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QIAGEN Launches QIAstat-Dx Gastrointestinal Panel 2 in the U.S. for Improved GI Infection Diagnosis

QIAGEN has introduced the QIAstat-Dx Gastrointestinal Panel 2 in the United States, following its clearance by the U.S. FDA. This new panel offers rapid and accurate identification of up to 16 common gastrointestinal pathogens, significantly enhancing the diagnosis and treatment of GI infections.

The QIAstat-Dx Gastrointestinal Panel 2, recently cleared by the U.S. Food and Drug Administration (FDA), represents a significant advancement in the diagnosis of gastrointestinal (GI) infections. This innovative panel can simultaneously detect up to 16 clinically relevant bacterial, viral, and parasitic pathogens that are responsible for most GI infections, delivering results in approximately one hour. This rapid turnaround is a notable improvement over traditional microbiological testing methods, which can take from 24 hours up to 10 days.
Utilizing real-time PCR technology, the QIAstat-Dx system quickly multiplies many genetic targets in the same reaction, providing easy-to-view cycle threshold (Ct) values and amplification curves. These features offer additional insights not available with end-point PCR or other techniques, facilitating a more accurate diagnosis.
Fernando Beils, Senior Vice President and Head of the Molecular Diagnostics Business Area at QIAGEN, highlighted the panel's ability to quickly identify GI pathogens, addressing the challenges of diagnosing overlapping symptoms and laborious testing methods. Romney Humphries, Ph.D., from Vanderbilt University Medical Center, emphasized the clinical utility of the panel in distinguishing between viral, bacterial, and parasitic causes of GI illness, noting the ease of setup and the valuable information provided by Ct values.
The introduction of the QIAstat-Dx Gastrointestinal Panel 2 expands QIAGEN's U.S. menu for syndromic testing, complementing the QIAstat-Dx Respiratory Panel Plus. Both panels are designed as cost-efficient, single-use cartridges for the QIAstat-Dx Analyzer 1.0, requiring less than a minute for setup and no precision pipetting.
This development is expected to significantly benefit healthcare providers by enabling quick and accurate diagnosis and treatment of patients, reducing the burden of unnecessary testing and treatment costs. Syndromic testing also improves the detection of co-infections and supports responsible antimicrobial stewardship by allowing healthcare providers to discontinue empiric antibiotic treatment when viral pathogens are detected.
QIAstat-Dx solutions, including the Gastrointestinal Panel 2, are available in over 100 countries, with more than 4,000 systems installed worldwide by the end of 2023. The system's cloud-based connectivity and epidemiological insights further enhance its utility, offering remote monitoring and real-time data analysis to support epidemiological surveillance and informed decision-making in healthcare settings.
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[1]
QIAGEN expands QIAstat-Dx syndromic testing menu in ...
corporate.qiagen.com · Jun 3, 2024

The U.S. FDA has approved QIAGEN's QIAstat-Dx Gastrointestinal Panel 2 for clinical use, enabling rapid identification o...

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