Stephanie Donauer
Cincinnati Children's Hospital Medical Center
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Clinical Infectious Diseases | 2013
Daniel C. Payne; Julie A. Boom; Mary Allen Staat; Kathryn M. Edwards; Peter G. Szilagyi; Eileen J. Klein; Rangaraj Selvarangan; Parvin H. Azimi; Christopher J. Harrison; Mary Moffatt; Samantha H. Johnston; Leila C. Sahni; Carol J. Baker; Marcia A. Rench; Stephanie Donauer; Monica M. McNeal; James D. Chappell; Geoffrey A. Weinberg; Azadeh Tasslimi; Jacqueline E. Tate; Mary E. Wikswo; Aaron T. Curns; Iddrisu Sulemana; Slavica Mijatovic-Rustempasic; Mathew D. Esona; Michael D. Bowen; Jon R. Gentsch; Umesh D. Parashar
BACKGROUND We assessed vaccine effectiveness (VE) for RotaTeq (RV5; 3 doses) and Rotarix (RV1; 2 doses) at reducing rotavirus acute gastroenteritis (AGE) inpatient and emergency department (ED) visits in US children. METHODS We enrolled children <5 years of age hospitalized or visiting the ED with AGE symptoms from November 2009-June 2010 and from November 2010-June 2011 at 7 medical institutions. Fecal specimens were tested for rotavirus by enzyme immunoassay and genotyped. Vaccination among laboratory-confirmed rotavirus cases was compared with rotavirus-negative AGE controls. Regression models calculated VE estimates for each vaccine, age, ethnicity, genotype, and clinical setting. RESULTS RV5-specific analyses included 359 rotavirus cases and 1811 rotavirus-negative AGE controls. RV1-specific analyses included 60 rotavirus cases and 155 rotavirus-negative AGE controls. RV5 and RV1 were 84% (95% confidence interval [CI], 78%-88%) and 70% (95% CI, 39%-86%) effective, respectively, against rotavirus-associated ED visits and hospitalizations combined. By clinical setting, RV5 VE against ED and inpatient rotavirus-associated visits was 81% (95% CI, 70%-84%) and 86% (95% CI, 74%-91%), respectively. RV1 was 78% (95% CI, 46%-91%) effective against ED rotavirus disease; study power was insufficient to evaluate inpatient RV1 VE. No waning of immunity was evident during the first 4 years of life for RV5, nor during the first 2 years of life for RV1. RV5 provided genotype-specific protection against each of the predominant strains (G1P[8], G2P[4], G3P[8], G12P[8]), while RV1 VE was statistically significant for the most common genotype, G3P[8]. CONCLUSIONS Both RV5 and RV1 significantly protected against medically attended rotavirus gastroenteritis in this real-world assessment.
Pediatrics | 2011
Mary Allen Staat; Daniel C. Payne; Stephanie Donauer; Geoffrey A. Weinberg; Kathryn M. Edwards; Peter G. Szilagyi; Marie R. Griffin; Caroline B. Hall; Aaron T. Curns; Jon R. Gentsch; Shelia Salisbury; Gerry Fairbrother; Umesh D. Parashar
OBJECTIVE: To determine the vaccine effectiveness (VE) of complete and partial vaccination with the pentavalent rotavirus vaccine (RV5) in the prevention of rotavirus acute gastroenteritis (AGE) hospitalizations and emergency department visits during the first 3 rotavirus seasons after vaccine introduction. METHODS: Active, prospective population-based surveillance for AGE and acute respiratory infection (ARIs) in inpatient and emergency department settings provided subjects for a case-control evaluation of VE in 3 US counties from January 2006 through June 2009. Children with laboratory-confirmed rotavirus AGE (cases) were matched according to date of birth and onset of illness to 2 sets of controls: children with rotavirus-negative AGE and children with ARI. The main outcome measure was VE with complete (3 doses) or partial (1 or 2 doses) RV5 vaccination. RESULTS: Of age-eligible children enrolled, 18% of cases, 54% of AGE controls, and 54% of ARI controls received ≥1 dose of RV5. The VE of RV5 for 1, 2, and 3 doses against all rotavirus genotypes with the use of rotavirus-negative AGE controls was 74% (95% confidence interval [CI]: 37%–90%), 88% (95% CI: 66%–96%), and 87% (95% CI: 71%–94%), respectively, and with the use of ARI controls was 73% (95% CI: 43%–88%), 88% (95% CI: 68%–95%), and 85% (95% CI: 72%–91%), respectively. The overall VE estimates were comparable during the first and second years of life and against AGE caused by different rotavirus strains. CONCLUSION: RV5 was highly effective in preventing severe rotavirus disease, even after a partial series, with protection persisting throughout the second year of life.
JAMA Pediatrics | 2008
Peter G. Szilagyi; Gerry Fairbrother; Marie R. Griffin; Richard Hornung; Stephanie Donauer; Ardythe L. Morrow; Mekibib Altaye; Yuwei Zhu; Sandra Ambrose; Kathryn M. Edwards; Katherine A. Poehling; Geraldine Lofthus; Michol Holloway; Lyn Finelli; Marika K. Iwane; Mary Allen Staat
OBJECTIVE To measure vaccine effectiveness (VE) in preventing influenza-related health care visits among children aged 6 to 59 months during 2 consecutive influenza seasons. DESIGN Case-cohort study estimating effectiveness of inactivated influenza vaccine in preventing inpatient/outpatient visits (emergency department [ED] and outpatient clinic). We compared vaccination status of laboratory-confirmed influenza cases with a cluster sample of children from a random sample of practices in 3 counties (subcohort) during the 2003-2004 and 2004-2005 seasons. SETTING Counties encompassing Rochester, New York, Nashville, Tennessee, and Cincinnati, Ohio. PARTICIPANTS Children aged 6 to 59 months seen in inpatient/ED or outpatient clinic settings for acute respiratory illnesses and community-based subcohort comparison. Main Exposure Influenza vaccination. MAIN OUTCOME MEASURES Influenza vaccination status of cases vs subcohort using time-dependent Cox proportional hazards models to estimate VE in preventing inpatient/ED and outpatient visits. RESULTS During the 2003-2004 and 2004-2005 seasons, 165 and 80 inpatient/ED and 74 and 95 outpatient influenza cases were enrolled, while more than 4500 inpatient/ED and more than 600 outpatient subcohorts were evaluated, respectively. In bivariate analyses, cases had lower vaccination rates than subcohorts. However, significant influenza VE could not be demonstrated for any season, age, or setting after adjusting for county, sex, insurance, chronic conditions recommended for influenza vaccination, and timing of influenza vaccination (VE estimates ranged from 7%-52% across settings and seasons for fully vaccinated 6- to 59-month-olds). CONCLUSION In 2 seasons with suboptimal antigenic match between vaccines and circulating strains, we could not demonstrate VE in preventing influenza-related inpatient/ED or outpatient visits in children younger than 5 years. Further study is needed during years with good vaccine match.
Vaccine | 2010
Gerry Fairbrother; Amy Cassedy; Ismael R. Ortega-Sanchez; Peter G. Szilagyi; Kathryn M. Edwards; Noelle-Angelique Molinari; Stephanie Donauer; Diana Henderson; Sandra Ambrose; Diane Kent; Katherine A. Poehling; Geoffrey A. Weinberg; Marie R. Griffin; Caroline B. Hall; Lyn Finelli; Carolyn B. Bridges; Mary Allen Staat
This study determined direct medical costs for influenza-associated hospitalizations and emergency department (ED) visits. For 3 influenza seasons, children <5 years of age with laboratory-confirmed influenza were identified through population-based surveillance. The mean direct cost per hospitalized child was
Pediatrics | 2011
Mary Allen Staat; Marilyn Rice; Stephanie Donauer; Sheena Mukkada; Michol Holloway; Amy Cassedy; Jennifer Kelley; Shelia Salisbury
5402, with annual cost burden estimated at
Pediatrics | 2010
Katherine A. Poehling; Gerry Fairbrother; Yuwei Zhu; Stephanie Donauer; Sandra Ambrose; Kathryn M. Edwards; Mary Allen Staat; Mila M. Prill; Lyn Finelli; Norma J. Allred; Barbara Bardenheier; Peter G. Szilagyi
44 to
Pediatric Infectious Disease Journal | 2013
Michelle Dickey; Marilyn Rice; Douglas G. Kinnett; Robin Lambert; Stephanie Donauer; Michael A. Gerber; Mary Allen Staat
163 million. Factors associated with high-cost hospitalizations included intensive care unit (ICU) admission and having an underlying high-risk condition. The mean medical cost per ED visit was
Vaccine | 2010
Mary Allen Staat; Laura Patricia Stadler; Stephanie Donauer; Indi Trehan; Marilyn Rice; Shelia Salisbury
512, with annual ED cost burden estimated at
Vaccine | 2011
Mary Allen Staat; Marie R. Griffin; Stephanie Donauer; Kathryn M. Edwards; Peter G. Szilagyi; Geoffrey A. Weinberg; Caroline B. Hall; Mila M. Prill; Sandra S. Chaves; Carolyn B. Bridges; Katherine A. Poehling; Gerry Fairbrother
62 to
Vaccine | 2013
Stephanie Donauer; Daniel C. Payne; Kathryn M. Edwards; Peter G. Szilagyi; Richard Hornung; Geoffrey A. Weinberg; James D. Chappell; Caroline B. Hall; Umesh D. Parashar; Mary Allen Staat
279 million. Implementation of the current vaccination policies will likely reduce the cost burden.