Thromb Haemost 1958; 02(01/02): 024-038
DOI: 10.1055/s-0038-1656262
Originalarbeiten — Original Articles — Travaux Originaux
Schattauer GmbH

The Stuart-Prower Factor Assay and its Clinical Significance[*]

F Bachmann
1   Coagulation laboratory (Prof. F. Koller) of the Department of Medicine (Prof. P. H. Rossier), University of Zurich, Switzerland
,
F Duckert
1   Coagulation laboratory (Prof. F. Koller) of the Department of Medicine (Prof. P. H. Rossier), University of Zurich, Switzerland
,
F Koller**
1   Coagulation laboratory (Prof. F. Koller) of the Department of Medicine (Prof. P. H. Rossier), University of Zurich, Switzerland
› Author Affiliations
Further Information

Publication History

Publication Date:
07 June 2018 (online)

Summary

A simple one-stage test for the determination of the Stuart-Prower factor is described. The method is a modification of the classical Factor VII complex assay, using a Russell’s viper venom (Stypven)-cephalin reagent instead of brain thromboplastin. The optimal conditions for the assay system have been systematically investigated. A high dilution of RVV (1 : 200 000) has given the best results. The system is not influenced by different concentrations of fibrinogen, prothrombin, Factor V, Factor VII and plasma thromboplastin precursors other than Stuart-Prower factor. Variations of lipoid and/or platelet contents of the plasma do not alter the results. Stuart-Prower factor is not activated by glass contact. The method has proved most valuable in the detection of heterozygous Stuart-Prower factor deficiencies. Comparison with a specific Stuart-Prower factor assay using patient’s plasma deficient in Stuart-Prower factor gave variations not greater than 15%. If determined simultaneously with the Quick one-stage ‘prothrombin time’, the test may provide a better control of patients under treatment with dicoumarol derivatives.

* This study was aided by grants from the ‘Emil Barell-Foundation for Medical Research.’


** With the technical assistance of Miss D. Gerber.


 
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