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1 acid in acute severe bleeding (traumatic and post-partum haemorrhage).
2 ics reduce death from bleeding in trauma and post-partum haemorrhage.
3 uitable first-line treatment alternative for post-partum haemorrhage.
4 Retained placenta is associated with post-partum haemorrhage.
5 d management of heavy menstrual bleeding and post-partum haemorrhage.
6 mental and caesarean births, infections, and post-partum haemorrhage.
7 labour and delivery, and are more at risk of post-partum haemorrhage.
8 in view of its relevance in time-to-death in post-partum haemorrhage.
9 tum haemorrhage (1.49, 1.01-2.20; I(2)=37%), post-partum haemorrhage (1.29, 1.13-1.49; I(2)=41%), hyp
10 d antibiotics to reduce maternal deaths from post-partum haemorrhage and sepsis could be a highly eff
11 timates from published work of occurrence of post-partum haemorrhage and sepsis, case fatality, and t
12 978 (10%) women were diagnosed with primary post-partum haemorrhage and were randomly assigned to re
15 is increasingly used ad hoc for treatment of post-partum haemorrhage; however, evidence is insufficie
16 ous to intravenous oxytocin for treatment of post-partum haemorrhage in women not exposed to oxytocin
17 ior to intravenous oxytocin for treatment of post-partum haemorrhage in women receiving prophylactic
18 tocin, the standard of care for treatment of post-partum haemorrhage, is not available in all setting
19 Oxytocin, the gold-standard treatment for post-partum haemorrhage, needs refrigeration, intravenou
20 aesarean section, or instrumental delivery); post-partum haemorrhage; neonatal death; low birthweight
22 estimated that of 2860 maternal deaths from post-partum haemorrhage or sepsis per year in Malawi, in
25 on of women in the placebo group with severe post-partum haemorrhage than those in the cholecalcifero