Table 5.
Study | Patient background | Pathogens | Oritavancin dose and duration | Outcome | Adverse effects |
---|---|---|---|---|---|
Schulz et al. [32] | 4 patients; median age 59 years (31–76); 25% male | MSSA |
3 patients: 1200 mg × 1 dose, then 800 mg weekly ≥ 2 doses 1 patient: 1200 mg × 2/week |
Success × 2 Improvement × 2 |
Anemia and leukopenia in 1 patient |
Chastain et al. [36] | 12 patients, median age 65 years (47–79), 67% male, 67% DM | MRSA |
3 patients = 1200 mg × 1 dose 9 patients = 1200 mg × ≥ 2 doses |
100% Success | None |
Foster et al. [37] | 57 y/o M with osteomyelitis secondary to prosthetic hip replacement | Daptomycin non-susceptible VRE | 1200 mg once weekly × 6 weeks | Success | None |
Delaportas et al. [31] | 49 y/o F with right tibial osteomyelitis secondary to retained intramedullary nail | MSSA | 1200 mg once weekly × 6 weeks | Success | None |
Ruggero et al. [33] | 46 y/o M with native vertebral osteomyelitis | MRSA | 1200 mg every 2 weeks × 4 doses, then 1200 mg 1 month later | Improvement | None |
Dahesh et al. [35] | 59 y/o M with hardware-associated vertebral osteomyelitis | Vancomycin-resistant and daptomycin NS E. faecium | 1200 mg weekly × 2 doses, then 800 mg weekly × 8 doses | Improvement | None |
Stewart et al. [34] | 26 y/o F with sacral joint osteomyelitis; IVDU | MSSA | 1200 mg × 1 dose | Failure | None |
CHROME Registry [38] | 18 patients; mean age 58.4 years, 38.9% male, 77.8% prior antibiotics, 50% failure prior antibiotics | MRSA, MSSA, coagulase-negative Staphylococcus, E. faecalis, E. faecium, S. pyogenes |
10 patients = 1200 mg × 1 dose 8 patients = 1200 mg × ≥ 2 doses |
Clinical success: Single dose: 90% Multi-dose: 87.5% |
Moderate, not serious infusion-related reaction (in multidose patient) |
M male, F female, y years, MSSA methicillin-sensitive Staphylococcus aureus, MRSA methicillin-resistant Staphylococcus aureus, VRE vancomycin-resistant Enterococcus, NS non-susceptible, DM diabetes mellitus, IVDU intravenous drug user