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1.
Epidemics ; 5(4): 197-207, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24267876

ABSTRACT

Haiti has been in the midst of a cholera epidemic since October 2010. Rainfall is thought to be associated with cholera here, but this relationship has only begun to be quantitatively examined. In this paper, we quantitatively examine the link between rainfall and cholera in Haiti for several different settings (including urban, rural, and displaced person camps) and spatial scales, using a combination of statistical and dynamic models. Statistical analysis of the lagged relationship between rainfall and cholera incidence was conducted using case crossover analysis and distributed lag nonlinear models. Dynamic models consisted of compartmental differential equation models including direct (fast) and indirect (delayed) disease transmission, where indirect transmission was forced by empirical rainfall data. Data sources include cholera case and hospitalization time series from the Haitian Ministry of Public Health, the United Nations Water, Sanitation and Health Cluster, International Organization for Migration, and Hôpital Albert Schweitzer. Rainfall data was obtained from rain gauges from the U.S. Geological Survey and Haiti Regeneration Initiative, and remote sensing rainfall data from the National Aeronautics and Space Administration Tropical Rainfall Measuring Mission. A strong relationship between rainfall and cholera was found for all spatial scales and locations examined. Increased rainfall was significantly correlated with increased cholera incidence 4-7 days later. Forcing the dynamic models with rainfall data resulted in good fits to the cholera case data, and rainfall-based predictions from the dynamic models closely matched observed cholera cases. These models provide a tool for planning and managing the epidemic as it continues.


Subject(s)
Cholera/epidemiology , Rain , Rural Population/statistics & numerical data , Urban Population/statistics & numerical data , Cholera/transmission , Haiti/epidemiology , Humans , Incidence , Mathematical Computing , Models, Statistical , Seasons
2.
Ann Intern Med ; 154(9): 593-601, 2011 May 03.
Article in English | MEDLINE | ID: mdl-21383314

ABSTRACT

BACKGROUND: Haiti is in the midst of a cholera epidemic. Surveillance data for formulating models of the epidemic are limited, but such models can aid understanding of epidemic processes and help define control strategies. OBJECTIVE: To predict, by using a mathematical model, the sequence and timing of regional cholera epidemics in Haiti and explore the potential effects of disease-control strategies. DESIGN: Compartmental mathematical model allowing person-to-person and waterborne transmission of cholera. Within- and between-region epidemic spread was modeled, with the latter dependent on population sizes and distance between regional centroids (a "gravity" model). SETTING: Haiti, 2010 to 2011. DATA SOURCES: Haitian hospitalization data, 2009 census data, literature-derived parameter values, and model calibration. MEASUREMENTS: Dates of epidemic onset and hospitalizations. RESULTS: The plausible range for cholera's basic reproductive number (R(0), defined as the number of secondary cases per primary case in a susceptible population without intervention) was 2.06 to 2.78. The order and timing of regional cholera outbreaks predicted by the gravity model were closely correlated with empirical observations. Analysis of changes in disease dynamics over time suggests that public health interventions have substantially affected this epidemic. A limited vaccine supply provided late in the epidemic was projected to have a modest effect. LIMITATIONS: Assumptions were simplified, which was necessary for modeling. Projections are based on the initial dynamics of the epidemic, which may change. CONCLUSION: Despite limited surveillance data from the cholera epidemic in Haiti, a model simulating between-region disease transmission according to population and distance closely reproduces reported disease patterns. This model is a tool that planners, policymakers, and medical personnel seeking to manage the epidemic could use immediately.


Subject(s)
Cholera/epidemiology , Cholera/transmission , Epidemics/prevention & control , Models, Statistical , Population Surveillance , Cholera/prevention & control , Haiti/epidemiology , Humans
3.
Influenza Other Respir Viruses ; 3(5): 215-22, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19702583

ABSTRACT

BACKGROUND: Between 5 and 25 April 2009, pandemic (H1N1) 2009 caused a substantial, severe outbreak in Mexico, and subsequently developed into the first global pandemic in 41 years. We determined the reproduction number of pandemic (H1N1) 2009 by analyzing the dynamics of the complete case series in Mexico City during this early period. METHODS: We analyzed three mutually exclusive datasets from Mexico City Distrito Federal which constituted all suspect cases from 15 March to 25 April: confirmed pandemic (H1N1) 2009 infections, non-pandemic influenza A infections and patients who tested negative for influenza. We estimated the initial reproduction number from 497 suspect cases identified prior to 20 April, using a novel contact network methodology incorporating dates of symptom onset and hospitalization, variation in contact rates, extrinsic sociological factors, and uncertainties in underreporting and disease progression. We tested the robustness of this estimate using both the subset of laboratory-confirmed pandemic (H1N1) 2009 infections and an extended case series through 25 April, adjusted for suspected ascertainment bias. RESULTS: The initial reproduction number (95% confidence interval range) for this novel virus is 1.51 (1.32-1.71) based on suspected cases and 1.43 (1.29-1.57) based on confirmed cases before 20 April. The longer time series (through 25 April) yielded a higher estimate of 2.04 (1.84-2.25), which reduced to 1.44 (1.38-1.51) after correction for ascertainment bias. CONCLUSIONS: The estimated transmission characteristics of pandemic (H1N1) 2009 suggest that pharmaceutical and non-pharmaceutical mitigation measures may appreciably limit its spread prior the development of an effective vaccine.


Subject(s)
Disease Outbreaks , Influenza A Virus, H1N1 Subtype/pathogenicity , Influenza, Human/transmission , Pandemics , Contact Tracing , Epidemiologic Methods , Humans , Influenza, Human/epidemiology , Influenza, Human/physiopathology , Influenza, Human/virology , Mexico/epidemiology , North America/epidemiology
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