Mary E. Wikswo
National Center for Immunization and Respiratory Diseases
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Publication
Featured researches published by Mary E. Wikswo.
The New England Journal of Medicine | 2013
Daniel C. Payne; Jan Vinjé; Peter G. Szilagyi; Kathryn M. Edwards; Mary Allen Staat; Geoffrey A. Weinberg; Caroline B. Hall; James D. Chappell; David I. Bernstein; Aaron T. Curns; Mary E. Wikswo; S. Hannah Shirley; Aron J. Hall; Benjamin A. Lopman; Umesh D. Parashar
BACKGROUND Cases of rotavirus-associated acute gastroenteritis have declined since the introduction of rotavirus vaccines, but the burden of norovirus-associated acute gastroenteritis in children remains to be assessed. METHODS We conducted active surveillance for laboratory-confirmed cases of norovirus among children younger than 5 years of age with acute gastroenteritis in hospitals, emergency departments, and outpatient clinical settings. The children resided in one of three U.S. counties during the years 2009 and 2010. Fecal specimens were tested for norovirus and rotavirus. We calculated population-based rates of norovirus-associated acute gastroenteritis and reviewed billing records to determine medical costs; these data were extrapolated to the U.S. population of children younger than 5 years of age. RESULTS Norovirus was detected in 21% of young children (278 of 1295) seeking medical attention for acute gastroenteritis in 2009 and 2010, with norovirus detected in 22% (165 of 742) in 2009 and 20% (113 of 553) in 2010 (P=0.43). The virus was also detected in 4% of healthy controls (19 of 493) in 2009. Rotavirus was identified in 12% of children with acute gastroenteritis (152 of 1295) in 2009 and 2010. The respective rates of hospitalization, emergency department visits, and outpatient visits for the norovirus were 8.6, 146.7, and 367.7 per 10,000 children younger than 5 years of age in 2009 and 5.8, 134.3, and 260.1 per 10,000 in 2010, with an estimated cost per episode of
Clinical Infectious Diseases | 2011
Daniel C. Payne; Mary Allen Staat; Kathryn M. Edwards; Peter G. Szilagyi; Geoffrey A. Weinberg; Caroline B. Hall; James D. Chappell; Aaron T. Curns; Mary E. Wikswo; Jacqueline E. Tate; Benjamin A. Lopman; Umesh D. Parashar
3,918,
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
435, and
Emerging Infectious Diseases | 2013
Aron J. Hall; Mary E. Wikswo; Karunya Manikonda; Virginia A. Roberts; Jonathan S. Yoder; L. Hannah Gould
151, respectively, in 2009. Nationally, we estimate that the average numbers of annual hospitalizations, emergency department visits, and outpatient visits due to norovirus infection in 2009 and 2010 among U.S. children in this age group exceeded 14,000, 281,000, and 627,000, respectively, with more than
The Journal of Infectious Diseases | 2013
Preeti Chhabra; Daniel C. Payne; Peter G. Szilagyi; Kathryn M. Edwards; Mary Allen Staat; S. Hannah Shirley; Mary E. Wikswo; W. Allan Nix; Xiaoyan Lu; Umesh D. Parashar; Jan Vinjé
273 million in treatment costs each year. CONCLUSIONS Since the introduction of rotavirus vaccines, norovirus has become the leading cause of medically attended acute gastroenteritis in U.S. children and is associated with nearly 1 million health care visits annually. (Funded by the Centers for Disease Control and Prevention.).
Clinical Infectious Diseases | 2011
Catherine Yen; Mary E. Wikswo; Ben Lopman; Jan Vinjé; Umesh D. Parashar; Aron J. Hall
BACKGROUND Routine rotavirus vaccination of US infants began in 2006. We conducted active, population-based surveillance for rotavirus gastroenteritis hospitalizations in 3 US counties to assess vaccine impact. METHODS Children <36 months old hospitalized with diarrhea and/or vomiting were enrolled from January through June each year during the period 2006-2009 and tested for rotavirus. Age-stratified rates of hospitalization for rotavirus infection were compared with corresponding vaccination coverage among a control group of children with acute respiratory illness. To assess direct and indirect benefits, vaccination coverage rates in the control group were multiplied by vaccine effectiveness estimates to calculate expected reductions in the rate of hospitalization for rotavirus infection. Rotavirus serotypes were compared across years. RESULTS Compared with 2006, a significant reduction in rates of hospitalization for rotavirus infection (P < .001) was observed in 2008 among all age groups. There was an 87% reduction in the 6-11-month-old age group (coverage, 77%), a 96% reduction in the 12-23-months-old age group (coverage, 46%), and a 92% reduction in the 24-35-month-old age group (coverage, 1%), which exceeded reductions expected on the basis of coverage and vaccine effectiveness estimates. Age-specific rate reductions were nearly equivalent to those expected on the basis of age-specific vaccine coverage in 2009. Predominant strains varied annually: G1P[8] (91%) in 2006; G1P[8] (45%) and G12P[8] (36%) in 2007; G1P[8] (89%) in 2008; and G3P[8] (43%), G2P[4] (34%), and G9P[8] (27%) in 2009. CONCLUSIONS Rotavirus vaccination has dramatically decreased rates of hospitalization for rotavirus infection among children in these US counties. In 2008, reductions were prominent among both vaccine-eligible age groups and older, largely unvaccinated children; the latter likely resulted from indirect protection. Although rates among age groups eligible for vaccination remained low in 2009, indirect benefits disappeared.
Journal of Medical Entomology | 2007
Mary E. Wikswo; Renjie Hu; Marco E. Metzger; Marina E. Eremeeva
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.
Journal of Medical Entomology | 2008
Mary E. Wikswo; Renjie Hu; Laura Krueger; Aaron Arugay; Keith Jones; Barry D. Hess; Stephen H. Bennett; Vicki Kramer; Marina E. Eremeeva
Implemented in 2009, the National Outbreak Reporting System provides surveillance for acute gastroenteritis outbreaks in the United States resulting from any transmission mode. Data from the first 2 years of surveillance highlight the predominant role of norovirus. The pathogen-specific transmission pathways and exposure settings identified can help inform prevention efforts.
Emerging Infectious Diseases | 2013
Eyal Leshem; Mary E. Wikswo; Leslie Barclay; Eric Brandt; William Storm; Ellen Salehi; Traci DeSalvo; Tim Davis; Amy Saupe; Ginette Dobbins; Hillary Booth; Christianne Biggs; Katie Garman; Amy M. Woron; Umesh D. Parashar; Jan Vinjé; Aron J. Hall
BACKGROUND Although rotavirus and norovirus cause nearly 40% of severe endemic acute gastroenteritis (AGE) in children <5 years of age in the United States, there are limited data on the etiologic role of other enteric viruses in this age group. METHODS We conducted active population-based surveillance in children presenting with AGE to hospitals, emergency departments, and primary care clinics in 3 US counties. Stool specimens from these children and from age-matched healthy controls collected between October 2008 and September 2009 were tested for enteric adenovirus, astrovirus, sapovirus, parechovirus, bocavirus, and aichivirus. Typing was performed by sequencing and phylogenetic analysis. RESULTS Adenovirus, astrovirus, sapovirus, parechovirus, bocavirus, and aichivirus were detected in the stool specimens of 11.8%, 4.9%, 5.4%, 4.8%, 1.4%, and 0.2% of patients with AGE and 1.8%, 3.0%, 4.2%, 4.4%, 2.4%, and 0% of healthy controls, respectively. Adenovirus (type 41), astrovirus (types 1, 2, 3, 4, and 8), sapovirus (genogroups I and II), parechovirus (types 1, 3, 4, and 5), and bocavirus (types 1, 2, and 3) were found cocirculating. CONCLUSIONS Adenovirus, astrovirus, and sapovirus infections were detected in 22.1% of the specimens from children <5 years of age who had medical visits for AGE and tested negative for rotavirus and norovirus. No causal role for parechovirus and bocavirus was found.
Clinical Infectious Diseases | 2009
Mary E. Wikswo; Nino Khetsuriani; Ashley Fowlkes; Xiaotian Zheng; Silvia Peñaranda; Natasha Verma; Stanford T. Shulman; Kanta Sircar; Christine C. Robinson; Terry Schmidt; David P. Schnurr; M. Steven Oberste
In October 2009, a new genogroup II, type 4 (GII.4) norovirus variant was identified in the United States. We collected norovirus outbreak data from 30 states to assess whether this new strain was associated with increased acute gastroenteritis activity. No increase in norovirus outbreaks was observed during the 2009-2010 winter.