http://orcid.org/0000-0002-8714-6162
Figures
Abstract
Introduction
Immunization is a cost-effective intervention that prevented more than 5 million deaths worldwide from 2010 to 2015. Despite increased vaccination coverage over the past four decades in many African countries, including Ethiopia, universal coverage has not yet been reached. Only 39% of children aged 12–23 months received full vaccinations in Ethiopia, according to the 2016 Ethiopian Demographic Health Survey. This study aimed to evaluate immunization coverage and identify individual and community factors that explain incomplete vaccination coverage among children aged 6–36 months in the Wonago district of southern Ethiopia.
Methods
We conducted a community-based, cross-sectional study in three randomly selected kebeles in the Wonago district from June to July 2017. Our nested sample of 1,116 children aged 6–36 months included 923 child-mother pairs (level 1) within kebeles (level 2). We conducted multilevel regression analysis using STATA software.
Results
Among participants, 85.0% of children aged 12–36 months received at least one vaccine, and 52.4% had complete immunization coverage. After controlling for several individual and community variables, we identified six significant predictor variables for complete immunization: Older mothers’ age (AOR = 1.05, 95% CI: 1.00–1.09), higher utilization of antenatal care (AOR = 1.36, 95% CI: 1.14–1.62), one or more tetanus-toxoid vaccination during pregnancy (AOR = 2.64, 95% CI: 1.43–4.86), mothers knowing the age at which to complete child’s vaccinations (AOR = 2.00, 95% CI: 1.25–3.20), being a female (AOR = 0.64, 95% CI: 0.43–0.95), and child receiving vitamin A supplementation within the last 6 months (AOR = 2.79, 95% CI: 1.59–4.90). We observed a clustering effect at the individual and community levels with an intra-cluster correlation coefficient of 48.1%.
Citation: Hailu S, Astatkie A, Johansson KA, Lindtjørn B (2019) Low immunization coverage in Wonago district, southern Ethiopia: A community-based cross-sectional study. PLoS ONE 14(7): e0220144. https://doi.org/10.1371/journal.pone.0220144
Editor: Italo Francesco Angelillo, University of Campania, ITALY
Received: March 4, 2019; Accepted: July 9, 2019; Published: July 24, 2019
Copyright: © 2019 Hailu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are with the manuscript files.
Funding: BL received funding by SENUPH Norwegian Program for Capacity Development in Higher Education and Research for Development. The fund number; ETH-13/0025; website: http://www.uib.no/en/cih. The funder had no role in study design,data collection and analysis,decision to publish or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Immunization is a cost–effective and lifesaving intervention that prevents sickness, disability, and death. Between 2010 and 2015, immunizations prevented more than 5 million deaths worldwide [1, 2]. In Ethiopia, vaccination programs averted 23% of deaths among children [3]. Vaccination coverage is an important indicator to monitor progress towards the United Nation’s Sustainable Development Goal 3 “Ensure healthy lives and promote well-being for all at all ages” [4, 5]. Specifically, this goal aims to eradicate preventable newborn and under-five mortality by 2030 and reduce under-five mortality to 25 per 1,000 live births [4, 5].
The World Health Organization (WHO) launched the global Expanded Program on Immunization (EPI) in 1974 to control and reduce vaccine-preventable disease and death among children throughout the world. For children under one year old, the program recommends country-level immunization rates of 90% and at least 80% within districts or equivalent administrative units [6–9]. From 2010 to 2016, global immunization coverage stalled at 86%. Worldwide, vaccine coverage remained high, but regional rates varied, particularly among children in low- and middle-income countries, such as sub-Saharan Africa [10, 11]. For example, using the diphtheria-pertussis-tetanus-3 vaccine as a key indicator (because it tends to largely be distributed through horizontal health programs and not vaccine campaigns such as supplementary immunization activities, it is the proxy for the completion of vaccination series and ability health system to reach children multiple times), the coverage among children younger than 1 year was 86% globally, 75% in Africa, and 96% in the western Pacific and Europe. Most children (14.8 million;68%) who did not receive this vaccine lived in 10 countries, including Ethiopia [12].
Ethiopia has a high burden of diarrheal diseases, vaccine-preventable diseases, and malnutrition [13]. In 1980, the Ethiopian Ministry of Health launched its own immunization program to increase vaccine coverage by 10% annually and reach 100% coverage among children younger than 2 years by 1990 [14]. These implementation guidelines were revised in 2015 to focus on children younger than one year and women of reproductive age (15–49 years) as the main targets for currently available vaccines in Ethiopia. Progress has been made [7]. Diphtheria-pertussis-tetanus-3 coverage reached 3% in 1980 and 49% in 1990 [15]. This coverage has gradually increased with the Reach Every District initiative, started in 2004, and the health extension program, implemented in 2003 [16]. Unfortunately, full immunization coverage has not been reached. The 2016 Ethiopian Demographic Health Survey reported only 39% vaccination rates in children aged 12–23 months and that rate varied substantially across geographical regions. For example, coverage in the Southern Nation, Nationalities, and Peoples’ Region was 47% [17]. Despite outreach strategies and supplementary immunization schedules, full coverage remains very low in some regions of Ethiopia (e.g. Afar and Somali).
To achieve the goal and reduce child mortality, vaccinating children should be maintained. So, understanding the level and factors that affect the coverage should be known. Previous studies evaluate the coverage and suggest that antenatal care, mothers’ tetanus vaccination status, place of birth, mother’s education, mother’s knowledge about vaccination, and household wealth can affect immunization coverage [18–27]. However, these studies focus on individual factors while neglecting community, household, and institutional factors. The objective of this study thus was to evaluate immunization coverage and to identify factors associated vaccination coverage at individual and community levels among children aged 6–36 months. Children age less than 11 months were focused to see the immunization coverage of children assessed for child immunized accordance to their age. We conducted this study in the Gedeo Zone of southern Ethiopia. The results would help policymakers, program implementers, and service providers to address issues that decrease vaccination rates.
Materials and methods
Ethical clearance
The institutional review board at the College of Medicine and Health Sciences of Hawassa University (reference number: HW/17/0668/15) and the regional ethical committee in Western Norway (reference number: 2016/1916/REK vest) provided ethical approval. Permission letters were obtained from Gedeo zone health department and Wonago district health office. Before the start of the study, community elders, health extension workers and kebele leaders were sensitized. Mothers or caretakers provided written and signed informed consent. Confidentiality was maintained and participants were informed that participation was voluntary and they had right to withdraw from the study at any time.
Study setting and design
We conducted community-based, cross-sectional study in Wonago district in southern Ethiopia from June 2017 to July 2017. Wonago is about 377 km south of Addis Ababa and 13 km south of Dilla, the capital of Gedeo. The district is 142 km2 and has 17 rural and 4 urban kebeles (the smallest administrative units) containing 29,227 households. Among the most densely populated areas in Ethiopia, it has 1,014 people per square kilometer. According to the 2007 census, the district’s population of 147,600 people included 22,140 (15%) children younger than five years [28, 29]. The majority of the population lives in the rural areas and agricultural is the dominant means of livelihood of Wonago district. Major cause of childhood illness is pneumonia and diarrhea. Wonago has 20 health posts, six governmental health center, two private clinics, and two drug stores. Expanded Program of Immunization (EPI) was all provided in health centers and health posts and supported by 34 outreach programs site with every week provision of immunization.
Study participants
Eligible participants included were all children aged 6 to 36 months and their mothers or guardians, who lived in Wonago for at least 6 months before data collection and who consented to participate in the study. We excluded those who had not lived in the study area for least 6 months prior to data collection. We calculated the sample size required for estimating immunization coverage using Open Epi software version 3.03 [30]. The calculation assumed a desired precision (sampling error) of 4% to get larger sample size with a 95% confidence interval (CI), a design effect of two to consider two stage sampling and to adjust the variance, and a 10% non-response rate. The anticipated proportion of full immunization coverage was 30.5% based on a study in Hosanna [20]. We thus calculated a sample size of 1,119 children aged 6 to 36 months old and their guardians.
A two-stage sampling technique was employed. In the first stage, we used a random sampling lottery method to select 3 of 17 total kebeles using the Statistical Package for Social Science (SPSS) version 20 complex sample method [31], we then randomly selected 12 villages from the selected kebeles based on probability proportional to size (number of households). Before the survey, we conducted a census in selected kebeles to obtain socio-demographic, household status information and to identify eligible children. The sample is distributed to selected villages based on probability proportional to size (number of eligible children). The first household was identified by randomly from the center of the village. Once first household was identified the interviewer went to the next household with the mother of children age group of 6–36 months. Subsequent sampling of household was conducted from selected villages until the desired sample size was attained. When two children from the same household were identified, both children were selected.
Study variables
The outcome variable in this study was full (complete) immunization. Individual-level factors included were mother’s age, mother’s occupation, parity, religion, ethnicity, women’s education(Mothers education has 5 categories, no formal education, primary(1–8 grade), secondary(9–10 grade), preparatory (11–12 grade) and college or university), antenatal care (antenatal care defines as number of visit that mother get care during pregnancy), delivery place, post-natal care, sex of child, number of children younger than five years in the household, birth order, family planning use, household family size, attitude of mothers towards immunization(Mothers attitude towards vaccination was assessed by six attitude related questions and using a 2-point scale (agree and disagree), where 1 = positive perception and 0 = negative perception. The mean score was computed and dichotomized into positive and negative: if mothers reacted score below the mean, they were labeled as having a negative attitude; if mother reacted to at the mean and above the mean, they were labeled as having a positive attitude), presence of child vaccination card and wealth index. The wealth index was assessed to capture households’ socio-economic statuses and constructed using principal component analysis based on household asset and amenities. The generated wealth score was grouped into quartiles as a measure of socioeconomic status, with the first quartile representing the poorest group and the fourth quartile the richest.
Community-level factors included were visits from healthcare workers, distance to healthcare facilities, access to health outreach (e.g. vitamin A supplementation) and families participating in food supporting programs(such as safety net program).
Table 1 summarizes the infant immunization schedule of recommended vaccines, including Bacillus Calmette–Guérin; oral polio; diphtheria, pertussis, and tetanus; hepatitis B and Hemophilus influenzae type B; pneumococcal conjugate; rotavirus; and measles) in the study area [14].
Data collection and quality control
The structured questionnaire was initially developed in English, translated into the local Gedeoffa language and then translated back to English to ensure consistency. Most questions were adopted from questionnaires in the Demographic and Health Survey of Ethiopia [5] and from literature reviews [15, 21, 23–25]. Before data collection the questionnaires reviewed by supervisors then we conducted pre-test on 56 children (6–36 months) in another kebele of Wonago district and that were not included in the study. Based on this pre-testing, we rephrased unclear questions, wording, and sequences. After data collection the data cleaned and checked for the consistency.
Eight trained data collectors and two supervisors conducted the interviews. Immunization data were collected from vaccination cards (i.e., doses and types) and mothers’ or guardians’ verbal reports. We confirmed the information given by checking children for Bacillus Calmette–Guérin (BCG) scars on upper arm. The principal investigator checked the data for completeness, and errors were corrected accordingly. To control for recall bias, we used standardized questionnaires and trained data collectors in facilitating participant recall.
We defined complete or full immunization among children aged 12–36 months as receiving one dose of BCG, three doses of polio, three doses of (Diphtheria, pertussis, tetanus, Hepatitis B and Hemophilus influenzae type B) and one dose of measles, as confirmed by immunization card or mother’s recall. We defined partial immunization as missing one or more of the recommended eight vaccines and children who were not vaccinated at recommended age. Children who never received any immunizations were classified as not vaccinated. We considered children younger than 11 months with complete vaccinations as completed immunization for age. We defined the age limit for immunization as nine months, by which each child should have had one dose of BCG, three doses of polio, three doses of pentavalent, and one dose of measles vaccinations. Immunization coverage by card was calculated based on card documentation only and excluded vaccinations confirmed by mothers’ recall. Immunization by card plus recall included card and verbal histories. An infant immunization card was yellow card that given to child when child starts vaccination and used for vaccination follow-up and monitoring.
Data analysis
Data were double-entered using EpiData version 3.1. STATA 15 software (Stata Corp) was used for analyses. We compiled descriptive statistics, such as frequencies, percentages, means, and ranges. Cross-tabulation was used to show proportions of different categories of each characteristic, with respect to immunization status. A two-level logistic regression model was applied to analyze the hierarchical structure. Child-mother pairs (level 1) were nested within communities or villages (level 2).
We used multilevel analysis to account for hierarchical and binary outcome variables. Four models were constructed. The first (null) model had no exposure or independent variables and was used to check there was variability in probability of children with fully immunized across the community. The second and third models comprised individual and community variables, respectively. The fourth multivariate, multilevel regression model adjusted for outcome variables and predictors that were significant at the individual or community level. The effects of individual and community level predictors on the dependent variable were assessed independently. Bivariate analysis was performed to test the effect of each independent variable on the immunization coverage. Only variables correlating with fully immunization (for our data set defined as all variables correlating with immunization with p-value of ≤ 0.25) were selected for the consecutive multivariate analysis[32]. Multicollinearity testing was performed using Variance Inflation Factors (VIF) and independent variables with VIF >5 were removed.
Estimated associations (fixed-effects) between the likelihood of full vaccination and various explanatory variables were expressed as adjusted odds ratios (AOR) with 95% CI. Variations (random effects) were reported as intra-cluster correlation coefficients, or the percentage of variance explained by the community-level variables [33].
The Akakie information criterion was used to estimate goodness-of-fit of the adjusted final model in comparison with the preceding individual- and community-level models. The model with the lowest value was considered the best-fit model [33]. All variables with P-values less than 0.25 in the bivariate analysis were included in the multivariate logistic regression.
Results
Among the 923 mothers who participated in this study, the mean age was 27.4 (15–50) years, 798 (86.7%) were housewives and 674 (73.0%) had no formal education. Nearly all (909; 98.5%) were married. More than half (564; 54.6%) had households of 6 or more people. Only 339 (43.2%) of households had been visited by health extension workers in the past month. Table 2 summarizes the results for the mothers and guardians who participated in the study.
Of the 1,116 (571 girls and 545 boys) children aged 6–36 months in this study, the mean age was 24.1 months. Most (799; 71.3%) were born at home, and 317 (28.7%) were born at a health institution. Mothers reported that 178 (15.9%) experienced illness in the two weeks preceding the survey. Table 3 summarizes the results for the children.
Maternal health care
Most (863; 77.3%) mothers had at least one antenatal care visit during pregnancy, 351 (40.6%) had three antenatal care visits, and 246 (28.5%) had four and more. More than half (766; 68.6%) were immunized against tetanus, and 766 (68.6%) received no postnatal care for the child who participated in the study. Table 4 summarizes the results for maternal health care.
Awareness of vaccinations among mothers and guardians
Of the 879 (94.7%) mothers who knew about vaccinations, 604 (68.0%) got the information from health workers and 128 (14.0%) from community volunteers. Only 130 (14.1%) women knew that vaccinations start at birth, but more than half (593; 64.2%) knew the age at which a child should complete immunization. Table 5 summarizes the results.
Immunization coverage
Based on immunization cards and mothers’ recall, 959 (85.9%) children had at least one vaccine dose (95% CI; 83.9, 87.9). Among vaccinated children, 585 (52.4%) were fully immunized, 333 (29.8%) were partially immunized, 158 (14.2%) were not immunized, and 40 (3.6%) had completed immunization-for-age at the time of the survey. Among fully vaccinated children, (151) 55.1% were 12–23 months old, and (434) 60.9% were 24–36 months old. Table 6 summarizes the results.
Only 202 (21.1%) children had vaccination cards, among whom 158 (78%) received the BCG vaccine. More children (200; 99%) received pentavalent #1 than pentavalent #3 (157; 77.7%). Oral polio vaccine #1 was recorded for 200 (99%) of children and oral polio vaccine #3 for 157 (77.7%). Measles vaccines were recorded for 102 (50.4%) children. The lowest coverage was for the oral polio vaccine #0 vaccine 16 (7.9%). Table 7 summarizes the results.
Among partially and unimmunized children, 198 (45.6%) mothers were unaware of the need for subsequent doses of vaccine, 111 (25.0%) were unaware of any need for immunization, and 100 (23.0%) could not remember the place or time of vaccination. Table 8 summarizes the results.
Bivariate multilevel analysis
In the bivariate analysis, correlation was computed between independent and dependent variables. Maternal age, maternal education and occupation, maternal tetanus immunization, maternal antenatal and prenatal care, sex of child, child birth place, and maternal knowledge about appropriate age to vaccinate, maternal attitude towards immunization, child immunization card, health extension worker visit, and vitamin A supplementation in the last six months were associated with complete immunization. Table 9 summarizes the bivariate analyses.
Measuring variation and association
The null model showed significant variability in the probability of children with complete immunization across kebeles (variance = 2.71, p < .005). The intra-cluster correlation (48.1%) of the variability in probability of complete immunization was related to kebele. Variation in complete immunization across models 1, 2, and 3 was significant. Variation in full immunization in model 4 remained significant (variance = 1.66, p < .001), with 37% of variance among observations attributed to community-level factors.
Table 10 summarizes the multilevel, multivariate logistic regression analysis. After adjusting for variables at the community and individual levels, we found that increase in maternal age corresponded with increase immunization coverage (AOR = 1.05, 95% CI: 1.00–1.09). Children born to mothers who received one or more doses of tetanus toxoid vaccine had significantly higher odds of being fully immunized (AOR = 2.64, 95% CI: 1.43–4.86). Child had higher odds of being fully immunized if their mothers had higher number antenatal care visits (AOR = 1.36, 95% CI: 1.14–1.62). Among children with mothers who knew the age at which a child should complete immunization, 60.9% were fully immunized (AOR = 2.00, 95% CI: 1.25–3.20). Full immunization status of children was higher (60%) among female children than males (AOR = 0.64, 95% CI: 0.43–0.95). Children who received vitamin A supplements in the last 6 months were more likely to be fully immunized (AOR = 2.79, 95% CI: 1.59–4.90).
Discussion
In examining immunization coverage based on individual and community-level characteristics in the Gedeo zone in southern Ethiopia, we found that 85.9% of children had at least one dose of vaccine, but full immunization coverage was low at 52.4%. Immunization coverage was associated with individual factors (e.g., maternal age, prenatal care, mother’s tetanus vaccination, mother’s knowledge about age to complete childhood immunizations, sex of the child), as well as community factors (e.g., vitamin A supplementation). We conducted a two-level, multivariate logistic regression of fixed effects of individual and community factors to show the association of predictors with fully immunization and random effects to explain between-cluster variations. The intra-cluster correlation coefficient was 48.1%, indicating a cluster effect at the individual and community levels. These means the same kebeles were likely to have the same or similar immunization statuses.
Our findings on immunization coverage are comparable to other studies of rural districts in Tigray, Bangladesh, Uganda, and India [34–36]. However, our results show lower coverage than that in other areas of Ethiopia, such as 73% in Arba Minch, 76% in North Gondar, 89% in Ghana, and 86% in Cameroon [18, 19, 22, 37]. The immunization coverage observed in study was higher than result obtained from the report of national demographic health survey (EDHS 2016) 39%, study conducted in Somalia Jijiga 36.5%, in Ambo 36% and in Hossanna 30% [20, 21, 38, 39].
For individual vaccines, 78% of participants in our study received the BCG, 99% received pentavalent #1, 77% received pentavalent #3, and 50% received the measles vaccine. Coverage decreased from the first to final vaccine doses (e.g., oral polio #1 to #3, pentavalent #1 to #3, BCG to measles). This decrease aligns with findings from Arbaminch, Hossana, Ambo, and Bale [19–21, 24]. The long intervals between the third dose of pentavalent and measles vaccines may contribute to low immunization coverage.
In our study, 25% of the children were partially immunized and 14% were never immunized. The main reasons for partial immunization was lack of knowledge among mothers and guardians about the need to return for subsequent doses and the need for immunization in general, as demonstrated by studies in Tigray [32]. Studies conducted in Ghana and Mali also show that insufficient information and inconvenience led to partial immunization among children [18, 40]. It also showed that, fear of side effects of vaccine and erroneous ideas of vaccine contraindications were some of possible the reasons for incomplete immunization. Vaccine hesitancy is defined as delay in acceptance or refusal of vaccine despite the availability of vaccination service, and is one the reason for incomplete immunization[41].Other studies from Ethiopia support this and mothers hesitate to vaccinate their children because of fear of side effects, excessive waiting time, hearing rumors about vaccination and fear of the vaccine needle[42, 43]. Vaccine hesitancy studies from Italy revealed that the main reasons for vaccine hesitancy was not trusting the information given about vaccines and that not vaccines are important [44, 45].
Children of older mothers were more likely to be fully immunized. As the maternal age increases the child immunization coverage also improved. This may because older mothers may have experience and better knowledge of the effect and importance of immunization compared to younger. This is also in agreement with studies from Ethiopia [25, 46] and other African countries [18, 47–49].
Our findings also show that use of antenatal care was associated with full immunization coverage, as mothers with one or more tetanus toxoid vaccines during pregnancy were more likely to be fully immunized. These results correspond with those documented elsewhere in Ethiopia [20, 21, 36, 50, 51] and Africa [37, 52–54]. Follow-up care at a health institution during pregnancy and having one or more tetanus toxoid vaccine creates opportunities to obtain adequate information to discuss vaccines and vaccine-preventable diseases and to encourage adherence to vaccine schedules [55–57].
Moreover, mothers who knew the age at which a child should complete immunizations tended to have children with high immunization coverage, as has been documented from Ethiopia [21, 22, 27] and Nigeria[49]. This may explain that mothers who know age at which the child should complete immunization is likely to be fully immunized and may get information from health facility or through media or other sources. We also found that girls had higher immunization coverage than boys, which is in line with findings of studies in Ethiopia and Ghana [5, 18, 53]. In other study, boys were more likely to be fully immunized[22]. However, the reason why there is variation in coverage with gender is not evident.
Community-level factors associated with vaccination were highlighted in this study. We observed significant difference in immunization coverage across communities. Specifically, children from the same kebele tended to have similar immunization status. Our study also showed that vitamin A supplementation was associated with higher vaccination status, as others have found [36]. Vitamin A campaigns in the community may increase awareness about vaccinations. Strengthening the outreach and campaign program will improve the immunization coverage.
The study has some limitations. The survey was cross-sectional, so causal relationships between variables of interest could not be assessed with certainty. Because the data were self-reported by the mothers, it is possible that responses were affected by recall and social desirability bias. The survey study may also have anon-response error. The study has failure to assess the degree to which non-response error is likely to have.
As study strength, the study is population based and used multilevel multivariate regression analysis.
Conclusions
There is low immunization coverage in the Wonago district of southern Ethiopia. We found that individual and community factors affect the childhood immunization. Our study suggests the need for policies that address low immunization coverage. These awareness programs should emphasize the importance of health care access and use for mothers and children and of immunization schedules.
Supporting information
S1 File. Questionnaire used to conduct assess immunization coverage data collection in Wonago district in southern Ethiopia, June 2017- July 2017.
https://doi.org/10.1371/journal.pone.0220144.s001
(ZIP)
Acknowledgments
We are grateful to the community members in the Wonago district, particularly those households that participated in the study. We also acknowledge our data collectors and supervisors for their involvement in the study. We are grateful to Hawassa University and the University of Bergen for their support.
References
- 1.
World Health Organization(WHO). 10 facts on immunization. World Health Organization, 2018. [updated March, 2018]. Available from: Available at https://www.who.int/features/factfiles/immunization/en/.
- 2.
WHO, UNICEF. WHO's vision and mission in immunization and vaccine 2015–2030. Geneva: World Health Organization; 2017.
- 3. Ruducha J, Mann C, Singh NS, Gemebo TD, Tessema NS, Baschieri A, et al. How Ethiopia achieved Millennium Development Goal 4 through multisectoral interventions: A Countdown to 2015 case study. The Lancet Global Health 2017;5(11):e1142–e51. pmid:29025635.
- 4.
World Health Organization(WHO). WHO UN sustainable Development Summit 2015. World Health Organization,2015. Available from: https://www.who.int/mediacentre/events/meetings/2015/un-sustainable-development-summit/en/.
- 5.
Central Statistical Agency (Ethiopia), ICF International. Ethiopia Demographic and Health Survey 2011. Addis Ababa, Ethiopia and Calverton,Maryland,USA: Central Statistical Agency/Ethiopia and ICF International, 2012. http://dhsprogram.com/pubs/pdf/FR255/FR255.pdf.
- 6.
World Health Organization(WHO). Immunization service delivery: Expanded Programme on Immunization (EPI): World Health organization, 2013. [updated December 1,2013]. Available from: www.who.int/immunization/programmes_systems/supply…of_immunization/en/.
- 7.
World Health Orgaization(WHO). World Health report 2005-Make every mother and child count. Geneva,Switzerland: World Health organization, 2005.
- 8.
Center of Disease Control(CDC). Global routine vaccination coverage,2013. Center of Disease Control, 2013. Contract No.: 46.
- 9.
WHO, UNICEF. Global Immunization vision and Strategy 2006–2015. Geneva: Department of immunization,vaccine and Bilolgicals, World Health Organization and the United Nation Children's Fund, 2005.
- 10. Feldstein LR, Mariat S, Gacic-Dobo M, Diallo MS, Conklin LM, Wallace AS. Global Routine Vaccination Coverage, 2016. MMWR Morbidity and mortality weekly report 2017;66(45):1252–5. pmid:29145357
- 11. Tao W, Petzold M, Forsberg BC. Routine vaccination coverage in low- and middle-income countries: further arguments for accelerating support to child vaccination services. Global Health Action 2013;6:20343. pmid:23639178.
- 12. Vakili R, Hashemi AG, Khademi G, Abbasi MA, Saeidi M. Immunization coverage in WHO regions. Int J,Pediatr 2015;15(3):111–8. https://doi.org/10.22038/ijp.2015.4157
- 13.
World Health Organization(WHO). Expanded program on immunization,WHO Africa Region Ethiopia Geneva: World Health Organiztion; 2018. Available from: www.who.int/countries/eth/areas/immunization/en/.
- 14.
Federal Ministry of Health Ethiopia. Ethiopia National Programme on Immunization; Comprehensive Multiyear plan 2016–2020. Addis Ababa,Ethiopia: Federal Minisitry Of Health; 2015.
- 15.
Yigzaw A. Overview of immunization service in Ethiopia. Presented to Malaria vaccine Decision Making Framework Meeting. Addis Ababa: WHO/EPI; 2007.
- 16. Belete H, Kidane T, Bisrat F, Molla M, Mounier-Jack S, Kitaw Y. Routine immunization in Ethiopia. Ethiop J Health Dev 2015;29(1).
- 17.
Central Statistical Agency (CSA)Ethiopia, ICF. Ethiopia Demographic and Health Sruvey 2016. Addis Ababa, Ethiopia and Maryland: CSA and ICF, 2017. http://dhsprogram.com/pubs/pdf/FR328/FR328.pdf
- 18. Adokiya MN, Baguune B. Evaluation of immunization coverage and its associated factors among children 12–23 months of age in Techiman Municipality,Ghana, 2016. Archives of Public Health 2017;75:28. pmid:28652913
- 19. Animaw W, Taye W, Merdekios B, Tilahun M, Ayele G. Expanded program of immunization coverage and associated factors among children age 12–23 months in Arba Minch town and Zuria District, Southern Ethiopia, 2013. BMC Public Health 2014;14:464. pmid:24884641
- 20. Ayano B. Factors Affecting Fully Immunization status of children Aged 12–23 Months in Hosanna Town,South Ethiopia. J Preg Child Health 2015;2(185). https://doi.org/10.4172/2376-127X.1000185
- 21. Etana B, Deressa W. Factors associated with complete immunization coverage in children aged 12–23 months in Ambo Woreda, Central Ethiopia. BMC Public Health 2012;12(1):566. pmid:22839418
- 22. Kassahun MB, Biks GA, Teferra AS. Level of immunization coverage and associated factors among children aged 12–23 months in Lay Armachiho District, North Gondar Zone, Northwest Ethiopia: Acommunity based cross sectional study. BMC research notes 2015;8:239. pmid:26071403
- 23. Lakew Y, Bekele A, Biadgilign S. Factors influencing full immunization coverage among 12–23 months of age children in Ethiopia: Evidence from the National Demographic and Health Survey in 2011. BMC Public Health 2015;15:728. pmid:26224089
- 24. Legesse E, Dechasa W. An assessment of child immunization coverage and its determinants in Sinana District, Southeast Ethiopia. BMC pediatrics 2015;15:31. pmid:25886255
- 25. Negussie A, Kassahun W, Assegid S, Hagan AK. Factors associated with incomplete childhood immunization in Arbegona district, southern Ethiopia: Acase—control study. BMC Public Health 2016;16:27. pmid:26757893
- 26. Asfaw AG, Koye DN, Demssie AF, Zeleke EG, Gelaw YA. Determinants of default to fully completion of immunization among children aged 12 to 23 months in south Ethiopia: Unmatched case-control study. The Pan African medical journal 2016;23:100. pmid:27222689
- 27. Tadesse H, Deribew A, Woldie M. Predictors of defaulting from completion of child immunization in south Ethiopia, May 2008: Acase control study. BMC Public Health 2009;9:150. pmid:19463164
- 28.
Centeral Statistical Authority (CSA). 2007 Population and Housing Census of Ethiopia, Admistrative report. Addis Ababa: Central Statistical Authority, 2012.
- 29.
Centeral Statistical Agency (CSA). Ethiopia-population and Housing Census of 2007. Centeral Statistical Agency-Ministry of Finance and Economic Development 2007.
- 30. Sullivan KM, Dean A, Soe MM. OpenEpi: A Web-based Epidemiologic and Statistical Calculator for Public Health. Public Health Reports 2009;124(3):471–4. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2663701/. pmid:19445426
- 31.
Kirkpatrick LA. A simple guide to IBM SPSS statistics for versions 20.0 & 21.0: Australia; Belmont, CA: Wadsworth, [2013] ©2013; 2013. https://search.library.wisc.edu/catalog/9910207028202121
- 32. 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 pmid:28953970
- 33. Merlo J, Yang M, Chaix B, Lynch J, Råstam L. A brief conceptual tutorial on multilevel analysis in social epidemiology: investigating contextual phenomena in different groups of people. Journal of epidemiology and community health 2005;59(9):729–36. pmid:16100308
- 34. Kidane T, Tekie M. Factors influencing child immunization coverage in a rural District of Ethiopia,2000. Ethiop J Health Dev 2003;17(2):105–10.
- 35. Perry H, Weierbach R, Hossain I, Islam R. Childhood immunization coverage in zone 3 of Dhaka City: the challenge of reaching impoverished households in urban Bangladesh. Bulletin of the World Health Organization 1998;76(6):565–73. pmid:10191552
- 36. Restrepo-Mendez MC, Barros AJ, Wong KL, Johnson HL, Pariyo G, Wehrmeister FC, et al. Missed opportunities in full immunization coverage: findings from low- and lower-middle-income countries. Global health action 2016;9(1):30963. pmid:27146444
- 37. Russo G, Miglietta A, Pezzotti P, Biguioh RM, Mayaka GB, Sobze MS, et al. 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 outbreak. BMC Public Health 2015;15:630. pmid:26156158.
- 38.
Central Statistical Agency—CSA/Ethiopia, ICF. Ethiopia Demographic and Health Sruvey 2016. Addis Ababa, Ethiopia and Maryland: CSA and ICF, 2017. http://dhsprogram.com/pubs/pdf/FR328/FR328.pdf.
- 39. Mohamud AN, Feleke A, Worku W, Kifle M, Sharma HR., Immunization coverage of 12–23 months old children and associated factors in Jigjiga District, Somali National Regional State, Ethiopia. BMC Public Health 2014;14: p. 865. pmid:25146502
- 40. Koumaré AK, Traore D, Haidara F, Sissoko F, Traoré I, Dramé S, et al. Evaluation of immunization coverage within the Expanded Program on Immunization in Kita Circle, Mali: A cross-sectional survey. BMC International Health Human Rights 2009;9(Suppl 1):S13–S. pmid:19828057
- 41. European Center of Disease Control(ECDC), Vaccine hesitancy among healthcare workers and their patients in Europe, 2015.
- 42. Masters NB, Tefera YA, Wagner AL. Vaccine hesitancy among caregivers and association with childhood vaccination timeliness in Addis Ababa, Ethiopia. 2018; 14(10): p. 2340–2347. pmid:29792555
- 43. Tefera YA, Wagner AL. Predictors and Barriers to Full Vaccination among Children in Ethiopia. 2018; 6(2). pmid:29642596
- 44. Napolitano F , D'Alessandro A, Angelillo IF. Investigating Italian parents' vaccine hesitancy: A cross-sectional survey. Human Vaccin immunoterapeutics 2018;14(7): p. 1558–1565. pmid:29641945
- 45. Bianco A, Mascaro V,Zucco R,Pavia M. Parent perspectives on childhood vaccination: How to deal with vaccine hesitancy and refusal? Vaccine 2019;37(7): p. 984–990. pmid:30655175
- 46. Beyene EZ, Worku A,Bisrat F,Fantahun M. Factors associated with immunization coverage among children age 12–23 months: the case of Zone 3, Afar Regional State, Ethiopia. Ethiop Med J 2013; 51 Suppl 1: p. 41–50. pmid:24380206
- 47. Adedokun ST, Uthman OA, Adekanmbi VT. Incomplete childhood immunization in Nigeria: a multilevel analysis of individual and contextual factors. BMC Public Health 2017; 17(1): p. 236. pmid:28270125
- 48. Adenike OB, Adejumoke J, Olufunmi O,Ridwan O. Maternal characteristics and immunization status of children in North Central of Nigeria. Pan Afr Med J 2017;26: p. 159. pmid:28588745
- 49. Odusanya OO, Alufohai EF, Meurice FP, Ahonkhai VI. Determinants of vaccination coverage in rural Nigeria. BMC Public Health 2008; 8:381. pmid:18986544
- 50. Gualu T, Dilie A. Vaccination Coverage and Associated Factors among Children Aged 12–23 Months in Debre Markos Town, Amhara Regional State, Ethiopia. Advances in Public Health 2017;2017:6. https://doi.org/10.1155/2017/5352847
- 51. Wado YD, Afework MF, Hindin MJ. Childhood vaccination in rural southwestern Ethiopia: the nexus with demographic factors and women's autonomy. The Pan African medical journal 2014;17 Suppl 1:9. pmid:24624243
- 52. Adedire EB, Ajayi I, Fawole OI, Ajumobi O, Kasasa S, Wasswa P, et al. Immunisation coverage and its determinants among children aged 12–23 months in Atakumosa-west district, Osun State Nigeria: a cross-sectional study. BMC Public Health 2016;16:905. pmid:27578303
- 53. Shrivastwa N, Gillespie BW, Kolenic GE, Lepkowski JM, Boulton ML. Predictors of Vaccination in India for Children Aged 12–36 Months. Am J Prev Med 2015;49(6 Suppl 4):S435–44. pmid:26297449.
- 54. Mbengue MAS, Sarr M, Faye A, Badiane O, Camara FBN, Mboup S, et al. Determinants of complete immunization among senegalese children aged 12–23 months: Evidence from the demographic and health survey. BMC Public Health 2017;17(1):630. pmid:28683781
- 55. D'Alessandro A, Napolitano F, D'Ambrosio A, Angelillo IF. Vaccination knowledge and acceptability among pregnant women in Italy. Hum Vaccin Immunother 2018;14(7): p. 1573–1579. pmid:29863958
- 56. Danchin MH, Costa-Pinto J, Attwell K, Willaby H, Wiley K, Hoq M, et al. Vaccine decision-making begins in pregnancy: Correlation between vaccine concerns, intentions and maternal vaccination with subsequent childhood vaccine uptake. Vaccine 2018; 36(44): p. 6473–6479. pmid:28811050
- 57. Rosso A, Massimi A, De Vito C, Adamo G, Baccolini V, Marzuillo C, et al. Knowledge and attitudes on pediatric vaccinations and intention to vaccinate in a sample of pregnant women from the City of Rome. Vaccine 2019; 37(14): p.1954–1963. pmid:30827733