Authors

D. A. Kalkowska; R. J. D. Tebbens; M. A. Pallansch; S. L. Cochi; S. G. F. Wassilak;K. M. Thompson

Comments

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Abbreviated Journal Title

BMC Infect. Dis.

Keywords

Disease outbreaks; Disease transmission; Models; Statistical; Poliomyelitis; Poliovirus; Surveillance; Risk assessment; Vaccination; AFFECTING DETECTION SENSITIVITY; DETECTING WILD POLIOVIRUS; ACUTE; FLACCID PARALYSIS; THEORETICAL FRAMEWORK; GLOBAL ERADICATION; POLICY; OPTIONS; POLIOMYELITIS; EPIDEMIOLOGY; CAMPAIGN; IMMUNITY; Infectious Diseases

Abstract

Background: Most poliovirus infections occur with no symptoms and this leads to the possibility of silent circulation, which complicates the confirmation of global goals to permanently end poliovirus transmission. Previous simple models based on hypothetical populations assumed perfect detection of symptomatic cases and suggested the need to observe no paralytic cases from wild polioviruses (WPVs) for approximately 3-4 years to achieve 95% confidence about eradication, but the complexities in real populations and the imperfect nature of surveillance require consideration. Methods: We revisit the probability of undetected poliovirus circulation using a more comprehensive model that reflects the conditions in a number of places with different characteristics related to WPV transmission, and we model the actual environmental WPV detection that occurred in Israel in 2013. We consider the analogous potential for undetected transmission of circulating vaccine-derived polioviruses. The model explicitly accounts for the impact of different vaccination activities before and after the last detected case of paralytic polio, different levels of surveillance, variability in transmissibility and neurovirulence among serotypes, and the possibility of asymptomatic participation in transmission by previously-vaccinated or infected individuals. Results: We find that prolonged circulation in the absence of cases and thus undetectable by case-based surveillance may occur if vaccination keeps population immunity close to but not over the threshold required for the interruption of transmission, as may occur in northwestern Nigeria for serotype 2 circulating vaccine-derived poliovirus in the event of insufficient tOPV use. Participation of IPV-vaccinated individuals in asymptomatic fecal-oral transmission may also contribute to extended transmission undetectable by case-based surveillance, as occurred in Israel. We also find that gaps or quality issues in surveillance could significantly reduce confidence about actual disruption. Maintaining high population immunity and high-quality surveillance for several years after the last detected polio cases will remain critical elements of the polio end game. Conclusions: Countries will need to maintain vigilance in their surveillance for polioviruses and recognize that their risks of undetected circulation may differ as a function of their efforts to manage population immunity and to identify cases or circulating live polioviruses.

Journal Title

Bmc Infectious Diseases

Volume

15

Publication Date

1-1-2015

Document Type

Article

Language

English

First Page

12

WOS Identifier

WOS:000350064500001

ISSN

1471-2334

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