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5374 citation(s) found for "St Louis, E K".

Possible Transmission of St. Louis Encephalitis Virus Through Blood Transfusion—Arizona, 2015
Venkat, Heather , Sunenshine, Rebecca, Levy, Craig, Kafenbaum, Tammy, Sylvester, Tammy, Adams, Laura E. , Smith, Kirk, Townsend, John, Dosmann, Melissa, Kamel, Hany , Patron, Roberto L. , Huskey, Janna L. , Khamash, Hasan , Krow-Lucal, Elizabeth, Rabe, Ingrid B., Krow‐Lucal, Elisabeth , Townsend, John

Mayo Clinic

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

10.1093/ofid/ofw172.1133 Get It

Choosing Ceftazidime/Avibactam and Ceftolozane/Tazobactam as Empiric Therapies against Pseudomonas aeruginosa (Pa) using Rapid Molecular Diagnostics (RMDs): PRIMERS IV
Tran, Thuy Tien T., Hujer, Andrea M. , Hill, Carol , Hujer, Kristine M., Mediavilla, José R. , Kreiswirth, Barry N , Pérez, Federico , Sampath, Rangarajan , Marzan, Christine, Fowler, Vance G. , Chambers, Henry F. , Evans, Scott , Manca, Claudia , Domitrovic, Tatiana , Patel, Robin , Jacobs, Michael R. , Chen, Liang , Hall, Thomas, Fowler, Vance G. , Bonomo, Robert A.

Mayo Clinic

Open Forum Infectious Diseases | February 1, 2017 | Volume: 3 | Issue: suppl_1 | Pages: No page available

10.1093/ofid/ofw172.1598 Get It

Efficacy and Safety of RBX2660 for the Prevention of Recurrent Clostridium difficile Infection: Results. of the PUNCH CD 2 Trial
Lee, Christine , Orenstein, Robert , Khanna, Sahil , Hecht, Gail , Fraiz, Joseph, Dubberke, Erik R. , Lee, Christine H.

Mayo Clinic

Open Forum Infectious Diseases | February 1, 2017 | Volume: 3 | Issue: suppl_1 | Pages: No page available

10.1093/ofid/ofw172.1044 Get It

Rapid Phenotypic Antibiotic Susceptibility Testing Using Forward-Angle Laser Light Scattering
Tomaras, Andrew P., Norgan, Andrew P.

Mayo Clinic

Open Forum Infectious Diseases | February 1, 2017 | Volume: 3 | Issue: suppl_1 | Pages: No page available

10.1093/ofid/ofw172.43 Get It

1657Who Seeks a Fecal Microbiota Transplant for Recurrent C. difficile Infection?: Patient Profile of the PUNCH CD Study
Orenstein, Robert , Griesbach, Cheryl L., Sobcinski, Mary Kay, Dubberke, Erik R.

Mayo Clinic

Open Forum Infectious Diseases | February 1, 2017 | Volume: 1 | Issue: suppl_1 | Pages: S443-S443

10.1093/ofid/ofu052.1203 Get It

Phase I/II study of the novel proteasome inhibitor delanzomib (CEP-18770) for relapsed and refractory multiple myeloma
Martin, Thomas G. , Vij, Ravi , Wu, Ka Lung , Delforge, Michel , Gasparetto, Cristina , Mikhael, Joseph R., Vogl, Dan T. , Hari, Parameswaran , Mıkhael, Joseph , Siegel, David S.

Mayo Clinic

Leukemia & Lymphoma | January 31, 2017 | Volume: 58 | Issue: 8 | Pages: 1872-1879

10.1080/10428194.2016.1263842 | PMID 28140719 Get It

Granulocytic Sarcoma (Chloroma) of the Epiglottis
Ferguson, Jonathan L., Maragos, Nicolas E., Weiland, Louis H.

Mayo Clinic

Otolaryngology–Head and Neck Surgery | January 28, 2017 | Volume: 97 | Issue: 6 | Pages: 588-590

10.1177/019459988709700613 | PMID 3124040 Get It

A phase 2 study incorporating sorafenib into the chemotherapy for older adults with FLT3-mutated acute myeloid leukemia: CALGB 11001
Uy, Geoffrey L. , Mandrekar, Sumithra J. , Laumann, Kristina, Marcucci, Guido , Zhao, Weiqiang , Baer, Maria R. , Powell, Bayard L., Westervelt, Peter, DeAngelo, Daniel J. , Sanford, Ben L. , Blum, William , Bloomfield, Clara D. , Stone, Richard M. , Levis, Mark J. , Klepin, Heidi D. , Stock, Wendy , Larson, Richard A. , Uy, Geoffrey , Deangelo, D. J.

Mayo Clinic

Blood Advances | January 25, 2017 | Volume: 1 | Issue: 5 | Pages: 331-340

10.1182/bloodadvances.2016003053 | PMID 29034366 Get It

Key Points The addition of sorafenib to chemotherapy for older adults with FLT3-ITD mutated AML is safe and may improve overall survival.
Gout Self‐Management in African American Veterans: A Qualitative Exploration of Challenges and Solutions From Patients' Perspectives
Singh, Jasvinder A. , Herbey, Ivan , Bharat, Aseem, Dinnella, Janet, Pullman‐Mooar, Sally, Eisen, Seth A. , Ivankova, Nataliya V. , Singh, Jasvinder A , Eisen, Seth

Mayo Clinic

Arthritis Care & Research | January 24, 2017 | Volume: 69 | Issue: 11 | Pages: 1724-1732

10.1002/acr.23202 | PMID 28118526 Get It

ObjectiveTo explore gout self‐management and associated challenges and solutions in African Americans.MethodsWe conducted semistructured interviews with 35 African American veterans with gout, who received health care at Birmingham or Philadelphia Veterans Affairs (VA) medical centers, had filled urate‐lowering therapy (ULT; most commonly allopurinol) for at least 6 months, and had a ULT medication possession ratio ≥80%. The interview protocol was constructed to explore key concepts related to gout self‐management, including initial diagnosis of gout, beginning medical care for gout, the course of the gout, ULT medication adherence, dietary strategies, comorbidity and side effects, and social support.ResultsThirty‐five African American male veterans with gout who had ≥80% ULT adherence (most commonly, allopurinol) were interviewed at Birmingham (n = 18) or Philadelphia (n = 17) VA medical centers. Mean age was 65 years, mean body mass index was 31.9 kg/m2, 97% had hypertension, 23% had coronary artery disease, and 31% had renal failure. The main themes motivating African American veterans to better gout self‐management were fear of pain, adherence to medications, self‐discipline, lifestyle changes, information gathering, and developing a positive outlook. Birmingham participants more frequently revealed skipping gout medications. More Philadelphia participants discussed lifestyle/diet changes to prevent gout flares, indicated limiting social activities that involved drinking, and sought more information about gout self‐management from health care providers and internet sources.ConclusionIdentified themes, including cultural differences by site, led to the development of a patient‐centered intervention to improve gout self‐management in African American men with gout.
Human Adipose‐Derived Mesenchymal Stem Cells for Osseous Rehabilitation of Induced Osteoradionecrosis: A Rodent Model
Janus, Jeffrey R. , Jackson, Ryan S. , Lees, Katherine A. , Voss, Stephen G. , Wilson, Zachary C., Remmes, Nicholas B. , Keeney, Michael, García, Joaquín J., Marina, Serban San, Keeney, Michael G., San Marina, Serban

Mayo Clinic

Otolaryngology–Head and Neck Surgery | January 24, 2017 | Volume: 156 | Issue: 4 | Pages: 616-621

10.1177/0194599816688647 | PMID 28116973 Get It

ObjectiveHuman adipose‐derived mesenchymal stem cells (ADSCs) were used to rehabilitate bone damaged by osteoradionecrosis (ORN) in an established animal model.Study DesignProspective animal study.SettingAcademic department laboratory.Subjects and MethodsAfter institutional review board and Institutional Animal Care and Use Committee approval, 24 athymic nude rats were divided into 5 groups: 4 groups irradiated (20 Gy) by brachytherapy catheter placed at the left hemimandible and 1 mock irradiation control (n = 4). For all groups, ORN was initiated by extraction of the central molar 1 week later. After 28 days, animals (n = 5/group) received injection at the extraction site with saline (SAL), ADSCs, platelet‐rich plasma and collagen (PRP/COL), or ADSCs + PRP/COL. Rats were sacrificed 28 days later and their mandibles harvested for histopathology analysis (osteoblasts, osteoclasts, and fibrosis) and bone volume measurement using 3‐dimensional micro–computed tomography.ResultsAll but 1 rat survived the experiment period (23/24). Radiographic and histological analysis revealed 60% bone loss in the SAL group compared with the nonirradiated control. Injection of ADSCs increased jaw region bone volume by up to 36% (P <. 01). All experimental groups (ADSC, PRP/COL, and ADSC + PRP/COL) showed dramatically decreased osteoclast counts (P <. 001) while injection of PRP/COL with or without ADSCs increased osteoblasts. Increased fibrosis was observed after ADSC injection (P <. 05).ConclusionThe application of human ADSCs to an induced mandibular osteoradionecrosis model in athymic rats results in increased deposition or preservation of bone, demonstrated both histologically and radiographically. This offers an encouraging possible treatment option for translational research in this difficult disease.