Table 3. Laboratory findings in critical patients with HFRS complicated by ARDS during the acute stage.
Variables | Survivors (n = 27) | Non-survivors (n = 21) | p value• |
Maximum leukocyte counts, ×109/L | 35.95±15.49* | 46.93±22.45* | 0.051 |
Nadir PLT, ×109/L | 11.81±12.93** | 15.29±10.94** | 0.330 |
Maximum HGB, g/L | 170.96±22.29* | 162.48±19.94 | 0.178 |
Maximum ALT, U/L | 208.07±256.04* | 350.33±324.42* | 0.096 |
Nadir serum ALB, g/L | 22.74±5.14** | 21.31±5.16** | 0.344 |
Maximum Scr, µmol/L | 788.95±236.27* | 411.88±197.49* | <0.001 |
Maximum UA, µmol/L | 543.20±213.00* | 433.76±154.57 | 0.054 |
Maximum glucose, mmol/L | 13.58±6.30* | 14.52±8.30* | 0.656 |
Longest PT, sec | 15.95±3.87* | 23.73±11.32* | 0.006 |
Longest APTT, sec | 50.92±16.16* | 63.58±20.13* | 0.020 |
Longest TT, sec | 25.19±6.79* | 26.44±7.49* | 0.554 |
Minimum Fib, g/L | 1.63±0.64** | 1.13±0.40** | 0.003 |
Maximum AST, U/L | 370.33±406.15* | 1271.9±1531.14* | 0.015 |
Reference values: Leukocyte count (3.2–9.7)×109/L; PLT (100–300)×109/L; HGB (120–160) g/L (male), (110–150) g/L (female); ALT (4–44) U/L; AST (8–38) U/L; serum ALB (35–55) g/L; serum Cr (53–97) µmol/L (male), (35–71) µmol/L (female); UA (210–430) µmol/L (male), (150–360) µmol/L (female); glucose (3.89–6.11) mmol/L; PT (8.8–13.8) sec; APTT (25.1–36.5) sec; TT (10.3–16.6) sec, and Fib (2.38–4.98) g/L.
PLT, platelet; HGB, hemoglobin; ALT, alanine aminotransferase; ALB, albumin; Scr, serum creatinine; UA, uric acid; PT, prothrombin time; APTT, activated partial thromboplastin time; TT, thrombin time; Fib, fibrinogen;AST, aspartate aminotransferase.
Survivors vs. non-survivors.
* Higher or longer than the reference value, P<0.05.
** Lower than the reference value, P<0.05.