TY - JOUR
T1 - Activity of ceftolozane-tazobactam against Gram-negative pathogens isolated from lower respiratory tract infections in the Asia-Pacific region
T2 - SMART 2015-2016
AU - the SMART Asia-Pacific Group
AU - Kuo, Shu Chen
AU - Liu, Chun Eng
AU - Lu, Po Liang
AU - Chen, Yao Shen
AU - Lu, Min Chi
AU - Ko, Wen Chien
AU - Hsueh, Po Ren
AU - Chuang, Yin Ching
AU - Wang, Fu Der
N1 - Funding Information:
Funding: This study was supported by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA and by a research grant from the Taipei Veterans General Hospital (V107C-169).
Funding Information:
Funding: This study was supported by Merck Sharp & Dohme Corp. a subsidiary of Merck & Co. Inc. Kenilworth, NJ, USA and by a research grant from the Taipei Veterans General Hospital (V107C-169). Competing Interests: None declared. Ethical Approval: The study was approved by the Institutional Review Boards and Ethical Committees of the participating centers, including the Taipei Veterans General Hospital (2018-07-025CC). The Ethical Committees waived the need for informed consent because limited private health information was collected and this research involved no risk to the subjects. We thank other investigators from the Asia-Pacific region for their participation in the SMART program; Tony Korman (Monash Medical Center, Australia), Justin Ellem (Westmead Hospital, Australia), Narelle George (Royal Brisbane Hospital, Australia), Geoffrey Coombs (Royal Perth Hospital, Australia), Geoffery Coombs (Fiona Stanley Hospital, Australia), Hiroshige Mikamo (Aichi Medical University Hospital, Japan), Shinya Kusachi (Toho University, Japan), Tetsu Mizutani (Osaka Police Hospital, Japan), Min-Ja Kim (Korea University Anam Hospital, South Korea), In-Gyu Bae (Gyeongsang National University Hospital, South Korea), Nurulhuda Binti Umur (Hospital Kuala Lumpur, Malaysia), Datin Ganeswrie Rajasekaram (Hospital Sultanah Aminah Johin Bahru, Malaysia), Susan Taylor (Middlemore Hosp. at Counties Manukau District, New Zealand), Sally Roberts (Auckland City Hospital, New Zealand), Koen van der Werff (Wellington Hospital, New Zealand), Dragana Drinkovic (North Shore Hospital, New Zealand), Evelina Lagamayo (St. Luke?s Medical Center, Philippines), Myrna Mendoza (Philippine General Hospital, Philippines), Thean Yen Tan (Changi General Hospital, Singapore), Prabha Krishnan (Tan Tock Seng Hospital, Singapore), Ellie Wang (National Cheng Kung University Hospital, Taiwan), Kwok-Woon Yu (Taipei Veterans General Hospital, Taiwan), Siripen Panthuwong (Songklanakarin Hospital, Thailand), Pattarachai Kiratisin (Siriraj Hospital, Thailand), Doan Mai Phuong (Bach Mai Hospital, Vietnam), Nguyen Thi Van (Benh Vien Viet Duc Hospital, Vietnam). The technical and molecular support for this study provided by IHMA, Inc. is gratefully acknowledged. We also thank Yi-Ju Luo and Mei-Chen Tan from the National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes for performing the WHONET analyses.
Publisher Copyright:
© 2020 Elsevier B.V. and International Society of Chemotherapy
PY - 2020/3
Y1 - 2020/3
N2 - The aim of this study was to investigate the susceptibility of respiratory Gram-negative bacteria to ceftolozane/tazobactam and other antibiotics in the Asia-Pacific region during 2015-2016. MICs were determined using the CLSI standard broth microdilution method and interpreted accordingly. Pseudomonas aeruginosa (1574 isolates), Klebsiella pneumoniae (1226), Acinetobacter baumannii (627) and Escherichia coli (476) accounted for 73.1% of 5342 Gram-negative respiratory pathogens. Susceptibility to ceftolozane/tazobactam of individual Enterobacteriaceae was >80%, except for Enterobacter cloacae (76.6%). Ceftolozane/tazobactam inhibited 81.9% of K. pneumoniae and 91.9% of E. coli, with respective MIC50/MIC90 values of 0.5/>32 and 0.25/2 mg/L. For carbapenem-susceptible, ESBL-producing K. pneumoniae and E. coli, susceptibility was 65.5% and 93.3%, respectively, and respective MIC50/MIC90 values were 2/>32 and 0.5/2 mg/L. BlaCTX-M-1 group was most prevalent in selected ESBL-producing K. pneumoniae (40 of 54 isolates) and E. coli (15 of 22 isolates), with ceftolozane/tazobactam susceptibility rates of 50% and 80%, respectively. BlaSHV-ESBL was the second most prevalent, and ceftolozane/tazobactam inhibited 20% of 20 K. pneumoniae isolates with blaSHV-ESBL. The only effective antibiotics for carbapenem-non-susceptible K. pneumoniae (111 isolates) and E. coli (24 isolates) were amikacin and colistin. Ceftolozane/tazobactam was effective against almost all tested P. aeruginosa and carbapenem-non-susceptible strains, with susceptibility of 92.3% and 72.8%, respectively; the respective MIC50/MIC90 values were 1/4 and 2/>32 mg/L. The high susceptibility of ceftolozane/tazobactam remained in different age groups, patient locations, recovery times and countries, except Vietnam. In conclusion, ceftolozane/tazobactam was effective against most respiratory Gram-negative pathogens in the Asia-Pacific region; however, the emergence of carbapenem resistance mandates ongoing surveillance.
AB - The aim of this study was to investigate the susceptibility of respiratory Gram-negative bacteria to ceftolozane/tazobactam and other antibiotics in the Asia-Pacific region during 2015-2016. MICs were determined using the CLSI standard broth microdilution method and interpreted accordingly. Pseudomonas aeruginosa (1574 isolates), Klebsiella pneumoniae (1226), Acinetobacter baumannii (627) and Escherichia coli (476) accounted for 73.1% of 5342 Gram-negative respiratory pathogens. Susceptibility to ceftolozane/tazobactam of individual Enterobacteriaceae was >80%, except for Enterobacter cloacae (76.6%). Ceftolozane/tazobactam inhibited 81.9% of K. pneumoniae and 91.9% of E. coli, with respective MIC50/MIC90 values of 0.5/>32 and 0.25/2 mg/L. For carbapenem-susceptible, ESBL-producing K. pneumoniae and E. coli, susceptibility was 65.5% and 93.3%, respectively, and respective MIC50/MIC90 values were 2/>32 and 0.5/2 mg/L. BlaCTX-M-1 group was most prevalent in selected ESBL-producing K. pneumoniae (40 of 54 isolates) and E. coli (15 of 22 isolates), with ceftolozane/tazobactam susceptibility rates of 50% and 80%, respectively. BlaSHV-ESBL was the second most prevalent, and ceftolozane/tazobactam inhibited 20% of 20 K. pneumoniae isolates with blaSHV-ESBL. The only effective antibiotics for carbapenem-non-susceptible K. pneumoniae (111 isolates) and E. coli (24 isolates) were amikacin and colistin. Ceftolozane/tazobactam was effective against almost all tested P. aeruginosa and carbapenem-non-susceptible strains, with susceptibility of 92.3% and 72.8%, respectively; the respective MIC50/MIC90 values were 1/4 and 2/>32 mg/L. The high susceptibility of ceftolozane/tazobactam remained in different age groups, patient locations, recovery times and countries, except Vietnam. In conclusion, ceftolozane/tazobactam was effective against most respiratory Gram-negative pathogens in the Asia-Pacific region; however, the emergence of carbapenem resistance mandates ongoing surveillance.
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U2 - 10.1016/j.ijantimicag.2020.105883
DO - 10.1016/j.ijantimicag.2020.105883
M3 - Article
C2 - 31923574
AN - SCOPUS:85078496364
SN - 0924-8579
VL - 55
JO - International journal of antimicrobial agents
JF - International journal of antimicrobial agents
IS - 3
M1 - 105883
ER -