Don't let gastrointestinal infections impact your laboratory's efficiency
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:
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?
Dive deeper into prevalence of bacterial, viral and parasitic infection in acute gastroenteritis and main diagnostic methods.
Learn more about the challenges of traditional diagnostic methods and how these inefficiencies can affect your laboratory workflow.
Rapid, accurate pathogen identification is crucial to minimising 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
Gain a greater understanding of the benefits of molecular testing in this evaluation comparing workflow and time-to-results with culture.
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
Make the step toward simplicity and cost-effectiveness with the BD MAX™ System.
How did the NHS Chesterfield Royal Hospital reduce diagnostic turnaround times and optimise bed management with the BD MAX™ System?
Learn more about the ease of specimen preparation on the BD MAX™ System and best practices in readying your samples.
Discover the full menu of assays for enteric testing and how your laboratory can benefit from the BD MAX™ System.
With hardware and software innovations, the enhanced BD MAX™ System is designed to be easy-to-use, provide even more consistent results and enhance laboratory efficiency and ergonomics.11
As a step toward the BD vision of integrating molecular testing into the automated BD Kiestra™ microbiology workflow, you can now consolidate your sample types across molecular and culture testing with FecalSwab™ now validated on the BD Enteric Portfolio for the BD MAX™ System.***