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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         Retained placenta is associated with post-partum haemorrhage.
4 mental and caesarean births, infections, and post-partum haemorrhage.
5 labour and delivery, and are more at risk of post-partum haemorrhage.
6 in view of its relevance in time-to-death in post-partum haemorrhage.
7 uitable first-line treatment alternative for post-partum haemorrhage.
8 tum haemorrhage (1.49, 1.01-2.20; I(2)=37%), post-partum haemorrhage (1.29, 1.13-1.49; I(2)=41%), hyp
9 d antibiotics to reduce maternal deaths from post-partum haemorrhage and sepsis could be a highly eff
10 timates from published work of occurrence of post-partum haemorrhage and sepsis, case fatality, and t
11  978 (10%) women were diagnosed with primary post-partum haemorrhage and were randomly assigned to re
12           809 (3%) women were diagnosed with post-partum haemorrhage and were randomly assigned to re
13 is increasingly used ad hoc for treatment of post-partum haemorrhage; however, evidence is insufficie
14 ous to intravenous oxytocin for treatment of post-partum haemorrhage in women not exposed to oxytocin
15 ior to intravenous oxytocin for treatment of post-partum haemorrhage in women receiving prophylactic
16 tocin, the standard of care for treatment of post-partum haemorrhage, is not available in all setting
17    Oxytocin, the gold-standard treatment for post-partum haemorrhage, needs refrigeration, intravenou
18 he key events leading to maternal death from post-partum haemorrhage or sepsis after delivery.
19  estimated that of 2860 maternal deaths from post-partum haemorrhage or sepsis per year in Malawi, in
20 ning, could reduce maternal mortality due to post-partum haemorrhage or sepsis.
21                                  Deaths from post-partum haemorrhage peaked 2-3 h after childbirth.
22 on of women in the placebo group with severe post-partum haemorrhage than those in the cholecalcifero

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