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Dive into the research topics where Maroya Spalding Walters is active.

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Featured researches published by Maroya Spalding Walters.


Morbidity and Mortality Weekly Report | 2015

Notes from the Field: Carbapenem-resistant Enterobacteriaceae Producing OXA-48-like Carbapenemases--United States, 2010-2015.

Meghan Lyman; Maroya Spalding Walters; David Lonsway; Kamile Rasheed; Brandi Limbago

Carbapenem-resistant Enterobacteriaceae (CRE) are bacteria that are often resistant to most classes of antibiotics and cause health care-associated infections with high mortality rates. Among CRE, strains that carry plasmid-encoded carbapenemase enzymes that inactivate carbapenem antibiotics are of greatest public health concern because of their potential for rapid global dissemination, as evidenced by the increasing distribution of CRE that produce the Klebsiella pneumoniae carbapenemase and the New Delhi metallo-β-lactamase. Newly described resistance in Enterobacteriaceae, such as plasmid-mediated resistance to the last-line antimicrobial colistin, recently detected in China, and resistance to the newly approved antimicrobial, ceftazidime-avibactam, identified from a U.S. K. pneumoniae carbapenemase-producing isolate, highlight the continued urgency to delay spread of CRE. Monitoring the emergence of carbapenemases is crucial to limiting their spread; identification of patients carrying carbapenemase-producing CRE should result in the institution of transmission-based precautions and enhanced environmental cleaning to prevent transmission.* The OXA-48 carbapenemase was first identified in Enterobacteriaceae in Turkey in 2001, and OXA-48-like variants have subsequently been reported around the world. The first U.S. reports of OXA-48-like carbapenemases were published in 2013 and included retrospectively identified isolates from 2009 and two isolates collected in 2012 from patients in Virginia who had recently been hospitalized outside the United States. Although there are limited additional published reports from the United States, CDC continues to receive reprots of these organisms. This report describes patients identified as carrying CRE producing OXA-48-like carbapenemases in the United States during June 2010-August 2015.


Morbidity and Mortality Weekly Report | 2015

Vancomycin-Resistant Staphylococcus aureus - Delaware, 2015.

Maroya Spalding Walters; Paula Eggers; Valerie Albrecht; Tatiana Travis; David Lonsway; Greg Hovan; Debra Taylor; Kamile Rasheed; Brandi Limbago

Vancomycin-resistant Staphylococcus aureus (VRSA) is a rare, multidrug-resistant bacterium of public health concern that emerged in the United States in 2002. VRSA (S. aureus with vancomycin minimum inhibitory concentration [MIC] ≥16 μg/mL) arises when vancomycin resistance genes (e.g., the vanA operon, which codes for enzymes that result in modification or elimination of the vancomycin binding site) from vancomycin-resistant enterococci (VRE) are transferred to S. aureus (1). To date, all VRSA strains have arisen from methicillin-resistant S. aureus (MRSA). The fourteenth VRSA isolate (VRSA 14) identified in the United States was reported to CDC in February 2015.


Morbidity and Mortality Weekly Report | 2016

Investigation of Escherichia coli Harboring the mcr-1 Resistance Gene — Connecticut, 2016

Amber Vasquez; Noelisa Montero; Mark Laughlin; Ehren Dancy; Russell Melmed; Lynn Sosa; Louise Francois Watkins; Jason P. Folster; Nancy A. Strockbine; Heather Moulton-Meissner; Uzma Ansari; Matthew L. Cartter; Maroya Spalding Walters

The mcr-1 gene confers resistance to the polymyxins, including the antibiotic colistin, a medication of last resort for multidrug-resistant infections. The mcr-1 gene was first reported in 2015 in food, animal, and patient isolates from China (1) and is notable for being the first plasmid-mediated colistin resistance mechanism to be identified. Plasmids can be transferred between bacteria, potentially spreading the resistance gene to other bacterial species. Since its discovery, the mcr-1 gene has been reported from Africa, Asia, Europe, South America, and North America (2,3), including the United States, where it has been identified in Escherichia coli isolated from three patients and from two intestinal samples from pigs (2,4-6). In July 2016, the Pathogen Detection System at the National Center for Biotechnology Information (Bethesda, Maryland) identified mcr-1 in the whole genome sequence of an E. coli isolate from a Connecticut patient (7); this is the fourth isolate from a U.S. patient to contain the mcr-1 gene.


PLOS Neglected Tropical Diseases | 2014

Shifts in Geographic Distribution and Antimicrobial Resistance during a Prolonged Typhoid Fever Outbreak — Bundibugyo and Kasese Districts, Uganda, 2009–2011

Maroya Spalding Walters; Janell Routh; Matthew Mikoleit; Samuel Kadivane; Caroline Ouma; Denis Mubiru; Ben Mbusa; Amos Murangi; Emmanuel Ejoku; Absalom Rwantangle; Uziah Kule; John Lule; Nancy M. Garrett; Jessica L. Halpin; Nikki Maxwell; Atek Kagirita; Fred Mulabya; Issa Makumbi; Molly M. Freeman; Kevin Joyce; Vince Hill; Robert Downing; Eric D. Mintz

Background Salmonella enterica serovar Typhi is transmitted by fecally contaminated food and water and causes approximately 22 million typhoid fever infections worldwide each year. Most cases occur in developing countries, where approximately 4% of patients develop intestinal perforation (IP). In Kasese District, Uganda, a typhoid fever outbreak notable for a high IP rate began in 2008. We report that this outbreak continued through 2011, when it spread to the neighboring district of Bundibugyo. Methodology/Principal Findings A suspected typhoid fever case was defined as IP or symptoms of fever, abdominal pain, and ≥1 of the following: gastrointestinal disruptions, body weakness, joint pain, headache, clinically suspected IP, or non-responsiveness to antimalarial medications. Cases were identified retrospectively via medical record reviews and prospectively through laboratory-enhanced case finding. Among Kasese residents, 709 cases were identified from August 1, 2009–December 31, 2011; of these, 149 were identified during the prospective period beginning November 1, 2011. Among Bundibugyo residents, 333 cases were identified from January 1–December 31, 2011, including 128 cases identified during the prospective period beginning October 28, 2011. IP was reported for 507 (82%) and 59 (20%) of Kasese and Bundibugyo cases, respectively. Blood and stool cultures performed for 154 patients during the prospective period yielded isolates from 24 (16%) patients. Three pulsed-field gel electrophoresis pattern combinations, including one observed in a Kasese isolate in 2009, were shared among Kasese and Bundibugyo isolates. Antimicrobial susceptibility was assessed for 18 isolates; among these 15 (83%) were multidrug-resistant (MDR), compared to 5% of 2009 isolates. Conclusions/Significance Molecular and epidemiological evidence suggest that during a prolonged outbreak, typhoid spread from Kasese to Bundibugyo. MDR strains became prevalent. Lasting interventions, such as typhoid vaccination and improvements in drinking water infrastructure, should be considered to minimize the risk of prolonged outbreaks in the future.


Vaccine | 2015

Economic evaluation of typhoid vaccination in a prolonged typhoid outbreak setting: the case of Kasese district in Uganda.

Cristina Carias; Maroya Spalding Walters; Edward Wefula; Kashmira Date; David L. Swerdlow; Maya Vijayaraghavan; Eric D. Mintz

BACKGROUND Vaccination has been increasingly promoted to help control epidemic and endemic typhoid fever in high-incidence areas. Despite growing recognition that typhoid incidence in some areas of sub-Saharan Africa is similar to high-incidence areas of Asia, no large-scale typhoid vaccination campaigns have been conducted there. We performed an economic evaluation of a hypothetical one-time, fixed-post typhoid vaccination campaign in Kasese, a rural district in Uganda where a large, multi-year outbreak of typhoid fever has been reported. METHODS We used medical cost and epidemiological data retrieved on-site and campaign costs from previous fixed-post vaccination campaigns in Kasese to account for costs from a public sector health care delivery perspective. We calculated program costs and averted disability-adjusted life years (DALYs) and medical costs as a result of vaccination, to calculate the cost of the intervention per DALY and case averted. RESULTS Over the 3 years of projected vaccine efficacy, a one-time vaccination campaign was estimated to avert 1768 (90%CI: 684-4431) typhoid fever cases per year and a total of 3868 (90%CI: 1353-9807) DALYs over the duration of the immunity conferred by the vaccine. The cost of the intervention per DALY averted was US


Infection Control and Hospital Epidemiology | 2016

Policies for Controlling Multidrug-Resistant Organisms in US Healthcare Facilities Reporting to the National Healthcare Safety Network, 2014.

Lindsey M. Weiner; Amy K Webb; Maroya Spalding Walters; Margaret A. Dudeck

484 (90%CI: 18-1292) and per case averted US


American Journal of Public Health | 2015

A Qualitative Inquiry About Pruno, an Illicit Alcoholic Beverage Linked to Botulism Outbreaks in United States Prisons

Maroya Spalding Walters; Nandini Sreenivasan; Bobbie Person; Mark Shew; Daniel Wheeler; Julia Hall; Linda Bogdanow; Karyn Leniek; Agam K Rao

341 (90%CI: 13-883). CONCLUSION We estimated the vaccination campaign in this setting to be highly cost-effective, according to WHOs cost-effective guidelines. Results may be applicable to other African settings with similar high disease incidence estimates.


Clinical Infectious Diseases | 2018

Outbreak of Botulism Due to Illicit Prison-Brewed Alcohol: Public Health Response to a Serious and Recurrent Problem

Agam K Rao; Maroya Spalding Walters; Julia M. Hall; Colleen Guymon; Richard M. Garden; Pauline Sturdy; Diana Thurston; Lori Smith; Melissa Dimond; Dagmar Vitek; Linda Bogdanow; Mary Hill; Neal H Lin; Carolina Lúquez; Patricia M. Griffin

We examined reported policies for the control of common multidrug-resistant organisms (MDROs) in US healthcare facilities using data from the National Healthcare Safety Network Annual Facility Survey. Policies for the use of Contact Precautions were commonly reported. Chlorhexidine bathing for preventing MDRO transmission was also common among acute care hospitals. Infect Control Hosp Epidemiol 2016:1-4.


Mbio | 2018

Genomic Analysis of a Pan-Resistant Isolate of Klebsiella pneumoniae, United States 2016

Tom J. B. de Man; Joseph D. Lutgring; David Lonsway; Karen F. Anderson; Julia A. Kiehlbauch; Lei Chen; Maroya Spalding Walters; Maria Sjölund-Karlsson; J. Kamile Rasheed; Alison Laufer Halpin

OBJECTIVES Since 2011, 3 outbreaks of botulism in US prisons have been attributed to pruno, which is an alcoholic beverage made by inmates. Following 1 outbreak, we conducted a qualitative inquiry to understand pruno brewing and its social context to inform outbreak prevention measures. METHODS We interviewed staff, inmates, and parolees from 1 prison about pruno production methods, the social aspects of pruno, and strategies for communicating the association between botulism and pruno. RESULTS Twenty-seven inmates and parolees and 13 staff completed interviews. Pruno is fermented from water, fruit, sugar, and miscellaneous ingredients. Knowledge of pruno making was widespread among inmates; staff were familiar with only the most common ingredients and supplies inmates described. Staff and inmates described inconsistent consequences for pruno possession and suggested using graphic health messages from organizations external to the prison to communicate the risk of botulism from pruno. CONCLUSIONS Pruno making was frequent in this prison. Improved staff recognition of pruno ingredients and supplies might improve detection of brewing activities in this and other prisons. Consistent consequences and clear messages about the association between pruno and botulism might prevent outbreaks.


Emerging Infectious Diseases | 2018

Carbapenem-Nonsusceptible Acinetobacter baumannii, 8 US Metropolitan Areas, 2012-2015.

Sandra N. Bulens; Sarah H. Yi; Maroya Spalding Walters; Jesse T. Jacob; Chris Bower; Jessica Reno; Lucy E. Wilson; Elisabeth Vaeth; Wendy Bamberg; Sarah J. Janelle; Ruth Lynfield; Paula Snippes Vagnone; Kristin M. Shaw; Marion Kainer; Daniel Muleta; Jacqueline Mounsey; Ghinwa Dumyati; Cathleen Concannon; Zintars G. Beldavs; P. Maureen Cassidy; Erin C. Phipps; Nicole Kenslow; Emily B. Hancock

Background Botulism is a rare, sometimes lethal neuroparalytic illness. On 2 October 2011, an inmate at prison A developed symptoms compatible with botulism after drinking pruno, an illicit, prison-brewed alcoholic beverage. Additional illnesses were identified within several days. We conducted an investigation to determine the cause and extent of the outbreak. Methods A case was defined as signs or symptoms of botulism in a prison A inmate with onset during 30 September-9 October 2011. Cases were identified through medical evaluations and interviews with inmates about recent pruno consumption. Laboratory testing was performed for Clostridium botulinum and botulinum neurotoxin. Ingredients, preparation, and sharing of the implicated pruno were investigated. Results Eight prisoners developed botulism; all drank pruno made with a potato. Three received mechanical ventilation. Culture of fluid from a sock that inmates reported using to filter the implicated pruno yielded C. botulinum type A. The implicated batch may have been shared between cells during delivery of meal trays. Challenges of the investigation included identifying affected inmates, overcoming inaccuracies in histories, and determining how the illicit beverage was shared. Costs to taxpayers were nearly

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David Lonsway

United States Department of Health and Human Services

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Heather Moulton-Meissner

Centers for Disease Control and Prevention

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Uzma Ansari

Centers for Disease Control and Prevention

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Amber Vasquez

Centers for Disease Control and Prevention

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Erin C. Phipps

University of New Mexico

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Ghinwa Dumyati

University of Rochester Medical Center

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J. Kamile Rasheed

Centers for Disease Control and Prevention

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Jeffrey P. Davis

Children's Hospital of Wisconsin

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Lina I Elbadawi

Centers for Disease Control and Prevention

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