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. 2024 Dec 21;11:2333794X241310487. doi: 10.1177/2333794X241310487

Childhood Vaccinations and Associated Factors in 35 Sub-Saharan African Countries: Secondary Analysis of Demographic and Health Surveys Data from 358 949 Under-5 Children

Michael Ekholuenetale 1,, Victor A Ochagu 2, Olayinka Stephen Ilesanmi 2, Okikiolu Badejo 3, Amit Arora 4,5,6,7,8
PMCID: PMC11663273  PMID: 39741897

Abstract

Objective. We examined childhood vaccinations coverage and its associated factors in sub-Saharan Africa (SSA) countries. Methods. We used demographic and health surveys (DHSs) data collected between 2008 and 2022 from 35 SSA countries. A sample of 358 949 under-5 children was analyzed. Percentage and multivariable binary logistic regression analyses were conducted. A 5% significance level was set. Results. Rwanda (7461/8092; 92.2%), Burundi (10 792/13 192; 81.8%), Gambia (6548/8362; 78.3%), Kenya (14 570/19 530; 74.6%), and Burkina Faso (8739/12 343; 70.8%) had the leading coverage of under-5 children who received all basic vaccinations in the first year of life. For every unit increase in the age of a child, there was 72% increase in the odds of vaccination. Children from older mothers had higher odds of vaccination, when compared with children with mothers aged 15 to 19 years. There was a 6% reduction in the odds of vaccination among children from rural residence, when compared with their urban counterparts. Children with educated mothers had over two times higher odds of vaccination, when compared with those from mothers with no formal education. Children from rich households had higher odds of vaccination, when compared with children from poorest household. There was a 13% increase in the odds of vaccination among children covered by health insurance, when compared with those not covered by health insurance. Conclusion. Vaccination uptake for children under-5 in SSA was found to be sub-optimal and associated with several factors. A health educational intervention for pregnant women could potentially increase the uptake of vaccines among children.

Keywords: immunization, vaccination, infant, under-5, sub-Saharan Africa, children

Background

Vaccination is a crucial public health intervention, protecting children from a variety of infectious diseases. 1 It is one of the most effective public health initiatives as it lowers the rates of mortality and morbidity associated with infectious diseases at a low cost. 2 It is a fundamental approach to ensuring the survival of children, and has been shown to prevent over 1.2 million child mortality annually. 3 To achieve the third Sustainable Development Goal (SDG-3.2), which aims to reduce under-5 mortality to at least as low as 25 per 1000 live births by 2030, is largely dependent on uptake of vaccinations. 4 Despite public health advancement, vaccine-preventable deaths, due to lower respiratory infections, meningitis, and measles, has constituted 21·7% of under-5 deaths globally. 5 In addition to the direct protection to those who have received vaccination, high vaccination rates offer indirect protection (herd immunity) to the remaining unvaccinated members of a population. However, there are significant differences in the duration of vaccine effects. While vaccines against measles, rotavirus, and pneumococcal disease have an immediate effect, the effects of vaccinations against human papillomavirus (HPV) and hepatitis B typically take longer to manifest in reduced adult morbidity and mortality. 1

World Health Organization (WHO) launched the Expanded Programme on Immunization (EPI) in 1974 with the aim of creating and growing vaccination regimens globally. 6 A goal was set in 1977 that all children worldwide will have access to poliomyelitis, tetanus, diphtheria, pertussis, measles, and tuberculosis vaccinations by 1990. Nonetheless, the goal has not been achieved because the program has faced a number of challenges, such as low public and governmental knowledge of the scope of the target diseases; poor program administration; inadequate tools and knowledge for handling and storing vaccines; vaccine hesitancy; and a lack of ways to track the program’s impact in terms of rising vaccination rates and falling incidence of the target diseases. In the first year of life, every child is required to receive one dose of BCG, oral polio vaccine (OPV0) at birth, hepatitis B vaccine (HBV1), penta1 and OPV1 at 6 weeks, penta2 and OPV2 at 10 weeks, penta3 and OPV3 at 14 weeks, measles and yellow fever at 9 months. 7

In sub-Saharan Africa (SSA), however, the full potential of vaccines has not been realized due to various factors including access, education, and cultural beliefs.8 -11 Vaccinations are essential in preventing illnesses such as measles, polio, and pneumonia, which are major causes of childhood morbidity and mortality. According to the WHO, vaccination prevents an estimated 2 to 3 million deaths globally. 12 Despite the proven benefits of vaccinations, several factors hinder their uptake. One of the primary challenges is the lack of access to healthcare services. 13 Many families in rural areas have limited access to vaccination clinics due to distance,14,15 making it difficult for them to get their children vaccinated. Additionally, the cost of transportation to vaccination centers can be a barrier for low-income families, 16 further reducing vaccine coverage rates. Parental education and health literacy plays a crucial role in vaccination uptake. 9 Cultural beliefs and practices also influence vaccination uptake. 11 With 52% of all deaths in this age group, SSA has the highest under-5 mortality rate globally, where the average under-5 mortality rate in 2018 was 78 deaths per 1000 live births, or 1 in 13 children dying before aged 5 years. 17

The objective of this study was to examine at childhood vaccinations coverage and associated factors among under-5 in SSA countries using demographic and health surveys (DHS) data. Over 85 countries have participated in this surveys, which have been conducted every 5 years since 1984. A major advantage of DHS is the same sampling technique used for data collection across all countries, which makes results comparable across borders. Although the DHS was created to supplement the demographic, family planning, and fertility data gathered by the Contraceptive Prevalence Surveys (CPSs) and World Fertility Surveys (WFSs), it has quickly expanded to become the most important population investigation basis for the tracking of population health guidelines, especially in areas with limited resources. Data from the DHS is useful in epidemiologic investigations to calculate prevalence and health inequalities. Information concerning DHS is available in literature. 18

Methods

Data Source

We examined nationally representative cross-sectional data from the 2008 to 2022 Demographic and Health Surveys (DHS) in SSA countries. The study examined data from: Angola, Benin, Burkina Faso, Burundi, Cameroon, Chad, Comoros, Congo, Congo Democratic Republic, Cote d’Ivoire, Eswatini, Ethiopia, Gabon, Gambia, Ghana, Guinea, Kenya, Lesotho, Liberia, Madagascar, Malawi, Mali, Mauritania, Namibia, Niger, Nigeria, Rwanda, Sao Tome and Principe, Senegal, Sierra Leone, South Africa, Tanzania, Togo, Zambia, and Zimbabwe. DHS data is publicly available and can be found at http://dhsprogram.com/data/available-datasets.cfm.

Sampling Technique

The selection of 35 out of 49 countries in SSA was based on the availability of relevant data on under-5 children between 2008 and 2022. This ensures that the analysis reflects recent estimates and includes a sufficient time span for meaningful comparisons. The choice of countries with available data allows for comprehensive coverage, representing diverse regions within SSA. Additionally, it ensures data consistency, reducing potential bias that may arise from incomplete or outdated information. By focusing on these countries, the analysis remains robust while providing actionable insights into childhood vaccination coverage across the countries.

Selection and Measurement of Variables

Outcome

According to EPI schedule, every child will receive one dose of Bacillus Calmette Guerin (BCG), Oral Polio Vaccine (OPV0), and Hepatitis B Vaccine (HBV1) at birth, Penta1 and OPV1 at 6 weeks of age, Penta2 and OPV2 at 10 weeks of age, Penta3 and OPV3 at 14 weeks of age and measles and yellow fever at 9 months of age. 7 The outcome variables of this study was measured as: “yes” versus “no” if a child received each of the essential vaccines. This was further measured as those who received all the basic vaccinations, those who received none or those who ever received vaccination.

Explanatory Variables

Sex of a child (male vs female); age of a child; mother’s age (15-19, 20-24, 25-29, 30-34, 35-39, 40-44, 45-49); place of residence (urban vs rural); mother’s education (no formal education, primary, secondary, higher); sex of household head (male vs female); mother’s exposure to magazine/newspaper (not at all, less than once a week, at least once a week, almost every day); mother’s exposure to radio (not at all, less than once a week, at least once a week, almost every day); mother’s exposure to tv (not at all, less than once a week, at least once a week, almost every day); mother’s age at first childbirth; health insurance coverage (yes vs no); mother’s marital status (not in union, married, widowed/separated/divorced); household wealth quintiles (poorest, poorer, middle, richer, richest). The DHS wealth index was kept because it can be found directly in the dataset. 19 The DHS wealth index for the household was constructed by utilizing ownership of asset data to generate a linear index, which was then measured using principal component analysis. The wealth index in the first survey was created by assigning a score to each household and ranking each member of the home according to their score. Subsequently, five equal category distributions were divided, with 20% of the population representing each category. These comprised data on economic indicators, housing standards, household amenities, the quantity of consumer items, and the amount of land holdings.

Statistical Analysis

With the use of Stata survey module (“svy”), sampling weights, clustering, and stratification were taken into consideration in data analysis. This ensures that individuals from underrepresented groups have a proportionate effect on the final estimates. Percentage was used to estimate the coverage of vaccinations. Furthermore, unadjusted or crude logistic regression was conducted to examine the association between childhood vaccination and associated factors at the bivariate analysis. Only the statistically significant factors in the crude or unadjusted regression models were included in the multivariable or adjusted logistic regression model. The adjusted or multivariable logistic regression model was used to determine the factors associated with vaccination. In the multivariable binary logistic regression model, we computed the standard errors of the parameter estimates through several steps. First, the model coefficients were estimated using maximum likelihood estimation. Then, the variance-covariance matrix of the coefficient estimates was computed, which accounts for the uncertainty in the parameter estimates. This matrix was used to calculate the standard errors of the parameter estimates. Finally, confidence intervals for the parameter estimates were constructed using the standard errors. This process accounts for the uncertainty in the estimates and allows for the assessment of the precision of the parameter estimates in the logistic regression model. We set the significant level at 5%. The analysis was performed in Stata 17.0 version (StataCorp, College Station, TX, USA).

To address potential confounding factors within the datasets, we carefully planned the analytical technique. First, we established that datasets were collected using consistent sampling methods and the variables extracted were defined the same way and similar instruments across countries. If variations existed, we would have adjusted for such differences during statistical analysis. In addition, we applied statistical methods such as multivariable logistic regression analysis and weighting to account for confounders. These methods helped adjust for differences in confounding variables between time points. By using these techniques, we controlled for confounding factors and enhance the reliability of our findings.

We used StatCompiler to create a geospatial map. This was done by first selecting the vaccination indicator from StatCompiler (https://www.statcompiler.com/en/) using available DHS data in SSA countries. We used visualization techniques such as color gradients to represent variations in vaccination coverage across SSA countries. We employed layers to show multiple data points of vaccination coverage and apply legends and labels for clarity. The map generated was exported in a compatible format.

Ethical Approval and Informed Consent

Population-based anonymized public domain datasets were examined in this work. MEASURE DHS/ICF International granted the authors permission to use the data. The DHS Program complies with all relevant regulations in regards to safeguarding respondents’ personal information. ICF International ensures that the survey complies with the Human Subjects Protection Act of the US Department of Health and Human Services. Prior to administering the surveys, the DHS team secured approval from the National Health Research Ethics Committees of multiple nations. For this inquiry, no further permissions were required. For more on our data and ethical standards, please see the link: http://goo.gl/ny8T6X.

Results

Table 1 shows the coverage of under-5 who received all and no basic vaccinations in SSA countries. From the results, Rwanda (92.2%), Burundi (81.8%), Gambia (78.3%), Kenya (74.6%), and Burkina Faso (70.8%) had the leading coverage of under-5 who received all basic vaccinations in the first year of life. Chad (70.8%), Congo Democratic Republic (52.5%), Niger (47.7%), Nigeria (43.0%), and Ethiopia (42.1%) had the leading coverage of under-5 who received no basic vaccinations in first year of life. In addition, the coverage of children 12 to 23 months who received all and no basic vaccinations in SSA countries is presented in Table 1. Rwanda (93.0%), Burundi (83.1%), Gambia (79.8%), Kenya (77.0%), Eswatini (73.7%), Burkina Faso (71.8%), Zambia (70.3%), and Malawi (70.0%) had the leading coverage of children 12 to 23 months who received all basic vaccinations in first year of life. Chad (60.5%), Congo Democratic Republic (50.3%), and Nigeria (39.8%) had the leading coverage of children aged 12 to 23 months who received no basic vaccinations in first year of life. See Table 1 below for the details.

Table 1.

Vaccination Coverage in 2008 to 2022 Demographic and Health Surveys in Sub-Saharan Africa (n = 358 949).

Country Survey year Number of children (n) Children under-5 who received all basic vaccinations in first year of life (%) Children aged 12-23 months who received all basic vaccinations in first year of life (%) Children under-5 who received no basic vaccinations in first year of life (%) Children aged 12-23 months who received no basic vaccinations in first year of life (%)
Angola 2015-2016 14 322 25.4 28.2 36.1 32.2
Benin 2017-2018 13 589 51.1 53.7 15.1 13.0
Burkina Faso 2021 12 343 70.8 71.8 3.7 2.6
Burundi 2016-2017 13 192 81.8 83.1 2.0 1.5
Cameroon 2018 9733 48.4 49.1 20.9 17.6
Chad 2014-2015 18 623 9.6 18.3 70.8 60.5
Comoros 2012 3149 26.5 52.8 24.6 16.3
Congo 2011-2012 9329 23.6 42.3 22.9 19.4
Congo Democratic Republic 2013-2014 18 716 22.0 41.2 52.5 50.3
Cote d’Ivoire 2021 10 645 30.3 32.9 13.5 12.9
Eswatini 2006-2007 2812 38.1 73.7 9.3 7.3
Ethiopia 2019 5753 38.3 40.2 42.1 36
Gabon 2019 6376 39.9 40.7 14.9 14.6
Gambia 2019-2020 8362 78.3 79.8 3.0 1.4
Ghana 2022 9353 66.5 68.9 4.2 3.8
Guinea 2018 7951 21.0 21.3 32.6 29.3
Kenya 2022 19 530 74.6 77.0 6.0 5.2
Lesotho 2014 3138 35.0 60.1 15.1 6.6
Liberia 2019-2020 5704 42.5 45.7 11.7 9.7
Madagascar 2021 12 499 43.7 44.6 30.7 28.5
Malawi 2015-2016 17 286 65.7 70.0 8.0 5.1
Mali 2018 9940 36.2 41.2 24.1 23.0
Mauritania 2019-2021 11 628 30.7 32.1 30.8 27.5
Namibia 2013 5046 30.8 62.6 13.7 9.8
Niger 2012 12 558 23.7 43.9 47.7 28.9
Nigeria 2018 33 924 26.4 28.3 43.0 39.8
Rwanda 2019-2020 8092 92.2 93.0 0.7 0.4
Sao Tome and Principe 2008-2009 1931 37.2 67.7 9.9 4.6
Senegal 2019 6125 65.3 67.5 7.0 6.0
Sierra Leone 2019 9899 44.9 49.1 6.4 5.2
South Africa 2016 3548 56.7 57.7 8.9 7.3
Tanzania 2022 10 783 50.4 48.7 12.4 10.6
Togo 2013-2014 6979 28.7 54.8 18.6 12.9
Zambia 2018 9959 66.7 70.3 7.8 6.8
Zimbabwe 2015 6132 67.3 69.0 24.8 20.5

Table 2 shows vaccinations in first year of life among children aged 12-23 months. From the results, there is a pattern of variations in the coverage of vaccines in first year of life across all SSA countries. In addition, the variations in coverage also exist for vaccines that should be taken at the same age schedule. The coverage of BCG and Polio 0 varied across all countries, even though these should be taken at the same time—at birth. For 6 weeks, 10 weeks, 14 weeks, and 9 months vaccinations coverage, there were within and between age schedule variations. Rwanda (95.5%), Burundi (92.0%), Kenya (85.9%), Zambia (85.6%), Malawi (85.5%), and Gambia (85.2%) had the leading vaccinations coverage at 9 months in first year of life.

Table 2.

Vaccinations in First Year of Life Among Children Aged 12 to 23 Months.

Country Survey year At birth At 6 weeks At 10 weeks At 14 weeks At 9 months
BCG vaccination received in first year Polio 0 vaccination received in first year DPT 1 vaccination received in first year Polio 1 vaccination received in first year DPT 2 vaccination received in first year Polio 2 vaccination received in first year DPT 3 vaccination received in first year Polio 3 vaccination received in first year Measles vaccination received in first year
Angola 2015-2016 70.4 64.3 67.1 65.8 49.7 53.3 38.1 39.9 51.2
Benin 2017-2018 88.1 86.3 84 81.9 77.9 76.7 72.2 64.8 64.5
Burkina Faso 2021 96.5 93.4 94.8 93.1 92.1 89.3 87.4 79.8 81.5
Burundi 2016-2017 97.5 90 99 98.5 98.4 97.3 95.9 91.5 92
Cameroon 2018 86.2 74.9 82.9 85 78.1 79.3 70.8 66.1 61.4
Chad 2014-2015 55.2 36.4 53.5 70.5 43.8 60.3 28.4 42.6 39.8
Comoros 2012 84.6 80.1 80.6 85.5 78.5 78.9 71.2 69.4 63.4
Congo 2011-2012 93.3 76 88 86.3 81.4 76.5 70.7 56.4 68.1
Congo Democratic Republic 2013-2014 82.8 49.5 79.6 89.6 71.9 82.2 58.2 62.9 64.4
Cote d’Ivoire 2021 86.8 69.3 69.5 80.8 62.3 73.4 53.6 61.7 55.1
Eswatini 2006-2007 97 92.8 95.4 96.3 93.8 94.6 90.2 85.9 82.7
Ethiopia 2019 70.4 31.6 75.1 76.7 70.3 70.6 60.3 58.4 54.8
Gabon 2019-2021 88.5 80.3 82.2 81.1 73.5 73.5 66.9 60.2 58.3
Gambia 2019-2020 98.8 98.2 98.2 97.4 96.1 95 92.1 89.8 85.2
Ghana 2022 95 76 96.9 95.4 94.1 91.1 87.9 83.1 80.4
Guinea 2018 72.9 68.6 61.7 64.1 49.4 51.2 39.1 38.6 35
Kenya 2022 96.7 86 97.1 96.5 93.9 94.1 88.9 77.9 85.9
Lesotho 2014 97.6 84.3 98.3 96 95 88.4 83.9 74.9 79.6
Liberia 2019-2020 89.3 85.9 90.9 86 82.5 76.7 67.8 62 68.2
Madagascar 2021 78.2 61.2 77.9 76.3 73.9 70.5 67.2 57.3 58.7
Malawi 2015-2016 97 72 97.2 96.6 95.7 93.2 91.9 79.7 85.5
Mali 2018 82.6 65.2 81.3 77.8 74.6 72.3 68.8 53.2 64.4
Mauritania 2019-2021 87.6 65.7 85.8 81.5 80.3 72.9 68.1 44.9 62.4
Namibia 2013 94.2 89.9 92.3 92.2 88.8 87.4 82.4 73.2 82.9
Niger 2012 82.6 56.4 84.4 90.8 76.8 82.3 64.8 71.1 57.5
Nigeria 2018 66 54.3 64.5 72.7 56.6 65.4 48.3 45.6 48.5
Rwanda 2019-2020 99.1 93.9 99.6 99.6 99.4 99.3 98.8 97.6 95.5
Sao Tome and Principe 2008-2009 95.2 90.3 93.6 94.6 89.4 90.2 86.4 85.7 75.3
Senegal 2019 93.3 79.9 96 95.3 94.5 93.1 91.1 83 76.6
Sierra Leone 2019 95.7 92.4 94.1 89.1 85.4 80.6 76.2 69.5 65.6
South Africa 2016 92.2 92.3 90.1 78 75.1 64.6 82
Tanzania 2022 90.4 51.1 94.5 88.3 92.9 77.2 89.2 58 81.3
Togo 2013-2014 95.1 86.9 93.1 93.9 89 88.8 81.6 73 66.2
Zambia 2018 97 66.4 97.6 96.2 95.4 92.9 91.4 80.6 85.6
Zimbabwe 2015 89.4 89.2 89.2 87.9 87.6 82 81 76.2

Table 3 shows vaccinations in first year of life among under-5 in SSA countries. From the results, there is a pattern of variations in the coverage of vaccines in first year of life across all SSA countries. Furthermore, the variations in coverage also exist for vaccines that should be taken at the same age schedule. The coverage of vaccines at birth, 6 weeks, 10 weeks, 14 weeks, and 9 months varied across all countries, even for vaccines that should be taken at the same time. The within and between age schedule variations was visible. Rwanda, Burundi, Eswatini, Gambia, Ghana, Kenya, Lesotho, Burkina Faso, Congo, Malawi, Namibia, and Zambia had the leading vaccinations coverage at 9 months in first year of life.

Table 3.

Vaccinations in First Year of Life Among Under-5.

Country Survey year At birth At 6 weeks At 10 weeks At 14 weeks At 9 months
BCG vaccination received in first year Polio 0 vaccination received in first year DPT 1 vaccination received in first year Polio 1 vaccination received in first year DPT 2 vaccination received in first year Polio 2 vaccination received in first year DPT 3 vaccination received in first year Polio 3 vaccination received in first year Measles vaccination received in first year
Angola 2015-2016 68.4 61.7 64.8 61.5 46.8 50.8 35.1 36.9 50.5
Benin 2017-2018 86.4 84.2 82.6 80.6 76.4 75.3 70.9 62.5 62.8
Burkina Faso 2021 96.1 92.7 93.7 92.5 90.6 88.5 86.1 77.7 81.7
Burundi 2016-2017 97.5 90.4 98.7 98.1 98.2 96.8 95.8 89.2 92.5
Cameroon 2018 84.3 72.6 81.8 83.7 76.7 78.3 69.7 63.4 63.6
Chad 2014-2015 54.7 28.9 50.1 69.6 42.6 61.4 28.9 47.4 41.7
Comoros 2012 80.9 74.1 75.5 79.6 71.6 70.9 62.9 56.8 64
Congo 2011-2012 93.1 75.4 88.6 89.5 83.1 80.4 72.8 56.2 73.6
Congo Democratic Republic 2013-2014 83.8 47.8 80.6 88.3 74.2 79.8 61.5 61.1 70.6
Cote d’Ivoire 2021 87 70.4 69.6 81.2 61.5 73.3 52.6 58.6 55.7
Eswatini 2006-2007 95.4 90.6 94.6 94.9 92.3 91.9 88.4 77.3 84.1
Ethiopia 2019 66.5 32 69.2 72.1 64.4 65.8 54.7 53.8 52.4
Gabon 2019-2021 87.8 81 82.2 80.7 74.5 73.8 66.3 59.1 59.3
Gambia 2019-2020 98.4 96.7 97.7 97.2 95.8 94.5 91 87.8 85.2
Ghana 2022 94.7 75.4 95.9 94.2 92.6 89.3 85.9 79.3 81
Guinea 2018 71 66 61.6 62.4 48.7 50.7 39 37.2 36.5
Kenya 2022 96 85.5 96.4 95.2 92.6 92.3 86.9 72.9 85.5
Lesotho 2014 96 79.5 96.9 95 92.3 87.1 83.5 70.9 84.8
Liberia 2019-2020 90 84 89.9 83.9 78.9 72.8 64.2 57.1 68.3
Madagascar 2021 77.3 60.8 76.8 75.3 72.7 69.6 66.9 55.7 58.9
Malawi 2015-2016 96.1 72.6 96.3 95.6 94.7 92 90.1 76.1 84.4
Mali 2018 82.1 65.6 80.9 76.8 74 70.4 67.1 48.3 62.8
Mauritania 2019-2021 86.6 63.9 84.1 79.1 77.7 70.4 66.6 42.1 63
Namibia 2013 93.5 86.2 91.8 91.6 85.1 84.8 76.4 65.6 83.3
Niger 2012 80.1 46.1 80.3 88.7 73.4 79 61.9 68.8 63.5
Nigeria 2018 64.7 52.4 62.5 71.2 54.6 64.3 46.9 43.7 49
Rwanda 2019-2020 99 94 99.5 99.4 99.1 98.8 98.4 96.7 95.5
Sao Tome and Principe 2008-2009 93.8 88.5 91.7 93.2 88.3 89.1 85.3 82.3 79.3
Senegal 2019 93.3 79.8 95.4 94 94 92.3 90.9 78.8 78.4
Sierra Leone 2019 94.7 91.7 93 86.8 83.5 77.5 73.4 64.2 65.8
South Africa 2016 91.4 89.9 88.5 75.9 72.7 63.3 79.7
Tanzania 2022 90.7 57.7 94.4 88.4 92.6 78.2 88.5 59.5 80.5
Togo 2013-2014 93.4 81.4 91.2 92.8 87.9 88 79.7 64.1 71.5
Zambia 2018 96.6 66.8 97.3 95.8 95 92.1 90.1 78 84.3
Zimbabwe 2015 87.8 87.6 87.7 86.1 85.8 80.4 79.3 74.5

Table 4 shows the sociodemographic factors associated with vaccination in SSA. For every unit increase in the age of a child, there was a 72% increase in the odds of vaccination (aOR = 1.72; 95% CI: 1.69-1.75). Children with older mothers had higher odds of vaccination, when compared with children with mothers aged 15 to 19 years. There was a 6% reduction in the odds of vaccination among children from rural residence, when compared with their urban counterparts (aOR = 0.94; 95% CI: 0.90-0.99). Children with educated mothers had over two times higher odds of vaccination, when compared with those from mothers with no formal education. Children from female headed households had a 9% higher odds of vaccination, when compared with children from male headed households (aOR = 1.09; 95% CI: 1.04-1.14). Children whose mothers were exposed to magazine/newspaper, radio, and tv had a higher odds of vaccination, when compared to children whose mothers were not exposed to media. Children from rich households had a higher odds of vaccination, when compared with children from poorest household. There was a 13% increase in the odds of vaccination among children covered by health insurance, when compared with those not covered by health insurance (aOR = 1.13; 95% CI: 1.02-1.25). Children from mothers that were formerly married had a 21% increase in the odds of vaccination, when compared with children from single women (aOR = 1.21; 95% CI: 1.09-1.33).

Table 4.

Demographic and Socioeconomic Factors Associated with Vaccinations in SSA.

Variable Unadjusted odds ratio 95% confidence interval Adjusted odds ratio 95% confidence interval
Sex of child
 Male 1.00
 Female 1.02 0.99-1.06
Age of child 1.62 1.60-1.64 1.72 1.69-1.75
Mother’s age
 15-19 1.00 1.00
 20-24 1.51 1.43-1.60 1.21 1.13-1.29
 25-29 1.54 1.45-1.62 1.26 1.18-1.35
 30-34 1.62 1.52-1.71 1.33 1.24-1.43
 35-39 1.62 1.52-1.72 1.35 1.25-1.46
 40-44 161 1.49-1.74 1.34 1.22-1.47
 45-49 1.46 1.30-1.64 1.19 1.03-1.37
Place of residence
 Urban 1.00 1.00
 Rural 0.52 0.50-0.54 0.94 0.90-0.99
Mother’s education
 No formal education 1.00 1.00
 Primary 2.21 2.14-2.29 2.06 1.98-2.15
 Secondary 3.50 3.35-3.65 2.54 2.41-2.69
 Higher 6.10 5.28-7.06 2.93 2.45-3.50
Sex of household head
 Male 1.00 1.00
 Female 1.25 1.20-1.29 1.09 1.04-1.14
Mother’s exposure to magazine/newspaper
 Not at all 1.00 1.00
 Less than once a week 2.91 2.67-3.17 1.17 1.06-1.29
 At least once a week 2.81 2.55-3.11 1.08 0.97-1.22
 Almost every day 2.08 1.49-2.88 0.58 0.41-0.83
Mother’s exposure to radio
 Not at all 1.00 1.00
 Less than once a week 1.78 1.70-1.86 1.39 1.32-1.46
 At least once a week 2.04 1.96-2.12 1.36 1.29-1.43
 Almost every day 2.33 2.08-2.61 1.34 1.17-1.52
Mother’s exposure to tv
 Not at all 1.00 1.00
 Less than once a week 1.72 1.62-1.82 1.10 1.02-1.17
 At least once a week 2.20 2.10-2.30 1.00 0.94-1.06
 Almost every day 3.01 2.64-3.44 1.24 1.07-1.44
Wealth index
 Poorest 1.00 1.00
 Poorer 1.26 1.22-1.31 1.13 1.08-1.18
 Middle 1.59 1.53-1.66 1.34 1.27-1.41
 Richer 2.08 1.98-2.18 1.58 1.48-1.67
 Richest 3.52 3.31-3.73 1.97 1.81-2.15
Mother’s age at first childbirth 1.03 1.02-1.04 1.00 0.99-1.01
Health insurance coverage
 Yes 1.67 1.53-1.83 1.13 1.02-1.25
 No 1.00 1.00
Mother’s marital status
 Not in union 1.00 1.00
 Married 0.74 0.70-0.79 1.03 0.96-1.11
 Widowed/separated/divorced 1.16 1.06-1.26 1.21 1.09-1.33

Discussion

From the findings of this study, Rwanda (92.2%), Burundi (81.8%), Gambia (78.3%), Kenya (74.6%), and Burkina Faso (70.8%) had the leading coverage of under-5 who received all basic vaccinations in the first year of life Conversely, Chad (70.8%), Congo Democratic Republic (52.5%), Niger (47.7%), Nigeria (43.0%), and Ethiopia (42.1%) had the leading coverage of under-5 who received no basic vaccinations in first year of life. This is consistent with the findings from previous studies.20,21 The objective of SDG-3.2 is to enhance child health and survival rates. This has led to notable adjustments in both public and private investments, with the goal of facilitating access to reasonably cost-effective programs that enhance children’s health, including vaccination schedules. 22 However, several factors have been identified as barriers to complete basic vaccinations.

Children from older mothers were more likely to have received vaccinations compared to children from mothers aged 15 to 19 years old. This could be due to the fact that older mothers learn over time on the importance and benefits of vaccinations and the consequences of having unvaccinated children. This is consistent with the findings from studies.23,24 As a child gets older, there was higher odds of being vaccinated. This is because, for various reasons the child visits health centers and the missed opportunities for vaccinations are addressed. The emphasis should be in timely vaccinations, as children will become susceptible to various vaccines preventable illnesses due to missed opportunities for vaccinations.

Furthermore, we found that, in comparison to their urban counterparts, children in rural areas had a lower likelihood of receiving vaccines. Africa’s population is primarily rural, with limited access to health care. 25 Vaccination programs in remote areas are hindered by inadequate workforce levels and inadequate logistical support. Furthermore, due to inadequate transportation infrastructure, around 16% of rural communities lack mobile vaccination programs, and over half of rural health centers face a vaccine shortage. 26 Compared to rural settings, urban vaccination campaigns have higher vaccination coverage due to the aforementioned challenges. These challenges were also reported in a previous study. 27 Variation in vaccination coverage between urban and rural areas in SSA can be attributed to the fact that urban areas generally have better healthcare infrastructure, including clinics and transportation systems, which facilitates easier access to vaccination services. In contrast, rural areas often suffer from inadequate healthcare facilities and poor transportation, making it difficult for residents to access vaccinations. Also, urban centers usually attract more healthcare professionals due to better working conditions and opportunities for career advancement. Rural areas may face shortages of healthcare workers, impacting the delivery and uptake of vaccination services. Urban areas typically benefit from higher education levels and greater awareness about the importance of vaccinations. In rural regions, lower levels of education and awareness can lead to misconceptions and lower vaccination rates. In addition, supply chain issues are more pronounced in rural areas, where transporting vaccines and maintaining proper storage conditions can be challenging. Urban areas benefit from more efficient logistics and better cold chain management. Furthermore, cultural beliefs and practices can influence vaccination rates. Urban areas might experience more diverse healthcare influences and acceptance, whereas rural areas may have more entrenched traditional beliefs that impact vaccination uptake.

In low-income countries, maternal education is considered to be a significant factor influencing vaccination uptake. Regardless of education level, mothers with higher levels of education have higher vaccination rates for their children, according to a recent systematic review. 9 Additionally, a previous population-based study, showed that mothers with only a primary education had a higher likelihood of their children being fully vaccinated than mothers with no formal education. 28 Furthermore, early marriages and pregnancies are two things that hinder the educational opportunities for women. Africa has a high percentage of child marriages globally, with 40% of females reportedly getting married before becoming 18 years old. 29 Due to cultural stigmatization, many girls are pressured into young marriages. 30 In an effort to keep girls in school longer and prevent early female marriages, many African countries have committed to implementing universal or mandatory primary education. Re-entry policies have been put in place by countries including South Africa, Cameroon, and Zambia to allow mothers to return to school after giving birth. Nonetheless, young mothers frequently experience social isolation in schools and lack the financial means to attend. 31 In the Ambo area of Ethiopia, for instance, a survey revealed that although the majority of mothers understood the value of vaccination, few of them were aware of the appropriate age to start vaccinating their children. 32

In this study, exposure to media such as magazine/newspaper, radio, and tv by mothers had higher odds of vaccinations among under-5. Exposure to media by mothers is a source of knowledge and enlightenment about availability and use for health care services. Previous studies have reported the importance of media as source of health information and promotes knowledge.33 -36 No doubt, this can promote good knowledge of child vaccination among mothers. Research evidence from Ethiopia highlights that maternal understanding of vaccination was found to be a predictor of vaccination uptake. 37 In comparison to children whose mothers had inadequate understanding of vaccination, children of mothers with good awareness of the disease were found to have a threefold higher likelihood of being fully immunized. 37 Similar findings has been reported in another study. 14 Mothers in Burkina Faso who were aware of the preventive benefits of vaccination were more likely to vaccinate their children than those who were not. 27 Poor maternal knowledge of vaccines was found to be the primary factor contributing to poor vaccination uptake, accounting for 50% of the reasons for non-vaccination in a household-level cluster survey of 7815 children conducted in 40 polio high-risk districts of Nigeria. 38 This highlights that exposure to media improves health literacy of the community on vaccinations.

The children from rich households had higher odds of vaccinations, when compared with the poorest counterparts. There exists a correlation between a parent’s primary economic pursuits and the completion of vaccinations. Unlike parents who have a job, parents who are poor or unemployed might not be able to afford health care costs. The results of the study indicate a relationship between vaccination coverage and household economic conditions. In most circumstances, household income disparities impact vaccination uptake. 7 A higher vaccination coverage exists in regions with a high economic quartile. A financial constraint has been stated by mothers as one of the reasons they do not vaccinate their children. There are certain countries with good health insurance policies, where access to medical services is convenient.7,39

Health insurance coverage has been reported to promote health care services uptake,40 -42 as was also found in this study to increase the odds of vaccinations. A collection of policy levers known as strategic health purchasing must be operationalized in order to direct the money raised via contributions (ie, pooled funds) for national health insurance towards vaccination. 43 It is necessary for these plans to exist in order to give the buyer (national health insurance) the ability to choose what services to acquire (such as vaccination services included in the health benefit package), from whom to purchase them, and how to pay for them. 44 One of the most significant roles in the system was seen to be played by the insurance system, and the introduction of strategic health care purchasing was done so to shield individuals from the financial risk that comes with illness. In addition, children from families headed by women were more likely than those headed by men to receive vaccinations. This may be due to enhanced women’s empowerment, decision-making power or high socioeconomic status.

Strengths and Limitations

This study estimated vaccination coverage of under-5. We conducted secondary analysis of nationally representative datasets This could encourage collaboration, new policies and initiatives, and a mobilization of people to support current efforts aimed at improving vaccine uptake. However, DHS did not collect data of income or expenditure, which are two common indicators of wealth. The wealth index used in this study is determined by collecting information on household asset, which is a proxy of the financial situation of households. The results of this index are not always comparable to those resulting from direct revenue and expenditure capacities. Another limitation to the study was the use of data across a 14-year period (2008-2022). For inter-country comparisons, this could be problematic, as it can fail to account for potential temporal trends and variations in demographic, health, and socioeconomic factors.

Conclusion

SSA countries need to prioritize funding for vaccine access, increase vaccine coverage storage, address vaccine hesitancy while identifying priority populations for vaccination in order to address their local vaccination failures and issues. To ensure complete vaccination coverage, extensive community engagement and efficient health communication are essential. While there have been many recommendations for ways to increase vaccination coverage in SSA countries, reaching the required levels to fully reap the advantages of vaccination remains a significant barrier. Healthcare systems and providers working together can do this, and it will benefit individuals as well as the communities and cultures in which they live.

Acknowledgments

The authors appreciate the MEASURE DHS project for the approval and access to the original data.

Footnotes

Author Contributions: Michael Ekholuenetale: Contributed to conception and design; Contributed to data curation, analysis and interpretation; Drafted the manuscript; Discussed the findings; critically revised the manuscript; Gave final approval; Agrees to be accountable for all aspects of work ensuring integrity and accuracy.

Victor A. Ochagu: Contributed to conception and design; Contributed to analysis; Drafted the manuscript; critically revised the manuscript; Gave final approval; Agrees to be accountable for all aspects of work ensuring integrity and accuracy.

Olayinka Stephen Ilesanmi: Contributed to conception and design; Contributed to analysis; Drafted the manuscript; critically revised the manuscript; Gave final approval; Agrees to be accountable for all aspects of work ensuring integrity and accuracy.

Okikiolu Badejo: Contributed to conception and design; Contributed to analysis; Drafted the manuscript; critically revised the manuscript; Gave final approval; Agrees to be accountable for all aspects of work ensuring integrity and accuracy.

Amit Arora: Contributed to conception and design; Contributed to analysis; Drafted the manuscript; critically revised the manuscript; Gave final approval; Agrees to be accountable for all aspects of work ensuring integrity and accuracy.

Availability of Data and Materials: Data for this study were sourced from Demographic and Health surveys (DHS) and available here: http://dhsprogram.com/data/available-datasets.cfm.

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.

Ethical Approval and Consent to Participate: This study is a secondary data analysis, which is publicly available, approval was sought from MEASURE DHS/ICF International and permission was granted for this use. The original DHS data were collected in conformity with international and national ethical guidelines. Written consent was obtained from mothers/caregivers and data were recorded anonymously at the time of data collection during the data collection. More details regarding DHS data and ethical standards are available at: http://dhsprogram.com/data/availabledatasets.cfm.

ORCID iD: Michael Ekholuenetale Inline graphic https://orcid.org/0000-0002-2372-3020

References

  • 1. Li X, Mukandavire C, Cucunubá ZM, et al. Estimating the health impact of vaccination against ten pathogens in 98 low-income and middle-income countries from 2000 to 2030: a modelling study. Lancet. 2021;397(10272):398-408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Ozawa S, Mirelman A, Stack ML, Walker DG, Levine OS. Cost-effectiveness and economic benefits of vaccines in low- and middle-income countries: a systematic review. Vaccine. 2012;31(1):96-108. [DOI] [PubMed] [Google Scholar]
  • 3. Wolfson LJ, Gasse F, Lee-Martin SP, et al. Estimating the costs of achieving the WHO-UNICEF global immunization vision and strategy, 2006-2015. Bull World Health Organ. 2008;86(1):27-39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Rosa W, ed. Transforming our world: the 2030 agenda for sustainable development. In: Rosa W, ed. A New Era in Global Health. Springer; 2017. Accessed February 25, 2021. http://connect.springerpub.com/lookup/doi/10.1891/9780826190123.ap02 [Google Scholar]
  • 5. Perin J, Mulick A, Yeung D, et al. Global, regional, and national causes of under-5 mortality in 2000-19: an updated systematic analysis with implications for the sustainable development goals. Lancet Child Adolesc Health. 2022;6(2):106-115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Keja K, Chan C, Hayden G, Henderson RH. Expanded programme on immunization. World Health Stat Q Rapp Trimest Stat Sanit Mond. 1988;41(2):59-63. [PubMed] [Google Scholar]
  • 7. Galadima AN, Zulkefli NAM, Said SM, Ahmad N. Factors influencing childhood immunisation uptake in Africa: a systematic review. BMC Public Health. 2021;21(1):1475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Olorunsaiye CZ, Langhamer MS, Wallace AS, Watkins ML. Missed opportunities and barriers for vaccination: a descriptive analysis of private and public health facilities in four African countries. Pan Afr Med J. 2017;27(Suppl. 3):6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. 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]
  • 10. Adetokunboh O, Iwu-Jaja CJ, Nnaji CA, Ndwandwe D. Missed opportunities for vaccination in Africa. Curr Opin Immunol. 2021;71:55-61. [DOI] [PubMed] [Google Scholar]
  • 11. Chambongo PE, Nguku P, Wasswa P, Semali I. Community vaccine perceptions and its role on vaccination uptake among children aged 12-23 months in the Ileje District, Tanzania: a cross section study. Pan Afr Med J. 2016;23(162):1-8. Accessed March 18, 2024. https://www.panafrican-med-journal.com/content/article/23/162/full [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. WHO. Children: improving survival and well-being. Accessed March 18, 2024. https://www.who.int/news-room/fact-sheets/detail/children-reducing-mortality
  • 13. Kaufman J, Tuckerman J, Bonner C, et al. Parent-level barriers to uptake of childhood vaccination: a global overview of systematic reviews. BMJ Glob Health. 2021;6(9):e006860. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Bangura JB, Xiao S, Qiu D, Ouyang F, Chen L. Barriers to childhood immunization in sub-Saharan Africa: a systematic review. BMC Public Health. 2020;20(1):1108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Essoh TA, Adeyanju GC, Adamu AA, Tall H, Aplogan A, Tabu C. Exploring the factors contributing to low vaccination uptake for nationally recommended routine childhood and adolescent vaccines in Kenya. BMC Public Health. 2023;23(1):912. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Jelle M, Seal AJ, Mohamed H, et al. Understanding multilevel barriers to childhood vaccination uptake among internally displaced populations (IDPs) in Mogadishu, Somalia: a qualitative study. BMC Public Health. 2023;23(1):2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. United Nations Inter-Agency Group for Child Mortality Estimation (UN IGME). Levels & Trends in Child Mortality: Report 2019, Estimates developed by the United Nations Inter-agency Group for Child Mortality Estimation. United Nations Children’s Fund; 2019. Accessed March 18, 2024. https://www.who.int/publications/m/item/levels-and-trends-in-child-mortality-report-2021 [Google Scholar]
  • 18. Corsi DJ, Neuman M, Finlay JE, Subramanian S. Demographic and health surveys: a profile. Int J Epidemiol. 2012;41(6):1602-1613. [DOI] [PubMed] [Google Scholar]
  • 19. Rutstein SO, Staveteig S. Making the Demographic and Health Surveys Wealth Index Comparable. DHS Methodological Reports No. 9. ICF International; 2014. [Google Scholar]
  • 20. Tesema GA, Tessema ZT, Tamirat KS, Teshale AB. 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 Public Health. 2020;20(1):1837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. 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]
  • 22. Asuman D, Ackah CG, Enemark U. Inequalities in child immunization coverage in Ghana: evidence from a decomposition analysis. Health Econ Rev. 2018;8(1):9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Mekonnen AG, Bayleyegn AD, Ayele ET. Immunization coverage of 12-23 months old children and its associated factors in Minjar-Shenkora district, Ethiopia: a community-based study. BMC Pediatr. 2019;19(1):198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Abebe AM, Mengistu T, Mekuria AD. 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):71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Malison MD, Sekeito P, Henderson PL, Hawkins RV, Okware SI, Jones TS. Estimating health service utilization, immunization coverage, and childhood mortality: a new approach in Uganda. Bull World Health Organ. 1987;65(3):325-330. [PMC free article] [PubMed] [Google Scholar]
  • 26. Kaboré S, Kaboré BYL, Ouédraogo SYYA, et al. Equity of access to immunization services in the Center-East health region in 2018, Burkina Faso. Sante Publiq Vandoeuvre Nancy Fr. 2020;32(2):263-272. [DOI] [PubMed] [Google Scholar]
  • 27. Sanou A, Simboro S, Kouyaté B, Dugas M, Graham J, Bibeau G. Assessment of factors associated with complete immunization coverage in children aged 12-23 months: a cross-sectional study in Nouna District, Burkina Faso. BMC Int Health Hum Rights. 2009;9(1):S1-S10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Kibreab F, Lewycka S, Tewelde A. Impact of mother’s education on full immunization of children aged 12-23 months in Eritrea: population and health survey 2010 data analysis. BMC Public Health. 2020;20(1):267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Mulenga J, Mulenga MC, Bwalya BB, Ngongola-Reinke C. Too young to be a wife! analysis of the factors influencing child marriages and its influence on the preferred number of children among women in Zambia. Afr Popul Stud. 2018;32(2):1210. Accessed March 18, 2024. https://aps.journals.ac.za/pub/article/view/1210 [Google Scholar]
  • 30. Lilian GK, Nancy IA, Odundo PA, Akondo JO, Ngaruiya B. Early and forced child marriage on girls’ education, in Migori County, Kenya: constraints, prospects and policy. World J Educ. 2015;5(4):72. [Google Scholar]
  • 31. Tuwor T, Sossou M. Gender discrimination and education in West Africa: strategies for maintaining girls in school. Int J Incl Educ. 2008;12(4):363-379. [Google Scholar]
  • 32. Tadesse H, Deribew A, Woldie M. Predictors of defaulting from completion of child immunization in south Ethiopia, May 2008—a case control study. BMC Public Health. 2009;9(1):150. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Acharya D, Khanal V, Singh JK, Adhikari M, Gautam S. Impact of mass media on the utilization of antenatal care services among women of rural community in Nepal. BMC Res Notes. 2015;8:1-6. Accessed January 18, 2020. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534014/ [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Babalola S, Figueroa ME, Krenn S. Association of mass media communication with contraceptive use in sub-Saharan Africa: a meta-analysis of demographic and health surveys. J Health Commun. 2017;22(11):885-895. Accessed March 21, 2019. https://www.tandfonline.com/doi/abs/10.1080/10810730.2017.1373874 [DOI] [PubMed] [Google Scholar]
  • 35. Odesanya A, Hassan S, Olaluwoye D. Mass media and maternal healthcare: a critical discourse. New Media Mass Commun. 2015;34:63-71. [Google Scholar]
  • 36. Zamawe COF, Banda M, Dube AN. The impact of a community driven mass media campaign on the utilisation of maternal health care services in rural Malawi. BMC Pregnancy Childbirth. 2016;16(1):21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Aregawi HG, Gebrehiwot TG, Abebe YG, Meles KG, Wuneh AD. Determinants of defaulting from completion of child immunization in Laelay Adiabo District, Tigray Region, Northern Ethiopia: a case-control study. PLoS One. 2017;12(9):e0185533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Gunnala R, Ogbuanu IU, Adegoke OJ, et al. Routine vaccination coverage in Northern Nigeria: results from 40 district-level cluster surveys, 2014-2015. PLoS One. 2016;11(12):e0167835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Nyandekwe M, Nzayirambaho M, Kakoma JB. Universal health insurance in Rwanda: major challenges and solutions for financial sustainability case study of Rwanda community-based health insurance part I. Pan Afr Med J. 2020;37(55):1-12. Accessed March 18. 2024. https://www.panafrican-med-journal.com/content/article/37/55/full [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Ayanore MA, Pavlova M, Kugbey N, et al. Health insurance coverage, type of payment for health insurance, and reasons for not being insured under the National Health Insurance Scheme in Ghana. Health Econ Rev. 2019;9(1):39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41. Wang W, Temsah G, Mallick L. The impact of health insurance on maternal health care utilization: evidence from Ghana, Indonesia and Rwanda. Health Policy Plan. 2017;32(3):366-375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42. Ekholuenetale M, Barrow A. Inequalities in out-of-pocket health expenditure among women of reproductive age: after-effects of national health insurance scheme initiation in Ghana. J Egypt Public Health Assoc. 2021;96(1):6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Cashin C, Nakhimovsky S, Laird K, et al. Strategic Health Purchasing Progress: A Framework for Policymakers and Practitioners. Health Finance & Governance Project, ABT Associates Inc, 2018. Accessed March 18, 2024. https://www.hfgproject.org/strategic-health-purchasing-progress-a-framework-for-policymakers-and-practitioners/ [Google Scholar]
  • 44. Abedi G, Shojaee J, Bastani P, Kabir MJ, Yazdani J. The comparative study of strategic purchasing of health services in selected countries: a review study. Bali Med J. 2018;7(1):1-6. [Google Scholar]

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