- Research article
- Open access
- Published:
The role of place of residency in childhood immunisation coverage in Nigeria: analysis of data from three DHS rounds 2003–2013
BMC Public Health volume 20, Article number: 123 (2020)
Abstract
Background
In 2017, about 20% of the world’s children under 1 year of age with incomplete DPT vaccination lived in Nigeria. Fully-immunised child coverage (FIC), which is the percentage of children aged 12–23 months who received all doses of routine infant vaccines in their first year of life in Nigeria is low. We explored the associations between child, household, community and health system level factors and FIC, in particular focussing on urban formal and slum, and rural residence, using representative Nigeria Demographic Health Survey (NDHS) data from 2003, 2008 and 2013.
Method
Multilevel logistic regression models were applied for quantitative analyses of NDHS 2003, 2008 and 2013 data, singly, pooled overall and stratified by rural/urban, and within urban by formal and slum. We also quantify Population Attributable Risk (PAR) of FIC.
Results
FIC for rural, urban formal and slum rose from 7.4, 25.6 and 24.9% respectively in 2003 to 15.8, 45.5 and 38.5% in 2013, and varied across sociodemographics. In pooled NDHS analysis, overall and stratified, final FIC adjusted odds (aOR) were: 1. Total population - delivery place (health facility vs home, aOR = 1.13, 95% CI = 0.73–1.73), maternal education (higher vs no education, aOR = 3.92, 95% CI = 1.79–8.59) and place of residence (urban vs rural, aOR = 1.69, 95% CI = 0.89–3.22). 2. Rural, urban formal and slum stratified: A.Rural – delivery place (aOR = 1.47, 95% CI = 1.12–1.94), maternal education (aOR = 4.99, 95% CI = 2.48–10.06). B.Urban formal - delivery place (aOR = 2.62, 95% CI = 1.43–4.79), maternal education level (aOR = 9.18, 95% CI = 3.05–27.64). C.Slums - delivery place (aOR = 5.39, 95% CI = 2.18–13.33), maternal education (aOR = 5.03, 95% CI = 1.52–16.65). The PAR revealed the highest percentage point increase in FIC would be achieved in all places of residence by maternal higher education: rural-38.15, urban formal-22.88 and slum 23.76, while non-attendance of antenatal care was estimated to lead to the largest reduction in FIC.
Conclusion
Although low FIC in rural areas may be largely due to lack of health facilities and immunisation education, the intra-urban disparity is mostly unexplained, and requires further qualitative and interventional research. We show the FIC point increase that can be achieved if specific sociodemographic variable (risk) are addressed in the various communities, thus informing prioritisation of interventions.
Background
Childhood immunisation is a cost-effective public health tool [1], resulting in the eradication of small pox, and elimination of polio in many countries, and drastically reducing morbidity and mortality caused by Diphtheria, Poliomyelitis, Pertussis, Tetanus, Measles and, more recently, Haemophilus influenzae type b, Streptococcus pneumoniae, Rotavirus, and Hepatitis B [1, 2]. However, the burden of vaccine-preventable child deaths remains substantial [3].
Nigeria has Africa’s largest under age 1 year population, but one of the lowest immunisation coverage [4, 5]; about 20% of the world’s children under 1 year of age with incomplete DPT vaccination in 2017 lived in Nigeria [4]. Maternal education, antenatal care attendance and place of delivery, religion and place of residence have been reported to be associated with childhood vaccination in Nigeria [6,7,8,9].
Immunisation rates are generally worse in rural than urban areas [6,7,8,9], and studies in Asia and the near East [10], India [11], Kenya [12] and Nigeria [13] have reported lower rates of immunisation coverage in slums than in formal urban areas. The rapid urbanisation in Nigeria may become a further barrier to childhood immunisation uptake, with growth of urban slums [14, 15], overstretched urban health facilities [16], leading to decreased health service quality and reduced access to health and immunisation services [13]. Hence the need to seek evidence to first, maintain and improve the relatively higher urban immunisation coverage compared to rural coverages, increase the rural coverages and lastly, reduce the prevalence of urban formal and slum immunisation disparity in Nigeria.
We will contribute to understanding of the associations between child, mother/family, community and health system level factors and immunisation coverage of routinely-provided immunisation in infancy, in particular focussing on urban formal and slum, and rural place of residence, in Nigeria, with the use of multilevel logistic regression and population attributable risk analyses on the available Nigeria Demographic Health Survey (NDHS) data from 2003, 2008 and 2013.
Method
Datasets
Nationally representative Demographic and Health Surveys (DHS) were carried out in Nigeria in 2003, 2008 and 2013. DHS population samples were randomly selected in a three-stage probability sampling process, with targeted number of households based on Nigeria’s population census [17,18,19]. These DHS reports are publicly available; datasets are accessible upon application including study aim and analytical plans from DHS MEASURE (https://www.dhsprogram.com/).
The outcome of interest here was fully immunised child coverage (FIC), a dichotomous variable defined as receipt of all routine infant vaccines (Bacillus Calmette Guerin (one dose), Oral Polio Vaccine (three doses), Diphtheria-Pertussis-Tetanus (three doses), Measles (one dose)) and reported for children aged 12–23 months [17,18,19]. This information was determined from the vaccination cards, and where not available from mothers’ recall. Sociodemographic variables were selected based on the reviewed literature and authors’ experience, and grouped into three levels: child, household and community; variables were either taken straight from the DHS or recoded as appropriate:
Child level
birth order (first, second and third, fourth and fifth, sixth or more), sex (female, male), place of delivery (health facility, and home/other), maternal antenatal care attendance (at least one ANC visit, none, don’t know/Missing).
Household factors
maternal education (no formal education/primary/secondary/higher), sex of household head (female/male), religion (Christianity/Islam/traditionalist and others) as provided in DHS. Maternal employment status (no/yes), maternal age at the child’s birth (14–19/20–29/30–39/40–49 year), maternal marital status (never married/married/no longer married), who decides on expenditure of maternal income (mother alone/mother and spouse/spouse alone/no income mother), media exposure (no/yes) and urban/rural-specific Household wealth (poor/middle/rich) were recoded from the raw DHS data.
Community level factors
place of residence (rural, urban formal, urban slum): two (improved water and sanitation) of the five UN HABITAT slum indicators (durable housing, overcrowding and security of tenure) [20, 21] were used to stratify the urban settlement. The absence of information on the house wall type in the 2003 DHS led to non-inclusion of the wall as an indicator. The roof or floor quality was not chosen because as people become richer, their roofs and floors may be changed irrespective of where they live and this indicator was thus considered less appropriate in this setting. With the culture of “co-sleeping” with children and polygamous families being common in all settings, overcrowding was deemed not appropriate to define a slum household. Finally, information on the indicator of security of tenure was not available in the DHS datasets. Regions: Northcentral, Northeast, Northwest, Southeast, Southsouth and Southwest. Distance to the nearest health facility was grouped as reported a big problem or no/not a big problem. Interaction terms were developed with place of residence as appropriate.
Statistical methods
The three DHS datasets were used in two ways: 1. Separate and pooled analyses of the three NDHS datasets to identify the patterns of association between the FIC and sociodemographic factors, quantifying the independent association with place of residence, and differences over time; 2.Stratified analysis (rural, urban formal and urban slums) of the pooled dataset.
Descriptive analysis was expressed as numbers, frequency and percentages; differences in immunisation coverage between categories of the sociodemographic variable were tested using the chi-square test.
The association between variables and the dependent variable, FIC, was assessed in logistic regression. Variables not statistically significantly (p-value > 0.05) associated with FIC in univariate analysis, or which displayed multicollinearity using the variance inflation factor (VIF) were not included in the regression models. In the pooled datasets for the first set of analyses, multilevel logistic regression included four models: Model 0 had place of residence and DHS year, Model 1 included child level factors, Model 2 child and household factors and the full Model 3 child, household, community factors and interaction terms for place of residence with maternal education level, household wealth, maternal ANC attendance, place of child delivery and mothers birth age. These five interaction terms were based on their significant association with full immunisation. In the stratified analyses, the three-level multilevel logistic regression included four models: Model 0 had only the dependent variable (FIC), Model 1 included child level factors, Model 2 child and household factors and the full Model 3 child, household and community factors. Model goodness of fit was assessed with the Akaike Information Criterion (AIC) [22, 23].
Finally, we estimated the population attributable risk (PAR) [22, 23] to explore the increase or decrease in FIC that can be achieved with optimum levels of specific sociodemographic variables (eg all mothers having higher education, all deliveries being in the health facilities) in any place of residence. PAR was calculated after fitting a simple logistic regression of FIC and each sociodemographic variable. The PAR values are presented in percentages and 95% significant confidence interval for each sociodemographic variable category in the different places of residence. All statistical analyses were done with STATA version 14.
Results
Description
The number of households interviewed rose from 7225 in 2003, to 34,070 in 2008, and 38,522 in 2013, with a total of 79,817 in the pooled dataset (Table 1). The number of children aged 12–23 months increased from 999 in 2003 to 5900 in 2013. In all three surveys, about two-thirds of the children resided in rural areas; 15.5% of all children aged 12–23 months in the pooled dataset resided in slum areas. FIC was lowest in rural areas, with slum FIC coverage higher than in rural but lower than in urban formal areas.
Multilevel analysis of the pooled dataset
Place of residence was significantly associated with FIC, with urban children more likely to be fully immunised than children in rural communities, and those in urban formal areas having higher odds than those in slums (Table 2). However, with the introduction of community variables and interaction terms in Model 3, FIC for an urban child (adjusted Odds Ratio (aOR) =1.60, 95% CI = 0.60–4.24) compared to the rural child remained higher, but was no longer statistically significant. FIC odds significantly increased over time, Model 0, with 2013 NDHS (aOR = 3.08, 95% CI = 2.21–4.29) higher than 2008 NDHS (aOR = 2.01, 95% CI = 1.46–2.77), which was higher than the reference, 2003 NDHS; this pattern was also seen in the subsequent models.
After controlling for child, household, community level variables and fitting interaction terms in model 3, odds and significance of the relationship between FIC and independent variables were reduced but with similar intra-variable trends. Maternal antenatal care attendance (aOR = 8.45, 95% CI = 5.21–13.69) increased FIC odds. Maternal education was also associated with FIC: compared to mothers without formal education, FIC odds of mothers with primary education was 77% higher (aOR = 1.77, 95% CI = 1.29–2.44), and for mothers with secondary and with higher education odds increased by 167% (aOR = 2.67, 95% CI = 1.64–4.36) and 292% (aOR = 3.92, 95% CI = 1.79–8.59) respectively. Children of Christian households (aOR = 2.36, 95% CI = 1.81–3.08) were more likely to be fully immunised than those from Muslim homes. FIC odds increased by at least 135% with maternal age 20 years and above compared to age 14–19 years. Children from media-exposed homes (aOR = 1.91, 95% CI = 1.50–2.41) were at higher odds of being fully immunised than peers from households that were not. Children whose mothers resided in Northeast (aOR = 0.56, 95% CI = 0.40–0.78) or Northwest (aOR = 0.30, 95% CI = 0.21–0.44), and those who saw distance to the health facility as a big problem were less likely to be fully immunised.
Of the interactions between place of residence and maternal education (aOR = 1.03, 95% CI = 0.91–1.17), household wealth (aOR = 0.90, 95% CI = 0.74–1.09), maternal antenatal care (aOR = 0.89, 95% CI = 0.69–1.13), place of delivery (aOR = 1.38, 95% CI = 1.08–1.76) and maternal age at birth (aOR = 0.92, 95% CI = 0.79–1.06), only the interaction between place of residence and place of delivery was significant.
Multilevel analysis of pooled NDHS dataset stratified by place of residence
The associations between FIC and sociodemographic variables were further explored in multilevel logistic regression analyses of the pooled dataset stratified by rural, formal urban and slum. Only Model 3 (final) is presented in Table 3 (with details on all Models in Additional file 1: Tables SA, SB and SC).
In each setting, factors significantly associated with FIC were place of delivery, maternal ANC attendance, maternal education level and region. FIC was significantly associated with birth order in urban formal and slums, religion in rural and slums, maternal age in rural and urban formal, media exposure and distance to the health facility in rural areas, and with current maternal marital status and decision-maker of maternal income in slums. FIC was not significantly associated in any setting with sex of the household head, mother employment status and household wealth.
The increased FIC odds for health facility delivery was higher among urban (urban formal and slums) than rural dwellers, which was also true for the birth order associations. In contrast, in rural areas, maternal ANC attendance appeared more important than in urban formal and slum areas.
FIC significantly increased with higher maternal education level in all areas, with the size of the association largest in urban areas. This was also seen for mothers’ age at birth of the child. Compared to a child of a Muslim mother, a Christian child had a significantly higher odds of being fully immunised, especially in the slums. The association between FIC and household media exposure was significant only in rural areas.
Almost half of all children resided in the Northeast and Northwest and these had the lowest odds of being fully immunised in all settings. Distance to the nearest health facility when seeking health care was significantly associated with FIC in rural areas only.
The odds of a child being fully immunised varied across households and communities in the rural, urban formal and slum areas, with household and community factors explaining 24.5 and 20.0% variation in rural, 9.0 and 9.5% in urban formal and 9.8 and 13.3% in the slums respectively.
Population attributable risk of the Sociodemographic variables on FIC in rural, urban formal and slum populations of Nigeria
To further understand the barriers of childhood immunisation, population attributable risk (PAR) analysis was deployed to investigate how the levels of FIC are associated with sociodemographic variables in a specific place of residence. Table 4 shows PARs for FIC in each place of residence for selected socio-demographic variables (PARs of all sociodemographic variables are in Additional file 1: Table SD). Non-attendance at antenatal care by mothers in urban formal areas reduced the average urban formal FIC percentage by 32 points. A 38 point increase over the average rural FIC percentage could be obtained if all rural mothers had higher education. Overall, variables had similar effect in each of the areas, either increasing or decreasing FIC, but with differing magnitude. FIC could be increased in rural, urban formal and slum by 19, 11 and 14 points respectively if all deliveries were at health facilities. FIC would be increased by 11, 5 and 4 points in rural, urban formal and slum populations respectively if all mothers had attended at least one antenatal care session.
However, maternal primary education would increase FIC by 6 points in rural areas but reduce FIC by 8 and 4 points in urban and slum populations respectively. The FIC of children with mothers aged 14–19 years was reduced by 7 to 21 points depending on place of residence. The effect of being exposed to media on increased FIC was felt more in the rural (6 points) and least in urban formal (3 points), while a 4 point percentage difference was achieved in the slums. Being resident in any of the 3 southern regions increased the FIC percentage, while in two (Northeast and Northwest) of the 3 Northern regions, the risk of reduced FIC was increased. Each percentage point represents tens of eligible children: 79 in rural (n = 7920), 21 in urban formal (n = 2087) and 18 in slum (1836).
Discussion
Using three national Demographic and Health surveys, 2003, 2008 and 2013, we quantify the associations between FIC and child, household and community factors in Nigeria. Allowing for child, household and community level factors, in multilevel logistic analysis of a pooled data set covering the three DHS, the odds of being fully immunised in 2008 was triple, and in 2013 it was 4.5-times that in 2003. FIC differed substantially by place of residence, with children in urban formal and slum areas being 69 and 45% respectively, more likely to be immunised than those in rural areas. Overall, and in each of the three place of residence strata separately, we found place of delivery, antenatal care, maternal education, maternal age at child birth, religion, place of residence, media exposure and distance to the health facility to be significantly associated with FIC. The pattern of the adjusted odds in overall pooled and stratified logistic models were similar, although the magnitude of odds varied. The pooled analyses provided quantification of changes over time, as well as reliable quantification of the associations with sociodemographic variables allowing for year and setting. Then stratified analyses allowed quantification of the association, highlighting potential differences by setting in these associations. In line with this adjusted odds, the PAR analysis quantified what could be achieved if these variables are optimised and provided more explanation of the FIC variation like health system related factors being more influential in the rural area compared to urban.
Overall, our results are in line with those from previous studies [6,7,8,9], based on more robust methodology we provided more details such as the association in the different places of residence and the improvement that could be obtained by ensuring all mothers obtain the level of the socio-demographic variable associated with optimum FIC.
Child level factors
Our finding that children of lower birth orders were more likely to be fully immunised than higher birth orders confirm evidence from studies in Nigeria and India [6, 24,25,26,27]. Competing demands for family resources and time with increasing number of children likely explains at least part of this association [28]. In our study FIC was higher among children delivered in a health facility than those delivered at home in all three settings, similar to earlier studies [6,7,8,9], which were criticised on methodological grounds for including the 1999 NDHS data in their analyses [29]. Health facility delivery would likely increase the uptake of birth dose vaccines, BCG, OPV and HBV, and the provision of immunisation health messages, including date and place for subsequent immunisation sessions [9, 27, 30, 31]. Further, non-delivery in a health facility may be suggestive of distrust and lack of confidence in modern medicine and its providers [32]. Similarly, children of mothers who attended antenatal care during their pregnancy independently had higher FIC coverage and significantly greater odds of being fully immunised than children whose mothers did not attend antenatal care. Adding to previously reported evidence [9, 26, 31], this study provided the strength and pattern of the significance of the association and residence disparity between antenatal care and fully immunised odds in Nigeria, with stratified multilevel analysis that showed the FIC adjusted odds of delivery in health facility was highest in the slums. PAR analysis estimated the percentage point increase in FIC that can be achieved if all mothers had attended antenatal care.
Household level factors
Maternal education level was consistently associated with FIC: as the mothers’ level of education increased, the child’s fully immunised odds increased, in line with results of several studies from Nigeria and elsewhere [6, 7, 17,18,19, 24, 25, 28, 32,33,34,35,36,37,38,39,40,41,42,43,44,45]. We additionally explored and quantified the pattern and trend of the association between maternal education and FIC status over the years in the general population and in each of the three settings and found its influence positive. Further analysis with PAR estimated that if maternal education was improved the whole population would benefit but the rural population stand to gain more. Increased maternal education is likely associated with increased health seeking behaviour, improved understanding of immunisation messages, knowledge of available immunisation delivery sites and having more money to cover the transport cost to health facilities [27, 46, 47].
Mother’s religion was also associated with the likelihood of the child to be fully immunised, such that a Christian child was several times more likely to be fully immunised than a Muslim child, with at least 25 point difference in their FIC irrespective of place of residence. This finding corroborated results from previous research in Nigeria and other countries [25, 48, 49]. Renne explained that Muslim leaders in Nigeria felt the vaccines were contaminated with HIV and anti-fertility substances aimed at reducing the Muslim population [48], while Taylor identified political and socioeconomic factors as reasons for acceptance or refusal of polio vaccine administration [49]. New evidence provided by this study was the lack of significance of the relationship between religion and fully immunised child odds in the urban formal areas. As found in earlier studies, the association between the age of the mother and fully immunised child status was significant [25, 41, 50]. Reasons suggested include lack of child care experience by young mother, experience gained by older mothers on the effectiveness of vaccines, and the effect of treating child illness on family income [6, 9]. Our study population was larger than those in previous studies, and nationally representative, thus increasing reliability of our findings.
Households with regular exposure to media had children with higher FIC than households without regular media exposure. This relationship had been documented as a determinant of childhood immunisation in previous research based on secondary analysis of NDHS datasets [9, 25]. The media provides information on the benefits of immunisation, health activities and location of health facilities, as such can serve as a tool to improve childhood immunisation [47].
Contrary to the findings of previous studies in Nigeria [9, 25], we found that the association between household wealth and childhood immunisation was not statistically significant, which may be attributed to the recoding of the wealth variable in this study to make it urban or rural relative, lest all rural population were classed as being poor relative to urban populations. Despite the free provision of immunisation services in public owned health facilities, there are still indirect costs that can be barriers, such as transport cost to the health facility that is far from the mothers, and for the low income earner's inability to be excused from work as a result of the considerable time spent for journey to and time spent in the health facility [8]. Also, the lack of money has been reported to hinder appropriate health care seeking behaviour [9].
Community level factors
Overall, the Northern regions (Northcentral, Northeast and Northwest) had lower FIC adjusted odds than the Southern (Southeast, Southsouth and Southwest) regions, also reported by others [17,18,19, 40, 43]. Reasons suggested include higher education level and higher household wealth in the South than in the North, northerners are mostly Muslims and the southerners predominantly Christian, and the recent Muslim insurgency in the Northeast [9, 25]. However, across the six regions in Nigeria, there was high variability in the likelihood of being fully immunised. The Northwest region which is the most populous had the lowest FIC coverage and least fully immunised child odds compared to the other regions, while the Southsouth region had the highest fully immunised children odds. As expected, children of mothers who felt the distance to the nearest health facility to seek health was a big problem had lower FIC coverage and lower fully immunised child odds than children with mothers who did not see the distance as a big problem. This finding is in line with the results of several studies in Nigeria [9, 25, 51].
Our novel contribution lies in the PAR estimates, which showed that the population FIC in each of the three areas of residence was dependent on key sociodemographic exposure. Simply, the PAR is the additional number of children that would have been vaccinated if the sociodemographic variable had been maximised. Though no particular PAR trend was found across the places of residence, variables such as maternal education and media exposure that are linked to building knowledge about immunisation had the greatest effects in the rural areas, next was the slums and least in the urban formal settings. The PAR estimated highest percentage point increase in FIC can be achieved in all places of residence by giving all mothers higher education: rural (38.15), urban formal (22.88) and slum (23.76). Also, with all households having regular media exposure, the PAR was rural (6.30), urban formal (2.81) and slum (3.56). Hence, PAR analysis makes planning more realistic since target setting can be more correctly done as the number of children to be reached to increase the FIC by a percent as well as the variable to minimise or maximise to achieve it in each residence is known.
Study limitations
The analyses are based on data from retrospective cross-sectional surveys; immunisation data was collected for children aged between 12 and 23 months from the child’s immunisation card, with the mother recalling the information if the card was not available. Maternal report may be subject to recall bias, especially as event could have occurred more than a year before the interview. Similarly, maternal education level has been reported to be associated with recall bias, with the mothers of more educated level being more likely to accurately recall the child’s immunisation history. Thus, adjusting for maternal education in the multilevel logistic models reduced the effect of maternal education on the recall bias [52]. The household wealth variable in NDHS is a proxy based on the presence or otherwise of a number of assets, rather than on direct measurement of household income [53]. However, contrary to earlier studies, we calculated household wealth relative to the area of residence rather than for the overall population, and our wealth variable thus indicates wealth relative to the wealth of others living in the same area. Some of the selected NDHS variables were not perfectly aligned to the research question, for example the variable, “distance to the nearest health facility when seeking health care”, does not specifically refer to child immunisation. As the NDHS data provides information only on urban and rural place of residence, we used UN HABITAT guidelines to recode the urban data into formal and slum households. This may have introduced selection bias, as the DHS sampling process was based on projections from general census held several years earlier, and as such may not be fully representative of the population when the DHS was conducted.
Conclusion
Nigeria’s fully immunised child coverage of about 23% is unacceptably low; utilisation of immunisation services is associated with sociodemographic variables acting at child, household, community and health system levels. However, even the most privileged sociodemographic groups do not achieve the recommended FIC coverage target. With this very low FIC coverage, the prevalence of vaccine preventable diseases will continue, leading to high child mortality rates and increased health expenditure by parents.
The pattern and coverage of being fully immunised across the sociodemographic variables were similar in all areas of residence (rural, urban formal and slum). The FIC was highest in urban formal, with the slums values slightly lower and the rural figures much lower. Although the very low rural coverages may be largely due to lack of health facilities and immunisation education as indicated by PAR analysis, the intra-urban disparity is mostly unexplained, and requires further qualitative and interventional research. But our epidemiological analysis has made it easier by estimating the risk as such quantifying the FIC point increase that can be achieved if specific sociodemographic variable (risk) are addressed in the various communities, thereby making prioritisation of interventions much easier.
In the meantime, pending further evidence, suggestions for improvement are location specific: Immunisation session reminders in the slums, engagement of Moslem leaders in slum and rural areas, improved immunisation education in all residences and re-establish outreach services in rural communities.
Availability of data and materials
The anonymised data of the Demographic and Health Surveys conducted in Nigeria in 2003, 2008 and 2013 are available at (www.measuredhs.com), after approval by Measure DHS, but the analyses are available from the corresponding author on reasonable request.
Abbreviations
- ANC:
-
Antenatal Care
- aOR:
-
Adjusted Odds Ratio
- DHS:
-
Demographic and Health Survey
- DPT:
-
Diphtheria Pertussis Tetanus
- FIC:
-
Fully Immunised Child
- NDHS:
-
Nigeria Demographic and Health Survey
- OR:
-
Odds Ratio
- PAR:
-
Population Attributable Risk
References
World Health Organisation:Media centre Factsheet [http://www.who.int/mediacentre/factsheets/fs378/en/]. Accessed 02 Jan 2019.
Tao W, Petzold M, Forsberg BC. Routine vaccination coverage in low- and middle-income countries: further arguments for accelerating support to child vaccination services. Glob Health Action. 2013;6:20343.
World Health Organisation:Surveillance and Burden [http://www.who.int/immunization/monitoring_surveillance/burden/estimates/en/]. Accessed 02 Jan 2019.
Feldstein LR, Mariat S, Gacic-Dobo M, Diallo MS, Conklin LM, Wallace AS. Global routine vaccination coverage, 2016. MMWR Morb Mortal Wkly Rep. 2017;66(45):1252–5.
World Bank: Nigeria Data [http://data.worldbank.org/country/nigeria]. Accessed 14 Aug 2018.
Antai D. Inequitable childhood immunization uptake in Nigeria: a multilevel analysis of individual and contextual determinants. BMC Infect Dis. 2009;9:181.
Adegboye OA, Kotze D, Adegboye OA. Multi-year trend analysis of childhood immunization uptake and coverage in Nigeria. J Biosoc Sci. 2014;46(2):225–39.
Olorunsaiye CZ, Degge H. Variations in the uptake of routine immunization in Nigeria: examining determinants of inequitable access. Global Health Commun. 2016;2(1):19–29.
Adedokun ST, Uthman OA, Adekanmbi VT, Wiysonge CS. Incomplete childhood immunization in Nigeria: a multilevel analysis of individual and contextual factors. BMC Public Health. 2017;17(1):236.
Fry S, Cousins B, Olivola K. Health of children living in urban slums in Asia and the near east: review of existing literature and data. Washington: Environmental Health Project, US Agency for International Development; 2002.
Agarwal S, Bhanot A, Goindi G. Understanding and addressing childhood immunization coverage in urban slums. Indian Pediatr. 2005;42(7):653–63.
Mutua MK, Kimani-Murage E, Ettarh RR. Childhood vaccination in informal urban settlements in Nairobi, Kenya: who gets vaccinated? BMC Public Health. 2011;11(1):6.
Dudu JE, Onokerhoraye AG. Barriers to effective immunization in urban slums of Warri and environs, Delta State Nigeria. Int J Humanit Soc Sci Invent. 2018;7(6):18–28.
Bobadoye SA, Fakere AA. Slum prevalence in Nigeria: what role for architects? World Environ. 2013;3(2):45–51.
Olotuah A, Bobadoye S. Sustainable housing provision for the urban poor: a review of public sector intervention in Nigeria. Built Human Environ Rev. 2009;2:51–63.
Lall SV, Henderson JV, Venables AJ. Africa's cities: opening doors to the world. Washington, DC: World Bank publications; 2017.
National Population Commission. Nigeria Demographic and Health Survey 2003. Calverton: National Population Commission and ORC Macro; 2004.
National Population Commission. Nigeria Demographic and Health Survey 2008. Abuja: National Population Commission and ICF Macro; 2009.
National Population Commission. Nigeria Demographic and Health Survey 2013. Abuja: National Population Commission and ICF International; 2014.
UN HABITAT. The Challenge of Slums:global report on human settlements 2003. In: Chapter 1: development Context and Millenium Agenda. Revised and Updated version; 2010.
UN HABITAT. Global Urban Observatory: guide to monitoring target11: improving the lives of 100 million slum dwellers. In. Nairobi: UN HABITAT; 2003.
Sober E. Bayesianism—Its scope and limits. In: Proceedings-British Academy: 2002. Oxford: Oxford University Press Inc; 2002. p. 21–38.
Forster MR. Predictive accuracy as an achievable goal of science. Philos Sci. 2002;69(S3):S124–34.
Antai D. Gender inequities, relationship power, and childhood immunization uptake in Nigeria: a population-based cross-sectional study. Int J Infect Dis. 2012;16(2):e136–45.
Chidiebere O, Uchenna E, Kenechi O. Maternal sociodemographic factors that influence full child immunisation uptake in Nigeria. South Afr J Child Health. 2014;08(04):5.
Babalola S, Lawan U. Factors predicting BCG immunization status in northern Nigeria: a behavioral-ecological perspective. J Child Health Care. 2009;13(1):46–62.
Mathew JL. Inequity in childhood immunization in India: a systematic review. Indian Pediatr. 2012;49(3):203–23.
Fatiregun AA, Okoro AO. Maternal determinants of complete child immunization among children aged 12-23 months in a southern district of Nigeria. Vaccine. 2012;30(4):730–6.
DHS MEASURE: Nigeria: Standard DHS, 1999 [https://dhsprogram.com/what-we-do/survey/survey-display-164.cfm]. Accessed 10 Sept 2018.
Kumar D, Aggarwal A, Gomber S. Immunization status of children admitted to a tertiary-care hospital of North India: reasons for partial immunization or non-immunization. J Health Popul Nutr. 2010;28(3):300–4.
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.
Ushie BA, Fayehun OA, Ugal DB. Trends and patterns of under-5 vaccination in Nigeria, 1990-2008: What manner of progress? Child Care Health Dev. 2014;40(2):267–74.
Gage AJ, Sommerfelt AE, Piani AL. Household structure and childhood immunization in Niger and Nigeria. Demography. 1997;34(2):295–309.
Antai D. Faith and child survival: the role of religion in childhood immunization in Nigeria. J Biosoc Sci. 2009;41(1):57–76.
Antai D. Migration and child immunization in Nigeria: individual- and community-level contexts. BMC Public Health. 2010;10:116.
Babalola S. Determinants of the uptake of the full dose of diphtheria-pertussis-tetanus vaccines (DPT3) in northern Nigeria: a multilevel analysis. Matern Child Health J. 2009;13(4):550–8.
Babalola S. Maternal reasons for non-immunisation and partial immunisation in northern Nigeria. J Paediatr Child Health. 2011;47(5):276–81.
Bonu S, Rani M, Razum O. Global public health mandates in a diverse world: the polio eradication initiative and the expanded programme on immunization in sub-Saharan Africa and South Asia. Health Pol. 2004;70(3):327–45.
Fatiregun AA, Adebowale AS, Ayoka RO, Fagbamigbe AF. Assessing full immunisation coverage using lot quality assurance sampling in urban and rural districts of Southwest Nigeria. Trans R Soc Trop Med Hyg. 2013;107(11):731–40.
Federal office of Statistics N. Nigeria Demographic and Health Survey 1990. Columbia, Maryland: Federal Office of Statistics and IRD Macro; 1992.
Mukherjee S, Madhivanan P, Li T, Albatineh A, Srinivas V, Jaykrishna P, Arun A, Krupp K. Correlates of completing routine vaccination among children in Mysore, India. J Infect Public Health. 2015;8(1):62–71.
Mushtaq MU, Majrooh MA, Ullah MZ, Akram J, Siddiqui AM, Shad MA, Waqas M, Abdullah HM, Ahmad W, Shahid U, et al. Are we doing enough? Evaluation of the Polio Eradication Initiative in a district of Pakistan's Punjab province: a LQAS study. Bmc Public Health. 2010;10:60.
National Population Commission. Nigeria Demographic and Health Survey 1999. Calverton, Maryland: National PopulationCommission and ORC Macro; 2000.
Obiajunwa PE, Olaogun AA. Childhood immunization coverage in south West Nigeria. Sudanese J Public Health. 2013;8(3):94–8.
Okoronkwo IL, Onwujekwe OE, Ani FO. The long walk to universal health coverage: patterns of inequities in the use of primary healthcare services in Enugu, Southeast Nigeria. BMC Health Services Res. 2014;14:132.
Singh PK. Trends in child immunization across geographical regions in India: focus on urban-rural and gender differentials. PLoS One. 2013;8(9):e73102.
Wiysonge CS, Uthman OA, Ndumbe PM, Hussey GD. Individual and contextual factors associated with low childhood immunisation coverage in sub-Saharan Africa: a multilevel analysis. PLoS One. 2012;7(5):e37905.
Renne E. Perspectives on polio and immunization in northern Nigeria. Soc Sci Med. 2006;63(7):1857–69.
Sebastin T. In: USAID, NPHCDA, editor. Perpestive of influence: understanding polio vaccination and immunisation in northern Nigeria. USAID and NPHCDA: Abuja; 2015.
Antai D. Rural-urban inequities in childhood immunisation in Nigeria: the role of community contexts. Afr J Prm Health Cae Fam Med. 2011;3(1):1–8.
Abdulraheem I, Onajole A, Jimoh A, Oladipo A. Reasons for incomplete vaccination and factors for missed opportunities among rural Nigerian children. J Public Health Epidemiol. 2011;3(4):194–203.
Kazembe LN, Muula AS, Simoonga C. Joint spatial modelling of common morbidities of childhood fever and diarrhoea in Malawi. Health Place. 2009;15(1):165–72.
Filmer D, Pritchett L: Estimating wealth effects without expenditure data—or tears: an application to educational enrollments in States of India. Demography. 2001;38(1):115–32.
Acknowledgements
Professor Nyovani Janet Madise provided technical support in the early stage of the study.
Funding
The authors received no financial support for the research and authorship of this article.
Author information
Authors and Affiliations
Contributions
OAO and MLN jointly conceptualised the study. OAO carried out the statistical analysis and reviewed by MLN. Both authors wrote, read and approved the final manuscript
Corresponding author
Ethics declarations
Ethics approval and consent to participate
This study conducted secondary analysis of anonymised data previously collected for the Demographic and Health Surveys conducted in Nigeria in 2003, 2008 and 2013 by the Monitoring and Evaluation to Assess and Use Results Demographic and Health Surveys (MEASURE DHS) project (www.measuredhs.com), in conjunction with the National Population Commission of Nigeria; approval for the use of the data was granted by Measure DHS. The surveys were carried out in line with best ethical practice with two ethical review approvals: 1. Institutional Review Board of Macro International in Calverton in the United States of America and 2. National Ethical Review Committees in Nigeria. During the NDHS, information was collected confidentially after written informed consent for participation had been obtained from all the participants.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Additional file 1: Table SA.
. Association between socio-demographic factors and full immunisation status (assessed at 12–23 months) in Rural Nigeria, Multilevel logistic regression analysis (DHS 2003, 2008 and 2013 data. Table SB. Association between socio-demographic factors and full immunisation status (assessed at 12–23 months) in Nigerian Urban formal Households, Multilevel logistic regression analysis (DHS 2003, 2008 and 2013 data. Table SC. Association between socio-demographic factors and full immunisation status (assessed at 12–23 months) in Nigerian Urban Slum Households, Multilevel logistic regression analysis (DHS 2003, 2008 and 2013 data. Table SD. Multivariate population attributable risk for fully immunised child coverage by place of residence.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Obanewa, O.A., Newell, M.L. The role of place of residency in childhood immunisation coverage in Nigeria: analysis of data from three DHS rounds 2003–2013. BMC Public Health 20, 123 (2020). https://doi.org/10.1186/s12889-020-8170-6
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12889-020-8170-6