Abstract
Background: The re-introduction of polio among children aged 12–23 months is likely to occur in Ethiopia due to the low vaccination rates against poliovirus. The study sought to examine the predictors of incomplete vaccination against polio among children aged 12–23 months in Ethiopia. Methods: The data used were obtained from the 2016 Ethiopia Demographic and Health Survey. Binary and Bayesian logistic regressions were used for the data analysis, with parameters estimated using classical maximum likelihood and the Bayesian estimation method. Results: The results revealed that 43.7% of the children were not fully vaccinated against polio in Ethiopia. Maternal age, educational level, household wealth index, exposure to mass media, place of residence, presence of nearby healthy facility, counseling on vaccination, and place of delivery were significant determinants of incomplete polio vaccination among children aged between 12 and 23 months in Ethiopia. Conclusion: Considerable numbers of children are not fully vaccinated against polio in Ethiopia. Individual and contextual factors significantly contributed to incomplete polio vaccination among children in the country. Therefore, the government and other stakeholders should pay particular attention to maternal education to increase mothers’ educational level in all regions and give training and counseling in all urban and rural parts of the country on child vaccination to overcome the problem of children’s incomplete polio vaccination and/or vaccination dropout.
Keywords: Bayesian logistic regression analysis, childhood vaccination, Ethiopia, polio, predictors
1. Introduction
Vaccination is a simple, safe, and effective way of protecting children against infectious diseases before they come into contact with them. Immunization is a worldwide health and improvement success history, saving millions of children’s lives every year and reducing the risk of getting a disease by working with your body’s natural defenses to build protection [1]. Immunization is the constituent of primary health care and an indubitable human right and it is critical to the prevention and control of infectious disease outbreaks. They also underpin global health security and will be a vital tool in the battle against antimicrobial resistance [2].
Globally, about two to three million childhood deaths annually could be averted through the use of vaccines [3,4]. Each year, approximately twenty million children fail to take all recommended vaccines, and almost two-thirds of these children come from just ten countries, including Ethiopia [4,5]. According to the World Health Organization’s (WHO) guidelines, children are considered as fully vaccinated against polio when they have received all recommended vaccination doses by the age of 12–23 months [6,7,8]. Poliovirus cases had reduced by over 99% since 1988, from a projected 350,000 cases in more than 125 endemic countries to 179 described cases in two countries in 2019 [9]. As a result of global eradication efforts, polio is now only endemic in Afghanistan, Nigeria, and Pakistan [10,11]. However, countries with low vaccination rates continue to be at risk for re-introduction of the virus due to imported cases resulting from travel. Unvaccinated travelers, especially children, pregnant women, and those with weakened immune system going to areas with polio outbreaks are at risk [11]. However, countries that have been cleared of the wild poliovirus, but at low vaccination rates and with weak and porous surveillance systems, continue to be at risk for re-introduction of the virus due to imported cases [12]. Again, surveillance evolves according to epidemiological changes and the indications on the performance of the surveillance system given by WHO may be susceptible to the integration of further systems of analysis [13].
The Ethiopia Demographic and Health Survey (EDHS) indicates that the percentage of children aged 12–23 months who are fully vaccinated increased by 15%, from 24% in 2011 to 39% in 2016 [14]. The Expanded Programme on Immunization (EPI) was established by the WHO in 1974 to control vaccine-preventable diseases [15]. Ethiopia has been realizing EPI free of charge aiming to immunize all children between the ages of 0 and 23 months against oral polio [16]. The findings of a recent study on factors associated with non-vaccination against polio has awakened the need for research to understand the vaccination status of children against polio in specific countries in Africa [11]. An extensive search of the literature on childhood vaccination in Ethiopia, where polio constitutes a major cause of death among children under five, shows that most studies conducted on childhood vaccination focused on the basic childhood vaccines together to determine whether a child was fully vaccinated or not. This approach makes it difficult to understand what the situation is with specific vaccines such as the polio vaccines. Due to inadequate information on childhood vaccination against polio in Ethiopia, the severity and the descriptions on it are quite scanty. Therefore, the purpose of the paper was to examine the factors associated with incomplete vaccination against polio among children aged between 12 and 23 months in Ethiopia to make recommendations that will help eradicate poliovirus from the country.
2. Materials and Methods
2.1. Source of Data
The data used for this study were obtained from the 2016 version of the EDHS on the polio vaccination status of children aged between 12 and 23 months. The sampling frame used for the 2016 EDHS is the Ethiopia Population and Housing Census (PHC), which was conducted in 2007 by the Ethiopia Central Statistical Agency. Administratively, Ethiopia is divided into nine geographical regions and two administrative cities. The sample for the 2016 EDHS was designed to provide estimates of key indicators for the country as a whole, for urban and rural areas separately, and for each of the nine regions and the two administrative cities. The survey was conducted from 18 January 2016 to 27 June 2016 [13]. Details of the EDHS methodology and sampling have been published in the EDHS report, which is also available online at https://dhsprogram.com/publications/publication-fr328-dhs-finalreports.cfm?cssearch=351226_1 (accessed on 25 July 2021).
2.2. Variables of the Study
2.2.1. Outcome Variable
Polio vaccination status was the outcome variable. Considering the WHO protocol, incomplete vaccination can be defined as children who missed at least one dose of the four vaccines between 12 and 23 months [5,6]. Polio vaccination was captured as a dichotomous variable and coded as 1 if a child aged between 12 and 23 months has missed at least one dose of the four basic doses of oral polio vaccine (polio 0 at birth, polio 1 at 6 weeks, polio 2 at 10 weeks, and polio 3 at 14 weeks) and 0 if otherwise [7,17,18,19].
2.2.2. Explanatory Variables
The explanatory variables used for this study were sex of the child (male and female), maternal age (15–24, 25–34, and 35–49), wealth index (poor, middle, and rich), maternal occupation (housewife, employee, daily labor market, and merchant) and educational level (no education, primary, and secondary/above). Other variables were exposure to mass media (not at all, once a week, and twice and more than a week), family size (1–3, 4–6, and 7 and above), place of residence (urban and rural), presence of nearby health facility (yes and no), type of nearby health facility (health center, health post, and private clinic), means of transport (on foot and transportations), counseling on vaccination (yes and no), and place of delivery (health facility and home). These variables were considered based on previous studies which found them associated with vaccination status among children aged between 12 and 23 months [7,17,18,19].
2.3. Data Analyses
2.3.1. Binary Logistic Regression
Binary logistic regression allows one to predict a dichotomous outcome, from a set of predictor variables that may be continuous, discrete, dichotomous, or a mix of any of these [20,21,22]. Therefore, this study used binary logistic regression; because the response variable, polio vaccination status has two categories or is dichotomous. The response variable was given as follows
Then, the conditional probability that the respondent’s polio vaccinated status given the X set of predictor variables is denoted by Prob ( = 1 ∣ X) = . The expression has the form:
where is the probability of child i is not fully vaccinated, Yi is the observed polio fully non-vaccination status of a child, and is a vector of fixed unknown coefficients.
The parameter was estimated by using the maximum likelihood estimation method. The estimated coefficients of variables, , the standard errors of estimates S.E(), Wald statistic, significance, the odds ratio (Exp()), and the 95% confidence interval for all predictor variables in the model are presented in the results section. The standard error of the estimate helps in computing the values of the Wald statistic, the significance of the Wald statistic indicates the importance of the predictor variable in the model, and the high value of the Wald statistic shows that the corresponding predictor variable was important. Since the covariates used in the model are categorical, to compute the odds ratio, a reference category (ref) was needed. The exp () is called the odds multiplier or odds ratio with an odds ratio of 1 for the reference category, and all other groups are compared based on the reference group.
2.3.2. Bayesian Logistic Regression
In Bayesian analysis, the three key ingredients are the likelihood function, which reflects information about the parameters contained in the data, the prior distribution, which quantifies what is known about the parameters before observing data, and the prior distribution and likelihood can be easily combined to form the posterior distribution, which represents total knowledge about the parameters after the data have been observed [23,24,25].
2.3.3. The Likelihood Function
In this study, Bayesian logistic regression specifies a dichotomous dependent variable as a function of a set of explanatory variables. The likelihood input from the subject follows Bernoulli distribution and given by:
where represents the probability of the event for subjects i who have covariate vector , and indicates the presence, = 1, or absence = 0 of the event for that subject.
where = the probability of child not fully vaccinated against polio, so that the likelihood contribution from the subject is given by
Since individual children are assumed to be independent, then, the likelihood function over a data set of n subjects is given by
2.3.4. The Prior Distribution
The prior distribution was a probability distribution that indicates the previous information related to the parameters of concern. In this study, a non-informative prior normal distribution was used, and the assigned normal prior distribution for the components of
where the common choice for µ is zero, and δ is usually chosen to be large enough to be considered as non-informative, common choices being in the range from δ = 10 to δ = 100.
2.3.5. The Posterior Distribution
From a specified likelihood of logistic regression and the prior distribution above, the posterior distribution of the Bayesian logistic regression contains a combination of both types of information, which were obtained from data (likelihood) and previous information obtained from the study area before data were collected (prior). Therefore, the posterior distribution was derived by multiplying the prior distribution over all parameters by the full likelihood function. Then, the posterior distribution was written in the form of:
Bayesian logistics model inference was based on samples drawn from the posterior distribution using the Gibbs sampler algorithms. The Gibbs sampling algorithm is one of the simplest Markov chain Monte Carlo (MCMC) algorithms that converge to the target density as the number of iterations become large. The posterior means of the parameters was estimated based on 50,000 iteration of MCMC samples.
2.4. Software Used
The statistical software used in this study was SPSS version 20 and WinBUGS14. SPSS was used for the descriptive and binary logistic analysis, and WinBUGS14 was used for the Bayesian analysis. The Bayesian logistic regression analysis using the Gibbs sampling method in the WinBUGS software was considered. The Bayesian model used normal–normal, in which the dependent variable, child polio non-vaccination status, is expected to follow a normal distribution with the prior of the coefficients normally distributed as non-informative priors. It is assumed that the regression parameters of concern will follow a normal distribution with mean = 0 and precision = 0.001. Three chains of parameters were simulated for 50,000 iterations each, and a total posterior sample of 90,000 is kept for summarization and convergence checks after discarding the first 20,000 iterations as burn-in. Evaluation of Model Convergence of MCMC was checked by a time-series plot, Gelman–Rubin statistic, autocorrelation plot, and kernel density plot, with all plots showing that the convergence of the model was achieved. The Bayesian approach usually reports either the mean or median of the posterior samples for each parameter of concern as a point estimate.
3. Results
3.1. Descriptive and Test of Association Results
Out of 2016 total children aged between 12 and 23 months included in the study, 881 of them (about 43.7%) were not fully vaccinated against polio at the time of the survey (Table 1). From the predictors included in the model shown in Table 1, the sex of the child, maternal age, maternal education, family wealth index, occupation, family size, exposure to mass media, presence of health facility nearby, means of transport, place of residence, counseling on vaccination, and place of delivery were statistically significantly associated with incomplete vaccination against polio.
Table 1.
Descriptive and test of association results on polio non-vaccination status with predictor variables.
| Variables | Categories | Polio Vaccination Status | Chi-Square | |||
|---|---|---|---|---|---|---|
| Not Fully Vaccinated | Fully Vaccinated | |||||
| Count | % | Count | % | |||
| Sex of child | Male | 409 | 43.7% | 525 | 56.3% | 53.98 * |
| Female | 473 | 43.7% | 609 | 56.3% | ||
| Maternal age | 15–24 | 300 | 48.4% | 320 | 51.6% | 69.35 ** |
| 25–34 | 352 | 43.8% | 452 | 56.2% | ||
| 35–49 | 230 | 38.9% | 362 | 61.1% | ||
| Wealth index | Poor | 704 | 58% | 200 | 42% | 84.65 ** |
| Middle | 249 | 39.1% | 388 | 60.9% | ||
| Rich | 177 | 34% | 298 | 66% | ||
| Occupation | House wife | 619 | 63.8% | 352 | 36.2% | 43.24 * |
| Employee | 56 | 27% | 148 | 73% | ||
| Daily labor worker | 175 | 48% | 189 | 52% | ||
| Merchant | 172 | 36% | 305 | 64% | ||
| Mother educational level | No education | 724 | 62.5% | 436 | 37.5% | 41.71 * |
| primary | 251 | 39.6% | 381 | 60.4% | ||
| Secondary and above | 66 | 29% | 158 | 71% | ||
| Exposure to mass media | Not at all | 216 | 58% | 158 | 42% | 55.25 * |
| Once a week | 349 | 41% | 501 | 59% | ||
| Twice and more a week | 253 | 32.1% | 536 | 67.9% | ||
| Family size | 1–3 | 370 | 49.8% | 372 | 50.2% | 47.18 * |
| 4–6 | 371 | 43.2% | 485 | 56.8% | ||
| Above 7 | 167 | 38.1% | 251 | 61.9% | ||
| Place of residence | Urban | 683 | 53.8% | 581 | 46.2% | 77.32 ** |
| Rural | 271 | 33.6% | 481 | 66.4% | ||
| Presence of nearby health facility | Yes | 381 | 35.9% | 678 | 64.1% | 65.84 ** |
| No | 492 | 51.5% | 465 | 48.5% | ||
| Type of nearby health facility | Health center | 319 | 42.3% | 435 | 57.7% | 2.56 |
| Health post | 341 | 39.2% | 528 | 60.8% | ||
| Private clinic | 195 | 49.6% | 198 | 50.4% | ||
| Means of transport | On walk | 497 | 48.3 | 532 | 51.7 | 36.17 * |
| Transportations | 387 | 39.1 | 600 | 60.9 | ||
| Counseling on vaccination | Yes | 311 | 22.2% | 1082 | 77.8% | 88.59 ** |
| No | 406 | 65.2% | 217 | 34.8% | ||
| Place of delivery | Health facility | 409 | 31.4% | 889 | 68.6% | 40.64 * |
| Home | 402 | 56% | 316 | 44% | ||
* Chi-square was significant at (p < 0.05) and ** Chi-square was significant at (p < 0.01).
3.2. Binary Logistic Regression Results
The results in Table 2 shows that maternal age, mother’s educational level, household wealth index, exposure to mass media, place of residence, presence of nearby healthy facility, counseling on vaccination, and place of delivery were the significant predictors of incomplete vaccination against polio among child aged between 12 and 23 months.
Table 2.
Results of binary logistic regression analysis.
| Variables | Categories | B | S.E | Wald | Sig | Exp (B) | 95%CI for Exp(B) | |
|---|---|---|---|---|---|---|---|---|
| Lower | Upper | |||||||
| Sex of child | Female (ref) Male |
−0.658 | 0.097 | −1.13 | 0.071 | |||
| 0.85 | 0.318 | 1.465 | ||||||
| Maternal age | 15–24 (ref) | |||||||
| 25–34 | −1.172 | 0.112 | −15.56 | 0.002 | 0.82 | 0.74 | 0.93 | |
| 35–49 | −1.195 | 0.164 | −17.42 | 0.001 | 0.77 | 0.62 | 0.94 | |
| Mother educational level |
No education (ref) | |||||||
| Primary school | −2.181 | 0.157 | −6.512 | 0.001 | 0.73 | 0.55 | 0.93 | |
| Secondary and above | −2.528 | 0.127 | −7.094 | 0.007 | 0.63 | 0.48 | 0.79 | |
| Poor (ref) | ||||||||
| Wealth index | Middle | −0.896 | 0.842 | −4.13 | 0.023 | 0.53 | 0.278 | 0.783 |
| Rich | −0.849 | 0.72 | −5.03 | 0.018 | 0.42 | 0.189 | 0.670 | |
| Occupation | House wife (ref) | |||||||
| Employed | −0.049 | 1.1088 | −0.92 | 0.146 | 0.650 | 0.24 | 1.060 | |
| Labor worker | 0.486 | 1.100 | 1.05 | 0.138 | 1.226 | 0.88 | 2.046 | |
| Merchant | 0.665 | 1.213 | 0.830 | 0.094 | 1.145 | 0.780 | 2.175 | |
| Family size | 1–3 (ref) | |||||||
| 4–6 | 1.001 | 0.846 | 1.39 | 0.083 | 1.767 | 0.570 | 1.131 | |
| Above 6 | 0.232 | 0.573 | 1.104 | 0.065 | 2.861 | 0.411 | 1.311 | |
| Expose to mass media | Not at all (ref) | |||||||
| Once a week | −0.172 | 0.089 | −3.16 | 0.019 | 0.821 | 0.729 | 0.915 | |
| twice and more a week | −0.293 | 0.094 | −4.41 | 0.002 | 0.684 | 0.534 | 0.836 | |
| Place of residence | Urban (ref) | |||||||
| Rural | −0.409 | 0.122 | −11.239 | 0.001 | 0.753 | 0.585 | 0.925 | |
| Presence of nearby health facility | Yes (ref) | |||||||
| No | 1.62 | 0.856 | 6.15 | 0.02 | 1.93 | 1.563 | 2.315 | |
| Means of transport | Transportations (ref) | |||||||
| On walk | 2.654 | 0.765 | 0.85 | 0.985 | 0.856 | 0.15 | 1.861 | |
| Counseling on vaccination | Yes (ref) | |||||||
| No | 1.49 | 0.196 | 3.65 | 0.035 | 2.35 | 2.14 | 2.59 | |
| Place of delivery | Health institution (ref) | |||||||
| Home | 0.870 | 0.791 | 4.21 | 0.029 | 3.14 | 2.95 | 3.45 | |
Children of mothers aged 25–34 and 35–49 were about 18% and 23% (OR = 0.82 with 95% CI = 0.74, 0.93) and OR = 0.77, with 95% CI (0.62, 0.94) less likely not to be fully vaccinated against polio compared to those of mothers in the age group 15–24. The result also indicates children of mothers who had primary and secondary and above education were about 27% (OR = 0.73 with 95% CI = 0.55, 0.93) and 37% (OR = 0.63 with 95% CI = 0.48, 0.79) less likely not to be fully vaccinated against polio compared those of mothers with no formal education. Concerning the household wealth index, children from medium and rich families were 47% (OR = 0.53 with 95% CI = 0.278, 0.873) and 58% (OR = 0.42 with 95% CI = 0.189, 0.670) less likely not to be fully vaccinated against polio compared to those from poor families. Similarly, children of mothers who are exposed to mass media once a week and twice and more a week were 17.9% (OR = 0.821 with 95% CI = 0.729, 0.915) and 32.6% (OR = 0.684 with 95% CI = 0.534, 0.836) less likely not to be fully vaccinated against polio compared to children of mothers who had no media exposure at all.
Incomplete polio vaccination among children aged 12–23 months from rural areas decreased by 24.7% (OR = 0.753 with 95% CI = 0.585, 0.925) compared with those from urban areas. The results also show that children from households that were not near a health facility were 93% (OR = 1.93 with 95% CI = 1.563, 2.315) more likely to have incomplete polio vaccination compared to children from households that were near a health facility. Similarly, children whose mothers were not counseled on child vaccination were more likely not to be fully vaccinated against polio compared to those whose mothers were counseled on vaccination (OR = 2.35 with 95% CI = 2.14, 2.59). We also found that children who were delivered at home were three times more likely not to be fully vaccinated against polio compared to those who were delivered at a health facility (OR = 3.14 with 95% CI = 2.95, 3.45) (Table 2).
3.3. Bayesian Logistic Regression Results
Approximately 2.5% and 97.5% percentiles of the posterior samples for each parameter provide a 95% posterior reliable interval (interval within which the parameter lies with probability of 0.95). The results of Table 3 indicate that maternal age, mother educational level, household wealth index, exposure to mass media, place of residence, presence of nearby healthy facility, counseling on vaccination, and place of delivery significantly contributed to the prediction of incomplete polio vaccination status among children aged between 12 and 23 months (since the credible intervals of these variables do not contain zero).
Table 3.
Results of Bayesian binary logistic regression analysis.
| Variables | Categories | Mode | Estimate | Sd | MC Error | 2.5% | Median | 97.5% |
|---|---|---|---|---|---|---|---|---|
| Intercept | Alpha | 0.1485 | 0.0728 | 0.007515 | 0.2970 | 0.5485 | 0.8535 | |
| Sex of child | Female (ref) | |||||||
| Male | beta [1] | −0.655 | 0.0920 | −1.025 | −0.659 | 0.175 | ||
| Maternal age | 15–24 (ref) | |||||||
| 25–34 | beta [2] | −1.14 | 0.112 | −1.82 | −1.138 | −0.456 | ||
| 35–49 | beta [3] | −1.186 | 0.158 | −1.43 | −1.185 | −0.940 | ||
| Mother educational level | No education (ref) | |||||||
| Primary | beta [4] | −2.181 | 0.0131 | 0.0001522 | −2.97 | −2.20 | −1.43 | |
| Secondary and above | beta [5] | −2.521 | 0.125 | 0.000532 | −2.82 | −2.53 | −2.240 | |
| Poor (ref) | ||||||||
| Wealth index | medium | beta [6] | −0.894 | 0.0839 | −0.983 | −0.885 | −0.787 | |
| Rich | beta [7] | −0.846 | 0.0721 | −0.989 | −0.848 | −0.707 | ||
| Occupation | House wife (ref) | |||||||
| Employed | beta [8] | −0.051 | 0.108 | 0.0002478 | −0.276 | −0.051 | 0.174 | |
| Labor worker | beta [9] | 0.487 | 0.105 | −0.258 | 0.456 | 0.979 | ||
| Merchant | beta [10] | 0.668 | 0.0211 | 0.000243 | −0.154 | 0.675 | 1.358 | |
| Family size | 1–3 (ref) | |||||||
| 4–6 | beta [11] | 1.001 | 0.0845 | −0.253 | 1.03 | 1.875 | ||
| Above 6 | beta [12] | 0.231 | 0.574 | −0.125 | 0.242 | 0.648 | ||
| Expose to mass media | Not at all (ref) | |||||||
| Once a week | beta [13] | −0.74 | 0.092 | −0.98 | −0.75 | −0.520 | ||
| Twice and more a week | beta [14] | −0.290 | 0.091 | −0.428 | −0.291 | −0.152 | ||
| Place of residence | Urban (ref) | |||||||
| Rural | beta [15] | −0.407 | 0.119 | −0.635 | −0.411 | −0.187 | ||
| Presence of nearby health facility | Yes (ref) | |||||||
| No | beta [16] | 1.67 | 0.449 | 0.00056 | 1.362 | 1.618 | 1.874 | |
| Means of transport | On walk (ref) | |||||||
| Transportations | beta [17] | 2.653 | 0.082 | 0.0007893 | −0.162 | 2.684 | 5.306 | |
| Counseling on vaccination | Yes (ref) | |||||||
| No | beta [18] | 1.46 | 0.0470 | 1.025 | 1.471 | 1.917 | ||
| Place of delivery | Health institution (ref) | |||||||
| Home | beta [19] | 0.864 | 0.0650 | 0.435 | 0.859 | 1.283 |
In Bayesian analysis, to have accurate posterior estimates, the simulation should be run until the Monte Carlo (MC) error for each parameter of interest is less than about 5% of the sample standard deviation. In Table 3, the MC errors for all the parameters were less than 5% of its posterior standard error. This approach suggests that the convergence and accuracy of the posterior estimates are achieved. Both the classical parameter estimation approach and Bayesian parameter estimation approach fit the data well and give almost consistent results, but most of the parameters in the Bayesian analysis had smaller errors than the corresponding classical binary logistic model, and the Bayesian analysis provides additional solutions as the posterior distribution of the parameters.
4. Discussion
This study examines the predictors of incomplete vaccination against polio among children between 12 and 23 months in Ethiopia. The results showed that maternal age, mother’s educational level, household wealth index, exposure to mass media, place of residence, presence of nearby healthy facility, counseling on vaccination, and place of delivery were associated with incomplete polio vaccination among children aged 12–23 months in Ethiopia.
Concerning maternal age, it was found that the odds of incomplete vaccination against polio decreases with increasing age. Hence, children born to younger women were more likely to have incomplete vaccination against polio compared to those born to older women. This finding is consistent with the findings of studies that have been carried out in Ethiopia [26,27] and other low-and middle-income countries [28,29,30,31], which found that young maternal age is a risk factor for incomplete childhood immunization. The possible reason for the finding could be the better understanding of the child’s health and the importance of vaccination among older women compared to younger women [30,31]. Younger women may also face challenges accessing health care to immunize their children including stigma, cost, and distance to health facilities [32,33,34]. This finding calls for the need to address barriers to maternal healthcare services utilization among young mothers. There is also the need to educate young mothers on the importance of vaccination against polio to a child’s survival.
Children of mothers with a higher educational level and wealth index were less likely to be incompletely immunized against polio compared with those with no formal education. High socio-economic status (wealth and educational level) has been found to be protective against incomplete childhood vaccination in several studies in low- and middle-income countries, including Ethiopia [26,27,28,29,30,31]. In explaining the relationship between socio-economic status and childhood vaccination, several authors have explained that higher socio-economic status enhanced health-care seeking for child health, including immunization [35,36,37]. Specifically, women with a higher level of education were considered as more knowledgeable of the risks associated with incomplete childhood vaccination and the importance of complete childhood vaccination [35,36,37]. The knowledge obtained by women with higher levels of education is available to them not only through schooling but also through exposure to media, where information about the risks associated with incomplete vaccination and the importance of complete childhood vaccination is available [35,36,37]. Those with a higher wealth quintile were found as having the economic empowerment to overcome the financial cost of accessing health care for their children and thus are able to access health care for their children [29,31,38]. Unless they live in areas where childhood vaccinations are offered to children in their homes, the place where a mother lives also plays a major role in the incomplete vaccination of children. However, in this study, children of mothers who lived in rural areas were less likely to be incompletely immunized compared to those who lived in urban areas. This finding contradicts previous studies that explained that access to nearby health facilities in urban areas reduced incomplete vaccination against polio [29,30,39,40]. The findings underscore the importance of addressing socio-economic inequalities in access to maternal and child health-care services. Special attention should be given to mothers of high socio-economic disadvantages by reducing the cost of child health care and educating those with no formal education on the importance of childhood vaccination against polio. Health-care workers in Ethiopia may consider providing community-based vaccination services that will target mothers who live in rural areas and far away from health facilities.
Children who were delivered at home were more likely to be incompletely vaccinated against polio compared to those who were delivered at the health facility. Previous studies have shown that maternal health-care utilization plays a key role in determining the complete vaccination status of children [26,30,35]. In relation to the observed association between place of delivery and incomplete vaccination against polio among children in Ethiopia, women who deliver at health facilities might be exposed to information about their health and that of their children [41]. Such information may include vaccination counseling [42], which was also found to decrease the likelihood of incomplete polio vaccination in the current study. Thus, women who deliver in health facilities are likely to receive adequate training from health professionals on the importance of childhood vaccinations, and this builds their confidence in using preventive health services [30]. This finding calls for the need to educate pregnant women during antenatal care attendance on the importance of health facility delivery for maternal and child health and its impact on childhood vaccination against polio specifically. Notwithstanding, as long as some women continue to deliver at home, special attention should be given to reach these children and provide them with the necessary vaccinations.
Strengths and Limitations
The robust analytical approaches employed in the analysis of data for the current study constitutes its key strength. We also followed a systematic methodological process in arriving at our findings and conclusion, making our findings and conclusions reliable. The use of nationally representative data also makes our findings generalizable. Nonetheless, our results should be interpreted with caution, since the cross-sectional nature of the data makes it impossible for us to establish causality. Some of the mothers also gave verbal responses about the vaccination status of their children, and this can be influenced by recall bias.
5. Conclusions
The purpose of the paper was to examine the factors associated with incomplete vaccination against polio among children aged between 12 and 23 months in Ethiopia in order to make recommendations that will help eradicate poliovirus from the country. The prevalence of polio incomplete vaccination against polio was 43.7%. Maternal age, mother’s educational level, household wealth index, exposure to mass media, place of residence, presence of nearby healthy facility, counseling on vaccination, and place of delivery were the significant predictors of incomplete vaccination against polio among child aged between 12 and 23. Thus, the stakeholders must give consideration to all significant predictors revealed in the results of this study. The study also shows that children born to mothers with no education have a high probability of not being fully vaccinated. Therefore, the government should pay attention to maternal education to increase mothers’ educational levels in all regions and give training and counseling in all urban and rural parts of the country on child vaccination to overcome the problems of child incomplete vaccination against polio or polio vaccination dropout.
Author Contributions
T.U.C. developed the study concept and performed the analysis portion. T.U.C., A.-A.S., J.E.H.J., R.G.A. and B.O.A. drafted and revised the manuscript for its intellectual content. All authors have read and agreed to the published version of the manuscript.
Funding
The authors sincerely thank Bielefeld University, Germany for providing financial support through the Institutional Open Access Publication Fund for the article processing charge.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
The dataset is available on the following website: https://dhsprogram.com/data/dataset/Ethiopia_Standard-DHS_2016.cfm?flag=0 (accessed on 6 October 2021).
Conflicts of Interest
The authors declare no conflict of interest.
Ethics Approval
Ethical clearance was obtained by the Institutional Review Board of ICF International. Permission was also sought from each woman during the fieldwork. The authors requested and officially received approval from the DHS Program to use the dataset for this study. Supplementary information about the DHS data usage and ethical standards are available at http://goo.gl/ny8T6X.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Eshete A., Shewasinad S., Hailemeskel S. Immunization coverage and its determinant factors among children aged 12–23 months in Ethiopia: A systematic review, and Meta- analysis of cross-sectional studies. BMC Pediatr. 2020;20:1–13. doi: 10.1186/s12887-020-02163-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Porth J.M., Wagner A.L., Tefera Y.A., Boulton M.L. Childhood Immunization in Ethiopia: Accuracy of Maternal Recall Compared to Vaccination Cards. Vaccines. 2019;7:48. doi: 10.3390/vaccines7020048. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.UNICEF Immunization Programme 2018. [(accessed on 27 July 2021)]. Available online: https://www.unicef.org/immunization.
- 4.Porth J.M., Wagner A.L., Teklie H., Abeje Y., Moges B., Boulton M.L. Vaccine non-receipt and refusal in Ethiopia: The expanded program on immunization coverage survey, 2012. Vaccine. 2019;37:2106–2121. doi: 10.1016/j.vaccine.2019.02.045. [DOI] [PubMed] [Google Scholar]
- 5.World Health Organization WHO Immunization Coverage 2018. [(accessed on 28 July 2021)]. Available online: https://www.who.int/news-room/fact-sheets/detail/immunization-coverage.
- 6.Chanie M.G., Ewunetie G.E., Molla A., Muche A. Determinants of vaccination dropout among children 12–23 months age in north Gondar zone, northwest Ethiopia, 2019. PLoS ONE. 2021;16:e0246018. doi: 10.1371/journal.pone.0246018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Abebe A.M., Mengistu T., Mekuria A.D. Measles case, immunization coverage and its determinant factors among 12–23 month children, in Bassona Worena Woreda, Amhara Region, Ethiopia, 2018. BMC Res. Notes. 2019;12:1–6. doi: 10.1186/s13104-019-4104-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Mohamud A.N., Feleke A., Worku W., Kifle M., Sharma H.R. Immunization coverage of 12–23 months old children and associated factors in Jigjiga District, Somali National Regional State, Ethiopia. BMC Pub. Health. 2014;14:1–9. doi: 10.1186/1471-2458-14-865. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Wiysonge C.S. How Ending Polio in Africa Has Had Positive Spinoffs for Public Health. 2020. [(accessed on 30 July 2021)]. The Conversation. Available online: https://theconversation.com/how-ending-polio-in-africa-has-had-positive-spinoffs-for-public-health-148857.
- 10.UNICEF . Polio Vaccination Campaigns Resume in Afghanistan and Pakistan after COVID-19 Disruptions Leave 50 Million Children Unimmunized. UNICEF; New York, NY, USA: 2020. [Google Scholar]
- 11.Uthman O., Ndwandwe D., Uthman M., Yaya S., Wiysonge C. Multilevel Analysis of Individual and Contextual Factors Associated with Polio Non-Vaccination in Africa: Further Analyses to Enhance Policy and Opportunity to Save More Lives. Vaccines. 2021;9:683. doi: 10.3390/vaccines9070683. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Okiror S., Ogange J., Shukla H., Lamoureau C., Monze M., Ismail A., Kazoka A., Nkowane B., Kamadjeu R., Igweonu O., et al. Surveillance Review System to Track Progress Towards Polio Eradication in the Horn of Africa. J. Immunol. Sci. 2021;2:136–145. doi: 10.29245/2578-3009/2021/S2.1111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Stefanelli P., Bellino S., Fiore S., Fontana S., Amato C., Buttinelli G. Hospital discharges-based search of acute flaccid paralysis cases 2007–2016 in Italy and comparison with the National Surveillance System for monitoring the risk of polio reintroduction. BMC Publ. Health. 2019;19:1532. doi: 10.1186/s12889-019-7617-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Federal Democratic Republic of Ethiopia . Ethiopia Demographic and Health Survey 2016. Central Statistical Agency; Addis Ababa, Ethiopia: The DHS Program; Rockville, MD, USA: 2017. [Google Scholar]
- 15.Machingaidze S., Wiysonge C.S., Hussey G.D. Strengthening the Expanded Programme on Immunization in Africa: Looking beyond 2015. PLoS Med. 2013;10:e1001405. doi: 10.1371/journal.pmed.1001405. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Federal Ministry of Health Ethiopia . Ethiopia National Expanded Programme on Immunization, Comprehensive MULTI-YEAR Plan 2016. Federal Ministry of Health Ethiopia; Addis Ababa, Ethiopia: 2015. [Google Scholar]
- 17.Mebrat A., Dube L., Kebede A., Aweke Z. Determinants of Incomplete Childhood Vaccination among Children Aged 12–23 Months in Gambela Region, Southwest Ethiopia: A Case Control Study. Ethiop. J. Health Sci. 2021;31:63–72. doi: 10.4314/ejhs.v31i1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Ntenda P.A.M. Factors associated with non- and under-vaccination among children aged 12–23 months in Malawi. A multinomial analysis of the population-based sample. Pediatr. Neonatol. 2019;60:623–633. doi: 10.1016/j.pedneo.2019.03.005. [DOI] [PubMed] [Google Scholar]
- 19.Tesfaye T.D., Temesgen W.A., Kasa A.S. Vaccination coverage and associated factors among children aged 12–23 months in Northwest Ethiopia. Hum. Vaccines Immunother. 2018;14:2348–2354. doi: 10.1080/21645515.2018.1502528. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Agresti A. Categorical Data Analysis. 2nd ed. John Wiley and Sons; New York, NY, USA: 2000. [Google Scholar]
- 21.Hosmer D.W., Lemeshow S. Applied Logistic Regression. 2nd ed. John Wiley and Sons; New York, NY, USA: 2000. [Google Scholar]
- 22.Menard S. Applied Logistic Regression Analysis. 2nd ed. Sage Publications; New York, NY, USA: 2002. [Google Scholar]
- 23.Brooks S.P., Gelman A. General Methods for Monitoring Convergence of Iterative Simulations. J. Comput. Graph. Stat. :1998. doi: 10.1080/10618600.1998.10474787. [DOI] [Google Scholar]
- 24.Gelman A., Carlin J., Stern H., Rubin D. Bayesian Data Analysis. Chapman & Hall; London, UK: 2004. [Google Scholar]
- 25.Xu Z., Akella R. A Bayesian Logistic Regression Model for Active Relevance Feedback; Proceedings of the 31st Annual International ACM SIGIR Conference on Research and Development in Information Retrieval; Singapore. 20–24 July 2008; pp. 227–234. [Google Scholar]
- 26.Negussie A., Kassahun W., Assegid S., Hagan A.K. Factors associated with incomplete childhood immunization in Arbegona district, southern Ethiopia: A case—Control study. BMC Pub. Health. 2015;16:1–9. doi: 10.1186/s12889-015-2678-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Zenbaba D., Sahiledengle B., Debela M.B., Tufa T., Teferu Z., Lette A., Gezahegn H., Solomon D., Tekalegn Y. Determinants of Incomplete Vaccination Among Children Aged 12 to 23 Months in Gindhir District, Southeastern Ethiopia: Unmatched Case—Control Study. Risk Manag. Healthc. Policy. 2021;14:1669–1679. doi: 10.2147/RMHP.S295806. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Kusuma Y.S., Kumari R., Pandav C.S., Gupta S.K. Migration and immunization: Determinants of childhood immunization uptake among socioeconomically disadvantaged migrants in Delhi, India. Trop. Med. Int. Health. 2010;15:1326–1332. doi: 10.1111/j.1365-3156.2010.02628.x. [DOI] [PubMed] [Google Scholar]
- 29.Budu E., Seidu A.-A., Ahinkorah B.O., Agbaglo E., Dadzie L.K., Yaya S. Determinants of complete immunizations coverage among children aged 12–23 months in Papua New Guinea. Child. Youth Serv. Rev. 2020;118:105394. doi: 10.1016/j.childyouth.2020.105394. [DOI] [Google Scholar]
- 30.Budu E., Ahinkorah B.O., Aboagye R.G., Armah-Ansah E.K., Seidu A.A., Adu C., Ameyaw E.K., Yaya S. Maternal healthcare utilisation and complete childhood vaccination in sub-Saharan Africa: A cross-sectional study of 29 nationally representative surveys. BMJ Open. 2021;11:e045992. doi: 10.1136/bmjopen-2020-045992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Khan M.T., Zaheer S., Shafique K. Maternal education, empowerment, economic status and child polio vaccination uptake in Pakistan: A population based cross sectional study. BMJ Open. 2017;7:e013853. doi: 10.1136/bmjopen-2016-013853. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Anderson E.L. Recommended Solutions to the Barriers to Immunization in Children and Adults. Mo. Med. 2014;111:344–348. [PMC free article] [PubMed] [Google Scholar]
- 33.Ferrer H.B., Trotter C., Hickman M., Audrey S. Barriers and facilitators to HPV vaccination of young women in high-income countries: A qualitative systematic review and evidence synthesis. BMC Pub. Health. 2014;14:700. doi: 10.1186/1471-2458-14-700. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Akwataghibe N.N., Ogunsola E.A., Broerse J.E.W., Popoola O.A., Agbo A.I., Dieleman M.A. Exploring Factors Influencing Immunization Utilization in Nigeria—A Mixed Methods Study. Front. Pub. Health. 2019;7 doi: 10.3389/fpubh.2019.00392. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Bugvi A.S., Rahat R., Zakar R., Zakar M.Z., Fischer F., Nasrullah M., Manawar R. Factors associated with non-utilization of child im-munization in Pakistan: Evidence from the Demographic and Health Survey 2006–07. BMC Pub. Health. 2014;14:232. doi: 10.1186/1471-2458-14-232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Russo G., Miglietta A., Pezzotti P., Biguioh R.M., Mayaka G.B., Sobze M.S., Stefanelli P., Vullo V., Rezza G. Vaccine coverage and determinants of incomplete vaccination in children aged 12–23 months in Dschang, West Region, Cameroon: A cross-sectional survey during a polio out-break. BMC Pub. Health. 2015;15:630. doi: 10.1186/s12889-015-2000-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Kawakatsu Y., Tanaka J., Ogawa K., Ogendo K., Honda S. Effects of three interventions and determinants of full vaccination among children aged 12–59 months in Nyanza province, Kenya. Public Health. 2015;129:1530–1538. doi: 10.1016/j.puhe.2015.07.008. [DOI] [PubMed] [Google Scholar]
- 38.Uthman O.A., Adedokun S.T., Olukade T., Watson S., Adetokunboh O., Adeniran A., Oyetoyan S.A., Gidado S., Lawoko S., Wiysonge C.S. Children who have received no routine polio vaccines in Nigeria: Who are they and where do they live? Hum. Vaccines Immunother. 2017;13:2111–2122. doi: 10.1080/21645515.2017.1336590. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Jani J.V., De Schacht C., Jani I.V., Bjune G. Risk factors for incomplete vaccination and missed opportunity for immunization in rural Mozambique. BMC Pub. Health. 2008;8:161–167. doi: 10.1186/1471-2458-8-161. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Adedokun S.T., Uthman O.A., Adekanmbi V.T., Wiysonge C.S. Incomplete childhood immunization in Nigeria: A multilevel analysis of individual and contextual factors. BMC Pub. Health. 2017;17:1–10. doi: 10.1186/s12889-017-4137-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Acharya P., Kismul H., Mapatano M.A., Hatloy A. Individual- and community-level determinants of child immunization in the Democratic Republic of Congo: A multilevel analysis. PLoS ONE. 2018;13:e0202742. doi: 10.1371/journal.pone.0202742. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Tesema G.A., Tessema Z.T., Tamirat K.S., Teshale A.B. Complete basic childhood vaccination and associated factors among children aged 12–23 months in East Africa: A multilevel analysis of recent demographic and health surveys. BMC Publ. Health. 2020;20:1–14. doi: 10.1186/s12889-020-09965-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The dataset is available on the following website: https://dhsprogram.com/data/dataset/Ethiopia_Standard-DHS_2016.cfm?flag=0 (accessed on 6 October 2021).
