2018
DOI: 10.1002/14651858.cd005456.pub3
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Prophylactic use of ergot alkaloids in the third stage of labour

Abstract: Analysis 1.4. Comparison 1 Ergot alkaloids (any route of administration) versus no uterotonic agents, Outcome 4 Maternal haemoglobin concentration at 24 to 48 hours postpartum (g/dL

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Cited by 34 publications
(24 citation statements)
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“…11 Some authorities consider methylergometrine as second line drug for AMTSL compared to oxytocin. 17 Studies have shown that Misoprostol is not as effective as Oxytocin for the prevention of PPH and that maternal pyrexia is a significant adverse effect. 14,16,[18][19][20] However, misoprostol is a suitable agent for management of the third stage of labour when other agents are not available for reasons of cost, storage, or difficulty of administration.…”
Section: Discussionmentioning
confidence: 99%
“…11 Some authorities consider methylergometrine as second line drug for AMTSL compared to oxytocin. 17 Studies have shown that Misoprostol is not as effective as Oxytocin for the prevention of PPH and that maternal pyrexia is a significant adverse effect. 14,16,[18][19][20] However, misoprostol is a suitable agent for management of the third stage of labour when other agents are not available for reasons of cost, storage, or difficulty of administration.…”
Section: Discussionmentioning
confidence: 99%
“…Intraumbilical administration of oxytocin was also found to cause significant reductions in blood loss [60,61]. Similarly for the use of other uterotonics, a 2011 review of ergot alkaloids containing six studies (RCTs and quasiRCTs) found a significant reduction of PPH when administered in third stage of labor [62].…”
Section: The International Confederation Of Midwives and Internationalmentioning
confidence: 96%
“…Lower abdominal pain may be mild to severe, accompanied by back pain and is described as throbbing, cramping and aching. Ergot alkaloids during the third stage of labour increased the requirement for analgesia for pain after birth due to persistent uterine contraction (RR 2.53; CI 1.34 to 4.78), but also decreased mean blood loss and the incidence of postpartum haemorrhage compared with no uterotonic drugs (Liabsuetrakul et al, 2007 Level I).…”
Section: Uterine Painmentioning
confidence: 99%