Determining a specific clinical diagnosis can benefit a patient with infectious diarrhoea by:
Directing appropriate therapy
Allowing the judicious use of antimicrobial agents
Improving patient satisfaction
Targeted molecular stool testing that decreases turnaround time, increases accuracy and aids in patient management
Because it can be difficult to differentiate the cause of gastrointestinal illness, targeted testing allows clinicians to accurately decide which tests are needed according to the patient’s clinical presentation and history.
The innovation of the BD MAX™ System offers you a fully integrated, automated real-time PCR platform with an array of targeted syndromic panels that provide improved rapid detection of bacterial, viral and parasitic pathogens responsible for ≥90% of infectious diarrhoea.1
Transitioning from culture to molecular testing, namely nucleic acid-based amplification tests (NAATs), has been shown to significantly improve the sensitivity, specificity, time to results of your laboratory’s gastroenteritis testing.2
When early detection or identification of pathogens can help lead to faster treatment decisions, reduce hospital length of stay, prevent unnecessary antibiotic use and most importantly, save lives, you need to implement the most rapid, reliable testing solution.3
~ 1.7 billion cases of children with infectious gastroenteritis each year4
Infectious diarrhoea is the 2nd leading cause of the death in children under 5 years of age4
Norovirus resulted in a total of $4.2 billion in direct health system costs5
Delayed results6
Difficulty growing certain organisms on culture media7
False results due to subjective interpretation of microscopy8
Poor sensitivity and specificity with immunoassays9
Directing appropriate therapy
Allowing the judicious use of antimicrobial agents
Improving patient satisfaction
Salmonella spp.
Campylobacter spp. (C. jejuni and C. coli)
Shigella spp and EIEC
Shiga toxin (stx1/stx2) genes (found in STEC)
Plesiomonas shigelloides
Vibrio spp. (V. vulnuficus, V. parahaemo lyticus, V. cholerae)
Enterotoxigenic E. coli (ETEC)
Yersinia entercolitica
Giardia lamblia
Cryptosporidium spp (C. hominis and C. parvum)
Entamoeba histolytica
Norovirus GI & GII
Rotavirus A
Adenovirus F40/41
Sapovirus (genogroups I, II, IV, V)
Human Astrovirus (hAstro
Norovirus GI & GII
Rotavirus A
EIEC, Enteroinvasive Escherichia coli; ETEC, Enterotoxigenic Escherichia coli; STEC, Shiga toxin–producing Escherichia coli.
Shigella dysenteriae can possess a Shiga toxin gene identical to the Shiga toxin 1 found in STEC.
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The BD MAX™ System, BD MAX™ Enteric Bacterial & Extended Enteric Bacterial Panels, BD MAX™ Enteric Viral Panel, BD MAX™ Enteric Viral Panel-NR, BD MAX™ Enteric Parasite Panel, BD MAX™ Vaginal Panel, BD MAX™ CPO, BD MAX™ MRSA XT, BD MAX™ StaphSR, BD MAX™ Cdiff, BD MAX™ MDR-TB, BD SARS-CoV-2 Reagents for BD MAX™ System, BD SARS-CoV-2/Flu for BD MAX™ System, BD Respiratory Viral Panel for BD MAX™ System, VIASURE SARS-CoV-2 (N1+N2) Real Time PCR Detection Kit for BD MAX™ System, VIASURE SARS-CoV-2 Variant Real Time PCR Detection Kit for BD MAX™, VIASURE SARS-CoV-2 Variant II Real Time PCR Detection Kit for BD MAX™, VIASURE SARS-CoV-2, Flu (A+B), RSV Real Time PCR Detection Kit for BD MAX™ System, VIASURE Flu A, Flu B & RSV Real Time PCR Detection Kit for BD MAX™ System, VIASURE VanR Real Time PCR Detection Kit for BD MAX™ System, VIASURE Pneumocystis jirovecci Real Time PCR Detection Kit for BD MAX™ System and VIASURE Bordetella Real Time PCR Detection Kit for BD MAX™ System are in vitro diagnostic medical devices bearing a CE mark.
The BD CTGC2 and BD CTGCTV2 assays for BD MAX™ System are in vitro diagnostic medical devices bearing a CE mark and are CE certified by BSI Group The Netherlands B.V. (Notified Body Number = 2797).