6 research outputs found
Projections of Ebola outbreak size and duration with and without vaccine use in Équateur, Democratic Republic of Congo, as of May 27, 2018.
As of May 27, 2018, 6 suspected, 13 probable and 35 confirmed cases of Ebola virus disease (EVD) had been reported in Équateur Province, Democratic Republic of Congo. We used reported case counts and time series from prior outbreaks to estimate the total outbreak size and duration with and without vaccine use. We modeled Ebola virus transmission using a stochastic branching process model that included reproduction numbers from past Ebola outbreaks and a particle filtering method to generate a probabilistic projection of the outbreak size and duration conditioned on its reported trajectory to date; modeled using high (62%), low (44%), and zero (0%) estimates of vaccination coverage (after deployment). Additionally, we used the time series for 18 prior Ebola outbreaks from 1976 to 2016 to parameterize the Thiel-Sen regression model predicting the outbreak size from the number of observed cases from April 4 to May 27. We used these techniques on probable and confirmed case counts with and without inclusion of suspected cases. Probabilistic projections were scored against the actual outbreak size of 54 EVD cases, using a log-likelihood score. With the stochastic model, using high, low, and zero estimates of vaccination coverage, the median outbreak sizes for probable and confirmed cases were 82 cases (95% prediction interval [PI]: 55, 156), 104 cases (95% PI: 58, 271), and 213 cases (95% PI: 64, 1450), respectively. With the Thiel-Sen regression model, the median outbreak size was estimated to be 65.0 probable and confirmed cases (95% PI: 48.8, 119.7). Among our three mathematical models, the stochastic model with suspected cases and high vaccine coverage predicted total outbreak sizes closest to the true outcome. Relatively simple mathematical models updated in real time may inform outbreak response teams with projections of total outbreak size and duration
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Modeling the transmission of Ebola and GU Chlamydia in Sub-Saharan African countries under both epidemic and endemic settings
In this dissertation, I used various methods to model the transmission of two infectious diseases, Ebola in an epidemic setting and GU Chlamydia in an endemic setting within in Sub-Saharan Africa. Since 2015, there have been five outbreaks of Ebola Virus Disease (EVD) in several dierent countries in Sub-Saharan Africa, one of which became the second largest EVD outbreak in history in the setting of a longstanding conflict zone. It is suspected that after violent events occur, EVD transmission will increase; however, empirical studies to understand the impact of violence on transmission are lacking. In my first chapter, I used spatial and temporal trends of EVD case counts to compare transmission rates between health zones that have versus have not experienced recent violent events during the outbreak. In my second chapter, I also sought to use modeling to make outbreak projections, looking at the 2020 outbreak in The Democratic Republic of Congo. I made short and long-term projections for the outbreak in an eort to assess the potential to provide more accurate forecasting for an ongoing outbreak. I also evaluated how the outbreak’s timing and course affected the accuracy of such forecasts. Lastly in my third chapter, I focused on trachoma endemic areas of Sub-Saharan Africa and modeling the impact of annual Trachoma Mass Drug Administration (MDA) with azithromycin upon the prevalence of genitourinary (GU) chlamydia using a compartmental model. Communities that are especially hard hit with Trachoma are almost exclusively poor commu- nities with poor access to sanitation, screening and antibiotics to treat the infection; conditions that may allow for STDs to maintain a high chain of transmission. The dosing of azithromycin for the Trachoma MDA is consistent with dosing given clinically to treat GU chlamydial (GUC) disease, and recent evidence has suggested it reduces the population prevalence.In my first chapter investigating the potential impact of violent events upon local instability and increased EVD transmission, I collected daily EVD case counts from DRC Ministry of Health for the 2018 outbreak in the Democratic Republic of Congo (DRC). A time-varying indicator of recent violence in each health zone was derived from events documented in the WHO situation reports. I used the Wallinga-Teunis technique to estimate the reproduction number R for each case by day per zone in the 2018–2019 outbreak. I fit an exponentially decaying curve to estimates of R overall and by health zone, for comparison to past outbreaks.As of 16 April 2019, the mean overall R for the entire outbreak was 1.11. I found evidence of an increase in the estimated transmission rates in health zones with recently reported violent events versus those without (p = 0.008). The average R was estimated as between 0.61 and 0.86 in regions not aected by recent violent events, and between 1.01 and 1.07 in zones aected by violent events within the previous 21 days, leading to an increase in R between 0.17 and 0.53. Within zones with recent violent events, the mean estimated quenching rate was lower than for all past outbreaks except the 2013–2016 West African outbreak. The difference in the estimated transmission rates between zones affected by recent violent events suggests that violent events contributed to increased transmission and the prolonged nature of the second largest EVD outbreak in history.In my second chapter performing EVD outbreak projections, several mathematical models were used to predict the final outbreak size and weekly incidence for the 2020 DRC outbreak. Projections were commenced prospectively mid-way through the outbreak, and retrospectively applied for the early out- break. Short-term forecasts were made using two different models: (i) a particle-filter branching-process model and (ii) a naive auto-regression. Final outbreak size predictions were made using four different models: (i) the particle-filter branching-process model, (ii) Theil-Sen regression, (iii) Gott’s Law and (iv) a novel Bayesian branching process model parameterized using prior outbreak sizes and contingent on the current outbreak size. The Bayesian model examined final size distributions across a range of current outbreak sizes, allowing for an examination of parameter fits.Overall, there were reasonable amounts of variability in the forecasts created by different models. For short-term, auto-regression models showed relatively stable steady-state growth in the outbreak, with somewhat larger confidence intervals while the particle-filter branching model projected an outbreak slowly ending in the same period. Final outbreak size predictions increased overall as the outbreak continued. The median expectation among models increased between 2.5–4.0 fold in September over initial expectations from June as the outbreak grew from 34 to 128 cases. The branching-process model was overall the most stable consistent performer, though the Bayesian model was a close second. Including the West Africa outbreak, easily the largest to date, increased the range of predicted outcomes for the DRC outbreak between 40–50%.In predicting the 2020 Ebola outbreak, the most consistent performing model was the branching process particle-filter model though the Bayesian model did nearly as well, despite being agnostic to the trajectory of the outbreak. Our short-term models consistently predicted the outbreak would grow, though models disagreed over the slowing pace; it will be important to evaluate the performance of these models in future outbreaks to understand these uncertainties. The growth of the outbreak to well over a hundred cases underscores the real risk EBOV poses to the region and the need for improved understanding of outbreak trajectories even with the presence of three approved vaccines.In my third chapter, I analyzed the impact of Trachoma MDA upon GUChlamydia prevalence using an extended compartmental SIS model, accounting for the natural history of GUC, risk structure, and gender. The model includes slowly developing partial immunity. MDA was modelled as an impulsively forced treatment with varying coverage and efficacy.My model showed that three years of MDA at current levels reduced the prevalence of GUC in all populations by at least 15%. Between annual MDA, the prevalence partially rebounded to pre-treatment levels. With Coverage x Efficacy ≥ 0.80, the time between MDA treatments was insufficient to sustain transmission, allowing for GUC burden to be suppressed below 1 in 10,000 after 5 rounds for starting prevalence less than 9.2%. When serial non-compliance is increased from 20% to 80%, this target is achieved for starting prevalences below 4.7%, down from 9.2%. Targeting azithromycin treatment only to high-risk individuals reduces the starting prevalences for which target is reached to 1.8%.My model suggests that MDA could reduce the prevalence of GUC to less than 1 in 10,000 within 5 years time. This reinforces the suggestions of potential additional health benefits of trachoma MDA and points to potential value of screening and disease treatment even in impoverished areas, and suggests testable hypotheses regarding prevalence in endemic areas under treatment
Lifecourse Educational Trajectories and Hypertension in Midlife: An Application of Sequence Analysis
BackgroundHigher educational attainment predicts lower hypertension. Yet, associations between nontraditional educational trajectories (eg, interrupted degree programs) and hypertension are less well understood, particularly among structurally marginalized groups who are more likely to experience these non-traditional trajectories.MethodsIn National Longitudinal Survey of Youth 1979 cohort data (N = 6 317), we used sequence and cluster analyses to identify groups of similar educational sequences-characterized by timing and type of terminal credential-that participants followed from age 14-48 years. Using logistic regression, we estimated associations between the resulting 10 educational sequences and hypertension at age 50. We evaluated effect modification by individual-level indicators of structural marginalization (race, gender, race and gender, and childhood socioeconomic status [cSES]).ResultsCompared to terminal high school (HS) diploma completed at traditional age, terminal GED (OR: 1.32; 95%CI: 1.04, 1.66) or Associate degree after ConclusionsBoth type and timing to terminal credential matter for hypertension but effects may vary by experiences of structural marginalization. Documenting the nuanced ways in which complex educational trajectories are associated with health could elucidate underlying mechanisms and inform systems-level interventions for health equity
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Understanding the benefits of different types and timing of education for mental health: A sequence analysis approach.
Individuals increasingly experience delays or interruptions in schooling; we evaluate the association between these non-traditional education trajectories and mental health. Using year-by-year education data for 7,501 National Longitudinal Survey of Youth 1979 participants, ages 14-48 (262,535 person-years of education data), we applied sequence analysis and a clustering algorithm to identify educational trajectory groups, incorporating both type and timing to credential. Linear regression models, adjusted for early-life confounders, evaluated relationships between educational trajectories and mental health component scores (MCS) from the 12-item short form instrument at age 50. We evaluated effect modification by race, gender, and race by gender. We identified 24 distinct educational trajectories based on highest credential and educational timing. Compared to high school (HS) diplomas, < HS (beta=-3.41, 95%CI:-4.74,-2.07) and general educational development credentials (GEDs) predicted poorer MCS (beta=-2.07,95%CI:-3.16,-0.98). The following educational trajectories predicted better MCS: some college immediately after High School (beta=1.52, 95%CI:0.68,2.37), Associate degrees after long interruptions (beta=1.73, 95%CI:0.27,3.19), and graduate school soon after Bachelor's completion (beta=1.13, 95%CI:0.21,2.06). Compared to White men, Black women especially benefited from educational credentials higher than HS in predicting MCS. Both type and timing of educational credential predicted mental health. Black women's mental higher especially benefited from higher educational credentials
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Estimating the impact of violent events on transmission in Ebola virus disease outbreak, Democratic Republic of the Congo, 2018-2019.
IntroductionAs of April 2019, the current Ebola virus disease (EVD) outbreak in the Democratic Republic of the Congo (DRC) is occurring in a longstanding conflict zone and has become the second largest EVD outbreak in history. It is suspected that after violent events occur, EVD transmission will increase; however, empirical studies to understand the impact of violence on transmission are lacking. Here, we use spatial and temporal trends of EVD case counts to compare transmission rates between health zones that have versus have not experienced recent violent events during the outbreak.MethodsWe collected daily EVD case counts from DRC Ministry of Health. A time-varying indicator of recent violence in each health zone was derived from events documented in the WHO situation reports. We used the Wallinga-Teunis technique to estimate the reproduction number R for each case by day per zone in the 2018-2019 outbreak. We fit an exponentially decaying curve to estimates of R overall and by health zone, for comparison to past outbreaks.ResultsAs of 16 April 2019, the mean overall R for the entire outbreak was 1.11. We found evidence of an increase in the estimated transmission rates in health zones with recently reported violent events versus those without (p = 0.008). The average R was estimated as between 0.61 and 0.86 in regions not affected by recent violent events, and between 1.01 and 1.07 in zones affected by violent events within the last 21 days, leading to an increase in R between 0.17 and 0.53. Within zones with recent violent events, the mean estimated quenching rate was lower than for all past outbreaks except the 2013-2016 West African outbreak.ConclusionThe difference in the estimated transmission rates between zones affected by recent violent events suggests that violent events are contributing to increased transmission and the ongoing nature of this outbreak