B·R·A·H·M·S Lab Solutions: Preeclampsia Management

Discover the power of biomarker testing on KRYPTOR for your laboratory

Benefits of B·R·A·H·M·S biomarkers for prenatal screening, including outstanding lot-to-lot stability, high precision with low interference, efficient workflow for short turnaround time, and more than 20 years of expertise.

Our B·R·A·H·M·S Biomarkers on the KRYPTOR platform offer cutting-edge and novel testing to enhance the care of preeclampsia and other life-threatening diseases. With our solution, you can improve clinical decision making while streamlining workflows and optimizing efficiencies in your laboratory.

 

Optimize your laboratory routine with biomarker testing on KRYPTOR for preeclampsia management

KRYPTOR compact PLUS analyzer

With Nobel Prize winning TRACE technology, Thermo Scientific B·R·A·H·M·S KRYPTOR compact PLUS and biotin-free assays provide results with low interference and high precision. This user-friendly bench-top instrument is easily integrated into any laboratory. Enhance biomarker testing in your lab with:

  • An easy and straightforward laboratory routine requiring less operator intervention
  • With the self-determining dilution factor, reduce human error with increased instrument autonomy
  • Cost reduction due to efficient sample processing
  • Low level of liquid and plastic waste for an environment friendly solution 

Get your sFlt-1/PlGF ratio result in 30 minutes and leverage the optimized workflow offered by the instrument.

 

The first and only FDA cleared biomarkers for the risk assessment and clinical management of preeclampsia

Thermo Scientific B·R·A·H·M·S sFlt-1/PlGF KRYPTOR Test System offers the highest level of compliance with FDA clearance on the B·R·A·H·M·S KRYPTOR compact PLUS.  

Intended use:

Chart illustrating the FDA approved clinical indication for B·R·A·H·M·S PlGF plus KRYPTOR and B·R·A·H·M·S sFlt-1 KRYPTOR. The action is to aid in the risk assessment of progression to preeclampsia with severe features. The patient type is for singleton pregnancy between gestation age 23+0 to 34+6/7 weeks as well as hospitalized for hypertensive disorders of pregnancy. In addition, this test can be used for patients hospitalized for hypertensive disorders of pregnancy. Timing is within next two weeks of presentation.

*As defined by American College of Obstetricians and Gynecologists (ACOG) guidelines

**Preeclampsia, chronic hypertension with or without superimposed preeclampsia, or gestaional hypertension

Interpreting results:

sFlt-1/PlGF < 40 (low risk)* sFlt-1/PlGF ≥ 40 (high risk)*
If the result of the ratio is lower than 40, the pregnant woman is at low risk for progression to preeclampsia with severe features within 2 weeks.  If the result of the ratio is higher or equal to 40, the pregnant woman is at high risk for progression to preeclampsia with severe features within 2 weeks.

 

Quantitative results for PlGF, sFlt-1, and sFlt-1/PlGF ratio are individually reported by the instrument.  These results for PlGF and sFlt-1 should only be used by laboratories to assess assay performance as part of a quality control program and are not intended for interpretation of results. It is recommended to only provide the sFlt-1/PlGF ratio on the laboratory report for healthcare practitioners.

*Interpretations may differ in regions outside of the US.

Learn from our customers

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Preeclampsia Risk Assessment Using Angiogenic Biomarkers in Hospitalized Patients

AACC Symposium - Dr. Anders Berg MD, PhD, Associate Professor of Pathology, Vice Chair of CLIA and Laboratory Operations, Cedars Sinai Medical Center, Los Angeles, CA

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KRYPTOR and TRACE are trademarks of Cisbio Bioassays, licensed for use by B·R·A·H·M·S GmbH, a part of Thermo Fisher Scientific. Nobel Prize is a registered trademark of the Nobel Foundation.