IN VITRO ANTIBIOTIC SYNERGY COLISTIN-RESISTANT KLEBSIELLA PNEUMONIAE
Colistin-resistant Klebsiella pneumoniae (coRKP) infections can cause problems with management, increasing risk for morbidity and mortality but it is unclear which antibiotic combinations are most effective in their treatment. In this study we aimed to determine the activity of individual antibiotic...
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Veröffentlicht in: | Southeast Asian journal of tropical medicine and public health 2019-07, Vol.50 (4), p.703-707 |
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description | Colistin-resistant Klebsiella pneumoniae (coRKP) infections can cause problems with management, increasing risk for morbidity and mortality but it is unclear which antibiotic combinations are most effective in their treatment. In this study we aimed to determine the activity of individual antibiotics and combinations of antibiotics against coRKP using minimum inhibitory concentrations (MICs) of individual antibiotics and the checkerboard technique, respectively. We used the broth microdilution technique to determine the MIC values for tigecycline, gentamicin, amikacin, fosfomycin, chloramphenicol, meropenem, imipenem, ciprofloxacin and colistin against coRKP. The studied coRKP isolates were obtained from patients treated at Phramongkutklao Hospital in Bangkok, Thailand during January 2016-December 2018. None of the isolates tested were susceptible to meropenem, imipenem, ciprofloxacin or colistin but all the isolates were susceptible to tigecycline, amikacin and gentamicin. During in vitro checkerboard testing, a synergistic effect was seen for the following combinations: fosfomycin plus gentamicin seen in 30% of isolates, fosfomycin plus tigecycline seen in 30% of isolates and tigecycline plus gentamicin seen in 13 % of isolates. In vivo studies are needed to determine if these combinations result in a significantly different outcome than treatment using individual antibiotics. To summarize, there were varying sensitivity to tested antibiotics among tested isolates. The combinations of fosfomycin plus gentamicin and fosfomycin plus tigecycline should be explored further for possible combination therapy of coRKP at the studied institution. |
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In this study we aimed to determine the activity of individual antibiotics and combinations of antibiotics against coRKP using minimum inhibitory concentrations (MICs) of individual antibiotics and the checkerboard technique, respectively. We used the broth microdilution technique to determine the MIC values for tigecycline, gentamicin, amikacin, fosfomycin, chloramphenicol, meropenem, imipenem, ciprofloxacin and colistin against coRKP. The studied coRKP isolates were obtained from patients treated at Phramongkutklao Hospital in Bangkok, Thailand during January 2016-December 2018. None of the isolates tested were susceptible to meropenem, imipenem, ciprofloxacin or colistin but all the isolates were susceptible to tigecycline, amikacin and gentamicin. During in vitro checkerboard testing, a synergistic effect was seen for the following combinations: fosfomycin plus gentamicin seen in 30% of isolates, fosfomycin plus tigecycline seen in 30% of isolates and tigecycline plus gentamicin seen in 13 % of isolates. In vivo studies are needed to determine if these combinations result in a significantly different outcome than treatment using individual antibiotics. To summarize, there were varying sensitivity to tested antibiotics among tested isolates. The combinations of fosfomycin plus gentamicin and fosfomycin plus tigecycline should be explored further for possible combination therapy of coRKP at the studied institution.</description><identifier>ISSN: 0125-1562</identifier><language>eng</language><publisher>Bangkok: Central Coordinating Board, SEAMEO-TROPMED Project</publisher><subject>Amikacin ; Antibiotics ; Chloramphenicol ; Chloromycetin ; Ciprofloxacin ; Colistin ; Fosfomycin ; Gentamicin ; Imipenem ; In vivo methods and tests ; Klebsiella ; Meropenem ; Minimum inhibitory concentration ; Morbidity ; Synergistic effect ; Tigecycline</subject><ispartof>Southeast Asian journal of tropical medicine and public health, 2019-07, Vol.50 (4), p.703-707</ispartof><rights>Copyright Central Coordinating Board, SEAMEO-TROPMED Project Jul 2019</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Prawang, Abhisit</creatorcontrib><creatorcontrib>Santimaleeworagun, Wichai</creatorcontrib><creatorcontrib>Changpradub, Dhitiwat</creatorcontrib><creatorcontrib>Thunyaharn, Sudaluck</creatorcontrib><creatorcontrib>Puttilerpong, Chankit</creatorcontrib><title>IN VITRO ANTIBIOTIC SYNERGY COLISTIN-RESISTANT KLEBSIELLA PNEUMONIAE</title><title>Southeast Asian journal of tropical medicine and public health</title><description>Colistin-resistant Klebsiella pneumoniae (coRKP) infections can cause problems with management, increasing risk for morbidity and mortality but it is unclear which antibiotic combinations are most effective in their treatment. In this study we aimed to determine the activity of individual antibiotics and combinations of antibiotics against coRKP using minimum inhibitory concentrations (MICs) of individual antibiotics and the checkerboard technique, respectively. We used the broth microdilution technique to determine the MIC values for tigecycline, gentamicin, amikacin, fosfomycin, chloramphenicol, meropenem, imipenem, ciprofloxacin and colistin against coRKP. The studied coRKP isolates were obtained from patients treated at Phramongkutklao Hospital in Bangkok, Thailand during January 2016-December 2018. None of the isolates tested were susceptible to meropenem, imipenem, ciprofloxacin or colistin but all the isolates were susceptible to tigecycline, amikacin and gentamicin. During in vitro checkerboard testing, a synergistic effect was seen for the following combinations: fosfomycin plus gentamicin seen in 30% of isolates, fosfomycin plus tigecycline seen in 30% of isolates and tigecycline plus gentamicin seen in 13 % of isolates. In vivo studies are needed to determine if these combinations result in a significantly different outcome than treatment using individual antibiotics. To summarize, there were varying sensitivity to tested antibiotics among tested isolates. The combinations of fosfomycin plus gentamicin and fosfomycin plus tigecycline should be explored further for possible combination therapy of coRKP at the studied institution.</description><subject>Amikacin</subject><subject>Antibiotics</subject><subject>Chloramphenicol</subject><subject>Chloromycetin</subject><subject>Ciprofloxacin</subject><subject>Colistin</subject><subject>Fosfomycin</subject><subject>Gentamicin</subject><subject>Imipenem</subject><subject>In vivo methods and tests</subject><subject>Klebsiella</subject><subject>Meropenem</subject><subject>Minimum inhibitory concentration</subject><subject>Morbidity</subject><subject>Synergistic effect</subject><subject>Tigecycline</subject><issn>0125-1562</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNotjctOAyEARVloYq3-A4nrSXgOsJyOWIkIZoaadNUAhUVjbO20_-8kurpncXLuDVggTHiDeUvuwP00HRBiCCu5AM_GwU8TBg87F8zK-GB6OG6dHtZb2HtrxmBcM-hxhtmAb1avRqOt7eCH05t370ynH8BtjV9TefzfJdi86NC_NtavTd_Z5oQlvTRMRakyq0hkWqrYyxRV5IIk2dJERcY4CpZFSZJWQSRvWSptVXQfc2KEVroET3_d0_n4cy3TZXc4Xs_f8-WOcMq5QIJh-gsqgT_i</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Prawang, Abhisit</creator><creator>Santimaleeworagun, Wichai</creator><creator>Changpradub, Dhitiwat</creator><creator>Thunyaharn, Sudaluck</creator><creator>Puttilerpong, Chankit</creator><general>Central Coordinating Board, SEAMEO-TROPMED Project</general><scope>3V.</scope><scope>7QL</scope><scope>7SS</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BVBZV</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope></search><sort><creationdate>20190701</creationdate><title>IN VITRO ANTIBIOTIC SYNERGY COLISTIN-RESISTANT KLEBSIELLA PNEUMONIAE</title><author>Prawang, Abhisit ; 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During in vitro checkerboard testing, a synergistic effect was seen for the following combinations: fosfomycin plus gentamicin seen in 30% of isolates, fosfomycin plus tigecycline seen in 30% of isolates and tigecycline plus gentamicin seen in 13 % of isolates. In vivo studies are needed to determine if these combinations result in a significantly different outcome than treatment using individual antibiotics. To summarize, there were varying sensitivity to tested antibiotics among tested isolates. The combinations of fosfomycin plus gentamicin and fosfomycin plus tigecycline should be explored further for possible combination therapy of coRKP at the studied institution.</abstract><cop>Bangkok</cop><pub>Central Coordinating Board, SEAMEO-TROPMED Project</pub><tpages>5</tpages></addata></record> |
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subjects | Amikacin Antibiotics Chloramphenicol Chloromycetin Ciprofloxacin Colistin Fosfomycin Gentamicin Imipenem In vivo methods and tests Klebsiella Meropenem Minimum inhibitory concentration Morbidity Synergistic effect Tigecycline |
title | IN VITRO ANTIBIOTIC SYNERGY COLISTIN-RESISTANT KLEBSIELLA PNEUMONIAE |
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