Abstract

BackgroundPostpartum haemorrhage (PPH) remains a leading cause of maternal mortality. Many trials assessing interventions to prevent PPH base their data on low risk women. It is important to consider the impact data collection methods may have on these results. This review aims to assess trials of PPH prophylaxis by grading trials according to the degree of risk status of the population enrolled in these trials and identify differences in the PPH rates of low risk and high risk populations.MethodsSystematic review and meta-analysis using a random-effects model. Trials were identified through CENTRAL. Trials were assessed for eligibility then graded according to antenatal risk factors and method of birth into five grades. The main outcomes were overall trial rate of minor PPH (blood loss ≥500 ml) and major PPH (> 1000 ml) and method of determining blood loss (estimated/measured).ResultsThere was no relationship between minor or major PPH rate and risk grade (Kruskal-Wallis: minor - T = 0.92, p = 0.82; major - T = 0.91, p = 0.92). There was no difference in minor or major PPH rates when comparing estimation or measurement methods (Mann-Whitney: minor - U = 67, p = 0.75; major - U = 35, p = 0.72). There was however a correlation between % operative births and minor PPH rate, but not major PPH (Spearman r = 0.32 v. Spearman r = 0.098).ConclusionsUsing data from trials using low risk women to generalise best practice guidelines might not be appropriate for all births, particularly complex births. Although complex births contribute disproportionately to PPH rates, this review showed they are often underrepresented in trials. Despite this, there was no difference in reported PPH rates between studies conducted in high and low risk groups. Method of birth was shown to be an important risk factor for minor PPH and may be a better predictor of PPH than antenatal risk factors. Women with operative births are often excluded from trials meaning a lack of data supporting interventions in these women. More focus on complex births is needed to ensure the evidence base is relevant to the target population.

Highlights

  • Postpartum haemorrhage (PPH) remains a leading cause of maternal mortality

  • Postpartum haemorrhage (PPH) remains a leading obstetric emergency, causing 25% maternal deaths worldwide [1]. It is defined by the Royal College of Obstetricians and Gynaecologists (RCOG) as blood loss from the genital tract within the first 24 h after birth of at least 500 ml and at least 1000 ml [2]

  • The RCOG recognize several risk factors for postpartum haemorrhage (PPH) (Table 1) [2], this is not an exhaustive list and associations have been found with other risk factors including foetal death, maternal age and history of bleeding during pregnancy

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Summary

Introduction

Postpartum haemorrhage (PPH) remains a leading cause of maternal mortality. Many trials assessing interventions to prevent PPH base their data on low risk women. Postpartum haemorrhage (PPH) remains a leading obstetric emergency, causing 25% maternal deaths worldwide [1]. It is defined by the Royal College of Obstetricians and Gynaecologists (RCOG) as blood loss from the genital tract within the first 24 h after birth of at least 500 ml (minor) and at least 1000 ml (major) [2]. Active management includes the use of uterotonic drugs and controlled cord traction. For women who progress to PPH, treatment involves further use of uterotonics, uterine massage, intravenous fluid, bladder emptying and controlled cord traction. Current evidence suggests the first line drug in this instance should be oxytocin, ergometrine or a combination of these [3]

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