Abstract

BackgroundFollowing the emergence of the A/H1N1 2009 influenza pandemic, public health interventions were activated to lessen its potential impact. Computer modelling and simulation can be used to determine the potential effectiveness of the social distancing and antiviral drug therapy interventions that were used at the early stages of the pandemic, providing guidance to public health policy makers as to intervention strategies in future pandemics involving a highly pathogenic influenza strain.MethodsAn individual-based model of a real community with a population of approximately 30,000 was used to determine the impact of alternative interventions strategies, including those used in the initial stages of the 2009 pandemic. Different interventions, namely school closure and antiviral strategies, were simulated in isolation and in combination to form different plausible scenarios. We simulated epidemics with reproduction numbers R0of 1.5, which aligns with estimates in the range 1.4-1.6 determined from the initial outbreak in Mexico.ResultsSchool closure of 1 week was determined to have minimal effect on reducing overall illness attack rate. Antiviral drug treatment of 50% of symptomatic cases reduced the attack rate by 6.5%, from an unmitigated rate of 32.5% to 26%. Treatment of diagnosed individuals combined with additional household prophylaxis reduced the final attack rate to 19%. Further extension of prophylaxis to close contacts (in schools and workplaces) further reduced the overall attack rate to 13% and reduced the peak daily illness rate from 120 to 22 per 10,000 individuals. We determined the size of antiviral stockpile required; the ratio of the required number of antiviral courses to population was 13% for the treatment-only strategy, 25% for treatment and household prophylaxis and 40% for treatment, household and extended prophylaxis. Additional simulations suggest that coupling school closure with the antiviral strategies further reduces epidemic impact.ConclusionsThese results suggest that the aggressive use of antiviral drugs together with extended school closure may substantially slow the rate of influenza epidemic development. These strategies are more rigorous than those actually used during the early stages of the relatively mild 2009 pandemic, and are appropriate for future pandemics that have high morbidity and mortality rates.

Highlights

  • Following the emergence of the A/H1N1 2009 influenza pandemic, public health interventions were activated to lessen its potential impact

  • We initially simulated an unmitigated epidemic within the Albany community to determine the illness attack rate that would result if no interventions were in place

  • The derived serial interval depends upon the latent and infectious durations and on the transmissibility of the virus. Our assumptions about these durations were based on seasonal influenza; when combined with a transmissibility calibrated to give an R0 of 1.5, the resulting serial interval of 2.47 days is consistent with estimates of 1.3 - 2.71 days for the 2009 pandemic [29,9]

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Summary

Introduction

Following the emergence of the A/H1N1 2009 influenza pandemic, public health interventions were activated to lessen its potential impact. Household quarantine and reduced workplace, social and community contacts are considered to be key non-pharmaceutical interventions which may readily be used for the early containment of an influenza epidemic These social distancing measures have been shown in modelling studies to delay the overall impact of a pandemic, as well as allowing time for antiviral drug administration and the development of appropriate vaccines [7,8]. Neuraminidase inhibitor antiviral drugs and appropriate vaccines are the key pharmaceutical interventions, with antiviral drugs being the only available pharmaceutical interventions available when faced with a novel strain of influenza virus in the early phase of pandemic, as has occurred in 2009 Social distancing measures, such as school closure, and antiviral drug strategies have been used in the initial stages of the A/H1N1 2009 pandemic in Australia and other parts of the world [9,10]

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