Skip to main content
Advertisement
  • Loading metrics

Enhancing birth weight outcomes through improved antenatal care in West African countries: Evidence from propensity score matching analysis

  • Aklilu Habte Hailegebireal ,

    Roles Conceptualization, Formal analysis, Methodology, Software, Writing – original draft, Writing – review & editing

    akliluhabte57@gmail.com

    Affiliations School of Public Health, College of Medicine and Health Sciences, Wachemo University, Hosanna, Ethiopia, Faculty of Health and Environmental Sciences, School of Clinical Sciences, Auckland University of Technology, Auckland, New Zealand

  • Habtamu Mellie Bizuayehu,

    Roles Methodology, Supervision, Writing – review & editing

    Affiliation First Nations Cancer and Wellbeing (FNCW) Research Program, School of Public Health, The University of Queensland, Brisbane, Queensland, Australia

  • Samuel Hailegebreal Gele,

    Roles Methodology, Software, Writing – review & editing

    Affiliations Department of Health Informatics, College of Medicine and Health Sciences, School of Public Health, Wachemo University, Hosanna, Ethiopia, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia

  • Angwach Abrham Asnake

    Roles Investigation, Methodology, Writing – review & editing

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, College of Health Sciences and Medicine, Wolaita Sodo University, Wolaita Sodo, Ethiopia

Abstract

While many underlying causes of low birth weight (LBW, < 2500 grams) are preventable through overall antenatal care (ANC) uptake, limited empirical evidence exists in West Africa quantifying the impact of the WHO-recommended four or more visits (ANC4+) and eight or more visits (ANC8+) models using rigorous causal inference techniques. Thus, this study aimed to examine the causal effect of those two models on birth weight outcomes in West African countries using propensity score matching (PSM). This study included a weighted sample of 51,455 women sourced from Demographic and Health Surveys (DHS) data from 14 West African countries (2012–2023). Covariates associated with treatments (ANC4+ and ANC8+) and birth weight were identified using Chi-square tests, one-way analysis of variance (ANOVA), and t-tests, and those deemed confounders were included in PSM. PSM was applied using a logit model to estimate the causal effects of ANC4+ and ANC8+ on birthweight. Average Treatment Effect on the Treated (ATT) and Average Treatment Effect (ATE) were calculated for each exposure. Quality of matching was assessed both statistically and graphically. Sensitivity analysis was done using Rosenbaum bounds to estimate unmeasured confounding and confirm the robustness of treatment effects. The mean birthweight was 3121.2 grams (±669.0), with 10.42% of newborns classified as LBW. Receiving ANC8+ and ANC4 + were associated with a birthweight increase of 102.36 and 83.89 grams, respectively. Across the entire population, ANC8+ and ANC4 + were linked to average birthweight increases of 89.09 and 75.81 grams, respectively. Of the weighted sample, 71.38% and 14.54% of women received ANC4+ and ANC8 + , respectively. All matching diagnostics demonstrated strong covariate balance and confirmed the validity of the treatment effect estimates. The treatment and control groups were well comparable for the baseline confounders after matching (p-value > 0.05). This study found that receiving ANC4+ or ANC8 + has a positive effect on birth weight, underscoring the importance of scaling up efforts to ensure comprehensive ANC coverage, especially ANC8 + , in the region to reduce LBW prevalence and improve neonatal survival.

Introduction

The birth weight of a newborn is the initial weight documented immediately after birth, preferably assessed within the first hours post-delivery [1]. The World Health Organization (WHO) defines low birth weight (LBW) as a birth weight of less than 2,500 grams [1,2].

Recent estimates showed that 19.8 million liveborn newborns (14.7% of all live births) globally were LBW [3]. The majority (91%) of these LBW births took place in low- and middle-income countries (LMICs), with almost half (48%) and a quarter (24%) of them occurring in southern Asia and sub-Saharan Africa, respectively [4].

LBW is associated with increased morbidity, mortality, and disability during childhood, and those who survived faced long-term consequences such as physical and neurological developmental delays, disabilities, and chronic health conditions, including type 2 diabetes, hypertension, and cardiovascular disease [513]. LBW babies were more likely to die during their first month of life [5,813].

Several maternal, fetal, and environmental factors contribute to LBW. Of fetal factors, preterm birth and intrauterine growth restriction are common causes of LBW. Maternal and environmental factors include maternal undernutrition [14,15], infections during pregnancy (e.g., malaria, polyparasitism, COVID-19) [1618], maternal anaemia [19,20], hypertensive disorders [2123], placental insufficiency [24,25], and multiple gestation [26,27]. Behavioral factors such as maternal smoking [2830] and alcohol or substance use [3133] further exacerbate the risk of LBW.

Many of those underlying causes and risk factors for LBW are largely preventable or manageable through the receipt of timely and adequate antenatal care (ANC) [3437]. ANC paves the way for receiving key services for a healthy pregnancy, which can help to prevent, identify, and treat the conditions that cause LBW and thus foster achievement of the World Health Assembly (WHA) nutrition target to reduce LBW by 30% between 2012 and 2030 [38,39]. It also plays a pivotal role in addressing underlying determinants of LBW, such as maternal malnutrition, undiagnosed health conditions, and limited health education [40]. The WHO originally endorsed the four-visit ANC model (ANC4+) as the recommended approach for antenatal care. In 2016, however, this was revised, with the new guidelines stipulating at least eight ANC (ANC8+) contacts as the minimum requirement [41,42].

Overall, equity in ANC coverage is vital for global public health because unequal access disproportionately affects vulnerable populations, contributing to higher rates of LBW, a key predictor of neonatal mortality and long-term health risks [38]. Thus, ensuring equitable ANC access and quality remains a strategic pathway for countries, especially in high-burden regions like West Africa, to achieve meaningful improvements in birth outcomes and meet international nutrition targets [38,39].

LBW continues to be a critical public health issue in West Africa, where uneven access to maternal healthcare leads to a heightened burden of LBW [43,44], contributing to persistent inequities in neonatal survival and long-term health outcomes. However, there is a dearth of empirical evidence linking ANC adequacy to birthweight. Especially, the evidence delineating the relative effects of ANC4+ versus ANC8 + remains limited, leaving a gap in understanding how the shift toward WHO’s new standard translates into measurable health benefits, such as reducing LBW. While some studies have reported associations between ANC quality and birth weight [40,4547], little is known with robust methods like propensity score matching (PSM) to estimate the actual causal effect.

This study addresses that evidence gap by exploring the impact of ANC adequacy on birth weight in West Africa, where access to quality ANC is often uneven [48]. The findings directly support global efforts to reduce preventable neonatal morbidity and mortality, align with Sustainable Development Goals (SDGs), and advance equity by informing policies that prioritize underserved communities in low-resource contexts. The analysis uses PSM to address confounding and selection bias inherent in observational data, allowing a robust comparison of the effect of the two ANC models (ANC4+ and ANC8+). Insights from this research carry important implications for tailoring ANC policies, enhancing service delivery strategies, and guiding resource allocation toward the most effective coverage benchmarks. Ultimately, findings could contribute to progress towards the Global Nutrition Target, which aims to reduce LBW by 30% by 2025, a goal now extended to 2030 due to slow progress.

Methods

Study design, period, and population

This study utilizes appended Demographic and Health Surveys (DHS) data from 14 West African countries, collected between 2012 and 2023. The analysis draws on the Individual Record (IR) files, which include women who had given birth within the five years preceding each survey. Women without documented data on ANC and/or birth weight were excluded from the study. We considered countries that had conducted DHS reports from 2010 onward, and we got countries with surveys conducted between 2012 and 2023. The final selection yielded a weighted sample of 51,455 eligible women, providing a robust foundation for the analysis (Table 1).

thumbnail
Table 1. List of countries included in the analysis with their respective weighted sample size, 2013–2023.

https://doi.org/10.1371/journal.pgph.0005367.t001

Sampling techniques and procedures.

The DHS employs a two-stage stratified sampling design: first selecting enumeration areas (EAs) with probability proportional to size (PPS), followed by systematic random sampling of households within selected EAs. Eligible women from each home were interviewed using a structured and standardized questionnaire. The details are mentioned in the Demographic and Health Survey Sampling and Household Listing Manual issued by ICF International [49,50].

Measurement of variables of the study

  1. Outcome variable:

The outcome variable is birthweight, which is the initial weight recorded immediately after birth, preferably within the first hours post-delivery, prior to any substantial postnatal weight reduction [1]. It is a continuous variable and recorded in grams as variable m19-1, indicating either recorded measurements from health cards or maternal recall. The analysis includes only children born within the five years preceding the survey who had valid birthweight data, excluding entries with standard placeholders used in the dataset to indicate specific types of missing or implausible responses (coded as 9996, 9997, or 9998). Using birthweight in continuous form allows for a more precise estimate of the effect of treatment (ANC4+ and ANC8+), enhances statistical power, and avoids information loss from categorizing the variable [51,52].

The exposure (treatment) variable‌‌.

Antenatal care (ANC) recorded as m14-1 is the main treatment variable, which is operationalised based on the number of visits a woman received during her last pregnancy. This discrete numeric variable captures the total ANC contacts, with values above 20 considered implausible and excluded. For analysis purposes, we grouped the treatment variable into two key groups: four or more visits (ANC4+) and eight or more visits (ANC8+), aligning with the previous [53,54] and current [41,42] WHO recommendations, respectively. Women with eight or more ANC visits were coded as Yes = 1; those with fewer were coded as No = 0. Similarly, women with four or more ANC visits were coded as Yes = 1; those with fewer were coded as No = 0. Two distinct models were fitted: Model 1 examined the causal effect of ANC8+ on birth weight, while Model 2 assessed the causal effect of ANC4+ on birth weight. The control groups for model 1 and model 2 were women without ANC8+ and ANC4 + , respectively.

Explanatory variables.

Given the observational nature of the DHS, random assignment of exposure was not applied, leading to inherent differences between treatment and control groups. To address potential selection bias in estimating the effects of ANC4+ and ANC8+ on birthweight, we identified maternal baseline characteristics that influence both the exposures and the outcome (birth weight) based on prior literature [27,41] (Table 2).

thumbnail
Table 2. Potential predictors of adequate ANC and birth weight.

https://doi.org/10.1371/journal.pgph.0005367.t002

Confounding variables.

Those variables significantly associated with both the exposures (ANC8+ and ANC4+) and birthweight were treated as confounders and were incorporated into the Propensity Score Matching (PSM). Those variables are maternal age, level of education, head of household, husband occupation, women’s occupation, place of residence, wealth index, family size, parity, contraceptive uptake, perceived distance to a health facility, ease of getting money for health care, permission to go to the health facility, listening to the radio, watching Television, reading newspaper, timing of first ANC visit, and visiting a health facility within the last 12 months. The hypothesized causal relationships among confounders, exposures (ANC4+ and ANC8+), and birthweight outcomes were illustrated using a Directed Acyclic Graph (DAG), developed in DAGitty version 3 (Fig 1).

thumbnail
Fig 1. A directed acyclic graph to show the relationship between treatment, outcome, and confounders.

https://doi.org/10.1371/journal.pgph.0005367.g001

Statistical analysis

Data management and statistical analyses were conducted using STATA version 18. All analyses were weighted using the DHS-provided sampling weight to ensure representativeness of the sample. We run chi-square tests to assess the association between the exposure variables (ANC8+ and ANC4+) and categorical covariates. In addition, one-way analysis of variance (ANOVA) and independent t-tests were used to assess the association between covariates and birth weight, to identify possible confounders for Propensity Score Matching (PSM). Accordingly, the observed covariates were classified into three categories based on their relationship with the exposure and outcome variables: those associated solely with the exposure assignment, those linked to both the exposure and the outcome—considered confounders—and those associated exclusively with the outcome (birth weight). Only covariates identified as confounders were incorporated into the propensity score model in this study.

Propensity score matching.

This study used data from DHS, an observational dataset in which treatment and control groups were not assigned randomly, resulting in baseline disparities and potential mismatches in confounding variables [55,56]. Such imbalances could bias the estimation of the causal effects of adequate antenatal care (ANC 8+ and ANC4+) on birth weight. Thus, a PSM was done to create a balanced comparison between treated and untreated groups, reducing confounding and improving the validity of the causal effect [57,58]. The matching was undertaken for each treatment using a logit model, and propensity scores (the conditional probability of receiving treatments-ANC4+ and ANC8+) were estimated using the pscore command. The propensity score is the likelihood of receiving treatments given all confounders, and that ranges from 0 to 1 [56,57].

After creating the matched samples, the effects of ANC4+ and ANC8 + were assessed independently by comparing the difference in birth weight (in grams) between the treated and control groups. Using logistic regression via the psmatch2 command, the study matched newborn birth weight to maternal exposure to ANC4+ and ANC8 + , enabling estimation of treatment effects within balanced comparison groups. The use of the logit model is due to the exposures being dichotomous (Yes = 1 or No = 0). In addition, covariate balance before and after matching was assessed using the pstest command, with p-values below 0.05 interpreted as evidence of imbalance. Conversely, a covariate with a p-value greater than 0.05 after matching is interpreted as evidence of adequate balance between the treatment and control groups [5961].

We seek to estimate the average effect of receiving treatments on birth weight independently. Let YiT denote the birth weight for the ith newborn whose mother received the treatments (either ANC4+ or ANC8+), and YiC represents the hypothetical birth weight for the same newborn had the mother not received the respective treatments. The treatment assignment indicator T equals 1 if the mother received ANC8 + , and 0 otherwise. The observed outcome can thus be described as: Yi = Ti Yi1 + (1 – Ti) Yi0 [62,63] Where

Yi: observed birth weight for individual i, Ti: treatment indicator (1 if exposed to treatment (ANC4+ or ANC8 + , 0 otherwise), Yi1: potential outcome if treated (exposed), and Yi0: potential outcome if not treated (unexposed)

The individual treatment effect is Y Yi1-Yi0, but since we can never observe both outcomes for the same individual, our interest shifts to the average effect of treatment on the treated (ATT):

ATT = E[Yi1- Yi0/Ti = 1] [62,63], where

Yi1: birth weight if the mother received ANC8+ (the treatment), Yi0: birth weight if the same mother had not received treatments (ANC8+ or ANC4+) (the counterfactual), and Ti: treatment indicator (1 if the mother received treatments, 0 if not)

Covariates were selected before treatments to minimize post-treatment bias. Key PSM assumptions, including common support and unconfoundedness (selection on observables), were evaluated both graphically and statistically. Matching was restricted to treated mothers whose propensity scores for birth weight fell within the range of controls. Nearest neighbor (with and without replacement) and radius matching (caliper = 0.01) were assessed using pstest for balance diagnostics (to ensure a high degree of similarity between matched units while retaining sufficient sample size). Treatment effects (ATT, ATU, ATE) were estimated via psmatch2, with the final model selected based on matching quality.

The quality of matching was evaluated using multiple diagnostics to ensure robustness of the propensity score model. These included assessments of standardized bias to examine covariate balance, model significance tests, and evaluation of the common support assumption. Additionally, a post-matching covariate balance plot was employed to visually inspect improvements in balance across groups (The details are mentioned in the results section).

To assess the robustness of the estimated treatment effect to potential unobserved confounding, a sensitivity analysis was conducted using Rosenbaum bounds (rosbounds) [64,65] for continuous outcomes, quantifying how strongly an unmeasured variable would need to influence treatment assignment to nullify the observed effect [57,66,67]. The sensitivity parameter Gamma (Γ) was used to represent the degree of departure from random assignment; values of Γ greater than 1 indicate increasing levels of potential hidden bias. The threshold at which the treatment effect becomes statistically insignificant provides insight into the strength of evidence for causality under unmeasured confounding [57,65].

Ethical approval and consent to participate.

This study is based on secondary analysis of publicly available data from the MEASURE DHS program. At the time of access, the dataset was available and unrestricted under the data use policies in effect prior to recent changes introduced by the current U.S. government. Ethical approval and informed consent were not required, as the dataset is fully anonymized and contains no identifiable personal or household information. Formal permission to download and use the data was granted through the DHS Program website, http://www.dhsprogram.com.

Results

Baseline characteristics of the study population

This analysis is based on a weighted sample of 51,455 women across 14 West African countries, with the largest proportions coming from Benin (11.28%), Nigeria (11.08%), and Burkina Faso (10.34%). The mean age of respondents was 29.26 years (±7.07), and nearly half were in the age group 25–34 years. The majority (44.7%) of women had no formal education, yet the vast majority were in a marital relationship (89.88%). Notably, over a quarter belonged to the richest wealth quintile. More than half (53.33%) of women were multiparous (Table 3).

thumbnail
Table 3. The distribution of sociodemographic characteristics of respondents across adequacy of ANC (ANC4+ and ANC8+) and birth weight in West African countries, 2012-2023.

https://doi.org/10.1371/journal.pgph.0005367.t003

The uptake of adequate ANC and mean birthweight showed significant variation across socioeconomic characteristics. Younger women (15–24) were less likely to reach ≥8 visits compared to those aged 35–49. ANC utilization increased with educational attainment; only 7.2% of women with no education had ≥ 8 visits, compared to 40.8% among those with higher education (p < 0.001). Urban residence, higher wealth, smaller family size, and female-headed households were all associated with better ANC coverage. Birthweight increased progressively with maternal age, education, urban residence, and parity (p < 0.001). The highest average birth weights were observed in Guinea and Mali, while Mauritania had the lowest (Table 3).

Adequate ANC uptake and birth weight across health service-related characteristics

Almost half (49.32%) of women initiated ANC early (within the first trimester). More than three-quarters (78.67%) of pregnancies were wanted at the time, though 17.2% were mistimed and 4.13% were unwanted. Over half of the women (51.76%) reported financial barriers as a major challenge to accessing maternity care, while about one-third faced issues related to distance (31.19%) (Table 4). The uptake of adequate ANC and neonatal birthweight showed significant variation across obstetric characteristics. Receipt of ANC4 + varied by parity, with primiparous women exhibiting the highest uptake at 73.64%, closely followed by multiparous women (72.49%). Notably, women who initiated their first ANC contact during the first trimester demonstrated markedly higher uptake, with ANC4+(84.27%) and ANC8+(20.69%). Multiparous and grand multiparous women exhibited greater mean birthweights of 3157.8 and 3163.1 grams, respectively, compared with nulliparous women (2901.7 grams) (Table 4).

thumbnail
Table 4. The distribution of health service-related characteristics of respondents across ANC4 + , ANC8 + , and birth weight in West African countries.

https://doi.org/10.1371/journal.pgph.0005367.t004

Adequate ANC uptake and birthweight in the region

The weighted prevalence of women who received at least four antenatal care visits (ANC4+) was 71.38% (95% CI: 70.9–71.7), whereas only 14.54% (95% CI: 14.15–14.92) received eight or more visits (ANC8+). The mean(±SD) birthweight was 3121.2 grams (±669.0), with 10.42% (95% CI: 10.10, 10.74) of newborns classified as LBW (<2500 g). Coverage of ANC4 + was highest in Ghana (92.36%), Liberia (91.68%), and Nigeria (85.94%). Similarly, Nigeria (44.52%), Ghana (42.52%), and Liberia (29.89%) reported the greatest proportions of women receiving ANC8+ (Fig 2).

thumbnail
Fig 2. Low birth weight and the uptake of adequate ANC (ANC4+ and ANC8+) in West African countries.

https://doi.org/10.1371/journal.pgph.0005367.g002

Estimation of propensity scores of treatment.

The variables that have a significant association with both treatments (ANC8+ and ANC4+) and outcome (birthweight) were considered for matching using the logit model (Table 5).

thumbnail
Table 5. Results of logit regression analysis of factors associated with treatments (ANC4+ and ANC8+) in West African countries.

https://doi.org/10.1371/journal.pgph.0005367.t005

Propensity score of receiving treatments.

For the treatment ANC4 + , the overall propensity score was 0.71, indicating a moderate level of variability in the likelihood of receiving treatment across the sample. Which means women in the sample had a 71% predicted probability of receiving treatment, given their covariates. This is supported by the histogram (Fig 3). Whereas the average estimated propensity score for receiving ANC8 + was 0.14, indicating that, based on observed covariates, the overall likelihood of receiving ANC8+ in the study population was 14%. The low average propensity score likely reflects the low proportion of women in the general population receiving ANC8+ (14.53%). The histogram below illustrates the distribution of propensity scores by treatment status, highlighting baseline differences in treatment probability between groups (Fig 4).

thumbnail
Fig 3. Histogram showing the distribution of estimated propensity scores by treatment status (ANC4 + vs. fewer visits).

https://doi.org/10.1371/journal.pgph.0005367.g003

thumbnail
Fig 4. Histogram showing the distribution of estimated propensity scores by treatment status (ANC8 + vs. fewer visits).

https://doi.org/10.1371/journal.pgph.0005367.g004

The causal effect of adequate ANC (ANC4+ and ANC8+) on birth weight.

The causal effects of two ANC interventions, ANC4+ and ANC8 + , on birth weight were assessed by estimating the mean difference in birth weight between the treated groups, those who received ANC4+ or ANC8 + , and their matched counterparts who received inadequate care (fewer than four or eight visits, respectively). The PSM analysis estimates the effect of the ANC4+ and ANC8+ on birth weight by adjusting for potential confounders (Table 6).

thumbnail
Table 6. A propensity score-matched analysis of the impact of Treatments (ANC4+ and ANC8+) on birth weight in West African countries, 20102-2023.

https://doi.org/10.1371/journal.pgph.0005367.t006

PSM was performed to estimate the Average Treatment Effect on the Treated (ATT) by comparing women who received the treatment (ANC4+ and ANC8+) with a matched group of similar women without treatment, based on observed covariates. It also estimates the Average Treatment Effect (ATE), reflecting the treatments’ impact across the entire women, including both treated and untreated groups. A radius matching approach with a 0.01 caliper width was employed to optimize match quality and estimate the average treatment effect (ATE) across the overall population, both exposed and unexposed groups.

Accordingly, the unmatched estimates indicated that receiving eight or more ANC visits (ANC8+) was associated with increases in birth weight of 130.92 grams. The ATE estimates of 89.09 showed that having ANC8 + was associated with increases in birth weight of 89.09 grams across the entire population. The ATT for ANC8 + was 102.36, which implies that after adjusting for confounders using PSM, women having ANC8 + had newborns with significantly higher birth weights by 102.36 grams compared to their matched counterparts (women who received fewer than eight visits). The Average Treatment Effect on the Untreated (ATU) was calculated to be 67.68 grams, implying that if women who did not receive ANC8 + had gotten the intervention, their newborns’ birth weights would have increased by about 67.68 grams.

Likely, the unmatched estimates indicated that receiving four or more antenatal care visits (ANC4+) was linked with increases in birth weight of 89.69 grams. The ATT was 83.89, which implies that after adjusting for confounders using PSM, women who received ANC4 + had newborns with significantly higher birth weights by 83.89 grams compared to their matched counterparts who received fewer than four visits. The ATE estimates showed that receiving ANC4 + was 75.81grams across the entire population. The Average Treatment Effect on the Untreated (ATU) was 56.20, meaning that if women lacking ANC4 + had received the intervention, the birth weight would have increased by an estimated 56.2 grams (Table 6).

Quality of matching.

Standard bias and model significance: The ability of the matching procedure to balance the distribution of relevant covariates between the treatment and control groups was evaluated. The pseudo-R² statistic was used to assess how well the covariates explained the likelihood of treatment assignment. For the first treatment (ANC8+), the pseudo-R² declined markedly from 0.134 in the unmatched sample to 0.001 post-matching, indicating a significant reduction in covariate imbalance between treatment and control groups. Additionally, the mean standardized bias decreased from 25.6% to 1.7%, while the median bias reduced from 19.1% to 01.4%, collectively demonstrating substantial improvement in covariate balance and suggesting that the matching procedure was successful. For the other treatment (ANC4+), the pseudo-R² value decreased markedly from 0.11 before matching to 0.001 post-matching, while the maximum absolute standardized bias (B) dropped from 84.8% to 7.3%, indicating a significant improvement in covariate balance (Table 7).

thumbnail
Table 7. Performance of the propensity score matching for the effect of ANC8+ and ANC4+ on birthweight.

https://doi.org/10.1371/journal.pgph.0005367.t007

* Ratio of Treated vs Untreated group.

Balancing test: The pstest command in Stata was employed to assess covariate balance between treated and control groups before and after matching. Before matching, most covariates exhibited substantial bias. Differences between the unmatched and matched samples were assessed using t-tests. The t-tests indicated there was a significant mean difference for each covariate before matching (p < 0.05), but after matching, the percentage bias for all covariates was reduced, and the results indicated no significant mean differences across nearly all factors (p > 0.05). In both cases, the matching process decreased the bias by more than 95% for each covariate. This demonstrates that the variables were adequately balanced (Tables 8 and 9).

thumbnail
Table 8. Quality of matching for the effect of ANC4+ on birthweight in the West African region, 2012-2023.

https://doi.org/10.1371/journal.pgph.0005367.t008

thumbnail
Table 9. Quality of matching for the effect of ANC8+ on birthweight in the West African region, 2012-2023.

https://doi.org/10.1371/journal.pgph.0005367.t009

Common support assumption: The common support assumption was assessed graphically and which revealed substantial overlap in the distribution of propensity scores between treated and control groups, substantiating the validity of the common support assumption. Visual inspection of the graph for ANC4 + revealed the propensity score of both treated and control groups concentrated between 0.4 and 0.8. This pattern suggests that a majority of individuals had a good predicted probability of receiving ANC4 + , and also, substantial overlap was evident, supporting the presence of common support within the matched sample (Fig 5). Visual inspection of the graph for ANC8 + revealed a markedly skewed distribution of estimated propensity scores, with both treated and control groups concentrated at the lower end of the scale (0–0.3) and tapering off toward higher values. This pattern suggests that a majority of individuals had a low predicted probability of receiving ANC8 + , yet substantial overlap was still evident, supporting the presence of common support within the matched sample (Fig 6).

thumbnail
Fig 5. Histogram of propensity score distribution across treatment (ANC4+) and control groups.

https://doi.org/10.1371/journal.pgph.0005367.g005

thumbnail
Fig 6. Histogram of propensity score distribution across treatment (ANC8+) and control groups.

https://doi.org/10.1371/journal.pgph.0005367.g006

Post-matching covariate balance plot: To evaluate the effectiveness of the PSM procedure for women who received eight or more antenatal care (ANC8+) visits, covariate balance was assessed using standardized percentage bias plots. This visual diagnostic compared pre- and post-matching standardized biases across key covariates. The resulting graph demonstrated a marked reduction in bias, with all post-matching values tightly clustered around zero and falling well within the conventional ±10% threshold. These findings confirm that the matching algorithm successfully eliminated systematic differences between treatment and control groups across observed covariates, thereby enhancing the validity of subsequent treatment effect estimates for ANC8+ on birthweight outcomes (Fig 7).

thumbnail
Fig 7. Standardized percentage bias in the distribution of confounders before and after matching for ANC8+.

https://doi.org/10.1371/journal.pgph.0005367.g007

Similarly, a covariate balance was assessed for ANC4 + , and the resulting balance plot demonstrated a marked reduction in standardized mean differences for all included covariates, with post-matching values falling well within the ± 10% threshold(-6–2). This indicates that the matching procedure successfully mitigated baseline differences, supporting the validity of subsequent treatment effect estimates on birthweight (Fig 8).

thumbnail
Fig 8. Standardized percentage bias in the distribution of confounders before and after matching for ANC4+.

https://doi.org/10.1371/journal.pgph.0005367.g008

Sensitivity analysis: In the presence of unobserved variables exerting simultaneous influence on both the assignment into exposure and the outcome variable, the emergence of ‘hidden bias’ becomes a concern. To handle this, the Rosenbaum bounding method was employed (as the outcome is a continuous variable) to ascertain the extent to which unmeasured variables, or hidden bias, impact the selection process and, consequently, the implications of the matching analysis. Strong evidence that ANC8+ and ANC4 + increase neonatal birthweight would be found in all of the analyses, in a study free of bias, that is, where Ґ = 1. The upper bound on the significance level for Ґ = 1.05, 1.1, 1.15……2. The final output demonstrated consistent robustness of the estimated treatment effects across both treatment groups (ANC8+ and ANC4+). For each specification, the upper and lower bounds remained statistically significant across a range of Γ values, suggesting that the observed associations are unlikely to be explained by unmeasured confounding, which enhances the credibility of the findings (Tables 10 and 11).

thumbnail
Table 10. Sensitivity analysis using Rosenbaum bounds for birthweight for ANC8+.

https://doi.org/10.1371/journal.pgph.0005367.t010

thumbnail
Table 11. Sensitivity analysis using Rosenbaum bounds for the effect of ANC8+ on birthweight.

https://doi.org/10.1371/journal.pgph.0005367.t011

Discussion

This study investigates the causal relationship between adequate antenatal care—defined by ANC4+ and ANC8 + contacts—and birthweight outcomes in West African countries, using PSM. Propensity score matching is widely recognized as a robust method for causal inference in observational studies, as it facilitates the construction of a comparable control group in the absence of randomization, thereby reducing selection bias [63,68].

The study revealed that 71.38% and 14.54% of women received ANC4+ and ANC8 + , respectively, and the weighted prevalence of LBW was 10.42%. Receiving ANC8 + was associated with an average increase of 102.37 grams (ATT = 102.37), while ANC4 + contacts led to an 83.90 grams (ATT = 83.9) gain compared to their respective control groups. These findings were comparable to the previous studies [35,69,70]. For example, a study conducted between 2019 and 2020 among 8,362 Gambian DHS newborns revealed that each additional ANC visit was linked to a 22-gram increase in birthweight, highlighting the incremental value of sustained maternal care throughout pregnancy [69]. The current finding was also in line with a recent systematic review and meta-analysis in Africa [35]. The birthweight increment associated with ANC4+ or ANC8 + could likely stem from enhanced maternal monitoring, early identification and management of pregnancy-related complications, and increased access to vital interventions, including nutritional counseling and supplementation, which facilitate fetal growth and weight gain during pregnancy [71,72]. In addition, as the number of ANC visits increases, so does the opportunity to detect and manage underlying conditions that contribute to maternal anaemia, such as nutritional deficiencies (by iron, folate), helminthic infections (by deworming), and endemic diseases like malaria, thereby improving birthweight outcomes [73].

Overall, the findings underscore the added value of expanding antenatal care coverage, particularly through the WHO-recommended ANC8 + model, which contributes to improved birthweight outcomes in the region. However, the observed lower rate of both ANC4+ (71.38%) and ANC8+ (14.54%) in the current study highlights a significant gap in optimal coverage. Given the demonstrated measurable benefits of ANC uptake at the population level, enhancing service uptake not only supports better birth outcomes but also reinforces equity-driven approaches by targeting vulnerable groups who are disproportionately affected by LBW. Therefore, integrating ANC expansion into existing health system reforms could serve as a pivotal strategy to reduce LBW and advance neonatal health equity across the region. These findings align with global health priorities, including the Sustainable Development Goal (SDG) 3.2, which aims to end preventable deaths of newborns and children under five by 2030 [7476]. Low birthweight is a major contributor to neonatal mortality, and its reduction via optimal prenatal care is critical to achieving this target.

The prevalence of LBW in this study was 10.42%, which is notably lower than the recent global estimate of 14.7% [3]. It aligns closely with findings from sub-Saharan Africa (10.44%) [77], though it exceeds another regional estimate of 9.76% [27]. In contrast, the LBW rate observed here is substantially lower than the average reported across Asian countries (16.64%) [76], and significantly lower than country-specific figures such as Pakistan (18%), Afghanistan (14%), Bangladesh (14%), and Nepal (11.3%) [78]. These observed disparities in the proportion of LBW might be attributed to variations in sample size, timing of data collection, and measurement methods, especially between self-reported birthweight and clinical records. From a policy perspective, these findings underscore the importance of strengthening maternal and neonatal health surveillance systems to ensure accurate data capture and comparability across regions. Moreover, the relatively lower LBW prevalence observed here may signal progress in maternal health service delivery, yet it also calls for targeted interventions to sustain and improve outcomes among vulnerable populations. Integrating LBW reduction strategies into regional health frameworks, especially those focused on equity and universal health coverage [79,80], can help address persistent gaps and ensure that improvements reach the most at-risk groups.

Policy implications

The study’s finding of a 10.42% LBW prevalence, notably below the global average of 14.7% indicates meaningful progress but also underscores the continued need to enhance maternal health services across West African countries. This progress may reflect growing alignment with the Global Nutrition Targets 2025, which aim to reduce LBW prevalence by 30% [39], and supports the broader objectives of Sustainable Development Goal (SDG) Target 3.2, which seeks to end preventable newborn deaths and lower neonatal mortality to at least 12 per 1,000 live births by 2030 [81].

The observed birthweight improvements associated with adequate ANC visits reaffirm the critical role of quality and timely maternal care in achieving optimal birth outcomes. Expanding access to comprehensive ANC, especially in line with the WHO-recommended ANC8 + contact model, presents a high-impact opportunity to further reduce LBW and ultimately advance maternal and neonatal health equity. Policymakers should prioritize interventions that strengthen ANC delivery systems, ensure early and comprehensive maternal monitoring, and address barriers to care among underserved populations to accelerate progress toward these global targets.

Strengths and limitations

This study presents several methodological and contextual strengths. By employing PSM, the analysis reduces selection bias inherent to observational data and allows for stronger causal inferences regarding the impact of adequate antenatal care (ANC4+ and ANC8+) on birth weight outcomes. The operational definition of ANC adequacy aligns with WHO guidelines, and the stratified examination of ANC4+ versus ANC8 + enhances interpretability and policy relevance. Additionally, the use of robust treatment effect estimates (ATT and ATE) enables a nuanced understanding of ANC’s effects across treated and total populations within diverse West African contexts. Overall, the study lies in the rigorous application of PSM complemented by thorough diagnostic analyses, which verified the robustness and quality of the matching process.

However, the study was not without limitations. Residual confounding from unobserved variables—such as nutritional status and environmental exposures—as the matching (PSM) was done for observable variables. Lastly, due to the cross-sectional nature of DHS data, the findings may be prone to social desirability and recall bias.

Conclusion

This study found that adequate ANC (ANC4 or ANC8+) contacts have a positive effect on birthweight outcomes in West African countries, which underscores the importance of scaling up efforts to ensure comprehensive ANC coverage, especially ANC8 + . These findings highlight the potential adherence to comprehensive ANC strategies to reduce LBW prevalence and improve neonatal outcomes. Thus, stakeholders in the health sector should work on strengthening ANC through integrated nutrition support, infection screening, and psychosocial intervention to reduce the risk of LBW.

References

  1. 1. Cutland CL, Lackritz EM, Mallett-Moore T, Bardají A, Chandrasekaran R, Lahariya C, et al. Low birth weight: Case definition & guidelines for data collection, analysis, and presentation of maternal immunization safety data. Vaccine. 2017;35(48 Pt A):6492–500. pmid:29150054
  2. 2. Organization WH. International statistical classification of diseases and related health problems: alphabetical index. World Health Organization; 2004.
  3. 3. Okwaraji YB, Krasevec J, Bradley E, Conkle J, Stevens GA, Gatica-Domínguez G, et al. National, regional, and global estimates of low birthweight in 2020, with trends from 2000: a systematic analysis. Lancet. 2024;403(10431):1071–80. pmid:38430921
  4. 4. Blencowe H, Krasevec J, de Onis M, Black RE, An X, Stevens GA, et al. National, regional, and worldwide estimates of low birthweight in 2015, with trends from 2000: a systematic analysis. Lancet Glob Health. 2019;7(7):e849–60. pmid:31103470
  5. 5. WHO, Low birth weight, 2024. https://www.who.int/data/nutrition/nlis/info/low-birth-weight
  6. 6. Negrato CA, Gomes MB. Low birth weight: causes and consequences. Diabetol Metab Syndr. 2013;5:49. pmid:24128325
  7. 7. Yaya S, Bishwajit G, Ekholuenetale M, Shah V. Inadequate Utilization of Prenatal Care Services, Socioeconomic Status, and Educational Attainment Are Associated with Low Birth Weight in Zimbabwe. Front Public Health. 2017;5:35. pmid:28321391
  8. 8. Linsell L, Malouf R, Morris J, Kurinczuk JJ, Marlow N. Prognostic Factors for Poor Cognitive Development in Children Born Very Preterm or With Very Low Birth Weight: A Systematic Review. JAMA Pediatr. 2015;169(12):1162–72. pmid:26457641
  9. 9. Applegate A, et al. Health conditions and impairments associated with low birth weight and their functional implications. Low birth weight babies and disability. National Academies Press (US); 2024.
  10. 10. Bianchi ME, Restrepo JM. Low Birthweight as a Risk Factor for Non-communicable Diseases in Adults. Front Med (Lausanne). 2022;8:793990. pmid:35071274
  11. 11. Zanetti D, Tikkanen E, Gustafsson S, Priest JR, Burgess S, Ingelsson E. Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease: Addressing the Barker Hypothesis With Mendelian Randomization. Circ Genom Precis Med. 2018;11(6):e002054. pmid:29875125
  12. 12. Eves R, Mendonça M, Baumann N, Ni Y, Darlow BA, Horwood J, et al. Association of Very Preterm Birth or Very Low Birth Weight With Intelligence in Adulthood: An Individual Participant Data Meta-analysis. JAMA Pediatr. 2021;175(8):e211058. pmid:34047752
  13. 13. Aboagye RG, Ahinkorah BO, Seidu A-A, Frimpong JB, Archer AG, Adu C, et al. Birth weight and nutritional status of children under five in sub-Saharan Africa. PLoS One. 2022;17(6):e0269279. pmid:35679306
  14. 14. Bilal JA, Rayis DA, AlEed A, Al-Nafeesah A, Adam I. Maternal Undernutrition and Low Birth Weight in a Tertiary Hospital in Sudan: A Cross-Sectional Study. Front Pediatr. 2022;10:927518. pmid:35799688
  15. 15. Young MF, Ramakrishnan U. Maternal Undernutrition before and during Pregnancy and Offspring Health and Development. Ann Nutr Metab. 2021:1–13. pmid:33524980
  16. 16. Muthiani Y, Hunter PJ, Näsänen-Gilmore PK, Koivu AM, Isojärvi J, Luoma J, et al. Antenatal interventions to reduce risk of low birth weight related to maternal infections during pregnancy. Am J Clin Nutr. 2023;117 Suppl 2:S118–33. pmid:37331759
  17. 17. Honkpéhèdji YJ, Adegbite BR, Zinsou JF, Dejon-Agobé JC, Edoa J-R, Zoleko Manego R, et al. Association of low birth weight and polyparasitic infection during pregnancy in Lambaréné, Gabon. Trop Med Int Health. 2021;26(8):973–81. pmid:33860600
  18. 18. Dileep A, ZainAlAbdin S, AbuRuz S. Investigating the association between severity of COVID-19 infection during pregnancy and neonatal outcomes. Sci Rep. 2022;12(1):3024. pmid:35194128
  19. 19. Khezri R, Rezaei F, Jahanfar S, Ebrahimi K. Association between maternal anemia during pregnancy with low birth weight their infants. Sci Rep. 2025;15(1):6446. pmid:39987181
  20. 20. Belete NK, Belete AG, Assefa DT, Sorrie MB, Teshale MY. Effects of maternal anemia on low-birth-weight in Sub-Sahara African countries: Systematic review and meta-analysis. PLoS One. 2025;20(6):e0325450. pmid:40560935
  21. 21. Liu W, Liu Q, Liu W, Qiu C. Maternal risk factors and pregnancy complications associated with low birth weight neonates in preterm birth. J Obstet Gynaecol Res. 2021;47(9):3196–202. pmid:34137133
  22. 22. Liu Y, Li N, An H, Li Z, Zhang L, Li H, et al. Impact of gestational hypertension and preeclampsia on low birthweight and small-for-gestational-age infants in China: A large prospective cohort study. J Clin Hypertens (Greenwich). 2021;23(4):835–42. pmid:33507600
  23. 23. Harper A, Rothberg A, Chirwa E, Sambu W, Mall S. Household Food Insecurity and Demographic Factors, Low Birth Weight and Stunting in Early Childhood: Findings from a Longitudinal Study in South Africa. Matern Child Health J. 2023;27(1):59–69. pmid:36169906
  24. 24. Hong J, Kumar S. Circulating biomarkers associated with placental dysfunction and their utility for predicting fetal growth restriction. Clin Sci (Lond). 2023;137(8):579–95. pmid:37075762
  25. 25. Preston M, Hall M, Shennan A, Story L. The role of placental insufficiency in spontaneous preterm birth: A literature review. Eur J Obstet Gynecol Reprod Biol. 2024;295:136–42. pmid:38359634
  26. 26. Cho H, Lee YW. Multiple births and low birth weight: Evidence from South Korea. Am J Hum Biol. 2022;34(3):e23648. pmid:34403549
  27. 27. Tessema ZT, Tamirat KS, Teshale AB, Tesema GA. Prevalence of low birth weight and its associated factor at birth in Sub-Saharan Africa: A generalized linear mixed model. PLoS One. 2021;16(3):e0248417. pmid:33705473
  28. 28. Delcroix M-H, Delcroix-Gomez C, Marquet P, Gauthier T, Thomas D, Aubard Y. Active or passive maternal smoking increases the risk of low birth weight or preterm delivery: Benefits of cessation and tobacco control policies. Tob Induc Dis. 2023;21:72. pmid:37256119
  29. 29. Di HK, et al. Maternal smoking status during pregnancy and low birth weight in offspring: systematic review and meta-analysis of 55 cohort studies published from 1986 to 2020. World Journal of Pediatrics. 2022;18(3):176–85.
  30. 30. Arabzadeh H, Doosti-Irani A, Kamkari S, Farhadian M, Elyasi E, Mohammadi Y. The maternal factors associated with infant low birth weight: an umbrella review. BMC Pregnancy Childbirth. 2024;24(1):316. pmid:38664680
  31. 31. Bandyopadhyay A, Jones H, Parker M, Marchant E, Evans J, Todd C, et al. Weighting of risk factors for low birth weight: a linked routine data cohort study in Wales, UK. BMJ Open. 2023;13(2):e063836. pmid:36764720
  32. 32. Baía I, Domingues RMSM. The Effects of Cannabis Use during Pregnancy on Low Birth Weight and Preterm Birth: A Systematic Review and Meta-analysis. Am J Perinatol. 2024;41(1):17–30. pmid:35901851
  33. 33. Hacker M, Firk C, Konrad K, Paschke K, Neulen J, Herpertz-Dahlmann B, et al. Pregnancy complications, substance abuse, and prenatal care predict birthweight in adolescent mothers. Arch Public Health. 2021;79(1):137. pmid:34325740
  34. 34. Weyori AE, Seidu A-A, Aboagye RG, Holmes FA-, Okyere J, Ahinkorah BO. Antenatal care attendance and low birth weight of institutional births in sub-Saharan Africa. BMC Pregnancy Childbirth. 2022;22(1):283. pmid:35382792
  35. 35. Engdaw GT, Tesfaye AH, Feleke M, Negash A, Yeshiwas A, Addis W, et al. Effect of antenatal care on low birth weight: a systematic review and meta-analysis in Africa, 2022. Front Public Health. 2023;11:1158809. pmid:37441651
  36. 36. Bountogo M, Sié A, Zakané A, Compaoré G, Ouédraogo T, Lebas E, et al. Antenatal care attendance and risk of low birthweight in Burkina Faso: a cross-sectional study. BMC Pregnancy Childbirth. 2021;21(1):825. pmid:34903190
  37. 37. Neupane S, Scott S, Piwoz E, Kim SS, Menon P, Nguyen PH. More is not enough: High quantity and high quality antenatal care are both needed to prevent low birthweight in South Asia. PLOS Glob Public Health. 2023;3(6):e0001991. pmid:37289728
  38. 38. UNICEF. The extension of the 2025 maternal, infant and young child nutrition targets to 2030. WHO; 2021.
  39. 39. WHO. Global nutrition targets 2025: low birth weight policy brief, 2025. https://www.who.int/publications/i/item/WHO-NMH-NHD-14.5
  40. 40. Uwimana G, Elhoumed M, Gebremedhin MA, Azalati MM, Nan L, Zeng L. Association between quality antenatal care and low birth weight in Rwanda: a cross-sectional study design using the Rwanda demographic and health surveys data. BMC Health Serv Res. 2023;23(1):558. pmid:37254102
  41. 41. Habte A, Tamene A, Melis T. Compliance towards WHO recommendations on antenatal care for a positive pregnancy experience: Timeliness and adequacy of antenatal care visit in Sub-Saharan African countries: Evidence from the most recent standard Demographic Health Survey data. PLoS One. 2024;19(1):e0294981. pmid:38271342
  42. 42. Organization, W.H. WHO recommendations on antenatal care for a positive pregnancy experience. In WHO recommendations on antenatal care for a positive pregnancy experience. 2016. p. 152.
  43. 43. Dwomoh D, et al. Secular trends in low birth weight and child undernutrition in West Africa: evidence from complex nationwide surveys, 1985–2019. Public Health Nutrition. 2022;25(9):2358–70.
  44. 44. He Z, Bishwajit G, Yaya S, Cheng Z, Zou D, Zhou Y. Prevalence of low birth weight and its association with maternal body weight status in selected countries in Africa: a cross-sectional study. BMJ Open. 2018;8(8):e020410. pmid:30158218
  45. 45. Wenling H, Jiangli D, Aiqun H, Wei Z, Huanqing H, Sidi C. Analysis of the relationship between the quality of antenatal care examinations and the incidence of preterm birth and low birth weight. BMC Public Health. 2024;24(1):3134. pmid:39533272
  46. 46. Aragaw FM, Amare T, Teklu RE, Tegegne BA, Alem AZ. Magnitude of unintended pregnancy and its determinants among childbearing age women in low and middle-income countries: evidence from 61 low and middle income countries. Front Reprod Health. 2023;5:1113926. pmid:37533507
  47. 47. Puthussery S, Tseng P, Li L. Risk of low birthweight and late antenatal care initiation in an ethnically diverse maternal cohort. European Journal of Public Health. 2023;33(Supplement_2).
  48. 48. Habte A, Hailegebreal S, Simegn AE. Predictors of maternal health services uptake in West African region: a multilevel multinomial regression analysis of demographic health survey reports. Reproductive Health. 2024;21(1):45.
  49. 49. DHS M. Demographic and health surveys. Calverton: Measure DHS; 2013.
  50. 50. ICF. ICF International, Demographic and health survey sampling and household listing manual. Maryland, USA: ICF International Calverton; 2012.
  51. 51. Clarke D, Oreffice S, Quintana‐Domeque C. On the Value of Birth Weight*. Oxf Bull Econ Stat. 2021;83(5):1130–59.
  52. 52. Oken E, Kleinman KP, Rich-Edwards J, Gillman MW. A nearly continuous measure of birth weight for gestational age using a United States national reference. BMC Pediatr. 2003;3:6. pmid:12848901
  53. 53. Muchie KF. Quality of antenatal care services and completion of four or more antenatal care visits in Ethiopia: a finding based on a demographic and health survey. BMC Pregnancy Childbirth. 2017;17(1):300. pmid:28893222
  54. 54. WHO. WHO, The Global Health Observatory, Antenatal care coverage - at least four visits. 2015.
  55. 55. Bezie MM, Fente BM, Asmare ZA, Asnake AA, Asebe HA, Negussie YM, et al. Impact of health facility delivery and antenatal care on neonatal mortality in Sub-Saharan Africa: a propensity score matching analysis. BMC Pregnancy Childbirth. 2025;25(1):440. pmid:40229788
  56. 56. Seifu BL, Asebe HA, Fente BM, Melkam M, Asmare ZA, Asnake AA, et al. The effect of maternal high-risk fertility behavior on child nutritional status in Sub-Saharan Africa: a propensity score-matched analysis. Front Public Health. 2025;13:1512392. pmid:40535436
  57. 57. Rosenbaum PR. Propensity score. Handbook of matching and weighting adjustments for causal inference. Chapman and Hall/CRC; 2023. p. 21–38.
  58. 58. Webster-Clark M, Stürmer T, Wang T, Man K, Marinac-Dabic D, Rothman KJ, et al. Using propensity scores to estimate effects of treatment initiation decisions: State of the science. Stat Med. 2021;40(7):1718–35. pmid:33377193
  59. 59. Li Y, Li L. Propensity score analysis methods with balancing constraints: A Monte Carlo study. Stat Methods Med Res. 2021;30(4):1119–42. pmid:33525962
  60. 60. Tesema GA, Worku MG, Alamneh TS, Teshale AB, Yeshaw Y, Alem AZ, et al. Estimating the impact of birth interval on under-five mortality in east african countries: a propensity score matching analysis. Arch Public Health. 2023;81(1):63. pmid:37085879
  61. 61. Zhang Z, Kim HJ, Lonjon G, Zhu Y, written on behalf of AME Big-Data Clinical Trial Collaborative Group. Balance diagnostics after propensity score matching. Ann Transl Med. 2019;7(1):16. pmid:30788363
  62. 62. Wan F. Propensity Score Matching: should we use it in designing observational studies? BMC Med Res Methodol. 2025;25(1):25. pmid:39875810
  63. 63. Guo S, Fraser M, Chen Q. Propensity Score Analysis: Recent Debate and Discussion. Journal of the Society for Social Work and Research. 2020;11(3):463–82.
  64. 64. Rosenbaum PR, Rosenbaum PR. Overt bias in observational studies. Springer; 2002.
  65. 65. Keele LJ. rbounds: Perform rosenbaum bounds sensitivity tests for matched data. R package version 0.1, 2008.
  66. 66. Data MC, et al. Sensitivity analysis and model validation. Secondary analysis of electronic health records. 2016;263–71.
  67. 67. Li L, Shen C, Wu AC, Li X. Propensity score-based sensitivity analysis method for uncontrolled confounding. Am J Epidemiol. 2011;174(3):345–53. pmid:21659349
  68. 68. Li CL. Propensity Score Matching in Observational Studies with Multiple Time Points. The Ohio State University; 2011.
  69. 69. Gautam S, Suso A, Wood E. Effect of antenatal care on birth outcomes in the Gambia: A propensity score matching analysis. PLOS Glob Public Health. 2025;5(6):e0003880. pmid:40531806
  70. 70. Zhou H, Wang A, Huang X, Guo S, Yang Y, Martin K, et al. Quality antenatal care protects against low birth weight in 42 poor counties of Western China. PLoS One. 2019;14(1):e0210393. pmid:30650127
  71. 71. Islam MM, Masud MS. Determinants of frequency and contents of antenatal care visits in Bangladesh: Assessing the extent of compliance with the WHO recommendations. PLoS One. 2018;13(9):e0204752. pmid:30261046
  72. 72. Nihal S, Shekhar C. An assessment of adequate quality antenatal care and its determinants in India. BMC Pregnancy Childbirth. 2024;24(1):698. pmid:39448927
  73. 73. Saapiire F, Dogoli R, Mahama S. Adequacy of antenatal care services utilisation and its effect on anaemia in pregnancy. J Nutr Sci. 2022;11:e80. pmid:36304821
  74. 74. Lawn JE, Bhutta ZA, Ezeaka C, Saugstad O. Ending Preventable Neonatal Deaths: Multicountry Evidence to Inform Accelerated Progress to the Sustainable Development Goal by 2030. Neonatology. 2023;120(4):491–9. pmid:37231868
  75. 75. Akseer N, Lawn JE, Keenan W, Konstantopoulos A, Cooper P, Ismail Z, et al. Ending preventable newborn deaths in a generation. Int J Gynaecol Obstet. 2015;131 Suppl 1:S43-8. pmid:26433505
  76. 76. Qian W. Global strategies to achieve SDG 3.2 for ending preventable deaths of children under-five: A realist review. Public Health. 2025;248:105967. pmid:40997514
  77. 77. Bezie MM, Tesema GA, Seifu BL. Multilevel multinomial regression analysis of factors associated with birth weight in sub-Saharan Africa. Sci Rep. 2024;14(1):9210. pmid:38649729
  78. 78. Ngo N, Bhowmik J, Biswas RK. Factors Associated with Low Birthweight in Low-and-Middle Income Countries in South Asia. Int J Environ Res Public Health. 2022;19(21):14139. pmid:36361018
  79. 79. Hone T, Gonçalves J, Seferidi P, Moreno-Serra R, Rocha R, Gupta I, et al. Progress towards universal health coverage and inequalities in infant mortality: an analysis of 4·1 million births from 60 low-income and middle-income countries between 2000 and 2019. Lancet Glob Health. 2024;12(5):e744–55. pmid:38614628
  80. 80. Sabo S, Wightman P, McCue K, Butler M, Pilling V, Jimenez DJ, et al. Addressing maternal and child health equity through a community health worker home visiting intervention to reduce low birth weight: retrospective quasi-experimental study of the Arizona Health Start Programme. BMJ Open. 2021;11(6):e045014. pmid:34135037
  81. 81. Pawar S. Global, regional, and national progress towards Sustainable Development Goal 3.2 for neonatal and child health: all-cause and cause-specific mortality findings from the Global Burden of Disease Study 2019. Available at SSRN 3939245, 2021.