|Year : 2015 | Volume
| Issue : 1 | Page : 27-29
Assessing the impact of polio eradication initiative and routine immunization in Zamfara State, North-West, Nigeria
KM Yusuf1, ED Jatau2, OS Olonitola2, SE Yakubu2, BS Ahmed2, ZA Gaiya2, AE Yahaya3, YY Pala4
1 Department of Disease Control and Immunization, National Primary Health Care Development Agency, Garki, Abuja, Nigeria
2 Department of Microbiology, Ahmadu Bello University, Zaria, Kaduna, Nigeria
3 Department of Mathematics and Statistics, Hassan Usman Katsina Polytechnic, Katsina, Nigeria
4 Veterinary Teaching Hospital, Ahmadu Bello University, Zaria, Kaduna, Nigeria
|Date of Web Publication||10-Dec-2015|
K M Yusuf
National Primary Health Care Development Agency. Plot 681/682, Port Harcourt Crescent off Gimbiya Street Area 11, Garki, Abuja
Source of Support: None, Conflict of Interest: None
Background: Evaluation of effectiveness of polio immunization has to be monitored continuously, particularly in endemic countries so that the immunity status can be precisely and effectively established. The aim of the present study was to determine the seroprevalence of poliovirus antibody in Zamfara State, Nigeria. Materials and Methods: This was a cross-sectional study of children aged 0–59 months. The children were randomly selected across the state. Blood samples collected from the children were tested for the presence of antibodies to poliovirus. Results: Blood samples from 63 (78.8%) of the 80 children had antibodies to all the three poliovirus serotypes. Seventy-five (93.8%), 68 (85.0%), and 75 (93.8%) of blood samples had antibodies to poliovirus serotypes 1, 2, and 3 respectively. All (100.0%) blood samples from children in the age group of 48–59 months tested positive for poliovirus. All (100.0%) the females had poliovirus antibody. In general, poliovirus antibody prevalence increased with increase in oral polio vaccine doses received. Urban children had higher poliovirus antibody prevalence of 81.0%, higher than their rural counterpart. Children whose fathers were educated up to tertiary level had 100.0% poliovirus antibody. There was no association among seroprevalence of poliovirus antibody and number of vaccine doses received and location of child's place of residence. Prevalence of poliovirus antibody was statistically significant based on age and father's educational level (χ = 0.1360, χ = 0.2923, respectively, P < 0.05). Conclusion: For the state to sustain the gains made in interrupting poliovirus transmission, more work need to be done so as to close the gap observed in the study.
Keywords: Antibodies, children, prevalence, Zamfara State
|How to cite this article:|
Yusuf K M, Jatau E D, Olonitola O S, Yakubu S E, Ahmed B S, Gaiya Z A, Yahaya A E, Pala Y Y. Assessing the impact of polio eradication initiative and routine immunization in Zamfara State, North-West, Nigeria. Niger J Health Sci 2015;15:27-9
|How to cite this URL:|
Yusuf K M, Jatau E D, Olonitola O S, Yakubu S E, Ahmed B S, Gaiya Z A, Yahaya A E, Pala Y Y. Assessing the impact of polio eradication initiative and routine immunization in Zamfara State, North-West, Nigeria. Niger J Health Sci [serial online] 2015 [cited 2022 Jan 16];15:27-9. Available from: https://www.chs-journal.com/text.asp?2015/15/1/27/171383
| Introduction|| |
The world has witnessed a remarkable reduction in paralytic poliomyelitis cases from 350,000 in more than 125 countries in 1988 to around 247 cases in 10 countries as on October 2014. The worldwide sustained use of polio vaccines since 1988 has led to a precipitous reduction in the number of cases of poliomyelitis by more than 99% globally. The cornerstone of the global polio eradication initiative is the immunization of children with multiple doses of oral poliovirus vaccine (OPV), through both routine immunization (RI) and supplementary immunization activities (SIAs). The key advantages in the usage of OPV are ease of administration and efficient induction of mucosal immunity, thereby limiting poliovirus shedding and person-to-person transmission poliovirus. With the use of OPV coupled with good surveillance, indigenous wild poliovirus (WPV) transmission has stopped in all but three countries. These are Nigeria, Pakistan, and Afghanistan.,
For many years, Nigeria had a high incidence of WPV cases due to the persistently low quality of both routine and SIAs, particularly in the Northern States of Nigeria. This had resulted in a major reservoir for WPV in some of the states in the Northern region., Low trivalent OPV coverage in the RI program, suspension of SIAs in some states in 2003–2004, and low coverage in SIAs had contributed to ongoing transmission of WPV. Reported cases of WPV in Nigeria, however, decreased from 798 in 2008 to 6 in 2014, representing 48% and 2% of global cases, respectively. The incidence of WPV cases in Nigeria had once reached an all-time low during January–June 2010 period, with only three reported cases of WPV accounting for <1% of 456 global cases. Despite substantial progress toward national eradication of polio, several challenges still remain.
Factors which contributed to suboptimal vaccination coverage in areas with on-going poliovirus circulation are varied. The most important ones include (a) poor political commitment and accountability, (b) poor quality micro-planning, (c) sub-optimal motivation of vaccination teams and supervisors as well as (d) low uptake of vaccination services in hard-to-reach and security compromised areas.
Since it is not all OPV recipients seroconvert, it is recommended and advised for any country where a comprehensive program to vaccinate children against polioviruses was being undertaken that from time to time, laboratory studies aimed at determining the immune status to polioviruses of eligible children or even the entire population has to be assessed.
| Materials and Methods|| |
This was a cross-sectional study, carried out between 3 March, 2012 and 27 June, 2012. Children aged 0–59 months were randomly selected in Zamfara State, Northern Nigeria. Children of mothers attending health facilities (HFs) across the state were enrolled where possible. The State Ethical Committee gave approval for the study. In addition, consent was sought and obtained from each caregiver before enrolling the child. Only children whose caregivers gave consents were enrolled for the study. Questionnaire was administered to capture all relevant information and bio-data of each participant. The estimated sample size for the study was 80 children.
About 5 ml of blood sample was collected from each child into a labeled plain tube. The tubes were transported to the laboratory in cold boxes in which ice-packs were placed to preserve the samples. Each tube with its content was centrifuged at 3000 revolutions/min for 5 min. Serum from the centrifuged sample was collected in another labeled tube and processed immediately or stored at −20°C, until analyzed on a later date.
The polio ELISA test kit (manufactured by antibodies-online GmbH) was used for the detection of specific antibodies against specific poliovirus in the sera.
Data were analyzed using Epi Info version 3.5.4 (Centers for Disease Control and Prevention, Atlanta, GA 30333, USA). Measure of independence and association was tested using Chi-square (χ2) test and linear regression, respectively. Statistically, significant level was set at P < 0.05.
| Discussion|| |
The relatively high prevalence of 78.8% antibodies to all the poliovirus serotypes observed in the present study compared to another study conducted by Adewumi et al. in the country, might be as a result of improved access to immunization services across the country by successive governments through constructing HFs that are effectively offering RI services. On the other hand, the seronegative rate 17.2% for all the poliovirus serotypes in the children sample was quite high, when compared with some studies conducted in Europe, where for example, not a single individual was reported as being seronegative. The highest seronegative rate of about 15.0% was observed for antibodies to poliovirus serotype 2. These relatively high seronegative rates may account for the pockets of polio being observed in parts of Northern Nigeria.
The age group with the highest prevalence of poliovirus antibodies was 48–59 months. Prevalence of poliovirus antibodies was found to be age-dependent. This might be as a consequence of antibody boosting through campaigns and probable exposure to the WPV through unsanitary habits. The findings in the present study agreed closely with that of Adewumi et al. Seropositivity was related to age except for 12–23 months age bracket. Moreover, the number of doses taken by a child had a direct bearing on the prevalence of poliovirus antibodies as in other studies. It was observed that the higher the number of doses of vaccine a child received, the higher the prevalence of poliovirus antibody. The much higher seronegative rates in age groups before 36 months means the younger children in the population surveyed were at a greater risk of infection with WPV. More effort must be made to increase vaccination in these age groups.
The reason for the higher prevalence of poliovirus antibodies in females when compared with their males counterpart, despite the fact that there was no special preference was given to either sex by the program implementers, is not clear. A previous study indicated there a complete absence of association between the sexes and prevalence of poliovirus antibodies.
Urban children were found to have higher poliovirus antibody prevalence than their rural counterparts. This was possibly due to close proximity of urban children to HFs rendering RI, which enabled mothers to take their children for services. On the other hand, outreach services might have helped to reach greater number of children in the rural areas, which may partly explain the association between and prevalence of poliovirus antibodies. These contrasting findings would probably explain why the difference in prevalence between the two areas was not statistically significant. The finding demonstrated that parents in both urban and rural areas had almost equal chance of accessing immunization services.
Children of fathers with a higher level of formal education had a higher prevalence of poliovirus antibody levels than those whose fathers' had lower levels of formal education. Level of awareness could have played a significant role, as most of the messages relating to immunization were broadcasted in English, with few translated into the local languages. From the result, it could be inferred that education had certainly helped in dispelling rumors and other negative things affecting OPV vaccine acceptance. This research underscores the fact that, the more knowledgeable the parents, the more the percentage positivity. More broadcast in the local language may, however, have a positive effect on the less educated parents.
It was surprising that those children whose parents live close to HFs rendering immunization services had a lower prevalence of poliovirus antibodies. The numbers involved were rather small for a valid conclusion. This observation might be purely behavioral, as such only mass education and awareness sensitization may possibly and positively change the parent's attitude toward vaccinating their children. Benefits of short distance from child's household to immunization point have been fully studied in Bangladesh, Nepal, and China.,, Bishai et al. reported that outreach services offered to clients by health workers in rural areas, who were far away from HFs rendering RI services, had reduced access problems among poor rural clients. The finding in the present study in this regard was in agreement with their finding. It was possible that those who were very close to the immunization sites took the services for granted, or possibly were not well sensitized as to see the reason for taking their children for immunization services, while more of those far away from HFs for RI were reached through outreach services by the immunization personnel or were more sensitized on the need to vaccinate their children.
The gaps observed in the prevalence of poliovirus antibody in the present study among the variables were of great concern. These might be as a result of not reaching all eligible children or other factors related to the vaccine usage and availability. Effects of lower immunogenicity of OPV had been documented in developing countries. This could as well be an important factor. That was why Anderson  advised for a high OPV vaccination coverage needed to block the transmission of poliovirus.
Serological studies are useful in defining the regions of suboptimal immunity, to enable special targeted vaccination campaigns to be mounted so as to close any noticeable gap. The results obtained in the present study were in agreement with the findings of other workers.
We acknowledge that more samples should have been taken if not for financial limitation faced in the present study. More samples would provide basis for more meaningful interpretation of results. Therefore, further studies in this and neighboring states are recommended involving larger samples to comprehensively evaluate the progress made so far, not only for polio eradication, but also for all vaccine-preventable diseases.
| Conclusion|| |
Identification of some children without detectable poliovirus antibodies in their sera, particularly in children younger than 36 months means that pockets of susceptible children were present within the population surveyed. Therefore, all efforts should be directed toward increase in vaccination coverage, so as to reduce the number of unvaccinated children in an effort to totally eradicate polio in the area.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
CDC. Progress towards poliomyelitis eradication – Nigeria, January 2009-July 2010. Morb Mortal Wkly Rep 2010;59:802-7.
Sutter RW, Kew OM, Cochi SL. Poliovirus vaccine – Live. In: Plotkin SA, Orenstein WA, Offit PA, editors. Vaccines. 5th
ed. Philadelphia: W.B. Saunders Company; 2008. p. 631-85.
Esteves K. Safety of oral poliomyelitis vaccine: Results of a WHO enquiry. Bull World Health Organ 1988;66:739-46.
Centers for Disease Control and Prevention (CDC). Progress toward interruption of wild poliovirus transmission – Worldwide, 2009. MMWR Morb Mortal Wkly Rep 2010;59:545-50.
Jenkins HE, Aylward RB, Gasasira A, Donnelly CA, Abanida EA, Koleosho-Adelekan T, et al.
Effectiveness of immunization against paralytic poliomyelitis in Nigeria. N Engl J Med 2008;359:1666-74.
Centers for Disease Control and Prevention (CDC). Progress toward interruption of wild poliovirus transmission – Worldwide, January 2005-March 2006. MMWR Morb Mortal Wkly Rep 2006;55:458-62.
WHO. Weekly Epidemiological Record. Geneva: WHO; 2009. p. 133-450.
Atkinson W, Hamborsky J, McIntyre L, Wolfe S. "Poliomyelitis" (PDF). Epidemiology and Prevention of Vaccine-Preventable Diseases. The Pink Book. 10th
ed. Washington, DC: Public Health Foundation; 2007. p. 101-14.
Pacsa AS, Al-Mufti S, El-Shazly A. Poliomyelitis: Immune status of the population of Kuwait. Med Princ Pract 1994;4:213-9.
Adewumi MO, Donbraye E, Odaibo GN, Bakarey AS, Opaleye OO, Olaleye DO. Neutralizing antibodies against poliovirus serotypes among children in southwest Nigeria. J Trop Pediatr 2006;52:92-5.
Affanni P, Veronesi L, Rizziero S, Bizzoco S, Bracchi MT, Tanzi ML. Status of immunity against poliomyelitis: A study among European and extra-European young immigrants living in Parma. Acta Biomed 2005;76:157-63.
Nishio O, Ishihara Y, Sakae K, Nonomura Y, Kuno A, Yasukawa S, et al.
The trend of acquired immunity with live poliovirus vaccine and the effect of revaccination: Follow-up of vaccinees for ten years. J Biol Stand 1984;12:1-10.
Chen RT, Hausinger S, Dajani AS, Hanfling M, Baughman AL, Pallansch MA, et al.
Seroprevalence of antibody against poliovirus in inner-city preschool children. Implications for vaccination policy in the United States. JAMA 1996;275:1639-45.
Jamil K, Bhuiya A, Streatfield K, Chakrabarty N. The immunization programme in Bangladesh: Impressive gains in coverage, but gaps remain. Health Policy Plan 1999;14:49-58.
Acharya LB, Cleland J. Maternal and child health services in rural Nepal: Does access or quality matter more? Health Policy Plan 2000;15:223-9.
Cui FQ, Gofin R. Immunization coverage and its determinants in children aged 12-23 months in Gansu, China. Vaccine 2007;25:664-71.
Bishai D, Suzuki E, McQuestion M, Chakraborty J, Koenig M. The role of public health programmes in reducing socioeconomic inequities in childhood immunization coverage. Health Policy Plan 2002;17:412-9.
Sutter RW, Suleiman AJ, Malankar P, Al-Khusaiby S, Mehta F, Clements GB, et al.
Trial of a supplemental dose of four poliovirus vaccines. N Engl J Med 2000;343:767-73.
Anderson RM. The concept of herd immunity and the design of community-based immunization programmes. Vaccine 1992;10:928-35.
Patriarca PA, Wright PF, John TJ. Factors affecting the immunogenicity of oral poliovirus vaccine in developing countries: Review. Rev Infect Dis 1991;13:926-39.