Thromb Haemost 1992; 67(04): 397-401
DOI: 10.1055/s-0038-1648459
Original Articles
Schattauer GmbH Stuttgart

Hypofibrinolysis in Patients with a History of Idiopathic Deep Vein Thrombosis and/or Pulmonary Embolism

Vito Grimaudo
The Hematology Division, Department of Medicine, University Hospital Center, Lausanne, Switzerland
,
Fedor Bachmann
The Hematology Division, Department of Medicine, University Hospital Center, Lausanne, Switzerland
,
Jacques Hauert
The Hematology Division, Department of Medicine, University Hospital Center, Lausanne, Switzerland
,
Maria-Adele Christe
The Hematology Division, Department of Medicine, University Hospital Center, Lausanne, Switzerland
,
Egbert K O Kruithof
The Hematology Division, Department of Medicine, University Hospital Center, Lausanne, Switzerland
› Author Affiliations
Further Information

Publication History

Received 02 July 1991

Accepted after revision 09 October 1991

Publication Date:
03 July 2018 (online)

Summary

An impaired fibrinolytic activity after a venous occlusion test is the most common abnormality associated with thomboembolic disease. To better characterize the causes of abnormal responses we have measured different fibrinolytic parameters, before and after 10 and 20 min of venous occlusion, in 77 patients with a history of idiopathic deep vein thrombosis and/or pulmonary embolism and in 38 healthy volunteers.

The patients had a lower mean fibrinolytic response to venous occlusion than the controls and higher antigen levels of tissue-type plasminogen activator (t-PA: Ag) and plasminogen activator inhibitor type 1 (PAI-1:Ag). Before venous occlusion, PAI-1 levels were at a molar excess over those of t-PA in all patients and controls. After 20 min of venous occlusion, the release of t-PA from the vascular endothelium resulted in a molar excess of t-PA over PAI-1 in the majority of controls (72%) but only in a minority of patients (39%).

To identify patients with fibrinolytic abnormalities, reference intervals (RI) for fibrinolytic activity, t-PA:Ag and PAI-1:Ag were established in healthy controls. None of the patients had low levels of t-PA:Ag, but 17 (22%) had elevated PAI-1:Ag levels before venous occlusion and 12 (16%) exhibited low fibrinolytic activity after 20 min of venous occlusion. Ten of these were among the 17 subjects with high PAI-1: Ag levels before venous occlusion. Thus, the measurement of PAI-1:Ag levels before venous occlusion (i.e. in samples taken without any stimulation) is a sensitive (83%) and specific (89%) assay for the detection of patients with an impaired fibrinolytic response to venous occlusion.

 
  • References

  • 1 Isacson S, Nilsson IM. Defective fibrinolysis in blood and vein walls in recurrent “idiopathic” venous thrombosis. Acta Chir Scand 1972; 138: 313-319
  • 2 Nilsson IM, Ljungner H, Tengborn L. Two different mechanisms in patients with venous thrombosis and defective fibrinolysis: low concentration of plasminogen activator or increased concentration of plasminogen activator inhibitor. Br Med J 1985; 290: 1453-1456
  • 3 Juhan-Vague I, Valadier J, Alessi MC, Aillaud MF, Ansaldi J, Philip-Joet C, Holvoet P, Serradimigni A, Collen D. Deficient t-PA release and elevated PA inhibitor levels in patients with spontaneous or recurrent deep venous thrombosis. Thromb Haemostas 1987; 57: 67-72
  • 4 Wiman B, Ljungberg B, Chmielewska J, Urden G, Blomback M, Johnsson H. The role of the fibrinolytic system in deep vein thrombosis. J Lab Clin Med 1985; 105: 265-270
  • 5 Stalder M, Hauert J, Kruithof EKO, Bachmann F. Release of vascular plasminogen activator (v-PA) after venous stasis: elec-trophoretic-zymographic analysis of free and complexed v-PA. Br J Haematol 1985; 61: 169-176
  • 6 Johansson L, Hedner U, Nilsson IM. A family with thromboembolic disease associated with deficient fibrinolytic activity in vessel wall. Acta Med Scand 1978; 203: 477-480
  • 7 Jprgensen M, Mortensen JZ, Madsen AG, Thorsen S, Jacobsen B. A family with reduced plasminogen activator activity in blood associated with recurrent venous thrombosis. Scand J Haematol 1982; 29: 217-223
  • 8 Stead NW, Bauer KA, Kinney TR, Lewis JG, Campbell EE, Shifman MA, Rosenberg RD, Pizzo SV. Venous thrombosis in a family with defective release of vascular plasminogen activator and elevated plasma factor VUI/von Willebrand’s factor. Am J Med 1983; 74: 33-39
  • 9 Clayton JK, Anderson JA, McNicol GP. Preoperative prediction of postoperative deep vein thrombosis. Br Med J 1976; 2: 910-912
  • 10 Korninger C, Lechner K, Niessner H, Gossinger H, Kundi M. Impaired fibrinolytic capacity predisposes for recurrence of venous thrombosis. Thromb Haemostas 1984; 52: 127-130
  • 11 Pizzo SV, Fuchs HE, Doman KA, Petruska DB, Berger jr H. Release of tissue plasminogen activator and its fast-acting inhibitor in defective fibrinolysis. Arch Intern Med 1986; 146: 188
  • 12 Jprgensen M, Bonnevie-Nielsen V. Increased concentration of the fast-acting plasminogen activator inhibitor in plasma associated with familial venous thrombosis. Br J Haematol 1987; 65: 175-180
  • 13 Engesser L, Brommer EJP, Kluft C, Briet E. Elevated plasminogen activator inhibitor (PAI), a cause of thrombophilia? - A study in 203 patients with familial or sporadic venous thrombophilia. Thromb Haemostas 1989; 62: 673-680
  • 14 Hamsten A, Walldius G, Szamosi A, Blomback M, de Faire U, Dahlen G, Landou C, Wiman B. Plasminogen activator inhibitor in plasma: risk factor for recurrent myocardial infarction. Lancet 1987; 2: 3-9
  • 15 Rocha E, Alfaro MJ, Paramo JA, Canadell JM. Preoperative identification of patients at high risk of deep venous thrombosis despite prophylaxis in total hip replacement. Thromb Haemostas 1988; 59: 93-95
  • 16 Grimaudo V, Bachmann F, Kruithof EKO. Plasminogen activator inhibitor type 1 antigen levels in citrated plasma. Determination of the contribution of platelets. Haemostasis 1990; 20: 329-333
  • 17 Kruithof EKO, Nicoloso G, Bachmann F. Plasminogen activator inhibitor 1: Development of a radioimmunoassay and observations on its plasma concentration during venous occlusion and after platelet aggregation. Blood 1987; 70: 1645-1653
  • 18 Kruithof EKO, Tran-Thang C, Gudinchet A, Hauert J, Nicoloso G, Genton C, Welti H, Bachmann F. Fibrinolysis in pregnancy: a study of plasminogen activator inhibitors. Blood 1987; 69: 460-466
  • 19 Langley R. Practical Statistics: Simply Explained. Dover Publications, Inc; New York: 1971
  • 20 Krieg AF, Gambino R, Galen RS. Why are clinical laboratory tests performed? When are they valid?. JAMA 1975; 233: 76-78
  • 21 Nguyen G, Horellou MH, Kruithof EKO, Conard J, Samama MM. Residual plasminogen activator inhibitor activity after venous stasis as a criterion for hypofibrinolysis: a study in 83 patients with confirmed deep venous thrombosis. Blood 1988; 72: 601-605
  • 22 Ellison RC, Brown J. Fibrinolysis in pulmonary vascular disease. Lancet 1965; i: 786
  • 23 Lackner H, Merskey C. Variation in fibrinolytic activity after acute myocardial infarction and after the administration of oral anticoagulant drugs and intravenous heparin. Br J Haematol 1960; 6: 402
  • 24 Bauer J, Bachmann F. Fibrinolysis and coumarin therapy: a possible relationship. Thromb Haemostas 1981; 46: 111 Abstract N° 338
  • 25 Grulich-Henn J, Loechelt K, Speiser W, Muller-Berghaus G. Increased tissue-plasminogen activator (t-PA) levels in patients under oral anticoagulant therapy. Blut 1989; 58: 39-43