Clinical Study

Fidaxomicin versus Vancomycin in the Treatment of Clostridium difficile Infection: Canadian Outcomes

Table 1

Patient and disease characteristics within the mITT population.

CharacteristicFidaxomicin
Vancomycin
Total

Female, number (%)127 (63.2)125 (61.0)252 (62.1)
UBMs per day, mean (SD)8.1 (4.2)7.8 (4.5)8.0 (4.3)
Inpatient, number (%)107 (53.2)105 (51.2)212 (52.2)
CDI antibiotics within previous 24 hours, number (%)59 (29.4)63 (30.7)122 (30.0)
Previous CDI episode, number (%)39 (19.4)37 (18.0)76 (18.7)
Severe CDI, number (%)83 (41.3)80 (39.0)163 (40.1)
Age ≥ 65 years, number (%)93 (46.3)92 (44.9)185 (45.6)
Antibiotic use, number (%)43 (21.4)37 (18.0)80 (19.7)
Cancer, number (%)23 (11.4)31 (15.1)54 (13.3)
Renal dysfunction, number (%)119 (59.2)107 (52.2)226 (55.7)
BI strain§, number (%)66 (40.0)67 (37.9)133 (38.9)

Severe CDI at baseline: ≥10 UBMs per day or white blood cell count > 15,000/mm3.
Other than CDI treatment, during either CDI treatment or follow-up period.
Renal impairment at baseline: creatinine clearance < 90 mL/min/1.73 m2.
§Percentages are calculated from all patients and not from the 342 patients for whom strain type was available.
BI, BI/NAP1/027; CDI, Clostridium difficile infection; mITT, modified intention-to-treat; SD, standard deviation; UBMs, unformed bowel movements.