Literature DB >> 31808846

Case-based discussion on the implications of exogenous estrogens in hemostasis and thrombosis: the hematologist's view.

Margaret V Ragni1.   

Abstract

In the childbearing years, hormonal therapy or hormonal changes in the menstrual cycle or the puerperium may be complicated by bleeding or thrombosis; however, among women with congenital disorders of hemostasis and thrombosis, the risk of bleeding or thrombosis may be increased. In women with congenital bleeding disorders, heavy menstrual bleeding is the most common bleeding symptom, and postpartum hemorrhage occurs despite treatment. Given the limitations of current therapy and the associated medical and psychological burden in women with bleeding disorders, better treatment approaches are needed to improve health outcomes and quality of life. In women with congenital thrombotic disorders, thromboembolism may complicate exogenous hormonal therapy and endogenous hormonal change during pregnancy and procedures, but risk differs by type of thrombophilia, procedure, time at risk, and thrombosis risk factors, all of which affect management. In this article, I shall consider a case-based discussion of current issues in women with congenital bleeding and clotting disorders, including heavy menstrual bleeding in a woman with VWD, postpartum hemorrhage risk in VWD, and thrombosis risk with oocyte retrieval in a woman with factor V Leiden and past thromboembolism. The goals are to review bleeding or thrombosis risk in these cases, current data, limitations of current treatment guidelines, and areas for future study.
© 2019 by The American Society of Hematology. All rights reserved.

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Year:  2019        PMID: 31808846      PMCID: PMC6913423          DOI: 10.1182/hematology.2019000022

Source DB:  PubMed          Journal:  Hematology Am Soc Hematol Educ Program        ISSN: 1520-4383


  50 in total

1.  Von Willebrand disease in the United States: perspective from the Zimmerman program.

Authors:  Veronica H Flood; Thomas C Abshire; Pamela A Christopherson; Kenneth D Friedman; Joan Cox Gill; Robert R Montgomery; Sandra L Haberichter
Journal:  Ann Blood       Date:  2018-01-26

Review 2.  Von Willebrand's Disease.

Authors:  Frank W G Leebeek; Jeroen C J Eikenboom
Journal:  N Engl J Med       Date:  2016-11-24       Impact factor: 91.245

Review 3.  Pharmacokinetics and Pharmacodynamics of Drugs Commonly Used in Pregnancy and Parturition.

Authors:  Jessica Ansari; Brendan Carvalho; Steven L Shafer; Pamela Flood
Journal:  Anesth Analg       Date:  2016-03       Impact factor: 5.108

Review 4.  Bleeding Assessment Tools: Limits and Advantages for the Diagnosis and Prognosis of Inherited Bleeding Disorders.

Authors:  Alberto Tosetto
Journal:  Semin Thromb Hemost       Date:  2016-04-20       Impact factor: 4.180

Review 5.  Pregnancy-Associated Changes in Pharmacokinetics: A Systematic Review.

Authors:  Gali Pariente; Tom Leibson; Alexandra Carls; Thomasin Adams-Webber; Shinya Ito; Gideon Koren
Journal:  PLoS Med       Date:  2016-11-01       Impact factor: 11.069

6.  Effect of early tranexamic acid administration on mortality, hysterectomy, and other morbidities in women with post-partum haemorrhage (WOMAN): an international, randomised, double-blind, placebo-controlled trial.

Authors: 
Journal:  Lancet       Date:  2017-04-26       Impact factor: 79.321

7.  Comparison of ferric Carboxymaltose and iron sucrose complex for treatment of iron deficiency anemia in pregnancy- randomised controlled trial.

Authors:  Ambily Jose; Reeta Mahey; Jai Bhagwan Sharma; Neerja Bhatla; Renu Saxena; Mani Kalaivani; Alka Kriplani
Journal:  BMC Pregnancy Childbirth       Date:  2019-02-04       Impact factor: 3.007

Review 8.  Physiologic and pharmacokinetic changes in pregnancy.

Authors:  Maged M Costantine
Journal:  Front Pharmacol       Date:  2014-04-03       Impact factor: 5.810

Review 9.  Current issues in diagnosis and treatment of von Willebrand disease.

Authors:  Daniel A Keesler; Veronica H Flood
Journal:  Res Pract Thromb Haemost       Date:  2017-12-12

10.  Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease.

Authors:  Ferdows Atiq; Karina Meijer; Jeroen Eikenboom; Karin Fijnvandraat; Eveline P Mauser-Bunschoten; Karin P M van Galen; Marten R Nijziel; Paula F Ypma; Joke de Meris; Britta A P Laros-van Gorkom; Johanna G van der Bom; Moniek P de Maat; Marjon H Cnossen; Frank W G Leebeek
Journal:  Br J Haematol       Date:  2018-05-16       Impact factor: 6.998

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