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. 2014 Oct 15;31(20):1721–1732. doi: 10.1089/neu.2014.3361

Table 1.

Study Population Characteristics

    Six-month mortality   Six-month neurological outcomeb  
Variable All patients (n=895) Survivors (n=684) Nonsurvivors (n=206) p valuea Favorable outcome (n=448) Unfavorable outcome (n=394) p valuec
Baseline characteristics
Age 58 (44–68) 55 (41–65) 65 (56–73) <0.001 51 (35–63) 63 (54–72) <0.001
Chronic comorbidity
 Cardiovascular 8 (1) 5 (1) 3 (2) 0.396d 2 (0) 6 (2) 0.156d
 Respiratory 10 (1) 7 (1) 3 (2) 0.705d 4 (1) 5 (1) 0.741d
 Hepatic 14 (2) 8 (1) 6 (3) 0.105d 6 (1) 8 (2) 0.591d
 Renal 2 (0) 1 (0) 1 (1) 0.410d 0 (0) 2 (1) 0.219d
 Immunosuppression 28 (3) 14 (2) 13 (6) 0.002 9 (2) 18 (5) 0.035
Admission GCS
 3–8 379 (43) 243 (35) 136 (66) <0.001 135 (30) 228 (58) <0.001
 9–12 210 (24) 168 (25) 42 (20)   111 (25) 88 (22)  
 13–15 301 (33) 273 (40) 28 (14)   202 (45) 78 (20)  
Admission motor score
 Obeys/localizes 584 (66) 502 (73) 82 (40) <0.001 347 (78) 197 (50) <0.001
 Normal/abnormal flexion 126 (14) 89 (13) 37 (18)   55 (12) 68 (17)  
 None/extension 180 (20) 93 (14) 87 (42)   46 (10) 129 (33)  
Admission GCS, median (IQR) 10 (6–13) 12 (7–14) 6 (3–11) <0.001 12 (8–14) 7 (4–12) <0.001
Admission motor score, median (IQR) 5 (4–6) 5 (4–6) 4 (1–5) <0.001 6 (5–6) 5 (2–6) <0.001
Worst 24-h GCS, median (IQR) 9 (4–12) 10 (7–12) 4 (3–9) <0.001 11 (8–13) 7 (3–10) <0.001
Worst 24-h motor score, median (IQR) 5 (2–6) 5 (4–6) 2 (1–5) <0.001 5 (4–6) 4 (1–5) <0.001
Pupils
 Both react 668 (74) 572 (83) 96 (47) <0.001 393 (88) 235 (60) <0.001
 One reacts 102 (12) 67 (10) 35 (17)   31 (7) 64 (16)  
 None react 120 (14) 45 (7) 75 (36)   42 (5) 95 (24)  
Hypotension 61 (7) 46 (7) 15 (7) 0.782 33 (7) 26 (7) 0.663
Hypoxia 131 (15) 86 (13) 45 (22) 0.001 49 (11) 76 (19) 0.001
Glucose (mmol/L) 7.3 (6.1–8.8) 7.0 (6.0–8.5) 8.1 (6.8–9.5) <0.001 7.0 (6.0–8.4) 7.6 (6.3–9.3) <0.001
Hemoglobin (g/dL) 12.5 (11.1–13.8) 12.8 (11.5–14.1) 11.6 (10.4–12.9) <0.001 13.0 (11.7–14.3) 11.9 (10.8–13.2) <0.001
Platelet count (109) 187 (136–235) 192 (142–236) 164 (116–231) 0.003 198 (147–242) 171 (129–228) <0.001
Base excess (mmol/L) –1.6 (–4.4–0.6) –1.4 (–4.1–0.7) –2.4 (–5.2–0.5) 0.017 –1.5 (–4.1–0.5) –1.8 (–4.7–0.9) 0.431
INR 1.1 (1.0–1.2) 1.1 (1.0–1.2) 1.1 (1.0–1.3) <0.001 1.0 (1.0–1.1) 1.1 (1.0–1.3) <0.001
Marshall CT
 DI I 15 (2) 15 (2) 0 (0) <0.001 12 (3) 2 (1) <0.001
 DI II 275 (30) 249 (36) 26 (12)   184 (41) 74 (19)  
 DI III–IV 67 (8) 49 (7) 18 (9)   32 (7) 33 (8)  
 EML/NEML 533 (60) 371 (55) 162 (79)   220 (49) 285 (72)  
Rotterdam CT
 1–2 206 (23) 178 (26) 28 (14) <0.001 130 (29) 59 (15) <0.001
 3–4 478 (54) 393 (58) 84 (41)   266 (59) 186 (47)  
 5–6 206 (23) 112 (16) 94 (45)   52 (12) 149 (38)  
Epidural hematoma 92 (10) 82 (12) 10 (5) 0.003 67 (15) 19 (5) <0.001
Traumatic SAH 504 (57) 379 (55) 125 (61) 0.181 237 (53) 243 (62) 0.010
Acute mass lesion evacuation 310 (35) 222 (33) 88 (43) 0.007 137 (31) 162 (41) 0.001
Length of stay (days)
 ICU 2 (1–6) 2 (1–6) 2 (1–5) 0.313 2 (1–5) 3 (1–7) 0.002
 Hospital 8 (4–5) 8 (5–15) 6 (2–14) <0.001 8 (5–13) 8 (3–17) 0.775
Predicted risk of death
IMPACT
 Core model 24 (15–35) 19 (12–24) 48 (24–68) <0.001 15 (12–24) 29 (19–55) <0.001
 Extended model 23 (15–41) 19 (12–34) 49 (28–75) <0.001 39 (27–53) 59 (46–85) <0.001
 Lab model 22 (13–35) 19 (11–26) 46 (26–66) <0.001 32 (18–44) 57 (38–82) <0.001
APACHE II 22 (12–34) 18 (12–28) 37 (28–52) <0.001 15 (9–25) 31 (20–45) <0.001
Observed outome
14-day mortality 99 (11) 0 (0) 99 (48) 0 (0) 99 (25)
6-month mortality 206 (23) 0 (0) 206 (100) 0 (0) 206 (52)
6-month unfavorable outcomeb 394 (47) 188 (30) 206 (100) 0 (0) 394 (100)

Continuous data presented as median (IQR), categorical data presented as n (%).

a

Between 6-month survivors and nonsurvivors.

b

Total of 842 patients.

c

Between 6-month favorable and unfavorable neurological outcome.

d

Fischer's exact test.

APACHE II, Acute Physiology and Chronic Health Evaluation II; CT, computerized tomography; DI, diffuse injury; GCS, Glasgow Coma Scale; INR, international normalized ratio; IMPACT, International Mission for Prognosis and Analysis of Clinical Trials in Traumatic Brain Injury; SAH, subarachnoid hemorrhage.