Use of the etonogestrel-releasing implant is associated with hypoactivation of the coagulation cascade

Hum Reprod. 2007 Aug;22(8):2196-201. doi: 10.1093/humrep/dem153. Epub 2007 Jun 13.

Abstract

Background: The role of progestogens in haemostasis is controversial. Our objective is to evaluate the haemostatic effects of an etonogestrel-releasing implant.

Methods: This open-label, self-controlled, longitudinal study involved 20 healthy women receiving subcutaneous etonogestrel-releasing implants. At baseline, 1, 3 and 6 months, we measured the following: activated partial thromboplastin time; prothrombin time; thrombin time; fibrinogen; coagulation factors II, V, VII, VIII, IX, X and XI; von Willebrand factor; activated protein C (APC); antithrombin; free protein S; plasminogen activator inhibitor type 1 (PAI-1); alpha2-antiplasmin; thrombin-antithrombin (TAT) complex; prothrombin fragment 1 + 2 (F1 + 2); D-dimers; APC resistance. Statistical analyses included the Friedman test and ANOVA.

Results: Levels of APC (P < 0.01), factor II (P = 0.02), factor VII (P = 0.006), factor X (P = 0.01) and F1 + 2 (P < 0.001) were reduced, whereas those of PAI-1 (P = 0.01) and factor XI (P = 0.006) were transitory increased. All of these values, however, remained within normal ranges. Surprisingly, TAT concentrations fell below the normal range (P < 0.001).

Conclusions: Our findings suggest that the etonogestrel-releasing implant does not induce a prothrombotic pattern during the first six months of use, and that its use is associated with a reduction in thrombin generation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antithrombins / metabolism
  • Blood Coagulation / drug effects*
  • Desogestrel / administration & dosage*
  • Desogestrel / pharmacology
  • Drug Implants
  • Female
  • Fibrin Fibrinogen Degradation Products / metabolism
  • Humans
  • Prospective Studies
  • Protein C / metabolism
  • Protein S / metabolism
  • Thromboembolism / prevention & control
  • Venous Thrombosis / prevention & control
  • alpha-2-Antiplasmin / metabolism

Substances

  • Antithrombins
  • Drug Implants
  • Fibrin Fibrinogen Degradation Products
  • Protein C
  • Protein S
  • alpha-2-Antiplasmin
  • fibrin fragment D
  • etonogestrel
  • Desogestrel