“…We recorded the following parameters: maternal age at time of birth, body mass index (BMI) at beginning of pregnancy, parity, ethnicity (Caucasian/non‐Caucasian), obstetric history (previous cesarean section and/or previous PPH), gestational age, mode of birth (vaginal birth, instrumental vaginal birth, elective cesarean section or emergency cesarean section), induction of labor, multiple pregnancy, preeclampsia in current pregnancy, blood loss (measured by weighing gauzes and by use of a suction system in the operating theater), number of packed red blood cells transfused, cause of hemorrhage (uterine atony, uterine rupture, placental pathology [including retained placenta, placental remnants, placenta previa, abnormally invasive placenta and placental abruption], laceration of the birth canal, uterine inversion and clotting disorder with or without amniotic fluid embolism) and management of hemorrhage (uterotonic agents [oxytocin, sulprostone, ergometrine, misoprostol], non‐uterotonic agents [tranexamic acid], intrauterine balloon tamponade, surgical interventions [B‐Lynch sutures, uterine artery ligation, hysterectomy] and uterine artery embolization). Furthermore, as major PPH can be the result of concurrent causes, we re‐examined all cases of massive transfusion due to PPH within the TeMpOH‐1 cohort, and only included multiple causes for an individual woman if those causes contributed significantly to the bleeding, as was previously done in the LEMMoN study . Causes of PPH in women who received massive transfusion were further analyzed by mode of birth and the number of packed red blood cells transfused, using the same cut‐off points described by Green et al in the UK: “moderate” (8‐12 units of packed red blood cells), “high” (13‐20 units of packed red blood cells) and “immense” (> 20 units of packed red blood cells).…”