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Dive into the research topics where Jessica D. Lewis is active.

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Featured researches published by Jessica D. Lewis.


Clinical Infectious Diseases | 2016

Influence of Minimum Inhibitory Concentration in Clinical Outcomes of Enterococcus faecium Bacteremia Treated With Daptomycin: Is it Time to Change the Breakpoint?

Bhavarth Shukla; Samuel A. Shelburne; Katherine Reyes; Mini Kamboj; Jessica D. Lewis; Sandra L. Rincon; Jinnethe Reyes; Lina P. Carvajal; Diana Panesso; Costi D. Sifri; Marcus J. Zervos; Eric G. Pamer; Truc T. Tran; Javier A. Adachi; Jose M. Munita; Rodrigo Hasbun; Cesar A. Arias

BACKGROUND Daptomycin has become a front-line antibiotic for multidrug-resistant Enterococcus faecium bloodstream infections (BSIs). We previously showed that E. faecium strains with daptomycin minimum inhibitory concentrations (MICs) in the higher end of susceptibility frequently harbor mutations associated with daptomycin resistance. We postulate that patients with E. faecium BSIs exhibiting daptomycin MICs of 3-4 µg/mL treated with daptomycin are more likely to have worse clinical outcomes than those exhibiting daptomycin MICs ≤2 µg/mL. METHODS We conducted a multicenter retrospective cohort study that included adult patients with E. faecium BSI for whom initial isolates, follow-up blood culture data, and daptomycin administration data were available. A central laboratory performed standardized daptomycin MIC testing for all isolates. The primary outcome was microbiologic failure, defined as clearance of bacteremia ≥4 days after the index blood culture. The secondary outcome was all-cause in-hospital mortality. RESULTS A total of 62 patients were included. Thirty-one patients were infected with isolates that exhibited daptomycin MICs of 3-4 µg/mL. Overall, 34 patients had microbiologic failure and 25 died during hospitalization. In a multivariate logistic regression model, daptomycin MICs of 3-4 µg/mL (odds ratio [OR], 4.7 [1.37-16.12]; P = .014) and immunosuppression (OR, 5.32 [1.20-23.54]; P = .028) were significantly associated with microbiologic failure. Initial daptomycin dose of ≥8 mg/kg was not significantly associated with evaluated outcomes. CONCLUSIONS Daptomycin MICs of 3-4 µg/mL in the initial E. faecium blood isolate predicted microbiological failure of daptomycin therapy, suggesting that modification in the daptomycin breakpoint for enterococci should be considered.


Infection Control and Hospital Epidemiology | 2014

Control of Simultaneous Outbreaks of Carbapenemase-Producing Enterobacteriaceae and Extensively Drug-Resistant Acinetobacter baumannii Infection in an Intensive Care Unit Using Interventions Promoted in the Centers for Disease Control and Prevention 2012 Carbapenemase-Resistant Enterobacteriaceae Toolkit

Kyle B. Enfield; Nujhat N. Huq; Megan F. Gosseling; Darla J. Low; Kevin C. Hazen; Denise M. Toney; Gavin Slitt; Heidi Zapata; Heather L. Cox; Jessica D. Lewis; John R. Kundzins; Amy J. Mathers; Costi D. Sifri

OBJECTIVE We describe the efficacy of enhanced infection control measures, including those recommended in the Centers for Disease Control and Preventions 2012 carbapenem-resistant Enterobacteriaceae (CRE) toolkit, to control concurrent outbreaks of carbapenemase-producing Enterobacteriaceae (CPE) and extensively drug-resistant Acinetobacter baumannii (XDR-AB). DESIGN Before-after intervention study. SETTING Fifteen-bed surgical trauma intensive care unit (ICU). METHODS We investigated the impact of enhanced infection control measures in response to clusters of CPE and XDR-AB infections in an ICU from April 2009 to March 2010. Polymerase chain reaction was used to detect the presence of blaKPC and resistance plasmids in CRE. Pulsed-field gel electrophoresis was performed to assess XDR-AB clonality. Enhanced infection-control measures were implemented in response to ongoing transmission of CPE and a new outbreak of XDR-AB. Efficacy was evaluated by comparing the incidence rate (IR) of CPE and XDR-AB before and after the implementation of these measures. RESULTS The IR of CPE for the 12 months before the implementation of enhanced measures was 7.77 cases per 1,000 patient-days, whereas the IR of XDR-AB for the 3 months before implementation was 6.79 cases per 1,000 patient-days. All examined CPE shared endemic blaKPC resistance plasmids, and 6 of the 7 XDR-AB isolates were clonal. Following institution of enhanced infection control measures, the CPE IR decreased to 1.22 cases per 1,000 patient-days (P = .001), and no more cases of XDR-AB were identified. CONCLUSIONS Use of infection control measures described in the Centers for Disease Control and Preventions 2012 CRE toolkit was associated with a reduction in the IR of CPE and an interruption in XDR-AB transmission.


World Journal of Hepatology | 2015

Hepatitis B in healthcare workers: Transmission events and guidance for management

Jessica D. Lewis; Kyle B. Enfield; Costi D. Sifri

Hepatitis B virus (HBV) is the most efficiently transmissible of the bloodborne viruses that are important in healthcare settings. Healthcare workers (HCWs) are at risk for exposure to HBV from infected patients and, if infected, are similarly at risk of transmitting HBV to patients. Published cases of HBV transmission from HCW to patient are relatively rare, having decreased in frequency following the introduction of standard (universal) precautions, adoption of enhanced percutaneous injury precautions such as double-gloving in surgery, and routine HBV vaccination of HCWs. Here we review published cases of HCW-to-patient transmission of HBV, details of which have helped to guide the creation of formal guidelines for the management of HBV-infected HCWs. We also compare the published guidelines for the management of HBV-infected HCWs from various governing bodies, focusing on their differences with regard to vaccination requirements, viral load limits, frequency of monitoring, and restrictions on practice. Importantly, while there are differences among the recommendations from governing bodies, no guidelines uniformly restrict HBV-infected HCWs from performing invasive or exposure-prone procedures.


Infection Control and Hospital Epidemiology | 2013

Admission Surveillance for Carbapenamase-Producing Enterobacteriaceae at a Long-Term Acute Care Hospital

Jessica D. Lewis; Matthew Bishop; Brenda Heon; Amy J. Mathers; Kyle B. Enfield; Costi D. Sifri

Carbapenemase-producing Enterobacteriaceae (CPE) are of increasing prevalence worldwide, and long-term acute care hospitals (LTACHs) have been implicated in several outbreaks in the United States. This prospective study of routine screening for CPE on admission to a LTACH demonstrates a high prevalence of CPE colonization in central Virginia.


Infection Control and Hospital Epidemiology | 2015

The Limits of Serial Surveillance Cultures in Predicting Clearance of Colonization with Carbapenemase-Producing Enterobacteriaceae

Jessica D. Lewis; Kyle B. Enfield; Amy J. Mathers; Eve T. Giannetta; Costi D. Sifri

An accepted practice for patients colonized with multidrug-resistant organisms is to discontinue contact precautions following 3 consecutive negative surveillance cultures. Our experience with surveillance cultures to detect persistent carbapenemase-producing Enterobacteriaceae (CPE) colonization suggests that extrapolation of this practice to CPE-colonized patients may not be appropriate.


Transplant Infectious Disease | 2016

A single‐center experience with infections due to daptomycin‐nonsusceptible Enterococcus faecium in liver transplant recipients

Jessica D. Lewis; Kyle B. Enfield; Heather L. Cox; Amy J. Mathers; Costi D. Sifri

Infections caused by vancomycin‐resistant Enterococcus faecium (VRE) are a major cause of morbidity and mortality in the liver transplant population. Daptomycin (DAP) is often used to treat infections caused by VRE, but DAP nonsusceptibility in Enterococcus is increasing.


Current Infectious Disease Reports | 2016

Multidrug-Resistant Bacterial Donor-Derived Infections in Solid Organ Transplantation

Jessica D. Lewis; Costi D. Sifri

Although rare, donor-derived infections (DDIs) caused by multidrug-resistant (MDR) bacteria can have devastating consequences for organ transplant recipients. Recognition of MDR bacterial DDIs can be challenging, as MDR bacteria are prevalent in most hospitals and distinguishing their transmission through transplantation from other, more typical routes of acquisition are difficult. New technologies such as whole genome sequencing have recently proven to be a powerful advance in the investigation of MDR bacterial DDIs. Once recognized, the optimal treatment of MDR bacterial DDIs is not clear. Herein, we review the clinical manifestations, outcomes, and management of MDR bacterial DDIs, and identify areas of uncertainty toward which the transplant community should direct further research efforts.


American Journal of Infection Control | 2017

Preparedness planning and care of patients under investigation for or with Ebola virus disease: A survey of physicians in North America.

Jessica D. Lewis; Kyle B. Enfield; Trish M. Perl; Costi D. Sifri

&NA; The West African Ebola virus disease (EVD) epidemic of 2014‐2015 required North American hospitals to undertake comprehensive planning and training for the potential need to care for patients with EVD. Here we describe physician contributions to EVD preparedness planning and the care of persons under investigation for or patients with EVD.


Transplant Infectious Disease | 2018

Comparison of risk factors and outcomes of daptomycin-susceptible and -nonsusceptible vancomycin-resistant Enterococcus faecium infections in liver transplant recipients

Jessica D. Lewis; A.J. Barros; Costi D. Sifri

Vancomycin‐resistant Enterococcus faecium (VRE) infections are common in liver transplant recipients (LTRs). Daptomycin (DAP) is an important treatment for such infections; however, DAP‐nonsusceptible VRE (DNS‐VRE) are increasingly frequent. The purpose of this study was to compare clinical characteristics and outcomes of LTRs with infections due to DNS‐VRE and DAP‐susceptible VRE (DS‐VRE).


American Journal of Infection Control | 2018

Septic arthritis due to oral streptococci following intra-articular injection: A case series

Stacy M. Cain; Kyle B. Enfield; Eve T. Giannetta; Costi D. Sifri; Jessica D. Lewis

Highlights69,540 joint injections/aspirations were performed over 9 years.4 cases of septic arthritis from common oral flora following injection were found.All case‐patients presented within 2‐5 days after joint injection.In 1 case the provider who performed the injection confirmed he did not wear a mask.All received treatment with irrigation and debridement and parenteral antibiotics. &NA; Oral streptococcal species are a rare cause of septic arthritis. We describe 4 cases of septic arthritis due to oral streptococcal species following joint injection. The routine use of face masks during joint injection may prevent this rare but serious complication.

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Costi D. Sifri

University of Virginia Health System

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Kyle B. Enfield

University of Virginia Health System

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Amy J. Mathers

University of Virginia Health System

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Eve T. Giannetta

University of Virginia Health System

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Samuel A. Shelburne

University of Texas MD Anderson Cancer Center

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Jose M. Munita

Universidad del Desarrollo

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