Thromb Haemost 1979; 42(01): 50
DOI: 10.1055/s-0039-1684381
Measurements in Fibrinolysis
Poster Board
Schattauer GmbH

Clinical Studies of the Use of a Fluorogenic Substrate Assay Method for the Determination of Plasminogen

Douglas A. Triplett
1   Department of Hematology, Ball Memorial Hospital, University of Indiana, Muncie, Indiana. U.S.A.
,
Cathy Harms
1   Department of Hematology, Ball Memorial Hospital, University of Indiana, Muncie, Indiana. U.S.A.
,
Lori Hermelin
1   Department of Hematology, Ball Memorial Hospital, University of Indiana, Muncie, Indiana. U.S.A.
,
Rolf M. Huseby
2   Department of Blood Coagulation and Hematology, Research and Development, DADE Division American Hospital Supply Corpora Mon, Miami, Florida, U.S.A.
,
Gary A. Mitchell
2   Department of Blood Coagulation and Hematology, Research and Development, DADE Division American Hospital Supply Corpora Mon, Miami, Florida, U.S.A.
,
Sharon P. Pochron
2   Department of Blood Coagulation and Hematology, Research and Development, DADE Division American Hospital Supply Corpora Mon, Miami, Florida, U.S.A.
› Author Affiliations
Further Information

Publication History

Publication Date:
18 April 2019 (online)

 

    Utilization of a recently reported method for the determination of plasminogen by fluorometrit technique (Ref. 3, Pochron, et. al., Thrombosis Research, Vol. 13, pg. 733, 1978) was compared with acceptable methodologies (e.g. the caseinolvtic and radial-immunodiffusion assays). Excellent results were seen with the normal range of 2.4–3.8 CTA U/ml of plasminogen by the synthetic substrate assay as compared to 8.7-14.3 mg/dl by the radial immunodiffusion assay. Normal ranges for the caseinolvtic assay were seen to be 2.2-4.0 CTA U/ml. Patients’ studies were performed on a general medical population but centered primarily on “pre” and “post” operative coronarv-pulmonary bypass patients. In all cases studied, a drop in Plasminogen level was noted in this group of patients following surgery (20–50%). Other clinical data will be presented indicating that the determination of plasminogen by the fluorometric assay procedure is sensitive and accurate for clinical situations.


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