A Community Survey of the Vaccination Status of Under-Five Children in a Community in Southern Nigeria : Nigerian Journal of Medicine

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A Community Survey of the Vaccination Status of Under-Five Children in a Community in Southern Nigeria

Ochei, Oboratare1,2,; Ntaji, Maureen Iru1,2; Adesoye, Oluwaseun Opeyemi2; Oserada, Nathaniel Ojitobo3; Ordiah, Sandra Nwanyemoghor3; Osaekete, Kojo Ifeoma3; Oshadiya, Ololade Christian3

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Nigerian Journal of Medicine 32(1):p 8-14, Jan–Feb 2023. | DOI: 10.4103/NJM.NJM_109_22
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Adequate nutrition, access to potable water, and good environmental hygiene remain essential for a child’s physical well-being, mental health, and excellent school performance. These measures together with vaccination against major childhood infections may optimize health.[1] Vaccination is expected to enhance a child’s ability to mount responses against many infectious diseases. It is a scientific technique of introducing a weakened or killed infectious agent or a fragment of the infectious agent or its toxin or a recombinant mRNA or a viral vector into an individual to activate the body’s immune cascade to produce humoral and cellular antibodies needed to fight the specific infectious agent, while immunisation is the ability of the body to promptly recognize and provide protection against infection on exposure to the infectious agent.[2]

The artificial immunisation of a child against an infectious agent helps strengthen the body’s ability to resist infection on exposure rather than allowing nature to take its course. When most of the population is immunised against a particular infectious agent, herd immunity is built, interrupting the spread of the infection in the population.[3] It also gives lifelong protection to families and individuals in the community, saves spending on treatment, and limits hospital visits and extended hospital admissions. The reduced hospital stay significantly improves productivity. Although vaccination does not always protect against the disease, it most often protects against serious forms of the disease. As reported in a study, the odds of vaccinated children dying from vaccine-related diseases compared to unvaccinated children was lower with a relative risk of 0.73 (95% confidence interval of 0.63–0.77).[4]

Childhood vaccination has been on for over a century.[5] It is said to be one important means of preventing millions of deaths and outbreaks of communicable diseases in a cluster of vaccinated children. Globally, it averts about 2–3 million deaths annually.[6] It is considered by the World Health Organisation (WHO) and United Nations Children’s Emergency Fund as the most cost-effective investment and one of the greatest phenomena ever discovered in medicine. The National Programme of Immunisation (NPI) in Nigeria presently vaccinates children against tuberculosis, poliomyelitis, diphtheria, pertussis, tetanus, Haemophilus influenzae type b, pneumococcal infection, hepatitis B, measles, yellow fever, and meningococcal disease.[7] This is comprised of a dose of Bacille Calmette–Guerin (BCG) vaccine, three doses of pentavalent vaccine, four doses of oral polio vaccine, a dose of inactivated polio vaccine, two doses of measles vaccine, a dose of yellow fever, and a dose of meningococcal vaccine.

In 2019, the WHO estimates of global childhood vaccine coverage were 75%; still, 14 million children had not had any vaccination.[8] Globally, the proportion of children who received the diphtheria–tetanus–pertussis 3 (DPT3) vaccine in 2019 was 85%, while in sub-Saharan Africa, vaccine uptake was 50% and 5% in hard-to-reach communities.[8] According to the 2018 National Demographic and Health Survey (NDHS), the percentage of children aged 12–23 months who had all vaccines stood at 31% and those with no vaccination was 19%. In the same document, the proportion of children who received all doses of polio vaccine was <50%, DPT1 (49.8%), DPT3 (38%), and measles (41.8%).[9] The bottom line is that Nigeria has made some progress in vaccine coverage, implementation of innovative ideas, and improved techniques in national immunisation program.[7] However, the country is yet to achieve the WHO’s equity in health for all people in the world. Low vaccine coverage, especially in hard-to-reach communities, may pose threat to vaccine-preventable diseases in children.[10] This may lead to many hospitalised, which in turn impinges on already dwindling health systems in developing countries.

A diversity of factors has been recognised to interfere with vaccine coverage, uptake, and the refusal to vaccinate in Nigeria. Factors cited include but are not limited to civil unrest, attacks on vaccination teams, the far distance of houses to the health facilities, low socioeconomic status of women, erratic supply of vaccines, low public acceptability of immunisation programs, late release of funds by the government, fear of its use as a weapon of bioterrorism, rumors of complications or harms, and fear of death from vaccination.[11] There are few disconcerting publications that may prevent parents from vaccinating their children. These researchers found an increased odds rate of neurodevelopmental delays, allergies, and ear infections in vaccinated children compared with the unvaccinated.[12,13] There are also increasing misconceptions about the dangers of childhood vaccination among parents. Thousands of parents linked vaccines with autism in their children after an article was published in Lancet in 1998 which was retracted 10 years after.[14] Furthermore, in May 2009, the New England Journal of Medicine published some frightening statistics on vaccine refusal.[15]

To reach the WHO vision for this decade: “a world where everyone, everywhere, at every age, fully benefits from vaccines for good health and well-being,” all people and nations need to respond, act, and support immunisation to advance a concrete rise in immunisation uptake and coverage.[8] By this vision, operational research to identify and scale up immunisation uptake and coverage in developing countries is needed. Although studies have been conducted in the past on the vaccination status of children, there is a need for continuous assessment of the prevalence of immunisation among children and the determinants of immunisation uptake as this will give a good understanding of trends that can be used for monitoring and evaluation and decision-making by policymakers.

Therefore, this study aimed to determine the proportion of children immunised in a community and the parental variables associated with immunisation in this community. The reasons for immunisation were also determined.


The study was conducted at Oghara, Delta State, Nigeria. Oghara is a semi-urban community in Delta State of Nigeria. It occupies an area of 1175 km2 within the tropical rainforest belt in the South-South geographical zone of Nigeria and lies approximately on longitude 5.7° West and latitude 5.916° South. It comprises five wards, including Ogharefe-one with a population of 178,455, Ogharefe-two with a population of 30,583, Oghara-three with a population of 22,923, Oghareki-one with a population of 27,017, and Ogharaeki-two with a population of 29,923. Oghara has primary health-care facilities, a secondary health-care facility at Ogharefe, and the Delta State University Teaching Hospital.

The study population included children aged 12–59 months and their parents who should have completed their routine immunisation in an Oghara community, Delta State. A cross-sectional study design was employed and a minimal sample size of 250 was estimated using the formula for a cross-sectional study.[16] The percentage of children who had completed their immunisation in Delta State was 34%–48%.[9] A multi-stage sampling technique was used at different stages to select respondents. In the first stage, each of the wards was divided into clusters based on natural landmarks, and thereafter, a cluster was then selected from each ward by balloting (there are five wards, thus five clusters were selected). In the second stage of the sampling, the sample size was divided uniformly among the five selected clusters, thus fifty households under-five were selected per cluster. In the third stage of the sampling, cluster sampling technique was used to select the fifty households for the study. All households with under-five children in the selected clusters were identified; in a household with more than one eligible child, balloting was used to select the child, and the selected child’s parent was then interviewed. This process continues until the desired sample size was reached. A semi-structured questionnaire was used to obtain and document the following information: child’s age, sex, birth order, sociodemographic data of parents/caregivers, awareness of vaccination, what is vaccination, its importance, current vaccination schedule in Nigeria, location of the immunisation centre and activities carried out at the vaccination centre, vaccines received by the child (this was accessed verbally and by sighting the child’s vaccination card), the age the child received the vaccines, the interval between vaccines, completion of vaccines, and reasons for and against immunisation. This information was obtained from their mother or both mother and father. Data were analysed using IBM Corp. Released 2013. IBM SPSS Statistics for Windows, Version 22.0 (Armonk, NY: IBM Corp). The percentage of children who had received all the required number of vaccines was computed irrespective of the age at which he/she received the vaccines. A child was considered to have completed immunisation if he/she had all vaccines in the NPI. Furthermore, the proportion of children who had BCG, OPV0, OPV1, OPV2, OPV3, IPV, PENTA 1, PENTA 2, PENTA 3, PCV1, PCV2, PCV3, VITAMIN A 1st DOSE, VITAMIN A 2nd DOSE, MEASLES 1st DOSE, MEASLES 2nd DOSE, YELLOW FEVER, and MENINGITIS were calculated.

Mother’s knowledge was assessed from the following questions: what is vaccination, its importance, the current vaccination schedule in Nigeria, the location of the immunisation centre, and activities carried out at the vaccination centre. Eighteen questions were used to assess knowledge, each correct response attracted one point, and the maximum points were 18. A mother with nine points and above was said to have good knowledge and a mother with <9 points was said to have poor knowledge.

The dropout rates were also calculated. The dropout rate is usually calculated using the formula provided by the National Primary Health Care Development Agency in the basic guide for routine immunisation for a service provider in Nigeria.[7] The dropout rate for PENTAVALENT vaccine was calculated by subtracting the number of children who had PENTA 3 from PENTA 1 divided by PENTA 1 multiplied by 100%. The dropout rate for BCG/measles was calculated by subtracting the number of children who had measles vaccine second dose from the BCG vaccine divided by BCG multiplied by 100%. Chi-square test was used to determine the association between parents’ sociodemographic characteristics and children’s vaccination status.


Table 1 shows the sociodemographic characteristics of the parents of the children sampled. They were more mothers with tertiary education 125 (50%), 216 (86.4%) mothers were ever married, 227 (90.8%) mothers were working, and about 175 (70%) were multiparous. They were more fathers with tertiary education 149 (59.6%), while 222 (88.8%) fathers were ever married [Table 1].

Table 1:
Sociodemographic characteristics of parents of the children

Table 2 shows the immunisation status of children in the study population. Of the 250 children under five years who participated in the study, 170 (68%) had all the vaccines; 44 (17.6%) did not complete their vaccines and 36 (14.4%) had no vaccine. About 207 (82.8%) had BCG vaccine, 199 (79.6%) had OPV0, 191 (76.4%) had OPV 1, 172 (68.8%) had OPV 2, and 177 (70.8%) had OPV 3. The number of children who had HBV0 was 196 (78.4%); pentavalent 1, 187 (74.8%); pentavalent 2, 188 (75.2%); pentavalent 3, 182 (72.8%); and IPV, 172 (68.8%). About 193 (77.2%) had PCV 1, 177 (70.8%) had PCV 2, and 174 (69.6%) had PCV 3. The number of children who took Vitamin A first dose was 177 (70.8%), and Vitamin A second dose was 171 (68.4%). Measles first and second doses were 174 (69.6%) and 170 (68%), respectively. About 174 (69.6%) took the yellow fever vaccine. The dropout rate for pentavalent vaccines was 2.7% and for BCG and measles 17.9% [Table 2].

Table 2:
Vaccination status of under-five children at Oghara

Table 3 shows the association between sociodemographic characteristics of parents and immunisation status of their children. About 82.4% of mothers had good knowledge and 17.6% had poor knowledge, of which 74.8% of mothers’ with good knowledge completed their children’s immunisation schedule, while 36.4% of mothers with poor knowledge of immunisation completed their children’s immunisation. Seventy-six percent (76%) of children whose mothers had tertiary education had complete vaccines compared to 40.4% whose mothers had primary education. Mothers who are grand multiparous (80%) had their children completely vaccinated when compared with mothers who are primiparous (53.3%). About 76.7% of fathers whose ages are >35 years of age completed their children’s immunisation schedule, compared to 47.6% of those <24 years. Seventy-six percent (76.5%) of children whose fathers had tertiary education had complete vaccines compared to 32.4% whose fathers had primary education. Maternal knowledge (P = 0.00001), maternal parity (P = 0.006), mother’s education (P = 0.00001), father’s education (P = 0.00001), and father’s age (P = 0.0002) were identified as variables associated with vaccine uptake within the community [Table 3].

Table 3:
Association between parent characteristics and child’s vaccination status

Table 4 shows the reasons for/against immunisation. About 48.8% of the mother’s said that vaccination protect their children against diseases, and 10% of the mother’s said it reduces severe forms of diseases. For reasons against immunisation, 3.2% of the mothers said that the vaccines had no effect on their children, and that the vaccines cause fever (10.8%) [Table 4].

Table 4:
Mother’s reason for/against immunisation


We assessed the proportion of children immunised in the community, the parental factors associated with immunisation, and the reasons for and against immunisation. In our study, the proportion of children that completed their vaccination was 68%. This was similar to a survey carried out in Imala, Ogun State, Nigeria, but was higher than the value (31%) obtained from the Nigeria National Demographic Health Survey.[9,17] This finding was also higher than reports obtained from a large-scale rural survey in Ethiopia, a rural setting in Western Nigeria, and a community-based study in Northwest Ethiopia.[18–20] This may be linked to the result that a greater number of mothers had good knowledge about immunisation and most parents in this study attained a tertiary level of education. The rate of complete vaccination of children is an important metric to assess progress toward attaining the United Nations Sustainable Development Goal 3.[21]

The coverage rates of the vaccines administered at birth (BCG and OPV0) were relatively higher than those administered at later periods of life (measles, yellow fever, and meningitis). A comparable pattern has been reported in other studies.[18,20,22,23] This variance has been associated with the duration between the first doses of vaccine and that of taking subsequent vaccines. In Nigeria, children require five contacts with health providers to complete the childhood vaccines.[7] Furthermore, in this study, the antigen with the highest rate of uptake was BCG. A likely reason is that this vaccine is usually given at birth in the health facility where the child is born and the hospital policy ensures that this vaccine is administered before the child is discharged from the hospital.

Comparing the two dropout rates from pentavalent 1/pentavalent 3 and BCG/measles vaccines, there was a marked difference between the two indices. This large difference may be attributable to the longer time between BCG and measles vaccination (about eight months), compared with the three-month time interval between the first and third doses of the pentavalent vaccine. The large time interval between BCG and measles vaccination may result in caregivers forgetting the measles vaccination date, hence a high dropout rate. This calls for the need to institute recalling mechanisms for mothers such as phone calls to remind them of the date for vaccination.

Unlike our study which showed a marked difference in the two metrics used for dropout rates, another study in a rural setting in East Africa showed very close similarity in the different metrics used for assessing dropout rates.[23] East Africa computed dropout rates using three metrics: OPV1 to OPV3, Penta1 to Penta3, and BCG to Measles. The reason that may have accounted for the disparity is that our study compared the dropout rate using BCG and the second dose of measles, while the East Africa study compared dropout rate using BCG and the first dose of measles.

There was a gradual and consistent reduction in the proportion of children who took the oral polio vaccine from OPV0 to OPV3. This may be related to the forgetfulness of vaccination dates by their caregivers due to the successive four weeks’ interval between the vaccine administrations. This draws attention to the need to include in the immunisation programs a means of reminding parents of the expected days for vaccination of their children. Some investigators have also suggested nursing mothers remind their husbands of their appointments, as a way of reducing forgetfulness during subsequent visits.[24]

There was a little above a four-fifths increase in the rate of BCG vaccination compared to the finding from NDHS 2018.[9] This may be an indication of improvement in BCG coverage which is highly commendable. High BCG vaccination is a key strategy for the prevention of tuberculosis infection. In this study, the coverage rate for BCG was more than eight in ten children, which was as high as nine in ten children who took the BCG vaccine in a similar study.[23]

Regarding uptake rate, the second dose of the measles vaccine had the lowest uptake rate. This is, in contrast, to a report by Hailu et al 2019, where the lowest uptake rate was in the administration of the oral polio vaccine at birth.[18] In this study, children without any vaccine were lower, almost three in twenty compared to the report of less than one in five from NDHS.[6] Abysmally low coverage rates were also documented in the North-west region of Nigeria.[25] This group of children without vaccination is significant and should be traced in the community as they may hinder the attainment of herd immunity.

About four-fifth of the mothers had good knowledge about immunisation. Conversely, less than a quarter of respondents were reported to have had good knowledge about immunisation in Mangalore, India.[26] A statistically significant association was found between mothers’ knowledge of immunisation and their children’s vaccination status. This corroborates findings from related studies showing a significant association between mothers’ knowledge about vaccination schedules and a child’s vaccination coverage.[19,20,27,28] This highlights the importance that educating mothers might have on childhood vaccination coverage. Messages related to the role of mothers as regards vaccination during antenatal care sessions and even in other fora which pertain to mothers of under-fives and those preparing for marriage will be beneficial.

There was a statistically significant association between immunisation status of children and educational level of mothers. In a related study, a similar observation was made.[23] This might reflect the importance of mothers’ education in achieving positive health outcomes in their children and within their families by extension. However, a study that was done in Al-Beida, Libya reported findings of a higher proportion of illiterate mothers whose children were fully immunised.[29] Our study portrayed that mothers’ knowledge about immunisation, educational status of mothers, maternal parity, and fathers’ age and educational level, were significantly associated with an increased uptake of immunisation.

Although there was no statistically significant association between child’s vaccination coverage and mother’s occupational status. Three-quarters of mothers not working completed their children’s vaccination when compared to two-thirds of those working. This may be because mothers who have no jobs have more flexible times to take their children for vaccination, whereas mothers who have jobs may be time-constrained due to busy work schedules, in addition to other reasons which could result in missing children’s vaccination dates. A contrary observation showed that a mother’s job did not affect the immunisation of their children.[29]

Most of the reasons given by respondents in this study for being against immunisation were factors associated with mothers’ experience at health facilities after vaccinating their children, such as fever and the inability of a child to move the leg after vaccination. This may imply that health-care providers may not be properly educating clients on the side effects of vaccines. Strengthening awareness about the side effects of vaccines needs to be embedded into the health education programs which should be done consistently before vaccine administration to prevent dropout rates during vaccinations.


Our study revealed that majority of the children in the community were fully vaccinated, but this coverage was below the expected national target. This signals a need to scale up attempts at creating awareness in the community as regards vaccination campaigns all year round. Furthermore, majority of the mothers had good knowledge of immunisation. Incentives should also be given to mothers who provide evidence of completed child health cards to further motivate other mothers within a community.

Mothers’ knowledge of immunisation, educational status of mothers, maternal parity, and fathers’ age and educational level were associated with uptake of immunisation. This discovery further reiterates the importance of improving the access to education and promoting gender equality for the achievement of sustained development within the society, with efforts geared toward reducing child morbidity and mortality.

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Conflicts of interest

There are no conflicts of interest.


1. Chaudhuri N. Interventions to improve children's health by improving the housing environment. Rev Environ Health 2004;19:197-222
2. Olufemi R, Adesina F. Immunisation coverage of the under-5 children in Akure north local government area of Ondo State. Ann Med Health Sci Res 2019;9:519-23
3. Mallory ML, Lindesmith LC, Baric RS. Vaccination-induced herd immunity: Successes and challenges. J Allergy Clin Immunol 2018;142:64-6
4. McGovern ME, Canning D. Vaccination and all-cause child mortality from 1985 to 2011: Global evidence from the demographic and health surveys. Am J Epidemiol 2015;182:791-8
5. Plotkin S. History of vaccination. Proc Natl Acad Sci U S A 2014;111:12283-7
6. World Health Organisation. Vaccines. World Health Organisation/Western Pacific Region. Published 2021. Available from: https://www.who.int/westernpacific/health-topics/vaccines-and-immunisation [Last accessed on 2023 Feb 15]
7. National Primary Health Care Development Agency. Basic Guide on Routine Immunisation for Service Providers in Nigeria. Facilitators Guide September 2017
8. World Health Organisation. Immunisation Coverage: Key Facts. Published 2020. Available from: https://www.who.int/news-room/fact-sheets/detail/immunisation-coverage [Last accessed on 2023 Feb 15]
9. National Population Commission [Nigeria] and ICF International. Nigeria Demographic and Health Survey 2018. Rockville, Maryland, USA: National Population Commission [Nigeria] and ICF International; 2018
10. Guerra FA. Delays in immunisation have potentially serious health consequences. Paediatr Drugs 2007;9:143-8
11. Nasir UN, Bandyopadhyay AS, Montagnani F, Akite JE, Mungu EB, Uche IV, et al. Polio elimination in Nigeria: A review. Hum Vaccin Immunother 2016;12:658-63
12. Hooker BS, Miller NZ. Analysis of health outcomes in vaccinated and unvaccinated children: Developmental delays, asthma, ear infections and gastrointestinal disorders. SAGE Open Med 2020;8:2050312120925344
13. Mawson AR, Ray BD, Bhuiyan AR, Jacob B. Pilot comparative study on the health of vaccinated and unvaccinated 6- to 12-year-old U.S. children. J Transl Sci 2017;3:1-12
14. Lee JW, Melgaard B, Clements CJ, Kane M, Mulholland EK, Olivé JM. Autism, inflammatory bowel disease, and MMR vaccine. Lancet 1998;351:905
15. Omer SB, Salmon DA, Orenstein WA, deHart MP, Halsey N. Vaccine refusal, mandatory immunisation, and the risks of vaccine-preventable diseases. N Engl J Med 2009;360:1981-8
16. Charan J, Biswas T. How to calculate sample size for different study designs in medical research?. Indian J Psychol Med 2013;35:121-6
17. Adediran AS, Onyire NB, Guvuoke VO, Obum E, Anyanwu OU. Immunisation status of under-5 children in a rural community in Nigeria. IOSR J Dent Med Sci 2017;16:126-30
18. Hailu S, Astatkie A, Johansson KA, Lindtjørn B. Low immunisation coverage in Wonago district, southern Ethiopia: A community-based cross-sectional study. PLoS One 2019;14:e0220144
19. 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
20. Tesfaye TD, Temesgen WA, Kasa AS. Vaccination coverage and associated factors among children aged 12–23 months in Northwest Ethiopia. Hum Vaccin Immunother 2018;14:2348-54
21. Stenberg K, Axelson H, Sheehan P, Anderson I, Gülmezoglu AM, Temmerman M, et al. Advancing social and economic development by investing in women's and children's health: A new global investment framework. Lancet 2014;383:1333-54
22. Sibeudu FT, Uzochukwu BS, Onwujekwe OE. Rural-urban comparison of routine immunisation utilisation and its determinants in communities in Anambra States, Nigeria. SAGE Open Med 2019;7:2050312118823893
23. Girmay A, Dadi AF. Full immunisation coverage and associated factors among children aged 12-23 months in a hard-to-reach areas of Ethiopia. Int J Pediatr 2019 2019;1924941
24. Onyiriuka A. Vaccination default rates among children attending a static immunisation clinic in Benin City, Nigeria. J Med Biomed Res 2009;4:71-7
25. Adeloye D, Jacobs W, Amuta AO, Ogundipe O, Mosaku O, Gadanya MA, et al. Coverage and determinants of childhood immunisation in Nigeria: A systematic review and meta-analysis. Vaccine 2017;35:2871-81
26. Jose J, Lobo M, Shilpa GS, Umarani J, Jose J. Awareness on immunisation among mothers of under-five children. Int J Innov Res Dev 2013;2:620-7
27. Libwea JN, Kobela M, Ollgren J, Emah I, Tchio R, Nohynek H. Predictors to parental knowledge about childhood immunisation/EPI vaccines in two health districts in Cameroon prior to the introduction of 13-valent Pneumococcal Conjugate Vaccines (PCV-13). Pan Afr Med J 2014;17:187
28. Ubajaka FC, Ukegbu AU, Okafor NJ, Ejiofor O. The prevalence of missed opportunities for immunisation among children utilizing immunisation services in Nnamdi Azikiwe University Teaching Hospital, Nnewi. J Biol Agric Healthc 2012;2:112-20
29. Bofarraj MAM. Knowledge, attitude and practices of mothers regarding immunisation of infants and preschool children at Al-Beida City, Libya 2008. Egypt J Pediatr Allergy Immunol 2011;9:29-34

Immunisation; parent education; South-southern Nigeria; under-five children; vaccination coverage

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