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Postpartum haemorrhage in anaemic women: assessing outcome measures for clinical trials

Trials volume 23, Article number: 220 (2022) Cite this article

Abstract

Background

Postpartum haemorrhage (PPH) is a leading cause of maternal mortality worldwide. Maternal anaemia greatly increases the risk of PPH, and over a third of all pregnant women are anaemic. Because anaemia reduces the oxygen-carrying capacity of the blood, anaemic women cannot tolerate the same volume of blood loss as healthy women. Yet the same blood loss threshold is used to define PPH in all women. The lack of an established PPH definition in anaemic women means the most appropriate outcome measures for use in clinical trials are open to question. We used data from the WOMAN-2 trial to examine different definitions of PPH in anaemic women and consider their appropriateness as clinical trial outcome measures.

Main body

The WOMAN-2 trial is assessing tranexamic acid (TXA) for PPH prevention in women with moderate or severe anaemia at baseline. To obtain an accurate, precise estimate of the treatment effect, outcome measures should be highly specific and reasonably sensitive. Some outcome misclassification is inevitable. Low sensitivity reduces precision, but low specificity biases the effect estimate towards the null. Outcomes should also be related to how patients feel, function, or survive. The primary outcome in the WOMAN-2 trial, a ‘clinical diagnosis of PPH’, is defined as estimated blood loss > 500 ml or any blood loss within 24 h sufficient to compromise haemodynamic stability. To explore the utility of several PPH outcome measures, we analysed blinded data from 4521 participants. For each outcome, we assessed its: (1) frequency, (2) specificity for significant bleeding defined as shock index ≥1.0 and (3) association with fatigue (modified fatigue symptom inventory [MFSI]), physical endurance (six-minute walk test) and breathlessness. A clinical diagnosis of PPH was sufficiently frequent (7%), highly specific for clinical signs of early shock (95% specificity for shock index ≥1) and associated with worse maternal functioning after childbirth.

Conclusion

Outcome measures in clinical trials of interventions for PPH prevention should facilitate valid and precise estimation of the treatment effect and be important to women. A clinical diagnosis of PPH appears to meet these criteria, making it an appropriate primary outcome for the WOMAN-2 trial.

Trial registration

ClinicalTrials.gov NCT03475342, registered on 23 March 2018; ISRCTN62396133, registered on 7 December 2017; Pan African Clinical Trial Registry PACTR201909735842379, registered on 18 September 2019.

Peer Review reports

Background

Postpartum haemorrhage (PPH) is a leading cause of maternal mortality worldwide, responsible for over 70,000 deaths annually [1]. Maternal anaemia greatly increases the risk of PPH [2, 3]. Over a third of all pregnant women (around 30 million) are anaemic, with a high prevalence in sub-Saharan Africa and South Asia [4]. Because anaemia reduces the oxygen-carrying capacity of the blood, anaemic women are more vulnerable to tissue hypoxia, morbidity and death after PPH [5, 6].

Primary PPH is usually defined as blood loss ≥500 ml from the genital tract within 24 h of a vaginal birth [7]. This definition, proposed by a WHO working group in 1989, uses the same threshold for all women. Despite recognising the need for an alternative definition in anaemic women, no specific criteria were proposed [8]. The core outcome set for PPH prevention trials does not consider anaemia [9].

Given the lack of an established definition of PPH in anaemic women, the most appropriate outcome measures for use in clinical trials are open to question. We used data from the WOMAN-2 trial to examine different definitions of PPH in anaemic women and consider their appropriateness as clinical trial outcome measures.

Criteria to assess PPH outcome measures

The WOMAN-2 trial is examining tranexamic acid (TXA) for PPH prevention in women with moderate (Hb 70–99 g/L, n = 3714, 82%) or severe (Hb < 70 g/L, n = 805, 18%) anaemia at baseline. Women are randomly allocated to receive 1 g of TXA or matching placebo as soon as possible after cord clamping. The primary outcome, a ‘clinical diagnosis of PPH’, may be defined as estimated blood loss > 500 ml or any blood loss within 24 h sufficient to compromise haemodynamic stability. Haemodynamic instability is based on clinical judgement and assessed using clinical signs (low systolic blood pressure, tachycardia, reduced urine output) that require an intervention (e.g. intravenous fluids)) [10].

In a clinical trial, the primary outcome should facilitate valid and precise estimation of the treatment effect and be related to how patients feel, function or survive [11, 12]. Some outcome misclassification is inevitable. Table 1 shows the potential impact of sensitivity and specificity on the relative risk (RR) in the WOMAN-2 trial. Assuming 6% of the placebo group have a PPH and TXA reduces this risk by 25% (RR = 0.75), a sample size of 10,000 should provide 90% power [10]. Low sensitivity (many false negatives) reduces precision but the RR remains the same, whereas low specificity (many false positives) biases the RR towards the null [13].

Table 1 Impact of sensitivity and specificity on the treatment effect estimate in a randomised trial. Hypothetical example based on the WOMAN-2 trial of 10,000 women (5000 per arm), assuming a true placebo group event rate of 6% and a true relative risk of 0.75
Full size table

To explore the utility of several PPH outcome measures, we analysed blinded data from 4521 participants recruited to 14th July 2021. For each outcome, we assessed its: (1) frequency, (2) specificity for significant bleeding and (3) importance to women. To assess frequency, we considered the sample size calculation for the trial—for 90% power to detect a 25% reduction in PPH with TXA, a minimum event rate of 6% in the placebo group is required, with an event rate of 4.5% in the TXA group and therefore 5.25% overall. To assess specificity, we used a shock index (postpartum heart rate/systolic blood pressure) ≥1.0 as the ‘gold standard’ for the cardiovascular impact of bleeding (see Table 2) [14,15,16,17]. To assess importance to women, we examined each outcome’s association with fatigue (modified fatigue symptom inventory [MFSI]), physical endurance (6-min walk test) and breathlessness (patient-reported outcome post-walk test), (see Table 3).

Table 2 Cumulative incidence of PPH outcome measures and their diagnostic accuracy for early shock defined as shock index ≥1
Full size table
Table 3 Association of PPH with measures of maternal functioning after birth
Full size table

Clinical diagnosis of PPH

In this population of anaemic women, 7% had a clinical diagnosis of PPH. When compared against shock index ≥1, this outcome measure had 95% specificity, meaning the false positive rate was 5% (see Table 2). Those with a clinical diagnosis of PPH had worse fatigue, reduced ability to exercise and were more breathless after exercise compared to those without this diagnosis (Table 3).

Estimated blood loss ≥500 ml

Blood loss was estimated to be ≥500 ml in 8% of women. When compared against shock index ≥1, this outcome had 93% specificity, meaning a false positive rate of 7% (see Table 2). Those with blood loss ≥500 ml had worse fatigue, reduced ability to exercise and were more breathless after exercise compared to those with blood loss < 500 ml (see Table 3).

Proportion of total blood volume lost

Height and weight determine total blood volume. The smaller the woman, the larger the proportion of total blood volume any given volume of blood loss represents. In pregnancy, blood volume per kilogram (kg) decreases with increasing body mass index (BMI) because fat tissue is relatively non-vascular [18]. BMI ranged from 13 to 68 kg/m2 in our study population (mean 26, SD 4; see Fig. 1). Based on the Advanced Trauma Life Support classification of hypovolaemic shock, we defined PPH as ≥15% total blood volume lost, which occurred in 3% of women. When compared against shock index ≥1, this outcome had 98% specificity, meaning a false positive rate of 2% (see Table 2). Women who lost ≥15% of their total blood volume had worse fatigue and were more breathless after exercise, with weak evidence of a reduced ability to exercise (see Table 3).

Fig. 1
figure 1

Body mass index and baseline haemoglobin level in the WOMAN-2 trial

Full size image

Peripartum haemoglobin change

Studies suggest that postpartum blood loss ≥500 ml confers a Hb drop ≥20 g/L, although this may vary between women and is affected by red blood cell (RBC) transfusion and intravenous (IV) fluids [19,20,21,22,23]. In the WOMAN-2 trial, 25% (n = 1143) and 44% (n = 2000) of women received a RBC transfusion or IV fluids (mostly crystalloids) between randomisation and their postpartum Hb test, respectively. In a multivariable linear regression model, one unit of RBC increased peripartum Hb by 7.7 g/L (95% CI 7.0 to 8.3), while 1 L of IV fluids reduced it by 1.5 g/L (95% CI − 2.2 to − 0.8), adjusting for baseline Hb and estimated blood loss. Mean Hb increment per unit of RBC transfused increased with lower baseline Hb (9 vs 6 g/L for Hb of 30 and 99 g/L). To correct postpartum Hb for RBC transfusion, we used coefficients from a predictive model of mean Hb increment derived from 23,194 patients in US hospitals who received one unit of RBC, which adjusted for possible effect modification by baseline Hb, BMI and age [22]. To correct for IV fluids, we applied the model coefficient from the WOMAN-2 data.

After correcting for RBC transfusion and IV fluid, 4% of women had a peripartum Hb drop ≥20 g/L. When compared against shock index ≥1, this outcome had 97% specificity, or a false positive rate of 3% (see Table 2). Because baseline Hb varied (mean = 8.1 g/dL, SD 1.4, range = 2.3–9.9; see Fig. 1), we analysed a relative Hb drop ≥10%, which occurred in 16% of women and had 85% specificity for shock index ≥1 or a 15% false positive rate (see Table 2). Women with a Hb drop ≥20 g/L or ≥ 10% had worse fatigue and breathlessness after exercise, but weak evidence of an increased ability to exercise compared to those with Hb drop < 20 g/L or < 10% (see Table 3).

Calculated blood loss ≥1000 ml

Another way to define PPH is using calculated blood loss (estimated total blood volume × proportional change in peripartum Hb) [24]. After correcting postpartum Hb for RBC transfusions and fluid resuscitation, 8% of women had calculated blood loss ≥1000 ml. When compared against shock index ≥1, this outcome had 93% specificity, or a 7% false positive rate (see Table 2). Women with calculated blood loss ≥1000 ml had worse fatigue and breathlessness after exercise, but weak evidence of an increased ability to exercise compared to those with calculated blood loss < 1000 ml (see Table 3).

Interventions for blood loss

Blood transfusion, intravenous fluid, TXA and uterotonics are common interventions for postpartum blood loss but are also routinely given for anaemia, dehydration or PPH prophylaxis. Interventions within 24 h after birth are more likely to be for primary PPH. In total, 25% of women had a blood transfusion within 24 h after giving birth, which had 76% specificity for shock index ≥1 (see Table 2). A total of 44% of women received IV fluid within 24 h after birth, which had 58% specificity for shock index ≥1 (see Table 2). In total, 6% of women received TXA within 24 h after birth, which had 96% specificity for shock index ≥1 (see Table 2). A total of 29% of women received postpartum uterotonics (oxytocin, carbetocin, misoprostol, prostaglandins and/or ergometrine), which had 72% specificity for shock index ≥1 (see Table 2). Women who received a blood transfusion had worse fatigue and a reduced ability to exercise, with weak evidence of increased breathlessness compared to those who did not receive a blood transfusion, whereas women who received IV fluids, TXA or postpartum uterotonics had worse fatigue, reduced ability to exercise and worse breathlessness (see Table 3).

Shock index ≥1

Although shock index was used as a gold standard measure of the cardiovascular impact of bleeding, we assessed its frequency and importance to women as an outcome measure. Shock index was ≥1 in 8% of women. Those with a shock index ≥1 had worse fatigue and breathlessness after exercise, but some evidence of an increased ability to exercise compared to those with shock index < 1 (Table 3).

Discussion

To obtain an accurate, precise estimate of the treatment effect, outcome measures should be highly specific and reasonably sensitive. To ensure that evidence of effectiveness translates into real benefit for mothers, the outcome should also be important to women. A clinical diagnosis of PPH, the primary outcome in the WOMAN-2 trial, appears to meet these criteria—it was sufficiently frequent, highly specific for clinical signs of early shock and predictive of maternal functioning after birth. Estimated blood loss and receipt of TXA within 24 h of birth also performed well against our criteria.

High-quality data on over 4500 anaemic pregnant women provided reliable estimates of PPH and its association with various factors. We were able to assess several PPH definitions and discern the sequence of events. Blood loss was estimated visually rather than measured as it is more practical and no worse at predicting adverse maternal outcomes [25]. The formula to estimate total blood volume was derived from pregnant women (blood volume = weight (kg) × 95 if BMI < 30, or 73 if BMI ≥30) but we did not collect data on pre-pregnancy weight [18]. Hb was measured with the Haemocue Hb 201 system which has reasonable accuracy [26]. We corrected postpartum Hb for RBC transfusion and IV fluid but not for time to postpartum Hb test, which had only a small effect (0.03 g/L drop in postpartum Hb for 1 h increase in time from childbirth to Hb test) [22, 23]. Although unlikely, women could possibly receive a RBC transfusion between their baseline Hb test and randomisation, which is not recorded in the trial. While heart rate and blood pressure can be accurately measured, shock index is an imperfect physiological marker of postpartum blood loss with low sensitivity for PPH [27]. Maternal cardiovascular compensatory mechanisms like haemoconcentration and increased cardiac output after childbirth may obscure early physiologic signs of postpartum bleeding. Shock can be caused by other conditions like sepsis, although this affected < 1% of trial participants.

By combining clinical judgement, physical signs of haemodynamic instability and estimated blood loss, a clinical diagnosis of PPH may be more specific for significant bleeding than estimated blood loss alone, particularly in anaemic women [28]. The TRAAP trial of TXA for the prevention of blood loss after vaginal birth found a 17% reduction in blood loss ≥500 ml with TXA (RR = 0.83, 95% CI 0.68–1.01) but a 26% reduction in clinically diagnosed PPH (RR = 0.74, 95% CI 0.61–0.91) [29]. Calculated blood loss combines peripartum Hb change and total blood volume. The TRAAP2 trial of TXA for PPH prevention in Caesarean births found a reduction in calculated blood loss ≥1000 ml or transfusion (RR = 0.84, 95% CI 0.75–0.94) [24]. However, surrogate measures of PPH based on Hb change may lack value to patients and clinical relevance. Of note, we found a non-significant increase in ability to exercise among women with PPH defined using peripartum Hb change. The relationship between Hb level and postpartum blood loss is not straightforward [20]. Dehydration during childbirth can cause haemoconcentration, increasing postpartum Hb [30]. Physiological adaptions of pregnancy like increased plasma volume and haemodilution may prevent a large drop in Hb with postpartum bleeding [20, 31]. Indeed, few women in the WOMAN-2 trial experienced a Hb drop ≥20 g/L.

Blood transfusion, IV fluid and uterotonics had low specificity, probably because some were given routinely for reasons other than bleeding or despite blood loss. The WOMAN trial of TXA for PPH showed that early treatment reduces death due to bleeding (RR = 0·69, 95% CI 0·52–0·91) but there was no effect on all-cause mortality or hysterectomy as TXA cannot influence non-bleeding causes of death (29% of all deaths) or hysterectomies planned before randomisation (38% of hysterectomies for bleeding occurred within an hour) [12, 32]. Careful consideration of the mechanism of action of the trial treatment, the natural history of the disease and potential sources of null bias is vital when selecting primary outcomes for clinical trials.

The WOMAN-2 trial will provide further insight into outcome measures for PPH research in anaemic women and evidence on the role of TXA for PPH prevention. Anaemia is a highly prevalent risk factor for PPH which needs more attention if we are to reduce the burden of PPH and its consequences for anaemic women and their babies [3, 6]. Large high-quality randomised trials are needed to find effective interventions for the treatment of anaemia in women of reproductive age.

Conclusions

Outcome measures in clinical trials of interventions for PPH prevention should facilitate valid and precise estimation of the treatment effect and be important to women. A clinical diagnosis of PPH is highly specific for the cardiovascular effects of significant postpartum bleeding, sufficiently common and associated with maternal functioning after birth, making it an appropriate primary outcome for the WOMAN-2 trial.

Availability of data and materials

The datasets generated and/or analysed during the current study are not publicly available because the WOMAN-2 trial is ongoing. After trial completion and publication of the planned primary and secondary analyses, the dataset will be made publicly available on the Free Bank of Injury and Emergency Research Data (freeBIRD) website, our data-sharing portal at https://ctu-app.lshtm.ac.uk/freebird/.

Abbreviations

CI:

Confidence interval

Hb:

Haemoglobin

MSFI:

Modified fatigue symptom inventory

PPH:

Postpartum haemorrhage

RR:

Relative risk/risk ratio

TXA:

Tranexamic acid

WHO:

World Health Organization

WOMAN-2 trial:

WOrld Maternal ANtifibrinolytic-2 trial

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Acknowledgements

The authors would like to thank the following people for their invaluable work on recruitment, data collection and research that contributed to this article: Collette Barrow, Amber Geer, Sumaya Huque, Olujide Okunade, Julio Gil-Onandia and Andrew Thayne. We would also like to thank all the study sites and staff around the world who are involved in making the WOMAN-2 trial happen and most importantly, the participating women, without whom the trial would not be possible.

Funding

The WOMAN-2 trial is funded by Wellcome and the Bill and Melinda Gates Foundation.

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Authors and Affiliations

  1. London School of Hygiene and Tropical Medicine, Clinical Trials Unit, Keppel Street, London, WC1E 7HT, UK

    Amy Brenner, Ian Roberts, Eni Balogun, Charlotte Fleming, Raoul Mansukhani, Danielle Prowse & Haleema Shakur-Still

  2. Department of Obstetrics and Gynaecology, University College Hospital, Ibadan, Oyo State, Nigeria

    Folasade Adenike Bello & Oladapo Olayemi

  3. Global Institute of Human Development, Shifa Tameer-e-Millat University, Islamabad, 44000, Pakistan

    Rizwana Chaudhri, Kiran Javaid & Aasia Kayani

  4. Women and Newborn Hospital, University Teaching Hospital, Department of Obstetrics and Gynaecology, Nationalist Road, Private Bag RW1X, 10101, Lusaka, Zambia

    Mwansa Ketty Lubeya & Bellington Vwalika

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  1. Amy Brenner
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HS-S and IR conceived and designed the WOMAN-2 trial. RC, KJ and AK coordinate the trial in Pakistan. FB and OO coordinate the trial in Nigeria. ML and BV coordinate the trial in Zambia. AB, IR and HS-S developed the concepts and conceived the analyses. AB and RM conducted the analyses. AB, IR and HS-S interpreted the data. AB and IR drafted the manuscript. EB, FB, RC, CF, KJ, AK, ML, RM, OO, DP, BV and HS-S provided important feedback, revised the manuscript and contributed to the final version. All authors read and approved the final manuscript.

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Correspondence to Amy Brenner.

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Ethics approval and consent to participate

Ethics approval was obtained from the London School of Hygiene and Tropical Medicine (ref: 15194), as well as all relevant national and local ethics committees. If women are in the active stage of labour and able to give fully informed consent, written consent is obtained. However, many women arrive at hospital in the second stage of labour. Because these women are more likely to be anaemic and more likely to have a PPH, it is important to include them in the trial. However, they may not have the physical/mental capacity to give fully informed consent due to the pain of labour, poor health, or the urgency of the situation. In these cases, a clinician will assess the capacity of the woman and the most appropriate consent procedure is used, which includes giving brief verbal information, obtaining witnessed verbal agreement and delaying written consent until women regain capacity. The patient information sheet and consent form can be found at https://woman2.lshtm.ac.uk/trial-materials-2/protocol/.

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Not applicable

Competing interests

The authors declare that they have no competing interests.

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Brenner, A., Roberts, I., Balogun, E. et al. Postpartum haemorrhage in anaemic women: assessing outcome measures for clinical trials. Trials 23, 220 (2022). https://doi.org/10.1186/s13063-022-06140-z

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