Picetti, R;
Miller, L;
Shakur-Still, H;
Pepple, T;
Beaumont, D;
Balogun, E;
Asonganyi, E;
Chaudhri, R;
El-Sheikh, M;
Vwalika, B;
et al.
Picetti, R; Miller, L; Shakur-Still, H; Pepple, T; Beaumont, D; Balogun, E; Asonganyi, E; Chaudhri, R; El-Sheikh, M; Vwalika, B; Arulkumaran, S; Roberts, I; WOMAN trial collaborators
(2020)
The WOMAN trial: clinical and contextual factors surrounding the deaths of 483 women following post-partum haemorrhage in developing countries.
BMC Pregnancy Childbirth, 20 (1).
p. 409.
ISSN 1471-2393
https://doi.org/10.1186/s12884-020-03091-8
SGUL Authors: Arulkumaran, Sabaratnam
Abstract
BACKGROUND: Post-partum haemorrhage (PPH) is a leading cause of maternal death worldwide. The WOMAN trial assessed the effects of tranexamic acid (TXA) on death and surgical morbidity in women with PPH. The trial recorded 483 maternal deaths. We report the circumstances of the women who died. METHODS: The WOMAN trial recruited 20,060 women with a clinical diagnosis of PPH after a vaginal birth or caesarean section. We randomly allocated women to receive TXA or placebo. When a woman died, we asked participating clinicians to report the cause of death and to provide a short narrative of the events surrounding the death. We collated and edited for clarity the narrative data. RESULTS: Case fatality rates were 3.0% in Africa and 1.7% in Asia. Nearly three quarters of deaths were within 3 h of delivery and 91% of these deaths were from bleeding. Women who delivered outside a participating hospital (12%) were three times more likely to die (OR = 3.12, 95%CI 2.55-3.81) than those who delivered in hospital. Blood was often unavailable due to shortages or because relatives could not afford to buy it. Clinicians highlighted late presentation, maternal anaemia and poor infrastructure as key contributory factors. CONCLUSIONS: Although TXA use reduces bleeding deaths by almost one third, mortality rates similar to those in high income countries will not be achieved without tackling late presentation, maternal anaemia, availability of blood for transfusion and poor infrastructure.
Item Type: |
Article
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Additional Information: |
© The Author(s). 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
Keywords: |
WOMAN trial collaborators, Obstetrics & Reproductive Medicine, 1114 Paediatrics and Reproductive Medicine, 1117 Public Health and Health Services, 1110 Nursing |
SGUL Research Institute / Research Centre: |
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) |
Journal or Publication Title: |
BMC Pregnancy Childbirth |
ISSN: |
1471-2393 |
Language: |
eng |
Dates: |
Date | Event |
---|
16 July 2020 | Published | 3 July 2020 | Accepted |
|
Publisher License: |
Creative Commons: Attribution 4.0 |
Projects: |
|
PubMed ID: |
32677911 |
 |
Go to PubMed abstract |
URI: |
https://openaccess.sgul.ac.uk/id/eprint/112168 |
Publisher's version: |
https://doi.org/10.1186/s12884-020-03091-8 |
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