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Article

Insights into Predictors of Vaccine Hesitancy and Promoting Factors in Childhood Immunization Programs—A Cross-Sectional Survey in Cameroon

by
Jonas Kemeugni Ngandjon
1,*,
Thomas Ostermann
2,
Virgile Kenmoue
3 and
Alfred Laengler
4
1
Institute of Pediatric, Faculty of Health, University of Witten/Herdecke, 58448 Witten, Germany
2
Department for Psychology and Statistics, Faculty of Health, University of Witten/Herdecke, 58448 Witten, Germany
3
Department for Human Medicine , Faculty of Health, Université des Montagnes, Bangangté BP 208, Cameroon
4
Department for Human Medicine, Institute of Pediatric, Faculty of Health, University of Witten/Herdecke, 58448 Witten, Germany
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(5), 2721; https://doi.org/10.3390/ijerph19052721
Submission received: 11 December 2021 / Revised: 1 February 2022 / Accepted: 16 February 2022 / Published: 26 February 2022

Abstract

:
Background: Vaccination is claimed to be a key intervention against the COVID-19 pandemic. A major challenge today is to increase vaccine acceptance as vaccine hesitancy has delayed the eradication of polio. This study aimed to identify predictors associated with vaccine acceptance in the context of the Expanded Program on Immunization among parents of children between the ages of 12 to 23 months in the Foumbot district, Cameroon. Methods: The design of this study is a cross-sectional survey. A total of 160 mothers of children between the ages of 12 to 23 months were selected using a simple random sampling technique. A pre-tested structured questionnaire was used for data collection. Incomplete vaccination status was considered “vaccine hesitancy”. Data was analyzed along with 95% confidence intervals and the p-value < 0.05. The results showed 60% vaccine acceptance and 40% vaccine hesitancy. Factors such as age-appropriate vaccination, knowledge of vaccine-preventable diseases (VPD), and religion were associated with vaccine acceptance. Conclusion: Poor knowledge of VPDs is a matter of concern as it contributes to vaccine hesitancy. The study findings provide the basis to heighten health education, the public perceived threat of the VPDs, and the consequences if no measures are taken to ensure health.

1. Background

Early vaccination success and necessities to eradicate communicable diseases brought widespread vaccine acceptance, and immunization programs have significantly decreased the incidence of numerous diseases in many parts of the world [1,2]. As the COVID-19 pandemic is threatening the world, the advent of COVID-19 vaccines was widely considered a key intervention in disease control. In addition to the Expanded Program on Immunization (EPI), which is a free immunization program to reach each child with polio, measles, tetanus, diphtheria, pertussis, and tuberculosis vaccines, governments in low-income countries have also launched the COVID-19 immunization program [2,3,4]. Reports from the World Health Organization (WHO) show that delays in polio eradication are linked to vaccine hesitancy among parents [2]. Therefore, the success of immunization programs depends not only on vaccines supply but also on vaccine acceptance. In 2020, many countries had still not achieved 80% polio herd immunity (three polio vaccine doses) despite the availability of vaccines: Cameroon (70%), the Democratic Republic of Congo (59%), Nigeria (57%), and Central African Republic (46%) [1]. During the COVID-19 pandemic, as COVID-19 vaccines arrived in Africa, Nigeria administered 48%, Cameroon 23%, and the Democratic Republic of Congo administered fewer than 5% of the vaccine doses that they received [5]. By December 2021, COVID-19 vaccine hesitancy was 84% among Cameroonians, and only 2.6% of the population had received two COVID-19 vaccine doses [1,6]. The sole provision of vaccines does not guarantee vaccine acceptance. Due to diverse reasons and factors, vaccine hesitancy remains a concern on the African continent, although immunization programs (EPI and COVID-19 vaccines) are free of charge. Vaccine hesitancy refers to a delay in acceptance or refusal of an available vaccine. Many vaccine-hesitant parents believe that vaccines contain suspicious products, which could endanger child health [4]. The feeling that sows doubt and mistrust, as well as the spread of misinformation, both lead to a community of vaccine hesitancy. Studies of recent outbreaks of vaccine-preventable diseases (VPDs) have reported that vaccine hesitancy among parents is linked to the outbreak of VPDs throughout African countries and internationally [7,8,9]. In 2013, outbreaks of polio were reported in Central Africa, particularly in Cameroon, where it was reported in nine districts, including the Foumbot district [10]. Despite the EPI in this district, children with polio had not received any vaccine by the age of two. A major challenge today is to increase vaccine acceptance.
Although evidence on encouraging vaccination, in general, is useful in the context of outbreaks, vaccine acceptance poses an enormous challenge. Understanding the process of vaccine acceptance can serve as an early warning system to take action to avoid declining vaccine confidence and acceptance. This study offers a baseline of confidence levels to assess vaccine acceptance among parents and help identify where further confidence-building is required to increase adoption of childhood vaccination and new vaccines such as COVID-19 vaccines.
However, data on vaccine acceptance from African countries, mainly from Central Africa, is substantially limited. This indicates a need for specific research in these regions to explore the factors that contribute to parental vaccine hesitancy. Evidence from western countries will not be applicable here due to the significant differences in social and cultural contexts. Therefore, this study aimed to identify, during the EPI, the factors influencing complete childhood vaccination by sociodemographics and knowledge on vaccination among parents in the Foumbot district in Cameroon to understand the gap in formulating a comprehensive immunization program.

2. Methods

2.1. Study Area

The Foumbot district is a rural area of about 1000 km2. It is located in the Noun Division, West Region of Cameroon. The population estimate is 62,776 inhabitants (from the 2013 Census), the majority being Bamum. The predominant religion is Islam. Farming is the main occupation. The district hosts the most important fresh food market in Cameroon. The EPI is provided free of charge at health facilities. In 2013, a polio outbreak was reported in the district [10].

2.2. Study Design

A cross-sectional survey of parents of children aged 12 to 23 months was conducted from 1st July to 31st October 2014. The EPI coverage and the factors associated with childhood vaccination were assessed. Only the parents of the children were interviewed. Survey participants were selected randomly according to coverage cluster survey sampling [11,12,13,14]. Vaccination coverage was evaluated by means of the vaccination booklet and the EPI registers.

2.3. Sample Size Determination

Using the sample size calculation methodology presented in the WHO Immunization Coverage Cluster Survey Reference Manual (WHO/IVB/04.23), the sample size required was determined using the coverage of 64% obtained in the western region, a precision of ± 10%, a type 1 error of 10%, and a design effect of 1.5, in conformity with the standard WHO methodology [12,13]. Thus, the calculated minimum number of children required was 147.

2.4. Participants

During the investigation, data from 160 children and 160 parents were randomly collected in the district. The sampling process was performed according to the simple random sample method [11,12]. The first household was randomly chosen from each selected cluster. Each household was chosen randomly, such that each household had the same probability in the cluster of being chosen during the sampling process [15].

2.5. Data Collection

The data was collected using a structured questionnaire. The questionnaire covers sociodemographic factors and parents’ knowledge of VPDs. Prior to data collection, the questionnaire was pretested on a 5% sample of a similar population. The vaccination status of the child was established by the records in the vaccination booklet, the records in the EPI registers, or by the presence of scar in the case of the BCG vaccine.

2.6. Independent Variables

The independent variables included sociodemographic characteristics and the parent’s knowledge regarding vaccination and VPDs. The sociodemographic variables included age group (<25, 25–34, >34), education (no formal education, primary, secondary, university), occupation (formal sector, informal sector), marital status (married, single, divorced, and widowed), religion (Catholic, Protestant, Muslim, and Animist). To collect data on knowledge about vaccination and VPDs, parents were asked if they knew the reason for vaccinating (prevent the occurrence of diseases, decrease the severity of diseases, no idea), had knowledge of VPDs (good knowledge, poor knowledge), knew age-appropriate vaccination (at birth, no idea, other date), were aware of the vaccination schedule (be aware), and if they retained the vaccination booklet (keep). The response was recorded as ‘Yes/No’.

2.7. Outcome Variable

A close-ended question inquiring whether the parent has completed the EPI was used as the outcome variable. The outcome variable for this study was complete vaccination. Complete vaccination was defined as a child who received one dose of BCG and measles and three doses of OPV before the age of two. Children missing one dose of these vaccines were defined as incomplete vaccination. Complete vaccination was considered ‘vaccine acceptance’, whereas incomplete vaccination and no vaccination were considered ‘vaccine hesitancy’.

2.8. Data Processing and Analysis

The data from the interview was coded and entered into a computer database using Microsoft Office Excel 2010. Descriptive statistics were performed by means of the statistical software program SPSS. The Fisher test was used, and the odds ratios (OR) were calculated along with 95% confidence intervals (CI). A bivariate analysis was conducted to examine the association of vaccination status with each independent variable. Based on this, only independent variables that had significant bivariate associations with vaccination status were considered for the multivariate logistic regression. The stepwise multivariate analysis was used. Models were generated according to the type “forward selection”. Akaike’s information criterion (AIC) and Schwarz’s Bayesian information criteria (BIC) were used to inform the selection of models and to assess the goodness of fit. The AIC and BIC values were compared in successive models, and the model with the lowest value was considered the best-fit model [16]. In addition, the likelihood ratio test and the area under receiver operating characteristics (AUC) curve were used to assess the predictive quality of the model.

2.9. Ethical Clearance

This study obtained authorization to be carried out from the Faculty of Medicine of the Université des Montagnes and the health authorities of the Foumbot district. Verbal informed consent was required for each participant prior to the administration of the questionnaire.

3. Results

3.1. Prevalence of Vaccine Acceptance

Table 1 present the vaccination coverage in the study area. It appears that 96 (60%) of the 160 respondents completed the EPI. About 62 (38.75%) of the respondents had not completed the EPI, and 2 (1.25%) of the respondents had not started with the EPI. Therefore, 64 (40%) of respondents indicated vaccine hesitancy. The dropout rate between the initial vaccine of BCG and the final vaccine of measles was 36%.

3.2. Barriers in Vaccine Acceptance

Table 2 present the reasons for missing vaccination among parents whose children had incomplete vaccination status. Eleven (17.2%) of the sixty-four vaccine hesitant parents declared a lack of information regarding childhood vaccination. Additionally, 11 (17.2%) reported a lack of confidence in the EPI, whereas 42 (65.6%) reported poor quality of vaccination services.

3.3. Sociodemographic in Vaccine Acceptance

Table 3 show the results of the bivariate analysis. The factors marital status, religion, knowledge of VPDs, age-appropriate vaccination, and being aware of the vaccination schedule were significantly associated with complete vaccination at p < 0.05. The odds of receiving a complete vaccination among children whose parents were single were 3.23 (OR = 3.23; 95% CI: 1.03, 10.09) times higher than children whose parents were married. Muslim parents had 0.27 (OR = 0.27; 95% CI: 0.12, 0.61) times lower odds of completely vaccinating their children than parents from other religions. Children whose parents started vaccination at birth were 2.5 (OR = 2.5; 95% CI: 1.12, 5.55) times more likely of being completely vaccinated compared to children whose parents started later. Parents who were aware of the vaccination schedule were 3.52 (OR = 3.52; 95% CI: 1.43, 8.65) times more likely to have completely vaccinated their child compared to parents who were not aware of it. The odds of being completely vaccinated among children whose parents had good knowledge of VDPs were 3.08 (OR = 3.08; 95% CI: 1.21, 7.85) times higher than children whose parents had poor knowledge of VPDs.

3.4. Multivariate Logistic Regressions

Table 4 present the results of the stepwise method based on forward selection to purposely assess the contribution of each independent variable towards the prediction of complete childhood vaccination. The effect of the variables (religion, age-appropriate vaccination, knowledge of VPDs) was statistically significant (that is with Sig. < 0.05). This means that the variables found in Table 4 contribute significantly to the explanatory power of parents’ decision to complete vaccination. However, the following variables (marital status and being aware of the vaccination schedule) were dropped from the final model with the stepwise method of forward selection since they did not contribute towards the prediction of complete vaccination in Supplementary Materials.
Table 5 depict the model fitting information for the inclusion of the three variables that were found significant in Table 4. The final model with the least log-likelihood (56.16), AIC (64.16), BIC (76.46), and a degree of freedom of 3 was highly significant at the 5% level of significance. This means the final model based on the likelihood ratio test confirms that the multivariate logistic regression comprising of the three predictors fits the data better and is more effective than by chance towards the prediction of childhood vaccination status. The predictive utility of the final model was fair, with an AUC of 0.73.

4. Discussion

This study examined the association and influence of sociodemographic factors and knowledge of VPDs on complete childhood vaccination. The complete childhood vaccine acceptance was 60% [Table 1]. This was high as compared to the three Cameroonian regions West (54%), Adamawa (38%), and North (36%) [17]. In total, 65.6% of the vaccine-hesitant parents mentioned barriers linked to the quality of vaccination services [Table 2]. Similar results were reported in studies carried out in Bangladesh, India, the Philippines, Ethiopia, and Malawi [18,19]. In these countries, shortcomings were identified at the interface between the vaccination provider and the parents. Thus, the pools of unvaccinated children increased. In 2015, Cameroon was still classified as having an acute shortage of health personnel [20]. Researchers in Vietnam observed that the advice of a healthcare professional was the major factor that changed the view of parents who had previously refused vaccination or had delayed vaccination [21,22]. Therefore, contact with a healthcare professional is an important factor in vaccine acceptance. The results of this study showed that age-appropriate vaccination was significantly associated with complete childhood vaccination. Once starting the vaccination program at birth, the likelihood to complete the EPI increased by 2.5 [OR = 2.5] [Table 3]. A study performed in 2000 in a rural community of the Edo State in Nigeria showed that early vaccination of children increases the awareness of the parents towards VPDs and vaccination [23]. Administering the first vaccine at birth is an important step for building confidence in medical interventions and raising parental awareness about VPDs and the role that the vaccination can play in promoting child health. However, we found that 36% of the children had not completed the vaccination program, although 98% had received the BCG vaccine at birth [Table 1]. This study revealed that 17.2% of the vaccine-hesitant parents had concerns about the quality of information on the vaccination. Additionally, 17.2% did not have trust in the vaccine [Table 2]. This indicates that the awareness towards VPDs was not reached, and the confidence in medical interventions was not established. This study also revealed that religion was significantly associated with complete childhood vaccination [Table 3]. Data from India, Kenya, and Nigeria showed that vaccination in countries with traditional societies was more often associated with religious leaders as they are key stakeholders in disease prevention [4,24,25,26,27,28,29,30]. In these countries, vaccine hesitancy was driven by religious leaders as they called for a boycott of polio vaccination campaigns citing safety concerns with vaccines so that medical interventions intersected with cultural perception [31,32,33,34,35]. Due to past experiences relating to the slave trade and the colonization of Africa, vaccination has become suspicious as it is often linked to the conspiracy theory that western countries want to depopulate the African continent. Furthermore, many people believe in vaccine-induced female infertility [4,24,26,27,34,35,36,37]. These previous studies showed that vaccine acceptance was not generated by religious principles but by how health information was conveyed, perceived, and understood. The results of this study showed that knowledge of VPDs was a significant predictor to complete the EPI. Parents with good knowledge of VPDs [OR = 3.08] had a higher likelihood of completing the EPI. This finding is similar to an international study carried out in five African countries (Democratic Republic of Congo, Benin, Uganda, Malawi, and Mali), which reported that during the COVID-19 pandemic, individuals who perceived taking the COVID-19 vaccine as important to protect themselves had the highest vaccine acceptance odd [36]. In these countries, vaccine acceptance was positively associated with COVID-19 knowledge and threat regarding COVID-19. However, as information that COVID-19 vaccine-induced death spread within communities [38], a study indicated a low-risk perception of COVID-19 among Sub-Sahara Africans [39]. Therefore, fear of adverse effects from vaccines “makes sense”. Having a perceived low risk of disease can make vaccination less of a requirement. According to the Health Believe Model (HBM), the understanding of diseases enables people to perceive threat and thus, vaccine acceptance increases [28,40,41,42]. With reference to studies carried out in Kenya, Nigeria, Senegal, Turkey, and Thailand [34,43,44,45,46,47], health education was best suited to fill existing knowledge gaps and motivate parents to get their children vaccinated; this was the primary influence on the participants’ decision on vaccination. Thereby, knowledge of VPDs raises parents’ awareness of the healthcare, prevention, and the consequences of diseases for the child if measures are not taken to ensure health. This finding showed that vaccine acceptance increases as parents’ knowledge of VPDs increases. Therefore, the implementation of health education programs may be most beneficial. At the same time, the local system of customs and values (background, tradition, healing concept, etc.) should be considered for people’s understanding and perception of VPDs [Figure 1].

5. Limitations of the Study

In this study, some limitations were expected because this is a cross-sectional study, and the sampling method is susceptible to selection bias. Although the sample size was small, it is representative of the population which it resamples as it was calculated using the simple random sampling (SRS) method. Unfortunately, this method lacks the use of available knowledge concerning the population. Only the participants that were present in the district at the time of the interview and that met the survey inclusion criteria were considered in the sample.

6. Conclusions

This study identified knowledge of vaccine-preventable diseases as a factor influencing vaccine acceptance among parents in the Foumbot district. The low perceived threat of diseases is a matter of concern as it contributes to vaccine hesitancy. Consequently, vaccine acceptance may or may not only be based directly on a knowledgeable comprehension of the vaccination but also on the understanding of vaccine-preventable disease and the interpretation of the received information in communities [Figure 1]. The findings of this study suggest investing in health education programs to raise parents’ perceived threat towards disease infections and thereby improve preventive health behaviors such as vaccination to avoid diseases. Health education programs should not exclusively be limited to avoiding diseases or how to cope with diseases. It should also consider the local understanding of health issues and diseases. Future research should investigate possibilities in understanding the dynamics of communities regarding health issues while tailoring immunization programs to the local context.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijerph19052721/s1, Table S1: Classification Table a,b—Model-Intercept.; Table S2: Variables in the Equation—Model-Intercept.; Table S3: Variables not in the Equation—Model-Intercept.; Table S4: Omnibus Test of Model Coefficients—Overall Chi-square test.; Table S5: Model Summary—Full Model.; Table S6: Variables in the Equation; Table S7: Classification Table a—Stepwise Regression; Table S8: Variable in the Equation—Stepwise Regression.; Table S9: Model Summary—Stepwise Regression.; Table S10: Step Summary—Information Criteria; Table S11: Information for Model Fitting Criteria; Figure S1: Receiver Operating Characteristic (ROC) curve—Final Model (step 3).; Table S12: Area Under the Curve—Test Result Variable(s)—Predicted probability.

Author Contributions

Conceptualization, J.K.N. and A.L.; Formal analysis, J.K.N. and T.O.; Investigation, V.K.; Methodology, J.K.N. and A.L.; Project administration, A.L.; Supervision, A.L. and T.O.; Validation, J.K.N., A.L. and T.O.; Writing—original draft, J.K.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The ethical approval Autorisation N° 2014/036/UdM/PR/CAB/CIE was obtained on the 30 June 2014 from the Institutional Ethic Committee of the Université des Montagnes. Before data collection, written consent was obtained from the respondents. No participant was below the age of 16 at the time of the study.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

AICAkaike’s Information Criterion
BCGBacillus Calmatte Guiren
BICBayesian Information Criterion
CIConfidence Interval
dfDegree of freedom
DPTDiphtheria, Pertussis, Tetanus
EPIExpanded Program on Immunization
EXPExponential
HBMHealth Belief Model
MCVMeasles-Containing Vaccine
OPVOral Polio Vaccine
OROdds Ratio
PCVPneumococcal Conjugate Vaccine
PolioPoliomyelitis
REFReference
S.E.Standard Error
Sig.Significance level
SRSSimple random sample
USAUnited States of America
VAAVaccin Anti Amaril (yellow fever vaccine)
VARVaccin Anti Rougeoleux (measles vaccine)
VPDVaccine-preventable disease
WHOWorld Health Organization

References

  1. World Health Organization (WHO). Global Health Observatory Data Repository. Available online: https://apps.who.int/gho/data/node.home (accessed on 28 December 2021).
  2. World Health Organization. Immunization Agenda 2030: A Global Strategy to Leave No One Behind. Available online: https://www.who.int/teams/immunization-vaccines-and-biologicals/strategies/ia2030 (accessed on 18 December 2021).
  3. Cameroon Ministry of Public Health. Cameroun-Comprehensive multi-year plan for 2011–2015. 2011. Available online: https://extranet.who.int/countryplanningcycles/sites/default/files/planning_cycle_repository/central_african_republic/cmyp_car_2011-2015_en.pdf (accessed on 18 May 2011).
  4. Njeru, I.; Ajack, Y.; Muitherero, C.; Onyango, D.; Musyoka, J.; Onuekusi, I.; Kioko, J.; Muraguri, N.; Davis, R. Did the call for boycott by the catholic bishops affect the polio vaccination coverage in Kenya in 2015? A cross-sectional study. Pan Afr. Med. J. 2016, 24, 120. [Google Scholar] [CrossRef] [PubMed]
  5. Adepoju, P. As COVID-19 Vaccines Arrive in Africa, Omicron is Reducing Supply and Increasing Demand. Available online: https://www.nature.com/articles/d41591-021-00073-x (accessed on 13 December 2021).
  6. Dinga, J.N.; Kouemou, L. Assessment of vaccine hesitanc to a COVID-19 vaccine in Cameroonian adults and its global implication. Vaccines 2021, 9, 175. [Google Scholar] [CrossRef] [PubMed]
  7. 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, 194–203. [Google Scholar]
  8. Gore, P.; Madhavan, S.; Curry, D.; McClung, G.; Castiglia, M.; Rosenbluth, S.A.; Smego, R.A. Predictors of childhood immunization completion in a rural population. Soc. Sci. Med. 1999, 48, 1011–1027. [Google Scholar] [CrossRef]
  9. Tanne, J.H. Measles: Two US outbreaks are blamed on low vaccination rates. BMJ 2019, 364, l312. [Google Scholar] [CrossRef] [PubMed]
  10. Ngandjon, J.K.; Laengler, A.; Ostermann, T. Community-based Programs for Childhood Immunization and Prevention of Childhood Diseases: Sustainable Support in Mothers’ Decision-Making—A Health Belief Model Approach. Available online: https://assets.researchsquare.com/files/rs-89501/v1/3ef95e7d-c286-4d5f-9f0a-b4f4c82ee450.pdf?c=1631857859 (accessed on 13 October 2020).
  11. World Health Organization. Vaccination Coverage Cluster Survey Reference Manual—WHO/IVB/04.23; World Health Organization: Geneve, Switzerland, 2005. [Google Scholar]
  12. World Health Organization. The EPI Coverage Survey—WHO/IVB/08.07. Available online: https://www.who.int/immunization/documents/MLM_module7.pdf (accessed on 12 December 2021).
  13. SCHWARTZ, D. Méthodes Statistiques à L’usage des Médecins et Biologists. 1969. Available online: https://bdsp-ehesp.inist.fr/vibad/index.php?action=getRecordDetail&idt=85872 (accessed on 12 May 2021).
  14. Bennett, S.; Woods, T.; Liyanage, W.; Smith, D. A simplified general method for cluster sample surveys of health in developing countries. World Health Stat. Q. 1991, 44, 98–106. [Google Scholar]
  15. United Nations. Designing Household Survey Samples: Practical Guidelines; United Nations: New York, NY, USA, 2005. [Google Scholar]
  16. Giancristofaro, R.A.; Salmaso, L. Model Performance Analysis and Model Validation in logistic Regression. Statistica 2003, 63, 375–396. [Google Scholar]
  17. Cameroon DHS, 2018—Cameroon 2018 Demographic and Health Survey—Summary Report. Available online: https://dhsprogram.com/publications/publication-sr266-summary-reports-key-findings.cfm (accessed on 18 December 2018).
  18. Etana, B. Factors Affecting Immunization Status of Children Aged 12–23 Months in Ambo Woreda, West Shewa Zone of Oromia Regional State. Available online: http://213.55.95.56/handle/123456789/6843 (accessed on 15 May 2011).
  19. Streefland, P.H.; Chowdhury, A.M.; Ramos-Jimenez, P. Quality of vaccination services and social demand for vaccination in Africa and Asia. Bull. World Health Organ. 1999, 77, 722. [Google Scholar] [PubMed]
  20. Tandi, T.E.; Cho, Y.; Akam AJ, C.; Afoh, C.O.; Ryu, S.H.; Choi, M.S.; Kim, K.; Choi, J.W. Cameroon public health sector: Shortage and inequalities in geographic distribution of health personnel. Int. J. Equity Health 2015, 14, 1–12. [Google Scholar] [CrossRef]
  21. Gust, D.A.; Darling, N.; Kennedy, A.; Schwartz, B. Parents with doubts about vaccines: Which vaccines and reasons why. Pediatrics 2008, 122, 718–725. [Google Scholar] [CrossRef]
  22. Dinh, T.A.; Rosenthal, S.L.; Doan, E.D.; Trang, T.; Pham, V.H.; Tran, B.D.; Tran, V.D.; Phan, G.A.B.; Chu, H.K.H.; Breitkopf, C.R. Attitudes of mothers in Da Nang, Vietnam toward a human papillomavirus vaccine. J. Adolesc. Health 2007, 40, 559–563. [Google Scholar] [CrossRef] [PubMed]
  23. Odusanya, O.O. Age-Appropriate Immunization Coverage in a Rural community in Edo State, Nigeria. J. Niger. Infect. Control Assoc. 2000, 3, 9. [Google Scholar] [CrossRef]
  24. Kapp, C. Surge in polio spreads alarm in northern Nigeria. Rumours about vaccine safety in Muslim-run states threaten WHO’s eradication program. Lancet 2003, 362, 1631. [Google Scholar] [CrossRef]
  25. IRIN. NIGERIA: Muslim Suspicion of Polio Vaccine Lingers on. 2013. Available online: https://www.thenewhumanitarian.org/report/48667/nigeria-muslim-suspicion-polio-vaccine-lingers#:~:text=The%20success%20of%20the%20global,used%20for%20immunisation%20in%20Nigeria (accessed on 19 February 2004).
  26. Muslim Clerics Finally Embrace Polio Campaign; Retrieved; Associated Press: New York, NY, USA, 2015; Available online: https://www.nbcnews.com/health/health-news/muslim-clerics-finally-embrace-polio-campaign-flna1c9450705 (accessed on 22 March 2002).
  27. Warraich, H.J. Religious Opposition to Polio Vaccination. Emerg. Infect. Dis. 2009, 15, 978. [Google Scholar] [CrossRef]
  28. Nichter, M. Special issue on the Debate on Selective or Comprehensive Primary Health Care. Soc. Sci. Med. 1998, 26, 877–878. [Google Scholar]
  29. Suk, J.E.; Lopalco, P. Hesitancy, Trust and Individualism in Vaccination Decision-Making. Available online: https://www.researchgate.net/publication/291368600_Measuring_vaccine_confidence_Introducing_a_global_Vaccine_Confidence_Index (accessed on 20 February 2015).
  30. Larson, H.J.; Schulz, W.S.; Tucker, J.D.; Smith, D.M. Measuring Vaccine Confidence: Introducing a Global Vaccine Confidence Index. PLoS Curr. 2015, 7. [Google Scholar] [CrossRef] [PubMed]
  31. Ambe, J.P.; Omotara, B.A.; Baba, M.M. Perceptions, beliefs and practices of mothers in sub-urban and rural areas towards measles and measles vaccination in Northern Nigeria. Trop. Dr. 2001, 31, 89–90. [Google Scholar] [CrossRef] [PubMed]
  32. Langwick, S.A. Bodies, Politics, and African Healing: The Matter of Maladies in Tanzania; Indiana University Press: Bloomington, IN, USA, 2011. [Google Scholar]
  33. Mokgobi, M.G. Understanding traditional African healing. Afr. J. Phys. Health Educ. Recreat. Danc. 2014, 20, 24–34. [Google Scholar]
  34. Odusanya, O.O.; Alufohai, E.F.; Meurice, F.P.; Ahonkhai, V.I. The determinants of vaccination coverage in rural Nigeria. BMC Public Health 2008, 8, 1–8. [Google Scholar] [CrossRef] [PubMed]
  35. Stilwell, S. The Imposition of Colonial Rule. Colonial Africa. Available online: https://www.bartleby.com/essay/The-Imposition-of-Colonialism-on-Africa-FKBRT6SQGDSX#:~:text=The%20imposition%20of%20colonialism%20on%20Africa%20drastically%20reconstructed%20the%20continent,people%2C%20culture%2C%20and%20resources. (accessed on 25 December 2021).
  36. Bono, S.A.; Faria de Moura Villela, E.; Siau, C.S.; Chen, W.S.; Pengpid, S.; Hasan, M.T.; Sessou, P.; Ditekemena, J.D.; Amodan, B.O.; Hosseinipour, M.C.; et al. Factors affecting COVID-19 vaccine acceptance: An international survey among low- and middle-income countries. Vaccines 2021, 9, 515. [Google Scholar] [CrossRef]
  37. Osuagwu, U.L.; Miner, C.A.; Bhattarai, D.; Mashige, K.P.; Oloruntoba, R.; Abu, E.K.; Ekpenyong, B.; Chikasirimobi, T.G.; Goson, P.C.; Ovenseri-Ogbomo, G.O.; et al. Misinformation About COVID-19 in Sub-Saharan Africa: Evidence from a Cross-Sectional Survey. Health Secur. 2021, 19, 44–56. [Google Scholar] [CrossRef]
  38. Sessa, F.; Salerno, M.; Esposito, M.; Di Nunno, N.; Zamboni, P.; Pomara, C. Autopsy Findings and Causality Relationship between Death and COVID-19 Vaccination: A Systematic Review. J. Clin. Med. 2021, 10, 5876. [Google Scholar] [CrossRef] [PubMed]
  39. Abu, E.K.; Oloruntoba, R.; Osuagwu, U.L.; Bhattarai, D.; Miner, C.A.; Goson, P.C.; Langsi, R.; Nwaeze, O.; Chikasirimobi, T.G.; Ovenseri-Ogbomo, G.O.; et al. Risk perception of COVID-19 among sub-Sahara Africans: A web-based comparative survey of local and diaspora residents. BMC Public Health 2021, 21, 1–13. [Google Scholar] [CrossRef] [PubMed]
  40. Sturm, L.A.; Mays, R.M.; Zimet, G.D. Parental beliefs and decision-making about child and adolescent immunization. J. Dev. Behav. Pediatrics 2005, 26, 441–452. [Google Scholar] [CrossRef] [PubMed]
  41. Teitler-Regev, S. Factors Affecting Intention among Students to Be vaccinated against A/H1N1 Influenza: A Health Belief Model Approach. Adv. Prev. Med. 2011, 2011, 353207. [Google Scholar] [CrossRef] [PubMed]
  42. Streefland, P.; Chowdhury, A.M.R.; Ramos-Jimenez, P. Patterns of vaccination acceptance. Soc. Sci. Med. 1999, 49, 1705–1716. [Google Scholar] [CrossRef]
  43. Ndiaye, N.M.; Ndiaye, P.; Diédhiou, A.; Guèye, A.S.; Tal-Dia, A. Facteurs d’abandon de la vaccination des enfants âgés de 10 à 23 mois à Ndoulo au Sénégal en 2005. Cah. D’études Rech. Francoph./St. 2009, 19, 9–13. [Google Scholar]
  44. Onsomu, E.O.; Abuya, B.A.; Okech, I.N.; Moore, D.; Collins-McNeil, J. Maternal Education and Immunization Status Among Children in Kenya. Matern. Child Health J. 2015, 19, 1724–1733. [Google Scholar] [CrossRef] [PubMed]
  45. Abuya, B.A.; Onsomu, E.O.; Kimani, J.K.; Moore, D. Influence of Maternal Education on Child Immunization and Stunting in Kenya. Matern. Child Health J. 2011, 15, 1389–1399. [Google Scholar] [CrossRef] [PubMed]
  46. Benninghoff, B.; Pereira, P.; Vetter, V. Role of healthcare practitioners in rotavirus disease awareness and vaccination—insights from a survey among caregivers. Hum. Vaccines Immunother. 2020, 16, 138–147. [Google Scholar] [CrossRef]
  47. Kumar, S.; Preetha, G.S. Health Promotion: An Effective Tool for Global Health. Indian J. Community Med. Off. Publ. Indian Assoc. Prev. Soc. Med. 2012, 37, 5. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Proposed community-based conceptual framework of parental decision-making.
Figure 1. Proposed community-based conceptual framework of parental decision-making.
Ijerph 19 02721 g001
Table 1. The EPI vaccines coverage of children 12–23 months from this study compared to data for Cameroon from the Sociodemographic Health Survey (DHS) in 2018.
Table 1. The EPI vaccines coverage of children 12–23 months from this study compared to data for Cameroon from the Sociodemographic Health Survey (DHS) in 2018.
VaccinesCasePercentagePercentage
Present StudyPresent StudyCameroon
(n = 160)(n = 160)DHS (2018)
Case%%
BCG15898.887.1
DPT 11449083
DPT 213483.879
DPT 312578.172
OPV 114389.486
OPV 213483.880
OPV 312477.567
VAA (Yellow Fever)10163.169.3
VAR (Measles)10163.165
Not vaccinated21.2510
Completely vaccinated966052
Table 2. Given reasons by parents for missing the EPI (n = 64).
Table 2. Given reasons by parents for missing the EPI (n = 64).
Barriers in Vaccine Acceptance:CasesPercentage
Missing InformationIgnores the necessity for vaccination617.2%
Ignores the necessity of the 2nd and 3rd dose3
Fear of adverse effects2
No interestDiscouraged by the entourage317.2%
Does not trust vaccination8
Quality of vaccination servicesAbsence of the vaccination personnel165.6%
Vaccines not available4
Long waiting time3
No flexible time schedule34
Table 3. Sociodemographic characteristics of participants (n = 160) and their associations with complete childhood immunization.
Table 3. Sociodemographic characteristics of participants (n = 160) and their associations with complete childhood immunization.
Independent VariablesComplete Vaccination Bivariate Analysis
YesNoTotalOR (95% CI)p-Value
n = 96 (%)n = 64 (%)n = 160 (%)
Maternal Age<25Yes53 (60.9)34 (39.1)87 (54.4)1.09 (0.57–2.05)0.461
No43 (58.9)30 (41.1)73 (45.6)
25 to 34Yes33 (60)22 (40)55 (34.4)1 (0.51–1.94)0.566
No63 (60)42 (40)105 (65.6)
>34Yes10 (55.6)8 (44.4)18 (11.3)0.81 (0.30–2.18)0.434
No86 (60.6)56 (39.4)142 (88.8)
EducationNo formal educationYes0 (0)2 (100)2 (1.3)00.158
No96 (60.8)62 (39.2)158 (98.8)
PrimaryYes37 (54.4)31 (45.6)68 (42.5)0.67 (0.35–1.26)0.141
No59 (64.1)33 (35.9)92 (57.5)
SecondaryYes57 (64.8)31 (35.2)88 (55)1.55 (0.82–2.94)0.115
No39 (54.2)33 (45.8)72 (45)
UniversityYes2 (100)02(1.3) 0.36
No94 (59.5)64 (40.5)15 (98.8)
Child Birth order1stYes27 (67.5)13 (32.5)40 (25)1.53 (0.72–3.26)0.176
No69 (57.5)51 (42.5)120 (75)
2ndYes32 (68.1)15 (31.9)47 (29.4)1.63 (0.79–3.34)0.121
No64 (56.6)49 (43.4)113 (70.6)
3rdYes14 (50)14 (50)28 (17.5)0.61 (0.26–1.38)0.164
No82 (62.1)50 (37.9)132 (82.5)
>3Yes23 (51.1)22 (48.9)45 (28.1)0.6 (0.29–1.20)0.105
No73 (63.5)42 (36.5)115 (71.9)
Marital StatusSingleYes17 (81)4 (19)21 (13.1)3.23 (1.03–10.09)0.028
No79(56.8)60 (43.2)139 (86.9)
MarriedYes79 (57.2)59 (42.8)138 (86.3)0.393 (0.13–1.12)0.06
No17 (77.3)5 (22.7)22 (13.8)
WidowYes01 (100)1 (0.6)00.4
No96 (60.4)63 (39.6)159 (99.4)
DivorcedNo96 (60)64 (40)160 (100)
ReligionCatholicYes12 (75)4 (25)16 (10)2.14 (0.65–6.96)0.1533
No84 (58.3)60 (41.7)144 (90)
ProtestantYes24 (82.8)5 (17.2)29 (18.1)3.93 (1.41–10.94)0.004
No72 (55)59 (45)131 (81.9)
MuslimYes60 (52.2)55 (47.8)115 (71.9)0.27 (0.12–0.61)0.001
No36 (80)9 (20)45 (28.1)
AnimistNo96 (60)64 (40)160 (100)
OccupationsFormal sectorYes8 (66.7)4 (33.3)12 (7.5)1.36 (0.39–4.73)0.434
No88 (59.5)60 (40.5)148 (92.5)
Informal SectorYes88 (59.5)60 (40.5)148 (92.5)0.73 (0.21–2.54)0.434
No8 (66.7)4 (33.3)12 (7.5)
Reason for vaccinatingPrevent the occurrence of diseasesYes64 (58.7)45 (41.3)109 (68.1)0.84 (0.42–1.67)0.379
No32 (62.7)19 (37.3)51 (31.9)
Decrease the severity of diseasesYes1 (50)1 (50)2 (1.2)0.66 (0.04–10.79)0.641
No95 (60.1)63 (39.9)158 (98.8)
No ideaYes31 (63.3)18 (36.7)49 (30.6)1.2 (0.61–2.4)0.35
No65 (58.6)46 (41.4)111 (69.4)
Knowledge of VPD and communicable diseasesGood knowledgeYes88 (63.7)50 (36.2)138 (86.2)3.08 (1.21–7.85)0.01
No8 (36.3)14 (63.6)22 (13.8)
Poor knowledgeYes8 (36.4)14 (63.6)22 (13.8)0.32 (0.12–0.82)0.014
No88 (63.8)50 (36.2)138 (86.3)
Age-appropriate vaccinationAt BirthYes83 (64.3)46 (35.7)129 (80.6)2.5 (1.12–5.55)0.02
No13 (41.9)18 (58.1)31 (19.4)
No ideaYes11 (44)14 (56)25 (15.6)0.4 (0.19 + 1.09)0.06
No85 (63)50 (37)135 (84.3)
Other dateYes2 (33.3)4 (66.6)6 (3.7)0.32 (0.06–1.79)0.17
No94 (60)60 (40)154 (96.9)
Be aware of the vaccination scheduleBe awareYes29 (80.6)7 (19.4)36 (22.5)3.52 (1.43–8.65)0.002
No67 (54)57 (46)124 (77.5)
Retention of the vaccination bookletKeepYes88 (62)54 (38)142 (88.8)2.04 (0.76–5.48)0.121
No8 (44.4)10 (55.6)18 (11.3)
Table 4. Information criteria of multivariate logistic regression analysis of vaccination decision-making in parents with children between 12 to 23 months (n = 160).
Table 4. Information criteria of multivariate logistic regression analysis of vaccination decision-making in parents with children between 12 to 23 months (n = 160).
ModelActionEffect(s)Model Fitting CriteriaEffect Selection Tests
AICBIC−2 Log-LikelihoodChi-square adf.Sig.
Step 0EnteredConstant85.7088.7883.70.
Step 1EnteredReligion76.5882.7372.5811.1210.001
Step 2EnteredAge-appropriate vaccination 67.7476.9761.7410.8410.001
Step 3EnteredKnowledge of VPDs64.1676.4656.145.5810.018
Stepwise Method: Forward Selection. The Chi-Square for entry is based on the likelihood ratio test.
Table 5. Model fitting information of multivariate logistic regression analysis of vaccination decision-making in parents with children between 12 to 23 months (n = 160).
Table 5. Model fitting information of multivariate logistic regression analysis of vaccination decision-making in parents with children between 12 to 23 months (n = 160).
ModelModel Fitting CriteriaLikelihood-Ratio-TestsAUC
AICBIC−2 Log-LikelihoodChi-Squaredf.Sig.
Only Intercept85.7088.7883.70
Final64.1676.4656.1627.5430.00010.73
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Kemeugni Ngandjon, J.; Ostermann, T.; Kenmoue, V.; Laengler, A. Insights into Predictors of Vaccine Hesitancy and Promoting Factors in Childhood Immunization Programs—A Cross-Sectional Survey in Cameroon. Int. J. Environ. Res. Public Health 2022, 19, 2721. https://doi.org/10.3390/ijerph19052721

AMA Style

Kemeugni Ngandjon J, Ostermann T, Kenmoue V, Laengler A. Insights into Predictors of Vaccine Hesitancy and Promoting Factors in Childhood Immunization Programs—A Cross-Sectional Survey in Cameroon. International Journal of Environmental Research and Public Health. 2022; 19(5):2721. https://doi.org/10.3390/ijerph19052721

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Kemeugni Ngandjon, Jonas, Thomas Ostermann, Virgile Kenmoue, and Alfred Laengler. 2022. "Insights into Predictors of Vaccine Hesitancy and Promoting Factors in Childhood Immunization Programs—A Cross-Sectional Survey in Cameroon" International Journal of Environmental Research and Public Health 19, no. 5: 2721. https://doi.org/10.3390/ijerph19052721

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