Oral-Only Linezolid-Rifampin Is Highly Effective Compared with Other Antibiotics for Periprosthetic Joint Infection: Study of a Mouse Model
The medical treatment of periprosthetic joint infection (PJI) involves prolonged systemic antibiotic courses, often with suboptimal clinical outcomes including increased morbidity and health-care costs. Oral and intravenous monotherapies and combination antibiotic regimens were evaluated in a mouse...
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Veröffentlicht in: | Journal of bone and joint surgery. American volume 2017-04, Vol.99 (8), p.656-665 |
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container_title | Journal of bone and joint surgery. American volume |
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creator | Thompson, John M. Saini, Vikram Ashbaugh, Alyssa G. Miller, Robert J. Ordonez, Alvaro A. Ortines, Roger V. Wang, Yu Sterling, Robert S. Jain, Sanjay K. Miller, Lloyd S. |
description | The medical treatment of periprosthetic joint infection (PJI) involves prolonged systemic antibiotic courses, often with suboptimal clinical outcomes including increased morbidity and health-care costs. Oral and intravenous monotherapies and combination antibiotic regimens were evaluated in a mouse model of methicillin-resistant Staphylococcus aureus (MRSA) PJI.
Oral linezolid with or without oral rifampin, intravenous vancomycin with oral rifampin, intravenous daptomycin or ceftaroline with or without oral rifampin, oral doxycycline, or sham treatment were administered at human-exposure doses for 6 weeks in a mouse model of PJI. Bacterial burden was assessed by in vivo bioluminescent imaging and ex vivo counting of colony-forming units (CFUs), and reactive bone changes were evaluated with radiographs and micro-computed tomography (μCT) imaging.
Oral-only linezolid-rifampin and all intravenous antibiotic-rifampin combinations resulted in no recoverable bacteria and minimized reactive bone changes. Although oral linezolid was the most effective monotherapy, all oral and intravenous antibiotic monotherapies failed to clear infection or prevent reactive bone changes.
Combination antibiotic-rifampin regimens, including oral-only linezolid-rifampin and the newer ceftaroline-rifampin combinations, were highly effective and more efficacious than monotherapies when used against a preclinical MRSA PJI.
This study provides important preclinical evidence to better optimize future antibiotic therapy against PJIs. In particular, the oral-only linezolid-rifampin option might reduce venous access complications and health-care costs. |
doi_str_mv | 10.2106/JBJS.16.01002 |
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Oral linezolid with or without oral rifampin, intravenous vancomycin with oral rifampin, intravenous daptomycin or ceftaroline with or without oral rifampin, oral doxycycline, or sham treatment were administered at human-exposure doses for 6 weeks in a mouse model of PJI. Bacterial burden was assessed by in vivo bioluminescent imaging and ex vivo counting of colony-forming units (CFUs), and reactive bone changes were evaluated with radiographs and micro-computed tomography (μCT) imaging.
Oral-only linezolid-rifampin and all intravenous antibiotic-rifampin combinations resulted in no recoverable bacteria and minimized reactive bone changes. Although oral linezolid was the most effective monotherapy, all oral and intravenous antibiotic monotherapies failed to clear infection or prevent reactive bone changes.
Combination antibiotic-rifampin regimens, including oral-only linezolid-rifampin and the newer ceftaroline-rifampin combinations, were highly effective and more efficacious than monotherapies when used against a preclinical MRSA PJI.
This study provides important preclinical evidence to better optimize future antibiotic therapy against PJIs. In particular, the oral-only linezolid-rifampin option might reduce venous access complications and health-care costs.</description><identifier>ISSN: 0021-9355</identifier><identifier>EISSN: 1535-1386</identifier><identifier>DOI: 10.2106/JBJS.16.01002</identifier><identifier>PMID: 28419033</identifier><language>eng</language><publisher>United States: The Journal of Bone and Joint Surgery, Inc</publisher><subject><![CDATA[Administration, Oral ; Animals ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - therapeutic use ; Ceftaroline ; Cephalosporins - administration & dosage ; Cephalosporins - therapeutic use ; Daptomycin - administration & dosage ; Daptomycin - therapeutic use ; Disease Models, Animal ; Doxycycline - administration & dosage ; Doxycycline - therapeutic use ; Drug Combinations ; Linezolid - administration & dosage ; Linezolid - therapeutic use ; Methicillin-Resistant Staphylococcus aureus ; Mice ; Prosthesis-Related Infections - drug therapy ; Rifampin - administration & dosage ; Rifampin - therapeutic use ; Scientific ; Staphylococcal Infections - drug therapy ; Treatment Outcome]]></subject><ispartof>Journal of bone and joint surgery. American volume, 2017-04, Vol.99 (8), p.656-665</ispartof><rights>The Journal of Bone and Joint Surgery, Inc.</rights><rights>Copyright © 2017 by The Journal of Bone and Joint Surgery, Incorporated 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3495-777d4599bd2d1388012db11e181a163f88ccdd178feccb2f07587bd1b9f3c55e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28419033$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thompson, John M.</creatorcontrib><creatorcontrib>Saini, Vikram</creatorcontrib><creatorcontrib>Ashbaugh, Alyssa G.</creatorcontrib><creatorcontrib>Miller, Robert J.</creatorcontrib><creatorcontrib>Ordonez, Alvaro A.</creatorcontrib><creatorcontrib>Ortines, Roger V.</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Sterling, Robert S.</creatorcontrib><creatorcontrib>Jain, Sanjay K.</creatorcontrib><creatorcontrib>Miller, Lloyd S.</creatorcontrib><title>Oral-Only Linezolid-Rifampin Is Highly Effective Compared with Other Antibiotics for Periprosthetic Joint Infection: Study of a Mouse Model</title><title>Journal of bone and joint surgery. American volume</title><addtitle>J Bone Joint Surg Am</addtitle><description>The medical treatment of periprosthetic joint infection (PJI) involves prolonged systemic antibiotic courses, often with suboptimal clinical outcomes including increased morbidity and health-care costs. Oral and intravenous monotherapies and combination antibiotic regimens were evaluated in a mouse model of methicillin-resistant Staphylococcus aureus (MRSA) PJI.
Oral linezolid with or without oral rifampin, intravenous vancomycin with oral rifampin, intravenous daptomycin or ceftaroline with or without oral rifampin, oral doxycycline, or sham treatment were administered at human-exposure doses for 6 weeks in a mouse model of PJI. Bacterial burden was assessed by in vivo bioluminescent imaging and ex vivo counting of colony-forming units (CFUs), and reactive bone changes were evaluated with radiographs and micro-computed tomography (μCT) imaging.
Oral-only linezolid-rifampin and all intravenous antibiotic-rifampin combinations resulted in no recoverable bacteria and minimized reactive bone changes. Although oral linezolid was the most effective monotherapy, all oral and intravenous antibiotic monotherapies failed to clear infection or prevent reactive bone changes.
Combination antibiotic-rifampin regimens, including oral-only linezolid-rifampin and the newer ceftaroline-rifampin combinations, were highly effective and more efficacious than monotherapies when used against a preclinical MRSA PJI.
This study provides important preclinical evidence to better optimize future antibiotic therapy against PJIs. In particular, the oral-only linezolid-rifampin option might reduce venous access complications and health-care costs.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Ceftaroline</subject><subject>Cephalosporins - administration & dosage</subject><subject>Cephalosporins - therapeutic use</subject><subject>Daptomycin - administration & dosage</subject><subject>Daptomycin - therapeutic use</subject><subject>Disease Models, Animal</subject><subject>Doxycycline - administration & dosage</subject><subject>Doxycycline - therapeutic use</subject><subject>Drug Combinations</subject><subject>Linezolid - administration & dosage</subject><subject>Linezolid - therapeutic use</subject><subject>Methicillin-Resistant Staphylococcus aureus</subject><subject>Mice</subject><subject>Prosthesis-Related Infections - drug therapy</subject><subject>Rifampin - administration & dosage</subject><subject>Rifampin - therapeutic use</subject><subject>Scientific</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Treatment Outcome</subject><issn>0021-9355</issn><issn>1535-1386</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUcGO0zAUjBCILQtHrshHLi5-cZw4HJCWamFbFRWxcLYS29kYErvYzlblF_hpnO2ygostzYxn_N5k2UsgyxxI-WbzfnO9hHJJgJD8UbYARhkGysvH2SIhgGvK2Fn2LITvhJCiINXT7CznBdSE0kX2e-ebAe_scERbY_UvNxiFv5iuGffGonVAV-amT-Rl12kZza1GKzfuG68VOpjYo13stUcXNprWuGhkQJ3z6LP2Zu9dSGTC0MYZG9Ha3lk4-xZdx0kdketQgz65Keh0Kj08z550zRD0i_v7PPv24fLr6gpvdx_Xq4stlrSoGa6qShWsrluVqzQoJ5CrFkADhwZK2nEupVJQ8RQn27wjFeNVq6CtOyoZ0_Q8e3fy3U_tqJXUNqYliL03Y-OPwjVG_M9Y04sbdyvKFJFzSAav7w28-znpEMVogtTD0FidxhHAeV1VnJc8SfFJKtM6gtfdQwwQMRco5gIFlOKuwKR_9e_fHtR_G0uC4iQ4uCFqH34M00F70etmiL0gc8dlTnFOoCLzEzxDjP4BurWojg</recordid><startdate>20170419</startdate><enddate>20170419</enddate><creator>Thompson, John M.</creator><creator>Saini, Vikram</creator><creator>Ashbaugh, Alyssa G.</creator><creator>Miller, Robert J.</creator><creator>Ordonez, Alvaro A.</creator><creator>Ortines, Roger V.</creator><creator>Wang, Yu</creator><creator>Sterling, Robert S.</creator><creator>Jain, Sanjay K.</creator><creator>Miller, Lloyd S.</creator><general>The Journal of Bone and Joint Surgery, Inc</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170419</creationdate><title>Oral-Only Linezolid-Rifampin Is Highly Effective Compared with Other Antibiotics for Periprosthetic Joint Infection: Study of a Mouse Model</title><author>Thompson, John M. ; Saini, Vikram ; Ashbaugh, Alyssa G. ; Miller, Robert J. ; Ordonez, Alvaro A. ; Ortines, Roger V. ; Wang, Yu ; Sterling, Robert S. ; Jain, Sanjay K. ; Miller, Lloyd S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3495-777d4599bd2d1388012db11e181a163f88ccdd178feccb2f07587bd1b9f3c55e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Ceftaroline</topic><topic>Cephalosporins - administration & dosage</topic><topic>Cephalosporins - therapeutic use</topic><topic>Daptomycin - administration & dosage</topic><topic>Daptomycin - therapeutic use</topic><topic>Disease Models, Animal</topic><topic>Doxycycline - administration & dosage</topic><topic>Doxycycline - therapeutic use</topic><topic>Drug Combinations</topic><topic>Linezolid - administration & dosage</topic><topic>Linezolid - therapeutic use</topic><topic>Methicillin-Resistant Staphylococcus aureus</topic><topic>Mice</topic><topic>Prosthesis-Related Infections - drug therapy</topic><topic>Rifampin - administration & dosage</topic><topic>Rifampin - therapeutic use</topic><topic>Scientific</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thompson, John M.</creatorcontrib><creatorcontrib>Saini, Vikram</creatorcontrib><creatorcontrib>Ashbaugh, Alyssa G.</creatorcontrib><creatorcontrib>Miller, Robert J.</creatorcontrib><creatorcontrib>Ordonez, Alvaro A.</creatorcontrib><creatorcontrib>Ortines, Roger V.</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Sterling, Robert S.</creatorcontrib><creatorcontrib>Jain, Sanjay K.</creatorcontrib><creatorcontrib>Miller, Lloyd S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bone and joint surgery. American volume</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thompson, John M.</au><au>Saini, Vikram</au><au>Ashbaugh, Alyssa G.</au><au>Miller, Robert J.</au><au>Ordonez, Alvaro A.</au><au>Ortines, Roger V.</au><au>Wang, Yu</au><au>Sterling, Robert S.</au><au>Jain, Sanjay K.</au><au>Miller, Lloyd S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral-Only Linezolid-Rifampin Is Highly Effective Compared with Other Antibiotics for Periprosthetic Joint Infection: Study of a Mouse Model</atitle><jtitle>Journal of bone and joint surgery. American volume</jtitle><addtitle>J Bone Joint Surg Am</addtitle><date>2017-04-19</date><risdate>2017</risdate><volume>99</volume><issue>8</issue><spage>656</spage><epage>665</epage><pages>656-665</pages><issn>0021-9355</issn><eissn>1535-1386</eissn><abstract>The medical treatment of periprosthetic joint infection (PJI) involves prolonged systemic antibiotic courses, often with suboptimal clinical outcomes including increased morbidity and health-care costs. Oral and intravenous monotherapies and combination antibiotic regimens were evaluated in a mouse model of methicillin-resistant Staphylococcus aureus (MRSA) PJI.
Oral linezolid with or without oral rifampin, intravenous vancomycin with oral rifampin, intravenous daptomycin or ceftaroline with or without oral rifampin, oral doxycycline, or sham treatment were administered at human-exposure doses for 6 weeks in a mouse model of PJI. Bacterial burden was assessed by in vivo bioluminescent imaging and ex vivo counting of colony-forming units (CFUs), and reactive bone changes were evaluated with radiographs and micro-computed tomography (μCT) imaging.
Oral-only linezolid-rifampin and all intravenous antibiotic-rifampin combinations resulted in no recoverable bacteria and minimized reactive bone changes. Although oral linezolid was the most effective monotherapy, all oral and intravenous antibiotic monotherapies failed to clear infection or prevent reactive bone changes.
Combination antibiotic-rifampin regimens, including oral-only linezolid-rifampin and the newer ceftaroline-rifampin combinations, were highly effective and more efficacious than monotherapies when used against a preclinical MRSA PJI.
This study provides important preclinical evidence to better optimize future antibiotic therapy against PJIs. In particular, the oral-only linezolid-rifampin option might reduce venous access complications and health-care costs.</abstract><cop>United States</cop><pub>The Journal of Bone and Joint Surgery, Inc</pub><pmid>28419033</pmid><doi>10.2106/JBJS.16.01002</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - therapeutic use Ceftaroline Cephalosporins - administration & dosage Cephalosporins - therapeutic use Daptomycin - administration & dosage Daptomycin - therapeutic use Disease Models, Animal Doxycycline - administration & dosage Doxycycline - therapeutic use Drug Combinations Linezolid - administration & dosage Linezolid - therapeutic use Methicillin-Resistant Staphylococcus aureus Mice Prosthesis-Related Infections - drug therapy Rifampin - administration & dosage Rifampin - therapeutic use Scientific Staphylococcal Infections - drug therapy Treatment Outcome |
title | Oral-Only Linezolid-Rifampin Is Highly Effective Compared with Other Antibiotics for Periprosthetic Joint Infection: Study of a Mouse Model |
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