Thromb Haemost 1998; 79(03): 567-570
DOI: 10.1055/s-0037-1614946
Review Articles
Schattauer GmbH

Sensitivity, Specificity and Predictive Value of Modified Assays for Activated Protein C Resistance in Children

Greg Brandt
1   The Division of Hematology/Oncology, S. Illinois University School of Medicine, Springfield, Illinois
,
Ralph Gruppo
2   The Division of Hematology/Oncology, Children’s Hospital Medical Center, Cincinnati, Ohio
,
Charles J. Glueck
3   The Cholesterol Center Jewish Hospital, Cincinnati, Ohio, USA
,
Davis Stroop
2   The Division of Hematology/Oncology, Children’s Hospital Medical Center, Cincinnati, Ohio
,
Ann Becker
2   The Division of Hematology/Oncology, Children’s Hospital Medical Center, Cincinnati, Ohio
,
Ann Pillow
2   The Division of Hematology/Oncology, Children’s Hospital Medical Center, Cincinnati, Ohio
,
Ping Wang
3   The Cholesterol Center Jewish Hospital, Cincinnati, Ohio, USA
› Author Affiliations
Further Information

Publication History

Received 18 April 1997

Accepted after resubmission 31 October 1997

Publication Date:
07 December 2017 (online)

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Summary

Very little data is available assessing the clinical utility of coagulation-based APC resistance assays compared to DNA-based analysis for the factor V Leiden mutation in children. Therefore, the clinical utility of four aPTT-based assays for APC resistance was evaluated in 169 children, ages 3 months through 16 years. The prevalence of the Arg506 to Gln mutation was 7/169 (4.1%). Using cutoff points derived from the normal PCR-screened population (n = 162), two assays for APC resistance (APC-SR and n-APC-SR) gave poor concordance with the PCR assay (sensitivity 29% and 57%, respectively). Two modified assays (FDAPC-SR and n-FDAPC-SR), in which patient plasma was prediluted 1:5 in factor V deficient plasma, gave excellent concordance (sensitivity 100%). The predictive value of a positive test was 0.25, 0.44, 1.00 and 0.88 for the APC-SR, n-APC-SR, FDAPC-SR and n-FDAPC-SR, respectively. The FDAPC-SR and n-FDAPC-SR tests gave excellent discrimination using cutoff values derived from the total population (n = 169) without regard to previous PCR screening results.