Point-of-Care Fibrinogen Testing in Pregnancy. Academic Article uri icon

Overview

abstract

  • Agreement between estimated fibrinogen concentration via thromboelastography and traditional assays is not established in the parturient. We therefore recruited 56 parturients and performed Clauss and functional fibrinogen level (FLEV) tests. Mean difference of measurements was 36.8 mg/dL (95% CI, 21.8-51.9) with a standard deviation of 52.8 mg/dL. Calculated limits of agreement were 140.2 mg/dL (95% CI, 166.3-114.6) and -66.6 mg/dL (95% CI, -40.8 to -92.5), within the maximum allowable difference of 165 mg/dL. We therefore conclude that while most measurements fell within the limits of agreement, more work is needed to clearly define the role of this test in the obstetric population.

publication date

  • September 1, 2019

Research

keywords

  • Fibrinogen
  • Point-of-Care Testing
  • Pre-Eclampsia
  • Pregnancy Trimester, Third

Identity

Scopus Document Identifier

  • 85066878972

Digital Object Identifier (DOI)

  • 10.1213/ANE.0000000000003301

PubMed ID

  • 31425220

Additional Document Info

volume

  • 129

issue

  • 3