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Rapid screening of positive blood cultures for extended-spectrum ß-lactamases and metallo-ß-lactamases using a drug susceptibility testing microfluidic method.
Yamagishi, Yuka; Nakayama, Norihisa; Doke, Akito; Iwame, Saya; Nishida, Yoshie; Arakawa, Yu; Mikamo, Hiroshige.
Afiliação
  • Yamagishi Y; Department of Clinical Infectious Diseases, Kochi Medical School, Kochi University, Kochi, Japan. Electronic address: y.yamagishi@mac.com.
  • Nakayama N; Fukoku Co. Ltd., Saitama, Japan.
  • Doke A; Division of Clinical Laboratory, Kochi Medical School Hospital, Kochi University, Kochi, Japan.
  • Iwame S; Division of Clinical Laboratory, Kochi Medical School Hospital, Kochi University, Kochi, Japan.
  • Nishida Y; Division of Clinical Laboratory, Kochi Medical School Hospital, Kochi University, Kochi, Japan.
  • Arakawa Y; Department of Clinical Infectious Diseases, Kochi Medical School, Kochi University, Kochi, Japan.
  • Mikamo H; Department of Clinical Infectious Diseases, Aichi Medical University, Aichi, Japan.
J Infect Chemother ; 2024 Apr 30.
Article em En | MEDLINE | ID: mdl-38697390
ABSTRACT

OBJECTIVES:

An increasing number of drug-resistant bacteria have been identified recently. In particular, drug-resistant bacteria have been linked to unfavorable prognoses in patients with bacteremia, highlighting the need for rapid testing. Our previous studies have focused on the utility of a drug susceptibility testing microfluidic (DSTM) method using microfluidic channels. A system with this DSTM method for screening for ß-lactamases can rapidly detect extended-spectrum ß-lactamases (ESBLs) and metallo-ß-lactamases (MBLs). In this study, we have evaluated the clinical utility of pre-treatment for screening positive blood cultures using the DSTM method.

METHODS:

A total of 178 positive blood cultures and five simulated samples of MBL-producing bacteria were prepared at Kochi University Hospital, Japan. The pretreatment consisted of a two-step centrifugation. The obtained sediments were screened with the DSTM method for the production of ß-lactamase based on morphological changes in the bacteria after 3 h of incubation.

RESULTS:

The pretreatment functioned properly for all samples. Of the 25 ESBL samples, 21 were positive for ESBLs. Four false-negative samples, all obtained from the same patient, contained CTX-M-2 enzyme-producing Proteus mirabilis and showed insusceptibility to an ESBL inhibitor. The simulated samples prepared for MBL screening were positive for MBLs.

CONCLUSIONS:

When combined with a method for rapidly identifying bacterial species, DSTM may enable patients with bloodstream infections to start receiving appropriate treatment within 4 h after positive blood cultures are screened.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article