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Dive into the research topics where Emily A. Burger is active.

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Featured researches published by Emily A. Burger.


PLOS ONE | 2014

Prevention of HPV-related cancers in Norway: cost-effectiveness of expanding the HPV vaccination program to include pre-adolescent boys.

Emily A. Burger; Stephen Sy; Mari Nygård; Ivar Sønbø Kristiansen; Jane J. Kim

Background Increasingly, countries have introduced female vaccination against human papillomavirus (HPV), causally linked to several cancers and genital warts, but few have recommended vaccination of boys. Declining vaccine prices and strong evidence of vaccine impact on reducing HPV-related conditions in both women and men prompt countries to reevaluate whether HPV vaccination of boys is warranted. Methods A previously-published dynamic model of HPV transmission was empirically calibrated to Norway. Reductions in the incidence of HPV, including both direct and indirect benefits, were applied to a natural history model of cervical cancer, and to incidence-based models for other non-cervical HPV-related diseases. We calculated the health outcomes and costs of the different HPV-related conditions under a gender-neutral vaccination program compared to a female-only program. Results Vaccine price had a decisive impact on results. For example, assuming 71% coverage, high vaccine efficacy and a reasonable vaccine tender price of


American Journal of Epidemiology | 2014

An Updated Natural History Model of Cervical Cancer: Derivation of Model Parameters

Nicole G. Campos; Emily A. Burger; Stephen Sy; Monisha Sharma; Mark Schiffman; Ana Cecilia Rodriguez; Allan Hildesheim; Rolando Herrero; Jane J. Kim

75 per dose, we found vaccinating both girls and boys fell below a commonly cited cost-effectiveness threshold in Norway (


Journal of the National Cancer Institute | 2017

Optimal Cervical Cancer Screening in Women Vaccinated Against Human Papillomavirus

Jane J. Kim; Emily A. Burger; Stephen Sy; Nicole G. Campos

83,000/quality-adjusted life year (QALY) gained) when including vaccine benefit for all HPV-related diseases. However, at the current market price, including boys would not be considered ‘good value for money.’ For settings with a lower cost-effectiveness threshold (


British Journal of Cancer | 2012

Cost-effectiveness of cervical cancer screening with primary human papillomavirus testing in Norway

Emily A. Burger; J Ortendahl; Stephen Sy; Ivar Sønbø Kristiansen; Jane J. Kim

30,000/QALY), it would not be considered cost-effective to expand the current program to include boys, unless the vaccine price was less than


The Lancet. Public health | 2016

Population-level impact, herd immunity, and elimination after human papillomavirus vaccination: a systematic review and meta-analysis of predictions from transmission-dynamic models

Marc Brisson; Élodie Bénard; Mélanie Drolet; Johannes A. Bogaards; Iacopo Baussano; Simopekka Vänskä; Mark Jit; Marie-Claude Boily; Megan A. Smith; Johannes Berkhof; Karen Canfell; Harrell W. Chesson; Emily A. Burger; Birgitte Freiesleben de Blasio; Sake J. de Vlas; Giorgio Guzzetta; Jan A.C. Hontelez; Johannes Horn; Martin Rudbeck Jepsen; Jane J. Kim; Fulvio Lazzarato; Suzette M. Matthijsse; Rafael T. Mikolajczyk; Andrew Pavelyev; M. Pillsbury; Leigh Anne Shafer; Stephen Tully; Hugo C. Turner; Cara Usher; Cathal Walsh

36/dose. Increasing vaccination coverage to 90% among girls was more effective and less costly than the benefits achieved by vaccinating both genders with 71% coverage. Conclusions At the anticipated tender price, expanding the HPV vaccination program to boys may be cost-effective and may warrant a change in the current female-only vaccination policy in Norway. However, increasing coverage in girls is uniformly more effective and cost-effective than expanding vaccination coverage to boys and should be considered a priority.


Annals of Internal Medicine | 2015

Inefficiencies and High-Value Improvements in U.S. Cervical Cancer Screening Practice: A Cost-Effectiveness Analysis

Jane J. Kim; Nicole G. Campos; Stephen Sy; Emily A. Burger; Jack Cuzick; Philip E. Castle; William C. Hunt; Alan G. Waxman; Cosette M. Wheeler

Mathematical models of cervical cancer have been widely used to evaluate the comparative effectiveness and cost-effectiveness of preventive strategies. Major advances in the understanding of cervical carcinogenesis motivate the creation of a new disease paradigm in such models. To keep pace with the most recent evidence, we updated a previously developed microsimulation model of human papillomavirus (HPV) infection and cervical cancer to reflect 1) a shift towards health states based on HPV rather than poorly reproducible histological diagnoses and 2) HPV clearance and progression to precancer as a function of infection duration and genotype, as derived from the control arm of the Costa Rica Vaccine Trial (2004-2010). The model was calibrated leveraging empirical data from the New Mexico Surveillance, Epidemiology, and End Results Registry (1980-1999) and a state-of-the-art cervical cancer screening registry in New Mexico (2007-2009). The calibrated model had good correspondence with data on genotype- and age-specific HPV prevalence, genotype frequency in precancer and cancer, and age-specific cancer incidence. We present this model in response to a call for new natural history models of cervical cancer intended for decision analysis and economic evaluation at a time when global cervical cancer prevention policy continues to evolve and evidence of the long-term health effects of cervical interventions remains critical.


Cancer | 2016

Racial and ethnic disparities in human papillomavirus-associated cancer burden with first-generation and second-generation human papillomavirus vaccines.

Emily A. Burger; Kyueun Lee; Mona Saraiya; Trevor D. Thompson; Harrell W. Chesson; Lauri E. Markowitz; Jane J. Kim

Background: Current US cervical cancer screening guidelines do not differentiate recommendations based on a womans human papillomavirus (HPV) vaccination status. Changes to cervical cancer screening policies in HPV‐vaccinated women should be evaluated. Methods: We utilized an individual‐based mathematical model of HPV and cervical cancer in US women to project the health benefits, costs, and harms associated with screening strategies in women vaccinated with the bivalent, quadrivalent, or nonavalent vaccine. Strategies varied by the primary screening test, including cytology, HPV, and combined cytology and HPV “cotesting”; age of screening initiation and/or switching to a new test; and interval between routine screens. Cost‐effectiveness analysis was conducted from the societal perspective to identify screening strategies that would be considered good value for money according to thresholds of


Preventive Medicine | 2015

Correlates of HPV vaccine uptake in school-based routine vaccination of preadolescent girls in Norway: A register-based study of 90,000 girls and their parents.

Bo Terning Hansen; Suzanne Campbell; Emily A. Burger; Mari Nygård

50 000 to


The Journal of Infectious Diseases | 2015

Too Late to Vaccinate? The Incremental Benefits and Cost-effectiveness of a Delayed Catch-up Program Using the 4-Valent Human Papillomavirus Vaccine in Norway

Emily A. Burger; Stephen Sy; Mari Nygård; Ivar Sønbø Kristiansen; Jane J. Kim

200 000 per quality‐adjusted life‐year (QALY) gained. Results: Among women fully vaccinated with the bivalent or quadrivalent vaccine, optimal screening strategies involved either cytology or HPV testing alone every five years starting at age 25 or 30 years, with cost‐effectiveness ratios ranging from


The Journal of Infectious Diseases | 2014

Too late to vaccinate? The incremental benefits and cost-effectiveness of a delayed catch-up program using the 4-valent HPV vaccine in Norway

Emily A. Burger; Stephen Sy; Mari Nygård; Ivar Sønbø Kristiansen; Jane J. Kim

34 680 to

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Mari Nygård

Oslo University Hospital

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Philip E. Castle

Albert Einstein College of Medicine

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Sveinung Wergeland Sørbye

University Hospital of North Norway

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