{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,1]],"date-time":"2025-11-01T13:56:10Z","timestamp":1762005370512,"version":"3.40.5"},"reference-count":39,"publisher":"Microbiology Society","issue":"4","funder":[{"DOI":"10.13039\/100009947","name":"Merck Sharp & Dohme Corp.","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100009947","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,4,22]]},"abstract":"<jats:p>\n                  <jats:bold>Introduction.<\/jats:bold> Ceftolozane\/tazobactam was approved by the Drug Office, Department of Health, Government of the Hong Kong Special Administrative Region in 2017.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Hypothesis\/Gap Statement.<\/jats:bold> Currently the <jats:italic>in vitro<\/jats:italic> activity of ceftolozane\/tazobactam against Gram-negative pathogens isolated from patients in Hong Kong is undocumented. It would be prudent to document the activity of ceftolozane\/tazobactam against <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2553\" xlink:type=\"simple\">Pseudomonas aeruginosa<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> and Enterobacterales isolated from hospitalized patients in Hong Kong.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Aim.<\/jats:bold> To describe the <jats:italic>in vitro<\/jats:italic> susceptibility of recent clinical isolates of <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2553\" xlink:type=\"simple\">P. aeruginosa<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> and the two most common Enterobacterales species (<jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.10789\" xlink:type=\"simple\">Klebsiella pneumoniae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>, <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3093\" xlink:type=\"simple\">Escherichia coli<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>) cultured from respiratory tract, intra-abdominal, urinary tract and bloodstream infection samples to ceftolozane\/tazobactam and other commonly used antimicrobial agents.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Methodology.<\/jats:bold> CLSI-defined broth microdilution MICs were determined and interpreted for Gram-negative isolates collected in Hong Kong from 2017 to 2019 by the SMART surveillance programme.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Results.<\/jats:bold> For <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2553\" xlink:type=\"simple\">P. aeruginosa<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>, 96.7\u200a% of isolates (<jats:italic>n<\/jats:italic>=210) were susceptible to ceftolozane\/tazobactam, while susceptibility rates were \u226514\u200a% lower to meropenem (82.9\u200a% susceptible), cefepime (82.4\u200a%), ceftazidime (81.4\u200a%), piperacillin\/tazobactam (76.7\u200a%) and levofloxacin (79.5\u200a%). Ceftolozane\/tazobactam inhibited 85.7\u200a% of piperacillin\/tazobactam-nonsusceptible isolates, 80.6\u201382.1\u200a% of cefepime-, ceftazidime- or meropenem-nonsusceptible isolates, and 75.9\u200a% of multidrug-resistant (MDR) isolates of <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2553\" xlink:type=\"simple\">P. aeruginosa<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>. For <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.10789\" xlink:type=\"simple\">K. pneumoniae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>, 96.1\u200a% of isolates (<jats:italic>n<\/jats:italic>=308) were susceptible to ceftolozane\/tazobactam compared with meropenem (99.0\u200a% susceptible), piperacillin\/tazobactam (93.8\u200a%), cefepime (85.7\u200a%) and ceftazidime (85.4\u200a%). The majority (88.3\u200a%) of ESBL (extended-spectrum \u03b2-lactamase) non-CRE (carbapenem-resistant Enterobacterales) phenotype isolates of <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.10789\" xlink:type=\"simple\">K. pneumoniae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> were susceptible to ceftolozane\/tazobactam, comparable to piperacillin\/tazobactam (85.0\u200a%) but lower than meropenem (100\u200a%). For <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3093\" xlink:type=\"simple\">E. coli<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>, 98.5\u200a% of isolates (<jats:italic>n<\/jats:italic>=609) were susceptible to ceftolozane\/tazobactam compared to meropenem (99.3\u200a% susceptible), piperacillin\/tazobactam (96.7\u200a%), ceftazidime (82.3\u200a%) and cefepime (76.5\u200a%). The majority (96.7\u200a%) of ESBL non-CRE phenotype isolates of <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3093\" xlink:type=\"simple\">E. coli<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> were susceptible to ceftolozane\/tazobactam, similar to both meropenem (100\u200a%) and piperacillin\/tazobactam (94.5\u200a%).<\/jats:p>\n               <jats:p>\n                  <jats:bold>Conclusions.<\/jats:bold> Overall, &gt;96\u200a% of clinical isolates of <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2553\" xlink:type=\"simple\">P. aeruginosa<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>, <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.10789\" xlink:type=\"simple\">K. pneumoniae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> and <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3093\" xlink:type=\"simple\">E. coli<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> collected in Hong Kong in 2017\u20132019 were susceptible to ceftolozane\/tazobactam, while the activity of several commonly prescribed \u03b2-lactams was reduced, especially for <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2553\" xlink:type=\"simple\">P. aeruginosa<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>. Continued surveillance of ceftolozane\/tazobactam and other agents is warranted.<\/jats:p>","DOI":"10.1099\/jmm.0.001487","type":"journal-article","created":{"date-parts":[[2022,4,22]],"date-time":"2022-04-22T15:17:36Z","timestamp":1650640656000},"source":"Crossref","is-referenced-by-count":6,"title":["Activity of ceftolozane\/tazobactam against Gram-negative isolates among different infections in Hong Kong: SMART 2017\u20132019"],"prefix":"10.1099","volume":"71","author":[{"given":"James A.","family":"Karlowsky","sequence":"first","affiliation":[{"name":"Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, MB, R3E 0J9, Canada"},{"name":"IHMA, Schaumburg, IL, 60173, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sibylle H.","family":"Lob","sequence":"additional","affiliation":[{"name":"IHMA, Schaumburg, IL, 60173, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aaron","family":"Khan","sequence":"additional","affiliation":[{"name":"Global Medical & Scientific Affairs, MSD (Asia) Ltd., Hong Kong"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wei-Ting","family":"Chen","sequence":"additional","affiliation":[{"name":"MSD, Taipei, Taiwan, ROC"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Patrick C. 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