Jason Kessler
New York University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Jason Kessler.
PLOS ONE | 2013
Jason Kessler; Julie E. Myers; Kimberly Nucifora; Nana Mensah; Alexis Kowalski; Monica Sweeney; Christopher Toohey; Amin Khademi; Colin W. Shepard; Blayne Cutler; R. Scott Braithwaite
Background New York City (NYC) remains an epicenter of the HIV epidemic in the United States. Given the variety of evidence-based HIV prevention strategies available and the significant resources required to implement each of them, comparative studies are needed to identify how to maximize the number of HIV cases prevented most economically. Methods A new model of HIV disease transmission was developed integrating information from a previously validated micro-simulation HIV disease progression model. Specification and parameterization of the model and its inputs, including the intervention portfolio, intervention effects and costs were conducted through a collaborative process between the academic modeling team and the NYC Department of Health and Mental Hygiene. The model projects the impact of different prevention strategies, or portfolios of prevention strategies, on the HIV epidemic in NYC. Results Ten unique interventions were able to provide a prevention benefit at an annual program cost of less than
The Lancet Global Health | 2014
Daniel Keebler; Paul Revill; Scott Braithwaite; Andrew N. Phillips; Nello Blaser; Annick Borquez; Valentina Cambiano; Andrea Ciaranello; Janne Estill; Richard Gray; Andrew Hill; Olivia Keiser; Jason Kessler; Nicolas A. Menzies; Kimberly Nucifora; Luisa Salazar Vizcaya; Simon Walker; Alex Welte; Philippa Easterbrook; Meg Doherty; Gottfried Hirnschall; Timothy B. Hallett
360,000, the threshold for consideration as a cost-saving intervention (because of offsets by future HIV treatment costs averted). An optimized portfolio of these specific interventions could result in up to a 34% reduction in new HIV infections over the next 20 years. The cost-per-infection averted of the portfolio was estimated to be
AIDS | 2014
Jason Kessler; Julie E. Myers; Kimberly Nucifora; Nana Mensah; Christopher Toohey; Amin Khademi; Blayne Cutler; Scott Braithwaite
106,378; the total cost was in excess of
Alcoholism: Clinical and Experimental Research | 2014
R. Scott Braithwaite; Kimberly Nucifora; Jason Kessler; Christopher Toohey; Sherry M. Mentor; Lauren Uhler; Mark S. Roberts; Kendall Bryant
2 billion (over the 20 year period, or approximately
AIDS | 2014
Ronald Scott Braithwaite; Kimberly Nucifora; Christopher Toohey; Jason Kessler; Lauren M. Uhler; Sherry M. Mentor; Daniel Keebler; Timothy B. Hallett
100 million per year, on average). The cost-savings of prevented infections was estimated at more than
Systematic Reviews | 2014
Holly Hagan; Joshua Neurer; Ashly E. Jordan; Don C. Des Jarlais; Jennifer Wu; Kirk Dombrowski; Bilal Khan; Ronald Scott Braithwaite; Jason Kessler
5 billion (or approximately
Medicine | 2017
Anik Patel; Jason Kessler; R. Scott Braithwaite; Kimberly Nucifora; Harsha Thirumurthy; Qinlian Zhou; Richard Lester; Carlo A. Marra
250 million per year, on average). Conclusions Optimal implementation of a portfolio of evidence-based interventions can have a substantial, favorable impact on the ongoing HIV epidemic in NYC and provide future cost-saving despite significant initial costs.
Alcoholism: Clinical and Experimental Research | 2015
Jason Kessler; Kelly V. Ruggles; Anik Patel; Kimberly Nucifora; Lingfeng Li; Mark S. Roberts; Kendall Bryant; R. Scott Braithwaite
BACKGROUND WHOs 2013 revisions to its Consolidated Guidelines on antiretroviral drugs recommend routine viral load monitoring, rather than clinical or immunological monitoring, as the preferred monitoring approach on the basis of clinical evidence. However, HIV programmes in resource-limited settings require guidance on the most cost-effective use of resources in view of other competing priorities such as expansion of antiretroviral therapy coverage. We assessed the cost-effectiveness of alternative patient monitoring strategies. METHODS We evaluated a range of monitoring strategies, including clinical, CD4 cell count, and viral load monitoring, alone and together, at different frequencies and with different criteria for switching to second-line therapies. We used three independently constructed and validated models simultaneously. We estimated costs on the basis of resource use projected in the models and associated unit costs; we quantified impact as disability-adjusted life years (DALYs) averted. We compared alternatives using incremental cost-effectiveness analysis. FINDINGS All models show that clinical monitoring delivers significant benefit compared with a hypothetical baseline scenario with no monitoring or switching. Regular CD4 cell count monitoring confers a benefit over clinical monitoring alone, at an incremental cost that makes it affordable in more settings than viral load monitoring, which is currently more expensive. Viral load monitoring without CD4 cell count every 6-12 months provides the greatest reductions in morbidity and mortality, but incurs a high cost per DALY averted, resulting in lost opportunities to generate health gains if implemented instead of increasing antiretroviral therapy coverage or expanding antiretroviral therapy eligibility. INTERPRETATION The priority for HIV programmes should be to expand antiretroviral therapy coverage, firstly at CD4 cell count lower than 350 cells per μL, and then at a CD4 cell count lower than 500 cells per μL, using lower-cost clinical or CD4 monitoring. At current costs, viral load monitoring should be considered only after high antiretroviral therapy coverage has been achieved. Point-of-care technologies and other factors reducing costs might make viral load monitoring more affordable in future. FUNDING Bill & Melinda Gates Foundation, WHO.
British Journal of Ophthalmology | 2016
Elisabeth J. Cohen; Jason Kessler
Objective:To compare the value and effectiveness of different prioritization strategies of pre-exposure prophylaxis (PrEP) in New York City (NYC). Design:Mathematical modelling utilized as clinical trial is not feasible. Methods:Using a model accounting for both sexual and parenteral transmission of HIV, we compare different PrEP prioritization strategies (PPS) with two scenarios – no PrEP and PrEP for all susceptible at-risk individuals. The PPS included PrEP for all MSM, only high-risk MSM, high-risk heterosexuals, and IDUs, and all combinations of these four strategies. Outcomes included HIV infections averted, and incremental cost-effectiveness (per-infection averted) ratios. Initial assumptions regarding PrEP included a 44% reduction in HIV transmission, 50% uptake in the prioritized population and an annual cost per person of
Value in Health | 2015
Jason Kessler; Kimberly Nucifora; Lingfeng Li; Lauren Uhler; Scott Braithwaite
9762. Sensitivity analyses on key parameters were conducted. Results:Prioritization to all MSM results in a 19% reduction in new HIV infections. Compared with PrEP for all persons at-risk, this PPS retains 79% of the preventive effect at 15% of the total cost. PrEP prioritized to only high-risk MSM results in a reduction in new HIV infections of 15%. This PPS retains 60% of the preventive effect at 6% of the total cost. There are diminishing returns when PrEP utilization is expanded beyond this group. Conclusion:PrEP implementation is relatively cost-inefficient under our initial assumptions. Our results suggest that PrEP should first be promoted among MSM who are at particularly high risk of HIV acquisition. Further expansion beyond this group may be cost-effective, but is unlikely to be cost-saving.