Rapid phenotypic antimicrobial susceptibility testing of Gram-negative rods directly from positive blood cultures using the novel Q-linea ASTar system

被引:9
|
作者
Esse, Jan [1 ,2 ]
Traeger, Johannes [1 ,2 ]
Valenza, Giuseppe [1 ,2 ]
Bogdan, Christian [1 ,2 ]
Held, Juergen [1 ,2 ]
机构
[1] Univ Klinikum Erlangen, Mikrobiol Inst, Klin Mikrobiol Immunol & Hyg, Erlangen, Germany
[2] Friedrich Alexander Univ FAU Erlangen Nurnberg, Erlangen, Germany
关键词
AST; RAST; sepsis; blood stream infection; VITEK; scum plate method; ESCHERICHIA-COLI; INITIATION; SURVIVAL; THERAPY;
D O I
10.1128/jcm.00549-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adequate and timely antibiotic therapy is crucial for the treatment of sepsis. Innovative systems, like the Q-linea ASTar, have been developed to perform rapid antimicrobial susceptibility testing (AST) directly from positive blood cultures (BCs). We conducted a prospective study to evaluate ASTar under real-life conditions with a focus on time-to-result and impact on antimicrobial therapy. Over 2 months, all positive BCs that showed Gram-negative rods upon microscopy were tested with the ASTar and our standard procedure (VITEK 2 from short-term culture). Additionally, we included multidrug-resistant Gram-negative bacteria from our archive. Both methods were compared to broth microdilution. In total, 78 bacterial strains (51 prospective and 27 archived) were tested. ASTar covered 94% of the species encountered. The categorical and essential agreement was 95.6% and 90.7%, respectively. ASTar caused 2.4% minor, 2.0% major, and 2.4% very major errors. The categorical agreement was similar to standard procedure. The average time between BC sampling and the availability of the antibiogram for the attending physician was 28 h 49 min for ASTar and 44 h 18 min for standard procedure. ASTar correctly identified all patients who required an escalation of antimicrobial therapy and 75% of those who were eligible for de-escalation. In conclusion, ASTar provided reliable AST results and significantly shortened the time to obtain an antibiogram. However, the percentage of patients that will profit from ASTar in a low-resistance setting is limited, and it is currently unclear if a change of therapy 29 h after BC sampling will have a significant impact on the patient's prognosis.
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页数:17
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