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. 2020 Jan 31;26(2):216–227. doi: 10.1111/hae.13927

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© 2020 The Authors. Haemophilia published by John Wiley & Sons Ltd.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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Prevalence of PPH according to the subtype of inherited platelet receptor defect and use of prophylactic treatment. ^No data available. GT, Glanzmann thrombasthenia; BSS, Bernard‐Soulier syndrome; PT‐VWD, platelet‐type von Willebrand disease; TxA2, thromboxane A2 receptor defects; P2Y12, ADP receptor defects. Prophylactic treatment for delivery is defined as measures taken to prevent PPH and could consist of blood products (erythrocytes, platelets, plasma, coagulation factors, plasmapheresis), recombinant Factor VIIa (rFVIIa), desmopressin (DDAVP), or other measures (preventive hysterectomy, antifibrinolytics, uterotonic agents, fibrinogen concentrate and steroids).