Publications by authors named "V I Smolenskiĭ"

The system of indication ofbiological pathogens that exists in our country allows to implement efficacious monitoring of epidemiologic situation, timely detect causative agents of infectious and parasitic diseases in material from humans and environmental samples, conduct their detailed identification and take appropriate means to ensure biosafety of the Russian Federation.

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An approach to increase effectiveness of epidemiological control of Crimean hemorrhagic fever, West Nile fever and Astrakhan spotted fever by building a prognostic model of epidemic activity based on contemporary information technologies of spatial and intellectual data analysis was developed and tested. Personified data on 4505 laboratory confirmed cases of natural-focal infectious diseases registered in the Russian Federation and database on 1999 - 2011 climatic observations were processed. A model implementing prognosis of epidemiological situation intensity level as a function of a combination of factors, maps of density of epidemic manifestations were built.

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In accordance with the established conceptual base for the up-to-date broad interpretation of biological safety, and IHR (2005), developed is the notional, terminological, and definitive framework, comprising 33 elements. Key item of the nomenclature is the biological safety that is identified as population safety (individual, social, national) from direct and (or) human environment mediated (occupational, socio-economic, geopolitical infrastructures, ecological system) exposures to hazardous biological factors. Ultimate objective of the biological safety provision is to prevent and liquidate aftermaths of emergency situations of biological character either of natural or human origin (anthropogenic) arising from direct and indirect impact of the biological threats to the public health compatible with national and international security hazard.

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Up to date there is a narrow and broad interpretation of the term biological safety (BS) the world over. In the narrow sense it is defined as availability of international regulations applied to diagnostic, manufacturing, or experimental works with pathogenic biological agents (PBA) in accordance with specified levels of biological hazard and BS. In a broader context it has no national, conceptual, terminological or defying basis.

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