Heavy menstrual bleeding in women with inherited bleeding disorders.

Claudia Djambas Khayat, Emna Gouider, Sylvia von Mackensen, Rezan Abdul Kadir

Journal: Haemophilia : the official journal of the World Federation of Hemophilia 2021;26 Suppl 3():16-19

PMID: 32356352

Abstract

Heavy menstrual bleeding (HMB) is the commonest bleeding symptom among women with inherited bleeding disorders (IBD). Since HMB starts at the very onset of menarche and continues throughout the reproductive life, the health related quality of life of these women is affected and they are at an increased risk of developing iron-deficiency anemia. Because of the entrenched stigma and taboos, women and girls are often reluctant to discuss the problem of HMB within their families and do not seek medical advice. Increased awareness and multidisciplinary management approach for the management of these women are essential in ensuring an optimal outcome. It is important to take a careful history and undertake a thorough gynecological assessment to exclude other underlying/concomitant causes of HMB. Iron supplementation is essential. Strategies for decreasing menstrual blood flow are similar to those used for HMB in general with the addition of desmopressin and replacement therapy and the exclusion of non-steroidal anti-inflammatory drugs. Tranexamic acid and/or hormonal intervention are usually recommended as first-line therapy. Treatment choice should be individualized taking into account whether the woman wishes to preserve her fertility, if she requires contraception, the type of IBD, the severity of bleeding, and her social and religious background as well as acceptability and availability of the treatment options.

© 2019 John Wiley & Sons Ltd.

Address: Hotel Dieu de France Beirut Saint Joseph University, Beirut, Lebanon.; Aziza Othmana Hospital, University Manar 2, Tunis, Tunisia.; Department of Medical Psychology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.; Royal Free NHS foundation Trust and institute of women's Health, UCL, London, UK.

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