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87 citation(s) found for "Schuetz, Audrey N".

Multicenter Performance Assessment of Carba NP Test
Cunningham, Scott A. , Limbago, Brandi, Traczewski, Maria M., Anderson, Karen, Hackel, Meredith , Hindler, Janet A., Sahm, Dan, Alyanak, Efe, Lawsin, Adrian , Man, Tom J. B. de , Mandrekar, Jayawant N. , Jenkins, Stephen G., Humphries, Romney M. , Palavecino, Elizabeth , Patel, Robin , Vasoo, Shawn , Gulvik, Christopher A. , Schuetz, Audrey N. , Patel, Robin , Humphries, Romney , Cunningham, Scott A

Mayo Clinic

Journal of Clinical Microbiology | April 13, 2017 | Volume: 55 | Issue: 6 | Pages: 1954-1960

10.1128/jcm.00244-17 | PMID 28404676 Get It

ABSTRACT Eighty Gram-negative bacilli (54 Enterobacteriaceae and 26 nonfermenting Gram-negative bacilli) obtained from multiple institutions in the United States were distributed in a blinded manner to seven testing laboratories to compare their performance of a test for detection of carbapenemase production, the Carba NP test. The Carba NP test was performed by all laboratories, following the Clinical and Laboratory Standards Institute (CLSI) procedure. Site-versus-site comparisons demonstrated a high level of consistency for the Carba NP assay, with just 3/21 site comparisons yielding a difference in sensitivity ( P < 0.05). Previously described limitations with bla OXA-48-like carbapenemases and bla OXA carbapenemases associated with Acinetobacter baumannii were noted. Based on these data, we demonstrate that the Carba NP test, when implemented with the standardized CLSI methodology, provides reproducible results across multiple sites for detection of carbapenemases.
Globicatella sanguinis Osteomyelitis and Bacteremia: Review of an Emerging Human Pathogen with an Expanding Spectrum of Disease
Buckwalter, Seanne P., Henry, Michael , Wu, Fann , Maloney, Katherine F., Abraham, Bisrat , Hartman, Barry J., Brause, Barry D. , Whittier, Susan , Walsh, Thomas J. , Miller, Andy , Schuetz, Audrey N.

Mayo Clinic

Open Forum Infectious Diseases | February 13, 2017 | Volume: 4 | Issue: 1 | Pages: No page available

10.1093/ofid/ofw277 | PMID 28480269 Get It

AbstractBackgroundGlobicatella sanguinis is an uncommon pathogen that may be misdiagnosed as viridans group streptococci. We review the literature of Globicatella and report 2 clinical cases in which catalase-negative Gram-positive cocci resembling viridans group streptococci with elevated minimum inhibitory concentrations (MICs) to ceftriaxone were inconsistently identified phenotypically, with further molecular characterization and ultimate identification of G sanguinis.MethodsTwo clinical strains (from 2 obese women; 1 with a prosthetic hip infection and the other with bacteremia) were analyzed with standard identification methods, followed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry, 16S recombinant ribonucleic acid (rRNA), and sodA polymerase chain reaction (PCR). The existing medical literature on Globicatella also was reviewed.ResultsStandard phenotypic methods failed to consistently identify the isolates. 16S PCR yielded sequences that confirmed Globicatella species. sodA sequencing provided species-level identification of G sanguinis. The review of literature reveals G sanguinis as an increasingly reported cause of infections of the urine, meninges, and blood. To our knowledge, this is the first reported case of an orthopedic infection caused by Globicatella sanguinis. A review of the 37 known cases of G sanguinis infection revealed that 83% of patients are female, and 89% are at the extremes of age (&lt;5 or &gt;65 years).ConclusionsGlobicatella sanguinis, an uncommon pathogen with elevated minimum inhibitory concentrations to third-generation cephalosporins, is difficult to identify by phenotypic methods and typically causes infections in females at the extremes of age. It may colonize skin or mucosal surfaces. Advanced molecular techniques utilizing 16S rRNA with sodA PCR accurately identify G sanguinis.
Clinical and Molecular Evidence of Atovaquone Resistance in Babesia microti Infection Associated With Rituximab
Simon, Matthew S. , Westblade, Lars F. , Furman, Richard R. , Jenkins, Stephen G., Schuetz, Audrey N. , Kirkman, Laura A.

Mayo Clinic

Open Forum Infectious Diseases | February 3, 2017 | Volume: 3 | Issue: suppl_1 | Pages: No page available

10.1093/ofid/ofw194.151 Get It

Clinical Impact of Rapid Molecular Diagnosis of Bloodstream Infections at an Academic Medical Center in New York City
Simon, Matthew S. , Loo, Angela, Satlin, Michael J. , Singh, Harjot , Holzer, Horatio , Galla, Naveen , Jenkins, Stephen A., Calfee, David P. , Chai, Christina L. L. , Dillon, John , Gerber, Linda M. , Chen, Zhengming , Schuetz, Audrey N.

Mayo Clinic

Open Forum Infectious Diseases | February 2, 2017 | Volume: 3 | Issue: suppl_1 | Pages: No page available

10.1093/ofid/ofw172.1428 Get It

Comparing Adenosine Triphosphate Luminescence Technology to Contact Plate-Based Microbiologic Sampling for the Assessment of Cleanliness of the Patient Care Environment
Salsgiver, Elizabeth , Bernstein, Daniel , Simon, Matthew S. , Greendyke, William , Robertson, Amy, Salter, Selma, Furuya, E. Yoko , Calfee, David P. , Jia, Haomiao , Schuetz, Audrey N. , Saiman, Lisa M.

Mayo Clinic

Open Forum Infectious Diseases | February 2, 2017 | Volume: 3 | Issue: suppl_1 | Pages: No page available

10.1093/ofid/ofw172.135 Get It

Activity of Tedizolid in Methicillin-Resistant Staphylococcus epidermidis Experimental Foreign Body-Associated Osteomyelitis
Greenwood‐Quaintance, Kerryl E. , Mandrekar, Jayawant N. , Patel, Robin , Park, Kyung Hwa , Schuetz, Audrey N. , Patel, Robin

Mayo Clinic

Antimicrobial Agents and Chemotherapy | November 15, 2016 | Volume: 61 | Issue: 2 | Pages: No page available

10.1128/aac.01644-16 | PMID 27855069 Get It

ABSTRACT We developed a rat model of methicillin-resistant Staphylococcus epidermidis (MRSE) foreign body-associated osteomyelitis and used it to compare tedizolid alone and in combination with rifampin against rifampin alone, vancomycin plus rifampin, and vancomycin alone. A clinical strain of MRSE was inoculated into the proximal tibia, and a stainless steel wire with a precolonized MRSE biofilm was implanted. Following a 1-week infection period, 92 rats received either no treatment ( n = 17) or 14 days of intraperitoneal tedizolid ( n = 15), tedizolid plus rifampin ( n = 15), rifampin ( n = 15), vancomycin plus rifampin ( n = 15), or vancomycin ( n = 15). Quantitative bone and wire cultures were performed after treatment completion and also 1 week after infection in a separate group of five rats. The median quantity of staphylococci in bone after the 1-week infection period was 4.89 log 10 CFU/g bone (interquartile range, 3.83 to 5.33 log 10 CFU/g bone); staphylococci were recovered from all associated wires. A median quantity of staphylococci of 3.70 log 10 CFU/g bone was detected in bones of untreated control rats after 3 weeks. Quantities of staphylococci in bones of all treatment groups except the group receiving vancomycin alone (2.78 log 10 CFU/g) were significantly lower than those for untreated controls, with no staphylococci being detected in the groups receiving rifampin monotherapy, tedizolid-plus-rifampin combination therapy, and vancomycin-plus-rifampin combination therapy. Quantities of staphylococci on wires from all treatment groups that included rifampin were significantly lower than those for untreated controls. No resistance to rifampin, tedizolid, or vancomycin was detected. Tedizolid combined with rifampin was active in a rat model of MRSE foreign body-associated osteomyelitis.
Iodamoeba butschlii in an anal pap test confirmed by iodine stain
Pritt, Bobbi S. , Schreiner, Andrew M., Schuetz, Audrey N. , Pritt, Bobbi S

Mayo Clinic

Diagnostic Cytopathology | October 25, 2013 | Volume: 42 | Issue: 9 | Pages: 775-777

10.1002/dc.23042 | PMID 24167099 Get It

We report the finding of Iodamoeba butschlii amebic cysts on a liquid‐based anal Pap smear from an HIV‐positive male. Iodine staining of the smear confirmed the diagnosis. It is important to distinguish I. butschlii from pathogenic ameobae and other organisms seen on anal Pap smears. Diagn. Cytopathol 2014;42:775–777. © 2013 Wiley Periodicals, Inc.