Abstract
Background and Aims
Childhood vaccination remains a cost‐effective strategy that has expedited the control and elimination of numerous diseases. Although coverage of new vaccines in low‐ and middle‐income countries increased exponentially in the last two decades, progress on expanding routine vaccination services to reach all children remains low, and coverage levels in many countries remains inadequate. This study aimed to examine the pattern of wealth and residence‐based related inequality in vaccination coverage through an equity lens.
Methods
We used data from the 2017−2018 Benin Demographic and Health Survey. Statistical and econometrics modeling were used to investigate factors associated with childhood vaccination. The Wagstaff decomposition analysis was used to disentangle the concentration index.
Results
A total of 1993 children were included, with 17% in the wealthiest quintile and 63% were living in rural areas. Findings showed that wealth is positively and significantly associated with vaccination coverage, particularly, for middle‐wealth households. A secondary or higher education level of women and partners increased the odds of vaccination compared to no education (p < 0.05). Women with more antenatal care visits, with multiple births, attending postnatal care and delivery in a health facility had increased vaccination coverage (p < 0.01). Inequalities in vaccination coverage are more prominent in rural areas; and are explained by wealth, education, and antenatal care visits.
Conclusion
Inequality in child vaccination varies according to socioeconomic and sociodemographic characteristics and is of interest to health policy. To mitigate inequalities in child vaccination coverage, policymakers should strengthen the availability and accessibility of vaccination and implement educational programs dedicated to vulnerable groups in rural areas.
Keywords: child, inequality, mother, vaccination, wealth
1. INTRODUCTION
Childhood vaccination remains a cost‐effective strategy that has aided to control and eliminate numerous diseases. 1 , 2 Since the beginning of the 20th century, numerous vaccine‐preventable diseases (VPDs) have been prevented or even eradicated in many countries through vaccination. Vaccination resulted in the eradication of wild‐type poliovirus in the Americas in 1990, the Western Pacific Region in 2000, and Europe in 2002, as well as the eradication of Hemophilus influenza type B in many countries within a few years of conjugate Hib vaccine introduction. 3 Measles, polio, and diphtheria−tetanus−pertussis vaccinations saved the lives of nearly 2.5 million children globally in the first decade of the 21st century. 4 Since 1924, 103 million instances of pediatric illnesses have been averted in the United States, with 26 million cases in the last decade. 5 In the United States, the number of instances of diphtheria, measles, paralytic poliomyelitis, and rubella decreased by more than 99% during the time before and after national vaccination recommendations. Mumps, pertussis, and tetanus cases decreased by more than 92%, while mortality decreased by 99% or more. 6 In Benin, pediatric bacterial meningitis is reported to have declined between 6.5% in 2012 to 1.0% in 2016 due to the introduction of the pneumococcal conjugate (PCV). 7
Although coverage of new vaccines increased exponentially in low‐ and middle‐income countries (LMICs) between 2000 and 2019, progress on expanding routine vaccination services to reach all children has stalled, and coverage levels in many countries remain below the 90% national coverage recommended by the World Health Organization. 8 , 9 In a review published in 2012 based on surveys dating back to 2007, 10% of all children living in LMICs were not vaccinated. 10 Given that vaccination is one of the most cost‐effective methods for averting child mortality globally, 2 this estimate was a startling discovery.
Consequently, some vaccine‐preventable illnesses such as measles, mumps, and pertussis have resurfaced and constitute a public health burden. 1 , 11 This re‐emergence has been connected in part to reduced vaccination coverage among children, especially in Sub‐Saharan Africa. 12 In LMICs, VPDs still constitute substantial causes of under‐five morbidity and mortality and are also associated with social and economic consequences. 1 There are still significant incidences of child mortality among regions, within nations, and across countries. 13 Sub‐Saharan Africa has the highest under‐five mortality rate in the world, accounting for 52% of all mortalities in this age range. In 2018, the region's average under‐five mortality rate was 78 deaths per 1000 live births. 13
Many factors have been marked as impeding vaccination coverage. Among these are reduced public confidence, and other social factors such as education and socioeconomic factors. 14 There also exist reports of inequalities in vaccine coverage. This discrepancy between LMICs can be narrowed if all children, regardless of their geographic, socioeconomic, or demographic makeup, have equitable access to vaccination and its associated benefits. 15 , 16 This is not always the case, since many children in various countries are either under‐vaccinated or unvaccinated. 17 As a result, vaccine‐preventable illnesses continue to be a cause of morbidity and mortality in many LMICs. To avoid VPD epidemics, prompt and high vaccination coverage devoid of inequalities is critical as herd immunity occurs from an under‐vaccinated and vulnerable population. 18
Inequality refers to the observed differences in coverage between different populations. Measuring and tracking these disparities might aid in the development of health treatments that give priority to the most vulnerable groups. 19 In countries like Benin, it is reported that the achievement of full vaccination among infants remains a challenge due to inadequate maternal healthcare utilization 20 possibly due to sociodemographic and socioeconomic inequalities and other factors. The study further reports religion, level of education, wealth, and place of residence as significant factors impeding full vaccination among infants. In another study, inequality in zero‐dose children was reported to be highest in Benin in a cohort of 25 Sub‐Saharan African countries. 13 However, there exists scant information on trends and determinants of inequalities associated with access to childhood vaccination among Beninese. Thus, the factors impeding full vaccination in Benin need to be explored.
A study of 21 national surveys conducted between 2000 and 2013 found that diphtheria−pertussis−tetanus vaccination coverage decreased with time in four countries, including Benin, however these analyses did not explore the influence of family wealth. 17 To this end, this study examined the pattern of wealth and residence‐based related inequality in vaccination coverage through an equity lens, focusing on the direction of inequality in vaccination coverage in Benin, using nationally‐representative data. The study also assesses the factors influencing the enormous socioeconomic and sociodemographic disparities in child vaccination coverage among Beninese. The findings of the present study would aid policymakers in developing equity‐focused vaccination strategies. This might also explain why some vaccination initiatives are more or less effective in reducing inequality in various circumstances.
2. METHODOLOGY
2.1. Data source and study design
Data for this study were obtained from the 2017−2018 Benin Demographic and Health Survey (BDHS). Specifically, the study used the individual record files of the DHS. BDHS is part of several surveys obtained from the MEASURE DHS Program, which contain information on several issues on population, health, and nutrition including childhood vaccination. The DHS is a comparatively nationally representative survey conducted in over 85 LMICs worldwide. DHS employed a descriptive cross‐sectional design. The survey adopted a two‐stage sampling design. The first stage was characterized by the selection of clusters across urban and rural locations from the entire nation. These constituted the enumeration areas for the study. The second stage involved the selection of households from the predefined clusters. Details of the methodologies employed in the various rounds of the surveys can be found in the final reports (National Institute of Statistics and Economic Analysis INSAE and ICF, 2019). Standardized structured questionnaires were used to collect data from the respondents on health indicators including vaccination. We included a total of 1993 children of married and cohabiting women. However, for size of the child at birth, there were 28 missing observations, resulting in a sample size of 1965 for that variable. The data set used is freely available upon request (https://dhsprogram.com/data/available-datasets.cfm). This manuscript was drafted with reference to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement guidelines.
2.1.1. Outcome variable
The study used complete vaccination as the outcome variable. In this study, complete and full vaccination coverage are used interchangeably. The information on vaccination coverage was collected from either vaccination cards or from mothers' verbal responses to these questions “Did (NAME) ever receive vaccination against Measles?,” “Did (NAME) ever receive vaccination against Polio?,” “Did (NAME) ever receive vaccination against BCG?,” and “Did (NAME) ever receive vaccination against DPT?.” Responses were “Yes,” “No,” and “Don't Know.” These were coded as “No” = 0, “Yes” = 1. For the purpose of the analysis, only women who provided definite responses (either “Yes” or “No”) were included in the study. According to the WHO guideline (2017), “complete or full vaccination” coverage is defined as a child that has received one dose of BCG, three doses of pentavalent, PCV, oral polio vaccines; two doses of Rotavirus and one dose of measles vaccine. We recoded each variable (vaccinations) as “0” and “1” for children who didn't take the recommended doses and those who took them, respectively. The complete vaccination was obtained by creating a dichotomous variable which comprised all the vaccines administered. To provide a binary outcome (model 1), the two responses were coded as follows: “Incomplete” = 0 and “Complete” = 1.”
For further analyses, we used a composite measure as a proxy for the vaccination scheme for robustness checks. Therefore, a composite index of vaccination (Model 2) of vaccination captures the level of vaccination coverage through a score or index. The principal component analysis (PCA) approach contributed to reducing the number of variables related to vaccination (eight dimensions) into a single. The first component of the PCA was related to the vaccination score given all different variables related to vaccination are highly correlated. Low values stand for individuals with a lower level of vaccination, whereas the highest value represents participants with a high vaccination. The Varimax rotation is used to maximize the variances of the sum of the loading. In the paper, we only retained the first component given that that axis exceeded 75% of the total explained intertia (Supporting Information: Files 1 and 2).
2.1.2. Explanatory variables
Wealth index and place of residence were the measures of inequality in this study. In the DHS, the wealth index is constructed using household assets and ownership through PCA as described in detail here and is comparable across all the survey years. The wealth index includes five quintiles (poorest, poorer, middle, richer, richest), where the first quintile stands for the less wealthy respondents. Place of residence is a description of an individual's geographical area and is grouped into urban and rural.
According to the literature related to vaccination, this study used 17 explanatory variables. These variables were the size of the child at birth, twin status, type of delivery, sex of the child, number of antenatal care attendance, postnatal care attendance, distance to the health facility, place of delivery, mother's age, marital status, employment status, exposure to mass media, ethnicity, number of live births, mother's education, partner's education, and religious affiliation. We performed the stepwise backward selection to investigate the variables most pertinent and associated with the vaccination. Afterwards, the most pertinent variables were retained for the final modeling.
2.2. Statistical and econometric analysis
We analyzed the data using Stata version 17. First, we presented the descriptive statistics of the vaccination across individual characteristics (Table 1). Second, using econometrics modeling, we examined the association between the measures of inequality, explanatory variables, and childhood vaccination (Equation 1). We applied the sample weights to obtain unbiased estimates according to the DHS guidelines. Also, the Stata survey command “svy” was used to adjust for the complex sampling structure of the data in the regression analyses.
(1) |
Where, represents the outcome variable; represents the residence area of the respondent (Urban/rural). variable is related to the five quintiles of the income category of the respondent. is related to the other explanatory variables; refers to the parameter estimate by the model. is the error term.
Table 1.
Vaccination coverage | |||||||
---|---|---|---|---|---|---|---|
Did not receive the full vaccination coverage (N = 859) | Received the full vaccination coverage (N = 1134) | Included population (N = 1993) | |||||
Frequency | Percentage | Frequency | Percentage | Frequency | Percentage | ||
Wealth | |||||||
Poorest | 249 | 29.0 | 189 | 16.7 | 438 | 22.0 | |
Poorer | 180 | 21.0 | 202 | 17.8 | 382 | 19.1 | |
Middle | 174 | 20.3 | 278 | 24.5 | 452 | 22.7 | |
Richer | 139 | 16.2 | 238 | 21.0 | 377 | 18.9 | |
Richest | 117 | 13.5 | 227 | 20.0 | 344 | 17.3 | |
Residence | |||||||
Urban | 286 | 33.3 | 455 | 40.1 | 741 | 37.2 | |
Rural | 573 | 66.7 | 679 | 59.9 | 1252 | 62.8 | |
Size of child at birth | |||||||
Larger than average | 237 | 28.1 | 323 | 28.8 | 560 | 28.5 | |
Average | 483 | 57.3 | 651 | 58.0 | 1134 | 57.7 | |
Smaller than average | 123 | 14.6 | 148 | 13.2 | 271 | 13.8 | |
Twin status | |||||||
Single birth | 850 | 99.0 | 1.101 | 97.1 | 1951 | 97.9 | |
Multiple birth | 9 | 1.0 | 33 | 2.9 | 42 | 2.1 | |
Type of delivery | |||||||
Vaginal birth | 825 | 96.0 | 1.068 | 94.2 | 1.893 | 95.0 | |
Cesarean birth | 34 | 4.0 | 66 | 5.8 | 100 | 5.0 | |
Gender | |||||||
Female | 458 | 53.3 | 539 | 47.5 | 997 | 50.0 | |
Male | 401 | 46.7 | 595 | 52.5 | 996 | 50.0 | |
Number of ANC visits | |||||||
Zero | 214 | 24.9 | 46 | 4.1 | 260 | 13.0 | |
One to three | 282 | 32.8 | 429 | 37.8 | 711 | 35.7 | |
Four+ | 363 | 42.3 | 659 | 58.1 | 1.022 | 51.3 | |
PNC attendance | |||||||
No | 695 | 80.9 | 882 | 77.8 | 1.577 | 79.1 | |
Yes | 164 | 19.1 | 252 | 22.2 | 416 | 20.9 | |
Distance to HF | |||||||
Not a big problem | 512 | 59.6 | 760 | 67.0 | 1.272 | 63.8 | |
Big problem | 347 | 40.4 | 374 | 33.0 | 721 | 36.2 | |
Place of delivery | |||||||
Home | 215 | 25.0 | 71 | 6.3 | 286 | 14.4 | |
Health facility | 644 | 75.0 | 1.063 | 93.7 | 1.707 | 85.6 | |
Mother's age | |||||||
15−19 | 49 | 5.7 | 49 | 4.3 | 98 | 4.9 | |
20−24 | 202 | 23.5 | 275 | 24.3 | 477 | 23.9 | |
25−29 | 270 | 31.4 | 377 | 33.2 | 647 | 32.5 | |
30−34 | 181 | 21.1 | 221 | 19.5 | 402 | 20.2 | |
35−39 | 105 | 12.2 | 148 | 13.1 | 253 | 12.7 | |
40−44 | 33 | 3.8 | 41 | 3.6 | 74 | 3.7 | |
45−49 | 19 | 2.3 | 23 | 2.0 | 42 | 2.1 | |
Marital status | |||||||
Married | 699 | 81.4 | 866 | 76.4 | 1.565 | 78.5 | |
Cohabiting | 160 | 18.6 | 268 | 23.6 | 428 | 21.5 | |
Employment status | |||||||
Not working | 183 | 21.3 | 170 | 15.0 | 353 | 17.7 | |
Working | 676 | 78.7 | 964 | 85.0 | 1.640 | 82.3 | |
Exposure to mass media | |||||||
Not exposed | 377 | 43.9 | 398 | 35.1 | 775 | 38.9 | |
Exposed | 482 | 56.1 | 736 | 64.9 | 1.218 | 61.1 | |
Ethnicity | |||||||
Adja and related | 115 | 13.4 | 142 | 12.5 | 257 | 12.9 | |
Bariba and related | 116 | 13.5 | 144 | 12.7 | 260 | 13.0 | |
Dendi and related | 54 | 6.3 | 64 | 5.6 | 118 | 5.9 | |
Fon and related | 240 | 27.9 | 447 | 39.4 | 687 | 34.5 | |
Yoa, lokpa and related | 25 | 2.9 | 40 | 3.5 | 65 | 3.3 | |
Betamaribe and related | 39 | 4.5 | 103 | 9.1 | 142 | 7.1 | |
Peulh and related | 168 | 19.6 | 81 | 7.1 | 249 | 12.5 | |
Yoruba and related | 102 | 11.9 | 113 | 10.1 | 215 | 10.8 | |
Number of live births | |||||||
One birth | 165 | 19.2 | 231 | 20.3 | 396 | 19.9 | |
Two births | 151 | 17.6 | 223 | 19.7 | 374 | 18.8 | |
Three births | 145 | 16.9 | 197 | 17.4 | 342 | 17.2 | |
Four+ | 398 | 46.3 | 483 | 42.6 | 881 | 44.1 | |
Mother education | |||||||
No education | 633 | 73.7 | 675 | 59.5 | 1.308 | 65.6 | |
Primary | 127 | 14.8 | 242 | 21.3 | 369 | 18.5 | |
Secondary+ | 99 | 11.5 | 217 | 19.2 | 316 | 15.9 | |
Partner education | |||||||
No education | 549 | 63.9 | 564 | 49.7 | 1.113 | 55.8 | |
Primary | 143 | 16.6 | 242 | 21.3 | 385 | 19.3 | |
Secondary+ | 167 | 19.5 | 328 | 29.0 | 495 | 24.9 | |
Religious affiliation | |||||||
Christianity | 349 | 40.6 | 626 | 55.2 | 975 | 48.9 | |
Islam | 354 | 41.2 | 309 | 27.2 | 663 | 33.3 | |
Other | 156 | 18.2 | 199 | 17.6 | 355 | 17.8 |
2.3. Measures of inequality
To estimate wealth inequalities in childhood vaccination, a concentration index, concentration curve (CC), and decomposition analysis, which represent the degree of inequality were employed. The CC was obtained by plotting the cumulative proportion of childhood vaccination on the y‐axis against the increasing percentage of the population ranked by the socioeconomic wealth index on the x‐axis. The curves show whether the wealth‐related inequality in childhood vaccination (on the x‐axis) prevails or not. If the curve is above the line of equality (45‐degree line), that means the index value is negative; hence it shows that childhood vaccination is disproportionally concentrated among the poor and vice‐versa. The concentration index measures the inequality of one variable (childhood vaccination) over the distribution of another variable (wealth index). The index ranges from −1 to +1, where the index value of 0 (zero) shows no socioeconomic inequality. Additionally, on either scale, the higher the value, the higher the extent of socioeconomic inequality. The study used Wagstaff decomposition analysis to decompose the concentration index. Wagstaff's decomposition demonstrated that the concentration index could be decomposed into the contributions of each factor to the wealth‐related inequalities. The results of the decomposition method were reported using elasticity, concentration index value, absolute contribution, and relative contribution. Elasticity refers to the change in the childhood vaccination that results from a one‐unit change in the explanatory variables. A positive or negative sign in the elasticity shows an increasing or decreasing trend in childhood vaccination due to a positive change in the explanatory variables. The distribution of the determinants in relation to the wealth quintiles is described using the concentration index values. A positive or negative concentration index value denotes whether childhood vaccination is more concentrated in rich or poor households. The percentage contribution indicates the relative contribution of each model component to the overall wealth‐related inequality in childhood vaccination. The observed wealth‐related inequality in childhood vaccination is increased by variables with positive percentage contributions and decreased by variables with a negative percentage contribution. 21
A multivariate nonlinear decomposition approach was used for the residence‐based inequality. In social science, it is common practice to quantify the contributions to group differences in the average predictions from multivariate models using a multivariate decomposition analysis. The method divides the components of a group difference in a statistic, such as a mean or proportion, into a component attributable to compositional differences between groups (i.e., differences in characteristics or endowments), and a component attributable to differences in the effects of characteristics. This technique was used to assess the variations in childhood vaccination between rural and urban women and identify how much each of the explanatory variables contributes to the variation. 22
3. RESULTS
3.1. Descriptive statistics
Table 1 shows that more than half of the children had average size at birth (57.7%). At least, 9 out of 10 were twins (97.9%) and were born vaginally (95.0%). Male and female children were equally represented (50.0%). More than half of the women had 4 or more ANC visits (51.3%) and 79.1% had no PNC. For 63.8% of the mothers, distance to health facilities was not a big problem and 85.6% gave birth in health facilities. About 3 out of 10 of the mothers were aged 25−29 (32.5%) and 78.5% were married. We noted that 82.3% were employed, 61.1% had media exposure, and 22.0% were poorest. Those belonging to Adja and related ethnicity constituted 12.9%. A significant proportion of the mothers had 4 or more live births (44.1%), no education (65.6%), had partners without formal education (55.8%), and were Christians (48.9%).
On the prevalence of childhood vaccination, it was evident that 58.0% of children who were larger than average at birth were vaccinated. Similarly, vaccination was profound among children who were products of single birth (91.1%) and those who were born through vaginal birth (94.2%). The analysis showed that 52.5% of male children, a greater proportion of those whose mothers had 4 or more ANC visits (58.1%) as well as those who had no PNC (77.8%) received the vaccination. Childhood vaccination dominated among children whose mothers reported that distance to the health facility was not a big problem (67.0%), children born in health facilities (93.7%), and children whose mothers were aged 25−29 (33.2%). In the same vein, vaccination was high among children of married women (76.4%), children whose mothers were working (85.0%), those whose mothers had media exposure (64.9%), and children of the richest women (20.0%). We also observed high vaccination among children of Fon and related ethnicity (39.4%), those whose mothers reported 4 births (42.6%) and were not educated (59.5%) as well as children of Christian women (55.2%).
3.2. Econometrics analyses of childhood vaccination among children
This section reports the significant findings from the adjusted model as shown in Table 2. Findings show that wealth is positively and significantly associated with vaccination coverage. Particularly, being a middle‐wealth household increased by 45% the access to vaccination (p < 0.01). Ethnicity was statistically associated with the vaccination for Bariba and related (p < 0.05), Fon and related (p < 0.01), and Betamaribe and related (p < 0.01). Women with multiple births were more likely to receive vaccination coverage (p < 0.01). A secondary or higher education level of women and partners increased the vaccination compared to not educated (p < 0.05). Women with more antenatal visits (4+) induced and increased children vaccination coverage (p < 0.01). PNC attendance was more likely to significantly increase children's vaccination (p < 0.01). The place of delivery for women (health facility) was significantly associated with vaccination coverage (p < 0.01).
Table 2.
(1) | (2) | |
---|---|---|
Variables | Model 1 | Model 2 |
Residence—rural | −0.075 | −0.099 |
(0.070) | (0.109) | |
Wealth—poorest | Ref. | Ref. |
Poorer | 0.055 | 0.192 |
(0.098) | (0.152) | |
Middle | 0.200** | 0.455*** |
(0.098) | (0.152) | |
Richer | 0.152 | 0.379** |
(0.106) | (0.166) | |
Richest | 0.073 | 0.362* |
(0.125) | (0.197) | |
Ethnicity—Adja and related | Ref. | Ref. |
Bariba and related | 0.189 | 0.387** |
(0.119) | (0.190) | |
Dendi and related | 0.138 | 0.101 |
(0.150) | (0.238) | |
Fon and related | 0.201** | 0.291* |
(0.096) | (0.154) | |
Yoa, lokpa, and related | 0.285 | 0.454 |
(0.185) | (0.290) | |
Betamaribe and related | 0.808*** | 0.853*** |
(0.149) | (0.223) | |
Peulh and related | 0.158 | −0.082 |
(0.137) | (0.212) | |
Yoruba and related | 0.003 | −0.204 |
(0.120) | (0.193) | |
Twin status—multiple birth | 0.641*** | 0.704** |
(0.224) | (0.323) | |
Mother's education—not educated | Ref. | Ref. |
Primary | 0.200** | 0.247* |
(0.084) | (0.133) | |
Secondary+ | 0.236** | 0.491*** |
(0.099) | (0.157) | |
Partner's education—not educated | Ref. | Ref. |
Primary | 0.105 | 0.290** |
(0.086) | (0.135) | |
Secondary+ | 0.086 | 0.327** |
(0.091) | (0.143) | |
ANC—zero visit | Ref. | Ref. |
One to three | 0.894*** | 2.348*** |
(0.118) | (0.178) | |
Four+ | 0.940*** | 2.445*** |
(0.119) | (0.181) | |
PNC attendance—yes | 0.003 | 0.357*** |
(0.074) | (0.116) | |
Distance to HF—big problem | 0.002 | 0.158 |
(0.066) | (0.104) | |
Place of delivery—health facility | 0.513*** | 1.648*** |
(0.110) | (0.168) | |
Constant | −1.960*** | −6.031*** |
(0.228) | (0.332) | |
N of observations | 1,993 | 1, 993 |
R 2 | 0.69a | 0.343 |
Note: This table contains findings after stepwise backward selection. Model 1 is the logistic model with the vaccination variable as a binary outcome. Model 2 (linear model) presents the findings of the secondary analyses with the composite index of vaccination. Standard errors in parentheses; Source: Authors based on the 2017−2018 Benin Demographic and Health Survey (BDHS).
Stands for the area under‐curve (AUC), indicating a good quality of the model.
p < 0.1
p < 0.05
p < 0.01.
3.3. Inequality analyses
3.3.1. Inequality in childhood vaccination by wealth quintile
As evidenced in Figure 1, childhood vaccination increased with wealth status, such that each increment in wealth status was associated with an increment in the proportion of children who had a vaccination. Clearly, whilst 66% of children from the richest households were vaccinated, less than half of those in the poorest wealth quintile (43%) were vaccinated.
In Figure 2, we presented the pictorial overview of the inequality in childhood vaccination by wealth quintile and place of residence using the CC. The straight diagonal line in red color depicts equality (i.e., equality line). The area around the equality line stands for the CC. The wider the gap between these two lines (green and yellow), the wider the disparity in childhood vaccination in favor of children from rich households. Therefore, the figure shows a higher concentration of childhood vaccination among the rich according to the residential areas. This means that children from the richest households in the urban area are more likely to benefit from vaccination compared with the poor living in the rural areas. The findings in Figure 2 confirms the positive concentration index among the richest (0.829) as shown in Table 3, thereby emphasizing higher concentration in childhood vaccination among children from rich households.
Table 3.
Variables | Elasticity | Concentration index | Absolute contribution | Percentage contribution | |
---|---|---|---|---|---|
Wealth index—poorest | |||||
Poorer | 0.0196 | −0.383 | −0.0075 | 1.97 | |
Middle | 0.072 | 0.0429 | 0.003 | 7.22 | |
Richer | 0.054 | 0.468 | 0.025 | 5.48 | |
Richest | 0.034 | 0.829 | 0.028 | 3.38 | |
Ethnicity—Adja and related | |||||
Bariba and related | 0.036 | −0.144 | −0.0053 | 3.68 | |
Dendi and related | 0.015 | −0.0127 | −0.0002 | 1.55 | |
Fon and related | 0.109 | 0.223 | 0.0243 | 10.92 | |
Yoa, loka, and related | 0.0122 | −0.008 | −0.0001 | 1.22 | |
Betamaribe and related | 0.067 | −0.324 | −0.021 | 6.75 | |
Peulh and related | 0.0110 | −0.536 | −0.0059 | 1.11 | |
Yoruba and related | 0.001 | 0.1703 | 0.0002 | 0.14 | |
Twin status—single birth | |||||
Multiple birth | 0.020 | −0.0642 | −0.0013 | 2.029 | |
Mother's educational level—no education | |||||
Primary | 0.052 | 0.205 | 0.010 | 5.1895 | |
Secondary/higher | 0.0528 | 0.4650 | 0.0245 | 5.280 | |
Partners educational level—no education | |||||
Primary | 0.037 | 0.138 | 0.005 | 3.72 | |
Secondary/higher | 0.04 | 0.396 | 0.0169 | 4.26 | |
Number of ANC visits—zero | |||||
One to three | 0.523 | −0.088 | −0.046 | 52.34 | |
Four+ | 0.833 | 0.148 | 0.123 | 83.36 | |
PNC attendance—yes | −0.003 | 0.121 | −0.0004 | −0.355 | |
Distance to health facility—big problem | −0.009 | −0.204 | 0.001 | −0.9516 |
3.3.2. Contribution of sociodemographic characteristics based on the decomposition of concentration index analysis for childhood vaccination
Table 3 shows the results of the decomposition analysis on the contribution of children and maternal sociodemographic characteristics toward the inequality in childhood vaccination. We presented the findings through concentration index (absolute) and adjusted percentage contribution of inequality (percentage contribution) as shown in Table 3. It was evident that concentration in childhood vaccination disfavored children from the poorest households, ethnicity (Bariba, Dendi, Yoa, loka, Betamaribe, Peulh, and related), children whose mothers had multiple births, mothers that reported one to three ANC visits, and for mothers experiencing big problem with the distance to the health facility.
3.3.3. Results of the residence‐based decomposition analysis
In Table 4, we presented the findings from the decomposition analysis as well as the contribution of the sociodemographic characteristics in relation to the inequality in childhood vaccination. The overall rural‐urban inequality attributable to variation in childhood and maternal characteristics represented 25.9% (and 74.1% for the difference due to the coefficient). The factors that contributed significantly toward this variation included Richer (6%), mother's education level (12%), partner's education level (11%), and four or more ANC visits (25%).
Table 4.
Variables | Difference dues to characteristics (E) | Difference dues to coefficient (C) | |||
---|---|---|---|---|---|
Coefficient | % | Coefficient | % | ||
Wealth index | |||||
Poorest | −0.004 | 4.770 | −0.010 | 13.320 | |
Poorer | −0.001 | 1.940 | 0.001 | −1.620 | |
Middle | 0.008* | −10.270 | 0.002 | −2.080 | |
Richer | −0.004** | 6.030 | 0.022** | −29.630 | |
Richest | 0.018 | −24.570 | −0.025 | 33.060 | |
Ethnicity | |||||
Adja and related | 0.001** | −1.400 | −0.002 | 2.620 | |
Bariba and related | 0.000 | −0.390 | −0.012 | 15.740 | |
Dendi and related | 0.005** | −6.770 | −0.023*** | 30.800 | |
Fon and related | −0.004 | 4.920 | 0.026 | −35.400 | |
Yoa, loka, and related | 0.000 | −0.640 | 0.007** | −8.880 | |
Betamaribe and related | 0.007*** | −9.410 | 0.002 | −3.090 | |
Peulh and related | −0.003 | 3.460 | 0.003 | −3.380 | |
Yoruba and related | −0.001 | 1.870 | 0.002 | −2.350 | |
Twin status | |||||
Single birth | 0.001** | −1.680 | 0.002 | −2.680 | |
Multiple birth | 0.001** | −1.680 | −0.000 | 0.040 | |
Mother's educational level | |||||
No education | −0.009* | 11.470 | 0.013 | −16.940 | |
Primary | −0.002 | 2.900 | 0.008 | −11.210 | |
Secondary/higher | −0.001 | 0.990 | −0.015 | 20.560 | |
Partners educational level | |||||
No education | −0.008* | 10.980 | −0.010 | 13.960 | |
Primary | −0.000 | 0.420 | 0.009 | −11.430 | |
Secondary/higher | −0.001 | 1.590 | −0.007 | 8.930 | |
Number of ANC visits | |||||
Zero | −0.014*** | 18.290 | −0.000 | 0.350 | |
One to three | 0.008*** | −10.710 | −0.007 | 9.940 | |
Four+ | −0.019*** | 25.390 | 0.016 | −21.220 | |
PNC attendance | |||||
No | 0.001 | −1.210 | 0.022 | −29.510 | |
Yes | 0.001 | −1.210 | −0.007 | 9.570 | |
Distance to health facility | |||||
Big problem | −0.000 | 0.420 | 0.001 | −0.740 | |
Not a big problem | −0.000 | 0.420 | −0.000 | 0.310 | |
% Total explained disparity | −0.019 | 25.90 | −0.055* | 74.10 |
Note: Source: Authors based on the 2017−2018 Benin Demographic and Health Survey (BDHS).
p < 0.1
p < 0.05
p < 0.01.
4. DISCUSSION
This study investigated the level and determinants of vaccination coverage in Benin and provides evidence of wealth and residence‐based inequalities in vaccination coverage. The findings of the present study highlights important issues worth the needed attention in the implementation of vaccination programs in Benin and other places in the world. Although child vaccination remains an important initiative in preventing many diseases, its implementation and success had been hampered by some sociodemographic and socioeconomic factors. 19 As a result, many LMICs continue to experience health‐related consequences due to vaccine‐preventable illnesses. 23
The level of vaccination coverage varies between countries and even within the same country and may be related to varying factors. 13 , 14 The present study showed that in 2018, approximately 58% of children were reported to have received full vaccination in Benin. 13 Full vaccine coverage reported in the present study was similar to a pooled prevalence of 59.40% in 9 Sub‐Saharan African countries 24 and reflects the generally low vaccine coverage in the region. Recent studies have reported full childhood vaccination coverage of 33.3% in Ethiopia, 25 45.3% in DR Congo, 26 70.96% in Senegal, 27 and 79.4% in Kenya. 28 Differences in vaccination coverage as observed between Benin and other countries may be a result of differences in vaccine uptake policies, sociodemographic and economic factors, individual beliefs, vaccine education, and access to vaccination services. 13 , 29 , 30
Even among the same population of Beninese, we observed disparities in vaccination, and these were associated with several factors. The findings show the presence of significant poor−rich, educated‐uneducated, among other differences in the probability of a child being fully vaccinated in Benin. We observed that vaccination coverage was associated with ANC visits, PNC attendance, deliveries in health facilities, and mother's wealth similar to that observed in other studies. 31 , 32 Particularly, the results showed that when compared to children born to mothers in the poorest wealth index, children born to mothers in the richest wealth index are about 40% more likely to receive full vaccination. Similar to the present observation, child vaccination is reported to be high among children born to rich mothers in Ghana 33 and many African countries. 13 Contrary to the report of decreased vaccination among children to highly educated mothers, children born to mothers who are highly educated are likely to be fully vaccinated in Ghana. 33 In India, compared to children born to mothers with no education, children born to mothers with higher education had 2.3 times the odds of being fully vaccinated. 34 This may be attributed to health knowledge of maternal education and vaccination and enhanced health seeking behavior. 34 , 35 Maternal education generally has a significant effect on improved child health. 36 , 37 These findings point to the need for complementary initiatives to enhance care usage across the care continuum, from reproductive health services to childhood and adolescence.
Socioeconomic inequalities in childhood vaccination seem to be a great challenge in achieving increased vaccine coverage in LMICs. Through concentration indices (C n) and decomposition analysis, we determined levels and determinants of inequalities in vaccination coverage at Benin. Vaccination coverage is pro‐rich in most LMICs. Particularly, in countries such as Nigeria (C n = 0.547), Pakistan (C n = 0.384), Yemen (C n = 0.34), Cambodia (C n = 0.296), and Cameroon (C n = 0.273), the situation is reported to be worse. 38 In Benin, we report an even more higher concentration index of 0.8265 among children from rich homes emphasizing higher concentration in childhood vaccination among children of the rich. This is about ninefolds increase over the C n of 0.091 from 2010 to 2015 Demographic and Health Survey data. 38 On the contrary, in some LMICs such as Gambia (C n = −0.101), the Kyrgyz Republic (C n = −0.097), and Namibia (C n = −0.161), vaccination in favor of those with lower socioeconomic status is reported. 39 These findings suggest that socioeconomic inequality in childhood vaccination is a huge problem in Benin and demands strategic interventions to curtail it. These disparities may be explained by differences in vaccine policies among these populations. For instance, the pro‐poor nature of vaccination in Gambia, the Kyrgyz Republic, and Namibia is attributed to the increased concentration of vaccination in rural compared to urban settings. 39 , 40 Reduced vaccination on the part of the poor may be a result of negative attitudes toward vaccination, remote settlement impeding vaccine access, and limited freedom in decision‐making. 21 Poor−rich inequalities in maternity care exist in most developing countries 22 and this could invariably contribute to wealth‐related inequality observed in this study.
The reasons for under‐ and non‐vaccination may be complex and dependent on many factors. Results from the decomposition analysis suggest that a substantial proportion of the disparities observed in this study may be explained by single birth, falling within the richest wealth quintile, having a mother without formal education, lack of education of the partner, and ANC visits. The majority of the determinants of inequality in vaccination coverage observed in this study may be described and understood using the Socioeconomic Determinants of Health (SDH) report. 41 These have also been recognized in a study conducted by Wiysonge, Uthman 42 to explain low child vaccination coverage in Sub‐Saharan Africa. This means that addressing the SDHs ‐ distribution of power, income, products, and services, as well as people's living conditions, such as access to healthcare, schools and education, working and leisure conditions, and the status of their home and surroundings would lead to significant improvements in vaccination coverage and reduce inequalities associated with it. 41 , 43
It is worth noting that achieving equality in child vaccination coverage is possible. In 2014, Vietnam achieved vaccination coverage among the rich and poor in almost equal coverage (C n = 0.009) and this was achieved by increased disbursement of Expanded Program on Immunization staff across all areas of the country to ensure complete free vaccination for both the rich and the poor. 21 In addition, vaccine coverage with little or no inequality was demonstrated by South Africa in 2016, Ghana in 2014, Burundi in 2016/2017, and Uganda in 2016 through increased vaccination coverage. 13
Our paper used nationally representative data; however, some limitations were identified through the analysis. First, the study is based on cross‐sectional data where the vaccination scheme did not capture how children have received different vaccines over a certain period. Second, the analysis did not permit us to draw evidence on how full vaccination coverage has contributed to reducing child and maternal mortality in the country. Further studies may investigate the value for money of vaccination programs in the country to adjust the coverage to support regions in need and reduce persisting inequalities. Researchers could also investigate the number of lives saved or deaths averted during the implementation of vaccination programs for vulnerable groups, especially children and women.
5. CONCLUSIONS
Inequality in childhood vaccination which is greatly driven by socioeconomic and sociodemographic variables as noted in Benin, is a cause for health policy concern. Policies aimed to improve child vaccination coverage among mothers in Benin may recognize these inequalities in vaccination coverage. Strategies such as increased availability and accessibility of vaccination as well as improved maternal education, and attention to the less privileged groups could be targeted to address this issue of concern.
AUTHOR CONTRIBUTIONS
Eugene Budu: Data curation; formal analysis; writing—original draft; writing—review & editing. Bright O. Ahinkorah: Formal analysis; investigation; validation; visualization; writing—original draft; writing—review & editing. Wilfried Guets: Formal analysis; methodology; writing—review & editing. Edward K. Ameyaw: Investigation; writing—review & editing. Mainprice A. Essuman: Investigation; writing—original draft. Sanni Yaya: Conceptualization; data curation; formal analysis; funding acquisition; investigation; methodology; project administration; resources; supervision; validation; visualization; writing—review & editing.
CONFLICT OF INTEREST STATEMENT
The authors declare no conflict of interest.
ETHICS STATEMENT
This was a secondary analysis of data and therefore no further approval was required since the data is available in the public domain. However, we sought for permission to use the data from MEASUREDHS. Further information about the DHS data usage and ethical standards is available at https://goo.gl/ny8T6X.
TRANSPARENCY STATEMENT
The lead author Sanni Yaya affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.
Supporting information
ACKNOWLEDGMENTS
The authors thank the MEASURE DHS project for their support and for free access to the original data.
Budu E, Ahinkorah BO, Guets W, Ameyaw EK, Essuman MA, Yaya S. Socioeconomic and residence‐based related inequality in childhood vaccination in Sub‐Saharan Africa: evidence from Benin. Health Sci Rep. 2023;6:e1198. 10.1002/hsr2.1198
DATA AVAILABILITY STATEMENT
The data sets generated and/or analyzed during the current study are available in DHS Program—available data sets (83).
REFERENCES
- 1. Wicker S, Maltezou HC. Vaccine‐preventable diseases in Europe: where do we stand? Expert Rev Vaccines. 2014;13(8):979‐987. [DOI] [PubMed] [Google Scholar]
- 2. Cata‐Preta BO, Santos TM, Mengistu T, Hogan DR, Barros AJD, Victora CG. Zero‐dose children and the immunisation cascade: understanding immunisation pathways in low and middle‐income countries. Vaccine. 2021;39(32):4564‐4570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Rémy V, Zöllner Y, Heckmann U. Vaccination: the cornerstone of an efficient healthcare system. J Mark Access Health Policy. 2015;3(1):27041. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Koppaka R. Ten great public health achievements—worldwide, 2001−2010. 2011.
- 5. Van Panhuis WG, Grefenstette J, Jung SY, et al. Contagious diseases in the United States from 1888 to the present. N Engl J Med. 2013;369:2152‐2158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Roush SW. Historical comparisons of morbidity and mortality for vaccine‐preventable diseases in the United States. JAMA. 2007;298(18):2155‐2163. [DOI] [PubMed] [Google Scholar]
- 7. Agossou J, Ebruke C, Noudamadjo A, et al. Declines in pediatric bacterial meningitis in the Republic of Benin following introduction of pneumococcal conjugate vaccine: epidemiological and etiological findings, 2011–2016. Clin Infect Dis. 2019;69(suppl ment_2):S140‐S147. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. VanderEnde K, Gacic‐Dobo M, Diallo MS, Conklin LM, Wallace AS. Global routine vaccination coverage—2017. MMWR Morb Mortal Wkly Rep. 2018;67(45):1261‐1264. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Cata‐Preta BO, Wehrmeister FC, Santos TM, Barros AJD, Victora CG. Patterns in wealth‐related inequalities in 86 low‐ and middle‐income countries: global evidence on the emergence of vaccine hesitancy. Am J Prev Med. 2021; 60(1, supplment 1):S24‐S33. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Bosch‐Capblanch X, Banerjee K, Burton A. Unvaccinated children in years of increasing coverage: how many and who are they? Evidence from 96 low‐and middle‐income countries. Tropical Me Int Health: TM & IH. 2012;17(6):697‐710. [DOI] [PubMed] [Google Scholar]
- 11. Kramarz P, Lopalco PL, Huitric E, Pastore Celentano L. Vaccine‐preventable diseases: the role of the European Centre for Disease Prevention and Control. Clin Microbiol Infect. 2014;20:2‐6. [DOI] [PubMed] [Google Scholar]
- 12. Kazungu JS, Adetifa IMO. Crude childhood vaccination coverage in West Africa: trends and predictors of completeness. Wellcome Open Res. 2017;2:12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Bobo FT, Asante A, Woldie M, Dawson A, Hayen A. Child vaccination in sub‐Saharan Africa: increasing coverage addresses inequalities. Vaccine. 2022;40(1):141‐150. [DOI] [PubMed] [Google Scholar]
- 14. Cata‐Preta BO, Wehrmeister FC, Santos TM, Barros AJD, Victora CG. Patterns in wealth‐related inequalities in 86 low‐and middle‐income countries: global evidence on the emergence of vaccine hesitancy. Am J Prev Med. 2021;60(1):S24‐S33. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. World Health Organization. State of Inequality: reproductive Maternal Newborn and Child Health: interactive Visualization of Health Data. World Health Organization; 2015. [Google Scholar]
- 16. World Health Organization . World Health Statistics 2016: monitoring Health for the SDGs Sustainable Development Goals. World Health Organization; 2016. [Google Scholar]
- 17. Hosseinpoor AR, Bergen N, Schlotheuber A, et al. State of inequality in diphtheria‐tetanus‐pertussis immunisation coverage in low‐income and middle‐income countries: a multicountry study of household health surveys. Lancet Global Health. 2016;4(9):e617‐e626. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Park Y‐J, Eom HS, Kim ES, Choe YJ, Bae GR, Lee DH. Reemergence of measles in South Korea: implications for immunization and surveillance programs. Jpn J Infect Dis. 2013;66(1):6‐10. [DOI] [PubMed] [Google Scholar]
- 19. Donfouet HPP, Agesa G, Mutua MK. Trends of inequalities in childhood immunization coverage among children aged 12‐23 months in Kenya, Ghana, and Côte d'Ivoire. BMC Public Health. 2019;19(1):988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Budu E, Seidu AA, Agbaglo E, et al. Maternal healthcare utilization and full immunization coverage among 12–23 months children in Benin: a cross sectional study using population‐based data. Arch Public Health. 2021;79(1):34. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Vo H‐L, Huynh LTB, Anh HNS, et al. Trends in socioeconomic inequalities in full vaccination coverage among Vietnamese children aged 12–23 months, 2000–2014: evidence for mitigating disparities in vaccination. Vaccines. 2019;7(4):188. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Houweling TA, Ronsmans C, Campbell OM, Kunst AE. Huge poor‐rich inequalities in maternity care: an international comparative study of maternity and child care in developing countries. Bull World Health Organ. 2007;85(10):745‐754. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Li Z, Hsiao Y, Godwin J, Martin BD, Wakefield J, Clark SJ. Changes in the spatial distribution of the under‐five mortality rate: small‐area analysis of 122 DHS surveys in 262 subregions of 35 countries in Africa. PLoS One. 2019;14(1):e0210645. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Fenta SM, Biresaw HB, Fentaw KD, Gebremichael SG. Determinants of full childhood immunization among children aged 12–23 months in sub‐Saharan Africa: a multilevel analysis using Demographic and Health Survey Data. Trop Med Health. 2021;49(1):29. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Geweniger A, Abbas KM. Childhood vaccination coverage and equity impact in Ethiopia by socioeconomic, geographic, maternal, and child characteristics. Vaccine. 2020;38(20):3627‐3638. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Acharya P, Kismul H, Mapatano MA, Hatløy A. Individual‐ and community‐level determinants of child immunization in the Democratic Republic of Congo: a multilevel analysis. PLoS One. 2018;13(8):e0202742. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Sarker AR, Akram R, Ali N, Chowdhury ZI, Sultana M. Coverage and determinants of full immunization: vaccination coverage among Senegalese children. Medicina. 2019;55(8):480. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Masters NB, Wagner AL, Carlson BF, Muuo SW, Mutua MK, Boulton ML. Childhood vaccination in Kenya: socioeconomic determinants and disparities among the Somali ethnic community. Int J Public Health. 2019;64(3):313‐322. [DOI] [PubMed] [Google Scholar]
- 29. Cooper S, Schmidt BM, Sambala EZ, et al. Factors that influence parents' and informal caregivers’ views and practices regarding routine childhood vaccination: a qualitative evidence synthesis. Cochrane Database Syst Rev. 2021;10(10):CD013265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Du F, Chantler T, Francis MR, et al. Access to vaccination information and confidence/hesitancy towards childhood vaccination: a cross‐sectional survey in China. Vaccines. 2021;9(3):201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Francis MR, Nohynek H, Larson H, et al. Factors associated with routine childhood vaccine uptake and reasons for non‐vaccination in India: 1998–2008. Vaccine. 2018;36(44):6559‐6566. [DOI] [PubMed] [Google Scholar]
- 32. Oleribe O, Kumar V, Awosika‐Olumo A, Taylor SD. Individual and socioeconomic factors associated with childhood immunization coverage in Nigeria. Pan African Med J. 2017;26:220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Budu E, Opoku Ahinkorah B, Okyere J, Seidu AA, Ofori Duah H. Inequalities in the prevalence of full immunization coverage among one‐year‐olds in Ghana, 1993–2014. Vaccine. 2022;40:3614‐3620. [DOI] [PubMed] [Google Scholar]
- 34. Forshaw J, Gerver SM, Gill M, Cooper E, Manikam L, Ward H. The global effect of maternal education on complete childhood vaccination: a systematic review and meta‐analysis. BMC Infect Dis. 2017;17(1):801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35. Vikram K, Vanneman R, Desai S. Linkages between maternal education and childhood immunization in India. Social Sci Med (1982). 2012;75(2):331‐339. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Grépin KA, Bharadwaj P. Maternal education and child mortality in Zimbabwe. J Health Econ. 2015;44:97‐117. [DOI] [PubMed] [Google Scholar]
- 37. Makate M, Makate C. The causal effect of increased primary schooling on child mortality in Malawi: universal primary education as a natural experiment. Social Sci Med (1982). 2016;168:72‐83. [DOI] [PubMed] [Google Scholar]
- 38. Hajizadeh M. Socioeconomic inequalities in child vaccination in low/middle‐income countries: what accounts for the differences? J Epidemiol Community Health. 2018;72(8):719‐725. [DOI] [PubMed] [Google Scholar]
- 39. Hajizadeh M. Decomposing socioeconomic inequality in child vaccination in the Gambia, the Kyrgyz Republic and Namibia. Vaccine. 2019;37(44):6609‐6616. [DOI] [PubMed] [Google Scholar]
- 40. Payne S, Townend J, Jasseh M, Lowe Jallow Y, Kampmann B. Achieving comprehensive childhood immunization: an analysis of obstacles and opportunities in The Gambia. Health Policy Plan. 2013;29(2):193‐203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41. Health, CoSDo . Closing the Gap in a Generation: health Equity through Action on the Social Determinants of Health: final Report of the Commission on Social Determinants of Health. World Health Organization; 2008. [DOI] [PubMed] [Google Scholar]
- 42. Wiysonge CS, Uthman OA, Ndumbe PM, Hussey GD. Individual and contextual factors associated with low childhood immunisation coverage in sub‐Saharan Africa: a multilevel analysis. PLoS One. 2012;7(5):e37905. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43. Ataguba JE, Ojo KO, Ichoku HE. Explaining socio‐economic inequalities in immunization coverage in Nigeria. Health Policy Plan. 2016;31(9):1212‐1224. [DOI] [PubMed] [Google Scholar]
- 44. Powers DA, Yoshioka H, Yun MS, Powers DA, Yoshioka H, Yun MS. mvdcmp: multivariate decomposition for nonlinear response models. Stata J: Promoting Communications statistics Stata. 2011;11(4):556‐576. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The data sets generated and/or analyzed during the current study are available in DHS Program—available data sets (83).