yes (%) | 8 (1.9) | 55 (11.3) |  < 0.001* |
 Use of invasive arterial blood pressure (IABP), yes (%) | 2 (0.5) | 46 (9.4) |  < 0.001* |
 Electroshock therapy, yes (%) | 2 (0.5) | 11 (2.3) | 0.025* |
 Acute tubular necrosis (ATN), yes (%) | 22 (5.1) | 241 (49.4) |  < 0.001* |
 Need for hemodialysis, yes (%) | 2 (0.5) | 72 (14.8) |  < 0.001* |
 Cerebral vascular accident (CVA), yes (%) | 2 (0.5) | 2 (0.4) | 0.903 |
 Drainage data, median (IQR) | 240 (180–320) | 450 (320–660) |  < 0.001* |
 Red-cell storage time, median (IQR) | 0.001 (0.001–12) | 18 (15–20) |  < 0.001* |
 Sleep quality in first night after surgery, ≤ 270 | 97 (22.5) | 378 (77.5) |  < 0.001* |
 Sleep quality in second night after surgery, ≤ 240 | 37 (8.6) | 201 (41.2) |  < 0.001* |
 Use of physical restraint, yes (%) | 423 (97.9) | 478 (98) | 0.971 |
 ICU-OH length of stay, ≥ 4 days | 26 (6) | 407 (83.4) |  < 0.001* |
 Hospital length of stay, ≥ 9 days | 50 (11.6) | 393 (80.5) |  < 0.001* |
Blood transfusion data | |||
 Blood product, packed red blood cells (PRBC) | 42 (9.7) | 266 (54.5) |  < 0.001* |
 Blood product, platelets | 390 (90.3) | 222 (45.5) |  |
Environmental factors | |||
 Lux measurement in the morning, ≥ 54 (%) | 368 (85.2) | 390 (79.9) | 0.036* |
 Lux measurement in the evening, ≥ 260 (%) | 409 (94.7) | 456 (93.4) | 0.431 |
 Lux measurement in the night, ≥ 271 (%) | 358 (82.9) | 415 (85) | 0.370 |
 Sound metrics in the morning, ≥ 41 (dB) | 29 (6.7) | 38 (7.8) | 0.532 |
 Sound metrics in the evening, ≥ 65 (dB) | 111 (25.7) | 153 (31.4) | 0.058 |
 Sound metrics in the night, ≥ 53 (dB) | 90 (20.8) | 124 (25.4) | 0.101 |
 Temperature, ≥ 27 °C | 260 (60.2) | 311 (63.7) | 0.269 |
 Humidity, ≥ 11% | 284 (65.7) | 322 (66) | 0.938 |
 Bed position, natural light (NL) group, near to window | 239 (55.3) | 229 (46.9) | 0.011* |
Medication data | |||
 Midazolam, ≥ 7 (%) | 103 (23.8) | 331 (67.8) |  < 0.001* |
 Morphine, ≥ 9 (%) | 72 (16.7) | 213 (43.6) |  < 0.001* |
 Fentanyl drip, ≥ 0.21 (%) | 188 (43.5) | 358 (73.4) |  < 0.001* |
 Dexmedetomidine, ≥ 400 (%) | 288 (66.7) | 275 (56.4) | 0.001* |
 Dexamethasone, ≥ 9 (%) | 145 (33.6) | 128 (26.2) | 0.015* |
 Norepinephrine, ≥ 1 (%) | 5 (1.2) | 110 (22.5) |  < 0.001* |
Laboratory data | |||
 Sodium levels in first day, ≥ 140 (mEq/L) | 235 (54.4) | 260 (53.3) | 0.734 |
 Sodium levels in second day, ≥ 140 (mEq/L) | 196 (45.4) | 255 (52.3) | 0.037* |
 Sodium levels in third day, ≥ 140 (mEq/L) | 219 (50.7) | 254 (52) | 0.692 |
 Potassium levels in first day, ≥ 4.21 (mEq/L) | 191 (44.2) | 256 (52.5) | 0.013* |
 Potassium levels in second day, ≥ 4.21 (mEq/L) | 185 (42.8) | 276 (56.6) |  < 0.001* |
 Potassium levels in third day, ≥ 4.21 (mEq/L) | 201 (46.5) | 291 (59.6) |  < 0.001* |
 Hematocrit levels in first day, ≥ 26.11 | 282 (65.3) | 171 (35) |  < 0.001* |
 Hematocrit levels in second day, ≥ 27.61 | 283 (65.5) | 182 (37.3) |  < 0.001* |
 Hematocrit levels in third day, ≥ 29.21 | 282 (65.3) | 186 (38.1) |  < 0.001* |
 Minimum blood glucose in first day, ≤ 175 (mg/dL) | 270 (62.5) | 186 (38.1) |  < 0.001* |
 Maximum blood glucose in first day, ≥ 242 (mg/dL) | 164 (38) | 312 (63.9) |  < 0.001* |
 Minimum blood glucose in second day, ≤ 155 (mg/dL) | 264 (61.1) | 194 (39.8) |  < 0.001* |
 Maximum blood glucose in second day, ≥217 (mg/dL) | 152 (35.2) | 309 (63.3) | <0.001* |
 Minimum blood glucose in third day, ≤133 (mg/dL) | 246 (56.9) | 211 (43.2) | <0.001* |
 Maximum blood glucose in third day, ≥176 (mg/dL) | 161 (37.3) | 304 (62.3) | <0.001* |
 Lactate levels in first day, ≥4.71 (mmol/L) | 129 (29.9) | 331 (67.8) | <0.001* |
 Lactate levels in second day, ≥3.1 (mmol/L) | 136 (31.5) | 343 (70.3) | <0.001 |
 Lactate levels in third day, ≥1.41 (mmol/L) | 117 (27.1) | 332 (68) | <0.001* |