PPH detection and first-response treatment bundle
A package for hospitals. Staff measure blood loss at vaginal births with a calibrated drape, and when heavy bleeding is detected they start a standard set of treatments straight away. The set covers uterine massage, a uterus-contracting medicine, tranexamic acid, fluids into a vein, a check for the source of bleeding and calling for more help. Staff training and feedback support the package.
Also called E-MOTIVE package · MOTIVE bundle
- Intervention
- In this atlas
Overview
Technical summary
The package combines objective blood-loss assessment with a calibrated drape, a first-response bundle (uterine massage, an oxytocic drug, tranexamic acid, intravenous fluids, examination of the genital tract and escalation of care) and an implementation strategy. WHO 2025 Recommendation 29 (Revalidated, Recommended) recommends it for all women having a vaginal birth. E-MOTIVE tested the whole package; the drape alone was not tested, and the effect cannot be assigned to any component. WHO says the supporting evidence comes largely from vaginal births in secondary-level facilities and that more research is needed before recommending bundle care at caesarean birth.
About this intervention
- Type
- Service
- Mechanism
- Early objective detection triggers a coordinated set of treatments, supported by training, audit and feedback and an emergency supply trolley or carry case (implementation strategy).
Claims and evidence
Context Patients having vaginal delivery in 80 secondary-level hospitals in Kenya, Nigeria, South Africa and Tanzania (E-MOTIVE)
- Recipient
- Maternal
- Population
- Patients having a vaginal delivery in the study hospitals. Hospitals were randomly assigned to the package or to usual care. The abstract reports results among hospitals and patients with data, not for all randomised deliveries. The registry describes its research participants as health care providers attending vaginal births, a different basis from the paper.
- Care setting
- Secondary-level hospitals.
- Geography
- Kenya, Nigeria, South Africa and Tanzania.
- Life stage
- Childbirth and the first hours after birth
- Gestational age
- Not reported
- Postnatal age
- Not reported
- Follow-up
- Not stated in the abstract.
Eligibility: 1 inclusion criterion; 1 exclusion criterion
- Included
- Patients having a vaginal delivery in a participating hospital
- Excluded
- Other criteria are not stated in the abstract
E-MOTIVE tested a package, not a single product. The package was a calibrated blood-collection drape for early detection, a bundle of first-response treatments, and a strategy to help hospitals use them. 80 secondary-level hospitals in Kenya, Nigeria, South Africa and Tanzania were randomly assigned to the package or to usual care. "Among hospitals and patients with data", severe bleeding (1000 mL or more), laparotomy for bleeding or death from bleeding occurred in 1.6% of patients with the package and 4.3% with usual care (risk ratio 0.40, 95% CI 0.32 to 0.50). Postpartum haemorrhage was detected in 93.1% against 51.1% (rate ratio 1.58, 1.41 to 1.76), and the bundle was used in 91.2% against 19.4% (rate ratio 4.94, 3.88 to 6.28).
Applies to Maternal- Patients having a vaginal delivery in the study hospitals. Hospitals were randomly assigned to the package or to usual care. The abstract reports results among hospitals and patients with data, not for all randomised deliveries. The registry describes its research participants as health care providers attending vaginal births, a different basis from the paper.
- Secondary-level hospitals.
- Kenya, Nigeria, South Africa and Tanzania.
- Childbirth and the first hours after birth
- Gestational age Not reported
- Postnatal age Not reported
- Certainty method
- Not assessed
- Limitations
- The effect belongs to the whole package (drape, bundle and implementation strategy) and cannot be split by component, so none of it is credited to the drape or to tranexamic acid alone. Randomisation was by hospital. Only the NEJM abstract was read, because the full text returned HTTP 403 and was not retrieved another way, so analysis methods are not described. The percentages are results among hospitals and patients with data and are not counts of individual patients. The registry gives 99659 enrolled (actual), describes the research participants as health care providers attending vaginal births, and lists no masking; the paper reports 210,132 vaginal deliveries. These are different bases and are not reconciled. The primary outcome is a composite, so the abstract gives no separate effect on maternal death.
- Last checked
- 2026-10-11
- Next evidence check due
- Not scheduled
Sources and citations (4)
-
Supports Randomized Trial of Early Detection and Treatment of Postpartum Hemorrhage
- Locator
- Abstract, METHODS: package and cluster design
- How it applies
- PubMed abstract; the full text was not retrieved.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
ac7a6b8ccd74b1e8eec860852401c1052be14e9cbe32a7f923b2be380a8662d0- Reuse basis
- Bibliographic metadata and short factual extraction from the PubMed abstract. The abstract belongs to the publisher, so it is not committed; only its sha256 is kept.
-
Supports Randomized Trial of Early Detection and Treatment of Postpartum Hemorrhage
- Locator
- Abstract, RESULTS: primary outcome, detection and bundle use
- How it applies
- PubMed abstract; results among hospitals and patients with data.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
ac7a6b8ccd74b1e8eec860852401c1052be14e9cbe32a7f923b2be380a8662d0- Reuse basis
- Bibliographic metadata and short factual extraction from the PubMed abstract. The abstract belongs to the publisher, so it is not committed; only its sha256 is kept.
-
- Locator
- protocolSection.designModule: enrollment count and masking
- How it applies
- Registry JSON; a different basis from the paper.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
0a7a1ede0bc051836032b9f2016627544ebe5a0c0093f178b25e94a4ab1a6a8f- Reuse basis
- Registry JSON. ClinicalTrials.gov terms of use have not been verified, so the bytes are not committed. Facts only. Public text is quote, following Ben's decision of 2026-10-13 (medical-atlas-core issue 2) that registries allow short quotations with attribution. This source's terms are unverified or reserve all rights, so any quotation stays short.
-
- Locator
- protocolSection.descriptionModule.detailedDescription: research participants
- How it applies
- Registry wording on who the participants are.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
0a7a1ede0bc051836032b9f2016627544ebe5a0c0093f178b25e94a4ab1a6a8f- Reuse basis
- Registry JSON. ClinicalTrials.gov terms of use have not been verified, so the bytes are not committed. Facts only. Public text is quote, following Ben's decision of 2026-10-13 (medical-atlas-core issue 2) that registries allow short quotations with attribution. This source's terms are unverified or reserve all rights, so any quotation stays short.
Context Women having a vaginal birth, objective assessment with a first-response bundle (WHO 2025 Recommendation 29)
- Recipient
- Maternal
- Population
- All women having a vaginal birth. WHO says the supporting evidence comes largely from vaginal births in secondary-level facilities and that more research is needed to recommend bundle care at caesarean birth.
- Care setting
- Health facilities. The evidence is largely from secondary-level facilities; WHO says recognition and treatment are equally relevant in primary care, community and home settings.
- Geography
- Global (WHO guidance intended to inform national and subnational policy).
- Life stage
- Childbirth and the first hours after birth
- Gestational age
- Not reported
- Postnatal age
- Not reported
- Follow-up
- Not applicable (recommendation context)
Eligibility: 1 inclusion criterion; exclusion criteria not stated
- Included
- Any woman having a vaginal birth
- Excluded
- None stated
WHO 2025 recommends a standardized and timely approach to managing postpartum haemorrhage for all women having a vaginal birth (Recommendation 29, category Recommended, Revalidated from the 2023 recommendation). The approach combines an objective assessment of blood loss with a treatment bundle supported by an implementation strategy. The first-line bundle includes rapid uterine massage, an oxytocic medicine and tranexamic acid, intravenous fluids, examination of the genital tract and escalation of care.
Applies to Maternal- All women having a vaginal birth. WHO says the supporting evidence comes largely from vaginal births in secondary-level facilities and that more research is needed to recommend bundle care at caesarean birth.
- Health facilities. The evidence is largely from secondary-level facilities; WHO says recognition and treatment are equally relevant in primary care, community and home settings.
- Global (WHO guidance intended to inform national and subnational policy).
- Childbirth and the first hours after birth
- Gestational age Not reported
- Postnatal age Not reported
- Certainty method
- Not assessed
- Limitations
- The supporting evidence is largely from vaginal births in secondary-level facilities; WHO says more research is needed before recommending bundle care at caesarean birth, although each treatment is separately recommended. The trial behind this recommendation included multiple implementation and health system strengthening strategies, so the recommended package is more than the drape and the medicines. WHO says its evidence on measuring blood loss comes largely from trials using calibrated drapes. WHO 2025 labels each recommendation with one of four categories and a development status. These are not GRADE strength labels, so the claim certainty is left not assessed.
- Last checked
- 2026-10-11
- Next evidence check due
- Not scheduled
Sources and citations (4)
-
Supports Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage
- Locator
- Recommendation 29: recommendation text and category
- How it applies
- WHO 2025 consolidated guideline, CC BY-NC-SA 3.0 IGO; short quotation with attribution.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
2049fb40dff7e97712c98cb58907ef662161627197a5e143ec50045abb1931de- Reuse basis
- Licensed CC BY-NC-SA 3.0 IGO, as stated in the PDF and in the IRIS record. Only short quotations with attribution are used, and neither the PDF nor the pages are committed. The non-commercial and share-alike terms need a licensing decision before any text is adapted.
-
Supports Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage
- Locator
- Recommendation 29, Remarks: implementation strategies, drape evidence, caesarean research need
- How it applies
- WHO 2025 consolidated guideline, CC BY-NC-SA 3.0 IGO; short quotation with attribution.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
2049fb40dff7e97712c98cb58907ef662161627197a5e143ec50045abb1931de- Reuse basis
- Licensed CC BY-NC-SA 3.0 IGO, as stated in the PDF and in the IRIS record. Only short quotations with attribution are used, and neither the PDF nor the pages are committed. The non-commercial and share-alike terms need a licensing decision before any text is adapted.
-
Background Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage
- Locator
- Summary list of recommendations, footnote to Recommendation 29: integrated from the 2023 recommendations
- How it applies
- WHO 2025 consolidated guideline, CC BY-NC-SA 3.0 IGO; short quotation with attribution.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
2049fb40dff7e97712c98cb58907ef662161627197a5e143ec50045abb1931de- Reuse basis
- Licensed CC BY-NC-SA 3.0 IGO, as stated in the PDF and in the IRIS record. Only short quotations with attribution are used, and neither the PDF nor the pages are committed. The non-commercial and share-alike terms need a licensing decision before any text is adapted.
-
- Locator
- Table 1, Recommendation 2: the same recommendation in 2023
- How it applies
- WHO 2023 recommendations, CC BY-NC-SA 3.0 IGO; history only.
- Retrieved
- Source effective date
- Not reported
- Source state
- Current
- Snapshot hash
36364aa61f4e3b6dc00561e5a5d6aff380639230952bda6cab1db58d81c66ad8- Reuse basis
- Licensed CC BY-NC-SA 3.0 IGO, as stated in the PDF and in the IRIS record. Only short quotations with attribution are used, and neither the PDF nor the pages are committed. The non-commercial and share-alike terms need a licensing decision before any text is adapted.
Guidance
Recommended: PPH detection and first-response treatment bundle
- All women having a vaginal birth. WHO says the supporting evidence comes largely from vaginal births in secondary-level facilities and that more research is needed to recommend bundle care at caesarean birth.
- Health facilities. The evidence is largely from secondary-level facilities; WHO says recognition and treatment are equally relevant in primary care, community and home settings.
- Global (WHO guidance intended to inform national and subnational policy).
- Childbirth and the first hours after birth
- Gestational age Not reported
- Postnatal age Not reported
- Issued by
- World Health Organization
- Guideline
- Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage, edition First edition, 2025. The date is the who.int page date, 5 October 2025, which the atlas uses for WHO sources and decisions; the WHO IRIS record lists an issue date of 2025-09-26 for the same document. The web annexes with the evidence base and the implementation guide were not read.
- Strength
- Recommended
- Effective
- 2025-10-05
- Jurisdiction
- Global (WHO guidance intended to inform national and subnational policy). Co-published with FIGO and ICM.
- Basis
- WHO 2025 recommends a standardized and timely approach to managing postpartum haemorrhage for all women having a vaginal birth (Recommendation 29, category Recommended, Revalidated from the 2023 recommendation). The approach combines an objective assessment of blood loss with a treatment bundle supported by an implementation strategy. The first-line bundle includes rapid uterine massage, an oxytocic medicine and tranexamic acid, intravenous fluids, examination of the genital tract and escalation of care.
Limitations. The supporting evidence is largely from vaginal births in secondary-level facilities; WHO says more research is needed before recommending bundle care at caesarean birth, although each treatment is separately recommended. The trial behind this recommendation included multiple implementation and health system strengthening strategies, so the recommended package is more than the drape and the medicines. WHO says its evidence on measuring blood loss comes largely from trials using calibrated drapes. WHO 2025 labels each recommendation with one of four categories and a development status. These are not GRADE strength labels, so the claim certainty is left not assessed.
Clinical links
Each link reports what one cited claim says about one population. "Evaluated for" means studied, not shown to work. These links do not show that anything is effective or right for you.
-
Claim, not a settled fact WHO 2025 Recommendation 29: recommended for vaginal birth: Postpartum haemorrhage
Applies to Maternal- All women having a vaginal birth. WHO says the supporting evidence comes largely from vaginal births in secondary-level facilities and that more research is needed to recommend bundle care at caesarean birth.
- Health facilities. The evidence is largely from secondary-level facilities; WHO says recognition and treatment are equally relevant in primary care, community and home settings.
- Global (WHO guidance intended to inform national and subnational policy).
- Childbirth and the first hours after birth
- Gestational age Not reported
- Postnatal age Not reported
WHO 2025 recommends a standardized and timely approach to managing postpartum haemorrhage for all women having a vaginal birth (Recommendation 29, category Recommended, Revalidated from the 2023 recommendation). The approach combines an objective assessment of blood loss with a treatment bundle supported by an implementation strategy. The first-line bundle includes rapid uterine massage, an oxytocic medicine and tranexamic acid, intravenous fluids, examination of the genital tract and escalation of care.Limitations. The supporting evidence is largely from vaginal births in secondary-level facilities; WHO says more research is needed before recommending bundle care at caesarean birth, although each treatment is separately recommended. The trial behind this recommendation included multiple implementation and health system strengthening strategies, so the recommended package is more than the drape and the medicines. WHO says its evidence on measuring blood loss comes largely from trials using calibrated drapes. WHO 2025 labels each recommendation with one of four categories and a development status. These are not GRADE strength labels, so the claim certainty is left not assessed.
-
Claim, not a settled fact Evaluated as a package in E-MOTIVE: Postpartum haemorrhage
Applies to Maternal- Patients having a vaginal delivery in the study hospitals. Hospitals were randomly assigned to the package or to usual care. The abstract reports results among hospitals and patients with data, not for all randomised deliveries. The registry describes its research participants as health care providers attending vaginal births, a different basis from the paper.
- Secondary-level hospitals.
- Kenya, Nigeria, South Africa and Tanzania.
- Childbirth and the first hours after birth
- Gestational age Not reported
- Postnatal age Not reported
E-MOTIVE tested a package, not a single product. The package was a calibrated blood-collection drape for early detection, a bundle of first-response treatments, and a strategy to help hospitals use them. 80 secondary-level hospitals in Kenya, Nigeria, South Africa and Tanzania were randomly assigned to the package or to usual care. "Among hospitals and patients with data", severe bleeding (1000 mL or more), laparotomy for bleeding or death from bleeding occurred in 1.6% of patients with the package and 4.3% with usual care (risk ratio 0.40, 95% CI 0.32 to 0.50). Postpartum haemorrhage was detected in 93.1% against 51.1% (rate ratio 1.58, 1.41 to 1.76), and the bundle was used in 91.2% against 19.4% (rate ratio 4.94, 3.88 to 6.28).Limitations. The effect belongs to the whole package (drape, bundle and implementation strategy) and cannot be split by component, so none of it is credited to the drape or to tranexamic acid alone. Randomisation was by hospital. Only the NEJM abstract was read, because the full text returned HTTP 403 and was not retrieved another way, so analysis methods are not described. The percentages are results among hospitals and patients with data and are not counts of individual patients. The registry gives 99659 enrolled (actual), describes the research participants as health care providers attending vaginal births, and lists no masking; the paper reports 210,132 vaginal deliveries. These are different bases and are not reconciled. The primary outcome is a composite, so the abstract gives no separate effect on maternal death.
Record details
- Record id
maternal:pph-detection-and-first-response-bundle- Content hash
b1ec619c447dd7ca865e7aecb03b1a7e551c7e7274102d14204b59e9ede6c2d3