4.6 Article

Congo Red Dot Paper Test for Antenatal Triage and Rapid Identification of Preeclampsia

Journal

ECLINICALMEDICINE
Volume 8, Issue -, Pages 47-56

Publisher

ELSEVIER
DOI: 10.1016/j.eclinm.2019.02.004

Keywords

Preeclampsia; Cohort study; Congophilia; Misfolded proteins; Point-of-care

Funding

  1. USAID
  2. National Institutes of Health/Eunice Kennedy Shriver National Instituteof Child Health and Human Development (NIH/NICHD)
  3. SLaB

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Background: Proteins in the urine of women with preeclampsia (PE) bind Congo Red dye (urine congophilia). We sought to determine the diagnostic performance of a paper-based point-of-care test detecting urine congophilia for rapid triage and diagnosis of PE. Methods: Prospective cohort study conducted in 346 consecutive pregnant women evaluated for PE in the Labour and Delivery triage unit at our institution. The Congo Red Dot (CRD) Paper Test (index test) was performed on fresh urine samples. The CRD Paper Test results were compared to an expert adjudicated diagnosis in each case. The accuracy of the CRD Paper Test was also compared to urine and serum analytes (placental growth factor and soluble fms-like tyrosine kinase-1) previously proposed as diagnostic aids for PE. Findings: During the first triage visit, 32% (112/346) of women received a clinical diagnosis of PE. Yet, 63% (217/ 346) were admitted for in-patient diagnostic work-up or delivery. The CRD Paper Test was positive in 25% (36/ 346) of the cases. Adjudication confirmed PE in 28% (96/346) of all cases. The CRD Paper Test outperformed measured serum and urine markers (80.2% sensitivity, 89.2% specificity, 92.1% negative predictive value, 86.7% accuracy). The pre-test, positive and negative post-test probabilities were 27.7%, 74.0%, and 8.0%, respectively. Of women who were discharged undelivered, 38% (133/346) had at least one additional triage visit and the interval between the last negative and first positive CRD Paper Test was 12 (interquartile range, [5-341) clays. Interpretation: The CRD Paper Test is a simple, non-invasive, sample-in, answer-out point -of-care clinical tool for rapid identification of PE. (C) 2020 The Authors. Published by Elsevier Ltd.

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