Comparison of the clinical efficacy between tigecycline plus extended-infusion imipenem and sulbactam plus imipenem against ventilator-associated pneumonia with pneumonic extensively drug-resistant Acinetobacter baumannii bacteremia, and correlation of clinical efficacy with in vitro synergy tests

Abstract Background/Purpose To compare the clinical efficacy between salvage antimicrobial regimen consisting of tigecycline plus extended-infusion imipenem/cilastatin (TIC) and regimen of sulbactam plus imipenem/cilastatin (SIC) for patients with ventilator-associated pneumonia and pneumonic bacter...

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Veröffentlicht in:Journal of microbiology, immunology and infection immunology and infection, 2016-12, Vol.49 (6), p.924-933
Hauptverfasser: Jean, Shio-Shin, Hsieh, Tai-Chin, Hsu, Chin-Wan, Lee, Wen-Sen, Bai, Kuan-Jen, Lam, Carlos
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container_end_page 933
container_issue 6
container_start_page 924
container_title Journal of microbiology, immunology and infection
container_volume 49
creator Jean, Shio-Shin
Hsieh, Tai-Chin
Hsu, Chin-Wan
Lee, Wen-Sen
Bai, Kuan-Jen
Lam, Carlos
description Abstract Background/Purpose To compare the clinical efficacy between salvage antimicrobial regimen consisting of tigecycline plus extended-infusion imipenem/cilastatin (TIC) and regimen of sulbactam plus imipenem/cilastatin (SIC) for patients with ventilator-associated pneumonia and pneumonic bacteremia due to extensively drug-resistant (XDR) Acinetobacter baumannii (Ab) isolates, and determine the correlation of results of in vitro tigecycline–imipenem synergy test with clinical efficacy. Methods The comparative survey was conducted at a medical center in Taiwan in 2013. Patients comprising the TIC group ( n  = 28) received tigecycline plus extended-infusion imipenem/cilastatin following unresponsiveness to 3-day sulbactam–imipenem/cilastatin therapy, and those in the SIC group ( n  = 56) received sulbactam–imipenem/cilastatin throughout the course. Univariate and multivariate analyses were applied to explore 30-day case-fatality independent predictors. Additionally, the checkerboard test and time-kill analysis were performed for the bloodstream XDR-Ab isolates from patients in the TIC group, and molecular characterization was done for the bloodstream XDR-Ab strains of all patients. Results We found that the TIC scheme has a significant benefit on improving patients' survival status (the mortality rate of TIC and SIC group patients was 14.3% and 64.3%, respectively), corresponding well with in vitro synergy or additivity results by the checkerboard test. Twenty TIC group cases had monomicrobial XDR-Ab cultured from tracheal aspirates after 10 days of tigecycline–imipenem/cilastatin therapy, but none developed subsequent pneumonia. However, breakthrough primary Burkholderia cepacia ( n  = 3) and Pseudomonas aeruginosa ( n  = 1) bacteremias were attributed to four TIC case fatalities. Shock, SIC regimen usage, and development of breakthrough bacteremia were independent predictors of 30-day in-hospital mortality. Conclusion Although the TIC regimen showed good efficacy, its value regarding managing XDR-Ab ventilator-associated pneumonia bacteremia needs further evaluation.
doi_str_mv 10.1016/j.jmii.2015.06.009
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Methods The comparative survey was conducted at a medical center in Taiwan in 2013. Patients comprising the TIC group ( n  = 28) received tigecycline plus extended-infusion imipenem/cilastatin following unresponsiveness to 3-day sulbactam–imipenem/cilastatin therapy, and those in the SIC group ( n  = 56) received sulbactam–imipenem/cilastatin throughout the course. Univariate and multivariate analyses were applied to explore 30-day case-fatality independent predictors. Additionally, the checkerboard test and time-kill analysis were performed for the bloodstream XDR-Ab isolates from patients in the TIC group, and molecular characterization was done for the bloodstream XDR-Ab strains of all patients. Results We found that the TIC scheme has a significant benefit on improving patients' survival status (the mortality rate of TIC and SIC group patients was 14.3% and 64.3%, respectively), corresponding well with in vitro synergy or additivity results by the checkerboard test. Twenty TIC group cases had monomicrobial XDR-Ab cultured from tracheal aspirates after 10 days of tigecycline–imipenem/cilastatin therapy, but none developed subsequent pneumonia. However, breakthrough primary Burkholderia cepacia ( n  = 3) and Pseudomonas aeruginosa ( n  = 1) bacteremias were attributed to four TIC case fatalities. Shock, SIC regimen usage, and development of breakthrough bacteremia were independent predictors of 30-day in-hospital mortality. Conclusion Although the TIC regimen showed good efficacy, its value regarding managing XDR-Ab ventilator-associated pneumonia bacteremia needs further evaluation.</description><identifier>ISSN: 1684-1182</identifier><identifier>EISSN: 1995-9133</identifier><identifier>DOI: 10.1016/j.jmii.2015.06.009</identifier><identifier>PMID: 26341302</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Acinetobacter baumannii - drug effects ; Acinetobacter baumannii - isolation &amp; purification ; Acinetobacter Infections - drug therapy ; Adult ; Aged ; Aged, 80 and over ; Anti-Bacterial Agents - therapeutic use ; Bacteremia - drug therapy ; Bacteremia - microbiology ; Cilastatin - therapeutic use ; combination regimen ; Drug Combinations ; Drug Resistance, Multiple, Bacterial ; Drug Synergism ; Drug Therapy, Combination - methods ; extensively drug-resistant Acinetobacter baumannii ; Female ; Hospital Mortality ; Humans ; imipenem ; Imipenem - therapeutic use ; Infectious Disease ; Male ; Medical Education ; Microbial Sensitivity Tests ; Middle Aged ; Minocycline - analogs &amp; derivatives ; Minocycline - therapeutic use ; Pneumonia, Ventilator-Associated - drug therapy ; Pneumonia, Ventilator-Associated - microbiology ; Salvage Therapy ; sulbactam ; Sulbactam - therapeutic use ; Taiwan ; tigecycline ; Treatment Outcome ; ventilator-associated pneumonia</subject><ispartof>Journal of microbiology, immunology and infection, 2016-12, Vol.49 (6), p.924-933</ispartof><rights>2015</rights><rights>Copyright © 2015. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-6ef0520312edd01b81e3f84c66003a9bd820a3484a30f4846b32f6a12a3d1d863</citedby><cites>FETCH-LOGICAL-c455t-6ef0520312edd01b81e3f84c66003a9bd820a3484a30f4846b32f6a12a3d1d863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jmii.2015.06.009$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,864,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26341302$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jean, Shio-Shin</creatorcontrib><creatorcontrib>Hsieh, Tai-Chin</creatorcontrib><creatorcontrib>Hsu, Chin-Wan</creatorcontrib><creatorcontrib>Lee, Wen-Sen</creatorcontrib><creatorcontrib>Bai, Kuan-Jen</creatorcontrib><creatorcontrib>Lam, Carlos</creatorcontrib><title>Comparison of the clinical efficacy between tigecycline plus extended-infusion imipenem and sulbactam plus imipenem against ventilator-associated pneumonia with pneumonic extensively drug-resistant Acinetobacter baumannii bacteremia, and correlation of clinical efficacy with in vitro synergy tests</title><title>Journal of microbiology, immunology and infection</title><addtitle>J Microbiol Immunol Infect</addtitle><description>Abstract Background/Purpose To compare the clinical efficacy between salvage antimicrobial regimen consisting of tigecycline plus extended-infusion imipenem/cilastatin (TIC) and regimen of sulbactam plus imipenem/cilastatin (SIC) for patients with ventilator-associated pneumonia and pneumonic bacteremia due to extensively drug-resistant (XDR) Acinetobacter baumannii (Ab) isolates, and determine the correlation of results of in vitro tigecycline–imipenem synergy test with clinical efficacy. Methods The comparative survey was conducted at a medical center in Taiwan in 2013. Patients comprising the TIC group ( n  = 28) received tigecycline plus extended-infusion imipenem/cilastatin following unresponsiveness to 3-day sulbactam–imipenem/cilastatin therapy, and those in the SIC group ( n  = 56) received sulbactam–imipenem/cilastatin throughout the course. Univariate and multivariate analyses were applied to explore 30-day case-fatality independent predictors. Additionally, the checkerboard test and time-kill analysis were performed for the bloodstream XDR-Ab isolates from patients in the TIC group, and molecular characterization was done for the bloodstream XDR-Ab strains of all patients. Results We found that the TIC scheme has a significant benefit on improving patients' survival status (the mortality rate of TIC and SIC group patients was 14.3% and 64.3%, respectively), corresponding well with in vitro synergy or additivity results by the checkerboard test. Twenty TIC group cases had monomicrobial XDR-Ab cultured from tracheal aspirates after 10 days of tigecycline–imipenem/cilastatin therapy, but none developed subsequent pneumonia. However, breakthrough primary Burkholderia cepacia ( n  = 3) and Pseudomonas aeruginosa ( n  = 1) bacteremias were attributed to four TIC case fatalities. Shock, SIC regimen usage, and development of breakthrough bacteremia were independent predictors of 30-day in-hospital mortality. Conclusion Although the TIC regimen showed good efficacy, its value regarding managing XDR-Ab ventilator-associated pneumonia bacteremia needs further evaluation.</description><subject>Acinetobacter baumannii - drug effects</subject><subject>Acinetobacter baumannii - isolation &amp; purification</subject><subject>Acinetobacter Infections - drug therapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Bacteremia - drug therapy</subject><subject>Bacteremia - microbiology</subject><subject>Cilastatin - therapeutic use</subject><subject>combination regimen</subject><subject>Drug Combinations</subject><subject>Drug Resistance, Multiple, Bacterial</subject><subject>Drug Synergism</subject><subject>Drug Therapy, Combination - methods</subject><subject>extensively drug-resistant Acinetobacter baumannii</subject><subject>Female</subject><subject>Hospital Mortality</subject><subject>Humans</subject><subject>imipenem</subject><subject>Imipenem - therapeutic use</subject><subject>Infectious Disease</subject><subject>Male</subject><subject>Medical Education</subject><subject>Microbial Sensitivity Tests</subject><subject>Middle Aged</subject><subject>Minocycline - analogs &amp; derivatives</subject><subject>Minocycline - therapeutic use</subject><subject>Pneumonia, Ventilator-Associated - drug therapy</subject><subject>Pneumonia, Ventilator-Associated - microbiology</subject><subject>Salvage Therapy</subject><subject>sulbactam</subject><subject>Sulbactam - therapeutic use</subject><subject>Taiwan</subject><subject>tigecycline</subject><subject>Treatment Outcome</subject><subject>ventilator-associated pneumonia</subject><issn>1684-1182</issn><issn>1995-9133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Ustu1TAQDQhES-EHWCAvkSAXPxIrV0KVqoqXVIkFsLYce3I7l8QOtnNL_oZv4ctwmrZIILEa23PmnJnxKYpnjG4YZfL1frMfEDecsnpD5YbS7f3imG23dbllQjzIZ9lUJWMNPyoex7intBK8lo-KIy5FxQTlx_denvth1AGjd8R3JF0CMT06NLon0HU5mpm0kK4AHEm4AzMveSBjP0UCPxI4C7ZE100RMwcOOIKDgWhnSZz6VpukhxX9J7fT6GIiB3AJe518KHWM3qBOYMnoYBq8Q02uMF3eXc2qFvEA_UxsmHZlgIgxaZfImck9Jb-oQSCtngbtHCJZH2BA_eq6I-NDgKyI67j_jnotie7XzwOm4EmcHYTdTBLEFJ8UDzvdR3h6E0-Kr-_efjn_UF58ev_x_OyiNFVdp1JCR2tOBeNgLWVtw0B0TWWkpFTobWsbTrWomkoL2uUgW8E7qRnXwjLbSHFSvFh5x-C_T1lZDRgN9L124Keo8odKKZismgzlK9QEH2OATo0BBx1mxahaTKL2ajGJWkyiqFTZJLno-Q3_1A5g70puXZEBb1YA5CkPCEFFg-AMWAxgkrIe_89_-lf57Z6_wQxx76fg8v4UU5Erqj4vNl1cympKG5a9-xvs_-2w</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Jean, Shio-Shin</creator><creator>Hsieh, Tai-Chin</creator><creator>Hsu, Chin-Wan</creator><creator>Lee, Wen-Sen</creator><creator>Bai, Kuan-Jen</creator><creator>Lam, Carlos</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>20161201</creationdate><title>Comparison of the clinical efficacy between tigecycline plus extended-infusion imipenem and sulbactam plus imipenem against ventilator-associated pneumonia with pneumonic extensively drug-resistant Acinetobacter baumannii bacteremia, and correlation of clinical efficacy with in vitro synergy tests</title><author>Jean, Shio-Shin ; Hsieh, Tai-Chin ; Hsu, Chin-Wan ; Lee, Wen-Sen ; Bai, Kuan-Jen ; Lam, Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-6ef0520312edd01b81e3f84c66003a9bd820a3484a30f4846b32f6a12a3d1d863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acinetobacter baumannii - drug effects</topic><topic>Acinetobacter baumannii - isolation &amp; purification</topic><topic>Acinetobacter Infections - drug therapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Bacteremia - drug therapy</topic><topic>Bacteremia - microbiology</topic><topic>Cilastatin - therapeutic use</topic><topic>combination regimen</topic><topic>Drug Combinations</topic><topic>Drug Resistance, Multiple, Bacterial</topic><topic>Drug Synergism</topic><topic>Drug Therapy, Combination - methods</topic><topic>extensively drug-resistant Acinetobacter baumannii</topic><topic>Female</topic><topic>Hospital Mortality</topic><topic>Humans</topic><topic>imipenem</topic><topic>Imipenem - therapeutic use</topic><topic>Infectious Disease</topic><topic>Male</topic><topic>Medical Education</topic><topic>Microbial Sensitivity Tests</topic><topic>Middle Aged</topic><topic>Minocycline - analogs &amp; derivatives</topic><topic>Minocycline - therapeutic use</topic><topic>Pneumonia, Ventilator-Associated - drug therapy</topic><topic>Pneumonia, Ventilator-Associated - microbiology</topic><topic>Salvage Therapy</topic><topic>sulbactam</topic><topic>Sulbactam - therapeutic use</topic><topic>Taiwan</topic><topic>tigecycline</topic><topic>Treatment Outcome</topic><topic>ventilator-associated pneumonia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jean, Shio-Shin</creatorcontrib><creatorcontrib>Hsieh, Tai-Chin</creatorcontrib><creatorcontrib>Hsu, Chin-Wan</creatorcontrib><creatorcontrib>Lee, Wen-Sen</creatorcontrib><creatorcontrib>Bai, Kuan-Jen</creatorcontrib><creatorcontrib>Lam, Carlos</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><jtitle>Journal of microbiology, immunology and infection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jean, Shio-Shin</au><au>Hsieh, Tai-Chin</au><au>Hsu, Chin-Wan</au><au>Lee, Wen-Sen</au><au>Bai, Kuan-Jen</au><au>Lam, Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the clinical efficacy between tigecycline plus extended-infusion imipenem and sulbactam plus imipenem against ventilator-associated pneumonia with pneumonic extensively drug-resistant Acinetobacter baumannii bacteremia, and correlation of clinical efficacy with in vitro synergy tests</atitle><jtitle>Journal of microbiology, immunology and infection</jtitle><addtitle>J Microbiol Immunol Infect</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>49</volume><issue>6</issue><spage>924</spage><epage>933</epage><pages>924-933</pages><issn>1684-1182</issn><eissn>1995-9133</eissn><abstract>Abstract Background/Purpose To compare the clinical efficacy between salvage antimicrobial regimen consisting of tigecycline plus extended-infusion imipenem/cilastatin (TIC) and regimen of sulbactam plus imipenem/cilastatin (SIC) for patients with ventilator-associated pneumonia and pneumonic bacteremia due to extensively drug-resistant (XDR) Acinetobacter baumannii (Ab) isolates, and determine the correlation of results of in vitro tigecycline–imipenem synergy test with clinical efficacy. Methods The comparative survey was conducted at a medical center in Taiwan in 2013. Patients comprising the TIC group ( n  = 28) received tigecycline plus extended-infusion imipenem/cilastatin following unresponsiveness to 3-day sulbactam–imipenem/cilastatin therapy, and those in the SIC group ( n  = 56) received sulbactam–imipenem/cilastatin throughout the course. Univariate and multivariate analyses were applied to explore 30-day case-fatality independent predictors. Additionally, the checkerboard test and time-kill analysis were performed for the bloodstream XDR-Ab isolates from patients in the TIC group, and molecular characterization was done for the bloodstream XDR-Ab strains of all patients. Results We found that the TIC scheme has a significant benefit on improving patients' survival status (the mortality rate of TIC and SIC group patients was 14.3% and 64.3%, respectively), corresponding well with in vitro synergy or additivity results by the checkerboard test. Twenty TIC group cases had monomicrobial XDR-Ab cultured from tracheal aspirates after 10 days of tigecycline–imipenem/cilastatin therapy, but none developed subsequent pneumonia. However, breakthrough primary Burkholderia cepacia ( n  = 3) and Pseudomonas aeruginosa ( n  = 1) bacteremias were attributed to four TIC case fatalities. Shock, SIC regimen usage, and development of breakthrough bacteremia were independent predictors of 30-day in-hospital mortality. Conclusion Although the TIC regimen showed good efficacy, its value regarding managing XDR-Ab ventilator-associated pneumonia bacteremia needs further evaluation.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>26341302</pmid><doi>10.1016/j.jmii.2015.06.009</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Acinetobacter baumannii - drug effects
Acinetobacter baumannii - isolation & purification
Acinetobacter Infections - drug therapy
Adult
Aged
Aged, 80 and over
Anti-Bacterial Agents - therapeutic use
Bacteremia - drug therapy
Bacteremia - microbiology
Cilastatin - therapeutic use
combination regimen
Drug Combinations
Drug Resistance, Multiple, Bacterial
Drug Synergism
Drug Therapy, Combination - methods
extensively drug-resistant Acinetobacter baumannii
Female
Hospital Mortality
Humans
imipenem
Imipenem - therapeutic use
Infectious Disease
Male
Medical Education
Microbial Sensitivity Tests
Middle Aged
Minocycline - analogs & derivatives
Minocycline - therapeutic use
Pneumonia, Ventilator-Associated - drug therapy
Pneumonia, Ventilator-Associated - microbiology
Salvage Therapy
sulbactam
Sulbactam - therapeutic use
Taiwan
tigecycline
Treatment Outcome
ventilator-associated pneumonia
title Comparison of the clinical efficacy between tigecycline plus extended-infusion imipenem and sulbactam plus imipenem against ventilator-associated pneumonia with pneumonic extensively drug-resistant Acinetobacter baumannii bacteremia, and correlation of clinical efficacy with in vitro synergy tests
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