4.5 Article

Uterotonics for prevention of postpartum haemorrhage: EN-BIRTH multi-country validation study

期刊

BMC PREGNANCY AND CHILDBIRTH
卷 21, 期 SUPPL, 页码 -

出版社

BMC
DOI: 10.1186/s12884-020-03420-x

关键词

Birth; Maternal; Coverage; Validity; Survey; Hospital records; Health management systems; Uterotonics; Postpartum haemorrhage

资金

  1. Children's Investment Fund Foundation (CIFF)
  2. Swedish Research Council
  3. CIFF
  4. London School of Hygiene & Tropical Medicine

向作者/读者索取更多资源

Postpartum haemorrhage is a leading cause of preventable maternal mortality worldwide, with the World Health Organization recommending uterotonic administration for every woman after birth. This study found high observed uterotonic coverage in five hospitals, but survey reports underestimated coverage and there were gaps in quality for timing and dose. Routine registers have the potential to track uterotonic coverage accurately, but standardization and further assessment are needed to improve data quality.
BackgroundPostpartum haemorrhage (PPH) is a leading cause of preventable maternal mortality worldwide. The World Health Organization (WHO) recommends uterotonic administration for every woman after birth to prevent PPH. There are no standardised data collected in large-scale measurement platforms. The Every Newborn Birth Indicators Research Tracking in Hospitals (EN-BIRTH) is an observational study to assess the validity of measurement of maternal and newborn indicators, and this paper reports findings regarding measurement of coverage and quality for uterotonics.MethodsThe EN-BIRTH study took place in five hospitals in Bangladesh, Nepal and Tanzania, from July 2017 to July 2018. Clinical observers collected tablet-based, time-stamped data. We compared observation data for uterotonics to routine hospital register-records and women's report at exit-interview survey. We analysed the coverage and quality gap for timing and dose of administration. The register design was evaluated against gap analyses and qualitative interview data assessing the barriers and enablers to data recording and use.ResultsObserved uterotonic coverage was high in all five hospitals (>99%, 95% CI 98.7-99.8%). Survey-report underestimated coverage (79.5 to 91.7%). Don't know replies varied (2.1 to 14.4%) and were higher after caesarean (3.7 to 59.3%). Overall, there was low accuracy in survey data for details of uterotonic administration (type and timing). Register-recorded coverage varied in four hospitals capturing uterotonics in a specific column (21.6, 64.5, 97.6, 99.4%). The average coverage measurement gap was 18.1% for register-recorded and 6.0% for survey-reported coverage. Uterotonics were given to 15.9% of women within the right time (1min) and 69.8% within 3min. Women's report of knowing the purpose of uterotonics after birth ranged from 0.4 to 64.9% between hospitals. Enabling register design and adequate staffing were reported to improve routine recording.ConclusionsRoutine registers have potential to track uterotonic coverage - register data were highly accurate in two EN-BIRTH hospitals, compared to consistently underestimated coverage by survey-report. Although uterotonic coverage was high, there were gaps in observed quality for timing and dose. Standardisation of register design and implementation could improve data quality and data flow from registers into health management information reporting systems, and requires further assessment.

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