Table 2.
Summary of primary and secondary outcomes
Primary Outcomes, n (%) | |
---|---|
Appropriateness outcomes (n = 111) | |
Appropriateness of indication | 106 (95.5) |
Appropriateness of duration | 105 (94.6) |
Clinical outcomes (n = 97) | |
Clinical success | 70 (72.2) |
Subsequent transition to oral amoxicillin-clavulanate | 54 (55.7) |
Reason(s) for inability to transition to oral amoxicillin-clavulanate on day 3 of IV amoxicillin-clavulanate (n = 55) a | |
Patient is not improving clinically | 29 |
Inability to swallow | 9 |
Pending specialist reassessment | 7 |
Pending further workup of infection(s) or imaging | 7 |
Patient non-compliant with oral medication | 2 |
Nonfunctioning GI tract | 1 |
Other | 4 |
Reason(s) for re-escalation to piperacillin-tazobactam or a carbapenem (n = 27) | |
Patients deteriorated clinically for the same indication | 18 (66.7) |
Inadequate source control | 5 (18.5) |
Grew subsequent resistant organisms | 3 (11.1) |
A different infection developed | 1 (3.7) |
Secondary outcomes ( n = 97), n (%) | |
Hospital readmission | 15 (15.5) |
Related to the same infection | 4 (26.7) |
Readmitted for other reasons | 11 (73.3) |
Mortality | 18 (18.6) |
Comfort care/end of life | 12 (66.7) |
Does not add up to 55, as patient can have > 1 reason