Frequency of inherited bleeding disorders in women with menorrhagia

Background Although menorrhagia is a common gynaecological symptom, a specific cause is identified in less than 50% of affected women. We investigated the frequency of inherited bleeding disorders in women with menorrhagia. Methods Women referred for investigation of menorrhagia whose pelvis was normal on clinical examination and who had an estimated menstrual blood loss of more than 80 mL were studied. A detailed menstrual history and history about other bleeding symptoms was taken. The activated partial thromboplastin time, factor VIII activity, von-Willebrand-factor antigen and activity, and factor XI (FXI) were measured in all patients; further tests were done when results were at or outside the limits of the assays. Findings 150 women were screened. An inherited bleeding disorder was diagnosed in 26 (17%) patients: the disorders were von Willebrandʹs disease of mild (15) or moderate severity (three), mild FXI deficiency (four), mild von Willebrandʹs disease and FXI deficiency (one), combined von Willebrandʹs disease, FXI deficiency, and factor X deficiency (one), carriage of haemophilia-A gene (one), and platelet dysfunction (one). The frequency of von Willebrandʹs disease and FXI deficiency were 13% (95% CI 7•9–18•8%) and 4% (1•5–8•5%), respectively. Menorrhagia since menarche was noted in 11 (8•9%) of 123 women without a bleeding disorder compared with 13 (65%) of 20 women with von Willebrandʹs disease (p=0•001) and four (66•7%) of six women with FXI deficiency (p<0•001). Interpretation Inherited bleeding disorders are found in a substantial proportion of women with menorrhagia and a normal pelvis examination. We suggest that such patients should be investigated for these disorders—especially von Willebrandʹs disease—before invasive procedures are done.