Thromb Haemost 2002; 88(04): 576-582
DOI: 10.1055/s-0037-1613258
Review Article
Schattauer GmbH

The Thrombogram in Rare Inherited Coagulation Disorders: Its Relation to Clinical Bleeding

Raed Al Dieri
1   Synapse Laboratory, Cardiovascular Research Institute (CARIM), University of Maastricht, The Netherlands
,
Flora Peyvandi
2   Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milano, Italy
,
Elena Santagostino
2   Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milano, Italy
,
Muriel Giansily
3   Laboratoire Central d’ Hematologie, Centre Hospitalier Universitaire, Montpellier, France
,
Pier Mannuccio Mannucci
2   Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milano, Italy
,
Jean François Schved
3   Laboratoire Central d’ Hematologie, Centre Hospitalier Universitaire, Montpellier, France
,
Suzette Béguin
1   Synapse Laboratory, Cardiovascular Research Institute (CARIM), University of Maastricht, The Netherlands
,
H. Coenraad Hemker
1   Synapse Laboratory, Cardiovascular Research Institute (CARIM), University of Maastricht, The Netherlands
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Publikationsverlauf

Received 11. Dezember 2001

Accepted after revision 03. Juni 2002

Publikationsdatum:
09. Dezember 2017 (online)

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Summary

We investigated the relation between clotting factor concentration, the parameters of the thrombin generation curve (the thrombogram) and the severity of clinically observed bleeding in patients with congenital deficiency of prothrombin (n = 21), factor V (n = 22), factor VII (n = 22), factor X (n = 10), factor XI (n = 7) and factor XII (n = 6). The parameters used were: area under the curve (endogenous thrombin potential, ETP), peak concentration of thrombin attained and lag time before manifest formation.

Peak height and ETP varied linearly with the concentration of prothrombin. For the other factors these parameters hyperbolically approached to the 100% limit with increasing clotting factor concentration. Half normal ETP was seen at about the following concentrations: prothrombin (50%), factor V (1%), factor VII (2%), factor X (5%) and factor XI (1%). As a rule, the peak height was somewhat more sensitive to clotting factor decrease than the ETP was.

In all the patients with severe bleeding symptoms the ETP was less than 20% of normal. Bleeding tendency was absent or mild in patients with an ETP of 30% or higher. This value (except for prothrombin) is already obtained at concentrations of clotting factor of 1%-2%, which corroborates the clinical observation that a severe bleeding tendency is only seen in severe clotting factor deficiencies (less than 1%). The one exception was a patient with factor VII deficiency and severe bleeding, who showed a normal ETP value, albeit with a decreased peak height and a prolonged lag-time.