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. Author manuscript; available in PMC: 2009 Dec 1.
Published in final edited form as: Clin Gastroenterol Hepatol. 2008 Dec;6(12):1354–1360. doi: 10.1016/j.cgh.2008.06.024

Table 2.

Univariate Analysis of Risk Factors Associated with Metronidazole Failure in the 2004–2006 Cohort

Variable Change to vancomycin (n = 14) Duration of diarrhea >10 days (n = 14) Total metronidazole failure (n = 28) No metronidazole failure (n = 51) P value*
Age (year), median (range) 83 (22–93) 74 (48–94) 76 (22–94) 68 (29–91) 0.09
 ≥65, n (%) 10 (71%) 11 (79%) 21 (75%) 30 (58%) 0.15
 ≥85, n (%) 5 (36%) 2 (14%) 7 (25%) 6 (12%) 0.14

Male sex, n (%) 7 (50%) 8 (57%) 15 (54%) 22 (42%) 0.29

White race, n (%) 13 (93%) 13 (93%) 26 (93%) 39 (75%) 0.06

Residence before admission, n (%)
Home 6 (43%) 7 (50%) 13 (46%) 34 (67%) 0.08
Nursing home or rehabilitation center 5 (36%) 3 (21%) 8 (29%) 11 (22%) 0.49
Other hospital 3 (21%) 4 (29%) 7 (25%) 6 (12%) 0.14

Prior CDI, n (%) 1 (7%) 2 (14%) 3 (11%) 7 (14%) 0.70

Number of recently used antibiotics, median (range) 3 (1–9) 3 (1–6) 3 (1–9) 2 (0–7) 0.20
Clindamycin, n (%) 2 (14%) 0 2 (7%) 7 (14%) 0.39
Metronidazole, n (%) 2 (14%) 2 (14%) 4 (14%) 9 (18%) 0.70
Vancomycin, n (%) 6 (43%) 6 (43%) 12 (43%) 21 (41%) 0.88
Penicillin, n (%) 2 (14%) 2 (14%) 4 (14%) 11 (22%) 0.43
Cephalosporin, n (%) 8 (57%) 9 (64%) 17 (61%) 15 (29%) 0.008
Carbopenem, n (%) 4 (29%) 1 (7%) 5 (18%) 6 (12%) 0.46
Macrolide, n (%) 2 (14%) 4 (29%) 6 (21%) 5 (10%) 0.16
Fluoroquinolone, n (%) 10 (71%) 8 (57%) 18 (64%) 26 (51%) 0.26
Aminoglycoside, n (%) 0 0 0 3 (6%) 0.98
Sulfonomide, n (%) 3 (21%) 0 3 (11%) 6 (12%) 0.89

Acid anti-secretory medication, n (%) 12 (86%) 11 (79%) 23 (82%) 38 (75%) 0.44
H-2RA 3 (21%) 1 (7%) 4 (14%) 7 (14%) 0.95
PPI 11 (79%) 10 (71%) 21 (75%) 36 (71%) 0.68

TPN, n (%) 0 1 (7%) 1 (4%) 4 (8%) 0.47

Tube feeding, n (%) 1 (7%) 0 1 (4%) 3 (6%) 0.66

Charlson score, median (range) 5 (1–11) 3 (0–10) 4 (0–11) 3 (0–10) 0.32

Horn’s index severe to fulminant, n (%) 5 (36%) 5 (36%) 10 (36%) 10 (20%) 0.12

Immunosuppression, n (%) 8 (57%) 5 (36%) 13 (46%) 18 (35%) 0.35

ICU admission before or at time of CDI diagnosis, n (%) 3 (21%) 5 (36%) 8 (29%) 14 (27%) 0.92

Length of stay before CDI diagnosis, median (range) 1, 0–11 2, 0–29 1 (0–29) 2 (0–27) 0.89

CDI on admission, n (%) 10 (71%) 8 (57%) 18 (64%) 22 (43%) 0.08

Severe CDI, n (%) 10 (71%) 1 (7%) 11 (39%) 18 (35%) 0.72

Albumin (g/dl), median (range) 2.6 (2.1–3.4) (n = 9) 2.9 (2.5–3.8) (n = 10) 2.8 (2.1–3.8) (n = 19) 3.1 (2–4.3) (n = 31) 0.08
 ≤2.5, n (%) 4 (44%) 1 (10%) 5 (26%) 6 (19%) 0.57

WBC (/μl), median (range) 18 (0.4–41.2) 14.3 (0.2–32.5) 16 (0.2–41.2) 12.3 (0.2–40.6) 0.15
 ≥15,000, n (%) 9 (64%) 6 (43%) 15 (54%) 16 (31%) 0.06
 ≥20,000, n (%) 6 (43%) 1 (7%) 7 (25%) 9 (18%) 0.44

Cr (mg/dl), median (range) 1.7 (0.7–11.5) 1.1 (0.6–5.7) 1.3 (0.6–11.5) 1.3 (0.4–9.9) (n = 50) 0.74
 ≥2.3, n (%) 5 (36%) 2 (14%) 7 (25%) 12 (24%) 0.92

Ileus, n (%) 2 (17%) (n = 12) 1 (25%) (n = 4) 3 (19%) (n = 16) 1 (4%) (n = 23) 0.18

Colitis, n (%) 9 (75%) (n = 12) 0 (n = 2) 9 (64%) (n = 14) 10 (48%) (n = 21) 0.34

Duration of diarrhea before CDI treatment (day), median (range) 2, 0–28 1, 0–14 2 (0–28) 2 (0–21) 0.85

Concurrent antibiotic use, n (%) 14 (100%) 9 (64%) 23 (82%) 37 (73%) 0.34

NAP-1, n (%) 3 (43%) (n = 7) 2 (17%) (n = 12) 5 (26%) (n= 19) 7 (21%) (n = 33) 0.67
*

P value for total metronidazole failure vs. no metronidazole failure