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Coagulation cascade, fibrinolytic system, antithrombin III, protein C and protein S in patients maintained on

N D Vaziri1, G M Shah, R L Winer

  • 1Department of Medicine, University of California, Irvine 92717.

Thrombosis Research
|January 15, 1989
PubMed

Insights

Patients on continuous ambulatory peritoneal dialysis (CAPD) show increased levels of clotting factors and protein S. However, key anticoagulants and fibrinolytic agents remain unchanged, suggesting potential hemostatic alterations in CAPD patients.

Area of Science:

  • Nephrology
  • Hematology
  • Clinical Chemistry

Background:

  • End-stage renal disease (ESRD) impacts hemostasis.
  • Continuous ambulatory peritoneal dialysis (CAPD) is a common ESRD treatment.
  • Understanding coagulation and fibrinolysis in CAPD patients is crucial.

Purpose of the Study:

  • To investigate the coagulation cascade, fibrinolytic system, and natural anticoagulants in CAPD patients.
  • To compare hemostatic markers in CAPD patients versus healthy volunteers.

Main Methods:

  • Studied 14 CAPD patients and 10 healthy controls.
  • Assessed plasma procoagulant activities of multiple coagulation factors (XII, XI, IX, VIII, VII, X, II, V).
  • Measured plasma concentrations of total and free protein S, fibrinogen, factor VIII-related antigen, protein C, antithrombin III, plasminogen, and alpha 2-antiplasmin.

Main Results:

  • Significantly elevated plasma procoagulant activities for factors XII, XI, IX, VIII, VII, X, and II in CAPD patients.
  • Increased plasma concentrations of total and free protein S, fibrinogen, and factor VIII-related antigen in CAPD patients.
  • No significant differences in plasma levels of protein C, antithrombin III, plasminogen, or alpha 2-antiplasmin between groups.

Conclusions:

  • CAPD patients exhibit a tendency towards increased levels of several coagulation factors and protein S.
  • Fibrinolytic and endogenous anticoagulant systems (antithrombin III, protein C) appear unaltered in CAPD patients.
  • The clinical significance and underlying mechanisms of these hemostatic changes warrant further investigation.

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