Improved blood culture workflow for faster identification of KPC-producing Enterobacterales.

改进血液培养工作流程,以更快地鉴定产 KPC 肠杆菌科细菌

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作者:Seco Bruna Mara Silva, Campos Juliana Coutinho, da Costa Rocha Darlan Augusto, de Lima Aline Valerio, de Oliveira Fernanda Filomena, Lemo Mara Elisa Borsato, Sampaio Suely Carlos Ferreira, Sampaio Jorge Luiz Mello
Carba-NP original report for blood cultures described the need of subculture and mechanical lysis before testing, reaching the turnaround time of approximately 4 hours for sample preparation. We tested 100 consecutive blood cultures positive for Gram-negative bacilli on the Gram stain from a large clinical laboratory. Bacterial pellets were prepared by centrifugation and submitted to Carba-NP and Blue-Carba tests and used further to prepare smears for Vitek MS. Results obtained with colonies grown on sheep blood agar using the same methodologies were used as the gold standard. Carbapenemase genes were confirmed by PCR and DNA sequencing. Vitek MS identified correctly 86% of the samples. Of note, 7% of the samples were incorrectly reported by the instrument as containing a single isolate. KPC-2 was the predominant carbapenemase detected. There was 100% concordance for both negative and positive results for Carba-NP. In contrast, for Blue-Carba the concordance for positive results was 92.8%, and 41% of strains negative for carbapenemases presented a yellowish color on control well turning the test non-interpretable. The turnaround time for sample preparation for preparing the pellet was 13 min, and no subculture or mechanical lysis is needed when detecting KPC production in Enterobacterales.

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