High-dose daptomycin therapy for left-sided infective endocarditis: a prospective study from the international collaboration on endocarditis.
dc.contributor.author | Carugati, Manuela | |
dc.contributor.author | Bayer, Arnold S | |
dc.contributor.author | Miró, Josè M | |
dc.contributor.author | Park, Lawrence P | |
dc.contributor.author | Guimarães, Armenio C | |
dc.contributor.author | Skoutelis, Athanasios | |
dc.contributor.author | Fortes, Claudio Q | |
dc.contributor.author | Durante-Mangoni, Emanuele | |
dc.contributor.author | Hannan, Margaret M | |
dc.contributor.author | Nacinovich, Francisco | |
dc.contributor.author | Fernández-Hidalgo, Nuria | |
dc.contributor.author | Grossi, Paolo | |
dc.contributor.author | Tan, Ru-San | |
dc.contributor.author | Holland, Thomas | |
dc.contributor.author | Fowler, Vance G | |
dc.contributor.author | Corey, Ralph G | |
dc.contributor.author | Chu, Vivian H | |
dc.contributor.author | International Collaboration on Endocarditis | |
dc.date.accessioned | 2024-01-25T16:12:56Z | |
dc.date.available | 2024-01-25T16:12:56Z | |
dc.date.issued | 2013-12 | |
dc.description.abstract | The use of daptomycin in Gram-positive left-sided infective endocarditis (IE) has significantly increased. The purpose of this study was to assess the influence of high-dose daptomycin on the outcome of left-sided IE due to Gram-positive pathogens. This was a prospective cohort study based on 1,112 cases from the International Collaboration on Endocarditis (ICE)-Plus database and the ICE-Daptomycin Substudy database from 2008 to 2010. Among patients with left-sided IE due to Staphylococcus aureus, coagulase-negative staphylococci, and Enterococcus faecalis, we compared those treated with daptomycin (cohort A) to those treated with standard-of-care (SOC) antibiotics (cohort B). The primary outcome was in-hospital mortality. Time to clearance of bacteremia, 6-month mortality, and adverse events (AEs) ascribable to daptomycin were also assessed. There were 29 and 149 patients included in cohort A and cohort B, respectively. Baseline comorbidities did not differ between the two cohorts, except for a significantly higher prevalence of diabetes and previous episodes of IE among patients treated with daptomycin. The median daptomycin dose was 9.2 mg/kg of body weight/day. Two-thirds of the patients treated with daptomycin had failed a previous antibiotic regimen. In-hospital and 6-month mortalities were similar in the two cohorts. In cohort A, median time to clearance of methicillin-resistant S. aureus (MRSA) bacteremia was 1.0 day, irrespective of daptomycin dose, representing a significantly faster bacteremia clearance compared to SOC (1.0 versus 5.0 days; P < 0.01). Regimens with higher daptomycin doses were not associated with increased incidence of AEs. In conclusion, higher-dose daptomycin may be an effective and safe alternative to SOC in the treatment of left-sided IE due to common Gram-positive pathogens. | |
dc.identifier | AAC.01563-13 | |
dc.identifier.issn | 0066-4804 | |
dc.identifier.issn | 1098-6596 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | American Society for Microbiology | |
dc.relation.ispartof | Antimicrobial agents and chemotherapy | |
dc.relation.isversionof | 10.1128/aac.01563-13 | |
dc.rights.uri | ||
dc.subject | International Collaboration on Endocarditis | |
dc.subject | Humans | |
dc.subject | Staphylococcus aureus | |
dc.subject | Enterococcus faecalis | |
dc.subject | Endocarditis, Bacterial | |
dc.subject | Daptomycin | |
dc.subject | Anti-Bacterial Agents | |
dc.subject | Prospective Studies | |
dc.subject | Aged | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.subject | Male | |
dc.title | High-dose daptomycin therapy for left-sided infective endocarditis: a prospective study from the international collaboration on endocarditis. | |
dc.type | Journal article | |
duke.contributor.orcid | Carugati, Manuela|0000-0002-3187-5905 | |
duke.contributor.orcid | Holland, Thomas|0000-0001-7745-9010 | |
duke.contributor.orcid | Fowler, Vance G|0000-0002-8048-0897 | |
pubs.begin-page | 6213 | |
pubs.end-page | 6222 | |
pubs.issue | 12 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Faculty | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Molecular Genetics and Microbiology | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Infectious Diseases | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.publication-status | Published | |
pubs.volume | 57 |
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