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Dive into the research topics where Aaron T. Fleischauer is active.

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Featured researches published by Aaron T. Fleischauer.


The American Journal of Medicine | 2003

Risk of malignancy in patients with celiac disease

Peter H. Green; Aaron T. Fleischauer; Govind Bhagat; Rishi K. Goyal; Bana Jabri; Alfred I. Neugut

PURPOSE Studies from Europe have demonstrated an increased risk of malignancy, especially non-Hodgkins lymphoma, in patients with celiac disease. However, there are no data on the risk for similar patients in the United States. Our aim was to estimate the risk of malignancy in a cohort of patients with celiac disease compared with the general U.S. population and to determine if a gluten-free diet is protective. METHODS Patients with celiac disease seen between July 1981 and January 2000 at a referral center were included. Standardized morbidity ratios (SMRs) (ratio of observed to expected) and corresponding 95% confidence intervals (CI) were calculated, using data from the National Cancer Institutes Surveillance, Epidemiology, and End Results Program. RESULTS Forty-three (11%) of 381 celiac disease patients had a diagnosis of cancer; 9 were after the diagnosis of celiac disease, 7 were simultaneous (during same month or admission), and 27 were before the diagnosis. The standardized morbidity ratio for all cancers combined was 1.5 (95% CI: 0.3 to 7.5), with significantly increased values for small bowel cancer (SMR = 34; 95% CI: 24 to 42), esophageal cancer (SMR = 12; 95% CI: 6.5 to 21), non-Hodgkins lymphoma (SMR = 9.1; 95% CI: 4.7 to 13), and melanoma (SMR = 5.0; 95% CI: 2.1 to 12). Following the diagnosis of celiac disease, patients were at increased risk of non-Hodgkins lymphoma only (SMR = 6.2; 95% CI: 2.9 to 14), despite adherence to a gluten-free diet. The non-Hodgkins lymphoma included both T-cell and B-cell types and occurred in both gastrointestinal (n = 5) and extraintestinal sites (n = 4). CONCLUSION In this cohort of patients with celiac disease, we observed increased risks of small intestinal adenocarcinoma, esophageal cancer, melanoma, and non-Hodgkins lymphoma. The risk of non-Hodgkins lymphoma persisted despite a gluten-free diet.


Journal of Clinical Oncology | 2002

Use of Adjuvant Chemotherapy and Radiation Therapy for Rectal Cancer Among the Elderly: A Population-Based Study

Alfred I. Neugut; Aaron T. Fleischauer; Vijaya Sundararajan; Nandita Mitra; Daniel F. Heitjan; Judith S. Jacobson; Victor R. Grann

PURPOSE Combined adjuvant fluorouracil (5-FU)-based chemotherapy with radiation is now the standard of care for locally advanced rectal cancer in the United States. We investigated the use of these treatments for stages II and III rectal cancer among the elderly and the effectiveness of these treatments on a population-based scale. PATIENTS AND METHODS The linked Surveillance, Epidemiology, and End-Results-Medicare database was used to identify 1,807 Medicare beneficiaries > or = 65 years of age with stage II or III rectal cancer who underwent surgical resection between 1992 and 1996. We excluded members of a health maintenance organization in the 12 months before or 4 months after their diagnosis and those who died within 4 months of diagnosis. We used multivariate analysis to identify factors associated with combined 5-FU and radiation therapy, and propensity score methodology to determine survival benefit for those treated. RESULTS We found that 37% of patients received both adjuvant 5-FU and radiation therapy, 11% 5-FU alone, and 14% radiation alone. Decreasing age, increasing lymph node positivity, comorbid conditions, and nonblack race were associated with increased probability of treatment with 5-FU and radiation. Combined chemotherapy/radiation therapy was associated with improved survival for stage III (relative risk, 0.71; 95% confidence interval, 0.56 to 0.90), but not for stage II rectal cancer (relative risk, 0.89; 95% confidence interval, 0.70 to 1.14). CONCLUSION The association of combined treatment with improved survival in node-positive disease was similar to that observed in other studies. In the absence of data from well-designed randomized controlled trials, our observational data support efforts on the part of clinicians to make appropriate referrals and provide combined treatment for elderly patients with stage III rectal cancer.


Emerging Infectious Diseases | 2005

Comparing Aberration Detection Methods with Simulated Data

Lori Hutwagner; Timothy Browne; G. Matthew Seeman; Aaron T. Fleischauer

We compared aberration detection methods requiring historical data to those that require little background by using simulated data. Methods that require less historical data are as sensitive and specific as those that require 3–5 years of data. These simulations can determine which method produces appropriate sensitivity and specificity.


The Journal of Infectious Diseases | 2011

Cluster of Oseltamivir-Resistant 2009 Pandemic Influenza A (H1N1) Virus Infections on a Hospital Ward among Immunocompromised Patients—North Carolina, 2009

Luke F. Chen; Natalie J. M. Dailey; Agam K Rao; Aaron T. Fleischauer; Ian Greenwald; Varough Deyde; Zack Moore; Deverick J. Anderson; Jonathan Duffy; Larisa V. Gubareva; Daniel J. Sexton; Alicia M. Fry; Arjun Srinivasan; Cameron R. Wolfe

BACKGROUND Oseltamivir resistance among 2009 pandemic influenza A (H1N1) viruses (pH1N1) is rare. We investigated a cluster of oseltamivir-resistant pH1N1 infections in a hospital ward. METHODS We reviewed patient records and infection control measures and interviewed health care personnel (HCP) and visitors. Oseltamivir-resistant pH1N1 infections were found with real-time reverse-transcription polymerase chain reaction and pyrosequencing for the H275Y neuraminidase (NA) mutation. We compared hemagglutinin (HA) sequences from clinical samples from the outbreak with those of other surveillance viruses. RESULTS During the period 6-11 October 2009, 4 immunocompromised patients within a hematology-oncology ward exhibited symptoms of pH1N1 infection. The likely index patient became febrile 8 days after completing a course of oseltamivir; isolation was instituted 9 days after symptom onset. Three other case patients developed symptoms 1, 3, and 5 days after the index patient. Three case patients were located in adjacent rooms. HA and NA sequences from case patients were identical. Twelve HCP and 6 visitors reported influenza symptoms during the study period. No other pH1N1 isolates from the hospital or from throughout the state carried the H275Y mutation. CONCLUSIONS Geographic proximity, temporal clustering, presence of H275Y mutation, and viral sequence homology confirmed nosocomial transmission of oseltamivir-resistant pH1N1. Diagnostic vigilance and prompt isolation may prevent nosocomial transmission of influenza.


PLOS ONE | 2010

Pneumonia Incidence and Mortality in Mainland China: Systematic Review of Chinese and English Literature, 1985–2008

Xuhua Guan; Benjamin J. Silk; Wenkai Li; Aaron T. Fleischauer; Xuesen Xing; Xiaoqing Jiang; Hongjie Yu; Sonja J. Olsen; Adam L. Cohen

Background Pneumonia is a leading infectious disease killer worldwide, yet the burden in China is not well understood as much of the data is published in the non-English literature. Methodology/Principal Findings We systematically reviewed the Chinese- and English-language literature for studies with primary data on pneumonia incidence and mortality in mainland China. Between 1985 and 2008, 37 studies met the inclusion criteria. The quality of the studies was highly variable. For children <5 years, incidence ranged from 0.06–0.27 episodes per person-year and mortality ranged from 184–1,223 deaths per 100,000 population. Overall incidence and mortality were stable or decreased over the study period and were higher in rural compared to urban areas. Conclusions/Significance Pneumonia continues to be a major public health challenge in young children in China, and estimates of pneumonia incidence and mortality vary widely. Reliable surveillance data and new prevention efforts may be needed to achieve and document additional declines, especially in areas with higher incidence and mortality such as rural settings.


Clinical Infectious Diseases | 2005

Evaluation of Human-to-Human Transmission of Monkeypox from Infected Patients to Health Care Workers

Aaron T. Fleischauer; James C. Kile; Molly Davidson; Marc Fischer; Kevin L. Karem; Robert Teclaw; Hans Messersmith; Pamela Pontones; Bradley Beard; Zachary Braden; Joanne Cono; James J. Sejvar; Ali S. Khan; Inger K. Damon; Matthew J. Kuehnert

BACKGROUND In 2003, human monkeypox was first identified in the United States. The outbreak was associated with exposure to infected prairie dogs, but the potential for person-to-person transmission was a concern. This study examines health care worker (HCW) exposure to 3 patients with confirmed monkeypox. METHODS Exposed HCWs, defined as HCWs who entered a 2-m radius surrounding case patients with confirmed monkeypox, were identified by infection-control practitioners. A self-administered questionnaire and analysis of paired serum specimens determined exposure status, immune response, and postexposure signs and symptoms of monkeypox. RESULTS Of 81 exposed HCWs, 57 (70%) participated in the study. Among 57 participants, 40 (70%) had > or =1 unprotected exposure; none reported signs or symptoms consistent with monkeypox illness. One exposed HCW (2%), who had been vaccinated for smallpox within the past year, had serological evidence of recent orthopoxvirus infection; acute- and convalescent-phase serum specimens tested positive for anti-orthopoxvirus IgM. No exposed HCWs had signs and symptoms consistent with monkeypox. CONCLUSION More than three-quarters of exposed HCWs reported at least 1 unprotected encounter with a patient who had monkeypox. One asymptomatic HCW showed laboratory evidence of recent orthopoxvirus infection, which was possibly attributable to either recent infection or smallpox vaccination. Transmission of monkeypox likely is a rare event in the health care setting.


Public Health Reports | 2012

Integration of Syndromic Surveillance Data into Public Health Practice at State and Local Levels in North Carolina

Erika Samoff; Anna E. Waller; Aaron T. Fleischauer; Amy Ising; Meredith K. Davis; Mike Park; Stephanie W. Haas; Lauren M. DiBiase; Pia D.M. MacDonald

Objectives. We sought to describe the integration of syndromic surveillance data into daily surveillance practice at local health departments (LHDs) and make recommendations for the effective integration of syndromic and reportable disease data for public health use. Methods. Structured interviews were conducted with local health directors and communicable disease nursing staff from a stratified random sample of LHDs from May through September 2009. Interviews captured information on direct access to the North Carolina syndromic surveillance system and on the use of syndromic surveillance information for outbreak management, program management, and the creation of reports. We analyzed syndromic surveillance system data to assess the number of signals resulting in a public health response. Results. Syndromic surveillance data were used for outbreak investigation (19% of respondents) and program management and report writing (43% of respondents); a minority reported use of both syndromic and reportable disease data for these purposes (15% and 23%, respectively). Receiving data from frequent system users was associated with using data for these purposes (p=0.016 and p=0.033, respectively, for syndromic and reportable disease data). A small proportion of signals (<25%) resulted in a public health response. Conclusions. Use of syndromic surveillance data by North Carolina local public health authorities resulted in meaningful public health action, including both case investigation and program management. While useful, the syndromic surveillance data system was oriented toward sensitivity rather than efficiency. Successful incorporation of new surveillance data is likely to require systems that are oriented toward efficiency.


Journal of Public Health Management and Practice | 2007

Direct cost associated with the development and implementation of a local syndromic surveillance system

Amy Kirkwood; Eric Guenther; Aaron T. Fleischauer; J. E. Gunn; Lori Hutwagner; M. Anita Barry

OBJECTIVE Enhancing public health surveillance to include electronic syndromic surveillance systems has received increased attention in recent years. Although cost continually serves as a critical factor in public health decision making, few studies have evaluated direct costs associated with syndromic surveillance systems. In this study, we calculated the direct costs associated with developing and implementing a syndromic surveillance system in Boston, Massachusetts, from the perspective of local, state, and federal governments. METHODS Between December 2003 and July 2005, the Boston Public Health Commission (BPHC), in collaboration with the Centers for Disease Control and Prevention (CDC), and the Massachusetts Department of Public Health developed a syndromic surveillance system in which limited demographic and chief complaint data are collected from all Boston acute care emergency departments every 24 hours. Costs were divided into three categories: development, operation, and upgrade. Within these categories, all fixed and variable costs incurred by both BPHC and CDC were assessed, including those associated with development of syndromic surveillance-related city regulations and system enhancements. RESULTS The total estimated direct cost of system development and implementation during the study period was


Public Health Reports | 2013

Improvements in timeliness resulting from implementation of electronic laboratory reporting and an electronic disease surveillance system.

Erika Samoff; Mary T. Fangman; Aaron T. Fleischauer; Anna E. Waller; Pia D.M. MacDonald

422,899 (


Emerging Infectious Diseases | 2013

Gastroenteritis Outbreak Associated with Unpasteurized Tempeh, North Carolina, USA

Stephanie E. Griese; Aaron T. Fleischauer; Jennifer K. MacFarquhar; Zackary Moore; Cris Harrelson; Anita Valiani; Sue Ellen Morrison; David Sweat; Jean-Marie Maillard; Denise Griffin; Debra Springer; Matthew Mikoleit; Anna E. Newton; Brendan R. Jackson; Thai-An Nguyen; Stacey Bosch; Megan Davies

396,716 invested by BPHC and

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Anna E. Waller

University of North Carolina at Chapel Hill

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Erika Samoff

Centers for Disease Control and Prevention

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Zack Moore

North Carolina Department of Health and Human Services

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Pia D.M. MacDonald

University of North Carolina at Chapel Hill

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Ali S. Khan

Centers for Disease Control and Prevention

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James J. Sejvar

Centers for Disease Control and Prevention

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Jessica Rinsky

Centers for Disease Control and Prevention

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Lori Hutwagner

Centers for Disease Control and Prevention

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