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Clinical experience with daptomycin in Europe: the first 2.5 years
To describe the patient populations and infections being treated with daptomycin, as well as the efficacy and safety outcomes. Data from the European Cubicin Outcomes Registry and Experience (EU-CORESM), retrospectively collected at 118 institutions between January 2006 and August 2008, were analyse...
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Published in: | Journal of antimicrobial chemotherapy 2011-04, Vol.66 (4), p.912-919 |
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description | To describe the patient populations and infections being treated with daptomycin, as well as the efficacy and safety outcomes.
Data from the European Cubicin Outcomes Registry and Experience (EU-CORESM), retrospectively collected at 118 institutions between January 2006 and August 2008, were analysed.
Daptomycin treatment was documented in 1127 patients with diverse infections, including complicated skin and soft tissue infections (33%), bacteraemia (22%), endocarditis (12%) and osteomyelitis (6%). It was used empirically, before microbiological results became available, in 53% of patients. Staphylococcus aureus was the most common pathogen (34%), with 52% of isolates resistant to methicillin; coagulase-negative staphylococci and enterococci were also frequent, with 22% of Enterococcus faecium isolates resistant to vancomycin. Daptomycin was used as first-line therapy in 302 (27%) patients. When used second line, the most common reasons for discontinuation of previous antibiotic were treatment failure and toxicity or intolerance. The use of concomitant antibiotics was reported in 65% of patients. Most frequent doses were 6 mg/kg (47%) and 4 mg/kg (32%). The median duration of daptomycin therapy was 10 days (range 1-246 days) in the inpatient setting and 13 days (range 2-189 days) in the outpatient setting. The overall clinical success rate was 79%, with a clinical failure rate of |
doi_str_mv | 10.1093/jac/dkq528 |
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Data from the European Cubicin Outcomes Registry and Experience (EU-CORESM), retrospectively collected at 118 institutions between January 2006 and August 2008, were analysed.
Daptomycin treatment was documented in 1127 patients with diverse infections, including complicated skin and soft tissue infections (33%), bacteraemia (22%), endocarditis (12%) and osteomyelitis (6%). It was used empirically, before microbiological results became available, in 53% of patients. Staphylococcus aureus was the most common pathogen (34%), with 52% of isolates resistant to methicillin; coagulase-negative staphylococci and enterococci were also frequent, with 22% of Enterococcus faecium isolates resistant to vancomycin. Daptomycin was used as first-line therapy in 302 (27%) patients. When used second line, the most common reasons for discontinuation of previous antibiotic were treatment failure and toxicity or intolerance. The use of concomitant antibiotics was reported in 65% of patients. Most frequent doses were 6 mg/kg (47%) and 4 mg/kg (32%). The median duration of daptomycin therapy was 10 days (range 1-246 days) in the inpatient setting and 13 days (range 2-189 days) in the outpatient setting. The overall clinical success rate was 79%, with a clinical failure rate of <10% for all infection types. Low failure rates were observed in first- and second-line therapy (6% and 8%, respectively). Daptomycin demonstrated a favourable safety and tolerability profile regardless of treatment duration.
Daptomycin has a relevant role in the treatment of Gram-positive infections.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkq528</identifier><identifier>PMID: 21393205</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - therapeutic use ; Antibiotics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Biological and medical sciences ; Child ; Child, Preschool ; Daptomycin - adverse effects ; Daptomycin - therapeutic use ; Enterococcus faecium ; Enterococcus faecium - drug effects ; Enterococcus faecium - isolation & purification ; Europe ; Female ; Gram-positive bacteria ; Gram-Positive Bacterial Infections - drug therapy ; Gram-Positive Bacterial Infections - microbiology ; Humans ; Infant ; Male ; Medical sciences ; Medical treatment ; Middle Aged ; Original Research ; Pharmacology. Drug treatments ; Retrospective Studies ; Staphylococcus - drug effects ; Staphylococcus - isolation & purification ; Staphylococcus aureus ; Staphylococcus infections ; Tissues ; Toxicity ; Treatment Outcome ; Young Adult</subject><ispartof>Journal of antimicrobial chemotherapy, 2011-04, Vol.66 (4), p.912-919</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright Oxford Publishing Limited(England) Apr 2011</rights><rights>The Author 2011. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-279f659544a57871a51726210615622e642b07d39a67835bfbea7a4829a3448f3</citedby><cites>FETCH-LOGICAL-c466t-279f659544a57871a51726210615622e642b07d39a67835bfbea7a4829a3448f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23976848$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21393205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GONZALEZ-RUIZ, Armando</creatorcontrib><creatorcontrib>BEIRAS-FERNANDEZ, Andres</creatorcontrib><creatorcontrib>LEHMKUHL, Hans</creatorcontrib><creatorcontrib>ANDREW SEATON, R</creatorcontrib><creatorcontrib>LOEFFLER, Juergen</creatorcontrib><creatorcontrib>CHAVES, Ricardo L</creatorcontrib><title>Clinical experience with daptomycin in Europe: the first 2.5 years</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>To describe the patient populations and infections being treated with daptomycin, as well as the efficacy and safety outcomes.
Data from the European Cubicin Outcomes Registry and Experience (EU-CORESM), retrospectively collected at 118 institutions between January 2006 and August 2008, were analysed.
Daptomycin treatment was documented in 1127 patients with diverse infections, including complicated skin and soft tissue infections (33%), bacteraemia (22%), endocarditis (12%) and osteomyelitis (6%). It was used empirically, before microbiological results became available, in 53% of patients. Staphylococcus aureus was the most common pathogen (34%), with 52% of isolates resistant to methicillin; coagulase-negative staphylococci and enterococci were also frequent, with 22% of Enterococcus faecium isolates resistant to vancomycin. Daptomycin was used as first-line therapy in 302 (27%) patients. When used second line, the most common reasons for discontinuation of previous antibiotic were treatment failure and toxicity or intolerance. The use of concomitant antibiotics was reported in 65% of patients. Most frequent doses were 6 mg/kg (47%) and 4 mg/kg (32%). The median duration of daptomycin therapy was 10 days (range 1-246 days) in the inpatient setting and 13 days (range 2-189 days) in the outpatient setting. The overall clinical success rate was 79%, with a clinical failure rate of <10% for all infection types. Low failure rates were observed in first- and second-line therapy (6% and 8%, respectively). Daptomycin demonstrated a favourable safety and tolerability profile regardless of treatment duration.
Daptomycin has a relevant role in the treatment of Gram-positive infections.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibiotics</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Daptomycin - adverse effects</subject><subject>Daptomycin - therapeutic use</subject><subject>Enterococcus faecium</subject><subject>Enterococcus faecium - drug effects</subject><subject>Enterococcus faecium - isolation & purification</subject><subject>Europe</subject><subject>Female</subject><subject>Gram-positive bacteria</subject><subject>Gram-Positive Bacterial Infections - drug therapy</subject><subject>Gram-Positive Bacterial Infections - microbiology</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medical treatment</subject><subject>Middle Aged</subject><subject>Original Research</subject><subject>Pharmacology. Drug treatments</subject><subject>Retrospective Studies</subject><subject>Staphylococcus - drug effects</subject><subject>Staphylococcus - isolation & purification</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus infections</subject><subject>Tissues</subject><subject>Toxicity</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpdkV1LG0EUhgdp0TTtjT-gLAURCqvz_eGFoCG1BaE3ej2cTGbNxM3uOrOr5t93QtJYCwfOxXl4Oec8CB0TfEawYedLcOfzxydB9QEaES5xSbEhH9AIMyxKxQU7Qp9SWmKMpZD6EB1RwgyjWIzQ9aQOTXBQF_618zH4xvniJfSLYg5d367WLjRFrukQ285fFP3CF1WIqS_omSjWHmL6jD5WUCf_ZdfH6P7H9G7ys7z9ffNrcnVbOi5lX1JlKimM4ByE0oqAIIpKSrAkQlLqJaczrObMgFSaiVk186CAa2qAca4rNkaX29xumK383Pmmj1DbLoYVxLVtIdj3kyYs7EP7bPMXtJA8B5zuAmL7NPjU21VIztc1NL4dkjWUEcMVMZn89h-5bIfY5OusltwYyvkG-r6FXGxTir7ar0Kw3YixWYzdisnw13-X36N_TWTgZAdAyjqqCI0L6Y1jRknNNfsD3q2Uyg</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>GONZALEZ-RUIZ, Armando</creator><creator>BEIRAS-FERNANDEZ, Andres</creator><creator>LEHMKUHL, Hans</creator><creator>ANDREW SEATON, R</creator><creator>LOEFFLER, Juergen</creator><creator>CHAVES, Ricardo L</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20110401</creationdate><title>Clinical experience with daptomycin in Europe: the first 2.5 years</title><author>GONZALEZ-RUIZ, Armando ; BEIRAS-FERNANDEZ, Andres ; LEHMKUHL, Hans ; ANDREW SEATON, R ; LOEFFLER, Juergen ; CHAVES, Ricardo L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-279f659544a57871a51726210615622e642b07d39a67835bfbea7a4829a3448f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibiotics</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Daptomycin - adverse effects</topic><topic>Daptomycin - therapeutic use</topic><topic>Enterococcus faecium</topic><topic>Enterococcus faecium - drug effects</topic><topic>Enterococcus faecium - isolation & purification</topic><topic>Europe</topic><topic>Female</topic><topic>Gram-positive bacteria</topic><topic>Gram-Positive Bacterial Infections - drug therapy</topic><topic>Gram-Positive Bacterial Infections - microbiology</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medical treatment</topic><topic>Middle Aged</topic><topic>Original Research</topic><topic>Pharmacology. Drug treatments</topic><topic>Retrospective Studies</topic><topic>Staphylococcus - drug effects</topic><topic>Staphylococcus - isolation & purification</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus infections</topic><topic>Tissues</topic><topic>Toxicity</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GONZALEZ-RUIZ, Armando</creatorcontrib><creatorcontrib>BEIRAS-FERNANDEZ, Andres</creatorcontrib><creatorcontrib>LEHMKUHL, Hans</creatorcontrib><creatorcontrib>ANDREW SEATON, R</creatorcontrib><creatorcontrib>LOEFFLER, Juergen</creatorcontrib><creatorcontrib>CHAVES, Ricardo L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GONZALEZ-RUIZ, Armando</au><au>BEIRAS-FERNANDEZ, Andres</au><au>LEHMKUHL, Hans</au><au>ANDREW SEATON, R</au><au>LOEFFLER, Juergen</au><au>CHAVES, Ricardo L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical experience with daptomycin in Europe: the first 2.5 years</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>66</volume><issue>4</issue><spage>912</spage><epage>919</epage><pages>912-919</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>To describe the patient populations and infections being treated with daptomycin, as well as the efficacy and safety outcomes.
Data from the European Cubicin Outcomes Registry and Experience (EU-CORESM), retrospectively collected at 118 institutions between January 2006 and August 2008, were analysed.
Daptomycin treatment was documented in 1127 patients with diverse infections, including complicated skin and soft tissue infections (33%), bacteraemia (22%), endocarditis (12%) and osteomyelitis (6%). It was used empirically, before microbiological results became available, in 53% of patients. Staphylococcus aureus was the most common pathogen (34%), with 52% of isolates resistant to methicillin; coagulase-negative staphylococci and enterococci were also frequent, with 22% of Enterococcus faecium isolates resistant to vancomycin. Daptomycin was used as first-line therapy in 302 (27%) patients. When used second line, the most common reasons for discontinuation of previous antibiotic were treatment failure and toxicity or intolerance. The use of concomitant antibiotics was reported in 65% of patients. Most frequent doses were 6 mg/kg (47%) and 4 mg/kg (32%). The median duration of daptomycin therapy was 10 days (range 1-246 days) in the inpatient setting and 13 days (range 2-189 days) in the outpatient setting. The overall clinical success rate was 79%, with a clinical failure rate of <10% for all infection types. Low failure rates were observed in first- and second-line therapy (6% and 8%, respectively). Daptomycin demonstrated a favourable safety and tolerability profile regardless of treatment duration.
Daptomycin has a relevant role in the treatment of Gram-positive infections.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>21393205</pmid><doi>10.1093/jac/dkq528</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Anti-Bacterial Agents - adverse effects Anti-Bacterial Agents - therapeutic use Antibiotics Antibiotics. Antiinfectious agents. Antiparasitic agents Biological and medical sciences Child Child, Preschool Daptomycin - adverse effects Daptomycin - therapeutic use Enterococcus faecium Enterococcus faecium - drug effects Enterococcus faecium - isolation & purification Europe Female Gram-positive bacteria Gram-Positive Bacterial Infections - drug therapy Gram-Positive Bacterial Infections - microbiology Humans Infant Male Medical sciences Medical treatment Middle Aged Original Research Pharmacology. Drug treatments Retrospective Studies Staphylococcus - drug effects Staphylococcus - isolation & purification Staphylococcus aureus Staphylococcus infections Tissues Toxicity Treatment Outcome Young Adult |
title | Clinical experience with daptomycin in Europe: the first 2.5 years |
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