We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Roche Diagnostics

Develops, manufactures, and markets a wide range of in vitro diagnostic systems, instruments, reagents, and tests read more Featured Products: More products

Download Mobile App




POC Bordetella Test Delivers PCR-Accurate Results in 15 Minutes

By LabMedica International staff writers
Posted on 03 Dec 2025

Whooping cough remains difficult to diagnose early because its first symptoms resemble other respiratory infections, leading clinicians to treat empirically and often too late. More...

With whooping cough cases rising due to disrupted vaccination schedules, waning immunity, and vaccine hesitancy, clinicians face increasing diagnostic pressure across all age groups. Now, a rapid point-of-care (POC) PCR test identifies and differentiates Bordetella infections within minutes, enabling targeted antibiotic therapy during the patient visit.

Roche Diagnostics’ (Basel, Switzerland) cobas liat Bordetella panel delivers results in just 15 minutes in primary care and emergency settings, allowing physicians to diagnose pertussis at POC and initiate immediate treatment to prevent severe complications and limit transmission. The test detects and differentiates three clinically important species: Bordetella pertussis, the cause of classic whooping cough; B. parapertussis, associated with a milder pertussis-like illness that may respond differently to treatment; and B. holmesii, an emerging pathogen known to complicate diagnosis.

The assay runs on the compact cobas liat platform and expands Roche’s existing menu of rapid PCR tests for SARS-CoV-2, Influenza A/B, RSV, and Group A Strep. By enabling multiple respiratory diagnoses directly during the consultation, the system reduces dependence on centralized laboratory testing and supports faster, more precise patient management. The cobas liat Bordetella panel has now received U.S. FDA 510(k) clearance, a CLIA waiver, and CE IVDR certification.

"Faster and more accurate clinical decisions are critical for reducing the risk of severe complications and ultimately stopping the transmission of Bordetella infections.” said Matt Sause, CEO of Roche Diagnostics. “This new test allows clinicians to quickly make a definitive and precise diagnosis to ensure patients get the right treatment earlier."


Gold Member
Quantitative POC Immunoassay Analyzer
EASY READER+
POC Helicobacter Pylori Test Kit
Hepy Urease Test
Gold Member
Hybrid Pipette
SWITCH
Alcohol Testing Device
Dräger Alcotest 7000
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Hematology

view channel
Image: Research has linked platelet aggregation in midlife blood samples to early brain markers of Alzheimer’s (Photo courtesy of Shutterstock)

Platelet Activity Blood Test in Middle Age Could Identify Early Alzheimer’s Risk

Early detection of Alzheimer’s disease remains one of the biggest unmet needs in neurology, particularly because the biological changes underlying the disorder begin decades before memory symptoms appear.... Read more

Microbiology

view channel
Image: The SMART-ID Assay delivers broad pathogen detection without the need for culture (Photo courtesy of Scanogen)

Rapid Assay Identifies Bloodstream Infection Pathogens Directly from Patient Samples

Bloodstream infections in sepsis progress quickly and demand rapid, precise diagnosis. Current blood-culture methods often take one to five days to identify the pathogen, leaving clinicians to treat blindly... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.