S_1420_3_MDx_ST_QIAstat_respi_plus_01
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QIAstat-Dx Respiratory Panel Plus

Cat. No. / ID:   691224

6 individually packaged cartridges containing all reagents needed for sample preparation and multiple RT-real time PCR plus internal control, including 6 transfer pipettes
ProductInstrumentProduct Type
QIAstat-Dx Respiratory Panel Plus
QIAstat-Dx Analyzer 2.0
QIAstat-Dx Operational Module PRO
QIAstat-Dx Respiratory Panel Mini
QIAstat-Dx Analyzer 1.0
QIAstat-Dx Analytical Module
QIAstat-Dx Operational Module
QIAstat-Dx Gastrointestinal Panel 2
QIAstat-Dx instruments and QIAstat-Dx panels are intended for in vitro diagnostic use. For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit instructions for use or user manual. QIAGEN instructions for use and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services (or your local distributor).
Virtual Demo
Explore the virtual tour to learn more and see this product in action.

Features

  • Intuitive workflow with minimal hands-on time
  • Uses real-time PCR to deliver comprehensive results in about an hour
  • Delivers Ct values and amplification curves for all detected pathogens directly on the instrument touchscreen
  • No precision pipetting required and unique direct swab protocol for input into the cartridge
  • QIAsphere-connected for real-time updates, proactive remote service and custom epidemiology reports*

 

Product Details

QIAstat-Dx simplifies infectious disease diagnostics so you can get faster results for your patients. All you need are a patient sample, a QIAstat-Dx assay cartridge and our intuitive QIAstat-Dx instrument. 

The QIAstat-Dx assay cartridges use multiplex PCR technology – also known as syndromic testing – to quickly survey many different pathogens in a single patient sample. The cartridges come ready with all reagents preloaded and use our trusted assay chemistry to provide comprehensive results in about an hour. 

The QIAstat-Dx Analyzer 1.0 is our flexible modular systems, perfect for labs of every size. Each instrument is made up of 1 Operational Module, which contains the intuitive touch-screen interface, and between 1 to 4 Analytical Modules, letting you test up to 4 samples at once (see "A flexible modular setup to meet your needs"). 

And now you can see critical results even faster with the QIAstat-Dx Analyzer 2.0. With our new Operational Module PRO at the helm, the QIAstat-Dx Analyzer 2.0 blends all the beloved QIAstat-Dx features with some exciting upgrades. This enhanced QIAstat-Dx instrument introduces our Remote Results Application, which merges lab accuracy with clinical speed. Now you can review and confirm patient results from any location, paving the way for effortless collaboration between central and regional labs. The QIAstat-Dx Analyzer 2.0 is more than just an upgrade – it’s a giant leap towards a smarter, more interconnected healthcare future. 

  • Break boundaries: Review and approve results from anywhere with the Remote Results Application, powered by QIAsphere.
  • Stay in the know: Automatically receive notifications and software updates on your instruments. 
  • Customize to your heart’s desire: Easily switch languages, user roles, instrument configurations and more. 

You’ll save even more time with QIAstat-Dx connectivity, powered by QIAsphere*. With QIAstat-Dx connectivity, you can remotely monitor your instruments in real-time and get on-demand epidemiology reports to support your institution-wide surveillance efforts. Simply install the QIAsphere app on your preferred tablet or smartphone or by accessing the QIAsphere web app through your laptop or desktop browser. 

Visit our resource hub to learn how syndromic testing with QIAstat-Dx can help you provide the best care possible for your patients.

*Some features require a QIAstat-Dx Connectivity plan. Flexible plans are available to meet your needs.

Principle

The QIAstat-Dx Analyzers 1.0 and 2.0, combined with QIAstat-Dx assay cartridges**, use real-time PCR to detect pathogen nucleic acids in human biological samples. The QIAstat-Dx Analyzers 1.0 and 2.0 and cartridges are designed as closed systems that contain all necessary reagents, enabling hands-off sample preparation. Detected real-time amplification signals are interpreted by the integrated software and are reported via an intuitive user interface. 

**QIAstat-Dx Respiratory Panel Mini is currently only available for QIAstat-Dx Analyzer 1.0. 

 

Procedure

Setting up and running a QIAstat-Dx test requires minimal hands-on time and just a few simple steps (see " Multiplex panel testing doesn't get easier than this").

  1. Add the patient sample to the main port of the QIAstat-Dx cartridge using the plastic pipette provided. This step is fast and easy to perform and requires no precision pipetting.
  2. Press the Run Test button on the QIAstat-Dx touch screen and scan the sample ID barcode.
  3. Scan the barcode of the cartridge you’re using.
  4. For our QIAstat-Dx Gastrointestinal Panel 2 test, select the sample type (Para-Pak C&S or FecalSwab).
  5. Position the cartridge on the instrument’s sample port. The cartridge will automatically move in and the test will start.
  6. After about an hour, view the comprehensive results.

 

See figures

Applications

QIAstat-Dx Respiratory Panel Plus: Our FDA-cleared test to analyze 21 viral and bacterial targets for common pathogens causing respiratory symptoms, including SARS-CoV-2.

QIAstat-Dx Respiratory Panel Plus – 21 bacterial and viral targets
Viruses Bacteria
  • Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2)
  • Influenza A
  • Influenza A H1
  • Influenza A H3
  • Influenza B
  • Human Coronavirus 229E
  • Human Coronavirus HKU1
  • Human Coronavirus NL63
  • Human Coronavirus OC43
  • Parainfluenza virus 1
  • Parainfluenza virus 2
  • Parainfluenza virus 3
  • Parainfluenza virus 4
  • Adenovirus
  • Respiratory syncytial virus
  • Human metapneumovirus
  • Human Rhinovirus/Enterovirus (not differentiated)
Mycoplasma pneumoniae
Bordetella pertussis
Chlamydophila pneumoniae

This version of our assay replaces the QIAstat-Dx Respiratory SARS-CoV-2 Panel. 

QIAstat-Dx Respiratory Panel Mini: Our FDA-cleared test to analyze 5 viral targets for common pathogens causing respiratory symptoms, including Human Rhinovirus. This targeted panel is ideal for low-risk patients.  

QIAstat-Dx Respiratory Panel Mini – 5 viral targets 
Viruses 
  • Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2)  
  • Influenza A  
  • Influenza B
  • Respiratory syncytial virus
  • Human Rhinovirus 

QIAstat-Dx Respiratory Panel Mini is currently only available for QIAstat-Dx Analyzer 1.0. 

 

QIAstat-Dx Gastrointestinal Panel 2: Our FDA-cleared test to analyze 16 bacterial, viral and parasitic targets for common pathogens causing gastrointestinal symptoms using preserved stool samples (Para-Pak C&S and FecalSwab)**.

QIAstat-Dx Gastrointestinal Panel 2 – 16 bacterial, viral and parasitic targets**
Bacteria Viruses Parasites
  • Campylobacter  (C. jejuni, C. coli and C. upsaliensisi)
  • Shigella/Enteroinvasive Escherichia coli (EIEC)
  • Enteropathogenic Escherichia coli (EPEC)
  • Enterotoxigenic Escherichia coli (ETEC) It/st
  • Shiga-like toxin-producing Escherichia coli (STEC) stx1/stx2 (including specific identification of E. coli O157 serogroup within STEC)
  • Salmonella
  • Plesiomonas shigelloides
  • Yersinia enterocolitica
  • Adenovirus F40/41
  • Astrovirus
  • Norovirus GI/GII
  • Rotavirus A
  • Cryptosporidium
  • Cyclospora cayetanensis
  • Entamoeba histolytica
  • Giardia lamblia***

** STEC and EPEC results are not reported for stool specimens collected in FecalSwab transport media.

***Also known as Giardia intestinalis and Giardia duodenalis.

 

Supporting data and figures

Resources

Application/Protocol Documents (1)
Operating Software (1)
For use with the QIAstat-Dx Analyzer and the DiagCORE Analyzer
Instrument User Manuals (4)
For use with software version 1.6.x

September 2024
For use with software version 1.2.x or higher
For use with software version 1.6.x

August 2024
Safety Data Sheets (1)
Certificates of Analysis (1)