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. 2017 Mar;18:16–28. doi: 10.1016/j.epidem.2017.02.006

Table 1.

Models studied and their characteristic features.

Model Infection dynamics in humans Infection dynamics in vectors Implementation Total number of parameters (number fitted)a Intervention (MDA or VC) Refs
EPIFIL Deterministic, age-structured Partial differential equations (PDE) Deterministic Ordinary differential equation (ODE) A Monte Carlo-based Bayesian Melding framework using a binomial likelihood function to fit data 28 (24) Random MDA coverage, with reduction in the biting rate as observed due to VCb where applicable Gambhir et al. (2010), Chan et al. (1998) and Norman et al. (2000)



LYMFASIM Stochastic, individual-based micro-simulation Deterministic non-linear A chi-squared statistic based fitting method 19 (3) MDA compliance is neither completely random nor completely systematic, with reduction in the biting rate as observed due to VCc where applicable Jambulingam et al. (2016), Plaisier et al. (1998) and Subramanian et al. (2004b)



TRANSFIL Individual-based micro-simulation Deterministic ODE An Approximate Bayesian Computation based fitting procedure 14 (3) Systematic non-compliance of MDA, with reduction in the biting rate as observed due to VCc where applicable Irvine et al. (2015)
a

Those parameters that are not fitted to data have fixed values.

b

In EPIFIL, the impact of IVM in Pondicherry was modelled using the equation: MBRVC = MBR0 exp[a1t], with a1 < 0 for ∀t when VC is ON, otherwise a1 > 0. Details can be found in part A of the SI text describing EPIFIL.

c

In both LYMFASIM and TRANSFIL, IVM in Pondicherry was modelled as the observed reduction in the average MBRs during the period 1981–1985.