Sabrina A. Assoumou
Boston University
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Publication
Featured researches published by Sabrina A. Assoumou.
PLOS ONE | 2014
Benjamin P. Linas; Devra M. Barter; Jared A. Leff; Sabrina A. Assoumou; Joshua A. Salomon; Milton C. Weinstein; Arthur Y. Kim; Bruce R. Schackman
Background As highly effective hepatitis C virus (HCV) therapies emerge, data are needed to inform the development of interventions to improve HCV treatment rates. We used simulation modeling to estimate the impact of loss to follow-up on HCV treatment outcomes and to identify intervention strategies likely to provide good value for the resources invested in them. Methods We used a Monte Carlo state-transition model to simulate a hypothetical cohort of chronically HCV-infected individuals recently screened positive for serum HCV antibody. We simulated four hypothetical intervention strategies (linkage to care; treatment initiation; integrated case management; peer navigator) to improve HCV treatment rates, varying efficacies and costs, and identified strategies that would most likely result in the best value for the resources required for implementation. Main measures Sustained virologic responses (SVRs), life expectancy, quality-adjusted life expectancy (QALE), costs from health system and program implementation perspectives, and incremental cost-effectiveness ratios (ICERs). Results We estimate that imperfect follow-up reduces the real-world effectiveness of HCV therapies by approximately 75%. In the base case, a modestly effective hypothetical peer navigator program maximized the number of SVRs and QALE, with an ICER compared to the next best intervention of
Sexually Transmitted Diseases | 2013
Sabrina A. Assoumou; Kenneth H. Mayer; Lori Panther; Benjamin P. Linas; Jane J. Kim
48,700/quality-adjusted life year. Hypothetical interventions that simultaneously addressed multiple points along the cascade provided better outcomes and more value for money than less costly interventions targeting single steps. The 5-year program cost of the hypothetical peer navigator intervention was
AIDS | 2014
Benjamin P. Linas; Devra M. Barter; Jared A. Leff; Madeline A. DiLorenzo; Bruce R. Schackman; C. R. Horsburgh; Sabrina A. Assoumou; Joshua A. Salomon; Milton C. Weinstein; Arthur Y. Kim; Kenneth A. Freedberg
14.5 million per 10,000 newly diagnosed individuals. Conclusions We estimate that imperfect follow-up during the HCV cascade of care greatly reduces the real-world effectiveness of HCV therapy. Our mathematical model shows that modestly effective interventions to improve follow-up would likely be cost-effective. Priority should be given to developing and evaluating interventions addressing multiple points along the cascade rather than options focusing solely on single points.
Open Forum Infectious Diseases | 2014
Sabrina A. Assoumou; Wei Huang; C. R. Horsburgh; Mari-Lynn Drainoni; Benjamin P. Linas
Background Anal cancer is one of the most common cancers affecting human immunodeficiency virus (HIV)–infected male patients. Currently, there is no consensus on posttreatment surveillance of HIV-infected men who have sex with men (MSM) who have been treated for high-grade intraepithelial neoplasia (HGAIN), the likely precursor to anal cancer. Objective The aim of this study was to assess the cost-effectiveness of a range of strategies for anal cancer surveillance in HIV-infected MSM previously treated for HGAIN. Methods We developed a Markov model to project quality-adjusted life expectancy, lifetime costs, and the incremental cost-effectiveness ratios of 5 strategies using high-resolution anoscopy (HRA) and/or anal cytology testing after treatment. Results Performing HRA alone at 6- and 12-month visits was associated with a cost-effectiveness ratio of
Clinical Infectious Diseases | 2018
Sabrina A. Assoumou; Abriana Tasillo; Jared A. Leff; Bruce R. Schackman; Mari-Lynn Drainoni; C. Robert Horsburgh; M. Anita Barry; Craig Regis; Arthur Y. Kim; Alison Marshall; Sheel Saxena; Peter C. Smith; Benjamin P. Linas
4446 per quality-adjusted life year gained. In comparison, combined HRA and anal cytology at both visits provided greater health benefit at a cost of
Open Forum Infectious Diseases | 2016
Benjamin P. Linas; Jake R. Morgan; Mai T. Pho; Jared A. Leff; Bruce R. Schackman; C. Robert Horsburgh; Sabrina A. Assoumou; Joshua A. Salomon; Milton C. Weinstein; Kenneth A. Freedberg; Arthur Y. Kim
17,373 per quality-adjusted life year gained. Our results were robust over a number of scenarios and assumptions including patients’ level of immunosuppression. Results were most sensitive to test characteristics and cost, as well as progression rates of normal to HGAIN and HGAIN to cancer. Conclusions Our results suggest that combined HRA and anal cytology at 6 and 12 months may be a cost-effective surveillance strategy after treatment of HGAIN in HIV-infected MSM.
Journal of Viral Hepatitis | 2016
Kraig L. Young; Wei Huang; C. R. Horsburgh; Benjamin P. Linas; Sabrina A. Assoumou
Objectives:To evaluate the effectiveness and cost–effectiveness of strategies to treat hepatitis C virus (HCV) in HIV/HCV coinfected patients in the United States. Participants:Simulated cohort of HIV/HCV genotype 1 coinfected, noncirrhotic, HCV treatment-naive individuals enrolled in US HIV guideline-concordant care. Design/interventions:Monte Carlo simulation comparing five strategies: no treatment; dual therapy with pegylated-interferon (PEG) and ribavirin (RBV); ‘PEG/RBV trial’ in which all patients initiate dual therapy and switch to triple therapy upon failure; ‘IL28B triage’ in which patients initiate either dual therapy or triple therapy based on their IL28B allele type; and PEG/RBV and telaprevir (TPV) triple therapy. Sensitivity analyses varied efficacies and costs and included a scenario with interferon (IFN)-free therapy. Main measures:Sustained virologic response (SVR), life expectancy, discounted quality-adjusted life expectancy (QALE), lifetime medical costs, and incremental cost-effectiveness ratios (ICERs) in
Journal of Health Care for the Poor and Underserved | 2017
Sabrina A. Assoumou; Wei Huang; Kraig L. Young; C. Robert Horsburgh; Benjamin P. Linas
/quality-adjusted life years (QALY) gained. Results:‘PEG/RBV trial,’ ‘IL28B triage,’ and ‘triple therapy’ each provided 72% SVR and extended QALE compared with ‘dual therapy’ by 1.12, 1.14, and 1.15 QALY, respectively. The ICER of ‘PEG/RBV trial’ compared with ‘dual therapy’ was
Journal of Health Care for the Poor and Underserved | 2014
Sabrina A. Assoumou; Wei Huang; C. Robert Horsburgh; Benjamin P. Linas
37 500/QALY. ‘IL28B triage’ and ‘triple therapy’ provided little benefit compared with ‘PEG/RBV trial,’ and both had ICERs exceeding
International Journal of Std & Aids | 2013
Sabrina A. Assoumou; Lori Panther; Kenneth H. Mayer
300 000/QALY. In sensitivity analyses, IFN-free treatment attaining 90% SVR had an ICER less than