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Dive into the research topics where Erin C. Phipps is active.

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Featured researches published by Erin C. Phipps.


The New England Journal of Medicine | 2015

Burden of Clostridium difficile Infection in the United States

Fernanda C. Lessa; Yi Mu; Wendy Bamberg; Zintars G. Beldavs; Ghinwa Dumyati; John R. Dunn; Monica M. Farley; Stacy M. Holzbauer; James Meek; Erin C. Phipps; Lucy E. Wilson; Lisa G. Winston; Jessica Cohen; Brandi Limbago; Scott K. Fridkin; Dale N. Gerding; L. Clifford McDonald

BACKGROUND The magnitude and scope of Clostridium difficile infection in the United States continue to evolve. METHODS In 2011, we performed active population- and laboratory-based surveillance across 10 geographic areas in the United States to identify cases of C. difficile infection (stool specimens positive for C. difficile on either toxin or molecular assay in residents ≥ 1 year of age). Cases were classified as community-associated or health care-associated. In a sample of cases of C. difficile infection, specimens were cultured and isolates underwent molecular typing. We used regression models to calculate estimates of national incidence and total number of infections, first recurrences, and deaths within 30 days after the diagnosis of C. difficile infection. RESULTS A total of 15,461 cases of C. difficile infection were identified in the 10 geographic areas; 65.8% were health care-associated, but only 24.2% had onset during hospitalization. After adjustment for predictors of disease incidence, the estimated number of incident C. difficile infections in the United States was 453,000 (95% confidence interval [CI], 397,100 to 508,500). The incidence was estimated to be higher among females (rate ratio, 1.26; 95% CI, 1.25 to 1.27), whites (rate ratio, 1.72; 95% CI, 1.56 to 2.0), and persons 65 years of age or older (rate ratio, 8.65; 95% CI, 8.16 to 9.31). The estimated number of first recurrences of C. difficile infection was 83,000 (95% CI, 57,000 to 108,900), and the estimated number of deaths was 29,300 (95% CI, 16,500 to 42,100). The North American pulsed-field gel electrophoresis type 1 (NAP1) strain was more prevalent among health care-associated infections than among community-associated infections (30.7% vs. 18.8%, P<0.001). CONCLUSIONS C. difficile was responsible for almost half a million infections and was associated with approximately 29,000 deaths in 2011. (Funded by the Centers for Disease Control and Prevention.).


Clinical Infectious Diseases | 2014

NAP1 Strain Type Predicts Outcomes from Clostridium difficile Infection

Isaac See; Yi Mu; Jessica Cohen; Zintars G. Beldavs; Lisa G. Winston; Ghinwa Dumyati; Stacy M. Holzbauer; John J. Dunn; Monica M. Farley; Carol Lyons; Helen Johnston; Erin C. Phipps; Rebecca Perlmutter; Lydia Anderson; Dale N. Gerding; Fernanda C. Lessa

BACKGROUND Studies are conflicting regarding the importance of the fluoroquinolone-resistant North American pulsed-field gel electrophoresis type 1 (NAP1) strain in Clostridium difficile infection (CDI) outcome. We describe strain types causing CDI and evaluate their association with patient outcomes. METHODS CDI cases were identified from population-based surveillance. Multivariate regression models were used to evaluate the associations of strain type with severe disease (ileus, toxic megacolon, or pseudomembranous colitis within 5 days; or white blood cell count ≥15 000 cells/µL within 1 day of positive test), severe outcome (intensive care unit admission after positive test, colectomy for C. difficile infection, or death within 30 days of positive test), and death within 14 days of positive test. RESULTS Strain typing results were available for 2057 cases. Severe disease occurred in 363 (17.7%) cases, severe outcome in 100 (4.9%), and death within 14 days in 56 (2.7%). The most common strain types were NAP1 (28.4%), NAP4 (10.2%), and NAP11 (9.1%). In unadjusted analysis, NAP1 was associated with greater odds of severe disease than other strains. After controlling for patient risk factors, healthcare exposure, and antibiotic use, NAP1 was associated with severe disease (adjusted odds ratio [AOR], 1.74; 95% confidence interval [CI], 1.36-2.22), severe outcome (AOR, 1.66; 95% CI, 1.09-2.54), and death within 14 days (AOR, 2.12; 95% CI, 1.22-3.68). CONCLUSIONS NAP1 was the most prevalent strain and a predictor of severe disease, severe outcome, and death. Strategies to reduce NAP1 prevalence, such as antibiotic stewardship to reduce fluoroquinolone use, might reduce CDI morbidity.


JAMA | 2015

Epidemiology of Carbapenem-Resistant Enterobacteriaceae in 7 US Communities, 2012-2013

Alice Guh; Sandra N. Bulens; Yi Mu; Jesse T. Jacob; Jessica Reno; Janine Scott; Lucy E. Wilson; Elisabeth Vaeth; Ruth Lynfield; Kristin M. Shaw; Paula Snippes Vagnone; Wendy Bamberg; Sarah J. Janelle; Ghinwa Dumyati; Cathleen Concannon; Zintars G. Beldavs; Margaret Cunningham; P. Maureen Cassidy; Erin C. Phipps; Nicole Kenslow; Tatiana Travis; David Lonsway; J. Kamile Rasheed; Brandi Limbago

IMPORTANCE Carbapenem-resistant Enterobacteriaceae (CRE) are increasingly reported worldwide as a cause of infections with high-mortality rates. Assessment of the US epidemiology of CRE is needed to inform national prevention efforts. OBJECTIVE To determine the population-based CRE incidence and describe the characteristics and resistance mechanism associated with isolates from 7 US geographical areas. DESIGN, SETTING, AND PARTICIPANTS Population- and laboratory-based active surveillance of CRE conducted among individuals living in 1 of 7 US metropolitan areas in Colorado, Georgia, Maryland, Minnesota, New Mexico, New York, and Oregon. Cases of CRE were defined as carbapenem-nonsusceptible (excluding ertapenem) and extended-spectrum cephalosporin-resistant Escherichia coli, Enterobacter aerogenes, Enterobacter cloacae complex, Klebsiella pneumoniae, or Klebsiella oxytoca that were recovered from sterile-site or urine cultures during 2012-2013. Case records were reviewed and molecular typing for common carbapenemases was performed. EXPOSURES Demographics, comorbidities, health care exposures, and culture source and location. MAIN OUTCOMES AND MEASURES Population-based CRE incidence, site-specific standardized incidence ratios (adjusted for age and race), and clinical and microbiological characteristics. RESULTS Among 599 CRE cases in 481 individuals, 520 (86.8%; 95% CI, 84.1%-89.5%) were isolated from urine and 68 (11.4%; 95% CI, 8.8%-13.9%) from blood. The median age was 66 years (95% CI, 62.1-65.4 years) and 284 (59.0%; 95% CI, 54.6%-63.5%) were female. The overall annual CRE incidence rate per 100<000 population was 2.93 (95% CI, 2.65-3.23). The CRE standardized incidence ratio was significantly higher than predicted for the sites in Georgia (1.65 [95% CI, 1.20-2.25]; P < .001), Maryland (1.44 [95% CI, 1.06-1.96]; P = .001), and New York (1.42 [95% CI, 1.05-1.92]; P = .048), and significantly lower than predicted for the sites in Colorado (0.53 [95% CI, 0.39-0.71]; P < .001), New Mexico (0.41 [95% CI, 0.30-0.55]; P = .01), and Oregon (0.28 [95% CI, 0.21-0.38]; P < .001). Most cases occurred in individuals with prior hospitalizations (399/531 [75.1%; 95% CI, 71.4%-78.8%]) or indwelling devices (382/525 [72.8%; 95% CI, 68.9%-76.6%]); 180 of 322 (55.9%; 95% CI, 50.0%-60.8%) admitted cases resulted in a discharge to a long-term care setting. Death occurred in 51 (9.0%; 95% CI, 6.6%-11.4%) cases, including in 25 of 91 cases (27.5%; 95% CI, 18.1%-36.8%) with CRE isolated from normally sterile sites. Of 188 isolates tested, 90 (47.9%; 95% CI, 40.6%-55.1%) produced a carbapenemase. CONCLUSIONS AND RELEVANCE In this population- and laboratory-based active surveillance system in 7 states, the incidence of CRE was 2.93 per 100<000 population. Most CRE cases were isolated from a urine source, and were associated with high prevalence of prior hospitalizations or indwelling devices, and discharge to long-term care settings.


Pediatrics | 2014

Clostridium difficile Infection Among Children Across Diverse US Geographic Locations

Joyanna Wendt; Jessica Cohen; Yi Mu; Ghinwa Dumyati; John R. Dunn; Stacy M. Holzbauer; Lisa G. Winston; Helen Johnston; James Meek; Monica M. Farley; Lucy E. Wilson; Erin C. Phipps; Zintars G. Beldavs; Dale N. Gerding; L. Clifford McDonald; Carolyn V. Gould; Fernanda C. Lessa

OBJECTIVE: Little is known about the epidemiology of Clostridium difficile infection (CDI) among children, particularly children ≤3 years of age in whom colonization is common but pathogenicity uncertain. We sought to describe pediatric CDI incidence, clinical presentation, and outcomes across age groups. METHODS: Data from an active population- and laboratory-based CDI surveillance in 10 US geographic areas during 2010–2011 were used to identify cases (ie, residents with C difficile–positive stool without a positive test in the previous 8 weeks). Community-associated (CA) cases had stool collected as outpatients or ≤3 days after hospital admission and no overnight health care facility stay in the previous 12 weeks. A convenience sample of CA cases were interviewed. Demographic, exposure, and clinical data for cases aged 1 to 17 years were compared across 4 age groups: 1 year, 2 to 3 years, 4 to 9 years, and 10 to 17 years. RESULTS: Of 944 pediatric CDI cases identified, 71% were CA. CDI incidence per 100 000 children was highest among 1-year-old (66.3) and white (23.9) cases. The proportion of cases with documented diarrhea (72%) or severe disease (8%) was similar across age groups; no cases died. Among the 84 cases interviewed who reported diarrhea on the day of stool collection, 73% received antibiotics during the previous 12 weeks. CONCLUSIONS: Similar disease severity across age groups suggests an etiologic role for C difficile in the high rates of CDI observed in younger children. Prevention efforts to reduce unnecessary antimicrobial use among young children in outpatient settings should be prioritized.


Clinical Infectious Diseases | 2013

Effect of Nucleic Acid Amplification Testing on Population-based Incidence Rates of Clostridium difficile Infection

Carolyn V. Gould; Jonathan R. Edwards; Jessica Cohen; Wendy Bamberg; Leigh Ann Clark; Monica M. Farley; Helen Johnston; Joelle Nadle; Lisa G. Winston; Dale N. Gerding; L. Clifford McDonald; Fernanda C. Lessa; Zintars G. Beldavs; Samir Hanna; Gary Hollick; Stacy M. Holzbauer; Carol Lyons; Erin C. Phipps; Lucy E. Wilson

Nucleic acid amplification testing (NAAT) is increasingly being adopted for diagnosis of Clostridium difficile infection (CDI). Data from 3 states conducting population-based CDI surveillance showed increases ranging from 43% to 67% in CDI incidence attributable to changing from toxin enzyme immunoassays to NAAT. CDI surveillance requires adjustment for testing methods.


Emerging Infectious Diseases | 2015

Improved Phenotype-Based Definition for Identifying Carbapenemase Producers among Carbapenem-Resistant Enterobacteriaceae

Nora Chea; Sandra N. Bulens; Thiphasone Kongphet-Tran; Ruth Lynfield; Kristin M. Shaw; Paula Snippes Vagnone; Marion Kainer; Daniel Muleta; Lucy E. Wilson; Elisabeth Vaeth; Ghinwa Dumyati; Cathleen Concannon; Erin C. Phipps; Karissa Culbreath; Sarah J. Janelle; Wendy Bamberg; Alice Guh; Brandi Limbago

A new, less restrictive definition increases detection of Klebsiella pneumoniae carbapenemase producers.


Open Forum Infectious Diseases | 2016

Burden of Nursing Home-Onset Clostridium difficile Infection in the United States: Estimates of Incidence and Patient Outcomes

Jennifer C. Hunter; Yi Mu; Ghinwa Dumyati; Monica M. Farley; Lisa G. Winston; Helen Johnston; James Meek; Rebecca Perlmutter; Stacy M. Holzbauer; Zintars G. Beldavs; Erin C. Phipps; John R. Dunn; Jessica Cohen; Johannetsy J. Avillan; Nimalie D. Stone; Dale N. Gerding; L. Clifford McDonald; Fernanda C. Lessa

Background. Approximately 4 million Americans receive nursing home (NH) care annually. Nursing home residents commonly have risk factors for Clostridium difficile infection (CDI), including advanced age and antibiotic exposures. We estimated national incidence of NH-onset (NHO) CDI and patient outcomes. Methods. We identified NHO-CDI cases from population-based surveillance of 10 geographic areas in the United States. Cases were defined by C difficile-positive stool collected in an NH (or from NH residents in outpatient settings or ≤3 days after hospital admission) without a positive stool in the prior 8 weeks. Medical records were reviewed on a sample of cases. Incidence was estimated using regression models accounting for age and laboratory testing method; sampling weights were applied to estimate hospitalizations, recurrences, and deaths. Results. A total of 3503 NHO-CDI cases were identified. Among 262 sampled cases, median age was 82 years, 76% received antibiotics in the 12 weeks prior to the C difficile-positive specimen, and 57% were discharged from a hospital in the month before specimen collection. After adjusting for age and testing method, the 2012 national estimate for NHO-CDI incidence was 112 800 cases (95% confidence interval [CI], 93 400–131 800); 31 400 (28%) were hospitalized within 7 days after a positive specimen (95% CI, 25 500–37 300), 20 900 (19%) recurred within 14–60 days (95% CI, 14 600–27 100), and 8700 (8%) died within 30 days (95% CI, 6600–10 700). Conclusions. Nursing home onset CDI is associated with substantial morbidity and mortality. Strategies focused on infection prevention in NHs and appropriate antibiotic use in both NHs and acute care settings may decrease the burden of NHO CDI.


Journal of Clinical Microbiology | 2014

Impact of Changes in Clostridium difficile Testing Practices on Stool Rejection Policies and C. difficile Positivity Rates across Multiple Laboratories in the United States

Jessica Cohen; Brandi Limbago; Ghinwa Dumyati; Stacy M. Holzbauer; Helen Johnston; Rebecca Perlmutter; John J. Dunn; Joelle Nadle; Carol Lyons; Erin C. Phipps; Zintars G. Beldavs; Leigh Ann Clark; Fernanda C. Lessa

ABSTRACT We describe the adoption of nucleic acid amplification tests (NAAT) for Clostridium difficile diagnosis and their impact on stool rejection policies and C. difficile positivity rates. Of the laboratories with complete surveys, 51 (43%) reported using NAAT in 2011. Laboratories using NAAT had stricter rejection policies and increased positivity rates.


Open Forum Infectious Diseases | 2015

Association between Outpatient Antibiotic Prescribing Practices and Community- Associated Clostridium difficile Infection

Raymund Dantes; Yi Mu; Lauri A. Hicks; Jessica Cohen; Wendy Bamberg; Zintars G. Beldavs; Ghinwa Dumyati; Monica M. Farley; Stacy M. Holzbauer; James Meek; Erin C. Phipps; Lucy E. Wilson; Lisa G. Winston; L. Clifford McDonald; Fernanda C. Lessa

A modest, 10% reduction in outpatient antibiotic prescribing among U.S. adults could result in a substantial 17% reduction in Clostridium difficile infections that originate in the community.


Open Forum Infectious Diseases | 2015

Risk Factors for Community-Associated Clostridium difficile Infection in Adults: A Case-Control Study

Alice Guh; Susan Hocevar Adkins; Qunna Li; Sandra N. Bulens; Monica M. Farley; Zirka Smith; Stacy M. Holzbauer; Tory Whitten; Erin C. Phipps; Emily B. Hancock; Ghinwa Dumyati; Cathleen Concannon; Marion Kainer; Brenda Rue; Carol Lyons; Danyel M Olson; Lucy E. Wilson; Rebecca Perlmutter; Lisa G. Winston; Erin Parker; Wendy Bamberg; Zintars G. Beldavs; Valerie Ocampo; Maria Karlsson; Dale N. Gerding; L. Clifford McDonald

Abstract Background An increasing proportion of Clostridium difficile infections (CDI) in the United States are community-associated (CA). We conducted a case-control study to identify CA-CDI risk factors. Methods We enrolled participants from 10 US sites during October 2014–March 2015. Case patients were defined as persons age ≥18 years with a positive C. difficile specimen collected as an outpatient or within 3 days of hospitalization who had no admission to a health care facility in the prior 12 weeks and no prior CDI diagnosis. Each case patient was matched to one control (persons without CDI). Participants were interviewed about relevant exposures; multivariate conditional logistic regression was performed. Results Of 226 pairs, 70.4% were female and 52.2% were ≥60 years old. More case patients than controls had prior outpatient health care (82.1% vs 57.9%; P < .0001) and antibiotic (62.2% vs 10.3%; P < .0001) exposures. In multivariate analysis, antibiotic exposure—that is, cephalosporin (adjusted matched odds ratio [AmOR], 19.02; 95% CI, 1.13–321.39), clindamycin (AmOR, 35.31; 95% CI, 4.01–311.14), fluoroquinolone (AmOR, 30.71; 95% CI, 2.77–340.05) and beta-lactam and/or beta-lactamase inhibitor combination (AmOR, 9.87; 95% CI, 2.76–340.05),—emergency department visit (AmOR, 17.37; 95% CI, 1.99–151.22), white race (AmOR 7.67; 95% CI, 2.34–25.20), cardiac disease (AmOR, 4.87; 95% CI, 1.20–19.80), chronic kidney disease (AmOR, 12.12; 95% CI, 1.24–118.89), and inflammatory bowel disease (AmOR, 5.13; 95% CI, 1.27–20.79) were associated with CA-CDI. Conclusions Antibiotics remain an important risk factor for CA-CDI, underscoring the importance of appropriate outpatient prescribing. Emergency departments might be an environmental source of CDI; further investigation of their contribution to CDI transmission is needed.

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Ghinwa Dumyati

University of Rochester Medical Center

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Lucy E. Wilson

Johns Hopkins University

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Stacy M. Holzbauer

Centers for Disease Control and Prevention

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Wendy Bamberg

Colorado Department of Public Health and Environment

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Yi Mu

Centers for Disease Control and Prevention

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Dale N. Gerding

Loyola University Chicago

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