Don't let gastrointestinal infections impact your laboratory's efficiency

Though among the most common global infectious diseases, gastrointestinal infections can create a major burden for the healthcare system, especially if your lab is lacking the resources, trained staff and equipment to detect certain pathogens.1

Traditional diagnostic methods such as culture, microscopy and immunoassay can take up to 3-5 days to identify the causative agents of infection, potentially impacting lab workflow, budget, clinical decision-making and patient outcomes. This inefficiency can lead to:

  • Delayed results2
  • Difficulty growing certain organisms on culture media1,3
  • False results due to subjective interpretation of microscopy4
  • The culture method in particular is labour intensive with poor sensitivity and low positive culture rates, requiring 3-5 days for pathogen detection.1,5

Can your lab afford the risks of inefficient enteric diagnostics?


Time-motion analysis: stool culture vs BD MAX™ Enteric Bacterial Panel

Gain a greater understanding of the benefits of molecular testing in this evaluation comparing workflow and time-to-results with culture.

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The BD MAX™ difference

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.9

Its automated workflow reduces manual tasks to achieve rapid, reliable results and facilitates off-hour testing, helping to offset molecular testing costs.*2,10:

  • Rapid results: 96 results available within the same day 
  • More time for value-added tasks: Less than 1.5 minutes of hands-on time with ready-to-use, room temperature reagents
  • All-inclusive package: All reagents and required tips are included in the assay kits of the BD MAX™ System
  • Easy to use: Snap, load and go system with limited training required and minimal daily set-up and intervention during the run
  • Concurrently test viral, bacterial and parasitic pathogens: Run and rack compatibility with most BD MAX™ assays**
  • Help reduce risks of contamination and human error: Fully automated sample processing and results interpretation
  • Make the step toward simplicity and cost-effectiveness with the BD MAX™ System

Additional Resources

Simplify Your GI Testing with Real-Time PCR

Hear from three respected key opinion leaders on how transitioning from traditional culture to molecular methods has created positive impact on their laboratory workflow and patients.


Watch the webinar


Advance diagnostic stewardship in GI testing

Hear from two experienced clinical microbiologists on their selection criteria for molecular panels for GI testing, the impact on the management of patients, and the role diagnostic stewardship plays in their laboratory testing practices.

Watch the webinar


The full BD MAX™ enteric testing menu


Discover the full menu of assays for enteric testing and how your laboratory can benefit from the BD MAX™ System.





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Let's have a conversation

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The BD MAX™ difference

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.9

Its automated workflow reduces manual tasks to achieve rapid, reliable results and facilitates off-hour testing, helping to offset molecular testing costs.*2,10

  • Rapid results: 96 results available within the same day
  • More time for value-added tasks: Less than 1.5 minutes of hands-on time with ready-to-use, room temperature reagents
  • All-inclusive package: All reagents and required tips are included in the assay kits of the BD MAX™ System
  • Easy to use: Snap, load and go system with limited training required and minimal daily set-up and intervention during the run
  • Concurrently test viral, bacterial and parasitic pathogens: Run and rack compatibility with most BD MAX™ assays**
  • Help reduce risks of contamination and human error: Fully automated sample processing and results interpretation
  • Make the step toward simplicity and cost-effectiveness with the BD MAX™ System.

Placeholder

H3 Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do

Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Habitant morbi tristique senectus et netus et malesuada fames. Bibendum est ultricies integer quis auctor elit sed. Magna eget est lorem ipsum dolor sit amet.

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Store Tab

360° rotation knob is effectively sized, contoured and located to enable easy instrument rotation.

360° rotation knob is effectively sized

360° rotation knob is effectively sized

360° rotation knob is effectively sized

More product details

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Make the move to molecular testing

Rapid, accurate pathogen identification is crucial to minimizing outbreak risk.6

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.7

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.1 It also allows easy differentiation between pathogenic and non-pathogenic species, such as Entamoeba histolytica and Entamoeba dispar8.

Thanks to NAATs, your laboratory can facilitate the rapid diagnosis, treatment and management of gastrointestinal infections.1

Gastroenteritis: The big picture


Dive deeper into prevalence of bacterial, viral and parasitic infection in acute gastroenteritis and main diagnostic methods.

READ THE ARTICLE

Evaluating the diagnostic methods for acute gastroenteritis

Learn more about the challenges of traditional diagnostic methods and how these inefficiencies can affect your laboratory workflow.

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Let's have a conversation

REFERENCES

1. Amjad M. An Overview of the Molecular Methods in the Diagnosis of Gastrointestinal Infectious Diseases. Int J Microbiol. 2020 Mar 24;2020:8135724. doi: 10.1155/2020/8135724
2. Mortensen JE, Ventrola C, Hanna S, Walter A. Comparison of time-motion analysis of conventional stool culture and the BD MAX™ Enteric Bacterial Panel (EBP). BMC Clin Pathol. 2015;15:9. https://doi.org/10.1186/s12907-015-0010-8
3. Anderson NW, Buchan BW, Ledeboer NA. Comparison of the BD MAX™ Enteric Bacterial Panel to Routine Culture Methods for Detection of Campylobacter, Enterohemorrhagic Escherichia coli (O157), Salmonella, and Shigella Isolates in Preserved Stool Specimens. J Clin Microbiol. 2014 Apr;52(4):1222-1224. doi: 10.1128/JCM.03099-13
4. Centers for Disease Control and Prevention. Parasites – Amebiasis – Entamoeba histolytica Infection. Available at: https://www.cdc.gov/parasites/amebiasis/index.html. Accessed 13 February, 2023.
5. Lee JY, Cho SY, Hwang HSH, et al. Diagnostic yield of stool culture and predictive factors for positive culture in patients with diarrheal illness. Medicine (Baltimore). 2017 Jul;96(30):e7641. doi: 10.1097/MD.0000000000007641.
6. Priyanka B, Patil RK, Dwarakanath S. A review on detection methods used for foodborne pathogens. Indian Journal of Medical Research. 2016 Sep;144(3):327-338. doi: 10.4103/0971-5916.198677.
7. NICE. BD MAX™ Enteric Bacterial Panel for Identifying Pathogens in Contagious Gastroenteritis Medtech Innovation Briefing.; 2015. www.nice.org.uk/guidance/mib32
8. Subhash et al. Laboratory methods of identification of Entamoeba histolytica and its differentiation from look-alike entamoeba spp, Trop Parasitol, 2014 Jul; 4(2):90-5
9. Sidoti F, Ritta M, Costa C, et al. Diagnosis of viral gastroenteritis: limits and potential pf currently available procedures. J Infect Dev Ctries 2015;9:551-561
10. Hirvonen JJ, et al. Comparison of BD Max Cdiff and GenomEra C. difficile molecular assays for detection of toxigenic Clostridium difficile from stools in conventional sample containers and in FecalSwabs. Eur J Clin Microbiol Infect Dis. 2015;34(5):1005-1009. doi: 10.1007/s10096-015-2320-2. Epub 2015 Jan 24.
11. Felder RA, Jackson KD, Walter AM. Process evaluation of an open architecture real-time molecular laboratory platform. J Lab Autom. 2014 Oct;19(5):468-73. doi: 10.1177/2211068214533195. Epub 2014 May 8.

*Time to results is assay dependent
**BD assays are run & rack compatible – Only MDR-TB is not run and rack compatible/Vaginal Panel, GBS and open systems’ assays are only run compatible.

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