Charles E. Begley
University of Texas Health Science Center at Houston
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Featured researches published by Charles E. Begley.
Epilepsia | 2011
David J. Thurman; Ettore Beghi; Charles E. Begley; Anne T. Berg; Jeffrey Buchhalter; Ding Ding; Dale C. Hesdorffer; W. Allen Hauser; Lewis E. Kazis; Rosemarie Kobau; Barbara L. Kroner; David M. Labiner; Kore Liow; Giancarlo Logroscino; Marco T. Medina; Charles R. Newton; Karen L. Parko; Angelia Paschal; Pierre-Marie Preux; Josemir W. Sander; Anbesaw W. Selassie; William H. Theodore; Torbjörn Tomson; Samuel Wiebe
Worldwide, about 65 million people are estimated to have epilepsy. Epidemiologic studies are necessary to define the full public health burden of epilepsy; to set public health and health care priorities; to provide information needed for prevention, early detection, and treatment; to identify education and service needs; and to promote effective health care and support programs for people with epilepsy. However, different definitions and epidemiologic methods complicate the tasks of these studies and their interpretations and comparisons. The purpose of this document is to promote consistency in definitions and methods in an effort to enhance future population‐based epidemiologic studies, facilitate comparison between populations, and encourage the collection of data useful for the promotion of public health. We discuss: (1) conceptual and operational definitions of epilepsy, (2) data resources and recommended data elements, and (3) methods and analyses appropriate for epidemiologic studies or the surveillance of epilepsy. Variations in these are considered, taking into account differing resource availability and needs among countries and differing purposes among studies.
Epilepsia | 2000
Charles E. Begley; Melissa Famulari; John F. Annegers; David R. Lairson; Thomas F. Reynolds; Sharon P. Coan; Stephanie Dubinsky; Michael E. Newmark; Cynthia L. Leibson; Elson L. So; Walter A. Rocca
Summary: Purpose: To provide 1995 estimates of the lifetime and annual cost of epilepsy in the United States using data from patients with epilepsy, and adjusting for the effects of comorbidities and socioeconomic conditions.
PharmacoEconomics | 2001
Charles E. Begley; John F. Annegers; Alan C. Swann; Christopher Lewis; Sharon P. Coan; William B. Schnapp; Lynda Bryant-Comstock
AbstractObjective: To develop a cost model that estimates the total and per case lifetime cost of bipolar disorder for 1998 incident cases in the US. Study design: Lifetime cost simulation model. Perspective: Societal. Methods: Age- and gender-specific incidence of bipolar disorder in 1998 was estimated by simulation based on existing prevalence data. The course of illness and mental health service cost of 6 clinically defined prognostic groups was estimated based on the research literature and the judgement of panels of experts. Excess cost of general medical care was estimated based on claims data from a large insurer. Indirect cost was projected including excess unemployment and reduced earnings reported in the National Comorbidity Survey. Comorbidity treatment and indirect cost related to alcohol (ethanol) and drug abuse was added based on a National Institute on Drug Abuse study. Results: The present value of the lifetime cost of persons with onset of bipolar disorder in 1998 was estimated at 24 billion US dollars (
Epilepsia | 1994
Charles E. Begley; John F. Annegers; David R. Lairson; Thomas F. Reynolds; W. Allen Hauser
US). Average cost per case ranged from
Epilepsia | 2002
Charles E. Begley; Ettore Beghi
US11 720 for personswith a single manic episode to
Epilepsia | 2009
Jorge G. Burneo; Nathalie Jette; William H. Theodore; Charles E. Begley; Karen L. Parko; David J. Thurman; Samuel Wiebe
US624 785 for persons with nonresponsive/chronic episodes. Conclusion: The model indicates the potential cost savings of preventing a case of bipolar disorder and underscores the importance of achieving a stable outcome in new cases to limit the economic consequences of the disorder.
Journal of Trauma-injury Infection and Critical Care | 2004
Charles E. Begley; YuChia Chang; Robert C. Wood; Arlo Weltge
Summary: A model of the clinical course of epilepsy from onset until remission or death has been developed for six prognostic groups, including survival, use and cost of medical care, and time lost from work and housekeeping. The model has been used to generate preliminary estimates of the lifetime cost of epilepsy for a cohort of persons diagnosed in 1990 in the United States. The distribution of incident cases among prognostic groups is derived from epidemiologic studies of prognosis in epilepsy. Direct cost is estimated by multiplying nationally representative unit costs by the expected type and frequency of medical care use. The latter were derived by an expert panel, based on inferences from existing literature and on their own clinical experiences. Indirect cost is estimated based on lost earnings associated with projections of restricted activity days, excess unemployment, and excess mortality. Total lifetime cost in 1990 dollars of all persons with epilepsy onset in 1990 was estimated at
Epilepsia | 2009
Charles E. Begley; Rituparna Basu; Thomas F. Reynolds; David R. Lairson; Stephanie Dubinsky; Michael E. Newmark; Forbes Barnwell; Allen Hauser; Dale C. Hesdorffer; Nora Hernandez; Steven Karceski; Tina Shih
3.0 billion, with indirect cost accounting for 62% of the total. Cost per patient ranged from
Epilepsy Research | 1999
Charles E. Begley; John F. Annegers; David R. Lairson; Thomas F. Reynolds
4,272 for persons with remission after initial diagnosis and treatment to
Journal of Health Care for the Poor and Underserved | 2006
Charles E. Begley; Rachel W. Vojvodic; Munseok Seo; Keith D. Burau
138,602 for persons with intractable and frequent seizures. Antiepileptic drug (AED) treatment is the most costly category of service. Different assumptions about the amount and type of drug administration cause major changes in overall cost estimates.