Thromb Haemost 1975; 34(02): 426-444
DOI: 10.1055/s-0038-1651402
Original Article
Schattauer GmbH

Use of a Lyophilized Reference Plasma to Compare Coagulation Test Procedures

Normotest, Simplastin-A and Thrombotest
J Kahan
1   Department of Clinical Chemistry, Södersjukhuset, 10064 Stockholm, and the Coagulation Laboratory, Karolinska sjukhuset, 10401, Stockholm, Sweden
,
I Nohén
1   Department of Clinical Chemistry, Södersjukhuset, 10064 Stockholm, and the Coagulation Laboratory, Karolinska sjukhuset, 10401, Stockholm, Sweden
› Author Affiliations
Further Information

Publication History

Received 20 January 1975

Accepted 06 June 1975

Publication Date:
24 July 2018 (online)

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Summary

In 4 collaborative trials, involving a varying number of hospital laboratories in the Stockholm area, the coagulation activity of different test materials was estimated with the one-stage prothrombin tests routinely used in the laboratories, viz. Normotest, Simplastin-A and Thrombotest. The test materials included different batches of a lyophilized reference plasma, deep-frozen specimens of diluted and undiluted normal plasmas, and fresh and deep-frozen specimens from patients on long-term oral anticoagulant therapy.

Although a close relationship was found between different methods, Simplastin-A gave consistently lower values than Normotest, the difference being proportional to the estimated activity. The discrepancy was of about the same magnitude on all the test materials, and was probably due to a divergence between the manufacturers’ procedures used to set “normal percentage activity”, as well as to a varying ratio of measured activity to plasma concentration. The extent of discrepancy may vary with the batch-to-batch variation of thromboplastin reagents.

The close agreement between results obtained on different test materials suggests that the investigated reference plasma could be used to calibrate the examined thromboplastin reagents, and to compare the degree of hypocoagulability estimated by the examined PIVKA-insensitive thromboplastin reagents.

The assigned coagulation activity of different batches of the reference plasma agreed closely with experimentally obtained values. The stability of supplied batches was satisfactory as judged from the reproducibility of repeated measurements. The variability of test procedures was approximately the same on different test materials.