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. 2013 May;51(5):1465–1473. doi: 10.1128/JCM.03352-12

Table 3.

Univariate and multivariate predictors of development of complicated CDAD (N = 335 patients)

Variablea,b Patients with:
Univariate analysis
Multivariate analysis
Uncomplicated CDAD Complicated CDAD OR (95% CI) P OR (95% CI) P
Age (yr)*c 72 (57–81) 77 (64–85) 1.03 (1.007–1.05) 0.010 1.028 (1.005–1.053) 0.019
Male sex 141/288 (49) 26/47 (55) 1.29 (0.69–2.40) 0.42
Community-acquired CDAD 46/288 (16) 1/47 (2) 0.11 (0.01–0.85) 0.03
Comorbidities
    Charlson comorbidity Index score* 2 (1–3) 3 (2–6) 1.28 (1.13–1.47) <0.001 1.265 (1.105–1.449) 0.001
    Malignancy 83/288 (29) 18/47 (38) 1.53 (0.81–2.91) 0.19
    Diabetes mellitus 62/288 (21) 15/47 (32) 1.71 (0.87–3.35) 0.12
    Chronic renal failure 42/288 (18) 15/47 (32) 2.75 (1.37–5.50) 0.004
    Chronic cardiac disease 43/288 (15) 9/47 (19) 1.35 (0.61–2.99) 0.46
    Chronic obstructive pulmonary disease 41/288 (14) 6/47 (13) 0.88 (0.35–2.21) 0.79
    Peripheral vascular disease 34/288 (12) 6/47 (13) 1.09 (0.43–2.76) 0.85
    Dementia 31/288 (11) 6/47 (13) 1.21 (0.48–3.09) 0.68
    Liver cirrhosis 21/288 (7) 6/47 (13) 1.86 (0.71–4.88) 0.21
    Transplant recipient 23/288 (8) 4/47 (8) 1.07 (0.35–3.25) 0.90
Predisposing factors 1 mo preceding diagnosis
    Prior antibiotic treatment 240/288 (83) 40/47 (85) 1.14 (0.48–2.71) 0.76
    Total length of AB treatment prior to CDAD diagnosis* 12 (7–21) 11 (7–20) 1.004 (0.97–1.04) 0.82
    Continued antibiotic use after CDAD diagnosis 62/288 (21) 17/47 (36) 2.066 (1.07–3.99) 0.02 2.009 (1.012–3.988) 0.046
    Prior PPI use 217/286 (76) 38/47 (81) 1.34 (0.62–2.91) 0.45
    PPI use after CDAD diagnosis 190/286 (66) 34/47 (72) 1.32 (0.66–2.62) 0.42
    Prior treatment with loperamide 27/288 (9) 1/47 (2) 0.21 (0.03–1.58) 0.09
    Prior treatment with laxatives 33/288 (11) 4/47 (8) 0.72 (0.24–2.13) 0.55
    Enteral feeding 21/288 (7) 7/47 (15) 2.225 (0.89–5.57) 0.81
    Parenteral feeding 18/288 (6) 4/47 (8) 1.39 (0.45–4.32) 0.56
    Prior immunosuppressive agent use 86/288 (30) 15/47 (32) 1.10 (0.57–2.14) 0.78
Clinical and biological markers at CDAD diagnosis
    Abdominal pain 117/288 (41) 17/47 (36) 0.83 (0.44–1.57) 0.56
    Fever 85/288 (29) 12/47 (25) 0.82 (0.40–1.65) 0.57
    Blood leukocyte count (cells/ml)* 10,600 (7,000–15,725) 12,510 (7,820–18,025) 1.00 (0.999–1.000) 0.18
    Albumin value (g/dl)* 2.82 (2.47–3.26) 2.11 (1.60–2.75) 0.22 (0.07–0.67) 0.008
    Creatinine value (mg/dl)* 0.93 (0.70–1.30) 1.14 (0.93–1.85) 1.18 (0.90–1.56) 0.23
CDAD treatment
    No specific CDAD treatmentd 276/288 (96) 43/47 (91) 0.47 (0.14–1.52) 0.19
    First CDAD treatment with metronidazole 249/288 (87) 36/47 (77) 0.49 (0.23–1.06) 0.07
    First CDAD treatment with vancomycine 26/288 (9) 7/47 (15) 1.84 (0.75–4.54) 0.18
a

All quantitative variables (those indicated with an asterisk) are expressed as the median and interquartile range (IQR), while the remaining variables are reported as the absolute number and percentage.

b

CDAD, Clostridium difficile-associated disease; AB, antibiotic; PPI, proton pump inhibitor.

c

Pediatric patients (n = 13) were excluded from the analysis.

d

Two patients were included in a blinded clinical trial on C. difficile treatment, and we did not know which CDAD treatment they received.

e

If first CDAD treatment included both metronidazole and vancomycin, the patient was included in the vancomycin group.