Evaluation of Effectiveness and Safety of High-Dose Daptomycin: Results from Patients Included in the European Cubicin® Outcomes Registry and Experience
| dc.creator | Seaton R.A., Menichetti F., Dalekos G., Beiras-Fernandez A., Nacinovich F., Pathan R., Hamed K. | en |
| dc.date.accessioned | 2023-01-31T09:54:51Z | |
| dc.date.available | 2023-01-31T09:54:51Z | |
| dc.date.issued | 2015 | |
| dc.identifier | 10.1007/s12325-015-0267-4 | |
| dc.identifier.issn | 0741238X | |
| dc.identifier.uri | http://hdl.handle.net/11615/78872 | |
| dc.description.abstract | Introduction: Daptomycin, a rapid concentration-dependent bactericidal antibiotic, is approved at a dose of 4 mg/kg/day for the treatment of complicated skin and soft tissue infections (cSSTI) and at a dose of 6 mg/kg/day for the treatment of Staphylococcus aureus right-sided infective endocarditis (RIE) and bacteremia associated with cSSTI and RIE. Studies have reported the successful use of high-dose daptomycin (>6 mg/kg/day) in patients with difficult-to-treat infections. The present analysis evaluated the effectiveness and safety of high doses (>6 mg/kg/day) of daptomycin for the treatment of different Gram-positive infections. Methods: European Cubicin® Outcomes Registry and Experience (EU-CORE) is a non-interventional, multicenter, retrospective, patient registry designed to collect real-world data from patients treated with daptomycin between 2006 and 2012. Clinical outcomes were assessed at the end of daptomycin treatment for three dose groups: ≤6, >6 to <8, and ≥8 mg/kg/day. Safety was assessed for up to 30 days post-daptomycin treatment. Results: Of the 6075 patients enrolled in EU-CORE, 4892 patients received daptomycin doses ≤6 mg/kg/day, while 1097 patients received high doses (>6 mg/kg/day). The primary infections with the largest proportion of patients treated with a high dose (>6 mg/kg/day) were osteomyelitis (37.1%), foreign body/prosthetic infection (31.6%), and endocarditis (27.6%). S. aureus was identified in 42.9% of patients with positive cultures treated with either ≤6 or >6 mg/kg/day. The overall clinical success rate was 82.0% (899/1097) with high doses (>6 mg/kg/day) and 80.3% (3928/4890) with doses ≤6 mg/kg/day. Numerically higher clinical success rate was observed for endocarditis and foreign body/prosthetic infection, as well as for coagulase-negative staphylococcal and enterococcal infections, with high-dose daptomycin treatment. There were no new or unexpected safety findings at doses >6 mg/kg/day. Conclusion: These results suggested that daptomycin at doses >6 mg/kg/day was effective and well tolerated. High-dose daptomycin is a potential therapeutic option in patients with difficult-to-treat Gram-positive infections. Funding: This study was funded by Novartis Pharma AG. © 2015, The Author(s). | en |
| dc.language.iso | en | en |
| dc.source | Advances in Therapy | en |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84951905947&doi=10.1007%2fs12325-015-0267-4&partnerID=40&md5=8fa2f0ba6b46a1343688480333e56b4b | |
| dc.subject | antibiotic agent | en |
| dc.subject | carbapenem derivative | en |
| dc.subject | cephalosporin derivative | en |
| dc.subject | creatine kinase | en |
| dc.subject | daptomycin | en |
| dc.subject | glycopeptide | en |
| dc.subject | penicillin derivative | en |
| dc.subject | antiinfective agent | en |
| dc.subject | daptomycin | en |
| dc.subject | adult | en |
| dc.subject | aged | en |
| dc.subject | Article | en |
| dc.subject | bacterium culture | en |
| dc.subject | clinical evaluation | en |
| dc.subject | coagulase positive Staphylococcus | en |
| dc.subject | connective tissue disease | en |
| dc.subject | creatine kinase blood level | en |
| dc.subject | creatinine clearance | en |
| dc.subject | dose response | en |
| dc.subject | drug dose comparison | en |
| dc.subject | drug efficacy | en |
| dc.subject | drug megadose | en |
| dc.subject | drug safety | en |
| dc.subject | drug tolerability | en |
| dc.subject | drug withdrawal | en |
| dc.subject | endocarditis | en |
| dc.subject | enterococcal infection | en |
| dc.subject | foreign body | en |
| dc.subject | Gram positive infection | en |
| dc.subject | human | en |
| dc.subject | major clinical study | en |
| dc.subject | male | en |
| dc.subject | mortality | en |
| dc.subject | multicenter study | en |
| dc.subject | muscle weakness | en |
| dc.subject | musculoskeletal disease | en |
| dc.subject | myalgia | en |
| dc.subject | myopathy | en |
| dc.subject | myositis | en |
| dc.subject | osteomyelitis | en |
| dc.subject | prosthesis infection | en |
| dc.subject | retrospective study | en |
| dc.subject | rhabdomyolysis | en |
| dc.subject | side effect | en |
| dc.subject | Staphylococcus aureus | en |
| dc.subject | statistical analysis | en |
| dc.subject | treatment outcome | en |
| dc.subject | treatment response | en |
| dc.subject | Europe | en |
| dc.subject | female | en |
| dc.subject | Gram-Positive Bacterial Infections | en |
| dc.subject | middle aged | en |
| dc.subject | register | en |
| dc.subject | Adult | en |
| dc.subject | Aged | en |
| dc.subject | Anti-Bacterial Agents | en |
| dc.subject | Daptomycin | en |
| dc.subject | Dose-Response Relationship, Drug | en |
| dc.subject | Europe | en |
| dc.subject | Female | en |
| dc.subject | Gram-Positive Bacterial Infections | en |
| dc.subject | Humans | en |
| dc.subject | Male | en |
| dc.subject | Middle Aged | en |
| dc.subject | Registries | en |
| dc.subject | Retrospective Studies | en |
| dc.subject | Treatment Outcome | en |
| dc.subject | Springer Healthcare | en |
| dc.title | Evaluation of Effectiveness and Safety of High-Dose Daptomycin: Results from Patients Included in the European Cubicin® Outcomes Registry and Experience | en |
| dc.type | journalArticle | en |
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