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Evaluation of real time methods for epidemic forecasting 4

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Chapter 4Discussion In this study, we aimed to model the inuenza A-H1N12009 epidemic in Singapore and to be able to perform predictions of number of individuals presenting ILIs per GP us

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Chapter 4

Discussion

In this study, we aimed to model the inuenza A-H1N1(2009) epidemic in Singapore and to be able to perform predictions of number of individuals presenting ILIs per GP using presently available data The results in Section 3.1 illustrate that the three models and methods that we proposed can be used for predictive purposes Of these, tting the stochastic SIR model using particle lter performed the best in terms of the prediction, as shown when superimposed with the daily observed data (Figure 3.7)

The predictions from the deterministic SIR model using MCMC together with importance sampling is satisfactory (Figure 3.5), as the model captures the general underlying dynamics of the disease, although the number of fected individuals is underestimated at the peak of the pandemic The in-accuracy in the estimated infected individuals might stem from the proposal distribution we used in the importance sampling algorithm, as the algorithm requires a proposal distribution which is close to the posterior distribution

to return good estimates (Christian and Casella, 2001) However, it should

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be noted that by running short MCMC chains to obtain a rough estimate

of the location and scale of the posterior distribution of the parameters of the deterministic SIR model, and then using these to build a multivariate normal proposal distribution for importance sampling, the prediction results are improved compared to performing only importance sampling

We observed that importance sampler on the Richards model (Figure 3.3) does not perform as well as the deterministic SIR and stochastic SIR models, for instance, the weekly peaks in the observed data at the end of the surveillance period is not captured in the predictions This shows that the Richards model proposed in this study might not be as representative of the disease dynamics as the SIR model We postulate this failure is because

it is not compartmental in nature Instead of dividing the population into dierent compartments throughout the pandemic and having several proba-bilities to govern the transitions between compartments, the Richards model has only key epidemiological parameters to describe the overall trend for the pandemic (Hsieh et al., 2010)

The scatterplot (Figure 3.6) shows that the weights associated with the parameters are generally well distributed, indicating that the algorithm worked well without weight degeneracy at the end of the iterations The scatter-plots for the Richards model (Figure 3.2) and the deterministic SIR model (Figure 3.4) also show that the importance sampling algorithms return well distributed weights for the parameters

From Section 3.2, we have chosen some commonly used functions of the

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71 estimator to compare how well the predictions fare across dierent data sub-sets used to perform the predictions and also across dierent models The result in Figure 3.11 shows that in most cases, the stochastic SIR model performs consistently the best as the absolute values it takes for most of the calculated functions are the lowest among the three models, with the exception of prediction using days 17 This result agrees with the graphical output from Section 3.1 which shows that particle lter on stochastic SIR model performs the best in generating predictions for the disease

Furthermore, from Figure 3.11 we can also see that, mostly, the absolute values for the ME, MAE, and MSE decrease as the number of days used for prediction grows Data subsets with larger number of days used for prediction perform better than data subset of shorter period because more information

is incorporated in the algorithm to produce more accurate predictions for the future

In Section 3.3, we compare the Richards model output generated using informative priors (Figure 3.3) with that generated using non-informative priors (Figure 3.12) and observe that apart from the underestimation at the

rst peak on the last week of June 2009, the output from non-informative priors actually performs very well Since the amount of information the priors carry does not aect the predictive performance of the Richards model, non-informative priors should be used in future epidemics with similar information content to permit accurate prediction

For the deterministic SIR model, informative priors (Figure 3.5) and

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non-informative priors (Figure 3.13) return similar results, possibly because the data play a bigger part in providing information for the algorithm to produce the posterior distribution For the stochastic SIR model, informative priors (Figure 3.7) perform much better than non-informative priors (Figure 3.14) The output from non-informative priors show an overestimation at the rst peak on the last week of June 2009, but is gradually corrected by mid July, however, the peak at the end of July is not captured Therefore, the informa-tive priors, which are constructed with input from previous study or expert opinion, is important in generating good predictions for the stochastic SIR model

We acknowledge that although the SIR model is adequate in explaining the disease dynamics in this context, other models, for instance, models which account for spatial spread (Mollison and Kuulasmaa, 1985), age-structure (Schenzle, 1984) or herd immunity (Starr et al., 1997), might provide more details on the evolution of the disease The assumptions imposed on the models, for example, homogeneous mixing between infected individuals and susceptible individuals, might not be an exact and realistic description of the disease dynamics in real life (Burr and Chowell, 2006) Nevertheless, the simple SIR model provides insights on how the dierent factors interact in the pandemic and forms a basis on which more assumptions details can be added to provide more sophisticated results and predictions

The dataset used in this study was obtained from a network of general practitioners or family doctors who submitted observations of ARIs among

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73 their patients on a voluntary basis, and therefore the data might not be representative of the actual numbers of infected individuals in the whole population of Singapore However, the simple surveillance system serves its intended purpose in disease tracking and forecasting in real-time (Ong et al., 2010), and estimates for the local outbreak size in terms of percentage of infected in the population from the deterministic model has a 95% credible interval of (5%, 20%) and that of the stochastic model has a 95% credi-ble interval of (7%, 21%), are consistent with estimates from independent serological studies (Chen et al., 2010; Lee et al., 2011)

Other limitations include the fact that we cannot fully account for the nature of patients in our study Studies (Hancock et al., 2009; Chi et al., 2010) show that the elderly are less susceptible to an epidemic because of pre-existing cross-reactive antibodies, however, we do not have access to past serological information to be incorporated into the predictions It might be more appropriate to incorporate age-structure in the models for this reason,

so that we can have more insight into the dierent eect of the pandemic on individuals in dierent age groups

We conclude from this study that stochastic SIR model with particle

lter is the most eective among our models and can be extended to per-form predictions for future pandemic outbreaks or other similar diseases in real-time Model selection and averaging can also be done within the frame-work of particle lter by including model as an element of the parameter set (Doucet et al., 2000) The deterministic SIR model performs well but

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requires more computational time compared to stochastic SIR model Al-though the Richards model does not return better predictions compared to compartmental models in our study, a two-phased Richards model which dis-tinguishes the turning point at the end of exponential growth and the turning point where the cumulative cases increases again has been shown to perform better than the simple Richards model (Hsieh et al., 2010) when applied to inuenza A-H1N1(2009) observations in Canada, and hence might be the topic of future investigations in the local setting

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Abramson J.S., 2011 The Pandemic is Declared: The First Wave Continues

to Spread Globally (June through Mid-August 2009) In: Inside the 2009 Inuenza Pandemic World Scientic Pub Co Inc, pp81

Ackerberg D.A., 2009 A new use of importance sampling to reduce compu-tational burden in simulation estimation Quant Mark Econ 7:343376 Alkema L., Raftery A.E., and Brown T., 2008 Bayesian melding for estimat-ing uncertainty in national HIV prevalence estimates Sexually transmitted infections 84(Suppl I):1116

Althaus C.L., Heijne J.C.M., Roellin A., and Low N., 2010 Transmission dy-namics of Chlamydia trachomatis aect the impact of screening programmes Epidemics 2(3):123131

Anderson R.M., May R.M., 1991 Infectious diseases of humans: Dynamics and contol Oxford: Oxford University Press pp757

Aparicio J.P and Pascual M., 2006 Building epidemiological models from R0: an implicit treatment of transmission in networks Proceedings of Royal Society Biological Sciences 274(1609):505512

Arulampalam M.S., Maskell S., Gordon N and Clapp T., 2002 A tutorial

on particle lters for online nonlinear/non-Gaussian Bayesian tracking Signal processing IEEE 50(2):174188

75

Trang 8

Beissinger S.R., Westphal M.I., On the Use of Demographic Models of Popu-lation Viability in Endangered Species Management The Journal of Wildlife Management 62(3):821841

Bolstad, W.M., 2010 Understanding Computational Bayesian statistics Wi-ley series in computational statistics, NJ, USA

Bouma A., Jong M.C.M., Kimman T.G., 1995 Transmission of pseudorabies virus within pig populations is independent of the size of the population Preventive Veterinary Medicine 23: 163172

Brauer F., Driessche P.V., Wu J., Allen L.J.S., 2008 Notes in Mathematical Epidemiology Springer, Berlin pp2122

Burr T.L., Chowell G., 2006 Observation and model error eects on param-eter estimates in susceptible-infected-recovered epidemic model Far East J Theor Stat 19(2): 163183

Bustad A., Terziivanov D., Leary R., Port R., Schumitzky A and Jellie R.,

2006 Parametric and nonparametric population methods: their comparative performance in analysing a clinical dataset and two Monte Carlo simulation studies Clinical Pharmacokinetics 45(8):851852

Carassco L.R., Lee V.J., Chen M.I., Matchar D.B., Thompson J.P., Cook A.R., 2011 Strategies for antiviral stockpiling for future inuenza pan-demics: a global epidemic-economic perspective J Roy Soc Interface 8(62): 13071313

Carlin B.P., and Louis T.A., 2000 Bayes and Empirical Bayes Methods for Data Analysis Second edition Chapman and Hall, New York pp129

Trang 9

77 Centers for Disease Control and Prevention (CDC), 2009 Outbreak of

Swine-Origin Inuenza A (H1N1) Virus Infection  Mexico, MarchApril 2009

Online Morbidity and Mortality Weekly Report, USA

Available from: http://www.cdc.gov/mmwr/preview/mmwrhtml/mm58d0430a2.htm [19 Aug 2011]

Chen M.I., Lee V.J., Lim W.Y., Barr I.G., Lin R.T.P., Koh G.C.H., Yap

J., Lin C., Cook A.R., Laurie K., Tan L.W.L., Tan B.H., Loh J., Shaw

R., Durrant C., Chow V.T.K., Kelso A., Chia K.S., Leo Y.S., 2010 2009

Inuenza A(H1N1) seroconversion rates and risk factors among distinct adult

cohorts in Singapore JAMA 303(14):13831391

Chi C.Y., Liu C.C., Lin C.C., Wang H.C., Cheng Y.T., Chang C.M., and

Wang J.R., 2010 Preexisting antibody response against 2009 pandemic

in-uenza H1N1 viruses in the Taiwanese population Clin Vaccine Immunol

17(12):19851986

Chow A., Ma S., Ling A.E., Chew S.K., 2006 Inuenza-associated deaths

in tropical Singapore Emerg Infect Dis 12(1):114121

Chowell G., Nishiura H and Bettencourt L.M.A., 2006 Comparative

esti-mation of the reproduction number for pandemic inuenza from daily case

notication data J Roy Soc Interface 4:155166

Christian R.P., Casella G., 2001 Monte Carlo statistical methods

Springer-Verlag, New York pp96

Cook A.R., Gibson G.J and Gilligan C.A., 2007 Optimal observation times

in experimental epidemic processes Biometrics 64:860868

Cook A.R., Lee H.C., Ong J., Chen M.I., 2010 Predicting the inuenza A

(H1N1-2009) epidemic in Singapore using inuenza-like-illness monitoring

Epidemiol News Bull 36:16

Trang 10

Cordova J.A., Hernandez M., Lopez-Gatell H., Bojorquez I., Palacios E., Rodriguez G., Rosa B., Ocampo R., Alpuche C., Flores R., Hernandez J.E., Tustin J., Watkins K., Stuart T.L., Kuschak T., Ströher U., Soule G., Bal-cewich B., Azziz-Baumgartner E., Lafond K., Mott J., Mahoney F., Uyeki T., McCarron M., Mounts A., Widdowson M.A., Xu X., Shu B., Lindstrom S., Klimov A., Katz J., Winchell J., Penaranda S., Dybdahl-Sissoko N., Ching K., Warner A., Etienne K., Waterman S., McAulie J., Dowell S., Chavez P.R., 2009 Update: Novel Inuenza A (H1N1) Virus Infection  Mex-ico, MarchMay, 2009 Centers for Disease Control and Prevention (CDC) Morbidity & Mortality Weekly Report 58(21):585589

Cox N.J and Subbarao K., 2000 Global epidemiology of inuenza: Past and Present Annu Rev Med 51:407421

Cutter J.L., Ang L.W., Lai F.Y.L., Subramony H., Ma S., James L., 2010 Outbreak of Pandemic Inuenza A (H1N1-2009) in Singapore, May to Septem-ber 2009 Ann Acad Med Singapore 39:273282

De Serres G., Rouleau I., Hamelin M.E., Quach C., Skowronski D., Fla-mand L., Boulianne N., Li Y., Carbonneau J., Bourgault A-M., Couillard M., Charest H., and Boivin G., 2010 Contagious period for pandemic (H1N1)

2009 Emerg Infect Dis 16(5):7838

Débarre F., Bonhoeer S and Regoes R.R., 2007 The eect of population structure on the emergence of drug resistance during inuenza pandemics J Roy Soc Interface 4(16): 893906

Domínguez-Cherit G., Lapinsky S.E., Macias A.E., Pinto R., Espinosa-Perez L., Torre A., Poblano-Morales M., Baltazar-Torres J.A., Bautista E., Mar-tinez A., MarMar-tinez M.A., Rivero E., Valdez R., Ruiz-Palacios G., Hernández M., Stewart T.E., Fowler R.A., 2009 Critically Ill Patients With 2009

In-uenza A(H1N1) in Mexico JAMA 302(17):18801887

Trang 11

Doraisingham S., Goh K.T., Ling A.E., and Yu M., 1988 Inuenza surveil-lance in Singapore: 1972-86 Bull Wld Hlth Org 66(1):5763

Doucet A., Gordon N., and Krishnamurthy V., 1999 Particle lters for state estimation of jump markov linear systems Technical report, Department of Engineering, Cambridge University

Doucet A., Godsill S and Andrieu C., 2000 On sequential Monte Carlo sam-pling methods for Bayesian ltering Statistics and Computing 10:197208

Dunson D.B., 2001 Commentary: Practical Advantages of Bayesian Analy-sis of Epidemiologic Data American Journal of Epidemiology 153(12):12221226

Emmanuel S.C., Phua H.P., Cheong P.Y., 2004 2001 survey on primary medical care in Singapore Singapore Med J 45(5): 199213

Gelman A., Carlin J.B., Stern H.S., Rubin D.B., 2003 Bayesian Data Anal-ysis 2nd ed London: Chapman & Hall

Ghosh J.K., Delampady M., Samanta T., 2006 An introduction to Bayesian analysis: theory and methods Springer, USA

Gibson G.J., and Renshaw E., 1998 Estimating parameters in stochastic compartmental models using Markov chain models IMA Journal of Mathe-matics Applied in Medicine and Biology 15(1):19940

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