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Proteases and antiproteases related to the coagulation system in plasma and ascites — Influence of dexamethasone

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Summary

Fibrinolysis induced by the infusion of plasminogen activators into the circulation has been shown to cause coagulation disorders in ascites retransfusion. Dexamethasone is known to inhibit the synthesis of plasminogen activators by peritoneal macrophages. We therefore assessed its potential in preventing the occurrence of fibrinolysis by injecting 16 mg dexamethasone intraperitoneally in 10 patients 24 h before ascites retransfusion was performed. In addition, the effect of dexamethasone upon the activity or concentration of several proteases and antiproteases related to coagulation in plasma and ascites was analyzed on 15 occasions. An increase of the activity of plasminogen, α2-antiplasmin, and antithrombin III, and in the concentration of α1-protease inhibitor in ascites was induced by the dexamethasone injection. However, the reaction was not identical in all patients. Those patients having an increase of plasminogen activities of 0.6 CTA U/ml or more did not show signs of fibrinolysis during retransfusion. The results obtained indicate that intraperitoneal injection of dexamethasone decreases the concentration of plasminogen activators in ascites and thereby reduces the risk of coagulation disorders during retransfusion procedures. Since the effect is variable and not sustained, assessment of preoperative plasminogen concentrations is mandatory in order to prevent complications.

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Abbreviations

α2AP:

α2-Antiplasmin

α1PI:

α1-Protease inhibitor

AT III:

Antithrombin III

CTA:

Committee on Thrombolytic Agents

DIC:

Disseminated intravascular coagulation

EAR:

Extracorporeal ascites retransfusion

FDP:

Fibrin(ogen) degradation products

FM:

Fibrin monomers

PVS:

Peritoneovenous shunt

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Schölmerich, J., Zimmermann, U., Köttgen, E. et al. Proteases and antiproteases related to the coagulation system in plasma and ascites — Influence of dexamethasone. Klin Wochenschr 65, 639–642 (1987). https://doi.org/10.1007/BF01875498

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  • DOI: https://doi.org/10.1007/BF01875498

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