Thromb Haemost 1978; 39(02): 455-465
DOI: 10.1055/s-0038-1646705
Original Article
Schattauer GmbH Stuttgart

Automation of Two-Stage Factor VIII Assay

Yvonne Stirling
The MRC-DHSS Epidemiology and Medical Care Unit, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJ, England
,
D J Howarth
The MRC-DHSS Epidemiology and Medical Care Unit, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJ, England
,
Marguerite Vickers
The MRC-DHSS Epidemiology and Medical Care Unit, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJ, England
,
W R S North
The MRC-DHSS Epidemiology and Medical Care Unit, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJ, England
,
T W Meade
The MRC-DHSS Epidemiology and Medical Care Unit, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJ, England
› Author Affiliations
Further Information

Publication History

Received 04 March 1977

Accepted 06 October 1977

Publication Date:
12 July 2018 (online)

Summary

Two automated methods for two-stage factor VIII assays have been compared with one another, and evaluated in practice. The Depex method records the clotting time when an electric circuit is completed by the formation of a fibrin thread across a hook-type electrode; the Electra method is based on an optical density technique of clot detection. The two methods gave comparable results for measured levels of factor VIII when haemophilic or “normal” plasmas were assayed. Results from the two methods in practice also suggest that both are valid at low and “normal” factor VIII levels. The Electra method is also probably suitable for assays of concentrates; however, the Depex method appears to give falsely high values in these circumstances, and experimental findings suggest that the reason may be that increased viscosity due to the high fibrinogen levels in factor VIII concentrates causes premature closure of the circuit between the two ends of the Depex electrode. The main advantage of the Depex method is that, provided 3 or 4 machines are available, a given number of assays can be completed more quickly than on Electra. The main advantages of Electra are that it is probably subject to less laboratory error than Depex, and that it is suitable for assaying concentrates as well as haemophilic and “normal” plasmas.

 
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