IMPACT: Google Scholar: H5-Index = 69; H5-Median = 102 (12th in the World in Public Health); Web of Science/Clarivate: Impact factor = 5.8 (5-year) / 5.5 (2-year); Scopus: Citescore = 6.2

Articles

Antenatal interventions to support newborn survival: updates for the Lives Saved Tool

Rahima Yasin1, Yvonne Tam2, Arjumand Rizvi1, Tyler Vaivada3, Ayesha Arshad Ali1, Robert E Black2, Jai K Das1 4, Zulfiqar A Bhutta1 3

1 Institute for Global Health and Development, The Aga Khan University, Karachi, Pakistan

2 Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA

3 Center for Global Child Health, Hospital for Sick Children, Toronto, Ontario, Canada

4 Department of Paediatrics and Child Health, The Aga Khan University, Karachi, Pakistan

DOI: 10.7189/jogh.16.04303
Cite as: Yasin R, Tam Y, Rizvi A, Vaivada T, Ali AA, Black RE, Das JK, Bhutta ZA. Antenatal interventions to support newborn survival: updates for the Lives Saved Tool. J Glob Health. 2026;16:04303.
Keywords: Lives Saved Tool, antenatal care, neonatal health, vaccination, nutrition, infectious disease

(14 pages)

Share:

Abstract

Background

Antenatal care strategies encompass a series of interventions delivered to expectant mothers to optimise both their health outcomes and those of their neonate. We summarise the most recent effect estimates for maternal immunisation, screening and management of infections, pre-existing chronic diseases such as hypertension and diabetes, nutrition, psychosocial interventions for smoking cessation, pre-term pre-labour rupture of membranes, administration of corticosteroids for foetal lung maturation, and induction of post-term labour.

Methods

We synthesised effect estimates for antenatal and intrapartum interventions using PubMed and CENTRAL searches (2022–2023) and in consultation with a technical advisory group to determine whether and how new meta-analysed effect estimates could be incorporated into the Lives Saved Tool (LiST) model, as well as which of these estimates should be updated and which should be retained.

Results

Tetanus toxoid vaccination during the antenatal period lead to a significant reduction in neonatal mortality. Antibiotics for pre-term pre-labour rupture of membranes and administration of corticosteroids for foetal lung maturation lead to significant reductions in neonatal mortality due to sepsis and prematurity, respectively. Nutritional interventions including balanced protein and energy supplementation and multiple micronutrient supplementation reduced the risks of small-for-gestational-age babies. Insecticide-treated bed-nets for malaria, antibiotic treatment of syphilis, and post-term induction of labour demonstrated significant reductions in the risks of stillbirth. The effect estimates for preterm births contributed to the LiST model for interventions including treatment of asymptomatic bacteriuria, omega-3 fatty acid supplementation, calcium supplementation, and provision of low-dose aspirin for pre-eclampsia, which projected significant reductions in the risks of small-for-gestational-age babies.

Conclusions

The evidence described here highlights the potential impact of implementing high-yield healthcare packages in context-specific settings to effectively improve neonatal survival. These estimates can be used as inputs to model the impact of antenatal care interventions using the LiST.

According to United Nations Children’s Fund (UNICEF) estimates, an estimated 1.9 million babies were stillborn in 2023, while 2.3 million infants died within the first month of life [1,2]. Perinatal health outcomes vary significantly between countries and regions, highlighting the need for better resource allocation and access to specialised services [3]. Although statistics, such as maternal mortality relative to neonatal and stillbirth deaths, have improved over the decades, disparities in perinatal healthcare persist, particularly in low- and middle-income countries [4]. The United Nations Sustainable Development Goal 3 calls for reducing neonatal mortality to less than 12 per 1000 live births and the maternal mortality ratio to less than 70 per 100,000 live births, as well as ensuring universal access to all aspects of reproductive healthcare services by 2030 [5].

World Health Organization (WHO) guidelines recommend at least eight contacts to a healthcare provider during the antenatal period to ensure access to essential healthcare interventions for the well-being of mothers and infants [6]. They also endorse a broad range of interventions for improving the utilisation and quality of antenatal care, including nutritional interventions, maternal and foetal assessment, preventive measures, interventions for common physiological symptoms, and health system interventions. Research has also called published evidence-based recommendations to address the multi-faceted challenges of neonatal health by improving quality of care, strengthening health systems, and increasing investments and policy support [7,8].

The Lives Saved Tool (LiST) is a modelling software developed [9] to estimate the potential impact of scaling up coverage of specific maternal, neonatal and child health interventions which could help reduce their mortality and morbidity. To achieve this, it utilises intervention efficacy estimates from meta-analyses to model the impact of the interventions in a consistent and transparent way. It is used by researchers, programme planners, policymakers, and other stakeholders to determine the most effective combination of evidence-based interventions to reduce maternal, neonatal and child mortality rates within a specific setting [10].

In this study, we document the literature derived from existing systematic reviews of interventions and their component trials and informs on the rationale for selecting effect estimates for specific interventions for a range of neonatal outcomes. A related paper examines the evidence for postnatal care interventions to be included in the updated LiST model [11].

METHODS

We build upon a previously published journal supplement [12–24] by providing a thorough synthesis of evidence on maternal interventions aimed at optimising outcomes for newborn health. We synthesised this evidence using different methodological techniques, which we summarise here and report in detail elsewhere [9,10,24].

Search and selection of reviews

We conducted a search in PubMed and Central between 2022 and 2023 to identify recent relevant systematic reviews of interventions offered to expectant mothers during the antenatal and intrapartum period, selected for inclusion in the LiST based on prior literature [8] and after consulting the technical advisory group (TAG) and the Johns Hopkins University team that manages LiST (Table S1 in the Online Supplementary Document). Details on this procedure are provided elsewhere [12,13,20,24].

The original set of interventions already included in the LiST model represented the foundation for this work [8]; here, we sought to revise these existing estimates (where applicable) using more up-to-date literature. We also identified new interventions that are already being delivered as part of maternal care, but whose effectiveness had not previously been quantified for inclusion in the LiST. The primary requirement was for the effect of antenatal or intrapartum intervention to have a pooled estimate reported for the outcome of neonatal mortality, preterm birth, low birth weight, stillbirth and small-for-gestational-age (SGA) ideally specifically from LMIC studies.

We grouped interventions into two packages, a basic package and an innovation package, to demonstrate the varying levels of feasibility, implementation capacity, and coverage within the LiST model. The basic package included well-established interventions that are backed by strong evidence of effectiveness and are already incorporated into routine maternal and newborn health services. These interventions, potentially scalable, are typically recommended in global guidelines and by the TAG. The innovation package includes interventions which have emerging data and are not proposed in any standard global guidelines. The evidence for these interventions is recent and mostly comes from high-income countries, meaning that they have not been fully tested or implemented in LMICs, but hold promise due to emerging evidence.

To align clinical evidence and pooled estimates with the LiST model, where applicable, we used effects on low birthweight (LBW) to model effects on term SGA, i.e. gestational growth, or preterm birth, depending on what was the likely cause of LBW. For interventions such as hypertensive disorder management and diabetes screening, where recent evidence was statistically insignificant or limited, we retained estimates derived from previous Delphi-consensus processes. These retentions were made based on the TAG’s recommendations as a final recourse in our evidence-selection hierarchy to maintain modelling stability for clinically established interventions, where robust systematic reviews or trial data was unavailable, either due to ethical considerations or a lack of high-quality experimental studies. We have flagged these consensus-based parameters in our results to distinguish them from newly updated empirical estimates.

Quantitative data synthesis

We extracted all relevant data and outcomes with effect estimates after identifying the most recent systematic review. We carried out subgroup analysis for all outcomes of interest reported in studies from LMICs, which we categorised in accordance with the World Bank’s list of countries for the corresponding years when the studies were carried out [25]. When we could not identify interventions from LMICs, we leveraged evidence from high-income or upper-middle income contexts to ensure a comprehensive analysis. We reported pooled statistics as the risk ratio (RR) between experimental and control groups with 95% confidence intervals (CIs). We performed all analyse using RevMan, version 5.1 (Cochrane, London, UK). Based on these effect estimates for relevant outcomes along with other considerations such as regional context and the generalisability of each intervention, we drafted recommendations for inclusion in the LiST model based on the guidelines proposed by Walker et al. [9,10] (Table S2 in the Online Supplementary Document). We extracted certainty of evidence assessments using the GRADE approach where explicitly reported in the included systematic reviews [26].

RESULTS

Of the interventions included and modelled, psychosocial interventions to reduce smoking has been added as a new intervention to the LiST model. Omega-3 fatty acids have been modelled as a part of the innovation care package. We retained previous LiST estimates for select interventions, including antibiotics for preterm pre-labour rupture of membranes, management of hypertensive disorders, and screening and management of diabetes. For the latter two interventions, estimates derived from a 2011 Delphi consensus process were maintained to ensure modelling stability. We applied standardised definitions for each intervention to ensure consistency during the modelling process (Table S3 in the Online Supplementary Document).

Interventions initiated during the early antenatal period

Tetanus toxoid vaccine

For tetanus toxoid vaccination, we selected a randomised controlled trial (RCT) conducted in Colombia assessing the effectiveness of two or three doses of tetanus toxoid vs. influenza vaccine for inclusion in LiST. Tetanus toxoid was associated with a 98% reduction in tetanus-related neonatal mortality (1 study, 688 participants, moderate quality evidence; RR = 0.02; 95% CI = 0.00–0.30) [27]. We propose using this effect estimate for the LiST, which similarly models a near-complete reduction in tetanus-related neonatal mortality as a result of tetanus toxoid vaccination (Table 1).

Table 1. Early antenatal period
Quality assessmentSummary of findings
DirectnessNumber of events
Study (year)Review approachNumber of studiesOutcomeDesignLimitationsConsistencyGeneralisability to population of interestGeneralisability to intervention of interestInterventionControlRR (95% CI)Previous LiST estimateLiST estimate
Tetanus toxoid vaccination
Demicheli et al. (2015) [27]As-is1Neonatal mortality due to tetanusRCTSignificant effect; fixed effects model used.Study shows significant benefits; GRADE certainty of evidence: moderateStudy conducted in Colombia (LMIC)Two or three doses of tetanus toxoid vs. influenza vaccine0 in 34127 in 3470.02 (0.00–0.30)0.94*0.98
Treatment of asymptomatic bacteriuria
Smaill et al. (2019) [28]As-is3Preterm birthRCT/quasi-experimental RCTSignificant effectTwo studies show benefit; GRADE certainty of evidence: lowAll studies are from developed countriesAntibiotics vs. no treatment for asymptomatic bacteriuria9 in 16029 in 1670.34 (0.13–0.88)0.430.66 (preterm AGA)
Prevention of malaria in pregnancy
Gamble et al. (2007) [29]As-is3LBWRCTInsignificant effectOne study shows significant benefitAll studies conducted in LMICsProvision of ITNs in pregnancyNANA0.80 (0.64–1.00)–0.20 (term SGA)
Syphilis detection and treatment
Tong et al. (2023) [30]As-is5StillbirthObservational studiesSignificant effect; fixed model usedAll studies showed consistent benefitAll studies are from LMICsTwo or more doses of penicillin vs. at least one dose of penicillin15 in 545137 in 5310.10 (0.06–0.17)0.82*0.90
As-is7Preterm birthObservational studiesSignificant effect; fixed model usedFour of seven studies showed consistent benefitAll studies are from LMICsTwo or more doses of penicillin vs. at least one dose of penicillin67 in 612205 in 5390.31 (0.24–0.40)0.51*0.69 (preterm AGA)
Multiple micronutrient supplementation
Keats et al. (2021) [31]As-is21StillbirthRCTSignificant effect; fixed effects model usedOne of twenty-five studies show benefitAll studies are from LMICsMultiple micronutrient supplementation on vs. iron and folic acid or placeboNANA0.91 (0.85–0.98)0.09*0.09
Wang et al. (2025) [32]As-is14Term SGARCTSignificant effect; fixed effects model usedThree of fourteen studies show benefitOne of fourteen studies is from a developed countryMultiple micronutrient supplementation on vs. iron and folic acid or placebo7321 in 19,3269155 in 23,2920.95 (0.93–0.97)0.05*0.05
As-is14Preterm SGARCTSignificant effect; fixed effects model usedOne of twelve studies show benefitOne of twelve studies is from a developed countryMultiple micronutrient supplementation on vs. iron and folic acid or placebo423 in 19326623 in 232920.71 (0.63–0.81)0.29*0.29
As-is14Preterm AGARCTSignificant effect; fixed effects model usedTwo of fourteen studies show benefitOne of fourteen studies is from a developed countryMultiple micronutrient supplementation on vs. iron and folic acid or placebo2638 in 19,3263144 in 23,2920.93 (0.89–0.97)0.07*0.07
Balanced protein and energy supplementation
Ota et al. (2015) [33]As-is4SGARCTSignificant effect; fixed effects model usedOne of four studies show benefitAll studies are from LMICsBalanced protein and energy supplementation vs. control or no intervention248 in 1325290 in 12190.80 (0. –0.92)0.29*0.2 (term SGA)
4StillbirthRCTSignificant effect; fixed effects model usedOne of four studies show benefitAll studies are from LMICsBalanced protein and energy supplementation vs. control or no intervention22 in 148939 in 13730.52 (0.31–0.88)0.61*0.48
Omega-3 fatty acids supplementation
Middleton et al. (2018) [34]As-is26Preterm birthRCTSignificant effect; fixed effects model usedOne of twenty-six studies shows significant benefit; GRADE certainty of evidence: high24 of 26 studies are from developed countriesOmega-3 vs. no omega-3608 in 5179685 in 51250.89 (0.81–0.97)0.10*0.11 (preterm AGA)
Calcium supplementation
Hofmeyr et al. (2018) [35]As-is6Preterm birthRCTSignificant effect; fixed effects model usedOne study showed benefit.All studies are from LMICsRoutine high-dose calcium supplementation vs. placebo in pregnancy452 in 4957515 in 50970.88 (0.78–0.99)0.19*0.12 (preterm AGA)
Low-dose aspirin provision for pre-eclampsia
Hoffman et al. (2020) [36]As-is1Preterm birthRCTSignificant effectN/AStudy is from LMICAspirin or placebo Tablets668 in 5780754 in 57640.89 (0.81–0.98)0.110.11 (preterm AGA)
Psychosocial interventions to reduce smoking
Chamberlain et al. (2017) [37]As-is18LBWRCT/quasiSignificant effect; fixed effects model usedNo studies show benefit; GRADE certainty of evidence: highAll studies are from developed countriesPsychosocial interventions to reduce smoking in pregnancy vs. control355 in 4743429 in 46590.83 (0.72–0.94)N/A; modelled as a new intervention (not currently a part of the LiST visualiser)0.17 (term SGA)

AGA – appropriate for gestational age, CI – confidence interval, LiST – Lives Saved Tool, LMICs – low- and middle-income country, RR – risk ratio, SGA – small for gestational age

*Previous estimates taken from the LiST visualiser.

Treatment of asymptomatic bacteriuria

We included this intervention for modelling via the list based on consultation with the TAG. Screening and treatment of genitourinary tract infection [28] significantly reduced preterm births in babies born appropriate for their gestational age (3 studies, 320 participants; RR = 0.34; 95% CI = 0.13–0.88) by 66%. All the included studies came from high- or upper-middle income countries. This pooled effect estimate showed a significant magnitude of effect and potential for clinical impact, and we used it to model the effect on preterm (Table 1).

Prevention of malaria

Insecticide treated bed-nets [29] did not demonstrate a significant impact on LBW (3 studies; RR = 0.80; 95% CI = 0.64–1.00). All trials included were from LMICs and the effect was marginally touching significance; for this reason, we used the LBW estimate in the LiST to model the effect on SGA (20% reduction) (Table 1).

Syphilis detection and treatment

Tong et al. [30] evaluated the effect of two or more doses of penicillin in comparison to at least one dose of penicillin for syphilis in pregnant women. While the systematic review included observational studies from high-, upper-, and lower-middle income countries, we conducted an analysis specifically for LMICs to assess the impact in those regions. Two or more doses of penicillin significantly reduced the risk of stillbirth (5 studies, 1076 participants; RR = 0.10; 95% CI = 0.06–0.17) by 90% and the risk of preterm birth (7 studies, 1151 participants; RR = 0.31; 95% CI = 0.24–0.40) in babies born appropriate for gestational age by 69%. This estimate showed a large magnitude of effect and potential for clinical impact, and we used these effect estimates for LiST to model the impact of detection and treatment of syphilis on stillbirth and preterm birth (Table 1).

Low-dose aspirin provision for pre-eclampsia

We identified one study [36] which evaluated the effect of low-dose aspirin in pregnant women between gestational ages of 6 weeks and 0 days of pregnancy and 13 weeks and 6 days of pregnancy. It was a large placebo-controlled trial and enrolled participants from six LMICs. Low-dose aspirin supplementation demonstrated a significant effect on preterm birth (1 study, 11,544 participants; RR = 0.89; 95% CI = 0.81–0.98). LiST uses this pooled effect estimate to model the effect of low-dose aspirin supplementation on preterm appropriate-for-gestational age babies (11% reduction) (Table 1).

Multiple micronutrient supplementation

Keats et al. [31] compared the effectiveness of multiple micronutrient supplementation with iron-folic acid supplementation; all the studies included were RCTs, and the former intervention demonstrated a 9% reduction on the risk of stillbirth (21 studies, 96,772 participants; RR = 0.91; 95% CI = 0.85–0.98; 21 studies, n = 96 772). We used these pooled effect estimates in the LiST to model the effect of MMS on term SGA, preterm SGA, and preterm non-SGA (Table 1).

We derived effect estimates for outcomes such as SGA and preterm birth from a meta-analysis of individual participant data [32]. Of the fourteen randomised trials included, one was conducted in Mexico (upper-middle income country). Prenatal multiple micronutrient supplementation reduced the risks of term SGA (14 studies, 42,618 participants; RR = 0.95; 95% CI = 0.93–0.97), preterm SGA (14 studies, 42,618 participants; RR = 0.71; 95% CI = 0.63–0.81), and preterm non-SGA (14 studies, 42,618 participants; RR = 0.93; 95% CI = 0.89–0.97) by 5%, 29%, and 7%, respectively. We used this pooled effect estimate in the LiST to model the effect on term SGA and stillbirth (Table 1).

Balanced protein and energy supplementation

Ota et al. [33] evaluated the impact of balanced protein and energy supplementation in pregnant women. We conducted an analysis specifically for LMICs to assess the impact in those regions. All the included studies were RCTs. Balanced protein and energy supplementation demonstrated a reduction in the risks of SGA (4 studies, 2544 participants; RR = 0.80; 95% CI = 0.69–0.92) by 20% and stillbirth (4 studies, 2862 participants; RR = 0.52; 95% CI = 0.31–0.88) by 48%. We used this pooled effect estimate to model the effect on term SGA and stillbirth (Table 1).

Omega-3 fatty acids supplementation

Omega-3 fatty acids supplementation in pregnancy has been identified by the TAG as a promising new nutrition-based intervention and has been added to the innovation package. Middleton et al. [34] assessed the impact of omega-3 fatty acids on preterm birth. RCTs from a mix of high-income, upper-middle income and LMICs were included. The intervention had a significant impact on preterm birth (26 studies, 10,304 participants; RR = 0.89; 95% CI = 0.81–0.97;), leading to an 11% reduction. We used this pooled effect estimate in the LiST to model the effect of omega-3 fatty acids on preterm babies born appropriate for their gestational age (Table 1).

Calcium supplementation in at-risk populations

Hofmeyr et al. [35] assessed the effect of calcium supplementation in women with low intake of calcium at population level. To assess the effect within LMICs, we conducted a subgroup analysis. The studies utilised a randomised controlled study design. Calcium supplementation during the antenatal period significantly reduced the risk of preterm birth by 12% (6 studies, 10,054 participants; RR = 0.88; 95% CI = 0.78–0.99). We used this pooled effect estimate in the LiST to model the effect of calcium supplementation on preterm babies born appropriate for their gestational age (Table 1).

Psychosocial interventions to reduce smoking

Chamberlain et al. [37] assessed the effectiveness of psychosocial interventions to reducing smoking in pregnant women. The review included RCTs and quasi-RCTs; all included studies were conducted in high-income countries. This intervention is included in the basic package of care and should be available and accessible by all expectant mothers. The intervention demonstrated a significant impact on low birth weight (18 studies, 9402 participants; RR = 0.83; 95% CI = 0.72–0.94). Based on the pooled estimate for LBW, the LiST model estimates a 17% reduction in term SGA babies (Table 1).

Interventions initiated during the late antenatal period

Hypertensive disorder case management

In consultation with the TAG, we opted to maintain the previous Every Newborn Action Plan [8] estimates for a 20% reduction in stillbirth applying to both, the antepartum (interquartile range (IQR) = 10–30) and intrapartum (IQR = 10–40) periods, respectively, from the use of antihypertensive agents in pregnancies with mild to moderate hypertension, which was based on the Delphi method (Table 2).

Table 2. Late antenatal period
Quality assessmentSummary of findings
DirectnessNumber of events
Study (year)Review approachNumber of studiesOutcomeDesignLimitationsConsistencyGeneralisability to population of interestGeneralisability to intervention of interestInterventionControlRR (95% CI)Previous LiST estimateNew LiST estimate
Hypertensive disorder case management
Magnesium sulfate vs. placebo0.20.2 (Delphi approach)
Antihypertensive drugs vs. control0.20.2 (Delphi approach)
Diabetes screening and management
Optimal control vs. suboptimal control of diabetes0.10.1 (Delphi approach)
Antibiotics for pre-term pre-labour rupture of membranes
Cousens et al. (2010) [38]As-is13Neonatal mortality due to sepsisRCTSignificant effect; fixed effects model usedTwo studies showed benefit; GRADE certainty of evidence: moderateTen of thirteen are from developed countriesAntibiotics for pre-term pre-labour rupture of membranes vs. control971630.61 (0.48–0.77)0.39*0.39
13Neonatal mortality due to prematurityRCTSignificant effect; fixed effects model usedTwo studies showed benefit; GRADE certainty of evidence: moderateAll trials are from developed countriesAntibiotics for pre-term pre-labour rupture of membranes vs. control5095960.88 (0.80–0.97)0.12*0.12
Antenatal corticosteroid administration for fetal lung maturation
McGoldrick et al. (2020) [39]As-is5Neonatal mortality due to prematurityRCTSignificant effect; random effects model usedThree of five studies show consistent benefitAll studies are from LMICsAntenatal corticosteroids for preterm labour312 in 1854397 in 18370.64 (0.43–0.97)0.15*0.36

AGA – appropriate for gestational age, CI – confidence interval, LiST – Lives Saved Tool, LMIC – low- and middle-income country, RCT – randomised controlled trial, RR – risk ratio, SGA – small for gestational age

*Previous estimates taken from the LiST visualiser.

Diabetes screening and management

In consultation with the TAG, we opted to maintain the previous 2014 Every Newborn Action Plan [8] estimate, where experts used the Delphi approach due to paucity of data from LMICs and determined a 10% reduction in stillbirth with optimal control of diabetes during the antepartum (IQR = 5–30) and intrapartum (IQR = 3.5–25) periods (Table 2).

Antibiotics for pre-term pre-labour rupture of membranes

Cousens et al. [38] evaluated the effectiveness of antibiotics for preterm pre-labour rupture of membranes based on data from RCTs. The intervention led to a 39% reduction in the risk of neonatal mortality due to sepsis (13 studies; RR = 0.61; 95% CI = 0.48–0.77), which we used in LiST. Additionally, the use of antibiotics for pre-term pre-labour rupture of membranes also demonstrated an effect on neonatal mortality due to prematurity (13 studies; RR = 0.88; 95% CI = 0.80–0.97). We used this 12% reduction in deaths from prematurity in the LiST (Table 2).

Antenatal corticosteroid administration for foetal lung maturation

McGoldrick et al. [39] evaluated the effect of antenatal corticosteroids for accelerating lung maturation in women at risk of preterm birth. All of the studies were RCTs. We conducted an analysis specifically for LMIC to assess the impact in those regions. Antenatal corticosteroids had a significant 36% reduction in neonatal mortality (5 studies, 3691 participants; RR = 0.64; 95% CI = 0.43–0.97). We used this effect estimate in the LiST to model the effect of antenatal corticosteroids on neonatal mortality due to prematurity (Table 2).

Interventions for the intrapartum period

Post-term induction of labour

Middleton et al. [40] evaluated the effect of inducing labour in pregnancies lasting over 41 weeks and identified a 76% reduction in the risk of stillbirth (15 studies, 10,909 participants; RR = 0.24; 95% CI = 0.08–0.78). All included studies were RCTs from a mix of high-, middle-, and lower-middle income countries with a potential for clinical impact. We used this effect in the LiST (Table 3).

Table 3. Intrapartum period
Quality assessmentSummary of findings
DirectnessNumber of events
Study (year)Review approachNumber of studiesOutcomeDesignLimitationsConsistencyGeneralisability to population of interestGeneralisability to intervention of interestInterventionControlRR (95% CI)Previous LiST estimateNew LiST estimate
Post-term induction of labour
Middleton et al. (2020) [40]As-is15StillbirthRCTSignificant result. Fixed model used.No studies show benefitTen of fifteen studies are from developed countriesInduction of labour for pregnancies lasting ≥41 weeks1 in 547212 in 54370.24 (0.08–0.78)0.7*0.76

CI – confidence interval, LiST – Lives Saved Tool, RCT – randomised controlled trial, RR – risk ratio

*Previous estimates taken from the LiST visualiser.

DISCUSSION

In this review, we evaluated 15 interventions implemented during the early and late antenatal period, and the intrapartum period, deriving the pooled effect estimates from clinical data within existing systematic reviews and meta-analyses. Our selection of the most recent systematic reviews, guided by consultations with the TAG, was based not solely on publication date, but also on a hierarchal assessment of methodological quality and the comprehensiveness of the review’s search strategy. Where possible, we derived the effect sizes from several robust randomised controlled trials, but such high-quality data were not consistently available for mortality outcomes for interventions such as treatment of bacteriuria and syphilis, which further emphasises the need for strengthened research efforts into this topic. Based on the TAG’s recommendations, we opted to maintain the previous 2014 Every Newborn Action Plan evidence base for interventions such as hypertensive case disorder management and diabetes screening and management, which employed pre-existing Delphi consensus estimates. For the management of preterm pre-labour rupture of membranes, we used historical studies to generate estimates, given the limited evidence from LMICs and ethical considerations, such as offering antibiotics to expectant mothers vs. providing little or no medical care, especially in low-resource settings.

While the LiST model estimates the potential impact of scaling up coverage of specific maternal health interventions which could help reduce maternal, neonatal and child mortality, morbidity and stillbirths, it has some inherent applicability and feasibility constraints for LMICs. For example, contextual differences such as baseline risk profiles, high comorbidity burdens, and variations in treatment quality in low-resource settings may alter real-world effect sizes relative to pooled estimates drawn from high-income settings. Furthermore, LMICs often face bottlenecks in their health systems, including limited referral capacity and reduced access to diagnostic infrastructure. Implementation in these settings, therefore, requires careful consideration of these contextual factors to ensure that scaling up coverage of specific interventions is sufficiently robust to deliver adequate neonatal care.

Psychosocial interventions to reduce smoking were newly added to the LiST model. These interventions leverage counselling, health education, financial incentives, and social support frameworks to reduce the risk of LBW. While the current evidence base relies on trials conducted in high-income countries [37], we believe the LiST model can still effectively project the impact of these interventions in LMICs. Additionally, while the evidence for omega-3 fatty acid supplementation demonstrating a significant reduction in preterm birth is mostly derived from high-income settings, it serves as a potentially effective and promising ‘innovative’ intervention for future modelling in LiST. However, additional trials in LMICs are required to warrant inclusion within the basic LiST package.

Evidence from LMICs was unavailable for interventions such as treatment of asymptomatic bacteriuria, psychosocial interventions to reduce smoking, hypertensive disorder case management, and screening and management of diabetes. To bridge this gap, we leveraged effect estimates from high- and upper-middle-income countries and the Delphi consensus. For interventions including omega-3 fatty acids supplementation, management of preterm pre-labour rupture of membranes and induction of labour, we utilised pooled data from a mix of high- and upper-middle income countries and LMICs.

Several studies [41–43] have assessed the optimal doses and time to administer the tetanus toxoid vaccine during pregnancy at which the maternal immune response and placental antibodies’ transfer is most efficient, providing a clear rationale for reinforcing vaccination requirements within the basic antenatal care packages. Serra et al. [44] and Sun et al. [45] did not find a reduced risk of preterm birth after omega-3 supplementation in pregnancy, but Abdelrahman et al. [46] observed decreases in risks of preeclampsia, low birthweight, and preterm birth. Romero et al. [47] and Conde-Agudelo et al. [48] reported decreased risks of preterm birth in singleton gestations with mid-trimester sonographic short cervix, but recommended more investigations on other perinatal outcomes. Strong evidence indicates multiple micronutrient supplementation improves key outcomes like preterm birth, SGA, and LBW compared to iron and folic acid supplementation [49], which is consistent with our findings. Chen et al. [50] compared low-dose aspirin combined with calcium supplementation to aspirin alone and reported the former to be more effective in prevention of preeclampsia and reduction of risk of preterm birth. Other reviews [51–53] also reported lower rates of preeclampsia with calcium supplementation, which is consistent with our results. However, more investigations are needed to determine the ideal dose for this intervention. Antenatal corticosteroids were reported by Ciapponi et al. [54] to be effective for improving neonatal outcomes among women at risk of preterm birth, with no significant differences in efficacy observed between different corticosteroid regimens. Simultaneously, Ninan et al. [55] found scarce data for comparing lower doses to standard double doses. Antibiotics for the management of preterm pre-labour rupture of membranes seem to be more effective than placebo in reducing the rate of chorioamnionitis, but Chatzakis et al. [56] reported that no single antibiotic is more superior to another, however the evidence is of low quality. Alkmark et al. [57] assessed induction of labour at 41 weeks and found improved perinatal outcomes compared with expectant management until 42 weeks in nulliparous women only. The interventions delivered in this research, however, are contextual and their quality varies across different regions, which affects the extent to which coverage translates into lives saved. Overall, our findings indicate that the implementation of the basic care package during the antenatal and the intrapartum period has the potential to translate to real-world impact.

CONCLUSIONS

We summarised the most recent and up-to-date evidence on a diverse range of essential interventions given to expectant mothers during the antenatal and the intrapartum period and subsequently synthesised the impact of a package of effective antenatal and intrapartum interventions for neonates for an updated LiST model. These updated effect estimates allow for a more precise estimation of how scaling up intervention coverages in LMICs can influence neonatal survival.

Additional material

Online Supplementary Document

Ethics statement: Ethical approval was not required for this study as it is a systematic review of previously published literature and did not involve primary data collection or direct interaction with human subjects.

Data availability: Data supporting the findings of this study are available within the article and its Online Supplementary Document.

Funding: This work was supported by a grant from the Gates Foundation (INV-042789). The funders did not contribute to the conceptualisation of this study, interpretation of the evidence, writing of this paper, or the decision to submit for publication.

Authorship contributions: ZAB conceptualised the study, acquired funding and oversaw the development of the final LiST model along with YT and REB. RY led the manuscript preparation. YT and AR provided ongoing technical guidance regarding the LiST and the required inputs. TV oversaw the review inputs into the updated LiST model and edits in the manuscript. AA contributed to various review components and manuscript writing. JKD provided supervision for each step and contributed to the critical revision of the manuscript. All authors approved the final version of the paper.

Disclosure of interest: The authors completed the ICMJE Disclosure of Interest Form (available upon request from the corresponding author) and disclose no relevant interests.

references

  1. United Nations Children’s Fund. Stillbirth. March 2025. Available: https://data.unicef.org/topic/child-survival/stillbirths/. Accessed: 17 December 2025.
  2. United Nations Children’s Fund. Neonatal mortality. March 2026. https://data.unicef.org/topic/child-survival/neonatal-mortality/. Accessed: 17 December 2025.
  3. Lawn JE, Blencowe H, Oza S, You D, Lee AC, Waiswa P, et al.. Every Newborn: progress, priorities, and potential beyond survival. Lancet. 2014;384:189–205. doi: 10.1016/S0140-6736(14)60496-7 PMID: 24853593
  4. Boerma T, Campbell OMR, Amouzou A, Blumenberg C, Blencowe H, Moran A, et al.. Maternal mortality, stillbirths, and neonatal mortality: a transition model based on analyses of 151 countries. Lancet Glob Health. 2023;11:e1024. doi: 10.1016/S2214-109X(23)00195-X PMID: 37349032
  5. United Nations – Women. SDG 3: Ensure healthy lives and promote well-being for all at all ages. Available: https://www.unwomen.org/en/news/in-focus/women-and-the-sdgs/sdg-3-good-health-well-being. Accessed: 17 December 2025.
  6. World Health Organization. New guidelines on antenatal care for a positive pregnancy experience. 7 November 2016. Available: https://www.who.int/news/item/07-11-2016-new-guidelines-on-antenatal-care-for-a-positive-pregnancy-experience. Accessed: 17 December 2025.
  7. Martines J, Paul VK, Bhutta ZA, Koblinsky M, Soucat A, Walker N, et al.. Neonatal survival: a call for action. Lancet. 2005;365:1189–97. doi: 10.1016/S0140-6736(05)71882-1 PMID: 15794974
  8. Bhutta ZA, Das JK, Bahl R, Lawn JE, Salam RA, Paul VK, et al.. Can available interventions end preventable deaths in mothers, newborn babies, and stillbirths, and at what cost? Lancet. 2014;384:347–70. doi: 10.1016/S0140-6736(14)60792-3 PMID: 24853604
  9. Walker N, Tam Y, Friberg IK. Overview of the Lives Saved Tool (LiST). BMC Public Health. 2013;13:S1. doi: 10.1186/1471-2458-13-S3-S1 PMID: 24564438
  10. Walker N, Fischer-Walker C, Bryce J, Bahl R, Cousens S, CHERG Review Groups on Intervention Effects. Standards for CHERG reviews of intervention effects on child survival. Int J Epidemiol. 2010;39:i21–s31. doi: 10.1093/ije/dyq036 PMID: 20348122
  11. Vaivada T, Tam Y, Dominguez G, Jiang L, Lee Him R, Muralidharan O, et al.. Postnatal interventions to support newborn survival: updates for the Lives Saved Tool (LiST). J Glob Health. Forthcoming 2026.
  12. Yasin R, Azhar M, Allahuddin Z, Das JK, Bhutta ZA. Antenatal Care Strategies to Improve Perinatal and Newborn Outcomes. Neonatology. 2025;122 Suppl 1:13–31. doi: 10.1159/000542702 PMID: 39581186
  13. Yasin R, Azhar M, Naseem HA, Ali AA, Das JK, Bhutta ZA. Near-Term and Intrapartum Care of Mothers for Perinatal and Newborn Outcomes. Neonatology. 2025;122 Suppl 1:42–51. doi: 10.1159/000543384 PMID: 39837301
  14. Azhar M, Yasin R, Hanif S, Bughio SA, Das JK, Bhutta ZA. Nutritional Management of Low Birth Weight and Preterm Infants in Low- and Low Middle-Income Countries. Neonatology. 2025;122 Suppl 1:209–23. PMID: 39591949
  15. Zaki U, Qazi SH, Shamim U, Fatima S, Das JK, Bhutta ZA. Optimal Strategies for Screening Common Birth Defects in Children of Low- and Middle-Income Countries: A Systematic Review. Neonatology. 2025;122 Suppl 1:224–44. PMID: 39462499
  16. Ali AA, Naseem HA, Allahuddin Z, Yasin R, Azhar M, Hanif S, et al.. The Effectiveness of Regionalization of Perinatal Care and Specific Facility-Based Interventions: A Systematic Review. Neonatology. 2025;122 Suppl 1:245–61. PMID: 39504943
  17. Jiang L, Lee Him R, Sihota D, Muralidharan O, Dominguez G, Harrison L, et al.. Supportive Care for Common Conditions in Small Vulnerable Newborns and Term Infants: The Evidence. Neonatology. 2025;122 Suppl 1:129–51. PMID: 39571565
  18. Lee Him R, Rehman S, Sihota D, Yasin R, Azhar M, Masroor T, et al.. Prevention and Treatment of Neonatal Infections in Facility and Community Settings of Low- and Middle-Income Countries: A Descriptive Review. Neonatology. 2025;122 Suppl 1:173–208. PMID: 39532080
  19. Dominguez G, Muralidharan O, Lee Him R, Harrison L, Vaivada T, Bhutta ZA. The Care of Preterm and Term Newborns with Respiratory Conditions: A Systematic Synthesis of Evidence from Low- and Middle-Income Countries. Neonatology. 2025;122 Suppl 1:152–72. doi: 10.1159/000542482 PMID: 39541964
  20. Yasin R, Jiang L, Das JK, Bhutta ZA. Interventions to Prevent and Manage Infections in Pregnancy. Neonatology. 2025;122 Suppl 1:32–41. doi: 10.1159/000543690 PMID: 39874953
  21. Jiang L, Dominguez G, Cummins A, Muralidharan O, Harrison L, Vaivada T, et al.. Immediate Care for Common Conditions in Term and Preterm Neonates: The Evidence. Neonatology. 2025;122 Suppl 1:106–28. PMID: 39532078
  22. Muralidharan O, Rehman S, Sihota D, Harrison L, Vaivada T, Bhutta ZA. Post-Asphyxial Aftercare and Management of Neonates in Low- and Middle-Income Countries: A Systematic Evidence Synthesis. Neonatology. 2025;122 Suppl 1:84–105. PMID: 39536730
  23. Sihota D, Lee Him R, Dominguez G, Harrison L, Vaivada T, Bhutta ZA. Effectiveness of Neonatal Resuscitation Training Programs, Implementation, and Scale-Up in Low- and Middle-Income Countries. Neonatology. 2025;122 Suppl 1:52–83. PMID: 39581184
  24. Harrison L, Vaivada T, Yasin R, Das JK, Bhutta ZA. Rationale and Approach to Evaluating Interventions for Newborn Care in Low- and Middle-Income Countries. Neonatology. 2025;122 Suppl 1:5–12. doi: 10.1159/000542754 PMID: 39653031
  25. Hamadeh N, Van Rompaey C, Metreau E, Eapen SG. New World Bank country classifications by income level: 2022–2023. World Bank. 1 July 2022. Available: https://blogs.worldbank.org/en/opendata/new-world-bank-country-classifications-income-level-2022-2023. Accessed: 17 December 2025.
  26. Guyatt GH, Oxman AD, Vist GE, Kunz R, Falck-Ytter Y, Alonso-Coello P, et al.. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336:924–6. doi: 10.1136/bmj.39489.470347.AD PMID: 18436948
  27. Demicheli V, Barale A, Rivetti A. Vaccines for women for preventing neonatal tetanus. Cochrane Database Syst Rev. 2015;(7):CD002959. doi: 10.1002/14651858.CD002959.pub4 PMID: 26144877
  28. Smaill FM, Vazquez JC. Antibiotics for asymptomatic bacteriuria in pregnancy. Cochrane Database Syst Rev. 2019;(11):CD000490. PMID: 31765489
  29. Gamble C, Ekwaru PJ, Garner P, Kuile FO. Insecticide-Treated Nets for the Prevention of Malaria in Pregnancy: A Systematic Review of Randomised Controlled Trials. PLoS Med. 2007;4:e107. doi: 10.1371/journal.pmed.0040107 PMID: 17388668
  30. Tong H, Heuer A, Walker N. The impact of antibiotic treatment for syphilis, chlamydia, and gonorrhoea during pregnancy on birth outcomes: A systematic review and meta-analysis. J Glob Health. 2023;13:04058. doi: 10.7189/jogh.13.04058 PMID: 37325885
  31. Oh C, Keats EC, Bhutta ZA. Vitamin and Mineral Supplementation During Pregnancy on Maternal, Birth, Child Health and Development Outcomes in Low- and Middle-Income Countries: A Systematic Review and Meta-Analysis. Nutrients. 2020;12:491. doi: 10.3390/nu12020491 PMID: 32075071
  32. Wang D, Liu E, Perumal N, Partap U, Cliffer IR, Costa JC, et al.. The effects of prenatal multiple micronutrient supplementation and small-quantity lipid-based nutrient supplementation on small vulnerable newborn types in low-income and middle-income countries: a meta-analysis of individual participant data. Lancet Glob Health. 2025;13:e298–308. doi: 10.1016/S2214-109X(24)00449-2 PMID: 39890230
  33. Ota E, Hori H, Mori R, Tobe-Gai R, Farrar D. Antenatal dietary education and supplementation to increase energy and protein intake. Cochrane Database Syst Rev. 2015;2015:CD000032. doi: 10.1002/14651858.CD000032.pub3 PMID: 26031211
  34. Middleton P, Gomersall JC, Gould JF, Shepherd E, Olsen SF, Makrides M. Omega-3 fatty acid addition during pregnancy. Cochrane Database Syst Rev. 2018;11:CD003402. PMID: 30480773
  35. Hofmeyr GJ, Lawrie TA, Atallah ÁN, Torloni MR. Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems. Cochrane Database Syst Rev. 2018;10:CD001059. doi: 10.1002/14651858.CD001059.pub5 PMID: 30277579
  36. Hoffman MK, Goudar SS, Kodkany BS, Metgud M, Somannavar M, Okitawutshu J, et al.. Low-dose aspirin for the prevention of preterm delivery in nulliparous women with a singleton pregnancy (ASPIRIN): a randomised, double-blind, placebo-controlled trial. Lancet. 2020;395:285–93. doi: 10.1016/S0140-6736(19)32973-3 PMID: 31982074
  37. Chamberlain C, O’Mara-Eves A, Porter J, Coleman T, Perlen SM, Thomas J, et al.. Psychosocial interventions for supporting women to stop smoking in pregnancy. Cochrane Database Syst Rev. 2017;2:CD001055. doi: 10.1002/14651858.CD001055.pub5 PMID: 28196405
  38. Cousens S, Blencowe H, Gravett M, Lawn JE. Antibiotics for pre-term pre-labour rupture of membranes: prevention of neonatal deaths due to complications of pre-term birth and infection. Int J Epidemiol. 2010;39:i134–43. doi: 10.1093/ije/dyq030 PMID: 20348116
  39. McGoldrick E, Stewart F, Parker R, Dalziel SR. Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth. Cochrane Database Syst Rev. 2020;12:CD004454. PMID: 33368142
  40. Middleton P, Shepherd E, Morris J, Crowther CA, Gomersall JC. Induction of labour at or beyond 37 weeks’ gestation. Cochrane Database Syst Rev. 2020;7:CD004945. PMID: 32666584
  41. Lima L, Molina MDGF, Pereira BS, Nadaf MLA, Nadaf MIV, Takano OA, et al.. Acquisition of specific antibodies and their influence on cell-mediated immune response in neonatal cord blood after maternal pertussis vaccination during pregnancy. Vaccine. 2019;37:2569–79. doi: 10.1016/j.vaccine.2019.03.070 PMID: 30955978
  42. Halperin BA, Morris A, Mackinnon-Cameron D, Mutch J, Langley JM, McNeil SA, et al.. Kinetics of the antibody response to tetanus-diphtheria-acellular pertussis vaccine in women of childbearing age and postpartum women. Clin Infect Dis. 2011;53:885–92. doi: 10.1093/cid/cir538 PMID: 21946190
  43. WHO. Pertussis vaccines: WHO position paper, August 2015–Recommendations. Vaccine. 2016;34:1423–5. doi: 10.1016/j.vaccine.2015.10.136 PMID: 26562318
  44. Serra R, Peñailillo R, Monteiro LJ, Monckeberg M, Peña M, Moyano L, et al.. Supplementation of Omega 3 during Pregnancy and the Risk of Preterm Birth: A Systematic Review and Meta-Analysis. Nutrients. 2021;13:1704. doi: 10.3390/nu13051704 PMID: 34069867
  45. Sun L, Li Y, Xie W, Xue X. Association between omega-3 fatty acid supplementation and lower risk of preterm delivery: a systematic review and meta-analysis. J Matern Fetal Neonatal Med. 2022;35:2294–303. doi: 10.1080/14767058.2020.1785423 PMID: 32942938
  46. Abdelrahman MA, Osama H, Saeed H, Madney YM, Harb HS, Abdelrahim MEA. Impact of n-3 polyunsaturated fatty acid intake in pregnancy on maternal health and birth outcomes: systematic review and meta-analysis from randomized controlled trails. Arch Gynecol Obstet. 2023;307:249–62. doi: 10.1007/s00404-022-06533-0 PMID: 35348829
  47. Romero R, Conde-Agudelo A, Da Fonseca E, O’Brien JM, Cetingoz E, Creasy GW, et al.. Vaginal progesterone for preventing preterm birth and adverse perinatal outcomes in singleton gestations with a short cervix: a meta-analysis of individual patient data. Am J Obstet Gynecol. 2018;218:161–80. doi: 10.1016/j.ajog.2017.11.576 PMID: 29157866
  48. Conde-Agudelo A, Romero R, Da Fonseca E, O’Brien JM, Cetingoz E, Creasy GW, et al.. Vaginal progesterone is as effective as cervical cerclage to prevent preterm birth in women with a singleton gestation, previous spontaneous preterm birth, and a short cervix: updated indirect comparison meta-analysis. Am J Obstet Gynecol. 2018;219:10–25. doi: 10.1016/j.ajog.2018.03.028 PMID: 29630885
  49. Hunter PJ, Muthiani Y, Näsänen-Gilmore PK, Koivu AM, Pörtfors P, Bastola K, et al.. A modular systematic review of antenatal interventions to address undernutrition during pregnancy in the prevention of low birth weight. Am J Clin Nutr. 2023;117 Suppl 2:S134–47. doi: 10.1016/j.ajcnut.2023.01.024 PMID: 37331760
  50. Chen WY, Sun SF. Clinical efficacy of low-dose aspirin combined with calcium in preventing preeclampsia: A systematic review and meta-analysis. Medicine (Baltimore). 2023;102:e34620. doi: 10.1097/MD.0000000000034620 PMID: 37653760
  51. Gunabalasingam S, De Almeida Lima Slizys D, Quotah O, Magee L, White SL, Rigutto-Farebrother J, et al.. Micronutrient supplementation interventions in preconception and pregnant women at increased risk of developing pre-eclampsia: a systematic review and meta-analysis. Eur J Clin Nutr. 2023;77:710–30. doi: 10.1038/s41430-022-01232-0 PMID: 36352102
  52. Woo Kinshella ML, Sarr C, Sandhu A, Bone JN, Vidler M, Moore SE, et al.. Calcium for pre-eclampsia prevention: A systematic review and network meta-analysis to guide personalised antenatal care. BJOG. 2022;129:1833–43. doi: 10.1111/1471-0528.17222 PMID: 35596262
  53. Sun X, Li H, He X, Li M, Yan P, Xun Y, et al.. The association between calcium supplement and preeclampsia and gestational hypertension: a systematic review and meta-analysis of randomized trials. Hypertens Pregnancy. 2019;38:129–39. doi: 10.1080/10641955.2019.1593445 PMID: 30935246
  54. Ciapponi A, Klein K, Colaci D, Althabe F, Belizán JM, Deegan A, et al.. Dexamethasone versus betamethasone for preterm birth: a systematic review and network meta-analysis. Am J Obstet Gynecol MFM. 2021;3:100312. doi: 10.1016/j.ajogmf.2021.100312 PMID: 33482400
  55. Ninan K, Morfaw F, Murphy KE, Beyene J, McDonald SD. Neonatal and Maternal Outcomes of Lower Versus Standard Doses of Antenatal Corticosteroids for Women at Risk of Preterm Delivery: A Systematic Review of Randomized Controlled Trials. J Obstet Gynaecol Can. 2021;43:74–81. doi: 10.1016/j.jogc.2020.02.127 PMID: 32660867
  56. Chatzakis C, Papatheodorou S, Sarafidis K, Dinas K, Makrydimas G, Sotiriadis A. Effect on perinatal outcome of prophylactic antibiotics in preterm prelabor rupture of membranes: network meta-analysis of randomized controlled trials. Ultrasound Obstet Gynecol. 2020;55:20–31. doi: 10.1002/uog.21884 PMID: 31633844
  57. Alkmark M, Keulen JKJ, Kortekaas JC, Bergh C, van Dillen J, Duijnhoven RG, et al.. Induction of labour at 41 weeks or expectant management until 42 weeks: A systematic review and an individual participant data meta-analysis of randomised trials. PLoS Med. 2020;17:e1003436. doi: 10.1371/journal.pmed.1003436 PMID: 33290410

Correspondence to:
Professor Zulfiqar A. Bhutta
Centre for Global Child Health, The Hospital for Sick Children
686 Bay Street, 11th Floor, Suite 11.9731, M5G 0A4, Toronto, Ontario
Canada
[email protected]