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AY,yTiG xsPhRN7V+M+Ȉ1-QV&Rb)d-֭ e#yJ#ž.!ju.JJ<3-@5Tȡzj%V] 'xQI8VɰQR)SRRRRRR,W4}bN(,kV(`  X eDocument Word.Document.80.Microsoft Word DocumentfDocument Word.Document.80.Microsoft Word DocumentTPicture Word.Picture.60,Microsoft Word PictureUPicture Word.Picture.60,Microsoft Word Picture,www.risk-modelling.com<http://www.risk-modelling.com/s_ Chart Excel.Chart.80*Microsoft Excel ChartvvDocument Word.Document.80.Microsoft Word DocumentywPicture Word.Picture.80,Microsoft Word Picturez Chart Excel.Chart.80*Microsoft Excel Chart{ Chart Excel.Chart.80*Microsoft Excel Chart} Chart Excel.Chart.80*Microsoft Excel Chart~ Chart Excel.Chart.80*Microsoft Excel Chart Chart Excel.Chart.80*Microsoft Excel Chart Chart Excel.Chart.80*Microsoft Excel Chart Chart Excel.Chart.80*Microsoft Excel Chart Chart Excel.Chart.80*Microsoft Excel Chart Chart Excel.Chart.80*Microsoft Excel Chart Chart Excel.Chart.80*Microsoft Excel Chart/0(  0;[0 0 000$([\{b00 000000000  0=] 0 0 0000 2 3 !A0C0E0G0I0c00000000000000000!%),.:;?]}acdeghijklmnop0DTimes New Roman0z[ 0DTahomaew Roman0z[ 0" DArialew Roman0z[ 0"0DSymbolew Roman0z[ 0@ .@  @@``  @n?" dd@  @@``  2   ##  $%& *+,-.12345 6 <=?@ABCDEFGHIJKMNOPQRTUt "$RűXӊ#2$] R|& 2$JwT"$Y;,&D"$qsIbZw ,2$@;m{)92$~-w,3/n2`?"$J=@~k q"$r})jkvNo{"$QSK*Mu#-"$$3Omq5:™ w"$Y"=Z"$v}?v2CS "$ M-UbX;\ $$"$g/`ȐRQ"$Z؃DBɷa$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$2$H$ۆKt= 0e0e A@A5%8c8c     ?1d0u0@Ty2 NP'p<'p@A)BCD|E?`^3@8  g4KdKd z[ 0ppp@ <4ddddL 0$:g4KdKd z[ 0Hp p ʚ;ʚ;<4!d!dL|- 08<4ddddL|- 08 0___PPT10 pp ___PPT9n {nqc)i?%@M?i.PNG  IHDR ex`PLTEƵֵƭƥ֭jhtRNS'4 5 cmPPJCmp0712Hs|IDATWUY Dq .11i # Ifp̄Šw.13,~'9;1Ք8|?UcN+ ͅYzsp~5O潦=M?$8xIENDB`nB)9K FEvPNG  IHDR [A0PLTEޥޜޜޔތތ֌քք{ss[ 7tRNS#] cmPPJCmp0712OmMIDATc pkJ> 2$0gM:3?[ڬ7I@i S@ gN1vIENDB` nX3WOj!7C- b tMicrobial risk assessment is a scientifically-based process consisting of four steps: Hazard Identification The identification of known or potential health affects associated with a particular agent; Exposure Assessment The qualitative and/or quantitative evaluation of the degree of intake likely to occur; Hazard Characterization The quantitative and/or qualitative evaluation of the nature of the adverse effects associated with biological, chemical and physical agents that may be present in food& For biological agents& a dose-response assessment should be performed if the data is available; Risk Characterization Integration of Hazard Identification, Hazard Characterization and Exposure Assessment into an estimation of the adverse effects likely to occur in a given population, including attendant uncertainties. W P" P PWcg3]cg3c+g)cg3cgcg3cg3cg3cg3Rc!gcc ; {OIE experience$%OIE produced guidelines for animal import risk assessments (for the management of disease spread) Now in its second edition Guidelines were offered as a way to help member (including developing) countries understand how to perform a r.a. First Ed. guidelines were used too literally, both by analysts and lawyers, and found to be often impractical or irrelevant to the risk question Lesson: keep guidelines non-specific, encourage understanding rather than prescribing a formulaic approach Popular interpretation of CODEX guidelines suffer similarly0&Zk3<:*(1) Risk analysis uses observations about what we know to make predictions about what we don t know. Risk analysis is a fundamentally science-based process that strives to reflect the realities of Nature in order to provide useful information for decisions about managing risks. Risk analysis seeks to inform, not to dictate, the complex and difficult choices among possible measures to mitigate risks...&3'3&3&&3&<&3 &`&3 &&3    &(2) Risk analysis seeks to integrate knowledge about the fundamental physical, biological, social, cultural, and economic processes that determine human, environmental, and technological responses to a diverse set of circumstances. Because decisions about risks are usually needed when knowledge is incomplete, risk analysts rely on informed judgment and on models reflecting plausible interpretations of the realities of Nature. We do this with a commitment to assess and disclose the basis of our judgments and the uncertainties in our knowledge. '&3&&3&&3&&34&z&3"  Current modelling, b  (Microbial QRA is a developing science We re making a lot of progress, but it is still in infancy Mostly producing  farm-to-fork Models the whole system but very poorly Not designed to model any decision question well Often relies on poor data, surrogates, and guesses Almost never is a decision question posed beforehand Assessors have probably over-sold QRA s usefulness Managers have expected too much&;H1&;+31  &d  , &F2F Achilles Heels, b Very little data available, system being modelled is hugely complex! Uncertainty, variability, inter-individual variablility Take too long to complete, too easy to make mistakes F2F considers only pathogen on the food source E.g. not E.coli produced during life of animal, appearing in water, vegetables, farmers exposure Predictive microbiology still unreliable Broth data doesn t translate well to food (usually overestimate, but some data  Tamplin, USDA  shows lag period can be shorter, e.g. E.coli in ground beef, Listeria in processed hams) Models often not based on physical/biological ideas, so we don t learn Attenuation may not be death, and ignores reactivation of bacteria D-R models inadequate Don t describe variability observed P(ill|dose, infected) = P(ill|infected)? Feeding trial data don t match epi data  can hugely underestimate the risk Little cost-benefit analysis effort made Including actions affecting several risk issues Requires enormous resources  impractical for many countriesEP8PdPbP)PDPPP)P0P=PE8db  )D)  0$$=((p   n    /         "   6Dutch observations on past QRA Havelaar, Jansen (2002):7 bThe lessons learnt from risk analysis experiences: Risk management has not always been an integral part of risk analysis so far; Risk managers should be trained to understand risk assessment, and risk assessors should be trained to explain their work; Available data are often of limited use for risk assessment and communication of data needs between risk assessors, food scientists and risk managers is a critical issue; The risk manager questions usually require rapid results, whereas (farm-to-fork) risk assessment projects require several years to complete. Solving this conflict requires open communication; Uncertainty is often large. \3 P"  3cPcc  FOur survey Internet based, voluntary participation, 39 valid responses>G  ;b   +Completion times of some farm-to-fork QRAs,,+cb"'  d9Salmonella dose-response Epi and feeding trial comparison:$!&   g$USDA-FSIS-FDA Salmonella EnteritidisP%c c c b $  Although the goal was to make the model comprehensive, it has some important limitations. It is a static model and does not incorporate possible changes in SE over time as either host, environment or agent factor change. For many variables, data were limited or nonexistent. Some obvious sources of contamination, such as food handlers, restaurant environment, or other possible sites of contamination on or in the egg (such as the yolk), were not included. And, as complex as the model is, it still represents a simplistic view of the entire farm-to-table continuum. Finally, the model does not yet separate our uncertainty from the inherent variability of the system. Much more work is needed to address this, and all other, limitations. @ Zc6cc  $USDA-FSIS-FDA Salmonella EnteritidisP%c c c b $  FDA Listeria risk assessment,c b .    Remedies: focusing on decisions>   b WConsider what is known about the risk problem, and data available immediately or within acceptable time frame Use epi data as much as possible Collect more epi data (e.g. Japan, Denmark) Consider what analysis could be done with this knowledge i.e. a risk-based reasoned argument for evaluating particular actions Estimate the possible magnitude of benefit for a risk action Note that it may not be possible to evaluate all actions Perform a cost-benefit analysis on these actions Perform a Value of Information analysis Determines whether it is worth collecting more data before making a decision Consider strategy to validate whether predicted improvement occurs Train data producers to supply maximally useful data E.g. microbiologists taken more than one cfu from a plate More inter-agency unity E.g. Farm (APHIS) Slaughter (FSIS) Retail (FDA)RnPMP9PFP=P:PYPNPxP:PP6PnM9F  =:YNx  :$$((,,,,,,,,,,Zr  '  Z  \ &Make it as simple as possible: example,'& b Risk: Human illness from SE in eggs A shell-egg selection system proposed that will reduce by 30% the number of contaminated eggs going to market Currently, 30,000 people a year suffer from SE from eggs What will be the reduction in cases if the new system is implemented? ,E3  h3An example of the way forward Havelaar, Jansen 2002P4 c cb6    Campylobacter Risk Management and Assessment Dutch proposal The main objectives of the project are to advise on the effectiveness and efficiency of measures aimed at reducing campylobacteriosis in the Dutch population. The two key questions are: What are the most important routes (quantifiable?)? Which (sets of) measures can be taken to reduce the exposure to Campylobacter, what is their expected efficiency and societal support?<  " ;g3g(3cc c  j.The way forward  cont., b [The target of the assessment is not limited to estimating the possible reduction in disease incidence but to evaluate both costs and benefits of possible interventions and to access their acceptance by stakeholders. Interventions with low social support will require more effort to uphold, which increases their costs and reduces their efficacy. \ \c \ >Danish Vet Service Salmonella QRA  A Bayesian Approach to Quantify the Contribution of Animal-food Sources to Human Salmonellosis - Hald, Vose, Koupeev (2002)L!ccccHW +   z7Fluoroquinolone-resistant Campylobacter risk assessment*8   7 xyReviewing a risk assessment$Risk assessment should be decision focused It is not appropriate to review a risk assessment independently from the question(s) the assessment is addressing Eg because a point is moot if the decision is insensitive to the argument It uses science but is not itself scientific research So we have to go with the best we ve got J6)J3),t  References a  /lmoq    P ` TTrff` TTrh-[ʬ` 333MMM` TTr8r-[ffV>` TTrQ[-[` TTrTz<7FӥaG|` TTr4eXQƄΗ|aHb>?" dd@,? 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