High-sensitivity Troponin Assay Access hsTnI

Access hsTnI (High Sensitivity Troponin I Assay)

The first true high-sensitivity troponin I assay cleared by the FDA

Confidently report accurate test results with Access hsTnI – quality results, optimal precision, easy interpretation. Plus, it provides sex-specific upper reference limits to enable more accurate identification of women with AMI.

This product may not be available in your country or region at this time. Please contact your Beckman Coulter sales representative or distributor for more information.
Overview
Specifications
Documents


A Highly-sensitive Assay

93.3 %
Concordance with PCR Minutes to first results Analyzers
 
25
Minutes to first results
2
Analyzers

High-quality

  • Delivers quality results with a new robust design to minimize the effects of pre-analytical variability and known interferences
  • Demonstrates optimal precision at concentrations ~10x lower than previous generations of assays

Accurate

  • Accurately identifies ≥94% of true acute myocardial infarction (AMI) patients in as little as one hour after presentation
  • Enables more accurate identification of women with AMI by providing separate sex-specific upper reference limits
  • Provides >99% confidence in ruling out AMI when a patient’s troponin result is below the URL

Timely

  • Enables easier interpretation of test results by using whole-number reporting
  • Increases testing flexibility as the only high-sensitivity assay to use either plasma or serum samples
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References:

iPretorius, C.J., et. al. “A critical evaluation of the Beckman Coulter Access hsTnI: Analytical performance, reference interval and concordance.” Clinical Biochemistry, vol. 55, 2018 May, pp. 49–55. https://doi.org/10.1016/j.clinbiochem.2018.03.003. Accessed 22 June 2018.