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1.
J Travel Med ; 27(3)2020 05 18.
Article de Anglais | MEDLINE | ID: mdl-32109273

RÉSUMÉ

BACKGROUND: Cruise ships carry a large number of people in confined spaces with relative homogeneous mixing. On 3 February, 2020, an outbreak of COVID-19 on cruise ship Diamond Princess was reported with 10 initial cases, following an index case on board around 21-25th January. By 4th February, public health measures such as removal and isolation of ill passengers and quarantine of non-ill passengers were implemented. By 20th February, 619 of 3700 passengers and crew (17%) were tested positive. METHODS: We estimated the basic reproduction number from the initial period of the outbreak using SEIR models. We calibrated the models with transient functions of countermeasures to incidence data. We additionally estimated a counterfactual scenario in absence of countermeasures, and established a model stratified by crew and guests to study the impact of differential contact rates among the groups. We also compared scenarios of an earlier versus later evacuation of the ship. RESULTS: The basic reproduction rate was initially 4 times higher on-board compared to the ${R}_0$ in the epicentre in Wuhan, but the countermeasures lowered it substantially. Based on the modeled initial ${R}_0$ of 14.8, we estimated that without any interventions within the time period of 21 January to 19 February, 2920 out of the 3700 (79%) would have been infected. Isolation and quarantine therefore prevented 2307 cases, and lowered the ${R}_0$ to 1.78. We showed that an early evacuation of all passengers on 3 February would have been associated with 76 infected persons in their incubation time. CONCLUSIONS: The cruise ship conditions clearly amplified an already highly transmissible disease. The public health measures prevented more than 2000 additional cases compared to no interventions. However, evacuating all passengers and crew early on in the outbreak would have prevented many more passengers and crew from infection.


Sujet(s)
Contrôle des maladies transmissibles/méthodes , Infections à coronavirus/épidémiologie , Infections à coronavirus/prévention et contrôle , Modèles statistiques , Pandémies/prévention et contrôle , Pneumopathie virale/épidémiologie , Pneumopathie virale/prévention et contrôle , Navires , Taux de reproduction de base , Betacoronavirus , COVID-19 , Humains , Incidence , Quarantaine , SARS-CoV-2
2.
Euro Surveill ; 19(8): 20718, 2014 Feb 27.
Article de Anglais | MEDLINE | ID: mdl-24602277

RÉSUMÉ

In 2012, Madeira reported its first major outbreak of dengue. To identify the origin of the imported dengue virus, we investigated the interconnectivity via air travel between dengue-endemic countries and Madeira, and compared available sequences against GenBank. There were 22,948 air travellers to Madeira in 2012, originating from twenty-nine dengue-endemic countries; 89.6% of these international travellers originated from Venezuela and Brazil. We developed an importation index that takes into account both travel volume and the extent of dengue incidence in the country of origin. Venezuela and Brazil had by far the highest importation indices compared with all other dengue-endemic countries. The importation index for Venezuela was twice as high as that for Brazil. When taking into account seasonality in the months preceding the onset of the Madeira outbreak, this index was even seven times higher for Venezuela than for Brazil during this time. Dengue sequencing shows that the virus responsible for the Madeira outbreak was most closely related to viruses circulating in Venezuela, Brazil and Columbia. Applying the importation index, Venezuela was identified as the most likely origin of importation of dengue virus via travellers to Madeira. We propose that the importation index is a new additional tool that can help to identify and anticipate the most probable country of origin for importation of dengue into currently non-endemic countries.


Sujet(s)
Virus de la dengue/isolement et purification , Dengue/épidémiologie , Épidémies de maladies/statistiques et données numériques , ARN viral/génétique , Voyage , Dengue/diagnostic , Dengue/transmission , Dengue/virologie , Virus de la dengue/génétique , Génotype , Humains , Épidémiologie moléculaire , Portugal/épidémiologie , Analyse de séquence d'ADN
3.
Clin Microbiol Infect ; 20(3): 235-41, 2014 Mar.
Article de Anglais | MEDLINE | ID: mdl-23742660

RÉSUMÉ

Hantaviruses are the causative agents of haemorrhagic fever with renal syndrome (HFRS) in Eurasia and of hantavirus cardiopulmonary syndrome (HCPS) in the Americas. The case fatality rate varies between different hantaviruses and can be up to 40%. At present, there is no specific treatment available. The hantavirus pathogenesis is not well understood, but most likely, both virus-mediated and host-mediated mechanisms are involved. The aim of the present study was to investigate the association among Puumala hantavirus (PUUV) viral RNA load, humoral immune response and disease severity in patients with HFRS. We performed a study of 105 PUUV-infected patients that were followed during the acute phase of disease and for up to 1-3 months later. Fifteen of the 105 patients (14%) were classified as having moderate/severe disease. A low PUUV-specific IgG response (p <0.05) and also a higher white blood cell count (p <0.001) were significantly associated with more severe disease. The PUUV RNA was detected in a majority of patient plasma samples up to 9 days after disease onset; however, PUUV RNA load or longevity of viraemia were not significantly associated with disease severity. We conclude that a low specific IgG response was associated with disease severity in patients with HFRS, whereas PUUV RNA load did not seem to affect the severity of HFRS. Our results raise the possibility of passive immunotherapy as a useful treatment for hantavirus-infected patients.


Sujet(s)
Fièvre hémorragique avec syndrome rénal/immunologie , Fièvre hémorragique avec syndrome rénal/virologie , Immunité humorale , Virus Puumala/immunologie , Charge virale , Adulte , Sujet âgé , Anticorps antiviraux/sang , Anticorps antiviraux/immunologie , Femelle , Fièvre hémorragique avec syndrome rénal/diagnostic , Fièvre hémorragique avec syndrome rénal/thérapie , Humains , Immunoglobuline A/sang , Immunoglobuline A/immunologie , Immunoglobuline G/sang , Immunoglobuline G/immunologie , Immunoglobuline M/sang , Immunoglobuline M/immunologie , Mâle , Adulte d'âge moyen , Virus Puumala/génétique , Indice de gravité de la maladie
4.
Epidemiol Infect ; 141(2): 412-7, 2013 Feb.
Article de Anglais | MEDLINE | ID: mdl-22651899

RÉSUMÉ

Dengue is the most frequent arboviral disease and is expanding geographically. Dengue is also increasingly being reported in travellers, in particular in travellers to Thailand. However, data to quantify the risk of travellers acquiring dengue when travelling to Thailand are lacking. Using mathematical modelling, we set out to estimate the risk of non-immune persons acquiring dengue when travelling to Thailand. The model is deterministic with stochastic parameters and assumes a Poisson distribution for the mosquitoes' biting rate and a Gamma distribution for the probability of acquiring dengue from an infected mosquito. From the force of infection we calculated the risk of dengue acquisition for travellers to Thailand arriving in a typical year (averaged over a 17-year period) in the high season of transmission. A traveller arriving in the high season of transmission and remaining for 7 days has a risk of acquiring dengue of 0·2% (95% CI 0·16-0·23), whereas the risk for travel of 15 and 30 days' duration is 0·46% (95% CI 0·41-0·50) and 0·81% (95% CI 0·76-0·87), respectively. Our data highlight that the risk of non-immune travellers acquiring dengue in Thailand is substantial. The incidence of 0·81% after a 1-month stay is similar to that reported in prospective seroconversion studies in Israeli travellers to Thailand, highlighting that our models are consistent with actual data. Risk estimates based on mathematical modelling offer more detailed information depending on various travel scenarios, and will help the travel medicine provider give better evidence-based advice for travellers to dengue-endemic countries.


Sujet(s)
Culicidae , Virus de la dengue/pathogénicité , Dengue/épidémiologie , Appréciation des risques/méthodes , Voyage , Animaux , Dengue/immunologie , Dengue/transmission , Humains , Incidence , Modèles théoriques , Études prospectives , Saisons , Processus stochastiques , Thaïlande/épidémiologie
5.
Environ Res ; 112: 218-24, 2012 Jan.
Article de Anglais | MEDLINE | ID: mdl-22226140

RÉSUMÉ

Extreme cold and heat waves, characterized by a number of cold or hot days in succession, place a strain on people's cardiovascular and respiratory systems. The increase in deaths due to these waves may be greater than that predicted by extreme temperatures alone. We examined cold and heat waves in 99 US cities for 14 years (1987-2000) and investigated how the risk of death depended on the temperature threshold used to define a wave, and a wave's timing, duration and intensity. We defined cold and heat waves using temperatures above and below cold and heat thresholds for two or more days. We tried five cold thresholds using the first to fifth percentiles of temperature, and five heat thresholds using the 95-99 percentiles. The extra wave effects were estimated using a two-stage model to ensure that their effects were estimated after removing the general effects of temperature. The increases in deaths associated with cold waves were generally small and not statistically significant, and there was even evidence of a decreased risk during the coldest waves. Heat waves generally increased the risk of death, particularly for the hottest heat threshold. Cold waves of a colder intensity or longer duration were not more dangerous. Cold waves earlier in the cool season were more dangerous, as were heat waves earlier in the warm season. In general there was no increased risk of death during cold waves above the known increased risk associated with cold temperatures. Cold or heat waves earlier in the cool or warm season may be more dangerous because of a build up in the susceptible pool or a lack of preparedness for extreme temperatures.


Sujet(s)
Changement climatique , Basse température/effets indésirables , Température élevée/effets indésirables , Mortalité/tendances , Humains , Modèles théoriques , Saisons , États-Unis/épidémiologie
7.
Eur Respir J ; 33(2): 245-51, 2009 Feb.
Article de Anglais | MEDLINE | ID: mdl-18799511

RÉSUMÉ

The present study aimed to investigate how the heat-related increase in deaths in summer and the extent of mortality displacement depend on influenza and other categories of mortality in the previous winter, which when low leaves a greater pool of susceptible individuals. Mortality data from Stockholm, Sweden, from 1990-2002 were stratified into a summer period and a winter period. A Poisson regression model was established for the daily mortality in the summer, with temperature and confounders as explanatory variables. In addition, indicators of total, respiratory, cardiovascular and influenza mortality of the winter period were incorporated as effect modifiers in the summer model, and lagged effects in strata defined by indicators were studied. A high rate of respiratory as well as cardiovascular mortality in winter reduced the heat effect the following summer, and influenza mortality tended to do so as well. The cumulative effect per degrees C increase was 0.79% below and 0.88% [corrected] above a threshold (21.3 degrees C) after a winter with low cardiovascular and respiratory mortality, but modified with -0.29% [corrected] below and -0.04% [corrected] above the threshold after a winter with high cardiovascular and respiratory mortality. The current study shows that high respiratory, cardiovascular and influenza mortality in winter leads to lower temperature effects in the following summer. It also suggests that persons for whom influenza may be fatal are often also susceptible to heat and this subgroup might, therefore, not benefit as much as expected from influenza vaccinations.


Sujet(s)
Grippe humaine/mortalité , Maladies de l'appareil respiratoire/mortalité , Sujet âgé , Pollution de l'air , Maladies cardiovasculaires/épidémiologie , Maladies cardiovasculaires/mortalité , Cause de décès , Humains , Grippe humaine/épidémiologie , Adulte d'âge moyen , Loi de Poisson , Analyse de régression , Maladies de l'appareil respiratoire/épidémiologie , Saisons , Suède , Température
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