Key issues in the persistence of poliomyelitis in Nigeria: a case-control study  Dr Tara D Mangal, PhD, R Bruce Aylward, MD, Michael Mwanza, BComm, Alex.

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Key issues in the persistence of poliomyelitis in Nigeria: a case-control study  Dr Tara D Mangal, PhD, R Bruce Aylward, MD, Michael Mwanza, BComm, Alex Gasasira, MBChB, Emmanuel Abanida, MBChB, Prof Muhammed A Pate, MD, Prof Nicholas C Grassly, PhD  The Lancet Global Health  Volume 2, Issue 2, Pages e90-e97 (February 2014) DOI: 10.1016/S2214-109X(13)70168-2 Copyright © 2014 Mangal et al. Open Access article distributed under the terms of CC BY-NC-SA Terms and Conditions

Figure 1 Effects of oral poliovirus vaccine use on poliomyelitis during 2001–12 (A) Monthly incidence of poliomyelitis associated with serotypes 1 and 3 wild poliovirus and cVDPV2. (B) Median estimated age-standardised vaccine-induced population immunity against poliomyelitis due to serotype 1, serotype 3, and cVDPV2 poliovirus on the basis of vaccination histories of children younger than 36 months with non-poliomyelitis AFP by year of onset of paralysis. Estimates not standardised to show geographic population distribution and therefore biased towards areas with a high incidence of non-poliomyelitis AFP. Bars=2·5th and 97·5th percentile intervals (95% CIs) based on bootstrap resampling. (C) Mean numbers of doses of OPV received by children younger than 36 months with non-poliomyelitis AFP, age-standardised to match underlying demography. Plot shows estimates under the assumption that all OPV doses were received via SIAs. Arrows depict timings of SIAs, with length of arrows proportional to number of local government areas that participated. AFP=acute flaccid paralysis. bOPV=bivalent oral poliovirus vaccine. cVDPV2=circulating vaccine-derived poliovirus type 2. mOPV= monovalent oral poliovirus vaccine. OPV=oral poliovirus vaccine. SIA=supplementary immunisation activity. tOPV=trivalent oral poliovirus vaccine. The Lancet Global Health 2014 2, e90-e97DOI: (10.1016/S2214-109X(13)70168-2) Copyright © 2014 Mangal et al. Open Access article distributed under the terms of CC BY-NC-SA Terms and Conditions

Figure 2 Serotype-specific vaccine-induced immunity by local government area in Nigeria and the spatial distribution of poliomyelitis cases during 2012 (A–C) Serotype-specific vaccine-induced immunity by LGA in Nigeria. LGAs with no shading had insufficient numbers of non-poliomyelitis AFP cases during 2012 to estimate population immunity. (D) Spatial distribution of poliomyelitis cases. Each poliomyelitis case is represented by one triangle, randomly placed within the LGA of residence. The 12 high-risk states published by the National Primary Health Care Development Agency of Nigeria are highlighted in green.6 AFP=acute flaccid paralysis. cVDPV2=circulating vaccine-derived poliovirus type 2. LGA=local government area. The Lancet Global Health 2014 2, e90-e97DOI: (10.1016/S2214-109X(13)70168-2) Copyright © 2014 Mangal et al. Open Access article distributed under the terms of CC BY-NC-SA Terms and Conditions

Figure 3 Reported reasons for missing oral poliovirus vaccine doses from routine and supplementary immunisation programmes between 2006 and 2012 Few data exist for routine immunisation during 2011 and so this year has been excluded. Data were obtained from the 60-day follow-up examinations and comprise only confirmed paralytic poliomyelitis cases. Numbers of observations are given above the bars (in the lower figure, reasons for children missing up to eight supplementary immunisation rounds are recorded). The Lancet Global Health 2014 2, e90-e97DOI: (10.1016/S2214-109X(13)70168-2) Copyright © 2014 Mangal et al. Open Access article distributed under the terms of CC BY-NC-SA Terms and Conditions