Quantifying Parameter and Structural Uncertainty of Dynamic Disease Transmission Models Using MCMC

Author:

Bilcke Joke12345,Chapman Ruth12345,Atchison Christina12345,Cromer Deborah12345,Johnson Helen12345,Willem Lander12345,Cox Martin12345,Edmunds William John12345,Jit Mark12345

Affiliation:

1. Centre for Health Economics Research & Modeling of Infectious Diseases (CHERMID), Vaccine and Infectious Disease Institute (VAXINFECTIO), University of Antwerp, Antwerp, Belgium (JB, LW)

2. Department of Infectious Diseases Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK (JB, HJ, WJE, MJ)

3. Modelling and Economics Unit, Public Health England, London, UK (RC, MJ)

4. Department of Primary Care and Public Health, School of Public Health, Imperial College, London, UK (CA)

5. Complex Systems in Biology Group, Centre for Vascular Research, UNSW Australia, Sydney, New South Wales, Australia (DC)

Abstract

Background. Two vaccines (Rotarix and RotaTeq) are highly effective at preventing severe rotavirus disease. Rotavirus vaccination has been introduced in the United Kingdom and other countries partly based on modeling and cost-effectiveness results. However, most of these models fail to account for the uncertainty about several vaccine characteristics and the mechanism of vaccine action. Methods. A deterministic dynamic transmission model of rotavirus vaccination in the United Kingdom was developed. This improves on previous models by 1) allowing for 2 different mechanisms of action for Rotarix and RotaTeq, 2) using clinical trial data to understand these mechanisms, and 3) accounting for uncertainty by using Markov Chain Monte Carlo. Results. In the long run, Rotarix and RotaTeq are predicted to reduce the overall rotavirus incidence by 50% (39%−63%) and 44% (30%−62%), respectively but with an increase in incidence in primary school children and adults up to 25 y of age. The vaccines are estimated to give more protection than 1 or 2 natural infections. The duration of protection is highly uncertain but has only impact on the predicted reduction in rotavirus burden for values lower than 10 y. The 2 vaccine mechanism structures fit equally well with the clinical trial data. Long-term postvaccination dynamics cannot be predicted reliably with the data available. Conclusion. Accounting for the joint uncertainty of several vaccine characteristics resulted in more insight into which of these are crucial for determining the impact of rotavirus vaccination. Data for up to at least 10 y postvaccination and covering older children and adults are crucial to address remaining questions on the impact of widespread rotavirus vaccination.

Publisher

SAGE Publications

Subject

Health Policy

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