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. 2015 Mar 29;2015:685476. doi: 10.1155/2015/685476

Table 2.

Laboratory examination data of Group A and Group B.

Reference range Total average (n = 182) Group A (n = 149) Group B (n = 33) P value
WBC (/µL) 2700–8800 7819.3 ± 4816.8 6238.6 ± 2213.6 15353.3 ± 6734.2 <0.001
Platelet (/µL) 14–34 21.4 ± 8.9 22.1 ± 8.5 18.6 ± 10.7 0.1009
AST (U/L) 8–38 136.0 ± 171.3 124.4 ± 164.3 197.4 ± 198.7 0.0884
ALT (U/L) 4–44 146.9 ± 184.9 146.9 ± 182.0 150.7 ± 206.2 0.9490
γ-GTP (U/L) 16–73 480.0 ± 609.6 484.6 ± 634.6 462.0 ± 487.9 0.7724
T-Bil (mg/dL) 0.2–1.2 4.0 ± 5.7 3.8 ± 5.9 4.6 ± 5.1 0.4991
ALB (g/dL) 3.9–5.3 3.1 ± 0.7 3.2 ± 0.7 2.7 ± 0.8 0.0006
CRP (mg/dL) <0.3 11.2 ± 73.8 10.6 ± 81.0 15.1 ± 7.1 0.6181

Group A: control group consisting of patients with mild acute cholangitis or without acute cholangitis.

Group B: more severe general condition group consisting of patients with severe or moderate acute cholangitis.

WBC: white blood cells, AST: aspartate aminotransferase, ALT: alanine aminotransferase, γ-GTP: γ-glutamyl transpeptidase, T-Bil: total bilirubin, ALB: albumin, and CRP: C-reactive protein.