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. 2017 Sep 14;8(1):35–41. doi: 10.1016/j.jceh.2017.08.007

Table 2.

Risk Factors of Infections in Patients With Decompensated Chronic Liver Disease.

Infection present (n = 60) No infection (n = 45) Odds ratio (95% CI) P value
Age (months) 78 (3–180) 87 (7–204) 0.92 (0.67–1.22) 0.24
Known CLDa 24 (40%) 13 (29%) 1.64 (0.71–3.74) 0.87
h/o prior decompensationb 19 (31.7%) 11 (24.4%) 1.43 (0.59–3.42) 0.41
On SBP prophylaxis 7 (11.7%) 2 (4.4%) 2.83 (0.56–14.38) 0.48
On Immuno-suppressive medicationsc 8 (13.3%) 4 (8.9%) 1.57 (0.44–5.60) 0.28
Gastrointestinal bleeding 10 (16.7%) 6 (13.3%) 1.30 (0.43–3.88) 0.59
Ascites 57 (95%) 42 (93.3%) 1.35 (0.26–7.06) 1.0
Hepatic encephalopathy 29 (48.3%) 15 (33.3%) 1.87 (0.84–4.16) 0.16
Invasive procedure 27 (45%) 15 (34%) 1.63 (0.73–3.64) 0.57
Serum bilirubin (0.2–1 mg/dL) 10.1 (0.5–33.5) 5.6 (0.4–45.5) 1.98 (0.32–6.77) 0.39
Serum albumin (3.5–5.5 g/dL) 2.4 (0.9–5.7) 2.9 (1.6–4.1) 0.64 (0.21–0.88) 0.001
INR (0.9–1.2) 2.2 (0.98–10) 1.7 (1–9.2) 1.44 (1.10–2.08) 0.01
Child–Pugh score 10 (6–14) 7 (6–14) 3.2 (1.77–5.10) 0.007

Continuous variables are shown as median (range); CI: Confidence Interval.

a

Known CLD: Patients who were diagnosed cases of chronic liver disease on follow-up and presented with decompensation.

b

h/o prior decompensation in the form of hepatic encephalopathy, gastrointestinal bleeding or ascites, from which the patient had recovered.

c

Autoimmune liver disease on therapy (n = 10), Langerhans cell histiocytosis (n = 1), Budd-Chiari Syndrome patient received prednisolone (2 mg/kg for 4 weeks) for unrelated cause; SBP-spontaneous bacterial peritonitis.