Table 4.
An overview of modelling studies of Ebola and study designs (Research aims: Parameter estimation and Trajectory prediction)
| Reference | Dataset/Factors | Description of Modelling Approaches | Compartments, if applicable | Assumption of population mixing, if applicable | Model fitting and calibration approach, if applicable | Sensitivity analysis, if applicable | Description of account for data bias, if applicable |
|---|---|---|---|---|---|---|---|
| Althaus et al. [27] | Case data from published reports. Parameters from previous EVD outbreaks | Transmission model with a set of ODEs and used Maximum likelihood estimates to determine model parameters (baseline transmission rate, rate at which control measures reduce transmission, case fatality rate) | SEIR | Assumed homogeneous mixing | Fitted a dynamic transmission model to data about reported cases and deaths of EVD during a small urban outbreak in Nigeria using Maximum likelihood methods | NA | NA |
| Barbarossa et al. [28] | Case data from WHO reports [1]. Parameters estimated from various studies | Compartmental population model based on Legrand's study [24] that distinguishes between community and hospitalised patients, and recognises importance of deceased individuals who can still transmit the virus at burials | Susceptible–latent–infectious–hospitalised–dead–buried–removed (SEIHBDR) | Model divided infectious population into those who exist in the community and those who exist in hospitals, and considered post-death transmission | Fitted model outcomes to the WHO reports for weekly case incidence. The data were fit with piecewise exponential curves | Studied the effects of model parameters on the basic reproduction number and on the final epidemic size. LHS is used to generate a representative sample set of test parameters from the ranges. Focused mostly on the sensitivity of the time of intervention. PRCCs analysis was reported | NA |
| Camacho et al. [49] | Case data from Sierra Leone Ministry of Health and Sanitation and WHO reports [1]. Data on ETCs, EHCs, CCCs from The Humanitarian Data Exchange. Proportion of symptomatic cases from the UN for Ebola Emergency Response and the National Emergency Response Centre | Transmission model with time-dependent transmission rate, accounting for hospitalisation and delay in case reporting | Susceptible–exposed1–exposed2–infectious–infectious (hospitalisation)–removed | Modelling individuals progressed through stages, including hospitalisation compartment | Fitted model to the time series of weekly reported cases using Bayesian approach | Sensitivity analysis was performed by taking averaged posterior distribution of R over a period of Jan 2015 | Assumed proportion of symptomatic cases reported at 60%, accounted for the potential variability in accuracy of reporting over time and accounted for over-dispersed delay between onset of symptoms and notification of reported cases |
| Chowell et al. [50] | Case data from WHO reports [1] | Logistic growth models fitted with the minimal amount of case data | NA | NA | Fitted logistic growth models to the cumulative number of cases using least-squares | NA | NA |
| Evans and Mammadov [51] | Case data from WHO [1] | Estimated the reproduction numbers for the total period of epidemic and for different consequent time intervals using simple linear model and considered the average infectious period as a time-dependent parameter | NA | NA | Fitted model outcome with the cumulative numbers of infected cases and deaths using global optimisation algorithm DSO | NA | NA |
| Fasina et al. [52] | Case data from WHO reports [1] and public source | Simplified version of Legrand's model [24] accounting for contribution of community and healthcare settings by adjusting baseline transmission rates, diagnostic rates, and enhancement of infection control measures | Susceptible–exposed–infectious–hospitalised–removed from isolation after recovery or death (SEIHP) | Model divided infectious individuals into groups in the community and isolation in a hospital | Assessed the timing of control interventions on the size of the EVD outbreak in Nigeria by extensive simulation runs | NA | NA |
| Fisman and Tuite [53] | Case data from WHO reports [1], Caitlin Rivers github website [19] | Incidence Decay with Exponential Adjustment (IDEA) model using maximum-likelihood methods to identify best-fit model parameters | NA | NA | Used maximum-likelihood methods to identify the optimal, best and worst case model parameters for the IDEA model | Sensitivity analysis were performed by varying vaccine efficacy | NA |
| Fisman et al. [54] | Case data from Caitlin Rivers github website [19], Virologically-confirmed case counts by date from the Virology Down Under blog [20] | IDEA model, a two parameter mathematical model describes exponential growth simultaneous decay, was used to project epidemic curve accounting for incidence decay | NA | NA | Model was fitted to time series data iteratively, using a progressively increasing number of outbreak generations. Best fit parameter values are estimated by fitting; – objective function: minimise the root mean-squared distance between model estimates and empirical data | Checked separate models to epidemic curves derived from reported deaths, curves based only on virologically confirmed cases, as well as curves based on varying assumptions about case-underreporting | Fitted separate models using assumptions about case underreporting (50% and 100%). |
| Lewnard et al. [55] | Montserrado case data, Number of Beds in Ebola Treatment Centres from Ministry of Health and Social Welfare, Liberia Ebola situation reports. Total population of Montserrado from Republic of Liberia 2008 Population and Housing Census. Time to burial, relative transmission rate from previous study. International SOS Hospital response and isolation/treatment centres also used to determine Number of Beds in ETCs | Developed a differential equation model which includes a latent population (L), two types of recovery populations (R), differentiation of ascertained (A) cases (which do not contribute to community transmission) | SEIR | Assumed homogeneous mixing | Modelled cumulative cases and mortality as a Poisson-distributed random variable. Model calibrated by sampling via Markov Chain Monte Carlo using a Metropolis–Hastings acceptance rule | NA | Addressed underreporting or delays in reporting by fitting model to estimate the delay between the beginning of the infectious period and time of ascertainment |
| Liu et al. [56] | Case data from WHO [1] | Logistic, Gompertz, Rosenzweg and Richards models were developed and compared | NA | NA | Fitted the model using precise estimates by Bayes factors and obtained model parameters | NA | NA |
| Meltzer et al. [9] | Infectious period from The World Bank website, CDC website. Likelihood of a patient going to an ETU and the number of days that a patient in each patient category would spend in the hospital. Actual number of beds in use – from expert opinion | EbolaResponse, a Markov chain model, categorises patient setting (i) hospitalised facility, (ii) home/community where there is reduced disease transmission, (iii) home with no effective isolation. Model also accounts for under-reporting of cases, and allows for imported cases or cases with no known contacts | Susceptible–infected–incubation–infectious–infectious (burial)–recovered | Considered those who die but whose burial provides risk for onward transmission. Patients were categorised into hospitalised in an Ebola treatment unit (ETU) or medical care facility, home or in a community setting and home with no effective isolation | Model parameters were altered to produce a matched outcome with the reported cases to date using goodness-of-fit test | NA | A underreporting correction factor of 2·5 was used to estimate future total cases |
| Nishiura and Chowell [57] | Case data form WHO reports [1] | Mathematical modelling considering time- and country-specific incidence data to estimate reproductive numbers, using likelihood-based method for real-time parameter estimation. Estimated daily incidence curves by fitting smoothing spline to county-specific cumulative curves of cases | NA | NA | Fitted a smoothing spline to cumulative reported cases by country and adjusted the spline function based on the daily incidence time series | Sensitivity analyses of reproduction number were carried out by varying the mean generation time | NA |
| Pandey et al. [30] | Demographic data from the 2008 National, Housing Census of Liberia. Case data from Liberian Ministry of Health and Social Welfare | Transmission model takes into account transmission within and between the community, hospitals and funerals | Susceptible–latent–infected–deceased–recovered–buried (SEIFRD) | Stratified epidemiological class into compartments that correspond to the general community, hospitals and funerals | Used weighted least-squares to fit the model to case data. Converted event-based stochastic model to a discrete-time difference equation model. Then evaluated the difference equation model, fitted the output to the data, and calculated the best-fit estimates of certain parameters by minimising the weighted least-squares difference between the model output and the data with the Quasi-Newton algorithm | Done extensive sensitivity analysis and elasticity analysis on intervention effectiveness to variation in epidemiological parameters. PRCCs was used | Refitted model to account for a range of plausible underreporting. Varied the levels of under-reporting of Ebola cases in both community and hospitals, as well as only communities |
| Rivers et al. [58] | Case data from WHO reports [1] and Ministry of Health of Liberia and Sierra Leone (available online from the Caitlin Rivers github website) [19] | Compartmental model adapted from Legrand's study [24]; stochastic model was implemented using Gillespie's algorithm | Susceptible–exposed–infectious–hospitalised–funeral–removed (SEIHFR) | Model accounted for those who are hospitalised and deceased individuals who can still transmit virus | A deterministic version of the model was fit and validated to the current outbreak data using least-squares optimisation. The last 15 days of reported cases were given one -quarter of the weight in the model to preferentially fit the most recent data | NA | NA |
| Shaman et al. [59] | Case data from WHO reports [1] | An ensemble Susceptible–exposed–infectious–recovered-X (SEIRX)–EAKF framework using observations, dynamic modelling and Bayesian inference to generate simulations | SEIRX | Additional X compartments were introduced to describe assimilation of mortality and case fatality rate | Fitted the model variables and parameters with weekly observations and allowed for time varying of variables and Rt parameters | Sensitivity analysis were performed by changing model structure, and varying population size and initial parameter ranges | NA |
| Shen et al. [60] | Case data from WHO [1] | Developed mathematical ODE model to study Ebola infection with isolation, media impact, post-death transmission and vaccination | Susceptible–vaccinated–latent (undetectable)–latent (detectable)–infectious with symptoms–isolated individuals–dead but have not been buried–recovered | Considered those who have died and are in the process of being buried | Fitted the model to epidemiological data of reported cumulative numbers of infected cases and deaths | Examined the most sensitive parameters to the R0 and the final epidemic size. LHS and PRCC methods were used |
NA |
| Siettos et al. [61] | Time series count data, including cumulative incidence, from WHO reports. Cumulative deaths data from Wikipedia and WHO case reports [1]. Demographic data from United Nations [22] | Agent-based model using a small-world network constructed using the Watts & Strogatz algorithm | Susceptible–exposed–infected–dead (but not yet buried)–dead (safely buried)–removed | Agent-based model considered individuals interact through a small-world network | Fitted two network characteristics and four epidemic rates with reported outbreak data | NA | NA |
| Towers et al. [62] | Case data from HealthMap, WHO reports [1] | Fitted piecewise exponential curves along the data time series to estimate the evolving rate of exponential rise (or decline) in cases. SEIR model developed to estimate the temporal patterns of the effective reproduction number for the outbreak in each country | SEIR | Assumed homogeneous mixing | Fitted piecewise exponential function to estimate rates of exponential rise from the average daily EVD incidence data | Sensitivity analyses were performed using LHS and PRCC methods to test the robustness of result with respect to the exact number of contiguous points used for the fits |
NA |
| Webb et al. [63] | Case data from WHO reports [1]. Parameters from various studies | Differential equations with compartments of the epidemic population that simulated forward projection of epidemic using Continuous Time Markov Chain. Model incorporates contact tracing of infectious cases. Both deterministic and stochastic models were run | SEICIIR | Modelling containment and isolation compartments | Parameters estimated using a least-squares curve fitting algorithm to obtain a choice of parameters with relatively accurate fit | Sensitivity analyses were performed in two contact tracing parameters. The contact tracing parameters were tested in sensitivity analysis | A ratio of unreported case of 1·78 is used for estimation |
| WHO [25] | Case data from investigation forms from confirmed, probable and suspected EVD cases identified in Guinea, Liberia, Nigeria, and Sierra Leone; also from informal case reports; data from diagnostic laboratories; data from burials | Projected case numbers using two methods: (i) regression method and (ii) stochastic branching process model | NA | NA | Epidemiological parameters were fitted with gamma probability distributions | Sensitivity analyses were performed by assuming different mean serial intervals of 11 and 13 and including suspected as well as confirmed and probable cases in the analysis | NA |
| WHO [64] | Case data from viral haemorrhagic fever data collection forms, treatment facilities, contact tracing forms | Reported summary statistics and prediction outcomes through simple model fitted to data. Used weighted average to estimate the duration reported of the observed means of the distributions of durations from hospitalisation to discharge and hospitalisation to death | NA | NA | Gamma distributions were fitted to confirmed and probable cases | NA | NA |