Skip to main content

Determinants of wealth-related inequalities in full vaccination coverage among children in Nepal: a decomposition analysis of nationally representative household survey data

Abstract

Background

Over the past two decades, child health indicators in Nepal have improved significantly at the national level. Yet, this progress hasn’t been uniform across various population subsets. This study identified the determinants associated with childhood full vaccination, assessed wealth-related inequalities, and delved into the key factors driving this inequality.

Methods

Data for this study were taken from the most recent nationally representative Nepal Demographic and Health Survey 2022. A total of 959 children aged 12–23 months who had received routine childhood basic antigens as per the national immunisation program were considered for analysis. Binary logistic regression models were conducted to identify the associated factors with outcome variable (uptake of full vaccination). The concentration curve and Erreygers normalized concentration index were used to assess inequality in full vaccination. Household wealth quintile index scores were used to measure wealth-related inequality and decomposition analysis was conducted to identify determinants explaining wealth-related inequality in the uptake of childhood vaccination.

Results

The coverage of full vaccination among children was 79.8% at national level. Several factors, including maternal health service utilisation variables (e.g., antenatal care, institutional delivery), financial challenges related to visiting health facilities, and mothers’ awareness of health mother group meetings within their ward, were associated with the uptake of full vaccination coverage among children. The concentration curve was below the line of equality, and the relative Erreygers normalized concentration index was 0.090, indicating that full vaccination was disproportionately higher among children from wealthy groups. The decomposition analysis identified institutional delivery (20.21%), the money needed to visit health facilities (14.25%), maternal education (16.79%), maternal age (8.53%), and caste (3.03%) were important contributors to wealth related inequalities in childhood full vaccination uptake.

Conclusions

There was notable wealth-related inequality in full vaccine uptake among children in Nepal. Multisectoral actions involving responsible stakeholders are pivotal in reducing the inequalities, including promoting access to maternal health services and improving educational attainment among mothers from socioeconomically disadvantaged communities.

Peer Review reports

Background

Child health improvement has been a global public health agenda for the last four decades [1]. Reducing child mortality has been a priority of global policy agendas including Sustainable Development Goals (SDGs) [2]. Immunisation is often regarded as a cost-effective public health intervention that can avert an estimated 4–5 million deaths in all age groups yearly from vaccine-preventable diseases (VPD) worldwide [3]. Moreover, 1.5 million deaths could be avoided if global vaccination achieved universal coverage [3]. The Global Vaccine Action Plan (GVAP) targeted 95% national coverage of the third dose of diphtheria, pertussis, and tetanus (DPT 3), vaccine a globally recognized proxy for vaccination system performance, and at least 80% DPT 3 coverage for subnational levels by 2015 [4]. Despite ongoing efforts, there was only an estimated 84% global DPT 3 coverage in 2022, leaving an estimated 20.5 million children incompletely vaccinated. Furthermore, the number of children who received no vaccinations has, concerningly, been trending upward, from 12.9 million in 2019 to 14.3 million in 2022, causing a decline in full vaccination coverage [5].

Historically, vaccination coverage has been measured by the proportion of children receiving all “basic” antigens. “A child is considered fully vaccinated against all basic antigens if they have received the Bacille Calmette-Guerin (BCG) vaccine, three doses of oral polio and DPT-containing vaccine, and a single dose of the measles-rubella (MR) vaccine” [6]. The proportion of children receiving all basic antigens is considered an important measure of vaccination coverage. In Nepal, several health policies, programs, strategies, and services related to immunisation programs are designed and implemented in Nepal aligning with global commitments. The BCG vaccine is given at birth or first clinic contact, while the OPV and DPT (given as pentavalent: DPT-HepB-Hib) vaccines are given together at 6, 10, and 14 weeks of age. The first dose of the MR vaccine is given at or soon after nine months, whereas the second dose is given at 15 months of age [6,7,8]. Nepal’s National Immunization Program (NIP) has made huge progress and is often regarded as one of the most successful public health programs [9]. Since its inception, this program has made significant achievements in controlling, eliminating, and eradicating several VPDs. For example, some successful examples of immunisation programs in Nepal include the eradication of smallpox (1977), elimination of maternal and neonatal tetanus (MNT) (2005), polio-free certification (2014), rubella control certification (2018), and certification of Hepatitis B control in children through immunisation (2019) [10]. Access to vaccination has improved in hard-to-reach areas and marginalised populations, including children from the lowest wealth quintile [11]. Furthermore, Nepal introduced the unique full immunisation declaration program in 2012/2013, with support from external development partners, and accelerated coverage and access to routine childhood vaccines by implementing full immunisation declaration guidelines [12]. As of November 2023, 72 out of 77 districts and 724 out of 753 local levels have achieved ‘full immunisation’ status [10].

These policy and programmatic efforts on childhood vaccination have contributed to the ongoing decline in child mortality, as evidenced by periodic survey reports. For instance, Nepal substantially improved under-five, infant, and neonatal mortality over the last two and half decades. Under-5, infant, and neonatal mortality declined by 72%, 64%, and 58%, respectively, between 1996 and 2022. Recent NDHS 2022 data indicate that the under-5 mortality rate (U5MR), infant mortality rate, and neonatal mortality rate are 33, 28, and 21 deaths per 1000 live births, respectively [6]. However, there is a significant socioeconomic disparity in the under-5 mortality rate, with 16 deaths per 1000 live births in the highest wealth quintile compared to 53 deaths per 1000 live births in the poorest wealth quintile [6]. The NIP has been crucial in preventing several VPDs responsible for avoidable under-five deaths [6, 8]. However, specific population groups in Nepal still have low coverage of full vaccination, with recent surveys indicating a decrease in full vaccination coverage [6]. Some marginalised groups, including internal migrants, neighbouring nearby India, specific ethnicities, low socioeconomic status, urban poor, and slum populations, face limited access to routine childhood vaccines [8]. These disparities in the utilization of immunisation services may present additional hurdles to universal coverage of vaccine uptake. Determinants of childhood vaccination coverage in low- and middle-income countries (LMICs), including Nepal, are not in limited numbers and are usually of a complex nature [13]. Household characteristics, including maternal education, socioeconomic status, and caste/ethnicity, are important predictors.

Moreover, factors associated with the immunisation service in Nepal, such as physical access to health facilities, availability of health professionals, cold chain maintenance system, and direct and indirect costs associated with vaccinations, also substantially impact vaccine uptake [9, 14, 15]. Most studies in LMICs, including Nepal, have documented inequality in vaccination coverage, favouring the privileged groups such as households with higher wealth status or maternal education [11, 16,17,18,19,20,21]. Children from poor households are more likely to experience a decline in vaccination coverage, making them more susceptible to VPDs and their consequences. This vulnerability can lead to catastrophic health expenditures, driving the affected households further into poverty [22, 23]. It is pivotal to examine vaccination inequality to achieve a relatively fair distribution of health outcomes. Appropriate strategies are needed to improve childhood vaccination coverage among children from disadvantaged communities and hard-to-reach areas. This aligns with the WHO’s goal of making immunization services accessible to everyone (leaving no one behind) [24] and the target of SDG3 of reducing U5MR by 2030 [25].

Assessing inequalities in full vaccination coverage, identifying gaps in routinely delivered immunisation services, and gathering valuable information to roll out effective strategies and policies are essential. Tracking those children who did not receive full vaccinations is important to develop an equity-oriented immunisation program to reach disadvantaged populations and reduce Nepal’s vaccine-preventable childhood morbidities and mortalities. Although previous studies in Nepal have addressed factors associated with full vaccination [11, 19, 26, 27], and another study [21] assessed the inequality of vaccination. Nonetheless, limited evidence is available on decomposition analysis of the determinants of socioeconomic inequality based on nationally representative data. The objective of this paper is threefold: (i) to analyse the determinants of full vaccination among children in Nepal using the data from the most recent nationally representative household survey; (ii) to measure socioeconomic inequality in the uptake of full vaccination; (iii) to identify the main components that explain socio-economic inequality in full vaccination uptake. Findings of this study provide important insights for the policymakers to develop evidence-based policy measures to address the inequitable distribution of these immunisation related cost-effective life-saving interventions.

Methods

Study population and data source

This study used the cross-sectional data from the NDHS 2022 survey from January 5th to June 22nd, 2022. The survey collected nationally representative samples from all seven provinces, further stratified by urban and rural areas. This survey used an updated urban and rural classification system based on structural changes made in the country on 17 April 2017 (post-federalization), which changed the nation into a pro-urban, accommodating 65% of the population. The NDHS adopted two stage sampling approach. In the first stage, 476 primary sampling units (PSUs) were selected using probability proportional to size, with 248 PSUs from urban areas and 228 from rural areas. In the second stage, 30 households were selected from each PSU, resulting in a total sample size of 14,280 households, consisting of 7,440 urban and 6,840 rural households. From these sampled households, 15,238 women aged 15–49 were eligible for interviews. Of these, 14,845 women were interviewed, yielding a response rate of 97.42%. The sample included 5,205 children under five years whose mothers were interviewed to determine vaccination status. Detailed sampling approach is described in original report of the NDHS 2022 [6].

The source population for this study was all children aged 12–23 months living in Nepal. This study’s term “children” refers to 12–23 months age group. The final sample included in the analysis were 959 children who were alive and living with the mother because they were the youngest children who had reached the age by which they should be fully vaccinated with the basic antigens (Fig. 1). For this study, we extracted the outcome and explanatory variables from the children, women, and household datasets of NDHS 2022. The survey data was collected using a structured and pretested questionnaire. Details about the sampled mother and children’s pair were collected using a woman’s questionnaire that primarily focused on the respondents’ background characteristics, vaccination and childhood illness, reproduction, and contraception. Another questionnaire was used to collect the sociodemographic details of everyone in the family, including inventory and asset information. Comprehensive information about the data collection tools and techniques for NDHS 2022 is available elsewhere [6].

Fig. 1
figure 1

Schematic representation of sampling procedure for study population in NDHS 2022

Study variables

The outcome variable of this study was children’s vaccination status with binary categories: “Fully Vaccinated” and “Not Fully Vaccinated.” The study considered a child who received one dose of the vaccine against tuberculosis (BCG), three doses each of the pentavalent (DPT-Hib, Hep-B) and OPVs, and a first dose of the Measles-Rubella (MR) vaccine any time before data collection as “fully vaccinated” and coded as “Yes = 1.” Conversely, a child who missed at least one dose of the recommended basic vaccines or didn’t receive any vaccines was considered “not fully vaccinated” and coded as “No = 0”. Before creating the outcome variable with two categories, We recoded the responses for each of the eight vaccine doses to indicate whether each dose was “vaccinated” or “not vaccinated” and then combined these to reflect “fully vaccinated.” The study obtained the vaccination status of children from the written vaccine records or the mother’s verbal report if cards were unavailable.

All seventeen explanatory variables of interest were based on the literature review [11, 15, 18, 21, 26,27,28,29,30,31,32,33,34] and the variables available in the dataset. The WHO framework on the epidemiology of nonvaccinated children [35,36,37] describes the factors influencing childhood vaccination into four main categories (Fig. 2): (a) health service immunisation system; (b) communication and information; (c) household characteristics; and (d) parental attitude, knowledge, and practices. In our study, the immunisation system category comprised the distance to a health facility and the money needed to visit a health facility. The communication and information category comprised exposure to mass media and awareness of HMG in the ward. Household characteristics included the following variables: maternal education, mother’s age, caste/ethnicity, wealth status, mother’s employment (in the past 12 months), birth order, child sex, household size, place of residence, province, and ecological zone. Variables such as ANC ≥ 4 visits and place of delivery represented the parental attitudes, knowledge, and practices.

Fig. 2
figure 2

Conceptual framework adapted from the WHO framework on the epidemiology of nonvaccinated child

Details about the description of categories of explanatory variables are explained in Supplementary Table S1. Socioeconomic status was measured using a household wealth index, a proxy measure of inequality without income, expenditure, and consumption data [38]. According to NDHS 2022, the household wealth index was derived using principal component analysis. Scores were assigned based on easily collectible data on household consumer goods (such as televisions, bicycles, and cars) and household characteristics (housing construction materials, water access, and sanitation facilities). Household wealth quintiles were then computed by assigning a household score to each household member, ranking each person in the household population by their score, and dividing the distribution into five equal categories comprising 20% of the population [39]. As the wealth index offers an ordinal interpretation, it served as a household ranking variable for measuring the inequality of childhood full vaccination [6].

Statistical analyses

The characteristics of the mother-child pairs included in this study were described using frequency and percentage. We followed Hosmer and Lemeshow’s (2000) [40] incremental process for specifying the initial model, refining the set of predictors, and determining the final form of the logistic regression model [41]. Multivariable binary logistic regression analysis examined the associations of full vaccination status (Yes/No) simultaneously with other variables. The study expressed the results as an odds ratio with a 95% confidence interval (CI). We ran the model fitness test using multiparameter Wald tests to determine the overall significance of each predictor. The multivariable binary logistic regression model included all the explanatory variables in the conceptual framework (Fig. 2), which we considered important based on previous studies [11, 15, 18, 21, 26,27,28,29,30,31,32,33,34]. The study dropped variables such as ecological zones following the multicollinearity check with a variance inflation factor (VIF) ≥ 5 [42]. Details about the VIF are presented in the supplementary Table 2. The Pearson goodness of fit test for the model accounting for survey design gave p = 0.873 (F-adjusted test statistic:0.50) with all the covariates in the multivariable model, which indicated no evidence of poor fit. Since the NDHS survey employed a two-stage stratified cluster sampling technique, the recommended sample weights provided by the NDHS 2022 were used for the analysis [6]. We adjusted the analysis by incorporating the sample weights, primary sampling units, and strata using the “SVY” command in STATA 18 to account for the complex survey design, which underestimated the variance.

Inequality measurement

The concentration curve (CC) and concentration index (CIX) in their relative formulation were employed to examine the inequality in the use of health services (childhood vaccination) across the socio-economic characteristics of the mother-child pair [43]. CIX, in its relative formulation, reflects horizontal inequity, assuming equal vaccination needs for all children. The CC plots the cumulative proportion of mothers ranked by wealth index score (x-axis) against the cumulative proportion of fully vaccinated children (y-axis). The 45-degree inclination from the origin showed perfect equality. If the CC coincides with the line of equality, vaccination uptake is equal among children. However, if the CC deviates from the line of equality, inequality in vaccination uptake exists and is biased towards mother-child pairs belonging to either low or high socioeconomic status. Although the concentration curve (CC) offers a graphical representation of inequality, it does not quantify the magnitude of the inequality numerically. Therefore, the Concentration Index (CIX) was utilized in this study to compute the degree of socioeconomic inequality in full vaccine uptake among children aged 12–23 months [21, 22, 44, 45]. The CIX quantifies the magnitude of wealth-related inequality, which is twice the area between the line of equality and CC [43]. The CIX ranges from − 1 to + 1, with zero indicating no inequality. A positive CIX implies a concentration of fully vaccinated children among higher socio-economic groups (pro-rich). In comparison, a negative CIX suggests a concentration among lower socio-economic groups (pro-poor). Provided that the outcome variable (full vaccination-yes/no) is binary, Erreygers’ normalized concentration index (ECIX) recommended for such cases was used in the study to assess the inequality of full vaccination among the children [46,47,48,49,50,51], as shown in Eq. 1.

$$\:ECI=\frac{8*cov\:\left({y}_{i,}{r}_{i}\right)}{b-a}$$
(1)

Where \(\:{y}_{i}\) is full vaccination uptake, \(\:{r}_{i}\) is the socioeconomic status ranking of individual mother-child pairs \(\:i\) by wealth index, \(\:cov\) is covariance, and ‘b’ and ‘denotes the upper and lower bound of the outcome variable, respectively. The range (\(\:b-a)\) become one for binary variables, like in our study. The glcurve (Lorenz as option) and conindex STATA commands were used to produce the CC and measure the ECIX, respectively [43].

Decomposition of the concentration index

While the ECI presents the extent of socioeconomic inequality in full vaccination uptake, it does not explain the factors behind these disparities. Identifying these factors is pivotal for formulating effective policy measures. Therefore, we used the decomposition analysis of ECI to identify the explanatory factors contributing to inequality in childhood full vaccinations [45, 52]. The selection of variables for the decomposition of ECIX was based on the results of multivariable binary logistic regression (statistical significance), policy relevance, and literature review of empirical studies [11, 15, 18, 21, 27, 29, 32, 34, 53, 54].

Let’s suppose that our outcome variable of interest, full vaccinee uptake \(\:{y}_{i}\), can be stated as a linear function of the explanatory variables as per the following multivariable linear regression Eq. 2.

$$\:{y}_{i=}\alpha\:+\:{{\Sigma\:}}_{k}{\beta\:}_{k}{\mathcal{X}}_{ki}+{\epsilon\:}_{i}$$
(2)

Where

\(\:{y}_{i}\) is full vaccine uptake (\(\:{y}_{i}\) = 1 if the child received all recommended eight basic antigens and \(\:{y}_{i}=0\:\) otherwise)

\(\:{\mathcal{X}}_{ki}\): a set of explanatory variables in the model for full vaccine uptake;

\(\:{\beta\:}_{k}\) : regression coefficient of explanatory variables \(\:{\mathcal{X}}_{k}\)

\(\:{\epsilon\:}_{i}\) : error term

After fitting the model, the ECIX for full vaccine uptake can be decomposed into the contribution of individual explanatory variables using the Eq. (3) [52].

$$\text{ECIX}=\:\left(\genfrac{}{}{0pt}{}{\sum\:}{k}{\beta\:}_{k}{\mathcal{X}}_{k}{C}_{k}+\:G{C}_{\epsilon\:}\right)$$
(3)

Where \(\:{\beta\:}_{k}\) is a partial regression coefficient of explanatory variables estimated from linear regression provided in Eq. (3), \(\:{\mathcal{X}}_{k}\) is the mean of the explanatory variable, and \(\:{C}_{k}\) is the concentration index of explanatory variables, and \(\:G{C}_{\epsilon\:}\) is generalised concentration index for the error term (\(\:\epsilon\:\)).

As shown in Eq. 3, ECIX combines the deterministic and residual components. The deterministic component \(\:\genfrac{}{}{0pt}{}{\sum\:}{k}{\beta\:}_{k}{\mathcal{X}}_{k}{C}_{k}\) comprises the sum of the contribution of each explanatory variable to inequality in childhood full vaccination uptake. The extent of contribution provided by explanatory variable (\(\:{\mathcal{X}}_{ki})\) to inequality varies according to its distribution by socioeconomic status (derived from its concentration index) and how it is associated with full vaccine uptake (measured by its regression coefficient \(\:{\beta\:}_{k}\)). The greater the value of \(\:{C}_{k}\) or \(\:{\beta\:}_{k}\) of the explanatory variable, the more significant its contribution to the observed overall inequality. The percentage contribution of each explanatory variable to overall inequality was derived by dividing its contribution by ECIX and multiplying by the hundreds. As Eq. (3) mentioned, the residual component \(\:G{C}_{\epsilon\:}\) represents the inequality of full vaccination not explained by a set of explanatory variables in the model. Although binary variables are best estimated by non-linear models, a generalized linear model (identity link) was fitted to our data in Eq. (3) as a linear assumption of decomposition analysis is fulfilled, and the results are easier to interpret relatively with a linear model. To check robustness, we performed the decomposition analysis using partial effects of logistic regression and found fairly consistent results, and the pattern remains unchanged (details are provided in Supplementary Table 4). This was concurrent with the previously published studies [51, 55].

Table 1 Background characteristics of mother and child (12–23 months) pair in NDHS 2022

During decomposition analysis, Erreygers and Kessels (2013) argued against including wealth status as an explanatory variable in the multivariable regression model [56]. Using the wealth status makes the residual component approximately null and causes the wealth quintile to dominate the explanation of inequality in full vaccination. Hence, we decided not to use the wealth status as an explanatory variable in the regression model in the decomposition analysis.

Results

Of the total children (weighted N = 959), 79.8% were fully vaccinated, and 20.2% were not. Table 1 presents descriptive statistics for the variables from the health service immunisation system, communication and information, household characteristics, and parental attitude, knowledge and practices, disaggregated by vaccination status. Most of the mothers belonged to Madhesh province, urban areas, terai ecological zone, who had primary education, who were aged 20–24 years, employed in the past 12 months, exposed to mass media weekly, had at least 4 ANC visits, and who delivered in health facilities. Similarly, most perceived financial and distance barriers to accessing health facilities and were unaware of HMG meetings in their ward. Further, most children were born in large households and were in the birth order of two to three. The proportion of fully vaccinated children was highest in Gandaki province, followed by Sudurpaschim, Lumbini, Karnali, Bagmati, Koshi, and Madhesh. Children from mountain ecological zones, wealthier households, and with one to three birth orders were more likely to be fully vaccinated. Similarly, children with mothers exposed to mass media weekly, receiving four or more ANC visits, employed in the past year, and delivering the child in health facilities were more likely to be fully vaccinated. Likewise, children whose mothers didn’t perceive financial or distance barriers to accessing health facilities and were aware of HMG meetings in the ward were also more likely to be fully vaccinated. Excluding place of residence, child sex, and mother’s age, most of the variables in the study showed evidence of association with full vaccination among children.

Table 2 Decomposition of concentration index (CIX) of full vaccination in Nepal, NDHS 2022

Determinants of childhood full vaccination

Figure 3 depicts the proportion of fully vaccinated children over household wealth index quintiles for the total number of children in the respective quintile. Around three-fourths (75.83%) of the children in the poorest wealth quintile got fully vaccinated compared to 82.3% of the children in the wealthiest counterpart. The graph demonstrates that the proportion of fully vaccinated children increases sharply while moving from the children in the poorest wealth quintile to the middle and richer wealth quintiles, then dropping slightly for children in the richest wealth quintile.

Fig. 3
figure 3

Childhood full vaccination status over the household wealth quintile index in NDHS 2022

Figure 4 shows the inequality in fully vaccinated children by wealth status. Since the concentration curve is below the line of equality, the proportion of fully vaccinated children was disproportionately higher among children from wealthy groups. A positive estimated relative CIX of 0.090 (standard error: 0.029; p < 0.01) indicates that the proportion of fully vaccinated children was relatively higher among wealthier households than their poor counterparts. However, the overlap of the line of equality and the concentration curve at both ends suggests equality at the extremes. This implies that full vaccination rates are similar among the poorest and wealthiest segments of the population.

Fig. 4
figure 4

Concentration curve for full vaccination status among children against wealth rank

Decomposition of the relative concentration index

The outputs of a decomposition analysis and each determinant’s contribution are depicted in Table 2. The determinants (excluding the wealth quintile) incorporated into the model explained 40% of socioeconomic inequality in childhood full vaccination uptake.

The major contribution to the inequality was from the place of delivery (20.21%), followed by maternal education (16.80%), money to reach health facilities (14.25%), and ANC ≥ 4 visits (8.92%). An explanatory variable such as caste contributed relatively little to the inequality in childhood full vaccination, accounting for only 3.03%. However, the percentage contribution of Dalits within the caste/ethnicity category was the highest (21.28%) for socioeconomic inequality. The residual contribution, including the wealth quintile, was around 60%. Mother’s employment (in the past 12 months) and awareness of HMG meetings in the ward were the factors that caused a reduction in wealth-related inequality by 19.25% and 12.96%, respectively, in the children who were fully vaccinated.

Discussion

This study analysed the determinants of full vaccination among children in Nepal using data from the NDHS 2022. The odds of Nepalese children being fully vaccinated with respect to variables from the health service immunisation system, communication and information, household characteristics, and paternal attitude, knowledge and practices were measured. Further, wealth-related inequality in fully vaccinated children was computed, and a decomposition analysis was performed to identify the determinants that explain the socioeconomic inequality [43]. Our analysis found that ANC ≥ 4 visits, awareness of HMG meetings in the ward, and household size were major determinants for full vaccination uptake among children. The proportion of fully vaccinated children was disproportionately higher among the children belonging to wealthy households. The concentration index decomposition showed that wealth-related inequality in childhood full vaccination was primarily explained by place of delivery, maternal education, money needed to each health facility, and ANC ≥ 4 visits.

Our study reported the socioeconomic inequality in childhood vaccine uptake from the poorest households. This finding was consistent with previously published studies from Nepal [11, 21]. As observed in earlier analysis conducted using four rounds of the NDHS (2001, 2006, 2011, 2016), the socio-economic inequality concerning full vaccination coverage between the socio-economic groups measured by relative CIX has, on average, narrowed over this period [21]. The relative CIX obtained from these four rounds of NDHS were 0.21, 0.20, 0.08, and 0.054, respectively [21]. The analysis presented in this paper using the data from NDHS 2022 has shown that the relative CIX for full vaccination has slightly increased to 0.090, signalling rise in socioeconomic inequality in vaccination uptake over the last one and half decades. Thus, identifying the factors driving the inequalities is a preliminary step in designing effective policy measures to reduce observed socioeconomic inequality.

The decomposition analysis revealed that maternal health service utilisation inequalities, including antenatal care and institutional delivery, largely explain inequalities in the uptake of full vaccinations. Both factors accounted for about 29% of the total inequality in full vaccination uptake. In Nepal, immunisation services are provided at the same health facility where maternal health care is provided, the utilisation of maternal health care can serve as a proxy indicator for accessibility of health facilities offering immunisation services. Observed inequality could be associated with disparity in access to immunisation services. Although maternal health care services are supposed to be provided free at public health facilities in Nepal, women with low socioeconomic status experience a financial burden for maternity care, as they have to pay not only for transportation, accommodation, and food but also loss earning due to absenteeism from work [57, 58]. This could impede the use of services among socioeconomically disadvantaged populations, especially those who rely predominantly on public health facilities for their health care requirement. Our findings are consistent with the findings from other studies which found antenatal check-ups a significant factor contributing to the inequality in childhood full vaccination [17, 51, 59]. From a policy perspective, targeted efforts are necessary to enhance maternal health service utilisation among the socioeconomically disadvantaged individuals and mitigate the inequality in vaccination uptake. Other studies are also reported a positive association of at least four ANC visits with childhood full vaccination in Nepal [11, 27, 60] and in Bangladesh [61], Indonesia [20], and Nigeria [62].

Furthermore, acute poverty reflected through the inability of the families to visit the health facility was a significant contributor (14.25%) to inequality in childhood full vaccination in this study. This finding corroborates a previous study that analysed inequalities in full childhood vaccination in Nepal based on the NDHS 2016 [60]. This is likely because the Government in Nepal has been offering free vaccines since the initiation of the Expanded Programme on Immunisation in 1979 [8]. Though vaccines are accessible through immunisation clinics throughout Nepal, poverty restricts some women’s ability to reach them. Mothers facing financial challenges were less likely to fully vaccinate to their children. Our findings suggest expanding the demand-side financing program for poor households to reward mothers vaccinating their children, alleviating financial obstacles to vaccination.

The mother’s education accounted for a relatively substantial portion of the inequality in childhood full vaccination (16.79%), which are consistent findings with earlier studies [16, 51]. In addition to improving health literacy, better education for mothers can transform women into financially independent, increase self-confidence, and ultimately empower them to address their and their children’s health needs [63]. Almost one-third (33.67%) of the poorest women had no education, relative to one among eighty women (1.22%) in the highest wealth quintile [64]. That’s why, besides improving women’s education equitably, the NIP can leverage and ensure the involvement of Female Community Health Volunteers (FCHVs) and other community health workers in communicating with problematic households at the community level in collaboration with local government. Previous studies in Nepal also identified maternal education as a potential determinant of full vaccination [19, 26].

It was also observed that caste/ethnicity accounts for some of the socioeconomic inequalities in the uptake of the full vaccines (3.03%) with significant portion of this contribution mainly stemmed from the Dalit caste (21.28%). These children were disproportionately concentrated among mothers from less wealthy households [64]. Meanwhile, the relatively lower literacy rate and sociocultural practice prevalence among the Dalit could be the reason behind the lower rate of full vaccination among the children in that group, as reported in previous studies [11, 32, 60, 65]. Additionally, community engagement can also be ensured through dialogue meetings by mobilizing and influencing persons among targeted groups at the local level to address misconceptions and concerns about vaccinations.

Decomposition analysis of this study also identified the awareness of HMG meetings as an important contributor to the reduction in socioeconomic inequality of full vaccine (-12.95%). The likelihood of full vaccination among children was greater among the children whose mothers were aware of the HMG meeting in their respective wards. This emphasizes the importance of the HMG, community groups led by FCHVs that bring together women of reproductive age (15–49 years) monthly to discuss and promote several areas of health, particularly related to maternal, newborn, and child health [66]. Additionally, we found approximately 60% of the socioeconomic inequality (excluding the wealth quintile) remained unexplained. This was inevitable as we did not consider supply-side factors, which have been explained as potential predictors in other studies for vaccination coverage, such as cold chain maintenance, availability of vaccines, and adequacy of staff in the facility [13, 14]. Furthermore, other demand-side factors might explain the socioeconomic inequality in childhood vaccination uptake, which needs to be assessed in future studies.

Strengths and limitations of the study

This study has some strengths and limitations. Strengths include rigorous statistical techniques applied to understand childhood full vaccination’s determinants. We applied the decomposition analysis to identify critical determinants of wealth-related inequality measured by the relative concentration index in the country’s childhood full vaccination uptake. However, this study has also some limitations. First, inclusion of the vaccination status of children based on the verbal response of mothers might have introduced differential misclassification into this study due to the potential under-reporting of children who were not fully vaccinated. This is because mothers can provide false reports about the immunization status of their children in the absence of health cards to appear socially acceptable. Second, vaccine stockouts, poor cold chain systems, and the non-readiness of health service providers to administer the vaccines during mothers’ use of maternal health services are some of the health system barriers to the child being fully vaccinated that were not captured in the data used for this study, which could have led to an underestimation of the impact of maternal health service use (ANC and place of delivery) on routine vaccine coverage found in this study. Thirdly, we could not consider the complex survey design while decomposing the socioeconomic inequality in vaccination uptake. This limitation resulted in underestimating the elasticity variance, leading to inaccuracies in the standard error, confidence interval, and p-value. However, it does not influence the point estimate since sampling weight was considered during the analysis.

Conclusion

This analysis found uptake of full vaccination among children is pro-wealthy in Nepal. Policymakers should recognize this disparity and implement equity-oriented policies to support socioeconomically disadvantaged groups. We recommend targeted interventions to enhance maternal healthcare services, financial access to health facilities, and educational attainment among socioeconomically disadvantaged mothers. These interventions can substantially reduce inequality in the childhood full vaccine uptake in Nepal.

Data availability

Data used in this study are publicly available secondary data obtained from the DHS (https://dhsprogram.com/data/available-datasets.cfm) program.

Abbreviations

ANC:

Antenatal care

AOR:

Adjusted odds ratio

BCG:

Bacillus Calmette-Guerin

CC:

Concentration curve

CI:

Confidence interval

CIX:

Concentration index

ECIX:

Erreygers normalized concentration index

COR:

Crude odds ratio

DPT:

Diphtheria, Pertussis, Tetanus

EDP:

External development partner

FCHV:

Female community health volunteers

FIDP:

Full immunisation declaration program

GVAP:

Global vaccine action plan

HMG:

Health mother group

MDG:

Millenium development goal

MMR:

Measles Mumps Rubella

MR:

Measles-Rubella

NDHS:

Nepal demographic and health Survey

NIP:

National immunisation program

OPV:

Oral Polio Vaccine

SDG:

Sustainable development goal

VIF:

Variance inflation factor

VPD:

Vaccine-preventable diseases

WHO:

World Health Organisation

References

  1. World Health Organization. Declaration of alma-ata: World Health Organization. Regional Office for Europe; 1978. https://www.who.int/teams/social-determinants-of-health/declaration-of-alma-ata

  2. Fukuda-Parr S. From the Millennium Development Goals to the Sustainable Development Goals: shifts in purpose, concept, and politics of global goal setting for development. Gend Dev. 2016;24(1):43–52. https://doi.org/10.1080/13552074.2016.1145895

    Article  Google Scholar 

  3. Immunization coverage [(https://www.who.int/en/news-room/fact-sheets/detail/immunization-coverage)].

  4. World Health Organization. Global vaccine Action Plan 2011–2020. In. USA: World Health Organization; 2013. p. 77.

    Google Scholar 

  5. Vaccination and immunization statistics. UNICEF data, 2021 [https://data.unicef.org/topic/child-health/immunization/]

  6. Ministry of Health and Population, New ERA, ICF International. Nepal Demographic and Health Survey 2022. Kathmandu, Nepal;; 2023. https://www.dhsprogram.com/pubs/pdf/FR379/FR379.pdf

  7. Shen AK, Fields R, McQuestion M. The future of routine immunization in the developing world: challenges and opportunities. Global Health Sci Pract. 2014;2(4):381–94. https://doi.org/10.9745/GHSP-D-14-00137

    Article  Google Scholar 

  8. Ministry of Health and Population: Annual Report 2021/2022. In. Kathmandu: Department of Health Services. 2022: 522.

  9. Hester KA, Sakas Z, Ellis AS, Bose AS, Darwar R, Gautam J, Jaishwal C, James H, Keskinocak P, Nazzal D, et al. Critical success factors for high routine immunization performance: a case study of Nepal. Vaccine: X. 2022;12:100214–100214. https://doi.org/10.1016/j.jvacx.2022.100214

    Article  PubMed  Google Scholar 

  10. Ministry of Health and Population. Annual Health Report 2079/2080. Kathmandu: Department of Health Services; 2024. http://dohs.gov.np/annual-health-report-2079-80/

    Google Scholar 

  11. Kc A, Nelin V, Raaijmakers H, Kim HJ, Singh C, Målqvist M. Increased immunization coverage addresses the equity gap in Nepal. Bull World Health Organ. 2017;95(4):261–9. https://doi.org/10.2471/BLT.16.178327

    Article  PubMed  PubMed Central  Google Scholar 

  12. Ministry of Health and Population. Full Immunization Declaration Guideline, third edition 2077. Kathmandu: Ministry of Health and Population; 2077. https://fwd.gov.np/wp-content/uploads/2023/02/FID-guideline-Revised-2023-2.pdf

  13. Phillips DE, Dieleman JL, Lim SS, Shearer J. Determinants of effective vaccine coverage in low and middle-income countries: a systematic review and interpretive synthesis. BMC Health Serv Res. 2017;17:1–17. https://doi.org/10.1186/s12913-017-2626-0

    Article  Google Scholar 

  14. Rainey JJ, Watkins M, Ryman TK, Sandhu P, Bo A, Banerjee K. Reasons related to non-vaccination and under-vaccination of children in low and middle income countries: findings from a systematic review of the published literature, 1999–2009. Vaccine. 2011;29(46):8215–21. https://doi.org/10.1080/21645515.2022.2076524

    Article  PubMed  Google Scholar 

  15. Ali HA, Hartner A-M, Echeverria-Londono S, Roth J, Li X, Abbas K, Portnoy A, Vynnycky E, Woodruff K, Ferguson NM, et al. Vaccine equity in low and middle income countries: a systematic review and meta-analysis. Int J Equity Health. 2022;21(1):82. https://doi.org/10.1186/s12939-022-01678-5

    Article  PubMed  PubMed Central  Google Scholar 

  16. Ataguba JE, Ojo KO, Ichoku HE. Explaining socio-economic inequalities in immunization coverage in Nigeria. Health Policy Plann. 2016;31(9):1212–24. https://doi.org/10.1093/heapol/czw053

    Article  Google Scholar 

  17. Debnath A, Bhattacharjee N. Wealth-based inequality in child immunization in India: a decomposition approach. J Biosoc Sci. 2018;50(3):312–25. https://doi.org/10.1017/S0021932017000402

    Article  PubMed  Google Scholar 

  18. Niveditha D, Suparna Ghosh J, Saket S, Elizabeth A, Anuraj HS, Sanjay Z. Determinants of childhood immunisation coverage in urban poor settlements of Delhi, India: a cross-sectional study. BMJ Open. 2016;6(8):e013015. http://bmjopen.bmj.com/content/6/8/e013015.abstract

    Article  Google Scholar 

  19. Patel PN, Hada M, Carlson BF, Boulton ML. Immunization status of children in Nepal and associated factors, 2016. Vaccine. 2021;39(40):5831–8. https://www.sciencedirect.com/science/article/pii/S0264410X21011075

    Article  PubMed  Google Scholar 

  20. Putri H, Abdel D. Determinants of immunisation coverage of children aged 12–59 months in Indonesia: a cross-sectional study. BMJ Open. 2017;7(12):e015790. http://bmjopen.bmj.com/content/7/12/e015790.abstract

    Article  Google Scholar 

  21. Acharya K, Paudel YR, Dharel D. The trend of full vaccination coverage in infants and inequalities by wealth quintile and maternal education: analysis from four recent demographic and health surveys in Nepal. BMC Public Health. 2019;19(1):1673–1673. https://doi.org/10.1186/s12889-019-7995-3

    Article  PubMed  PubMed Central  Google Scholar 

  22. Riumallo-Herl C, Chang AY, Clark S, Constenla D, Clark A, Brenzel L, Verguet S. Poverty reduction and equity benefits of introducing or scaling up measles, rotavirus and pneumococcal vaccines in low-income and middle-income countries: a modelling study. BMJ Global Health. 2018;3(2):e000613. https://gh.bmj.com/content/bmjgh/3/2/e000613.full.pdf

    Article  PubMed  PubMed Central  Google Scholar 

  23. Rodrigues CMC, Plotkin SA. Impact of vaccines; Health, Economic and Social perspectives. Front Microbiol. 2020;11:1526. https://doi.org/10.3389/fmicb.2020.01526

    Article  PubMed  PubMed Central  Google Scholar 

  24. Wallace A, Ryman T, Privor-Dumm L, Morgan C, Fields R, Garcia C, Sodha S, Lindstrand A, Lochlainn LN. Leaving no one behind: defining and implementing an integrated life course approach to vaccination across the next decade as part of the immunization agenda 2030. Vaccine. 2022. https://doi.org/10.1016/j.vaccine.2022.11.039

    Article  PubMed  Google Scholar 

  25. United Nations. The Sustainable Development Goals 2016. Newyork: United Nations; 2016. https://unstats.un.org/sdgs/report/2016/the sustainable development goals report 2016.pdf

    Google Scholar 

  26. Pandey S, Lee H. Determinants of child immunization in Nepal: the role of women’s empowerment. Health Educ J. 2011;71(6):642–53. https://doi.org/10.1177/0017896911419343

    Article  Google Scholar 

  27. Acharya K, Lacoul M, Bietsch K. Factors affecting vaccination coverage and retention of vaccination cards in Nepal. DHS further analysis reports no 121. Maryland, USA: ICF;: Rockville; 2019.

    Google Scholar 

  28. Abegaz MY, Seid A, Awol SM, Hassen SL. Determinants of incomplete child vaccination among mothers of children aged 12–23 months in Worebabo district, Ethiopia: unmatched case-control study. PLOS Global Public Health. 2023;3(8):e0002088. https://doi.org/10.1371/journal.pgph.0002088

    Article  PubMed  PubMed Central  Google Scholar 

  29. Asresie MB, Dagnew GW, Bekele YA. Changes in immunization coverage and contributing factors among children aged 12–23 months from 2000 to 2019, Ethiopia: multivariate decomposition analysis. PLoS ONE. 2023;18(9):e0291499. https://doi.org/10.1371/journal.pone.0291499

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Hu Y, Liang H, Wang Y, Chen Y. Inequities in childhood vaccination coverage in Zhejiang, province: evidence from a decomposition analysis on two-round surveys. Int J Environ Res Public Health. 2018;15(9):2000. https://doi.org/10.3390/ijerph15092000

    Article  PubMed  PubMed Central  Google Scholar 

  31. Noh J-W, Kim Y-m, Akram N, Yoo K-B, Park J, Cheon J, Kwon YD, Stekelenburg J. Factors affecting complete and timely childhood immunization coverage in Sindh, Pakistan; a secondary analysis of cross-sectional survey data. PLoS ONE. 2018;13(10):e0206766. https://doi.org/10.1371/journal.pone.0206766

    Article  PubMed  PubMed Central  Google Scholar 

  32. Paul AM, Nepal S, Upreti K, Lohani J, Rimal RN. The last stretch: barriers to and facilitators of full immunization among children in Nepal’s Makwanpur District, results from a qualitative study. PLoS ONE. 2022;17(1):e0261905. https://doi.org/10.1371/journal.pone.0261905

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Pandey S, Ranjan A, Singh CM, Kumar P, Ahmad S, Agrawal N. Socio-demographic determinants of childhood immunization coverage in rural population of Bhojpur district of Bihar, India. J Family Med Prim Care. 2019;8(7):2484–9. https://doi.org/10.4103/jfmpc.jfmpc_356_19

    Article  PubMed  PubMed Central  Google Scholar 

  34. Bhusal UP. Predictors of wealth-related inequality in institutional delivery: a decomposition analysis using Nepal multiple Indicator Cluster survey (MICS) 2019. BMC Public Health. 2021;21(1):2246. https://doi.org/10.1186/s12889-021-12287-2

    Article  PubMed  PubMed Central  Google Scholar 

  35. World Health Organization. Epidemiology of the unimmunized child: findings from the Grey Literature. Geneva: WHO; 2009. https://www.mchip.net/sites/default/files/Epid. of the Unimmunized child-Grey lit review.pdf

    Google Scholar 

  36. Croft TN, Allen CK, Zachary BW, Blake W. ea: guide to DHS statistics. Rockville, Maryland, USA: ICF; 2003.

    Google Scholar 

  37. Barrow A, Afape AO, Cham D, Azubuike PC. Uptake and determinants of childhood vaccination status among children aged 0–12 months in three west African countries. BMC Public Health. 2023;23(1):1093. https://doi.org/10.1186/s12889-023-15863-w

    Article  PubMed  PubMed Central  Google Scholar 

  38. McKenzie DJ. Measuring inequality with asset indicators. J Popul Econ. 2005;18:229–60.

    Article  Google Scholar 

  39. Rutstein SO, aKJ. The DHS Wealth Index. DHS Comparative Reports No. 6. Calverton, Maryland, USA; 2004. https://dhsprogram.com/pubs/pdf/CR6/CR6.pdf

  40. Hosmer DW Jr, Lemeshow S, Sturdivant RX. Applied logistic regression: Wiley; 2013.

  41. Heeringa SG, West BT, Berglund PA. Applied survey data analysis. CRC; 2017.

  42. Kim JH. Multicollinearity and misleading statistical results. Korean J Anesthesiol. 2019;72(6):558–69. https://doi.org/10.4097/kja.19087

    Article  PubMed  PubMed Central  Google Scholar 

  43. O’Donnell OvD E, Wagstaff A, Lindelow M, Washington DC. World Bank Group; 2007. https://documents.worldbank.org/en/publication/documents-reports/documentdetail/633931468139502235/analyzing-health-equity-using-household-survey-data-a-guide-to-techniques-and-their-implementation

  44. Wagstaff A, Paci P, Van Doorslaer E. On the measurement of inequalities in health. Soc Sci Med. 1991;33(5):545–57. https://doi.org/10.1016/0277-9536(91)90212-U

    Article  CAS  PubMed  Google Scholar 

  45. Wagstaff A, O’Donnell O, Van Doorslaer E, Lindelow M. Analyzing health equity using household survey data: a guide to techniques and their implementation. World Bank; 2007. http://documents.worldbank.org/curated/en/633931468139502235/Analyzing-health-equity-using-household-survey-data-a-guide-to-techniques-and-their-implementation

  46. Erreygers G. Correcting the concentration index. J Health Econ. 2009;28(2):504–15. https://doi.org/10.1016/j.jhealeco.2008.02.003

    Article  PubMed  Google Scholar 

  47. Erreygers G, Van Ourti T. Measuring socioeconomic inequality in health, health care and health financing by means of rank-dependent indices: a recipe for good practice. J Health Econ. 2011;30(4):685–94. https://doi.org/10.1016/j.jhealeco.2011.04.004

    Article  PubMed  PubMed Central  Google Scholar 

  48. Kjellsson G, Gerdtham UG. On correcting the concentration index for binary variables. J Health Econ. 2013;32(3):659–70. https://doi.org/10.1016/j.jhealeco.2012.10.012

    Article  PubMed  Google Scholar 

  49. Zhu D, Guo N, Wang J, Nicholas S, Wang Z, Zhang G, Shi L, Wangen KR. Socioeconomic inequality in Hepatitis B vaccination of rural adults in China. Hum Vaccin Immunother 2018, 14(2):464-470.10.1080/21645515.2017.1396401.

  50. Ngandu NK, Van Malderen C, Goga A, Speybroeck N. Wealth-related inequality in early uptake of HIV testing among pregnant women: an analysis of data from a national cross-sectional survey, South Africa. BMJ Open. 2017;7(7):e013362. https://doi.org/10.1136/bmjopen-2016-013362

    Article  PubMed  PubMed Central  Google Scholar 

  51. Wondimu A, van der Schans J, van Hulst M, Postma MJ. Inequalities in Rotavirus Vaccine Uptake in Ethiopia: A Decomposition Analysis. International Journal of Environmental Research and Public Health 2020, 17(8):2696. https://www.mdpi.com/1660-4601/17/8/2696

  52. Wagstaff A, Van Doorslaer E, Watanabe N. On decomposing the causes of health sector inequalities with an application to malnutrition inequalities in Vietnam. J Econ. 2003;112(1):207–23. https://doi.org/10.1016/S0304-4076(02)00161-6

    Article  Google Scholar 

  53. Glatman-Freedman A, Nichols K. The effect of social determinants on immunization programs. Hum Vaccines Immunotherapeutics. 2012;8(3):293–301. https://doi.org/10.4161/hv.19003

    Article  Google Scholar 

  54. Roy D, Debnath A, Sarma M, Roy D, Das K. A decomposition analysis to understand the wealth-based inequalities in child vaccination in Rural Southern Assam: a cross-sectional study. Indian J Community Med. 2023;48(1):112–25. https://doi.org/10.4103/ijcm.ijcm_422_22

    Article  PubMed  PubMed Central  Google Scholar 

  55. Van de Poel E, O’Donnell O, Van Doorslaer E. Urbanization and the spread of diseases of affluence in China. Econ Hum Biology. 2009;7(2):200–16. https://www.sciencedirect.com/science/article/pii/S1570677X09000434

    Article  Google Scholar 

  56. Erreygers G, Kessels R. Regression-based decompositions of rank-dependent indicators of socioeconomic inequality of health. Health and inequality. Volume 21. edn.: Emerald Group Publishing Limited; 2013. pp. 227–59. https://repository.uantwerpen.be/docman/irua/b1458d/e47122fc.pdf

  57. Khatri RB, Karkee R. Social determinants of health affecting utilisation of routine maternity services in Nepal: a narrative review of the evidence. Reprod Health Matters. 2018;26(54):32–46. https://doi.org/10.1080/09688080.2018.1535686

    Article  PubMed  Google Scholar 

  58. Simkhada P, van Teijlingen E, Sharma G, Simkhada B, Townend J. User costs and informal payments for care in the largest maternity hospital in Kathmandu, Nepal. Health Sci J. 2012;6(2):317–34. https://eprints.bournemouth.ac.uk/19868/1/6212.pdf

    Google Scholar 

  59. Hajizadeh M. Socioeconomic inequalities in child vaccination in low/middle-income countries: what accounts for the differences? J Epidemiol Community Health. 2018;72(8):719–25. https://doi.org/10.1136/jech-2017-210296

    Article  PubMed  Google Scholar 

  60. Song IH, Palley E, Atteraya MS. Inequalities in complete childhood immunisation in Nepal: results from a population-based cross-sectional study. BMJ open. 2020;10(9):e037646. https://doi.org/10.1136/bmjopen-2020-037646

    Article  PubMed  PubMed Central  Google Scholar 

  61. Boulton ML, Carlson BF, Power LE, Wagner AL. Socioeconomic factors associated with full childhood vaccination in Bangladesh, 2014. Int J Infect Dis. 2018;69:35–40. https://doi.org/10.1016/j.ijid.2018.01.035

    Article  PubMed  Google Scholar 

  62. Onyekachi Ibenelo A, Benedict Oppong A. The impact of maternal health care utilisation on routine immunisation coverage of children in Nigeria: a cross-sectional study. BMJ Open. 2019;9(6):e026324. http://bmjopen.bmj.com/content/9/6/e026324.abstract

    Article  Google Scholar 

  63. Ensor T, Cooper S. Overcoming barriers to health service access: influencing the demand side. Health Policy Plann. 2004;19(2):69–79. https://doi.org/10.1093/heapol/czh009

    Article  Google Scholar 

  64. Singh B.K., Khatri R., Mahasheth S., Paudel K.P., and Church R. 2024. Trends and Determinants of Vaccination among Children Aged 12–23 Months in Nepal: Insights from the Further Analysis of Recent Nepal Demographic and Health Surveys (draft). DHS Further Analysis Report No. 156. Rockville, Maryland, USA: ICF.

    Google Scholar 

  65. Shrestha S, Shrestha M, Wagle RR, Bhandari G. Predictors of incompletion of immunization among children residing in the slums of Kathmandu Valley, Nepal: a case-control study. BMC Public Health. 2016;16(1):970–970. https://doi.org/10.1186/s12889-016-3651-3

    Article  PubMed  PubMed Central  Google Scholar 

  66. New ERA. Family planning, maternal, newborn and child health situation in rural Nepal: A mid-term survey for NFHP II: Kathmandu; 2010. http://103.69.126.140:8080/handle/20.500.14356/560.

Download references

Acknowledgements

Not applicable.

Funding

No funding was received for the development of this manuscript.

Author information

Authors and Affiliations

Authors

Contributions

BKS and RBK conceived the study. BKS performed data analysis, prepared the first draft of the manuscript, and interpreted the findings. RBK supervised the study and provided critical comments in revising the manuscript. Both authors agreed to and approved the final version of the manuscript.

Corresponding author

Correspondence to Barun Kumar Singh.

Ethics declarations

Declarations

The authors declare that the research was conducted without any commercial or financial relationships that could be construed as a potential conflict of interest.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Singh, B.K., Khatri, R.B. Determinants of wealth-related inequalities in full vaccination coverage among children in Nepal: a decomposition analysis of nationally representative household survey data. BMC Public Health 24, 1990 (2024). https://doi.org/10.1186/s12889-024-19456-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12889-024-19456-z

Keywords