| Literature DB >> 26404176 |
Evi Struble1, Wafa Harrouk2, Albert DeFelice3, Belay Tesfamariam3.
Abstract
Pregnancy is a hypercoagulable state which carries an excess risk of maternal venous thrombosis. Endothelial injury, alterations in blood flow and activation of the coagulation pathway are proposed to contribute to the hypercoagulability. The risk for thrombosis may be accentuated by certain drugs and device implants that directly or indirectly affect the coagulation pathway. To help ensure that these interventions do not result in adverse maternal or fetal outcomes during pregnancy, gravid experimental animals can be exposed to such treatments at various stages of gestation and over a dosage range that would identify hazards and inform risk assessment. Circulating soluble biomarkers can also be evaluated for enhancing the assessment of any increased risk of venous thrombosis during pregnancy. In addition to traditional in vivo animal testing, efforts are under way to incorporate reliable non-animal methods in the assessment of embryofetal toxicity and thrombogenic effects. This review summarizes hemostatic balance during pregnancy in animal species, embryofetal development, biomarkers of venous thrombosis, and alterations caused by drug-induced venous thrombosis.Entities:
Keywords: biomarkers; drugs/biologics; embryofetal toxicity assessment; nonclinical evaluation; pregnancy; venous thrombosis
Mesh:
Substances:
Year: 2015 PMID: 26404176 PMCID: PMC5628500 DOI: 10.1002/bdrc.21111
Source DB: PubMed Journal: Birth Defects Res C Embryo Today ISSN: 1542-975X