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Dive into the research topics where Kathleen E. Wirth is active.

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Featured researches published by Kathleen E. Wirth.


Pediatrics | 2007

Cost-effectiveness of routine childhood vaccination for hepatitis A in the United States.

David B. Rein; Katherine A. Hicks; Kathleen E. Wirth; Kaafee Billah; Lyn Finelli; Anthony E. Fiore; Thomas J. Hoerger; Beth P. Bell; Gregory L. Armstrong

OBJECTIVES. Economic analysis is an important component in formulating national policy. We evaluated the economic impact of hepatitis A vaccination of all US children ages 12 to 23 months as compared with no vaccination and with current implementation of the preexisting (issued in 1999), regional policy. METHODS. We developed a Markov model of hepatitis A that followed a single cohort from birth in 2005 through death or age 95 years. From the societal perspective, the model compared the outcomes that resulted from routine vaccination at age 1 year to 2 scenarios: no hepatitis A vaccination and hepatitis A vaccination at levels observed in 2003 under the preexisting policy. We evaluated the economic impact of vaccination nationwide, in areas where vaccination was already recommended, and in areas where no previous recommendation existed. RESULTS. Without childhood vaccination, the ∼4 million children in the 2005 birth cohort would be expected over their lifetimes to have 199000 hepatitis A virus infections, including 74000 cases of acute hepatitis A and 82 deaths, resulting in


The Lancet HIV | 2016

Botswana's progress toward achieving the 2020 UNAIDS 90-90-90 antiretroviral therapy and virological suppression goals: a population-based survey

Tendani Gaolathe; Kathleen E. Wirth; Molly Pretorius Holme; Joseph Makhema; Sikhulile Moyo; Unoda Chakalisa; Etienne Kadima Yankinda; Quanhong Lei; Mompati Mmalane; Vlad Novitsky; Lillian Okui; Erik van Widenfelt; Kathleen M. Powis; Nealia Khan; Kara Bennett; Hermann Bussmann; Scott Dryden-Peterson; Refeletswe Lebelonyane; Shenaaz El-Halabi; Lisa A. Mills; Tafireyi Marukutira; Rui Wang; Eric J. Tchetgen Tchetgen; Victor DeGruttola; Max Essex; Shahin Lockman

134 million in hepatitis A–related medical costs and productivity losses. Compared with no vaccination, routine vaccination at age 1 year would prevent 172000 infections, at a cost of


Ophthalmology | 2009

The cost-effectiveness of routine office-based identification and subsequent medical treatment of primary open-angle glaucoma in the United States.

David B. Rein; John S. Wittenborn; Paul P. Lee; Kathleen E. Wirth; Stephen W. Sorensen; Thomas J. Hoerger; Jinan B. Saaddine

28000 per quality-adjusted life year saved. Compared with maintaining the levels of hepatitis A vaccination under the preexisting regional policy, routine vaccination at age 1 year would prevent an additional 112000 infections, at a cost of


Pediatrics | 2007

The Economics of Routine Childhood Hepatitis A Immunization in the United States: The Impact of Herd Immunity

Gregory L. Armstrong; Kaafee Billah; David B. Rein; Katherine A. Hicks; Kathleen E. Wirth; Beth P. Bell

45000 per quality-adjusted life year saved. CONCLUSIONS. The cost-effectiveness of nationwide hepatitis A vaccination compared with no vaccination, and the incremental cost-effectiveness of this recommendation compared with preexisting recommendations, is similar to that of other accepted public health interventions. In October 2005, the Advisory Committee on Immunization Practices recommended extending hepatitis A immunization to all US children ages 12 to 23 months.


Journal of Adolescent Health | 2008

The Influence of Adolescent Body Mass Index, Physical Activity, and Tobacco Use on Blood Pressure and Cholesterol in Young Adulthood

Carol A. Ford; James Nonnemaker; Kathleen E. Wirth

BACKGROUND HIV programmes face challenges achieving high rates of HIV testing and treatment needed to optimise health and to reduce transmission. We used data from the Botswana Combination Prevention Project study survey to assess Botswanas progress toward achieving UNAIDS targets for 2020: 90% of all people living with HIV knowing their status, 90% of these receiving sustained antiretroviral therapy (ART), and 90% of those having virological suppression (90-90-90). METHODS A population-based sample of individuals was recruited and interviewed in 30 rural and periurban communities from Oct 30, 2013, to Nov 24, 2015, as part of a large, ongoing community-randomised trial designed to assess the effect of a combination prevention package on HIV incidence. A random sample of about 20% of households in each community was selected. Consenting household residents aged 16-64 years who were Botswana citizens or spouses of citizens responded to a questionnaire and had blood drawn for HIV testing in the absence of documentation of positive HIV status. Viral load testing was done in all HIV-infected participants, irrespective of treatment status. We used modified Poisson generalised estimating equations to obtain prevalence ratios, corresponding Huber robust SEs, and 95% Wald CIs to examine associations between individual sociodemographic factors and a binary outcome indicating achievement of the three individual and combined overall 90-90-90 targets. The study is registered at ClinicalTrials.gov, number NCT01965470. FINDINGS 81% of enumerated eligible household members took part in the survey (10% refused and 9% were absent). Among 12 610 participants surveyed, 3596 (29%) were infected with HIV, and 2995 (83·3%, 95% CI 81·4-85·2) of these individuals already knew their HIV status. Among those who knew their HIV status, 2617 (87·4%, 95% CI 85·8-89·0) were receiving ART (95% of those eligible by national guidelines, and 73% of all infected people). Of the 2609 individuals receiving ART with a viral load measurement, 2517 (96·5%, 95% CI 96·0-97·0) had viral load of 400 copies per mL or less. Overall, 70·2% (95% CI 67·5-73·0) of HIV-infected people had virological suppression, close to the UNAIDS target of 73%. INTERPRETATION UNAIDS 90-90-90 targets are achievable even in resource-constrained settings with high HIV burden. FUNDING US Presidents Emergency Plan for AIDS Relief through the Centers for Disease Control and Prevention.


JAMA Pediatrics | 2011

Gender-based disparities in infant and child mortality based on maternal exposure to spousal violence: The heavy burden borne by Indian girls

Jay G. Silverman; Michele R. Decker; Debbie M. Cheng; Kathleen E. Wirth; Niranjan Saggurti; Heather L. McCauley; Kathryn L. Falb; Balaiah Donta; Anita Raj

OBJECTIVE To estimate the incremental cost-effectiveness of routine glaucoma assessment and treatment under current eye care visit and treatment patterns and different levels of treatment effectiveness (from randomized trials). DESIGN We compared the costs and benefits of routine glaucoma assessment and treatment compared with no treatment using conservative and optimistic assumptions regarding treatment efficacy and including and excluding prediagnostic assessment costs. PARTICIPANTS AND CONTROLS Computer simulation of 20 million people followed from age 50 years to death or age 100 years. METHODS With the use of a computer model, we simulated glaucoma incidence, natural progression, diagnosis, and treatment. We defined glaucoma incidence conservatively as a mean deviation of -4 decibels (dB) on visual field testing in either eye for all diagnoses to be both clinically meaningful and unambiguous. We simulated the annual probability of subsequent progression and the quantity of visual field lost when progression occurred. MAIN OUTCOME MEASURES Visual field loss, ophthalmologic and nursing home costs, quality-adjusted life years (QALYs), cost per QALY gained, and cost per year of sight gained. Costs and QALYs were discounted to 2005 values using a 3% rate. RESULTS Compared with no treatment and when including diagnostic assessment costs, the incremental cost-effectiveness of routine assessment and treatment was


Infection Control and Hospital Epidemiology | 2011

Moving CLABSI Prevention beyond the Intensive Care Unit: Risk Factors in Pediatric Oncology Patients

Matthew S. Kelly; Margaret Conway; Kathleen E. Wirth; Gail Potter-Bynoe; Amy L. Billett; Thomas J. Sandora

46,000 per QALY gained, assuming conservative treatment efficacy, and


Journal of Acquired Immune Deficiency Syndromes | 2013

A randomized trial of Mogen clamp versus Plastibell for neonatal male circumcision in Botswana.

Rebeca M. Plank; Nnamdi Ndubuka; Kathleen E. Wirth; Janet T. Mwambona; Poloko Kebaabetswe; Barbara Bassil; Chiapo Lesetedi; Jane Magetse; Maggie Nkgau; Joseph Makhema; Mompati Mmalane; Tracy Creek; Kathleen M. Powis; Roger L. Shapiro; Shahin Lockman

28,000 per QALY gained, assuming optimistic treatment efficacy. Compared with no treatment and when excluding diagnostic assessment costs, the incremental cost-effectiveness of routine assessment and treatment was


American Journal of Epidemiology | 2013

How Does Sex Trafficking Increase the Risk of HIV Infection? An Observational Study From Southern India

Kathleen E. Wirth; Eric J. Tchetgen Tchetgen; Jay G. Silverman; Megan Murray

20,000 per QALY gained, assuming conservative treatment efficacy, and


Journal of the Pediatric Infectious Diseases Society | 2015

Treatment Failures and Excess Mortality Among HIV-Exposed, Uninfected Children With Pneumonia

Matthew S. Kelly; Kathleen E. Wirth; Andrew P. Steenhoff; Coleen K. Cunningham; Tonya Arscott-Mills; Sefelani Boiditswe; Mohamed Z. Patel; Samir S. Shah; Rodney Finalle; Ishmael Makone; Kristen A. Feemster

11,000 per QALY gained, assuming optimistic treatment efficacy. The cost-effectiveness was most sensitive to the treatment costs and the value of QALY losses assigned to visual field losses. CONCLUSIONS Glaucoma treatment was highly cost-effective when the costs of diagnostic assessments were excluded or when we assumed optimistic treatment efficacy. The cost was reasonable and in line with other health interventions even when diagnostic assessment costs were included and assuming conservative efficacy. FINANCIAL DISCLOSURE(S) The author(s) have no proprietary or commercial interest in any materials discussed in this article.

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Andrew P. Steenhoff

Children's Hospital of Philadelphia

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