Updates on Combination Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia
Purpose of Review Methicillin-resistant Staphylococcus aureus (MRSA) bacteremia is associated with a large clinical burden and high rates of treatment failure with first-line treatment options. Literature for combination antimicrobial therapies for initial treatment or salvage therapy in the setting...
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description | Purpose of Review
Methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia is associated with a large clinical burden and high rates of treatment failure with first-line treatment options. Literature for combination antimicrobial therapies for initial treatment or salvage therapy in the setting of persistent bacteremia is developing.
Recent Findings
Various combination strategies have emerged for the treatment of MRSA bacteremia, including vancomycin or daptomycin in combination with either anti-staphylococcal penicillins, early- and late-generation cephalosporins, ceftaroline, trimethoprim-sulfamethoxazole, or fosfomycin. When used as second-line or salvage therapy, evidence suggests use of these combinations shorten the duration of bacteremia. More recently, data have emerged evaluating this strategy for initial therapy, although results are conflicting.
Summary
Use of combination therapy for MRSA bacteremia may shorten bacteremia duration, but the optimal combination, doses, timing of use, and exact impact on clinical outcomes are still evolving. |
doi_str_mv | 10.1007/s11908-020-00737-8 |
format | Article |
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Methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia is associated with a large clinical burden and high rates of treatment failure with first-line treatment options. Literature for combination antimicrobial therapies for initial treatment or salvage therapy in the setting of persistent bacteremia is developing.
Recent Findings
Various combination strategies have emerged for the treatment of MRSA bacteremia, including vancomycin or daptomycin in combination with either anti-staphylococcal penicillins, early- and late-generation cephalosporins, ceftaroline, trimethoprim-sulfamethoxazole, or fosfomycin. When used as second-line or salvage therapy, evidence suggests use of these combinations shorten the duration of bacteremia. More recently, data have emerged evaluating this strategy for initial therapy, although results are conflicting.
Summary
Use of combination therapy for MRSA bacteremia may shorten bacteremia duration, but the optimal combination, doses, timing of use, and exact impact on clinical outcomes are still evolving.</description><identifier>ISSN: 1523-3847</identifier><identifier>EISSN: 1534-3146</identifier><identifier>DOI: 10.1007/s11908-020-00737-8</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Antibiotics ; Antimicrobial Development and Drug Resistance (KC Claeys and J Smith ; Combination therapy ; Drug resistance ; Endocarditis ; Infectious Diseases ; Medicine ; Medicine & Public Health ; Mortality ; Penicillin ; Section Editors ; Staphylococcus infections ; Topical Collection on Antimicrobial Development and Drug Resistance</subject><ispartof>Current infectious disease reports, 2020-10, Vol.22 (10), Article 28</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2348-b23ccfbcd1dcc4cce853555af524f03f16151dcfbf8a235e1434390febde1c823</citedby><cites>FETCH-LOGICAL-c2348-b23ccfbcd1dcc4cce853555af524f03f16151dcfbf8a235e1434390febde1c823</cites><orcidid>0000-0001-7905-2417</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11908-020-00737-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11908-020-00737-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Blackman, Alison L.</creatorcontrib><creatorcontrib>Rubin, Ellen C.</creatorcontrib><creatorcontrib>Broadbent, Eleanor K.</creatorcontrib><creatorcontrib>Brade, Karrine D.</creatorcontrib><title>Updates on Combination Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia</title><title>Current infectious disease reports</title><addtitle>Curr Infect Dis Rep</addtitle><description>Purpose of Review
Methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia is associated with a large clinical burden and high rates of treatment failure with first-line treatment options. Literature for combination antimicrobial therapies for initial treatment or salvage therapy in the setting of persistent bacteremia is developing.
Recent Findings
Various combination strategies have emerged for the treatment of MRSA bacteremia, including vancomycin or daptomycin in combination with either anti-staphylococcal penicillins, early- and late-generation cephalosporins, ceftaroline, trimethoprim-sulfamethoxazole, or fosfomycin. When used as second-line or salvage therapy, evidence suggests use of these combinations shorten the duration of bacteremia. More recently, data have emerged evaluating this strategy for initial therapy, although results are conflicting.
Summary
Use of combination therapy for MRSA bacteremia may shorten bacteremia duration, but the optimal combination, doses, timing of use, and exact impact on clinical outcomes are still evolving.</description><subject>Antibiotics</subject><subject>Antimicrobial Development and Drug Resistance (KC Claeys and J Smith</subject><subject>Combination therapy</subject><subject>Drug resistance</subject><subject>Endocarditis</subject><subject>Infectious Diseases</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mortality</subject><subject>Penicillin</subject><subject>Section Editors</subject><subject>Staphylococcus infections</subject><subject>Topical Collection on Antimicrobial Development and Drug Resistance</subject><issn>1523-3847</issn><issn>1534-3146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kEtLAzEUhYMoWKt_wNWA62ieTbrU4gsqgrYLVyGTSWzKdDImmUX_vakjuHN1z-Wecy58AFxidI0REjcJ4zmSEBEEy0oFlEdggjllkGI2Oz5oQiGVTJyCs5S2qDiRkBPwse4bnW2qQlctwq72nc6-6NXGRt3vKxdi9WLzxhvftr6Dbzb5lHWXq_es-82-DSYYM6RKD9GWcadNttHuvD4HJ063yV78zilYP9yvFk9w-fr4vLhdQkMok7Am1BhXmwY3xjBjrOSUc64dJ8wh6vAM83JytZOaUG4xo4zOkbN1Y7GRhE7B1djbx_A12JTVNgyxKy8V4YLNGRICFxcZXSaGlKJ1qo9-p-NeYaQOCNWIUBUw6gehkiVEx1Aq5u7Txr_qf1LfKbp1vg</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Blackman, Alison L.</creator><creator>Rubin, Ellen C.</creator><creator>Broadbent, Eleanor K.</creator><creator>Brade, Karrine D.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><orcidid>https://orcid.org/0000-0001-7905-2417</orcidid></search><sort><creationdate>20201001</creationdate><title>Updates on Combination Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia</title><author>Blackman, Alison L. ; Rubin, Ellen C. ; Broadbent, Eleanor K. ; Brade, Karrine D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2348-b23ccfbcd1dcc4cce853555af524f03f16151dcfbf8a235e1434390febde1c823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antibiotics</topic><topic>Antimicrobial Development and Drug Resistance (KC Claeys and J Smith</topic><topic>Combination therapy</topic><topic>Drug resistance</topic><topic>Endocarditis</topic><topic>Infectious Diseases</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mortality</topic><topic>Penicillin</topic><topic>Section Editors</topic><topic>Staphylococcus infections</topic><topic>Topical Collection on Antimicrobial Development and Drug Resistance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blackman, Alison L.</creatorcontrib><creatorcontrib>Rubin, Ellen C.</creatorcontrib><creatorcontrib>Broadbent, Eleanor K.</creatorcontrib><creatorcontrib>Brade, Karrine D.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Current infectious disease reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blackman, Alison L.</au><au>Rubin, Ellen C.</au><au>Broadbent, Eleanor K.</au><au>Brade, Karrine D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Updates on Combination Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia</atitle><jtitle>Current infectious disease reports</jtitle><stitle>Curr Infect Dis Rep</stitle><date>2020-10-01</date><risdate>2020</risdate><volume>22</volume><issue>10</issue><artnum>28</artnum><issn>1523-3847</issn><eissn>1534-3146</eissn><abstract>Purpose of Review
Methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia is associated with a large clinical burden and high rates of treatment failure with first-line treatment options. Literature for combination antimicrobial therapies for initial treatment or salvage therapy in the setting of persistent bacteremia is developing.
Recent Findings
Various combination strategies have emerged for the treatment of MRSA bacteremia, including vancomycin or daptomycin in combination with either anti-staphylococcal penicillins, early- and late-generation cephalosporins, ceftaroline, trimethoprim-sulfamethoxazole, or fosfomycin. When used as second-line or salvage therapy, evidence suggests use of these combinations shorten the duration of bacteremia. More recently, data have emerged evaluating this strategy for initial therapy, although results are conflicting.
Summary
Use of combination therapy for MRSA bacteremia may shorten bacteremia duration, but the optimal combination, doses, timing of use, and exact impact on clinical outcomes are still evolving.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s11908-020-00737-8</doi><orcidid>https://orcid.org/0000-0001-7905-2417</orcidid></addata></record> |
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subjects | Antibiotics Antimicrobial Development and Drug Resistance (KC Claeys and J Smith Combination therapy Drug resistance Endocarditis Infectious Diseases Medicine Medicine & Public Health Mortality Penicillin Section Editors Staphylococcus infections Topical Collection on Antimicrobial Development and Drug Resistance |
title | Updates on Combination Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia |
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