Clinical Study

Urine β-2-Microglobulin, Osteopontin, and Trefoil Factor 3 May Early Predict Acute Kidney Injury and Outcome after Cardiac Arrest

Table 3

Univariate analyses of risk factors for mortality in resuscitated, comatose out-of-hospital cardiac arrest patients.

Survivors ()Nonsurvivors ()Risk factor for mortalityCrude OR (95% CI) for mortality value

Baseline data
Age (years)59.1 ± 13.161.4 ± 14.1Age ≥ 60 years1.37 (0.77 to 2.41)0.283
Weight (kg)a ()83.0 (75.0 to 93.0)85.0 (75.0 to 90.0)Weight ≥ 85 kg1.35 (0.73 to 2.51)0.335
Male (sex)94 (87.9)71 (80.7)Female sex1.73 (0.79 to 3.80)0.167
Witnessed CAa ()101 (95.3)68 (77.3)Unwitnessed CA5.94 (2.13 to 16.59)<0.001
Bystander CPR94 (87.9)77 (87.5)Not bystander CPR1.03 (0.44 to 2.44)0.941
ROSC time (min)a ()19.0 (12.0 to 29.0)30.0 (23.0 to 44.0)Time to ROSC ≥ 25 min3.28 (1.68 to 6.40)<0.001
Initial VF/VTa ()86 (81.1)42 (48.3)Not initial VF/VT4.61 (2.42 to 8.76)<0.001
SAPS II (score)68.3 ± 10.473.0 ± 10.0SAPS II score ≥ 691.62 (0.91 to 2.87)0.099

Admission day
Diuresis (L/day)2.03 (1.75 to 2.84)1.81 (1.43 to 2.45)Diuresis < 1.93 L/day1.99 (1.12 to 3.53)0.018
Fluid balance (L/day)4.05 (2.37 to 5.74)4.75 (3.50 to 6.39)Fluid balance ≥ 4.45 L/day1.92 (1.08 to 3.39)0.025
S-Creatinine (μ·mol/L)98.0 (84.0 to 114.0)107.5 (94.3 to 140.0)S-Creatinine ≥ 101 μ·mol/L1.76 (1.00 to 3.11)0.051
S-Urea (mmol/L)6.3 (5.1 to 7.7)7.3 (5.8 to 9.7)S-Urea  ≥ 6.7 mmol/L1.93 (1.09 to 3.43)0.023
B-HCO3 (mmol/L)20.6 (18.9 to 22.4)19.0 (16.6 to 21.2)B-HCO3  < 19.0 mmol/L2.82 (1.55 to 5.14)0.001
B-BE (mmol/L)−5.7 (−8.4 to −3.7)−8.8 (−12.4 to −6.0)B-BE < −7.0 mmol/L3.51 (1.94 to 6.35)<0.001
B-Lactate (mmol/L)3.3 (1.7 to 5.9)5.2 (2.9 to 9.3)B-Lactate ≥ 4.1 mmol/L2.48 (1.39 to 4.43)0.002
SOFA (score)10.0 (8.0 to 11.0)11.0 (10.0 to 12.0)SOFA score ≥ 104.26 (2.07 to 8.75)<0.001

Urine biomarkers ( at admission and at day three)
Adm. β2M (ng/mL)1840 (361 to 5356)4840 (1117 to 9415)Adm. β2M ≥ 2769 ng/mL2.27 (1.28 to 4.05)0.005
Day 3 β2M (ng/mL)a628 (90 to 4678)617 (67 to 4884)Day 3 β2M ≥ 627 ng/mL1.04 (0.56 to 1.95)0.898
Adm. osteopontin (ng/mL)1876 (1334 to 2588)2553 (1814 to 3251)Adm. osteopontin ≥ 2068 ng/mL1.99 (1.12 to 3.53)0.018
Day 3 osteopontin (ng/mL)a1345 (590 to 2539)2386 (1317 to 4397)Day 3 osteopontin ≥ 1683 ng/mL2.69 (1.41 to 5.15)0.002
Adm. TFF3 (ng/mL)2010 (1066 to 3964)3400 (1827 to 5110)Adm. TFF3, ng/mL ≥ 2694 ng/mL2.17 (1.22 to 3.85)0.008
Day 3 TFF3 (ng/mL)a2447 (1045 to 987)3784 (2384 to 5969)Day 3 TFF3, ng/mL ≥ 2910 ng/mL3.61 (1.86 to 7.02)<0.001

Outcome
Hospital RRT3 (2.8)5 (5.7)Treatment with RRT2.09 (0.48 to 9.01)0.314
AKI within 3 days32 (29.9)56 (63.6)Presence of AKI4.10 (2.52 to 7.46)<0.001
PNO at 6 months8 (7.5)88 (100.0)Poor neurological outcomen.a.

Categorical data are presented as number (percent), continuous data with skewed distribution as median (interquartile range), and continuous data with normal distribution as mean (±standard deviation). Presented values are from univariate Pearson’s chi square analysis. OR: odds ratio; CI: confidence interval; : number; CA: cardiac arrest; CPR: cardiopulmonary resuscitation; ROSC: return of spontaneous circulation; VF/VT: ventricular fibrillation/ventricular tachycardia; SAPS: simplified acute physiology score; S: serum; B: whole blood; HCO3: bicarbonate; BE: base excess; SOFA: sequential organ failure assessment; Adm.: admission; β2M: β-2-microglobulin; TFF3: trefoil factor 3; RRT: renal replacement therapy; AKI: acute kidney injury; PNO: poor neurological outcome defined as cerebral performance category (CPC) 3–5; n.a.: not applicable. aData from some patients are missing.