Table 4.
Variable | No. of Patients a | % | 95% CI |
---|---|---|---|
Characteristics of Ceftaroline Therapy | |||
Empirical Therapy b | 2/12 | 17 | 3–46 |
Targeted Therapy | 10/12 | 83 | 54–97 |
First-Line Therapy | 3/12 | 25 | 7–54 |
Salvage Therapy | 9/12 | 75 | 46–93 |
Monotherapy | 7/12 | 58 | 29–82 |
Combination Therapy c | 5/12 | 42 | 18–71 |
Time to Ceftaroline Initiation in Days, Median (IQR) | 6 (2–10) | 2–10 | |
Duration of Ceftaroline Therapy in Survivors, Median (IQR) | 13 (11–14) | 5–16 | |
Type Of Infection | |||
Isolated BSI | 4/12 | 33 | 12–63 |
BSI With Metastatic Foci of Infection d | 8/12 | 67 | 37–88 |
Early Source Control e | |||
Performed or Unnecessary | 7/12 | 58 | 29–82 |
No f | 5/12 | 42 | 18–71 |
Follow-Up Cultures At 72 H After Ceftaroline Initiation | |||
Follow-Up Cultures Performed | 9/12 | 75 | 46–93 |
Microbiological Success g | 6/9 | 67 | 32–90 |
Clinical Outcomes | |||
Favorable Response at the End of Ceftaroline Therapy | 8/12 | 67 | 37–88 |
Mortality at the End of Ceftaroline Therapy | 2/12 | 17 | 3–46 |
28-Day Mortality | 4/12 | 33 | 12–63 |
BSI, bloodstream infection; CI, confidence intervals; IQR, interquartile range; MRSA, methicillin-resistant Staphylococcus aureus. a Results are presented as No. of patients/Total of patients unless otherwise indicated; b Etiological diagnosis made after ceftaroline initiation; c With other agents with anti-MRSA activity: daptomycin (n = 5); d Endocarditis (n = 3); pneumonia (n = 1), septic arthritis (n = 1), vertebral osteomyelitis (n = 1), pneumonia plus septic arthritis (n = 1), pneumonia plus vertebral osteomyelitis (n = 1); e Performed within 24 h from BSI onset (defined as the time when the first positive blood culture was drawn); f central venous catheter removed later than 24 h after BSI onset (n = 3), infective endocarditis deemed as inoperable by the cardiac surgeon (n = 2); g Defined as negative blood cultures at 72 h after ceftaroline initiation.