Why the study?
Does oestriol succinate affect haemostatic function in postmenopausal women treated for osteoporosis?
Does oestriol succinate affect haemostatic function in postmenopausal women treated for osteoporosis?
Long-term therapy with oestriol succinate in postmenopausal women does not significantly alter plasma coagulation factors, suggesting a potentially favorable safety profile regarding thromboembolic risk.
Answers are grounded in this paper and cite their sources.
May support haemostatic safety of oestriol succinate in osteoporosis; leaves open confirmation of thromboembolic outcomes in RCTs.
Summary In a previous report we showed that oestriol succinate administered to post‐menopausal women caused fewer changes in haemostatic function over a four‐month period than ethinyloestradiol. Potential longer‐term effects were studied in postmenopausal women treated for osteoporosis with oestriol succinate for up to 12 months. Over this period there was no significant change in concentration of plasma coagulation factors, an increase in plasminogen concentration and euglobulin lysis activity, and an inconsistent increase in platelet sensitivity to aggregation induced by ADP and collagen. The relative lack of effect of oestriol succinate on coagulation function is encouraging with regard to the future incidence of thromboembolic complications of therapy. We thank the Special Trustees of the General Infirmary, Leeds, for their financial support. Organon Laboratories Limited gave generous financial assistance and provided oestriol succinate tablets. We are grateful to Professor B. E. C. Nordin for allowing us to study patients under his care. Mrs G. Fieldhouse, Mrs B. Griffin, Mrs A. Spencer and Mr J. Leek gave valuable technical assistance.
No takes yet. Share an insight, caveat, or question.
Toy et al. (1978) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: