Colin W. Shepard
Centers for Disease Control and Prevention
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Publication
Featured researches published by Colin W. Shepard.
Lancet Infectious Diseases | 2005
Colin W. Shepard; Lyn Finelli; Miriam J. Alter
Hepatitis C virus (HCV) is a major cause of liver disease worldwide and a potential cause of substantial morbidity and mortality in the future. The complexity and uncertainty related to the geographic distribution of HCV infection and chronic hepatitis C, determination of its associated risk factors, and evaluation of cofactors that accelerate its progression, underscore the difficulties in global prevention and control of HCV. Because there is no vaccine and no post-exposure prophylaxis for HCV, the focus of primary prevention efforts should be safer blood supply in the developing world, safe injection practices in health care and other settings, and decreasing the number of people who initiate injection drug use.
Emerging Infectious Diseases | 2002
Colin W. Shepard; Montse Soriano-Gabarró; Elizabeth R. Zell; James A. Hayslett; Susan L. Lukacs; Susan T. Goldstein; Stephanie Factor; Joshua D. Jones; Renee Ridzon; Ian T. Williams; Nancy E. Rosenstein
We collected data during postexposure antimicrobial prophylaxis campaigns and from a prophylaxis program evaluation 60 days after start of antimicrobial prophylaxis involving persons from six U.S. sites where Bacillus anthracis exposures occurred. Adverse events associated with antimicrobial prophylaxis to prevent anthrax were commonly reported, but hospitalizations and serious adverse events as defined by Food and Drug Administration criteria were rare. Overall adherence during 60 days of antimicrobial prophylaxis was poor (44%), ranging from 21% of persons exposed in the Morgan postal facility in New York City to 64% of persons exposed at the Brentwood postal facility in Washington, D.C. Adherence was highest among participants in an investigational new drug protocol to receive additional antibiotics with or without anthrax vaccine—a likely surrogate for anthrax risk perception. Adherence of <60 days was not consistently associated with adverse events.
Pediatrics | 2005
Colin W. Shepard; Ismael R. Ortega-Sanchez; R. Douglas Scott; Nancy E. Rosenstein
Context. The US Food and Drug Administration approved a meningococcal conjugate A/C/Y/W-135 vaccine (MCV-4) for use in persons aged 11 to 55 years in January, 2005; licensure for use in younger age groups is expected in 2 to 4 years. Objective. To evaluate and compare the projected health and economic impact of MCV-4 vaccination of US adolescents, toddlers, and infants. Design. Cost-effectiveness analysis from a societal perspective based on data from Active Bacterial Core Surveillance (ABCs) and other published and unpublished sources. Sensitivity analyses in which key input measures were varied over plausible ranges were performed. Setting and Patients. A hypothetical 2003 US population cohort of children 11 years of age and a 2003 US birth cohort. Interventions. Hypothetical routine vaccination of adolescents (1 dose at 11 years of age), toddlers (1 dose at 1 year of age), and infants (3 doses at 2, 4, and 6 months of age). Each vaccination scenario was compared with a “no-vaccination” scenario. Main Outcome Measures. Meningococcal cases and deaths prevented, cost per case prevented, cost per life-year saved, and cost per quality-adjusted life-year saved. Results. Routine MCV-4 vaccination of US adolescents (11 years of age) would prevent 270 meningococcal cases and 36 deaths in the vaccinated cohort over 22 years, a decrease of 46% in the expected burden of disease. Before program costs are counted, adolescent vaccination would reduce direct disease costs by
Clinical Infectious Diseases | 2004
Colin W. Shepard; Maryam I. Daneshvar; Robyn M. Kaiser; David A. Ashford; David Lonsway; Jean B. Patel; Roger E. Morey; Jean G. Jordan; Robbin S. Weyant; Marc Fischer
18 million and decrease productivity losses by
Journal of the American Geriatrics Society | 2006
Lauri A. Hicks; Colin W. Shepard; Phyllis H. Britz; Dean D. Erdman; Marc Fischer; Brendan Flannery; Angela J. Peck; Xiaoyan Lu; W. Lanier Thacker; Robert F. Benson; Maria L. Tondella; Mària Moll; Cynthia G. Whitney; Larry J. Anderson; Daniel R. Feikin
50 million. At a cost per vaccination (average public-private price per dose plus administration fees) of
The Journal of Infectious Diseases | 2005
Joseph J. Amon; Rose A. Devasia; Guoliang Xia; Omana V. Nainan; Stephanie Hall; Brian Lawson; Julie S. Wolthuis; Pia D.M. MacDonald; Colin W. Shepard; Ian T. Williams; Gregory L. Armstrong; Julie A. Gabel; Paul C. Erwin; Lorinda Sheeler; Wendi L. Kuhnert; Priti Patel; Gilberto Vaughan; Andre Weltman; Allen S. Craig; Beth P. Bell; Anthony E. Fiore
82.50, adolescent vaccination would cost society
Pediatric Infectious Disease Journal | 2005
Colin W. Shepard; Lyn Finelli; Anthony E. Fiore; Beth P. Bell
633000 per meningococcal case prevented and
Emerging Infectious Diseases | 2002
Marc S. Traeger; Steven Wiersma; Nancy E. Rosenstein; Jean M. Malecki; Colin W. Shepard; Pratima L. Raghunathan; Segaran P. Pillai; Tanja Popovic; Conrad P. Quinn; Richard F. Meyer; Sharif R. Zaki; Savita Kumar; Sherrie M. Bruce; James J. Sejvar; Peter M. Dull; Bruce C. Tierney; Joshua D. Jones; Bradley A. Perkins
121000 per life-year saved. Key variables influencing results were disease incidence, case-fatality ratio, and cost per vaccination. The cost-effectiveness of toddler vaccination is essentially equivalent to adolescent vaccination, whereas infant vaccination would be much less cost-effective. Conclusions. Routine MCV-4 vaccination of US children would reduce the burden of disease in vaccinated cohorts but at a relatively high net societal cost. The projected cost-effectiveness of adolescent vaccination approaches that of recently adopted childhood vaccines under conditions of above-average meningococcal disease incidence or at a lower cost per vaccination.
Clinical Infectious Diseases | 2008
Ismael R. Ortega Sanchez; Martin I. Meltzer; Colin W. Shepard; Elizabeth R. Zell; Mark L. Messonnier; Oleg O. Bilukha; Xinzhi Zhang; David S. Stephens; Nancy E. Messonnier
Bordetella holmesii is a recently identified gram-negative bacterial species associated with bacteremia, endocarditis, and respiratory illness, mainly in immunocompromised patients. From isolates submitted to the Centers for Disease Control and Prevention from 1983 through 2000 for further identification, we identified 30 patients with B. holmesii bacteremia. Of the 26 patients for whom data were available, 22 (85%) were anatomically or functionally asplenic. In 25 (96%) of the 26 patients, B. holmesii was the only organism isolated from blood samples, and 14 patients (54%) had B. holmesii recovered from > or =2 blood cultures. The clinical course of the infection was generally characterized by a nonspecific febrile illness. Twenty-one patients (81%) were treated with various antimicrobial agents, and 20 (77%) were admitted to the hospital. There were no deaths. Our findings support evidence that B. holmesii may be a true pathogen associated with bacteremia among asplenic patients.
Pediatric Infectious Disease Journal | 2003
Colin W. Shepard; Nancy E. Rosenstein; Marc Fischer
Objectives: To characterize illness and identify the etiology for two nursing home outbreaks of respiratory illness.
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National Center for Immunization and Respiratory Diseases
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