Lisa McGarry
ARIAD Pharmaceuticals, Inc.
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Publication
Featured researches published by Lisa McGarry.
Hepatology | 2012
Lisa McGarry; Vivek Pawar; Hemangi R. Panchmatia; Jaime L Rubin; Gary L. Davis; Zobair M. Younossi; James C. Capretta; Michael J. O'Grady; Milton C. Weinstein
Recent research has identified high hepatitis C virus (HCV) prevalence among older U.S. residents who contracted HCV decades ago and may no longer be recognized as high risk. We assessed the cost‐effectiveness of screening 100% of U.S. residents born 1946‐1970 over 5 years (birth‐cohort screening), compared with current risk‐based screening, by projecting costs and outcomes of screening over the remaining lifetime of this birth cohort. A Markov model of the natural history of HCV was developed using data synthesized from surveillance data, published literature, expert opinion, and other secondary sources. We assumed eligible patients were treated with pegylated interferon plus ribavirin, with genotype 1 patients receiving a direct‐acting antiviral in combination. The target population is U.S. residents born 1946‐1970 with no previous HCV diagnosis. Among the estimated 102 million (1.6 million chronically HCV infected) eligible for screening, birth‐cohort screening leads to 84,000 fewer cases of decompensated cirrhosis, 46,000 fewer cases of hepatocellular carcinoma, 10,000 fewer liver transplants, and 78,000 fewer HCV‐related deaths. Birth‐cohort screening leads to higher overall costs than risk‐based screening (
Vaccine | 2010
Jaime L Rubin; Lisa McGarry; David Strutton; Keith P. Klugman; Stephen I. Pelton; Kristen E. Gilmore; Milton C. Weinstein
80.4 billion versus
Human Vaccines & Immunotherapeutics | 2014
K Clements; Genevieve Meier; Lisa McGarry; Narin Pruttivarasin; Derek Misurski
53.7 billion), but yields lower costs related to advanced liver disease (
Pediatric Infectious Disease Journal | 1999
David R. Thompson; Gerry Oster; Lisa McGarry; Jerome O. Klein
31.2 billion versus
Clinical Therapeutics | 2004
Lisa McGarry; David R. Thompson
39.8 billion); birth‐cohort screening produces an incremental cost‐effectiveness ratio (ICER) of
Thrombosis Journal | 2006
Lisa McGarry; Michael Stokes; David R. Thompson
37,700 per quality‐adjusted life year gained versus risk‐based screening. Sensitivity analyses showed that reducing the time horizon during which health and economic consequences are evaluated increases the ICER; similarly, decreasing the treatment rates and efficacy increases the ICER. Model results were relatively insensitive to other inputs. Conclusion: Birth‐cohort screening for HCV is likely to provide important health benefits by reducing lifetime cases of advanced liver disease and HCV‐related deaths and is cost‐effective at conventional willingness‐to‐pay thresholds. (HEPATOLOGY 2012)
PLOS ONE | 2014
Lisa McGarry; Girishanthy Krishnarajah; Gregory Hill; Cristina Masseria; Michelle Skornicki; Narin Pruttivarasin; Bhakti Arondekar; Julie Roiz; Stephen I. Pelton; Milton C. Weinstein
The 7-valent pneumococcal conjugate vaccine (PCV7) has dramatically decreased pneumococcal disease incidence, and the 13-valent vaccine (PCV13) protects against 6 additional Streptococcus pneumoniae serotypes. A decision-analytic model was constructed to evaluate the impact of infant vaccination with PCV13 versus PCV7 on pneumococcal disease incidence and mortality as well as the incremental benefit of a serotype catch-up program. PCV13 effectiveness was extrapolated from observed PCV7 data, using assumptions regarding serotype prevalence and PCV13 protection against additional serotypes. The model predicts that PCV13 is more effective and cost saving compared with PCV7, preventing 106,000 invasive pneumococcal disease (IPD) cases and 2.9 million pneumonia cases, and saving
BMC Infectious Diseases | 2010
Jaime L Rubin; Lisa McGarry; Keith P. Klugman; David Strutton; Kristen E. Gilmore; Milton C. Weinstein
11.6 billion over a 10-year period. The serotype catch-up program would prevent an additional 12,600 IPD cases and 404,000 pneumonia cases, and save an additional
Leukemia Research | 2015
Jeffrey H. Lipton; Peter Bryden; M.K. Sidhu; Hui Huang; Lisa McGarry; Stephanie Lustgarten; Stuart Mealing; Beth Woods; J. Whelan; Neil Hawkins
737 million compared with no catch-up program.
Cancer | 2017
Franck E. Nicolini; Grzegorz W. Basak; Dong-Wook Kim; Eduardo Olavarria; Javier Pinilla-Ibarz; Jane F. Apperley; Timothy P. Hughes; Dietger Niederwieser; Michael J. Mauro; Charles Chuah; Andreas Hochhaus; Giovanni Martinelli; Maral DerSarkissian; Mei Sheng Duh; Lisa McGarry; Hagop M. Kantarjian; Jorge Cortes
To address influenza B lineage mismatch and co-circulation, several quadrivalent inactivated influenza vaccines (IIV4s) containing two type A strains and both type B lineages have recently been approved in the United States. Currently available trivalent inactivated vaccines (IIV3s) or trivalent live attenuated influenza vaccines (LAIV3s) comprise two influenza A strains and one of the two influenza B lineages that have co-circulated in the United States since 2001. The objective of this analysis was to evaluate the cost-effectiveness of a policy of universal vaccination with IIV4 vs. IIV3/LAIV3 during 1 year in the United States. On average per influenza season, IIV4 was predicted to result in 30 251 fewer influenza cases, 3512 fewer hospitalizations, 722 fewer deaths, 4812 fewer life-years lost, and 3596 fewer quality-adjusted life-years (QALYs) lost vs. IIV3/LAIV3. Using the Fluarix QuadrivalentTM (GlaxoSmithKline) prices and the weighted average IIV3/LAIV3 prices, the model predicts that the vaccination program costs would increase by