Your browser doesn't support javascript.
loading
Comparison of novel rapid diagnostic of blood culture identification and antimicrobial susceptibility testing by Accelerate Pheno system and BioFire FilmArray Blood Culture Identification and BioFire FilmArray Blood Culture Identification 2 panels.
Sze, Dorothy T T; Lau, Candy C Y; Chan, Tsz-Ming; Ma, Edmond S K; Tang, Bone S F.
Afiliación
  • Sze DTT; Department of Pathology, Hong Kong Sanatorium and Hospital, Hong Kong, Special Administrative Region, China.
  • Lau CCY; Department of Pathology, Hong Kong Sanatorium and Hospital, Hong Kong, Special Administrative Region, China.
  • Chan TM; Department of Pathology, Hong Kong Sanatorium and Hospital, Hong Kong, Special Administrative Region, China.
  • Ma ESK; Department of Pathology, Hong Kong Sanatorium and Hospital, Hong Kong, Special Administrative Region, China.
  • Tang BSF; Department of Pathology, Hong Kong Sanatorium and Hospital, Hong Kong, Special Administrative Region, China. bonetang@hksh.com.
BMC Microbiol ; 21(1): 350, 2021 12 18.
Article en En | MEDLINE | ID: mdl-34922463
ABSTRACT

BACKGROUND:

Conventional turnaround time (TAT) for positive blood culture (PBC) identification (ID) and antimicrobial susceptibility testing (AST) is 2-3 days. We evaluated the TAT and ID/AST performance using clinical and seeded samples directly from PBC bottles with different commercial approaches (1) Accelerate Pheno® system (Pheno) for ID/AST; (2) BioFire® FilmArray® Blood Culture Identification (BCID) Panel and/ or BCID2 for ID; (3) direct AST by VITEK® 2 (direct AST); and (4) overnight culture using VITEK® 2 colony AST.

RESULTS:

A total of 141 PBC samples were included in this evaluation. Using MALDI-TOF (Bruker MALDI Biotyper) as the reference method for ID, the overall monomicrobial ID sensitivity/specificity are as follows Pheno 97.9/99.9%; BCID 100/100%; and BCID2 100/100%, respectively. For AST performance, broth microdilution (BMD) was used as the reference method. For gram-negatives, overall categorical and essential agreements (CA/EA) for each method were Pheno 90.3/93.2%; direct AST 92.6/88.5%; colony AST 94.4/89.5%, respectively. For gram-positives, the overall CA/EAs were as follows Pheno 97.2/98.89%; direct AST 97.2/100%; colony AST 97.2/100%, respectively. The BCID/BCID2 and direct AST TATs were around 9-20 h (1/9-19 h for ID with resistance markers/AST), with 15 min/sample hands-on time. In comparison, Pheno TATs were around 8-10 h (1.5/7 h for ID/AST) with 2 min/sample hands-on time, maintains a clinically relevant fast report of antibiotic minimal inhibitory concentration (MIC) and allows for less TAT and hands-on time.

CONCLUSION:

In conclusion, to the best of our knowledge, this is the first study conducted as such in Asia; all studied approaches achieved satisfactory performance, factors such as TAT, panel of antibiotics choices and hands-on time should be considered for the selection of appropriate rapid ID and AST of PBC methods in different laboratory settings.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pruebas de Sensibilidad Microbiana / Cultivo de Sangre Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: BMC Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pruebas de Sensibilidad Microbiana / Cultivo de Sangre Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: BMC Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: China