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. 2011 May-Jun;17(3):174–179. doi: 10.4103/1319-3767.80379

Table 3.

Baseline characteristics of trial participants

Characteristic Antioxidant group(n=19) Control group (n=20) P value
Organ dysfunction# (day 7) 7 (37) 8 (40) 1.0
MODS (IQR)+ 1.59 (0–3) 1.26 (0–3) 0.08
Length of hospital stay (days)
Mean (SD)* 12.8 (3.9) 15.1 (5.43) 0.29
Median (range) 13 (9–21) 15 (3–22)
Duration of pain, days
Median (range) 5 (2–7) 5 (2–8) -
Improvement at day 7 (based on clinical and laboratory parameters)# 9/14 6/15 0.06
Target organ dysfunction (day 7) Renal insufficiency# 4 4 1.0
Pulmonary insufficiency# 1 3 0.60
Abscess# 2 4 0.65
Difference in complication scores at outcome (SD)$ 7.2 (12.9) .71 (1.26) .034
Laboratory markers (change from day 0 to day 7), mean (SD)*
MDA (μmol/l) –1.6 (1.9) –1.5 (1.75) 6.4 (8.9)
GSH (mmol/l) 1.1 (0.7) 1.3 (1.7) 0.68
SOD (IU/dl) 5.4 (7.5) 0.64 0.74
Patient outcome,(%)
Discharge 14 (100) 13 (86) 0.48
Death# 0 (0) 2 (14)
$

Adjusted for differences at baseline, compared by Univariate analysis

*

Student’s unpaired t test

#

Fisher exact test

+

Mann-Whitney U test. MDA: malondialdehyde; GSH: reduced glutathione; SOD: superoxide dismutase