Misoprostol for treating postpartum haemorrhage: A randomized controlled trial [ISRCTN72263357]

被引:30
作者
Hofmeyr G.J. [1 ]
Ferreira S. [1 ]
Nikodem V.C. [2 ]
Mangesi L. [1 ]
Singata M. [1 ]
Jafta Z. [1 ]
Maholwana B. [1 ]
Mlokoti Z. [3 ]
Walraven G. [4 ]
Gülmezoglu A.M. [5 ]
机构
[1] Effective Care Research Unit, Univ. of Witwatersrand and Fort Hare, East London Hospital Complex, East London
[2] Department of Nursing, University of the Western Cape, Cape Town
[3] Tembisa Hosp. Effective Care Res. U., Tembisa
[4] Aga Khan Health Services, Aiglemont
[5] HRP/RHR, World Health Organisation, Geneva
关键词
Oxytocin; Maternal Death; Misoprostol; Postpartum Haemorrhage; Uterine Atony;
D O I
10.1186/1471-2393-4-16
中图分类号
学科分类号
摘要
Background: Postpartum haemorrhage remains an important cause of maternal death despite treatment with conventional therapy. Uncontrolled studies and one randomised comparison with conventional oxytocics have reported dramatic effects with high-dose misoprostol, usually given rectally, for treatment of postpartum haemorrhage, but this has not been evaluated in a placebo-controlled trial. Methods: The study was conducted at East London Hospital Complex, Tembisa and Chris Hani Baragwanath Hospitals, South Africa. Routine active management of the third stage of labour was practised. Women with more than usual postpartum bleeding thought to be related to inadequate uterine contraction were invited to participate, and to sign informed consent. All routine treatment was given from a special 'Postpartum Haemorrhage Trolley'. In addition, participants who consented were enrolled by drawing the next in a series of randomised treatment packs containing either misoprostol 5 × 200 μg or similar placebo, which were given 1 orally, 2 sublingually and 2 rectally. Results: With misoprostol there was a trend to reduced blood loss ≥500 ml in 1 hour after enrolment measured in a flat plastic 'fracture bedpan', the primary outcome (6/117 vs 11/120, relative risk 0.56; 95% confidence interval 0.21 to 1.46). There was no difference in mean blood loss or haemoglobin level on day 1 after birth < 6 g/dl or blood transfusion. Side-effects were increased, namely shivering (63/116 vs 30/118; 2.14, 1.50 to 3.04) and pyrexia > 38.5°C (11/114 vs 2/118; 5.69, 1.29 to 25). In the misoprostol group 3 women underwent hysterectomy of whom 1 died, and there were 2 further maternal deaths. Conclusions: Because of a lower than expected incidence of the primary outcome in the placebo group, the study was underpowered. We could not confirm the dramatic effect of misoprostol reported in several unblinded studies, but the results do not exclude a clinically important effect. Larger studies are needed to assess substantive outcomes and risks before misoprostol enters routine use. © 2004 Justus Hofmeyr et al; licensee BioMed Central Ltd.
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页数:7
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