Stenotrophomonas maltophilia: Results of Antimicrobial Susceptibility Testing and In Vitro Activity of the Combination of Ceftazidime and Moxifloxacin/Stenotrophomonas maltophilia: Antimikrobik Duyarlilik Testi Sonuclari ve Seftazidimin Moksifloksasinle Kombinasyonunun In Vitro Etkinligi
Objective: Recommended combination for the treatment of serious Stenotrophomonas maltophilia infections is ticarcillin-clavulanate and co-trimoxazole (SXT). However, first agent is not available in our country, and the second component may be a matter of antimicrobial resistance or intolerance. Ther...
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description | Objective: Recommended combination for the treatment of serious Stenotrophomonas maltophilia infections is ticarcillin-clavulanate and co-trimoxazole (SXT). However, first agent is not available in our country, and the second component may be a matter of antimicrobial resistance or intolerance. Therefore, we aimed to evaluate antimicrobial susceptibility testing results of S. maltophilia and in vitro activity of ceftazidime and moxifloxacin as a potential therapeutic alternative. Methods: S. maltophilia strains isolated from clinical samples in Infectious Diseases and Clinical Microbiology Laboratory between 1 October 2007-23 November 2017 were included in the study. Disk diffusion antimicrobial susceptibility test results of the strains were evaluated retrospectively. The in vitro activity of combination of ceftazidime and moxifloxacin against 24 of these strains was investigated by Etest[R]. Results: During the study period, 649 S. maltophilia strains were isolated from 649 different patients, and 94%, 93%, 92%, 81%, 60%, 55%, 45%, 41%, 38% of the strains were susceptible to tigecycline, moxifloxacin, SXT, ciprofloxacin, cefoperazone-sulbactam, ceftazidime, netilmicin, gentamicin and amikacin, respectively. For the 24 strains included in the combination study, the moxifloxacin minimal inhibitory concentration [(MIC).sub.50]/[MIC.sub.90] values were defined as 0.064/0.125 [micro]g/mL (MIC range 0.023-4 [micro]g/mL) and ceftazidime [MIC.sub.50]/[MIC.sub.90] values were defined as 32/256 [micro]g/mL (MIC range 1.5-256 [micro]g/mL). According to the results of fractional inhibitor concentration (FIC) index; ceftazidime and moxifloxacin combination displayed synergism, additivity and indifference for 1 (4%), 18 (75%) and 5 (21%) strains, respectively and there was no antagonism. The [FIC.sub.50]/[FIC.sub.90] value is calculated as 0.75/1.01 (FIC range 0.5-1.01). Conclusions: SXT resistance in S. maltophilia strains is below 10%, but it should be closely monitored because of the limited treatment options. Tigecycline and moxifloxacin can be among the treatment alternatives because of their high sensitivity rates similar to SXT. The combination of moxifloxacin plus ceftazidime demonstrated in vitro synergism or additivity against majority of the strains. So, this combination may be used as an alternative for the treatment of patients with S. maltophilia infections if there is resistance or side effects to the antibiotics used as the first option. Key Words: Ste |
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fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_infotracmisc_A583990514</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A583990514</galeid><sourcerecordid>A583990514</sourcerecordid><originalsourceid>FETCH-LOGICAL-g674-288b8400a99af502f98f960ffeb02991620c9dde257db8b1224066d20325be633</originalsourceid><addsrcrecordid>eNp9kU1PAjEQhtdEEwly8RdM4hnodj_YeiOISsSYCDHeSHe3hXG7LaGFgL_erhj1YOwcms7MO-_TTBBchqSXhAntV2WPkpD1SHYatMKIhN0wjl7Pg461b6Q5AzKIk9YJzJzQxm3MemVqo7mFmivnX6iQX8OzsFvlLBgJQ-2wxmJjcuQKZltbiLXD3Pe5A8yFdaiXwHUJEw0v6CfCsHC4a6pe7VYCRqbOUXOHRjepkZCOv2OJtfjUPZo9SmX2vEDd_x_ryFI1LBXcbA98o3yhOmLAzOhtofgGYSdg9u2C2ltUtvGoLLeolYCHI5I9eImPH_axq3wDLvEiOJNcWdH5utvB_HY8H913p093k9Fw2l2mg7hLsyzPYkI4Y1wmhEqWSZYSKUVOKGNhSknBylLQZFDmWR5SGpM0LSmJaJKLNIrawdVx7JIrsUAt_ed5UaMtFsMkixgjiV9gO-j90eWjFH41RguJPv9L8AHpfKzz</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Stenotrophomonas maltophilia: Results of Antimicrobial Susceptibility Testing and In Vitro Activity of the Combination of Ceftazidime and Moxifloxacin/Stenotrophomonas maltophilia: Antimikrobik Duyarlilik Testi Sonuclari ve Seftazidimin Moksifloksasinle Kombinasyonunun In Vitro Etkinligi</title><source>EZB Electronic Journals Library</source><creator>Sadic, Betul ; Basaran, Seniha ; Simsek-Yavuz, Serap ; Cagatay, Atahan ; Ozsut, Halit ; Eraksoy, Haluk</creator><creatorcontrib>Sadic, Betul ; Basaran, Seniha ; Simsek-Yavuz, Serap ; Cagatay, Atahan ; Ozsut, Halit ; Eraksoy, Haluk</creatorcontrib><description>Objective: Recommended combination for the treatment of serious Stenotrophomonas maltophilia infections is ticarcillin-clavulanate and co-trimoxazole (SXT). However, first agent is not available in our country, and the second component may be a matter of antimicrobial resistance or intolerance. Therefore, we aimed to evaluate antimicrobial susceptibility testing results of S. maltophilia and in vitro activity of ceftazidime and moxifloxacin as a potential therapeutic alternative. Methods: S. maltophilia strains isolated from clinical samples in Infectious Diseases and Clinical Microbiology Laboratory between 1 October 2007-23 November 2017 were included in the study. Disk diffusion antimicrobial susceptibility test results of the strains were evaluated retrospectively. The in vitro activity of combination of ceftazidime and moxifloxacin against 24 of these strains was investigated by Etest[R]. Results: During the study period, 649 S. maltophilia strains were isolated from 649 different patients, and 94%, 93%, 92%, 81%, 60%, 55%, 45%, 41%, 38% of the strains were susceptible to tigecycline, moxifloxacin, SXT, ciprofloxacin, cefoperazone-sulbactam, ceftazidime, netilmicin, gentamicin and amikacin, respectively. For the 24 strains included in the combination study, the moxifloxacin minimal inhibitory concentration [(MIC).sub.50]/[MIC.sub.90] values were defined as 0.064/0.125 [micro]g/mL (MIC range 0.023-4 [micro]g/mL) and ceftazidime [MIC.sub.50]/[MIC.sub.90] values were defined as 32/256 [micro]g/mL (MIC range 1.5-256 [micro]g/mL). According to the results of fractional inhibitor concentration (FIC) index; ceftazidime and moxifloxacin combination displayed synergism, additivity and indifference for 1 (4%), 18 (75%) and 5 (21%) strains, respectively and there was no antagonism. The [FIC.sub.50]/[FIC.sub.90] value is calculated as 0.75/1.01 (FIC range 0.5-1.01). Conclusions: SXT resistance in S. maltophilia strains is below 10%, but it should be closely monitored because of the limited treatment options. Tigecycline and moxifloxacin can be among the treatment alternatives because of their high sensitivity rates similar to SXT. The combination of moxifloxacin plus ceftazidime demonstrated in vitro synergism or additivity against majority of the strains. So, this combination may be used as an alternative for the treatment of patients with S. maltophilia infections if there is resistance or side effects to the antibiotics used as the first option. Key Words: Stenotrophomonas maltophilia, antimicrobial susceptibility, drug combinations, moxifloxacin, ceftazidime. Amac: Ciddi Stenotrophomonas maltophilia infeksiyonlarinin kombinasyon tedavisinde ilk secenek olarak onerilen tikarsilin-klavulanat ve kotrimoksazol (SXT)'den, ilki ulkemizde bulunmamakta, ikincisi icin de direnc veya intolerans soz konusu olabilmektedir. Bu nedenle S. maltophilia suslarinin antibiyotik duyarlilik testi sonuclarini ve bu suslara karsi potansiyel bir tedavi secenegi olarak seftazidimin moksifloksasinle kombinasyonunun in vitro etkinligini degerlendirmeyi amacladik. Yontemler: Calismaya 1 Ekim 2017-23 Kasim 2017 tarihleri arasinda Infeksiyon Hastaliklari ve Klinik Mikrobiyoloji Laboratuvari'na gelen klinik orneklerde ureyen S. maltophilia suslari dahil edildi. Suslarin disk difuzyon yontemiyle yapilmis antimikrobiyal duyarlilik testi sonuclari retrospektif olarak degerlendirildi. Bu suslardan 24'une karsi seftazidim-moksifloksasin kombinasyonunun etkinligi Etest[R] yontemiyle in vitro arastirildi. Bulgular: Calisma suresince laboratuvarimizda toplam 649 ayri hastadan 649 S. maltophilia susu izole edildi. Suslarin %94'u tigesikline, %93'u moksifloksasine, %92'si SXT'ye, %81'i siprofloksasine, %60'i sefoperazon-sulbaktama, %55'i seftazidime, %45'i netilmisine, %41'i gentamisine ve %38'i amikasine duyarli olarak bulundu. Kombinasyon calismasina alinan 24 sus icin moksifloksasin minimum inhibitor konsantrasyon [(MIC).sub.50]/[MIC.sub.90] degerleri 0.064/0.125 [micro]g/ml (MIC araligi 0.023-4 [micro]g/ml) ve seftazidim [MIC.sub.50]/[MIC.sub.90] degerleri 32/256 [micro]g/ml (MIC araligi 1.5-256 [micro]g/ml) olarak hesaplandi. Fraksiyonel inhibitor konsantrasyon (FIC) indeksi sonuclarina gore, seftazidim ve moksifloksasin kombinasyonu suslarin 1 (%4)' inde sinerjik, 18 (%75)'inde aditif, 5 (%21)'inde indiferan etkinlik gosterdi. Bu kombinasyonla antagonist etkinlik gorulmedi. [FIC.sub.50]/[FIC.sub.90] degeri ise 0.75/1.01 (FIC araligi 0.5-1.01) olarak hesaplandi. Sonuclar: S. maltophilia suslarinda SXT direnci %10'un altindadir; ancak tedavi seceneklerinin sinirli olmasi nedeniyle yakindan izlenmelidir. Tigesiklin ve moksifloksasin, SXT kadar yuksek duyarlilik oranlari olmasi nedeniyle tedavi secenekleri arasinda yer alabilir. Moksifloksasin ve seftazidim kombinasyonu, suslarin coguna karsi in vitro sinerjik veya aditif etkinlik gostermistir. Bu nedenle S. maltophilia infeksiyonlarinin tedavisinde, yan etkiler veya direnc nedeniyle ilk secenek rejimlerin kullanilamadigi durumlarda bu kombinasyon bir secenek olabilir. Anahtar Sozcukler: Stenotrophomonas maltophilia, antimikrobik duyarliligi, ilac kombinasyonlari, moksifloksasin, seftazidim.</description><identifier>ISSN: 1301-143X</identifier><identifier>DOI: 10.5152/kd.2019.08</identifier><language>eng</language><publisher>AVES</publisher><subject>Amikacin ; Aminoglycosides ; Antibacterial agents ; Ceftazidime ; Clavulanate ; Combination drug therapy ; Communicable diseases ; Dosage and administration ; Gram-negative bacteria ; Infection ; Medical research ; Microbiology ; Moxifloxacin ; Sulbactam ; Ticarcillin ; Tigecycline</subject><ispartof>KLIMIK dergisi, 2019-04, Vol.32 (1), p.29</ispartof><rights>COPYRIGHT 2019 AVES</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Sadic, Betul</creatorcontrib><creatorcontrib>Basaran, Seniha</creatorcontrib><creatorcontrib>Simsek-Yavuz, Serap</creatorcontrib><creatorcontrib>Cagatay, Atahan</creatorcontrib><creatorcontrib>Ozsut, Halit</creatorcontrib><creatorcontrib>Eraksoy, Haluk</creatorcontrib><title>Stenotrophomonas maltophilia: Results of Antimicrobial Susceptibility Testing and In Vitro Activity of the Combination of Ceftazidime and Moxifloxacin/Stenotrophomonas maltophilia: Antimikrobik Duyarlilik Testi Sonuclari ve Seftazidimin Moksifloksasinle Kombinasyonunun In Vitro Etkinligi</title><title>KLIMIK dergisi</title><description>Objective: Recommended combination for the treatment of serious Stenotrophomonas maltophilia infections is ticarcillin-clavulanate and co-trimoxazole (SXT). However, first agent is not available in our country, and the second component may be a matter of antimicrobial resistance or intolerance. Therefore, we aimed to evaluate antimicrobial susceptibility testing results of S. maltophilia and in vitro activity of ceftazidime and moxifloxacin as a potential therapeutic alternative. Methods: S. maltophilia strains isolated from clinical samples in Infectious Diseases and Clinical Microbiology Laboratory between 1 October 2007-23 November 2017 were included in the study. Disk diffusion antimicrobial susceptibility test results of the strains were evaluated retrospectively. The in vitro activity of combination of ceftazidime and moxifloxacin against 24 of these strains was investigated by Etest[R]. Results: During the study period, 649 S. maltophilia strains were isolated from 649 different patients, and 94%, 93%, 92%, 81%, 60%, 55%, 45%, 41%, 38% of the strains were susceptible to tigecycline, moxifloxacin, SXT, ciprofloxacin, cefoperazone-sulbactam, ceftazidime, netilmicin, gentamicin and amikacin, respectively. For the 24 strains included in the combination study, the moxifloxacin minimal inhibitory concentration [(MIC).sub.50]/[MIC.sub.90] values were defined as 0.064/0.125 [micro]g/mL (MIC range 0.023-4 [micro]g/mL) and ceftazidime [MIC.sub.50]/[MIC.sub.90] values were defined as 32/256 [micro]g/mL (MIC range 1.5-256 [micro]g/mL). According to the results of fractional inhibitor concentration (FIC) index; ceftazidime and moxifloxacin combination displayed synergism, additivity and indifference for 1 (4%), 18 (75%) and 5 (21%) strains, respectively and there was no antagonism. The [FIC.sub.50]/[FIC.sub.90] value is calculated as 0.75/1.01 (FIC range 0.5-1.01). Conclusions: SXT resistance in S. maltophilia strains is below 10%, but it should be closely monitored because of the limited treatment options. Tigecycline and moxifloxacin can be among the treatment alternatives because of their high sensitivity rates similar to SXT. The combination of moxifloxacin plus ceftazidime demonstrated in vitro synergism or additivity against majority of the strains. So, this combination may be used as an alternative for the treatment of patients with S. maltophilia infections if there is resistance or side effects to the antibiotics used as the first option. Key Words: Stenotrophomonas maltophilia, antimicrobial susceptibility, drug combinations, moxifloxacin, ceftazidime. Amac: Ciddi Stenotrophomonas maltophilia infeksiyonlarinin kombinasyon tedavisinde ilk secenek olarak onerilen tikarsilin-klavulanat ve kotrimoksazol (SXT)'den, ilki ulkemizde bulunmamakta, ikincisi icin de direnc veya intolerans soz konusu olabilmektedir. Bu nedenle S. maltophilia suslarinin antibiyotik duyarlilik testi sonuclarini ve bu suslara karsi potansiyel bir tedavi secenegi olarak seftazidimin moksifloksasinle kombinasyonunun in vitro etkinligini degerlendirmeyi amacladik. Yontemler: Calismaya 1 Ekim 2017-23 Kasim 2017 tarihleri arasinda Infeksiyon Hastaliklari ve Klinik Mikrobiyoloji Laboratuvari'na gelen klinik orneklerde ureyen S. maltophilia suslari dahil edildi. Suslarin disk difuzyon yontemiyle yapilmis antimikrobiyal duyarlilik testi sonuclari retrospektif olarak degerlendirildi. Bu suslardan 24'une karsi seftazidim-moksifloksasin kombinasyonunun etkinligi Etest[R] yontemiyle in vitro arastirildi. Bulgular: Calisma suresince laboratuvarimizda toplam 649 ayri hastadan 649 S. maltophilia susu izole edildi. Suslarin %94'u tigesikline, %93'u moksifloksasine, %92'si SXT'ye, %81'i siprofloksasine, %60'i sefoperazon-sulbaktama, %55'i seftazidime, %45'i netilmisine, %41'i gentamisine ve %38'i amikasine duyarli olarak bulundu. Kombinasyon calismasina alinan 24 sus icin moksifloksasin minimum inhibitor konsantrasyon [(MIC).sub.50]/[MIC.sub.90] degerleri 0.064/0.125 [micro]g/ml (MIC araligi 0.023-4 [micro]g/ml) ve seftazidim [MIC.sub.50]/[MIC.sub.90] degerleri 32/256 [micro]g/ml (MIC araligi 1.5-256 [micro]g/ml) olarak hesaplandi. Fraksiyonel inhibitor konsantrasyon (FIC) indeksi sonuclarina gore, seftazidim ve moksifloksasin kombinasyonu suslarin 1 (%4)' inde sinerjik, 18 (%75)'inde aditif, 5 (%21)'inde indiferan etkinlik gosterdi. Bu kombinasyonla antagonist etkinlik gorulmedi. [FIC.sub.50]/[FIC.sub.90] degeri ise 0.75/1.01 (FIC araligi 0.5-1.01) olarak hesaplandi. Sonuclar: S. maltophilia suslarinda SXT direnci %10'un altindadir; ancak tedavi seceneklerinin sinirli olmasi nedeniyle yakindan izlenmelidir. Tigesiklin ve moksifloksasin, SXT kadar yuksek duyarlilik oranlari olmasi nedeniyle tedavi secenekleri arasinda yer alabilir. Moksifloksasin ve seftazidim kombinasyonu, suslarin coguna karsi in vitro sinerjik veya aditif etkinlik gostermistir. Bu nedenle S. maltophilia infeksiyonlarinin tedavisinde, yan etkiler veya direnc nedeniyle ilk secenek rejimlerin kullanilamadigi durumlarda bu kombinasyon bir secenek olabilir. Anahtar Sozcukler: Stenotrophomonas maltophilia, antimikrobik duyarliligi, ilac kombinasyonlari, moksifloksasin, seftazidim.</description><subject>Amikacin</subject><subject>Aminoglycosides</subject><subject>Antibacterial agents</subject><subject>Ceftazidime</subject><subject>Clavulanate</subject><subject>Combination drug therapy</subject><subject>Communicable diseases</subject><subject>Dosage and administration</subject><subject>Gram-negative bacteria</subject><subject>Infection</subject><subject>Medical research</subject><subject>Microbiology</subject><subject>Moxifloxacin</subject><subject>Sulbactam</subject><subject>Ticarcillin</subject><subject>Tigecycline</subject><issn>1301-143X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNp9kU1PAjEQhtdEEwly8RdM4hnodj_YeiOISsSYCDHeSHe3hXG7LaGFgL_erhj1YOwcms7MO-_TTBBchqSXhAntV2WPkpD1SHYatMKIhN0wjl7Pg461b6Q5AzKIk9YJzJzQxm3MemVqo7mFmivnX6iQX8OzsFvlLBgJQ-2wxmJjcuQKZltbiLXD3Pe5A8yFdaiXwHUJEw0v6CfCsHC4a6pe7VYCRqbOUXOHRjepkZCOv2OJtfjUPZo9SmX2vEDd_x_ryFI1LBXcbA98o3yhOmLAzOhtofgGYSdg9u2C2ltUtvGoLLeolYCHI5I9eImPH_axq3wDLvEiOJNcWdH5utvB_HY8H913p093k9Fw2l2mg7hLsyzPYkI4Y1wmhEqWSZYSKUVOKGNhSknBylLQZFDmWR5SGpM0LSmJaJKLNIrawdVx7JIrsUAt_ed5UaMtFsMkixgjiV9gO-j90eWjFH41RguJPv9L8AHpfKzz</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Sadic, Betul</creator><creator>Basaran, Seniha</creator><creator>Simsek-Yavuz, Serap</creator><creator>Cagatay, Atahan</creator><creator>Ozsut, Halit</creator><creator>Eraksoy, Haluk</creator><general>AVES</general><scope/></search><sort><creationdate>20190401</creationdate><title>Stenotrophomonas maltophilia: Results of Antimicrobial Susceptibility Testing and In Vitro Activity of the Combination of Ceftazidime and Moxifloxacin/Stenotrophomonas maltophilia: Antimikrobik Duyarlilik Testi Sonuclari ve Seftazidimin Moksifloksasinle Kombinasyonunun In Vitro Etkinligi</title><author>Sadic, Betul ; Basaran, Seniha ; Simsek-Yavuz, Serap ; Cagatay, Atahan ; Ozsut, Halit ; Eraksoy, Haluk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g674-288b8400a99af502f98f960ffeb02991620c9dde257db8b1224066d20325be633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amikacin</topic><topic>Aminoglycosides</topic><topic>Antibacterial agents</topic><topic>Ceftazidime</topic><topic>Clavulanate</topic><topic>Combination drug therapy</topic><topic>Communicable diseases</topic><topic>Dosage and administration</topic><topic>Gram-negative bacteria</topic><topic>Infection</topic><topic>Medical research</topic><topic>Microbiology</topic><topic>Moxifloxacin</topic><topic>Sulbactam</topic><topic>Ticarcillin</topic><topic>Tigecycline</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sadic, Betul</creatorcontrib><creatorcontrib>Basaran, Seniha</creatorcontrib><creatorcontrib>Simsek-Yavuz, Serap</creatorcontrib><creatorcontrib>Cagatay, Atahan</creatorcontrib><creatorcontrib>Ozsut, Halit</creatorcontrib><creatorcontrib>Eraksoy, Haluk</creatorcontrib><jtitle>KLIMIK dergisi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sadic, Betul</au><au>Basaran, Seniha</au><au>Simsek-Yavuz, Serap</au><au>Cagatay, Atahan</au><au>Ozsut, Halit</au><au>Eraksoy, Haluk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stenotrophomonas maltophilia: Results of Antimicrobial Susceptibility Testing and In Vitro Activity of the Combination of Ceftazidime and Moxifloxacin/Stenotrophomonas maltophilia: Antimikrobik Duyarlilik Testi Sonuclari ve Seftazidimin Moksifloksasinle Kombinasyonunun In Vitro Etkinligi</atitle><jtitle>KLIMIK dergisi</jtitle><date>2019-04-01</date><risdate>2019</risdate><volume>32</volume><issue>1</issue><spage>29</spage><pages>29-</pages><issn>1301-143X</issn><abstract>Objective: Recommended combination for the treatment of serious Stenotrophomonas maltophilia infections is ticarcillin-clavulanate and co-trimoxazole (SXT). However, first agent is not available in our country, and the second component may be a matter of antimicrobial resistance or intolerance. Therefore, we aimed to evaluate antimicrobial susceptibility testing results of S. maltophilia and in vitro activity of ceftazidime and moxifloxacin as a potential therapeutic alternative. Methods: S. maltophilia strains isolated from clinical samples in Infectious Diseases and Clinical Microbiology Laboratory between 1 October 2007-23 November 2017 were included in the study. Disk diffusion antimicrobial susceptibility test results of the strains were evaluated retrospectively. The in vitro activity of combination of ceftazidime and moxifloxacin against 24 of these strains was investigated by Etest[R]. Results: During the study period, 649 S. maltophilia strains were isolated from 649 different patients, and 94%, 93%, 92%, 81%, 60%, 55%, 45%, 41%, 38% of the strains were susceptible to tigecycline, moxifloxacin, SXT, ciprofloxacin, cefoperazone-sulbactam, ceftazidime, netilmicin, gentamicin and amikacin, respectively. For the 24 strains included in the combination study, the moxifloxacin minimal inhibitory concentration [(MIC).sub.50]/[MIC.sub.90] values were defined as 0.064/0.125 [micro]g/mL (MIC range 0.023-4 [micro]g/mL) and ceftazidime [MIC.sub.50]/[MIC.sub.90] values were defined as 32/256 [micro]g/mL (MIC range 1.5-256 [micro]g/mL). According to the results of fractional inhibitor concentration (FIC) index; ceftazidime and moxifloxacin combination displayed synergism, additivity and indifference for 1 (4%), 18 (75%) and 5 (21%) strains, respectively and there was no antagonism. The [FIC.sub.50]/[FIC.sub.90] value is calculated as 0.75/1.01 (FIC range 0.5-1.01). Conclusions: SXT resistance in S. maltophilia strains is below 10%, but it should be closely monitored because of the limited treatment options. Tigecycline and moxifloxacin can be among the treatment alternatives because of their high sensitivity rates similar to SXT. The combination of moxifloxacin plus ceftazidime demonstrated in vitro synergism or additivity against majority of the strains. So, this combination may be used as an alternative for the treatment of patients with S. maltophilia infections if there is resistance or side effects to the antibiotics used as the first option. Key Words: Stenotrophomonas maltophilia, antimicrobial susceptibility, drug combinations, moxifloxacin, ceftazidime. Amac: Ciddi Stenotrophomonas maltophilia infeksiyonlarinin kombinasyon tedavisinde ilk secenek olarak onerilen tikarsilin-klavulanat ve kotrimoksazol (SXT)'den, ilki ulkemizde bulunmamakta, ikincisi icin de direnc veya intolerans soz konusu olabilmektedir. Bu nedenle S. maltophilia suslarinin antibiyotik duyarlilik testi sonuclarini ve bu suslara karsi potansiyel bir tedavi secenegi olarak seftazidimin moksifloksasinle kombinasyonunun in vitro etkinligini degerlendirmeyi amacladik. Yontemler: Calismaya 1 Ekim 2017-23 Kasim 2017 tarihleri arasinda Infeksiyon Hastaliklari ve Klinik Mikrobiyoloji Laboratuvari'na gelen klinik orneklerde ureyen S. maltophilia suslari dahil edildi. Suslarin disk difuzyon yontemiyle yapilmis antimikrobiyal duyarlilik testi sonuclari retrospektif olarak degerlendirildi. Bu suslardan 24'une karsi seftazidim-moksifloksasin kombinasyonunun etkinligi Etest[R] yontemiyle in vitro arastirildi. Bulgular: Calisma suresince laboratuvarimizda toplam 649 ayri hastadan 649 S. maltophilia susu izole edildi. Suslarin %94'u tigesikline, %93'u moksifloksasine, %92'si SXT'ye, %81'i siprofloksasine, %60'i sefoperazon-sulbaktama, %55'i seftazidime, %45'i netilmisine, %41'i gentamisine ve %38'i amikasine duyarli olarak bulundu. Kombinasyon calismasina alinan 24 sus icin moksifloksasin minimum inhibitor konsantrasyon [(MIC).sub.50]/[MIC.sub.90] degerleri 0.064/0.125 [micro]g/ml (MIC araligi 0.023-4 [micro]g/ml) ve seftazidim [MIC.sub.50]/[MIC.sub.90] degerleri 32/256 [micro]g/ml (MIC araligi 1.5-256 [micro]g/ml) olarak hesaplandi. Fraksiyonel inhibitor konsantrasyon (FIC) indeksi sonuclarina gore, seftazidim ve moksifloksasin kombinasyonu suslarin 1 (%4)' inde sinerjik, 18 (%75)'inde aditif, 5 (%21)'inde indiferan etkinlik gosterdi. Bu kombinasyonla antagonist etkinlik gorulmedi. [FIC.sub.50]/[FIC.sub.90] degeri ise 0.75/1.01 (FIC araligi 0.5-1.01) olarak hesaplandi. Sonuclar: S. maltophilia suslarinda SXT direnci %10'un altindadir; ancak tedavi seceneklerinin sinirli olmasi nedeniyle yakindan izlenmelidir. Tigesiklin ve moksifloksasin, SXT kadar yuksek duyarlilik oranlari olmasi nedeniyle tedavi secenekleri arasinda yer alabilir. Moksifloksasin ve seftazidim kombinasyonu, suslarin coguna karsi in vitro sinerjik veya aditif etkinlik gostermistir. Bu nedenle S. maltophilia infeksiyonlarinin tedavisinde, yan etkiler veya direnc nedeniyle ilk secenek rejimlerin kullanilamadigi durumlarda bu kombinasyon bir secenek olabilir. Anahtar Sozcukler: Stenotrophomonas maltophilia, antimikrobik duyarliligi, ilac kombinasyonlari, moksifloksasin, seftazidim.</abstract><pub>AVES</pub><doi>10.5152/kd.2019.08</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1301-143X |
ispartof | KLIMIK dergisi, 2019-04, Vol.32 (1), p.29 |
issn | 1301-143X |
language | eng |
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source | EZB Electronic Journals Library |
subjects | Amikacin Aminoglycosides Antibacterial agents Ceftazidime Clavulanate Combination drug therapy Communicable diseases Dosage and administration Gram-negative bacteria Infection Medical research Microbiology Moxifloxacin Sulbactam Ticarcillin Tigecycline |
title | Stenotrophomonas maltophilia: Results of Antimicrobial Susceptibility Testing and In Vitro Activity of the Combination of Ceftazidime and Moxifloxacin/Stenotrophomonas maltophilia: Antimikrobik Duyarlilik Testi Sonuclari ve Seftazidimin Moksifloksasinle Kombinasyonunun In Vitro Etkinligi |
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