Book contents
- Frontmatter
- Contents
- Introduction
- Participants
- Non-Participant Contributors
- Part 1 Transmissible diseases with long development times and vaccination strategies
- Overview of data analysis: diseases with long development times
- HPV and cervical cancer
- An age-structured model for measles vaccination
- Invited Discussion
- Invited Discussion
- Piece-wise constant models to estimate age- and time-specific incidence of toxoplasmosis from age- and time-specific seroprevalence data
- New methodology for AIDS back calculation
- Imperfect HIV vaccines, the consequences for epidemic control and clinical trials
- Feasibility of prophylactic HIV-vaccine trials: some statistical issues
- The design of immunisation programmes against hepatitis B virus in developing countries
- The effect of different mixing patterns on vaccination programs
- Optimal vaccination patterns in age-structured populations I: the reproduction number
- Optimal vaccination patterns in age-structured populations II: optimal strategies
- Part 2 Dynamics of immunity (development of disease within individuals)
- Part 3 Population heterogeneity (mixing)
- Part 4 Consequences of treatment interventions
- Part 5 Prediction
The effect of different mixing patterns on vaccination programs
Published online by Cambridge University Press: 04 August 2010
- Frontmatter
- Contents
- Introduction
- Participants
- Non-Participant Contributors
- Part 1 Transmissible diseases with long development times and vaccination strategies
- Overview of data analysis: diseases with long development times
- HPV and cervical cancer
- An age-structured model for measles vaccination
- Invited Discussion
- Invited Discussion
- Piece-wise constant models to estimate age- and time-specific incidence of toxoplasmosis from age- and time-specific seroprevalence data
- New methodology for AIDS back calculation
- Imperfect HIV vaccines, the consequences for epidemic control and clinical trials
- Feasibility of prophylactic HIV-vaccine trials: some statistical issues
- The design of immunisation programmes against hepatitis B virus in developing countries
- The effect of different mixing patterns on vaccination programs
- Optimal vaccination patterns in age-structured populations I: the reproduction number
- Optimal vaccination patterns in age-structured populations II: optimal strategies
- Part 2 Dynamics of immunity (development of disease within individuals)
- Part 3 Population heterogeneity (mixing)
- Part 4 Consequences of treatment interventions
- Part 5 Prediction
Summary
Introduction
This paper is concerned with evaluation of vaccination programs for viral diseases such as measles, mumps, rubella and hepatitis A. For such diseases an individual starts off susceptible, at some stage catches the disease and after a short infectious period becomes permanently immune. Vaccines for measles, mumps and rubella are currently in use and vaccines for hepatitis A are not yet widely available but are currently undergoing testing. The aim of this paper is to look at the evaluation of vaccination programs and their sensitivity to different mixing assumptions.
Mathematical models which accurately describe the spread of a disease must take into account the age-structure of the population amongst whom the disease is spreading. Anderson and May (1985) describe an age-structured mathematical model using partial differential equations, which is the basis of the one which we shall use. Age-structured data for these diseases is available in the form of case reports, or more reliably age-serological profiles. Anderson and May divide the population into discrete age classes and use computer simulation methods to evaluate different vaccination programs for measles, mumps and rubella.
Method
The force of infection at time t, λ(a, t), is defined as the probability per unit time that a susceptible individual of age a will become infected. We follow Keiding's non-parametric maximum likelihood method to estimate the force of infection assuming that the disease has settled down to its longterm equilibrium value. We use age-structured serological profiles for hepatitis A in Bulgaria given by Keiding (1991).
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- Chapter
- Information
- Models for Infectious Human DiseasesTheir Structure and Relation to Data, pp. 86 - 89Publisher: Cambridge University PressPrint publication year: 1996
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