Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Saki Takahashi is active.

Publication


Featured researches published by Saki Takahashi.


PLOS Medicine | 2011

Predicting the Epidemic Sizes of Influenza A/H1N1, A/H3N2, and B: A Statistical Method

Edward Goldstein; Sarah Cobey; Saki Takahashi; Joel C. Miller; Marc Lipsitch

Using weekly influenza surveillance data from the US CDC, Edward Goldstein and colleagues develop a statistical method to predict the sizes of epidemics caused by seasonal influenza strains. This method could inform decisions about the most appropriate vaccines or drugs needed early in the influenza season.


Science | 2015

Reduced vaccination and the risk of measles and other childhood infections post-Ebola

Saki Takahashi; C. J. E. Metcalf; Matthew J. Ferrari; William J. Moss; Shaun Truelove; Andrew J. Tatem; Bryan T. Grenfell; Justin Lessler

Vaccinate children despite Ebola During the medical emergency caused by the Ebola virus outbreak in West Africa, routine childhood vaccination programs have been suspended. If vaccination is not resumed soon, there could be even more deaths. Measles is highly infectious, and outbreaks are a sign of health care systems in trouble. Using mathematical modelling, Takahashi et al. estimate that about a million children across Liberia, Sierra Leone, and Guinea are vulnerable to measles. Aggressive public health programs are vital for this region to minimize harm, not only from measles but also from polio, malaria, tuberculosis, and other childhood infections. Science, this issue p. 1240 Ebola is terrible, but childhood vaccination needs to resume in West Africa to prevent more deaths from common infections. The Ebola epidemic in West Africa has caused substantial morbidity and mortality. The outbreak has also disrupted health care services, including childhood vaccinations, creating a second public health crisis. We project that after 6 to 18 months of disruptions, a large connected cluster of children unvaccinated for measles will accumulate across Guinea, Liberia, and Sierra Leone. This pool of susceptibility increases the expected size of a regional measles outbreak from 127,000 to 227,000 cases after 18 months, resulting in 2000 to 16,000 additional deaths (comparable to the numbers of Ebola deaths reported thus far). There is a clear path to avoiding outbreaks of childhood vaccine-preventable diseases once the threat of Ebola begins to recede: an aggressive regional vaccination campaign aimed at age groups left unprotected because of health care disruptions.


PLOS Medicine | 2016

Hand, Foot, and Mouth Disease in China: Modeling Epidemic Dynamics of Enterovirus Serotypes and Implications for Vaccination.

Saki Takahashi; Qiaohong Liao; Thomas P. Van Boeckel; Weijia Xing; Junling Sun; Victor Y. Hsiao; C. Jessica E. Metcalf; Zhaorui Chang; Fengfeng Liu; Jing Zhang; Joseph T. Wu; Benjamin J. Cowling; Gabriel M. Leung; Jeremy Farrar; H. Rogier van Doorn; Bryan T. Grenfell; Hongjie Yu

Background Hand, foot, and mouth disease (HFMD) is a common childhood illness caused by serotypes of the Enterovirus A species in the genus Enterovirus of the Picornaviridae family. The disease has had a substantial burden throughout East and Southeast Asia over the past 15 y. China reported 9 million cases of HFMD between 2008 and 2013, with the two serotypes Enterovirus A71 (EV-A71) and Coxsackievirus A16 (CV-A16) being responsible for the majority of these cases. Three recent phase 3 clinical trials showed that inactivated monovalent EV-A71 vaccines manufactured in China were highly efficacious against HFMD associated with EV-A71, but offered no protection against HFMD caused by CV-A16. To better inform vaccination policy, we used mathematical models to evaluate the effect of prospective vaccination against EV-A71-associated HFMD and the potential risk of serotype replacement by CV-A16. We also extended the model to address the co-circulation, and implications for vaccination, of additional non-EV-A71, non-CV-A16 serotypes of enterovirus. Methods and Findings Weekly reports of HFMD incidence from 31 provinces in Mainland China from 1 January 2009 to 31 December 2013 were used to fit multi-serotype time series susceptible–infected–recovered (TSIR) epidemic models. We obtained good model fit for the two-serotype TSIR with cross-protection, capturing the seasonality and geographic heterogeneity of province-level transmission, with strong correlation between the observed and simulated epidemic series. The national estimate of the basic reproduction number, R 0, weighted by provincial population size, was 26.63 for EV-A71 (interquartile range [IQR]: 23.14, 30.40) and 27.13 for CV-A16 (IQR: 23.15, 31.34), with considerable variation between provinces (however, predictions about the overall impact of vaccination were robust to this variation). EV-A71 incidence was projected to decrease monotonically with higher coverage rates of EV-A71 vaccination. Across provinces, CV-A16 incidence in the post-EV-A71-vaccination period remained either comparable to or only slightly increased from levels prior to vaccination. The duration and strength of cross-protection following infection with EV-A71 or CV-A16 was estimated to be 9.95 wk (95% confidence interval [CI]: 3.31, 23.40) in 68% of the population (95% CI: 37%, 96%). Our predictions are limited by the necessarily short and under-sampled time series and the possible circulation of unidentified serotypes, but, nonetheless, sensitivity analyses indicate that our results are robust in predicting that the vaccine should drastically reduce incidence of EV-A71 without a substantial competitive release of CV-A16. Conclusions The ability of our models to capture the observed epidemic cycles suggests that herd immunity is driving the epidemic dynamics caused by the multiple serotypes of enterovirus. Our results predict that the EV-A71 and CV-A16 serotypes provide a temporary immunizing effect against each other. Achieving high coverage rates of EV-A71 vaccination would be necessary to eliminate the ongoing transmission of EV-A71, but serotype replacement by CV-A16 following EV-A71 vaccination is likely to be transient and minor compared to the corresponding reduction in the burden of EV-A71-associated HFMD. Therefore, a mass EV-A71 vaccination program of infants and young children should provide significant benefits in terms of a reduction in overall HFMD burden.


Epidemiology and Infection | 2015

Transport networks and inequities in vaccination: remoteness shapes measles vaccine coverage and prospects for elimination across Africa

C. J. E. Metcalf; Andrew J. Tatem; Ottar N. Bjørnstad; Justin Lessler; K. O'Reilly; Saki Takahashi; Felicity Cutts; Bryan T. Grenfell

SUMMARY Measles vaccination is estimated to have averted 13·8 million deaths between 2000 and 2012. Persisting heterogeneity in coverage is a major contributor to continued measles mortality, and a barrier to measles elimination and introduction of rubella-containing vaccine. Our objective is to identify determinants of inequities in coverage, and how vaccine delivery must change to achieve elimination goals, which is a focus of the WHO Decade of Vaccines. We combined estimates of travel time to the nearest urban centre (⩾50 000 people) with vaccination data from Demographic Health Surveys to assess how remoteness affects coverage in 26 African countries. Building on a statistical mapping of coverage against age and geographical isolation, we quantified how modifying the rate and age range of vaccine delivery affects national coverage. Our scenario analysis considers increasing the rate of delivery of routine vaccination, increasing the target age range of routine vaccination, and enhanced delivery to remote areas. Geographical isolation plays a key role in defining vaccine inequity, with greater inequity in countries with lower measles vaccine coverage. Eliminating geographical inequities alone will not achieve thresholds for herd immunity, indicating that changes in delivery rate or age range of routine vaccination will be required. Measles vaccine coverage remains far below targets for herd immunity in many countries on the African continent and is likely to be inadequate for achieving rubella elimination. The impact of strategies such as increasing the upper age range eligible for routine vaccination should be considered.


PLOS Medicine | 2016

Routine Pediatric Enterovirus 71 Vaccination in China: a Cost-Effectiveness Analysis

Joseph T. Wu; Mark Jit; Yaming Zheng; Kathy Leung; Weijia Xing; Juan Yang; Qiaohong Liao; Benjamin J. Cowling; Bingyi Yang; Eric H. Y. Lau; Saki Takahashi; Jeremy Farrar; Bryan T. Grenfell; Gabriel M. Leung; Hongjie Yu

Background China accounted for 87% (9.8 million/11.3 million) of all hand, foot, and mouth disease (HFMD) cases reported to WHO during 2010–2014. Enterovirus 71 (EV71) is responsible for most of the severe HFMD cases. Three EV71 vaccines recently demonstrated good efficacy in children aged 6–71 mo. Here we assessed the cost-effectiveness of routine pediatric EV71 vaccination in China. Methods and Findings We characterized the economic and health burden of EV71-associated HFMD (EV71-HFMD) in China using (i) the national surveillance database, (ii) virological surveillance records from all provinces, and (iii) a caregiver survey on the household costs and health utility loss for 1,787 laboratory-confirmed pediatric cases. Using a static model parameterized with these data, we estimated the effective vaccine cost (EVC, defined as cost/efficacy or simply the cost of a 100% efficacious vaccine) below which routine pediatric vaccination would be considered cost-effective. We performed the base-case analysis from the societal perspective with a willingness-to-pay threshold of one times the gross domestic product per capita (GDPpc) and an annual discount rate of 3%. We performed uncertainty analysis by (i) accounting for the uncertainty in the risk of EV71-HFMD due to missing laboratory data in the national database, (ii) excluding productivity loss of parents and caregivers, (iii) increasing the willingness-to-pay threshold to three times GDPpc, (iv) increasing the discount rate to 6%, and (v) accounting for the proportion of EV71-HFMD cases not registered by national surveillance. In each of these scenarios, we performed probabilistic sensitivity analysis to account for parametric uncertainty in our estimates of the risk of EV71-HFMD and the expected costs and health utility loss due to EV71-HFMD. Routine pediatric EV71 vaccination would be cost-saving if the all-inclusive EVC is below US


Vaccine | 2018

High resolution age-structured mapping of childhood vaccination coverage in low and middle income countries

C. Edson Utazi; Julia Thorley; Victor A. Alegana; Matthew J. Ferrari; Saki Takahashi; C. Jessica E. Metcalf; Justin Lessler; Andrew J. Tatem

10.6 (95% CI US


Scientific Reports | 2016

Hand, Foot, and Mouth Disease in China: Critical Community Size and Spatial Vaccination Strategies

Thomas P. Van Boeckel; Saki Takahashi; Qiaohong Liao; Weijia Xing; Shengjie Lai; Victor Y. Hsiao; Fengfeng Liu; Yaming Zheng; Zhaorui Chang; Chen Yuan; C. Jessica E. Metcalf; Hongjie Yu; Bryan T. Grenfell

9.7–US


PLOS ONE | 2011

Estimating Incidence Curves of Several Infections Using Symptom Surveillance Data

Edward Goldstein; Benjamin J. Cowling; Allison E. Aiello; Saki Takahashi; Gary King; Ying Lu; Marc Lipsitch

11.5) and would remain cost-effective if EVC is below US


Proceedings of the National Academy of Sciences of the United States of America | 2018

The seasonality of nonpolio enteroviruses in the United States: Patterns and drivers

Margarita Pons-Salort; M. Steven Oberste; Mark A. Pallansch; Glen R. Abedi; Saki Takahashi; Bryan T. Grenfell; Nicholas C. Grassly

17.9 (95% CI US


Vaccine | 2017

Demographics, epidemiology and the impact of vaccination campaigns in a measles-free world – Can elimination be maintained?

J.M. Prada; C. J. E. Metcalf; Saki Takahashi; Justin Lessler; Andrew J. Tatem; Matthew J. Ferrari

16.9–US

Collaboration


Dive into the Saki Takahashi's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Justin Lessler

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

Andrew J. Tatem

University of Southampton

View shared research outputs
Top Co-Authors

Avatar

Matthew J. Ferrari

Pennsylvania State University

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Qiaohong Liao

Chinese Center for Disease Control and Prevention

View shared research outputs
Top Co-Authors

Avatar

Weijia Xing

Chinese Center for Disease Control and Prevention

View shared research outputs
Top Co-Authors

Avatar

Yaming Zheng

Chinese Center for Disease Control and Prevention

View shared research outputs
Researchain Logo
Decentralizing Knowledge