MICROBIOLOGY REAGENTSMolecular syndromic testing

Comprehensive and effective approach to sepsis and antimicrobial resistance

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REAGENTSMolecular syndromic testing

Same-day results providing a significant improvement in patient treatment

With a high morbidity and mortality rate, ranging from 30% to 50%, sepsis and antimicrobial resistance pose a threat to global public health. Their treatment faces the challenge of increasing mechanisms of resistance, largely fuelled by the indiscriminate use of antibiotics. Accurate microbiological identification of the offending pathogens has become crucial for optimal treatment management. Response to treatment is directly linked to the time that elapses before appropriate antimicrobial therapy is administered.

In response to this critical public health challenge, Vitro has developed hybridisation reagents for molecular syndromic testing. Our kits allow bacteria, fungi and the most common antibiotic resistance genes to be detected in a single assay. Notably, it enables the direct analysis of clinical samples without the need to extract DNA, facilitating the process and enabling the efficient screening of infected and colonised patients for clinical management and infection control.

This innovative approach includes the detection of genes associated with multidrug-resistant Enterobacteriaceae (CRE, ESBL), vancomycin-resistant Enterococci (VRE) and methicillin-resistant Staphylococcus aureus (MRSA). It is also important to note that our kit and detection method are patent-protected (patent no. WO2014102761A3).

Vitro is breaking new ground by providing antibiotic resistance results on the same day as a positive blood culture, significantly improving patient management and treatment.

DNA FLOW for molecular syndromic testing

Detects multidrug-resistant pathogens by using multiplex PCR and reverse hybridisation.MDR Direct Flow Chip Kit

Ref: MAD-003946M-HS12 - 24 determinations
Ref: MAD-003946M-HS - 24 determinations

Kit details
It can detect 5 bacterial species (S. aureus, K. pneumoniae, P. aeruginosa, E. coli and A. baumannii) and a total of 56 resistance markers: beta-lactams, glycopeptides, oxazolidinones, macrolides, aminoglycosides, sulphonamides, fluoroquinolones, polymyxins, chloramphenicol, as well as point mutations most frequently detected in fluoroquinolone-resistant strains of E. coli and P. aeruginosa.

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Detection of antibiotic resistance markers via multiplex PCR and reverse hybridisation.AMR Direct Flow Chip Kit

Ref: MAD-003937M-HS12 - 24 determinations
Ref: MAD-003937M-HS - 24 determinations

Kit details
It can detect Staphylococcus aureus and 20 antibiotic resistance markers, including the detection of point mutations of the blaSHV gene.

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Detection of bacteria, fungi and antibiotic resistance markers via multiplex PCR and reverse hybridisation.Sepsis Flow Chip Kit

Ref: MAD-003936M-HS - 24 determinaciones
Ref: MAD-003936M-HS12-24 - 24 determinations
Ref: MAD-003936M-HS12-48 - 48 determinations
Ref: MAD-003936M-HS24-24 - 24 determinations
Ref: MAD-003936M-HS24-48 - 48 determinations

Kit details
Simultaneous detection of the main pathogens that cause sepsis and resistance genes to antibiotics commonly used in hospitals. It can detect 36 bacterial species and a total of 20 antibiotic resistance markers. It can detect Streptococcus spp., Streptococcus pneumoniae, Streptococcus pyogenes, Streptococcus agalactiae, Coagulase-negative staphylococci, Staphylococcus aureus, Listeria monocytogenes, Enterococcus spp., Neisseria meningitidis, Acinetobacter baumannii, Serratia marcescens, Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Enterobacter spp., Proteus spp./ Morganella morganii, Candida spp., Candida albicans and a total of 20 antibiotic resistance markers: Methicillin: mecA, Vancomycin: vanA and vanB, Carbapenemase: KPC, SME, NMC/IMI GES, VIM, GIM, SPM, NDM, SIM, IMP3, 15, 19_like, OXA-23_like, OXA-24_like, OXA-48_like, OXA-51_like, OXA-58_like, ß-lactamases: SHV and CTX-M

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Our kits include a panel that provides maximum coverage, designed to predict antibiotic resistance phenotypes by identifying known genes that encode specific mechanisms of resistance. As well as providing crucial information for targeted treatment, this approach also yields valuable epidemiological data.

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