82 results on '"Katherine Reyes"'
Search Results
2. Treatment with hydroxychloroquine, azithromycin, and combination in patients hospitalized with COVID-19
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Samia Arshad, Paul Kilgore, Zohra S. Chaudhry, Gordon Jacobsen, Dee Dee Wang, Kylie Huitsing, Indira Brar, George J. Alangaden, Mayur S. Ramesh, John E. McKinnon, William O’Neill, Marcus Zervos, Varidhi Nauriyal, Asif Abdul Hamed, Owais Nadeem, Jennifer Swiderek, Amanda Godfrey, Jeffrey Jennings, Jayna Gardner-Gray, Adam M. Ackerman, Jonathan Lezotte, Joseph Ruhala, Raef Fadel, Amit Vahia, Smitha Gudipati, Tommy Parraga, Anita Shallal, Gina Maki, Zain Tariq, Geehan Suleyman, Nicholas Yared, Erica Herc, Johnathan Williams, Odaliz Abreu Lanfranco, Pallavi Bhargava, and Katherine Reyes
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Hydroxychloroquine ,Mortality ,COVID-19 ,SARS-COV-2 ,Coronavirus ,Therapy ,Infectious and parasitic diseases ,RC109-216 - Abstract
Significance: The United States is in an acceleration phase of the COVID-19 pandemic. Currently there is no known effective therapy or vaccine for treatment of SARS-CoV-2, highlighting urgency around identifying effective therapies. Objective: The purpose of this study was to evaluate the role of hydroxychloroquine therapy alone and in combination with azithromycin in hospitalized patients positive for COVID-19. Design: Multi-center retrospective observational study. Setting: The Henry Ford Health System (HFHS) in Southeast Michigan: large six hospital integrated health system; the largest of hospitals is an 802-bed quaternary academic teaching hospital in urban Detroit, Michigan. Participants: Consecutive patients hospitalized with a COVID-related admission in the health system from March 10, 2020 to May 2, 2020 were included. Only the first admission was included for patients with multiple admissions. All patients evaluated were 18 years of age and older and were treated as inpatients for at least 48 h unless expired within 24 h. Exposure: Receipt of hydroxychloroquine alone, hydroxychloroquine in combination with azithromycin, azithromycin alone, or neither. Main outcome: The primary outcome was in-hospital mortality. Results: Of 2,541 patients, with a median total hospitalization time of 6 days (IQR: 4–10 days), median age was 64 years (IQR:53–76 years), 51% male, 56% African American, with median time to follow-up of 28.5 days (IQR:3–53). Overall in-hospital mortality was 18.1% (95% CI:16.6%–19.7%); by treatment: hydroxychloroquine + azithromycin, 157/783 (20.1% [95% CI: 17.3%–23.0%]), hydroxychloroquine alone, 162/1202 (13.5% [95% CI: 11.6%–15.5%]), azithromycin alone, 33/147 (22.4% [95% CI: 16.0%–30.1%]), and neither drug, 108/409 (26.4% [95% CI: 22.2%–31.0%]). Primary cause of mortality was respiratory failure (88%); no patient had documented torsades de pointes. From Cox regression modeling, predictors of mortality were age>65 years (HR:2.6 [95% CI:1.9–3.3]), white race (HR:1.7 [95% CI:1.4–2.1]), CKD (HR:1.7 [95%CI:1.4–2.1]), reduced O2 saturation level on admission (HR:1.5 [95%CI:1.1–2.1]), and ventilator use during admission (HR: 2.2 [95%CI:1.4–3.3]). Hydroxychloroquine provided a 66% hazard ratio reduction, and hydroxychloroquine + azithromycin 71% compared to neither treatment (p
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- 2020
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3. Risk Factors for 30-Day Mortality in Patients with Methicillin-Resistant Staphylococcus aureus Bloodstream Infections
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Pedro Ayau, Ana C. Bardossy, Guillermo Sanchez, Ricardo Ortiz, Daniela Moreno, Pamela Hartman, Khulood Rizvi, Tyler C. Prentiss, Mary B. Perri, Meredith Mahan, Vanthida Huang, Katherine Reyes, and Marcus J. Zervos
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risk factors ,30-day mortality ,blood stream infection ,Methicillin-resistant Staphylococcus aureus ,Infectious and parasitic diseases ,RC109-216 - Abstract
Objectives: Methicillin-resistant Staphylococcus aureus (MRSA) blood stream infections (BSI) are a major health care problem accounting for a large percentage of nosocomial infections. The aim of this study was to identify risk factors associated with 30-day mortality in patients with MRSA BSI. Methods: This was a retrospective study performed in Southeast Michigan. Over a 9- year period, a total of 1,168 patients were identified with MRSA BSI. Patient demographics and clinical data were retrieved and evaluated using electronic medical health records. Results: 30-day mortality during the 9-year study period was 16%. Significant risk factors for 30-day mortality were age, cancer, heart disease, neurologic disease, nursing home residence and Charlson score >3 with Odds Ratio (OR) of 1.03 (CI 1.02–1.04), 2.29 (CI 1.40–3.75), 1.78 (CI 1.20–2.63), 1.65 (CI 1.08–2.25), 1.66 (CI 1.02 − 2.70) and 1.86 (CI 1.18 − 2.95) correspondingly. Diabetes mellitus, peripheral vascular disease (PVD), and readmission were protective factors for 30-day mortality with OR of 0.53 (CI 0.36–0.78), 0.46 (CI 0.26–0.84) and 0.13 (CI0.05 − 0.32) respectively. Conclusions: Our study identified significant risk factors for 30-day mortality in patients with MRSA BSI. Interestingly, diabetes mellitus, PVD and readmission were protective effects on 30-day mortality. There was no statistically significant variability in 30-day mortality over the 9-year study period.
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- 2017
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4. Microbiological testing of adults hospitalised with community-acquired pneumonia: an international study
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Manuela Carugati, Stefano Aliberti, Luis Felipe Reyes, Ricardo Franco Sadud, Muhammad Irfan, Cristina Prat, Nilam J. Soni, Paola Faverio, Andrea Gori, Francesco Blasi, Marcos I. Restrepo, Patricia Karina Aruj, Silvia Attorri, Enrique Barimboim, Juan Pablo Caeiro, María I. Garzón, Victor Hugo Cambursano, Adrian Ceccato, Julio Chertcoff, Florencia Lascar, Fernando Di Tulio, Ariel Cordon Díaz, Lautaro de Vedia, Maria Cristina Ganaha, Sandra Lambert, Gustavo Lopardo, Carlos M. Luna, Alessio Gerardo Malberti, Nora Morcillo, Silvina Tartara, Claudia Pensotti, Betiana Pereyra, Pablo Gustavo Scapellato, Juan Pablo Stagnaro, Florencio Varela, Sonali Shah, Felix Lötsch, Florian Thalhammer, Kurt Anseeuw, Camille A. Francois, Eva Van Braeckel, Jean Louis Vincent, Marcel Zannou Djimon, Jules Bashi, Roger Dodo, Simone Aranha Nouér, Peter Chipev, Milena Encheva, Darina Miteva, Diana Petkova, Adamou Dodo Balkissou, Eric Walter Pefura Yone, Bertrand Hugo Mbatchou Ngahane, Ning Shen, Jin-fu Xu, Carlos Andres Bustamante Rico, Ricardo Buitrago, Fernando Jose Pereira Paternina, Jean-Marie Kayembe Ntumba, Vesna Vladic Carevic, Marko Jakopovic, Mateja Jankovic, Zinka Matkovic, Ivan Mitrecic, Marie-Laure Bouchy Jacobsson, Anette Bro Christensen, Uffe Christian Heitmann Bødtger, Christian Niels Meyer, Andreas Vestergaard Jensen, Gertrud Baunbæk-Knudsen, Pelle Trier Petersen, Stine Andersen, Ibrahim El-Said Abd El-Wahhab, Nesreen Elsayed Morsy, Hanaa Shafiek, Eman Sobh, Kedir Abdella Abdulsemed, Fabrice Bertrand, Christian Brun-Buisson, Etienne de Montmollin, Muriel Fartoukh, Jonathan Messika, Pierre Tattevin, Abdo Khoury, Bernard Ebruke, Michael Dreher, Martin Kolditz, Matthias Meisinger, Mathias W. Pletz, Stefan Hagel, Jan Rupp, Tom Schaberg, Marc Spielmanns, Petra Creutz, Norton Suttorp, Beatrice Siaw-Lartey, Katerina Dimakou, Dimosthenis Papapetrou, Evdoxia Tsigou, Dimitrios Ampazis, Evangelos Kaimakamis, Mina Gaga, Mohit Bhatia, Raja Dhar, George D'Souza, Rajiv Garg, Parvaiz A. Koul, P.A. Mahesh, B.S. Jayaraj, Kiran Vishnu Narayan, Hirennappa B. Udnur, Shashi Bhaskara Krishnamurthy, Surya Kant, Rajesh Swarnakar, Sneha Limaye, Sundeep Salvi, Keihan Golshani, Vera M. Keatings, Ignacio Martin-Loeches, Yasmin Maor, Jacob Strahilevitz, Salvatore Battaglia, Maria Carrabba, Piero Ceriana, Marco Confalonieri, Antonella d'Arminio Monforte, Bruno Del Prato, Marino De Rosa, Riccardo Fantini, Giuseppe Fiorentino, Maria Antonia Gammino, Francesco Menzella, Giuseppe Milani, Stefano Nava, Gerardo Palmiero, Roberta Petrino, Barbra Gabrielli, Paolo Rossi, Claudio Sorino, Gundi Steinhilber, Alessandro Zanforlin, Fabio Franzetti, Manuela Morosi, Elisa Monge, Mauro Carone, Vincenzo Patella, Simone Scarlata, Andrea Comel, Kiyoyasu Kurahashi, Zeina Aoun Bacha, Daniel Barajas Ugalde, Omar Ceballos Zuñiga, José F. Villegas, Milic Medenica, E.M.W. van de Garde, Deebya Raj Mihsra, Poojan Shrestha, Elliott Ridgeon, Babatunde Ishola Awokola, Ogonna N.O. Nwankwo, Adefuye Bolanle Olufunlola, Segaolu Olumide, Kingsley N. Ukwaja, Lukasz Minarowski, Skoczyński Szymon, Felipe Froes, Pedro Leuschner, Mariana Meireles, Sofia B Ravara, Victoria Brocovschii, Chesov Ion, Doina Rusu, Cristina Toma, Daniela Chirita, Carmen Mihaela Dorobat, Alexei Birkun, Anna Kaluzhenina, Abdullah Almotairi, Zakeya Abdulbaqi Ali Bukhary, Jameela Edathodu, Amal Fathy, Abdullah Mushira Abdulaziz Enani, Nazik Eltayeb Mohamed, Jawed Ulhadi Memon, Abdelhaleem Bella, Nada Bogdanović, Branislava Milenkovic, Dragica Pesut, Charles Feldman, Ho Kee Yum, Luis Borderìas, Noel Manuel Bordon Garcia, Hugo Cabello Alarcón, Catia Cilloniz, Antoni Torres, Vicens Diaz-Brito, Xavier Casas, Alicia Encabo González, Maria Luisa Fernández-Almira, Miguel Gallego, Inmaculada Gaspar-GarcÍa, Juan González del Castillo, Patricia Javaloyes Victoria, Elena Laserna Martínez, Rosa Malo de Molina, Pedro J. Marcos, Rosario Menéndez, Ana Pando-Sandoval, Cristina Prat Aymerich, Jordi Rello, Silvia Moyano, Francisco Sanz, Oriol Sibila, Ana Rodrigo-Troyano, Jordi Solé-Violán, Ane Uranga, Job F.M. van Boven, Ester Vendrell Torra, Jordi Almirall Pujol, Arnauld Attannon Fiogbe, Ferdaous Yangui, Semra Bilaceroglu, Levent Dalar, Ufuk Yilmaz, Artemii Bogomolov, Naheed Elahi, Devesh J. Dhasmana, Andrew Feneley, Rhiannon Ions, Julie Skeemer, Gerrit Woltmann, Carole Hancock, Adam T. Hill, Banu Rudran, Silvia Ruiz-Buitrago, Marion Campbell, Paul Whitaker, Alexander Youzguin, Anika Singanayagam, Karen S. Allen, Veronica Brito, Jessica Dietz, Claire E. Dysart, Susan M. Kellie, Ricardo A. Franco-Sadud, Garnet Meier, Thomas L. Holland, Stephen P. Bergin, Fayez Kheir, Mark Landmeier, Manuel Lois, Girish B. Nair, Hemali Patel, Katherine Reyes, William Rodriguez-Cintron, Shigeki Saito, Julio Noda, Cecilia I. Hinojosa, Stephanie M. Levine, Luis F. Angel, Antonio Anzueto, K. Scott Whitlow, John Hipskind, Kunal Sukhija, Vicken Totten, Richard G. Wunderink, Ray D. Shah, Kondwelani John Mateyo, Lorena Noriega, Ezequiel Alvarado, Mohamed Aman, and Lucía Labra
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Medicine - Abstract
This study aimed to describe real-life microbiological testing of adults hospitalised with community-acquired pneumonia (CAP) and to assess concordance with the 2007 Infectious Diseases Society of America (IDSA)/American Thoracic Society (ATS) and 2011 European Respiratory Society (ERS) CAP guidelines. This was a cohort study based on the Global Initiative for Methicillin-resistant Staphylococcus aureus Pneumonia (GLIMP) database, which contains point-prevalence data on adults hospitalised with CAP across 54 countries during 2015. In total, 3702 patients were included. Testing was performed in 3217 patients, and included blood culture (71.1%), sputum culture (61.8%), Legionella urinary antigen test (30.1%), pneumococcal urinary antigen test (30.0%), viral testing (14.9%), acute-phase serology (8.8%), bronchoalveolar lavage culture (8.4%) and pleural fluid culture (3.2%). A pathogen was detected in 1173 (36.5%) patients. Testing attitudes varied significantly according to geography and disease severity. Testing was concordant with IDSA/ATS and ERS guidelines in 16.7% and 23.9% of patients, respectively. IDSA/ATS concordance was higher in Europe than in North America (21.5% versus 9.8%; p
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- 2018
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5. Trends in US Hospital Admissions for Skin and Soft Tissue Infections
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John Edelsberg, Charu Taneja, Marcus Zervos, Nadia Haque, Carol Moore, Katherine Reyes, James Spalding, Jenny Jiang, and Gerry Oster
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Skin infections ,soft tissue infections ,hospital admissions ,staphylococci ,methicillin-resistant Staphylococcus aureus ,MRSA ,Medicine ,Infectious and parasitic diseases ,RC109-216 - Abstract
Using data from the 2000–2004 US Healthcare Cost and Utilization Project National Inpatient Sample, we found that total hospital admissions for skin and soft tissue infections increased by 29% during 2000–2004; admissions for pneumonia were largely unchanged. These results are consistent with recent reported increases in community-associated methicillin-resistant Staphylococcus aureus infections.
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- 2009
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6. Rights and responsibilities in Darfur
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Katherine Reyes
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forced migration ,displacement ,refugee ,Darfur ,IDP ,Social history and conditions. Social problems. Social reform ,HN1-995 - Abstract
A combined UN-military-police-humanitarian initiative hasbeen promoting civic rights and responsibilities among IDPsin order to increase security throughout Kalma camp and itssurroundings.
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- 2009
7. Hemorragia en el parto y en el embarazo
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Stefany Alexandra Erazo Flores, Karen Katherine Reyes Murillo, Ana Karen Bermúdez Rojas, and María Fernanda Erazo Carabajo
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General Medicine - Abstract
La muerte materna es un grave problema de salud pública mundial. Las cifras de muertes maternas son inaceptablemente altas en todo el mundo, en especial en los países en desarrollo. Cada día mueren en todo el mundo unas 830 mujeres por complicaciones relacionadas con el embarazo o el parto. El diagnóstico temprano y manejo oportuno mediante la utilización de medidas generales de soporte vital aunado a medidas específicas de contención del sangrado, a través de la creación de estrategias y protocolos por los servicios de salud, corresponde a la medida más efectiva para disminuir los eventos adversos derivados, y reducir la morbimortalidad materna general. En consecuencia, el objetivo de la presente revisión es compendiar los aspectos generales de la hemorragia en el embarazo y el parto. La investigación se realizó bajo una metodología de tipo documental bibliográfica, bajo la modalidad de revisión. Las principales causas de la hemorragia en el embarazo son el desprendimiento prematuro de placenta normoinserta, la placenta previa, la rotura uterina y la rotura de vasa previa. Mientras que las causas de la hemorragia en el parto son la inercia o atonía uterina, los restos placentarios, el acretismo placentario, la inversión uterina y el trauma de canal del parto. La hemorragia en el embarazo y parto representa una importante causa de mortalidad y morbilidad materna, en consecuencia, resulta fundamental conocer la forma cómo se presenta, sus síntomas, factores de riesgo, causas, a los fines de realizar los diagnósticos precisos y tempranos y realizar la intervención precoz que mejoren el pronóstico de estas pacientes.
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- 2022
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8. Ecuador: Efecto de la presión fiscal sobre la recaudación tributaria. Estimación de la curva de Laffer, periodo 2000-2020
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María Martínez-Quevedo, Katherine Reyes-Mesones, and Flor Vega-Jaramillo
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General Medicine - Abstract
Para Ecuador las recaudaciones tributarias desempeñan un rol preponderante dentro del financiamiento del Estado, debido a que dichos ingresos permiten sostener el gasto público gubernamental. Durante los últimos años las reformas tributarias se han encaminado a aumentar la carga tributaria con la finalidad de aumentar los ingresos impositivos, sin embargo, el incremento de impuestos según la teoría, no necesariamente permite obtener resultados positivos. Por tal motivo, el objetivo del presente estudio consiste en estimar el efecto de la presión fiscal sobre la recaudación tributaria, mediante la aplicación empírica y econométrica de la curva de Laffer, para determinar el punto de maximización de los ingresos fiscales en la economía ecuatoriana durante el periodo 2000 a 2020. Se aplican las metodologías de Mínimos Cuadrados Ordinarios (MCO) y cointegración de Johansen y Juselius (1990) juntamente con un modelo de corrección de error. Los resultados son estadísticamente significativos y el signo de los coeficientes corresponden a la teoría, por lo tanto, se ratifica la validez de la curva de Laffer para Ecuador, de tal forma que, en el corto plazo el nivel óptimo de presión fiscal es 19,71% así mismo, los hallazgos encontrados a largo plazo y mediante MCO señalan que el punto óptimo de presión fiscal que maximiza las recaudaciones tributarias está entre 25,39% y 26,49%. Una implicación de política económica es que a corto plazo se puede aumentar la presión fiscal 0,21% y a largo plazo en promedio puede incrementar 6,44%. Dicho incremento debería estar orientado hacia los impuestos progresivos.
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- 2022
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9. Equidad social para la inclusión: derechos de niños y niñas con discapacidad
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García, Eyder Alex Castillo, Cuba, Claudia Katherine Reyes, and Delgado, Georgina July Campos
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Derechos Humanos ,Niños con Discapacidad ,Sociedades Democráticas - Abstract
Se insiste en el papel del Estado como entidad que cuida el bienestar social en la medida que considera y atiende la condición humana plural; desde esta habilidad configura acciones que reivindica la dignidad implícita en la vida. La investigación tiene el propósito de analizar la equidad social como capacidad que permite la inclusión al expresar los derechos de niños y niñas con discapacidad. Es un estudio bibliográfico de carácter diacrónico desde el enfoque racionalista deductivo. Concluye que vencer los egoísmos característicos de las sociedades inhabitables, al configurar relaciones equitativas, exige la humanización de las convivencias en la medida que se instruye, capacita y expresa solidaridad y compasión. La justicia se presenta como característica de las democracias al disponer los medios y recursos que condescienden mayor inclusión.
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- 2023
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10. Perspectives of multisectoral community stakeholders on Arab American cancer patients’ needs and suggested interventions
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Karriem S. Watson, Naoko Muramatsu, Perla Chebli, Marian L. Fitzgibbon, Sarah Abboud, Katherine Reyes, and Yamile Molina
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medicine.medical_specialty ,business.industry ,Nursing research ,Psychological intervention ,Ethnic group ,Medically Underserved Area ,Language barrier ,Stakeholder engagement ,Stigma (botany) ,Qualitative property ,United States ,Arabs ,03 medical and health sciences ,0302 clinical medicine ,Cancer Survivors ,Oncology ,Neoplasms ,030220 oncology & carcinogenesis ,Family medicine ,Health care ,medicine ,Humans ,030212 general & internal medicine ,business ,Minority Groups - Abstract
Multilevel barriers can arise after a cancer diagnosis, especially in underserved racial/ethnic minority patient populations, raising the need for diverse and contextually adapted interventions. However, limited data exists on Arab American (ArA) cancer patients’ needs, partly due to their racial/ethnic misclassification as Whites. This study leveraged the perspectives of cancer survivors and community stakeholders (i.e., healthcare and community leaders) to identify ArA cancer patients’ needs, as well as their preferred intervention strategies to address them. Using a hybrid inductive-deductive content analysis approach, we analyzed qualitative data from interviews with 18 ArA community stakeholders recruited through community partners in Chicago. Participants associated cancer stigma to ArA patients’ concealment of their diagnosis and aversion to cancer support groups. Economic and language barriers to treatment were emphasized. A lack of resources for ArA cancer patients was also noted and was partly attributed to their misclassification as White. In response to these needs, participants suggested peer mentorship programs to overcome privacy concerns, hospital-based patient navigation to address language and economic barriers in healthcare, diversification of the healthcare workforce to overcome language barriers, and community coalitions to recognize ArA as an ethnic group and increase cancer support resources. Such advocacy will be essential to accurately characterize patients’ cancer burden and obtain funding to support community programs and resources. Our findings suggest that multilevel interventions at the patient, healthcare, and community levels are needed to address ArA cancer patients’ needs.
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- 2021
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11. Ecological and environmental stability in offshore Southern California Marine Basins through the Holocene
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Hannah M Palmer, Tessa M Hill, Esther Kennedy, Peter D Roopnarine, Sonali Langlois, Katherine Reyes, and Lowell Stott
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Atmospheric Science ,Paleontology ,Oceanography - Published
- 2022
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12. Intentional Storytelling to Sustain Low-cost/Free Breast Cancer Services: A Latina Example of Community-driven Advocacy
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Ayokunle Olagoke, Katherine Reyes, Liliana G. San Miguel, Paola Torres, Casandra Robledo, William Kling, Maria Medina, Juanita Arroyo, Carmen Garcia, Nora Coronado, Olivia Hernandez, Araceli Lucio, Hunter T. Norris, Vida Henderson, and Yamilé Molina
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Community-Based Participatory Research ,Health (social science) ,Sociology and Political Science ,Humans ,Medically Underserved Area ,Breast Neoplasms ,Female ,General Medicine ,Hispanic or Latino ,Vulnerable Populations ,Education - Abstract
Community-based public health advocacy efforts are crucial to sustaining the low-cost/free breast cancer services that support underserved populations.We introduce two ways in which narrative theory may be a useful tool for developing advocacy materials and provide an example, using a community-academic partnership to promote Latina breast health in Chicago, Illinois.Community and academic partners 1) engaged 25 Spanish-speaking Latinas in an advocacy workshop, 2) leveraged narrative theory to develop multi-media advocacy materials, and 3) disseminated materials to policymakers.Our project highlights 1) that narrative theory may be useful to describe how Latinas engage policy-makers in relation to their needs and cultural norms, 2) the importance of flexibility and offering community members multiple options to engage policymakers, and 3) the importance of leveraging partners' complementary strengths.Narrative theory may be a useful tool for developing advocacy materials in community-academic partnerships.
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- 2022
13. Diagnóstico y síntomas de una anemia hemolítica
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Marjorie Monserrate Romero Burgos, Gilberth Alexander Montes Mendoza, María Katherine Reyes Mera, and Valeria Melissa Mero Barcia
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Gynecology ,Hemolytic anemia ,medicine.medical_specialty ,education.field_of_study ,Anemia ,business.industry ,Strategy and Management ,Mechanical Engineering ,Population ,Metals and Alloys ,medicine.disease ,Industrial and Manufacturing Engineering ,World health ,Peripheral blood ,medicine.anatomical_structure ,Folic acid ,Reticulocyte ,medicine ,education ,business ,Hyperchromia - Abstract
espanolRESUMEN Segun la Organizacion Mundial Salud, la anemia afecta en todo el mundo, cerca de 1620 millones de personas, lo que corresponde al 24,8% de la poblacion, la anemia es una situacion compleja, que puede indicar decenas de enfermedades. Por medio del diagnostico laboratorio clinico se puede determinar la causa y el tipo de anemia. En la anemia hemolitica, se produce una reduccion de la vida media de los hematies por destruccion anormalmente elevada (hemolisis). La medula osea intenta compensarla aumentando la produccion eritroide, respuesta mediada por la eritropoyetina. Como consecuencia, se incrementa el porcentaje de reticulocitos en sangre periferica (>2%) y se elevan los indices reticulocitarios. La metodologia de la investigacion, es una revision bibliografica, apoyada en medios electronicos como fuente primaria de obtencion de la informacion. La anemia hemolitica tiene diferentes ramas como se ha podido leer en la presente investigacion, esta claro que es una afeccion que involucra a la sangre y todos sus elementos relacionados como los globulos rojos y la medula osea. Sin embargo, independientemente del tipo de anemia que se llegue a padecer, la prueba de laboratorio en sangre por medio del hemograma, es uno de las pruebas mas rutinarias, donde se podra detectar baja de hemoglobina y existencia de macrocitosis e hipercromia, asi como la valoracion de otros elementos como niveles de acido folico y bilirrubina EnglishAccording to the World Health Organization, anemia affects around the world, about 1.62 billion people, which corresponds to 24.8% of the population, anemia is a complex situation, which can indicate dozens of diseases. Through clinical labora-tory diagnosis, the cause and type of anemia can be determined. In hemolytic anemia, there is a reduction in the half-life of the red cells due to abnormally high destruction (hemolysis). The bone marrow tries to compensate by increasing erythroid production, a response mediated by erythropoietin. As a consequence, the percentage of reticulocytes in peripheral blood increases (> 2%) and reticulocyte indices rise. The research methodology is a bibliographic review, supported by electron-ic media as the primary source for obtaining information. Hemolytic anemia has different branches, as has been read in the present investigation, it is clear that it is a condition that involves the blood and all its related elements such as red blood cells and bone marrow. However, regardless of the type of anemia that is suffered, the laboratory test in blood through the hemogram is one of the most routine tests, where low hemoglobin and the existence of macrocytosis and hyperchromia can be detected, as well as the assessment of other elements such as levels of folic acid and bilirubin
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- 2021
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14. Treatment with hydroxychloroquine, azithromycin, and combination in patients hospitalized with COVID-19
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Gordon Jacobsen, Owais Nadeem, Kylie Huitsing, Johnathan Williams, Indira Brar, Amit Vahia, Odaliz Abreu Lanfranco, Jayna Gardner-Gray, Nicholas Yared, Samia Arshad, William W. O'Neill, Amanda Godfrey, Joseph Ruhala, Mayur Ramesh, Jeffrey H. Jennings, Gina Maki, Erica Herc, John E. McKinnon, Tommy Parraga, Marcus J. Zervos, Zain Tariq, Pallavi Bhargava, Geehan Suleyman, Adam M. Ackerman, George Alangaden, Jennifer Swiderek, Smitha Gudipati, Varidhi Nauriyal, Zohra S Chaudhry, Jonathan Lezotte, Paul E. Kilgore, Asif Abdul Hamed, Dee Dee Wang, Anita Shallal, Raef Fadel, and Katherine Reyes
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0301 basic medicine ,Microbiology (medical) ,medicine.medical_specialty ,030106 microbiology ,SARS-COV-2 ,Azithromycin ,lcsh:Infectious and parasitic diseases ,03 medical and health sciences ,0302 clinical medicine ,Pharmacotherapy ,Internal medicine ,medicine ,lcsh:RC109-216 ,030212 general & internal medicine ,Mortality ,business.industry ,Proportional hazards model ,Hazard ratio ,COVID-19 ,Retrospective cohort study ,Hydroxychloroquine ,General Medicine ,mortality ,hydroxychloroquine ,therapy ,Coronavirus ,medicine.disease ,Pneumonia ,Infectious Diseases ,Respiratory failure ,Therapy ,business ,medicine.drug - Abstract
Significance The United States is in an acceleration phase of the COVID-19 pandemic. Currently there is no known effective therapy or vaccine for treatment of SARS-CoV-2, highlighting urgency around identifying effective therapies. Objective The purpose of this study was to evaluate the role of hydroxychloroquine therapy alone and in combination with azithromycin in hospitalized patients positive for COVID-19. Design Multi-center retrospective observational study. Setting The Henry Ford Health System (HFHS) in Southeast Michigan: large six hospital integrated health system; the largest of hospitals is an 802-bed quaternary academic teaching hospital in urban Detroit, Michigan. Participants Consecutive patients hospitalized with a COVID-related admission in the health system from March 10, 2020 to May 2, 2020 were included. Only the first admission was included for patients with multiple admissions. All patients evaluated were 18 years of age and older and were treated as inpatients for at least 48 h unless expired within 24 h. Exposure Receipt of hydroxychloroquine alone, hydroxychloroquine in combination with azithromycin, azithromycin alone, or neither. Main outcome The primary outcome was in-hospital mortality. Results Of 2,541 patients, with a median total hospitalization time of 6 days (IQR: 4–10 days), median age was 64 years (IQR:53–76 years), 51% male, 56% African American, with median time to follow-up of 28.5 days (IQR:3–53). Overall in-hospital mortality was 18.1% (95% CI:16.6%–19.7%); by treatment: hydroxychloroquine + azithromycin, 157/783 (20.1% [95% CI: 17.3%–23.0%]), hydroxychloroquine alone, 162/1202 (13.5% [95% CI: 11.6%–15.5%]), azithromycin alone, 33/147 (22.4% [95% CI: 16.0%–30.1%]), and neither drug, 108/409 (26.4% [95% CI: 22.2%–31.0%]). Primary cause of mortality was respiratory failure (88%); no patient had documented torsades de pointes. From Cox regression modeling, predictors of mortality were age > 65 years (HR:2.6 [95% CI:1.9–3.3]), white race (HR:1.7 [95% CI:1.4–2.1]), CKD (HR:1.7 [95%CI:1.4–2.1]), reduced O2 saturation level on admission (HR:1.5 [95%CI:1.1–2.1]), and ventilator use during admission (HR: 2.2 [95%CI:1.4–3.3]). Hydroxychloroquine provided a 66% hazard ratio reduction, and hydroxychloroquine + azithromycin 71% compared to neither treatment (p Conclusions and relevance In this multi-hospital assessment, when controlling for COVID-19 risk factors, treatment with hydroxychloroquine alone and in combination with azithromycin was associated with reduction in COVID-19 associated mortality. Prospective trials are needed to examine this impact.
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- 2020
15. Estratificación del pie diabético en el Hospital General Guasmo Sur período 2018 - 2019
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Katiuska Patricia Cervantes Moyano, Alexandra Elizabeth Delgado Rivera, Karen Katherine Reyes Murillo, and Lida Stefania Veloz Estrada
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Pediatrics ,medicine.medical_specialty ,business.industry ,Mortality rate ,Emergency department ,medicine.disease ,Diabetic foot ,Health promotion ,Diabetes mellitus ,medicine ,General Earth and Planetary Sciences ,Observational study ,Correlation index ,Complication ,business ,General Environmental Science - Abstract
Antecedentes: El pie diabético es la entidad clínica que se representa como la principal complicación de la diabetes, un 20% de los diabéticos necesitará una internación anual y de esta el 25% es a causa del pie diabético. El objetivo principal del estudio fue presentar y establecer las características demográficas mediante escalas de clasificación del pie diabético en los pacientes que acuden al departamento de Emergencias del Hospital General Guasmo Sur. Métodos: Se realizó un estudio retrospectivo, descriptivo, observacional en pacientes con pie diabético durante el año 2018 y 2019. Se analizó edad, género, tiempo de evolución para presentar pie diabético, características clínicas según la escala de Wagner y Texas. Se usó Microsoft Excel y se procesó la información para obtención de porcentajes de variables cualitativa y cuantitativa, se empleó el índice de correlación de Pearson para cada clasificación. Resultados: Se evaluó 70 pacientes con pie diabético, de género masculino el 60%, grupo etario predominante de 51 a 60 años con el 36%. Tipo de diabetes mellitus 2 con el 86%, el tiempo de evolución para presentación clínica del pie diabético con mayor frecuencia de 16 a 20 años con el 36%. Se usó la escala de Texas y Wagner para las características clínicas, las tasas de mortalidad se encontraron a favor con mayor porcentaje para la escala de Wagner con el 17% vs 5% para Texas. Conclusiones: La estadificación del pie diabético de acuerdo a las escalas empleadas, y las características clínicas encontradas tiene importancia médica, la promoción de salud, la prevención de la diabetes mellitus y un buen manejo de las complicaciones es decisivo desde el primer nivel de atención en salud.
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- 2020
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16. Urbanismo y turismo: una mirada legal al desarrollo sostenible en Perú
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Gil, Mariano Miguel Blas, Cuba, Claudia Katherine Reyes, and Peralta, Ena Cecilia Obando
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sustainable urban planning ,sustainable tourism ,Agenda 2030 ,law ,decree ,urbanismo sostenible ,turismo sostenible ,ley ,decreto - Abstract
El objetivo de este artículo es discutir el estado actual de los aspectos conceptuales, teóricos y jurídicos sobre urbanismo y turismo sostenible en Perú para encarar los retos de la Agenda 2030 de Naciones Unidas. A partir de la reciente promulgación de la Ley de Desarrollo Urbano Sostenible y del Decreto Supremo que aprueba el Código Técnico de Construcción Sostenible, las construcciones están orientadas al levantamiento de espacios incluyentes, que preserven la armonía con la naturaleza y el desarrollo social del ser humano. Por otro lado, el turismo sostenible en el país se sustenta en la Ley General del Turismo, que promueve planes nacionales y regionales orientados al desarrollo social y económico local, representando estos preceptos, las bases legales para el cumplimiento de las metas de la Agenda 2030. La investigación se ejecutó bajo el enfoque metodológico documental para luego contrastar la norma jurídica con el estado actual de las variables estudiadas.
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- 2022
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17. Ideología de género en perspectiva crítica intercultural
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Johanson, Katherin Pozo, Cuba, Claudia Katherine Reyes, and Peralta, Ena Cecilia Obando
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Gender Ideology ,Interculturality ,Equity, Multiculturalism ,Intercultural Dialogue ,ideología de género ,interculturalidad ,equidad ,multiculturalidad ,diálogo intercultural - Abstract
La violencia que se ha construido en torno al género afecta las dinámicas sociales y las formas de comprender el mundo. Si bien es cierto, el papel de la mujer en la construcción de la cultura es vital, las relaciones con el otro, con el sexo masculino, han sido de asimetrías, cosificación e implementación de lógicas patriarcales dominantes. Por esta razón, el artículo analiza las categorías de género, equidad, multiculturalidad e interculturalidad, señalando la necesaria trascendencia de los enfoques multiculturales, que esconden patrones discriminatorios hegemónicos hacia la mujer y la cultura, ya que no es suficiente con el reconocimiento o tolerancia hacia el otro, se requiere de la instauración de diálogos simétricos, equitativos, que tiendan hacia la justicia social. El trabajo se desarrolló siguiendo los lineamientos la metodología hermenéutica-documental. Se concluye en el reconocimiento de la heterogeneidad de géneros, culturas y saberes, a denunciar los patrones discriminatorios en enfoques multiculturales, que fomentan el maltrato hacia la identidad divergente, tendiendo hacia la consolidación de un sistema ético-normativo sustentado en un diálogo intercultural genuino.
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- 2022
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18. Contemporary Clinical and Molecular Epidemiology of Vancomycin-Resistant Enterococcal Bacteremia: A Prospective Multicenter Cohort Study (VENOUS I)
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German A Contreras, Jose M Munita, Shelby Simar, Courtney Luterbach, An Q Dinh, Kirsten Rydell, Pranoti V Sahasrabhojane, Rafael Rios, Lorena Diaz, Katherine Reyes, Marcus Zervos, Helina M Misikir, Gabriela Sanchez-Petitto, Catherine Liu, Yohei Doi, Lilian M Abbo, Luis Shimose, Harald Seifert, Carlota Gudiol, Fernanda Barberis, Claudia Pedroza, Samuel L Aitken, Samuel A Shelburne, David van Duin, Truc T Tran, Blake M Hanson, and Cesar A Arias
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Infectious Diseases ,Malalties bacterianes ,Oncology ,Epidemiology ,Drug resistance ,Bacterial diseases ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,Epidemiologia ,Resistència als medicaments - Abstract
Background Vancomycin-resistant enterococci (VRE) are major therapeutic challenges. Prospective contemporary data characterizing the clinical and molecular epidemiology of VRE bloodstream infections (BSIs) are lacking. Methods The Vancomycin-Resistant Enterococcal BSI Outcomes Study (VENOUS I) is a prospective observational cohort of adult patients with enterococcal BSI in 11 US hospitals. We included patients with Enterococcus faecalis or Enterococcus faecium BSI with ≥1 follow-up blood culture(s) within 7 days and availability of isolate(s) for further characterization. The primary study outcome was in-hospital mortality. Secondary outcomes were mortality at days 4, 7, 10, 12, and 15 after index blood culture. A desirability of outcome ranking was constructed to assess the association of vancomycin resistance with outcomes. All index isolates were subjected to whole genome sequencing. Results Forty-two of 232 (18%) patients died in hospital and 39 (17%) exhibited microbiological failure (lack of clearance in the first 4 days). Neutropenia (hazard ratio [HR], 3.13), microbiological failure (HR, 2.4), VRE BSI (HR, 2.13), use of urinary catheter (HR, 1.85), and Pitt BSI score ≥2 (HR, 1.83) were significant predictors of in-hospital mortality. Microbiological failure was the strongest predictor of in-hospital mortality in patients with E faecium bacteremia (HR, 5.03). The impact of vancomycin resistance on mortality in our cohort changed throughout the course of hospitalization. Enterococcus faecalis sequence type 6 was a predominant multidrug-resistant lineage, whereas a heterogeneous genomic population of E faecium was identified. Conclusions Failure of early eradication of VRE from the bloodstream is a major factor associated with poor outcomes.
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- 2021
19. MÉTODO AUTOMÁTICO PARA LA MEDIDA DE LA VELOCIDAD DE FLUJO DE HEMOSUSTITUTOS EN ARTERIOLAS MEDIANTE PROCESAMIENTO DE IMÁGENES
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Manuel Guillermo Forero Vargas, Paula Katherine Reyes Garibello, Nicolás Ramírez Polanía, Sandra Liliana Cancino Suárez, and Homero Fernando Pastrana Rendón
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En algunos casos médicos, como cirugías y tratamiento de enfermedades cardiovasculares, o traumatismos es necesario el uso de la transfusión de sangre debido al riesgo o la presencia de hemorragia. Sin embargo, puede haber inconvenientes como la disponibilidad limitada de sangre, por falta de donantes, así como incompatibilidad de grupo sanguíneo o factor Rh, el riesgo de transmisión de enfermedades a través de la transfusión o el rechazo del procedimiento por parte del paciente. Por ello, se ha hecho necesario desarrollar sustancias denominadas hemosustituto, o hemoglobinas modificadas, que puedan sustituir a la sangre en su función de transporte de oxígeno. Uno de los fenómenos a evaluar para determinar la seguridad de los hemosustitutos, es el esfuerzo cortante sobre el endotelio. Tanto los esfuerzos elevados como muy bajos pueden generar daños en la función del endotelio produciendo arterias rígidas cuando se tiene un esfuerzo cortante elevado o el colapso de la arteria cuando el esfuerzo cortante disminuye o tiende a cero. Este fenómeno puede observarse mediante secuencias de imágenes de microscopía. En esta evaluación se requiere un grado importante de experticia, ya que los vasos capilares son muy pequeños y determinar la velocidad del flujo sanguíneo es difícil manualmente. Por ello, en este trabajo se propone una nueva técnica para la medición del flujo sanguíneo, desarrollada como un plugin para el programa imageJ. Emplea el canal de color con mayor entropía, sobre el que se realiza una detección de simetría y una transformación de producto de gradiente para la extracción del eje central y la estimación de la velocidad del flujo arteriolar hemostático. Los resultados fueron comparados con los obtenidos manualmente, presentando una mayor precisión y una estimación más rápida al permitir una mejor localización del punto por el que transita el hemosustituto en un tiempo determinado.
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- 2021
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20. Cuidados del bebe recién nacido sano
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Doris Fabiola Guallpa Lema, María Katherine Reyes Mera, Jonathan Gerardo Aguirre Mendoza, Mayra Andrea Santos Briones, Mónica Mariana Casanova Castillo, and Luis Enrique Ponce Quijije
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Strategy and Management ,Mechanical Engineering ,Metals and Alloys ,Industrial and Manufacturing Engineering - Abstract
Los ninos menores de cinco anos que fallecen cada ano son al menos 40% lactantes recien nacidos, muchos de estos casos son previsibles. El cuidado del feto desde su concepcion y durante el embarazo es requerido, asi como los cuidados inmediatos que se suministran al momento del parto y posterior a este. Revisar los cuidados en todas sus fases desde el parto y consecutivos, analizar los cuidados tanto en el centro de salud como los que deben procurarse en casa, son los principales objetivos planteados por este estudio, la revision documental permite recopilar recomendaciones y mejores practicas en el cuidado del recien nacido para incidir en la formacion y futuras investigaciones y en consecuencia dar a conocer la importancia de los cuidados del Neonato.
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- 2020
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21. Estudio comparativo de la isquemia en apendicectomia convencional vs laparoscópica. Factores de riesgo y complicaciones
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Karen Katherine Reyes Murillo, Yalixa lissette Macias cedeño, Katiuska Patricia Cervantes Moyano, and Lida Stefania Veloz Estrada
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Strategy and Management ,Mechanical Engineering ,Metals and Alloys ,Industrial and Manufacturing Engineering - Abstract
Este articulo busca comparar la isquemia en apendicetomia convencional vs laparoscopica, factores de riesgos y complicaciones, por ello, se hace una revision previa de diferentes documentos para asi relacionarla con la investigacion documental y al mismo tiempo permite indicar que en el campo de las urgencias medicas las sintomatologias relacionada con el abdomen especificamente con el apendice se convierte en una practica con alta frecuencia, esto lleva a realizar una intervencion quirurgica conocida como apendicetomia, aplicado ante la presencia de una apendicitis aguda, la misma puede ser efectuada de manera convencional; es decir, se realiza una incision en el lado inferior derecho para extirpar el apendices. Asimismo, existe una cirugia minimamente invasiva (laparoscopica) que representa un avance reciente en la apendicetomia, utiliza una sola incision menos invasiva y utiliza un unico puerto multiluminal o puertos multiples monoluminales, a traves de una unica incision en la piel. Sin embargo, hoy se dan controversias cientificas en relacion a estos procedimientos quirurgicos, el convencional o abierta, ha sido durante mas de un siglo, el mas utilizado para resolver el cuadro clinico, y ha probado largamente su eficacia. Entre las complicaciones comunes en ambas tecnicas, pueden mencionarse la aparicion de abscesos intraabdominales, dehiscencia del munon apendicular, obstruccion intestinal por bridas e infecciones de las heridas quirurgicas. Asimismo, se puede aportar que dichas tecnicas no ofrecen mayores ventajas con respecto al tiempo de internacion, recuperacion del transito intestinal, dolor postoperatorio entre otros. En consecuencia, su eleccion depende del cirujano. Para concluir, que la utilizacion de las tecnicas citadas se encuentra directamente relacionadas con el diagnostico medico y su seleccion es responsabilidad del especialista, pues, ambas de acuerdo a diferentes estudios cientificos presentan ventajas, complicaciones y factores de riesgos que pueden ser debidamente canalizados por el medico.
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- 2019
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22. Aspiration Risk Factors, Microbiology, and Empiric Antibiotics for Patients Hospitalized With Community-Acquired Pneumonia
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Judith Marin-Corral, Sergi Pascual-Guardia, Francesco Amati, Stefano Aliberti, Joan R Masclans, Nilam Soni, Alejandro Rodriguez, Oriol Sibila, Francisco Sanz, Giovanni Sotgiu, Antonio Anzueto, Katerina Dimakou, Roberta Petrino, Ewoudt van de Garde, Marcos I Restrepo, GLIMP investigators, Patricia Karina Aruj, Silvia Attorri, Enrique Barimboim, Juan Pablo Caeiro, María I Garzón, Victor Hugo Cambursano, V H Dr Cazaux A Adrian Ceccato, Julio Chertcoff, Florencia Lascar, Fernando Di Tulio, Ariel Cordon Díaz, Lautaro de Vedia, Maria Cristina Ganaha, Sandra Lambert, Gustavo Lopardo, Carlos M Luna, Alessio Gerardo Malberti, Nora Morcillo, Silvina Tartara, Claudia Pensotti, Betiana Pereyra, Pablo Gustavo Scapellato, Juan Pablo Stagnaro, Sonali Shah, Felix Lötsch, Florian Thalhammer, Kurt Anseeuw, Camille A Francois, Eva Van Braeckel, Jean Louis Vincent, Marcel Zannou Djimon, Jules Bashi, Roger Dodo, Simone Aranha Nouér, Peter Chipev, Milena Encheva, Darina Miteva, Diana Petkova, Adamou Dodo Balkissou, Eric Walter Pefura Yone, Bertrand Hugo Mbatchou Ngahane, Ning Shen, Jin-Fu Xu, Carlos Andres Bustamante Rico, Ricardo Buitrago, Fernando Jose Pereira Paternina, Jean-Marie Kayembe Ntumba, Vesna Vladic Carevic, Marko Jakopovic, Mateja Jankovic, Zinka Matkovic, Ivan Mitrecic, Marie-Laure Bouchy Jacobsson, Anette Bro Christensen, Uffe Christian Heitmann Bødtger, Christian Niels Meyer, Andreas Vestergaard Jensen, Gertrud Baunbæk-Knudsen, Pelle Trier Petersen, Stine Andersen, Ibrahim El-Said Abd El-Wahhab, Nesreen Elsayed Morsy, Hanaa Shafiek, Eman Sobh, Kedir Abdella Abdulsemed, Fabrice Bertrand, Christian Brun-Buisson, Etienne de Montmollin, Muriel Fartoukh, Jonathan Messika, Pierre Tattevin, Abdo Khoury, Bernard Ebruke, Michael Dreher, Martin Kolditz, Matthias Meisinger, Mathias W Pletz, Stefan Hagel, Jan Rupp, Tom Schaberg, Marc Spielmanns, Petra Creutz, Norton Suttorp, Beatrice Siaw-Lartey, Dimosthenis Papapetrou, Evdoxia Tsigou, Dimitrios Ampazis, Evangelos Kaimakamis, Mohit Bhatia, Raja Dhar, George D'Souza, Rajiv Garg, Parvaiz A Koul, P A Mahesh, B S Jayaraj, Kiran Vishnu Narayan, Hirennappa B Udnur, Shashi Bhaskara Krishnamurthy, Surya Kant, Rajesh Swarnakar, Sneha Limaye, Sundeep Salvi, Keihan Golshani, Vera M Keatings, Ignacio Martin-Loeches, Yasmin Maor, Jacob Strahilevitz, Paola Faverio, Salvatore Battaglia, Maria Carrabba, Piero Ceriana, Marco Confalonieri, Antonella d'Arminio Monforte, Bruno Del Prato, Marino De Rosa, Riccardo Fantini, Giuseppe Fiorentino, Maria Antonia Gammino, Francesco Menzella, Giuseppe Milani, Stefano Nava, Gerardo Palmiero, Barbra Gabrielli, Paolo Rossi, Claudio Sorino, Gundi Steinhilber, Alessandro Zanforlin, Ospedale San Luca, Fabio Franzetti, Manuela Carugati, Manuela Morosi, Elisa Monge, Mauro Carone, Vincenzo Patella, Simone Scarlata, Andrea Comel, Kiyoyasu Kurahashi, Zeina Aoun Bacha, Daniel Barajas Ugalde, Omar Ceballos Zuñiga, José F Villegas, Milic Medenica, Deebya Raj Mihsra, Poojan Shrestha, Elliott Ridgeon, Babatunde Ishola Awokola, Ogonna N O Adefuye Bolanle Olufunlola, Segaolu Olumide, Kingsley N Ukwaja, Muhammad Irfan, Lukasz Minarowski, Skoczyński Szymon, Felipe Froes, Pedro Leuschner, Mariana Meireles, Cláudia Ferrão, João Neves, Abel Salazar, Sofia B Ravara, Victoria Brocovschii, Doina Rusu, Cristina Toma, Daniela Chirita, Carmen Mihaela Dorobat, Alexei Birkun, Anna Kaluzhenina, Abdullah Almotairi, Zakeya Abdulbaqi Ali Bukhary, Jameela Edathodu, Amal Fathy, Abdullah Mushira Abdulaziz Enani, Nazik Eltayeb Mohamed, Jawed Ulhadi Memon, Abdelhaleem Bella, Serbia Nada Bogdanović, Branislava Milenkovic, Dragica Pesut, Luis Borderìas, Noel Manuel Bordon Garcia, Hugo Cabello Alarcón, Catia Cilloniz, Antoni Torres, Vicens Diaz-Brito, Xavier Casas, Alicia Encabo González, Maria Luisa Fernández-Almira, Medicina Interna, Miguel Gallego, Inmaculada Gaspar-GarcÍa, Juan González Del Castillo, Patricia Javaloyes Victoria, Elena Laserna Martínez, Rosa Malo de Molina, Pedro J Marcos, Rosario Menéndez, Ana Pando-Sandoval, Cristina Prat Aymerich, Alicia Lacoma de la Torre, Ignasi García-Olivé, Jordi Rello, Silvia Moyano, Ana Rodrigo-Troyano, Jordi Solé-Violán, Ane Uranga, Job Fm van Boven, Ester Vendrell Torra, Jordi Almirall Pujol, Charles Feldman, Ho Kee Yum, Inje Univ Arnauld Attannon Fiogbe, Ferdaous Yangui, Semra Bilaceroglu, Izmir Dr Levent Dalar, Ufuk Yilmaz, Artemii Bogomolov, Naheed Elahi, Devesh J Dhasmana, Andrew Feneley, Adam T Hill, Banu Rudran, Silvia Ruiz-Buitrago, Marion Campbell, Paul Whitaker, Alexander Youzguin, Anika Singanayagam, C Hancock, David Villafuerte, Karen S Allen, Veronica Brito, Jessica Dietz, Claire E Dysart, Susan M Kellie, Clement J Ricardo A Franco-Sadud, Garnet Meier, Mina Gaga, Thomas L Holland, Stephen P Bergin, Fayez Kheir, Mark Landmeier, Manuel Lois, Girish B Nair, Hemali Patel, Katherine Reyes, William Rodriguez-Cintron, Shigeki Saito, Julio Noda, Cecilia I Hinojosa, Stephanie M Levine, Luis F Reyes, Luis F Angel, K Scott Whitlow, John Hipskind, Kunal Sukhija, Vicken Totten, Richard G Wunderink, Ray D Shah, Kondwelani John Mateyo, Lorena Noriega, Ezequiel Alvarado, Mohamed Aman, Lucía Labra, Marin-Corral J., Pascual-Guardia S., Amati F., Aliberti S., Masclans J.R., Soni N., Rodriguez A., Sibila O., Sanz F., Sotgiu G., Anzueto A., Dimakou K., Petrino R., van de Garde E., Restrepo M.I., Aruj P.K., Attorri S., Barimboim E., Caeiro J.P., Garzon M.I., Cambursano V.H., Adrian Ceccato V.H.D.C.A., Chertcoff J., Lascar F., Di Tulio F., Diaz A.C., de Vedia L., Ganaha M.C., Lambert S., Lopardo G., Luna C.M., Malberti A.G., Morcillo N., Tartara S., Pensotti C., Pereyra B., Scapellato P.G., Stagnaro J.P., Shah S., Lotsch F., Thalhammer F., Anseeuw K., Francois C.A., Van Braeckel E., Vincent J.L., Djimon M.Z., Bashi J., Dodo R., Nouer S.A., Chipev P., Encheva M., Miteva D., Petkova D., Balkissou A.D., Pefura Yone E.W., Mbatchou Ngahane B.H., Shen N., Xu J.-F., Bustamante Rico C.A., Buitrago R., Pereira Paternina F.J., Kayembe Ntumba J.-M., Carevic V.V., Jakopovic M., Jankovic M., Matkovic Z., Mitrecic I., Bouchy Jacobsson M.-L., Christensen A.B., Heitmann Bodtger U.C., Meyer C.N., Jensen A.V., Baunbaek-knudsen G., Petersen P.T., Andersen S., El-Said Abd El-Wahhab I., Morsy N.E., Shafiek H., Sobh E., Abdulsemed K.A., Bertrand F., Brun-Buisson C., de Montmollin E., Fartoukh M., Messika J., Tattevin P., Khoury A., Ebruke B., Dreher M., Kolditz M., Meisinger M., Pletz M.W., Hagel S., Rupp J., Schaberg T., Spielmanns M., Creutz P., Suttorp N., Siaw-Lartey B., Papapetrou D., Tsigou E., Ampazis D., Kaimakamis E., Bhatia M., Dhar R., D'Souza G., Garg R., Koul P.A., Mahesh P.A., Jayaraj B.S., Narayan K.V., Udnur H.B., Krishnamurthy S.B., Kant S., Swarnakar R., Limaye S., Salvi S., Golshani K., Keatings V.M., Martin-Loeches I., Maor Y., Strahilevitz J., Faverio P., Battaglia S., Carrabba M., Ceriana P., Confalonieri M., Monforte A.D., Del Prato B., De Rosa M., Fantini R., Fiorentino G., Gammino M.A., Menzella F., Milani G., Nava S., Palmiero G., Gabrielli B., Rossi P., Sorino C., Steinhilber G., Zanforlin A., San Luca O., Franzetti F., Carugati M., Morosi M., Monge E., Carone M., Patella V., Scarlata S., Comel A., Kurahashi K., Bacha Z.A., Ugalde D.B., Zuniga O.C., Villegas J.F., Medenica M., Mihsra D.R., Shrestha P., Ridgeon E., Awokola B.I., Adefuye Bolanle Olufunlola O.N.O., Olumide S., Ukwaja K.N., Irfan M., Minarowski L., Szymon S., Froes F., Leuschner P., Meireles M., Ferrao C., Neves J., Abel Salazar, Ravara S.B., Brocovschii V., Rusu D., Toma C., Chirita D., Dorobat C.M., Birkun A., Kaluzhenina A., Almotairi A., Ali Bukhary Z.A., Edathodu J., Fathy A., Abdulaziz Enani A.M., Mohamed N.E., Memon J.U., Bella A., Bogdanovic S.N., Milenkovic B., Pesut D., Borderias L., Bordon Garcia N.M., Alarcon H.C., Cilloniz C., Torres A., Diaz-Brito V., Casas X., Gonzalez A.E., Fernandez-Almira M.L., Interna M., Gallego M., Gaspar-GarcIa I., Gonzalez del Castillo J., Victoria P.J., Martinez E.L., Malo de Molina R., Marcos P.J., Menendez R., Pando-Sandoval A., Aymerich C.P., Lacoma de la Torre A., Garcia-Olive I., Rello J., Moyano S., Rodrigo-Troyano A., Sole-Violan J., Uranga A., van Boven J.F., Torra E.V., Pujol J.A., Feldman C., Yum H.K., Arnauld Attannon Fiogbe I.U., Yangui F., Bilaceroglu S., Levent Dalar I.D., Yilmaz U., Bogomolov A., Elahi N., Dhasmana D.J., Feneley A., Hill A.T., Rudran B., Ruiz-Buitrago S., Campbell M., Whitaker P., Youzguin A., Singanayagam A., Hancock C., Villafuerte D., Allen K.S., Brito V., Dietz J., Dysart C.E., Kellie S.M., Ricardo A. Franco-Sadud C.J., Meier G., Gaga M., Holland T.L., Bergin S.P., Kheir F., Landmeier M., Lois M., Nair G.B., Patel H., Reyes K., Rodriguez-Cintron W., Saito S., Noda J., Hinojosa C.I., Levine S.M., Reyes L.F., Angel L.F., Whitlow K.S., Hipskind J., Sukhija K., Totten V., Wunderink R.G., Shah R.D., Mateyo K.J., Noriega L., Alvarado E., Aman M., Labra L., Marin-Corral, Judith, Pascual-Guardia, Sergi, Amati, Francesco, Aliberti, Stefano, R Masclans, Joan, Soni, Nilam, Rodriguez, Alejandro, Sibila, Oriol, Sanz, Francisco, Sotgiu, Giovanni, Anzueto, Antonio, Dimakou, Katerina, Petrino, Roberta, van de Garde, Ewoudt, I Restrepo, Marco, Investigators, Glimp, Karina Aruj, Patricia, Attorri, Silvia, Barimboim, Enrique, Pablo Caeiro, Juan, I Garzón, María, Hugo Cambursano, Victor, A Adrian Ceccato, V H Dr Cazaux, Chertcoff, Julio, Lascar, Florencia, Di Tulio, Fernando, Cordon Díaz, Ariel, de Vedia, Lautaro, Cristina Ganaha, Maria, Lambert, Sandra, Lopardo, Gustavo, M Luna, Carlo, Gerardo Malberti, Alessio, Morcillo, Nora, Tartara, Silvina, Pensotti, Claudia, Pereyra, Betiana, Gustavo Scapellato, Pablo, Pablo Stagnaro, Juan, Shah, Sonali, Lötsch, Felix, Thalhammer, Florian, Anseeuw, Kurt, A Francois, Camille, Van Braeckel, Eva, Louis Vincent, Jean, Zannou Djimon, Marcel, Bashi, Jule, Dodo, Roger, Aranha Nouér, Simone, Chipev, Peter, Encheva, Milena, Miteva, Darina, Petkova, Diana, Dodo Balkissou, Adamou, Walter Pefura Yone, Eric, Hugo Mbatchou Ngahane, Bertrand, Shen, Ning, Xu, Jin-Fu, Andres Bustamante Rico, Carlo, Buitrago, Ricardo, Jose Pereira Paternina, Fernando, Kayembe Ntumba, Jean-Marie, Vladic Carevic, Vesna, Jakopovic, Marko, Jankovic, Mateja, Matkovic, Zinka, Mitrecic, Ivan, Bouchy Jacobsson, Marie-Laure, Bro Christensen, Anette, Christian Heitmann Bødtger, Uffe, Niels Meyer, Christian, Vestergaard Jensen, Andrea, Baunbæk-Knudsen, Gertrud, Trier Petersen, Pelle, Andersen, Stine, El-Said Abd El-Wahhab, Ibrahim, Elsayed Morsy, Nesreen, Shafiek, Hanaa, Sobh, Eman, Abdella Abdulsemed, Kedir, Bertrand, Fabrice, Brun-Buisson, Christian, de Montmollin, Etienne, Fartoukh, Muriel, Messika, Jonathan, Tattevin, Pierre, Khoury, Abdo, Ebruke, Bernard, Dreher, Michael, Kolditz, Martin, Meisinger, Matthia, W Pletz, Mathia, Hagel, Stefan, Rupp, Jan, Schaberg, Tom, Spielmanns, Marc, Creutz, Petra, Suttorp, Norton, Siaw-Lartey, Beatrice, Papapetrou, Dimostheni, Tsigou, Evdoxia, Ampazis, Dimitrio, Kaimakamis, Evangelo, Bhatia, Mohit, Dhar, Raja, D'Souza, George, Garg, Rajiv, A Koul, Parvaiz, A Mahesh, P, S Jayaraj, B, Vishnu Narayan, Kiran, B Udnur, Hirennappa, Bhaskara Krishnamurthy, Shashi, Kant, Surya, Swarnakar, Rajesh, Limaye, Sneha, Salvi, Sundeep, Golshani, Keihan, M Keatings, Vera, Martin-Loeches, Ignacio, Maor, Yasmin, Strahilevitz, Jacob, Faverio, Paola, Battaglia, Salvatore, Carrabba, Maria, Ceriana, Piero, Confalonieri, Marco, d'Arminio Monforte, Antonella, Del Prato, Bruno, De Rosa, Marino, Fantini, Riccardo, Fiorentino, Giuseppe, Antonia Gammino, Maria, Menzella, Francesco, Milani, Giuseppe, Nava, Stefano, Palmiero, Gerardo, Gabrielli, Barbra, Rossi, Paolo, Sorino, Claudio, Steinhilber, Gundi, Zanforlin, Alessandro, San Luca, Ospedale, Franzetti, Fabio, Carugati, Manuela, Morosi, Manuela, Monge, Elisa, Carone, Mauro, Patella, Vincenzo, Scarlata, Simone, Comel, Andrea, Kurahashi, Kiyoyasu, Aoun Bacha, Zeina, Barajas Ugalde, Daniel, Ceballos Zuñiga, Omar, F Villegas, José, Medenica, Milic, Raj Mihsra, Deebya, Shrestha, Poojan, Ridgeon, Elliott, Ishola Awokola, Babatunde, O Adefuye Bolanle Olufunlola, Ogonna N, Olumide, Segaolu, N Ukwaja, Kingsley, Irfan, Muhammad, Minarowski, Lukasz, Szymon, Skoczyński, Froes, Felipe, Leuschner, Pedro, Meireles, Mariana, Ferrão, Cláudia, Neves, João, Salazar, Abel, B Ravara, Sofia, Brocovschii, Victoria, Rusu, Doina, Toma, Cristina, Chirita, Daniela, Mihaela Dorobat, Carmen, Birkun, Alexei, Kaluzhenina, Anna, Almotairi, Abdullah, Abdulbaqi Ali Bukhary, Zakeya, Edathodu, Jameela, Fathy, Amal, Mushira Abdulaziz Enani, Abdullah, Eltayeb Mohamed, Nazik, Ulhadi Memon, Jawed, Bella, Abdelhaleem, Nada Bogdanović, Serbia, Milenkovic, Branislava, Pesut, Dragica, Borderìas, Lui, Manuel Bordon Garcia, Noel, Cabello Alarcón, Hugo, Cilloniz, Catia, Torres, Antoni, Diaz-Brito, Vicen, Casas, Xavier, Encabo González, Alicia, Luisa Fernández-Almira, Maria, Interna, Medicina, Gallego, Miguel, Gaspar-GarcÍa, Inmaculada, González Del Castillo, Juan, Javaloyes Victoria, Patricia, Laserna Martínez, Elena, Malo de Molina, Rosa, J Marcos, Pedro, Menéndez, Rosario, Pando-Sandoval, Ana, Prat Aymerich, Cristina, Lacoma de la Torre, Alicia, García-Olivé, Ignasi, Rello, Jordi, Moyano, Silvia, Rodrigo-Troyano, Ana, Solé-Violán, Jordi, Uranga, Ane, Fm van Boven, Job, Vendrell Torra, Ester, Almirall Pujol, Jordi, Feldman, Charle, Kee Yum, Ho, Univ Arnauld Attannon Fiogbe, Inje, Yangui, Ferdaou, Bilaceroglu, Semra, Dr Levent Dalar, Izmir, Yilmaz, Ufuk, Bogomolov, Artemii, Elahi, Naheed, J Dhasmana, Devesh, Feneley, Andrew, T Hill, Adam, Rudran, Banu, Ruiz-Buitrago, Silvia, Campbell, Marion, Whitaker, Paul, Youzguin, Alexander, Singanayagam, Anika, Hancock, C, Villafuerte, David, S Allen, Karen, Brito, Veronica, Dietz, Jessica, E Dysart, Claire, M Kellie, Susan, A Franco-Sadud, Clement J Ricardo, Meier, Garnet, Gaga, Mina, L Holland, Thoma, P Bergin, Stephen, Kheir, Fayez, Landmeier, Mark, Lois, Manuel, B Nair, Girish, Patel, Hemali, Reyes, Katherine, Rodriguez-Cintron, William, Saito, Shigeki, Noda, Julio, I Hinojosa, Cecilia, M Levine, Stephanie, F Reyes, Lui, F Angel, Lui, Scott Whitlow, K, Hipskind, John, Sukhija, Kunal, Totten, Vicken, G Wunderink, Richard, D Shah, Ray, John Mateyo, Kondwelani, Noriega, Lorena, Alvarado, Ezequiel, Aman, Mohamed, Labra, Lucía, Marin-Corral, J, Pascual-Guardia, S, Amati, F, Aliberti, S, Masclans, J, Soni, N, Rodriguez, A, Sibila, O, Sanz, F, Sotgiu, G, Anzueto, A, Dimakou, K, Petrino, R, van de Garde, E, Restrepo, M, Aruj, P, Attorri, S, Barimboim, E, Caeiro, J, Garzon, M, Cambursano, V, Adrian Ceccato, V, Chertcoff, J, Lascar, F, Di Tulio, F, Diaz, A, de Vedia, L, Ganaha, M, Lambert, S, Lopardo, G, Luna, C, Malberti, A, Morcillo, N, Tartara, S, Pensotti, C, Pereyra, B, Scapellato, P, Stagnaro, J, Shah, S, Lotsch, F, Thalhammer, F, Anseeuw, K, Francois, C, Van Braeckel, E, Vincent, J, Djimon, M, Bashi, J, Dodo, R, Nouer, S, Chipev, P, Encheva, M, Miteva, D, Petkova, D, Balkissou, A, Pefura Yone, E, Mbatchou Ngahane, B, Shen, N, Xu, J, Bustamante Rico, C, Buitrago, R, Pereira Paternina, F, Kayembe Ntumba, J, Carevic, V, Jakopovic, M, Jankovic, M, Matkovic, Z, Mitrecic, I, Bouchy Jacobsson, M, Christensen, A, Heitmann Bodtger, U, Meyer, C, Jensen, A, Baunbaek-knudsen, G, Petersen, P, Andersen, S, El-Said Abd El-Wahhab, I, Morsy, N, Shafiek, H, Sobh, E, Abdulsemed, K, Bertrand, F, Brun-Buisson, C, de Montmollin, E, Fartoukh, M, Messika, J, Tattevin, P, Khoury, A, Ebruke, B, Dreher, M, Kolditz, M, Meisinger, M, Pletz, M, Hagel, S, Rupp, J, Schaberg, T, Spielmanns, M, Creutz, P, Suttorp, N, Siaw-Lartey, B, Papapetrou, D, Tsigou, E, Ampazis, D, Kaimakamis, E, Bhatia, M, Dhar, R, D'Souza, G, Garg, R, Koul, P, Mahesh, P, Jayaraj, B, Narayan, K, Udnur, H, Krishnamurthy, S, Kant, S, Swarnakar, R, Limaye, S, Salvi, S, Golshani, K, Keatings, V, Martin-Loeches, I, Maor, Y, Strahilevitz, J, Faverio, P, Battaglia, S, Carrabba, M, Ceriana, P, Confalonieri, M, Monforte, A, Del Prato, B, De Rosa, M, Fantini, R, Fiorentino, G, Gammino, M, Menzella, F, Milani, G, Nava, S, Palmiero, G, Gabrielli, B, Rossi, P, Sorino, C, Steinhilber, G, Zanforlin, A, San Luca, O, Franzetti, F, Carugati, M, Morosi, M, Monge, E, Carone, M, Patella, V, Scarlata, S, Comel, A, Kurahashi, K, Bacha, Z, Ugalde, D, Zuniga, O, Villegas, J, Medenica, M, Mihsra, D, Shrestha, P, Ridgeon, E, Awokola, B, Adefuye Bolanle Olufunlola, O, Olumide, S, Ukwaja, K, Irfan, M, Minarowski, L, Szymon, S, Froes, F, Leuschner, P, Meireles, M, Ferrao, C, Neves, J, Abel, S, Ravara, S, Brocovschii, V, Rusu, D, Toma, C, Chirita, D, Dorobat, C, Birkun, A, Kaluzhenina, A, Almotairi, A, Ali Bukhary, Z, Edathodu, J, Fathy, A, Abdulaziz Enani, A, Mohamed, N, Memon, J, Bella, A, Bogdanovic, S, Milenkovic, B, Pesut, D, Borderias, L, Bordon Garcia, N, Alarcon, H, Cilloniz, C, Torres, A, Diaz-Brito, V, Casas, X, Gonzalez, A, Fernandez-Almira, M, Interna, M, Gallego, M, Gaspar-GarcIa, I, Gonzalez del Castillo, J, Victoria, P, Martinez, E, Malo de Molina, R, Marcos, P, Menendez, R, Pando-Sandoval, A, Aymerich, C, Lacoma de la Torre, A, Garcia-Olive, I, Rello, J, Moyano, S, Rodrigo-Troyano, A, Sole-Violan, J, Uranga, A, van Boven, J, Torra, E, Pujol, J, Feldman, C, Yum, H, Arnauld Attannon Fiogbe, I, Yangui, F, Bilaceroglu, S, Levent Dalar, I, Yilmaz, U, Bogomolov, A, Elahi, N, Dhasmana, D, Feneley, A, Hill, A, Rudran, B, Ruiz-Buitrago, S, Campbell, M, Whitaker, P, Youzguin, A, Singanayagam, A, Villafuerte, D, Allen, K, Brito, V, Dietz, J, Dysart, C, Kellie, S, Ricardo, A, Meier, G, Gaga, M, Holland, T, Bergin, S, Kheir, F, Landmeier, M, Lois, M, Nair, G, Patel, H, Reyes, K, Rodriguez-Cintron, W, Saito, S, Noda, J, Hinojosa, C, Levine, S, Reyes, L, Angel, L, Whitlow, K, Hipskind, J, Sukhija, K, Totten, V, Wunderink, R, Shah, R, Mateyo, K, Noriega, L, Alvarado, E, Aman, M, and Labra, L
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Male ,Pulmonary and Respiratory Medicine ,medicine.drug_class ,Aspiration risk ,Antibiotics ,Nursing home resident ,Settore MED/10 - Malattie Dell'Apparato Respiratorio ,Critical Care and Intensive Care Medicine ,Microbiology ,anaerobic ,aspiration ,bacteria ,pneumonia ,risk factors ,Cohort Studies ,03 medical and health sciences ,0302 clinical medicine ,Community-acquired pneumonia ,Taverne ,Anti-Bacterial Agent ,medicine ,Humans ,Community-Acquired Infection ,030212 general & internal medicine ,Stroke ,Aged ,Aged, 80 and over ,business.industry ,Respiratory Aspiration ,Middle Aged ,medicine.disease ,Antibiotic coverage ,Anti-Bacterial Agents ,Community-Acquired Infections ,Hospitalization ,Pneumonia ,030228 respiratory system ,Risk factors ,risk factor ,Female ,Underweight ,medicine.symptom ,business ,Cardiology and Cardiovascular Medicine - Abstract
Background: Aspiration community-acquired pneumonia (ACAP) and community-acquired pneumonia (CAP) in patients with aspiration risk factors (AspRFs) are infections associated with anaerobes, but limited evidence suggests their pathogenic role. Research Question: What are the aspiration risk factors, microbiology patterns, and empiric anti-anaerobic use in patients hospitalized with CAP? Study Design and Methods: This is a secondary analysis of GLIMP, an international, multicenter, point-prevalence study of adults hospitalized with CAP. Patients were stratified into three groups: (1) ACAP, (2) CAP/AspRF+ (CAP with AspRF), and (3) CAP/AspRF- (CAP without AspRF). Data on demographics, comorbidities, microbiological results, and anti-anaerobic antibiotics were analyzed in all groups. Patients were further stratified in severe and nonsevere CAP groups. Results: We enrolled 2,606 patients with CAP, of which 193 (7.4%) had ACAP. Risk factors independently associated with ACAP were male, bedridden, underweight, a nursing home resident, and having a history of stroke, dementia, mental illness, and enteral tube feeding. Among non-ACAP patients, 1,709 (70.8%) had CAP/AspRF+ and 704 (29.2%) had CAP/AspRF-. Microbiology patterns including anaerobes were similar between CAP/AspRF-, CAP/AspRF+ and ACAP (0.0% vs 1.03% vs 1.64%). Patients with severe ACAP had higher rates of total gram-negative bacteria (64.3% vs 44.3% vs 33.3%, P =.021) and lower rates of total gram-positive bacteria (7.1% vs 38.1% vs 50.0%, P 50% in all groups) independent of AspRFs or ACAP received specific or broad-spectrum anti-anaerobic coverage antibiotics. Interpretation: Hospitalized patients with ACAP or CAP/AspRF+ had similar anaerobic flora compared with patients without aspiration risk factors. Gram-negative bacteria were more prevalent in patients with severe ACAP. Despite having similar microbiological flora between groups, a large proportion of CAP patients received anti-anaerobic antibiotic coverage.
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- 2021
23. MEDICIÓN DE LA VARIACIÓN DEL DIÁMETRO EN ARTERIOLAS MEDIANTE LA CIRCULACIÓN DE HEMOSUSTITUTOS A PARTIR DE PROCESAMIENTO DE IMÁGENES
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Manuel Guillermo Forero Vargas, Paula Katherine Reyes Garibello, Nicolás Ramírez Polanía, Homero Fernando Pastrana Rendón, and Sandra Liliana Cancino Suárez
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En algunas situaciones médicas como cirugías y tratamiento de enfermedades cardiovasculares, traumas o hemorragias, se hace necesario el procedimiento de la transfusión sanguínea. Sin embargo, este procedimiento puede presentar inconvenientes como no tener disponibilidad suficiente de sangre, una posible incompatibilidad en el grupo sanguíneo o el factor Rh, el riesgo de contagio de enfermedades a través de la transfusión, y el rechazo por parte del paciente o sus familiares al procedimiento de transfusión debido a creencias personales. Por esta razón, se hace necesario desarrollar sustancias denominadas hemosustitutos, o hemoglobinas modificadas, que puedan reemplazar la sangre en su función de transportar oxígeno a las células y tejidos del cuerpo a través de las vías circulatorias. Para evaluar la eficiencia de los hemosustitutos, se estudia el efecto de estos fluidos sobre el endotelio de arteriolas en modelos animales como son los conejos. Se observa si se producen lesiones o daños vasculares, debido al esfuerzo cortante derivado de la velocidad del flujo sanguíneo y la variación del diámetro de las arteriolas. Este fenómeno puede ser observado a través de secuencias de imágenes de microscopía, y por medio de técnicas de procesamiento de imágenes es posible implementar una herramienta semi-automática que permita realizar el análisis cuantitativo de las características del hemosustituto de forma rápida y objetiva. El presente trabajo introduce un nuevo método basado en técnicas de procesamiento digital de imágenes para la identificación de las arteriolas en el modelo animal, para la medición de la variación de su diámetro a lo largo del tiempo y para la estimación de la velocidad de flujo del hemosustituto.
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- 2020
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24. Safety and efficacy of combining genotype-guided irinotecan (Iri) with 5FU, leucovorin (LV), oxaliplatin (Ox), and docetaxel (Tax) (gFOLFOXIRITAX): The I-FLOAT phase 1 dose-escalation study for advanced upper GI cancers
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Koosha Paydary, Aurelie Desgardin, Chih-Yi Liao, Ardaman Shergill, Natalie Marie Reizine, Stephanie Moya, Bryan Peterson, Katherine Reyes, Chanelle Robinzine, Belen Martinez-Caro Aguado, Christine Racette, Elena Ignatiev, Anu Radha Neerukonda, Yuan Ji, Blase N. Polite, and Daniel V.T. Catenacci
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Cancer Research ,Oncology - Abstract
316 Background: 5FU, Ox, Iri, and Tax are each active in upper GI cancers. Triplet cytotoxic therapies (txs) improved survival compared to doublets/singlets. However, combination of all 4 agents (FOLFOXIRITAX) has not been studied. UGT1A1 polymorphisms reduce UGT enzymatic activity predisposing to Iri toxicity. We sought to determine the maximum tolerated dose (MTD) in the 1st month of tx among each of the low (L), intermediate (I) and high (H) risk UGT1A1 genotype (UGT) groups. Methods: Previously untx’d advanced upper GI cancer patients (pts) with ECOG PS 0/1 received gFOLFOXIRITAX (+ trastuzumab if HER2+) with pegfilgrastim. 5FU 2400mg/m2 over 46 hrs, LV 400mg/m2, Ox 85mg/m2, and Tax 25mg/m2 were given IV Q14 days. UGT-L, I, and H risk groups received starting Iri dose levels (DL1) of 120, 105 and 45mg/m2, respectively; Iri doses were escalated in each UGT group by 15mg/m2 increments and Tax to DL2 of 37.5mg/m2 using a I3+3 novel design (Liu & Ji. J Biopharm Stat 2020). Other endpoints included overall safety (thru up to 8 cycles before maintenance 5FU +/- Iri/tras), ORR (RECIST1.1), & ctDNA response (> 50% decrease in highest MAF) by G360 (Guardant Health). Results: From 6/30/2020-8/6/2021 20 pts (8F, 12M) enrolled: median age 50 (range 21-76); 8 ECOG PS 1, UGT-L:I:H with 3:14:3 pts; 10 esophageal, 6 gastric, 2 pancreatic, 1 unknown GI primary and 1 bile duct cancer; 2 pts HER2+; 18 metastatic, 2 locally advanced unresectable. The median (range) of albumin and neutrophil-to-lymphocyte ratio (NLR) were 3.9 mg/dL (3.3-4.6) and 4.28 (1.89-27.6), respectively; 80% (16/20) of pts had a NLR > 2.88, a poor prognostic marker. Dose limiting toxicities (DLTs) were seen in 4 pts: one G3 diarrhea (UGT-H, DL1/DL1 Iri/Tax), two G3 sepsis not neutropenic (one UGT-I, DL2/DL2 Iri/Tax; and one UGT-I, DL3/DL1 Iri/Tax) and one G3 fatigue (UGT-I DL2/DL2 Iri/Tax). MTD has not been reached in any UGT TAX DL1 cohorts to date; currently enrolling UGT-H Iri/Tax DL1/DL1, UGT-I DL4/DL1, & UGT-L DL3/DL1. Any Gr tx related toxicities in ³ 10% pts thru up to 8 cycles: nausea (70%), fatigue (70%, 5% G3), diarrhea (65%, 5% G3), anorexia (50%), peripheral neuropathy (30%, 5% G3), anemia (30%), thrombocytopenia (25%), elevated LFTs (25%), hyponatremia (25%), vomiting (20%), mucositis (20%, 5% G3), hyperglycemia (20%), edema (15%), alopecia (15%), hypocalcemia (15%) and dysgeusia (10%). Of evaluable pts across all cohorts, PR/CR was seen in 13/16 (81%) patients, with 2 (12.5%) SD and 1 (6.25%) PD for a disease control rate of 94%. Of evaluable pts, best ctDNA response was seen in 12/13 (92%). Conclusions: gFOLFOXIRITAX demonstrated tolerability at initial dose levels of Iri/Tax, with dose escalation continuing. Efficacy is promising and could be an aggressive approach in upper GI cancers having high relapse risk in curative-intent settings. Clinical trial information: NCT04361708.
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- 2022
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25. Abstract PO-028: Successful implementation of Latina breast health programs: A multi-stakeholder analysis to answer a multilevel question
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Yamilé Molina, Perla Chebli, Stephanie A. Torres, Joanna Olazar, Jeanette Olazar, Katherine Reyes, Juanita Arroyo, Maria Medina, Nora Coronado, Araceli Lucio, Garth H. Rauscher, Lauren Green, Pamela Ganschow, Candyce H. Kroenke, and Marc Atkins
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Oncology ,Epidemiology - Abstract
Background: Multiple interventions have been developed to address Latina-White breast cancer (BC) disparities. Yet, little is known about what drives successful implementation, resulting in limited and less successful translation to practice. Engaging participants, community staff, and academicians in program evaluation may enhance identification of factors driving implementation, given differences in lived experience and intervention roles. Objective: We engaged 20 Latina participants, 3 community health workers (CHWs), and 3 research staff to identify determinants of: (1) intervention appropriateness (extent to which interventions addressed BC disparities), (2) feasibility (extent to which intervention delivery/participation was possible), and (3) acceptability (extent to which interventions were satisfactory). Method: The “Empowering Latinas to Obtain Breast Cancer Screenings” trial compared the efficacy of two interventions on BC screening uptake among 142 Latinas who were non-adherent to US Preventive Services Task Force (USPSTF) BC screening guidelines. Both interventions employed CHWs with personal/family history of BC to deliver 3 group sessions and refer patients to navigation services. The current study focuses on a qualitative program evaluation of the trial. All participants completed audio-recorded semi-structured interviews. A sample question was “What helped make it possible to participate in/lead the intervention?.” We conducted deductive content analysis, guided by the Consolidated Framework for Implementation Science, on verbatim transcripts. Results: Emergent themes suggest distinct multilevel determinants of different implementation outcomes. Intervention acceptability and appropriateness were driven by (1) characteristics at intervention (e.g., adaptability to personal needs – e.g., personalized literacy assistance; addressing diverse barriers to BC screening); (2) characteristics of the CHW interventionists (e.g., information delivered via BC survivors' personal experiences); and, (3) characteristics of organizations (e.g., trusted service providers). Intervention feasibility was driven by (1) organizational (e.g., intervention compatibility with mission; clear delineated a priori tasks for intervention delivery) and (2) partnership characteristics (e.g., strength of relationships between academics, community leaders, and clinical navigation BC services). Differences in stakeholder perspectives aligned with their lived experiences. For example, participants' personal challenges with BC screening, CHWs' past experiences leading BC programs, and researchers' awareness of past research on BC disparities affected perceptions about intervention appropriateness. Conclusions: Our findings highlight the value of multi-stakeholder analysis and specify the types of intervention and study team characteristics that are needed to make interventions appropriate, acceptable, and feasible for Latina-White BC equity. Citation Format: Yamilé Molina, Perla Chebli, Stephanie A. Torres, Joanna Olazar, Jeanette Olazar, Katherine Reyes, Juanita Arroyo, Maria Medina, Nora Coronado, Araceli Lucio, Garth H. Rauscher, Lauren Green, Pamela Ganschow, Candyce H. Kroenke, Marc Atkins. Successful implementation of Latina breast health programs: A multi-stakeholder analysis to answer a multilevel question [abstract]. In: Proceedings of the AACR Virtual Conference: 14th AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2021 Oct 6-8. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2022;31(1 Suppl):Abstract nr PO-028.
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- 2022
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26. Risk Factors for 30-Day Mortality in Patients with Methicillin-Resistant Staphylococcus aureus Bloodstream Infections
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Ricardo Ortiz, Daniela Moreno, Meredith Mahan, Tyler Prentiss, Katherine Reyes, Pedro Ayau, Ana C. Bardossy, Vanthida Huang, Mary Beth Perri, Guillermo Sanchez, Khulood Rizvi, Pamela Hartman, and Marcus J. Zervos
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Male ,0301 basic medicine ,Microbiology (medical) ,Pediatrics ,medicine.medical_specialty ,Heart disease ,030106 microbiology ,30-day mortality ,blood stream infection ,Bacteremia ,medicine.disease_cause ,Staphylococcal infections ,lcsh:Infectious and parasitic diseases ,03 medical and health sciences ,Cause of Death ,Diabetes mellitus ,medicine ,Electronic Health Records ,Humans ,risk factors ,lcsh:RC109-216 ,Aged ,Retrospective Studies ,Cause of death ,Cross Infection ,business.industry ,Retrospective cohort study ,General Medicine ,Odds ratio ,Middle Aged ,Staphylococcal Infections ,medicine.disease ,Methicillin-resistant Staphylococcus aureus ,Infectious Diseases ,Female ,Methicillin Resistance ,business - Abstract
Summary Objectives Methicillin-resistant Staphylococcus aureus (MRSA) blood stream infections (BSI) are a major health care problem accounting for a large percentage of nosocomial infections. The aim of this study was to identify risk factors associated with 30-day mortality in patients with MRSA BSI. Methods This was a retrospective study performed in Southeast Michigan. Over a 9- year period, a total of 1,168 patients were identified with MRSA BSI. Patient demographics and clinical data were retrieved and evaluated using electronic medical health records. Results 30-day mortality during the 9-year study period was 16%. Significant risk factors for 30-day mortality were age, cancer, heart disease, neurologic disease, nursing home residence and Charlson score >3 with Odds Ratio (OR) of 1.03 (CI 1.02–1.04), 2.29 (CI 1.40–3.75), 1.78 (CI 1.20–2.63), 1.65 (CI 1.08–2.25), 1.66 (CI 1.02 − 2.70) and 1.86 (CI 1.18 − 2.95) correspondingly. Diabetes mellitus, peripheral vascular disease (PVD), and readmission were protective factors for 30-day mortality with OR of 0.53 (CI 0.36–0.78), 0.46 (CI 0.26–0.84) and 0.13 (CI0.05 − 0.32) respectively. Conclusions Our study identified significant risk factors for 30-day mortality in patients with MRSA BSI. Interestingly, diabetes mellitus, PVD and readmission were protective effects on 30-day mortality. There was no statistically significant variability in 30-day mortality over the 9-year study period.
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- 2017
27. 273. Comparative Effectiveness of Ampicillin in the Treatment of Enterococcus faecalis Bloodstream Infections in Patients With Cancer
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J P Sanchez, German Contreras, Truc T Tran, Shelby Simar, Blake Hanson, Kayleigh Marx, Marcus Zervos, Katherine Reyes, Jose M Munita, Samuel A Shelburne, Cesar A Arias, and Samuel L Aitken
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biology ,business.industry ,medicine.drug_class ,Antibiotics ,Cancer ,medicine.disease ,biology.organism_classification ,Enterococcus faecalis ,Microbiology ,chemistry.chemical_compound ,AcademicSubjects/MED00290 ,Infectious Diseases ,Oncology ,chemistry ,Ampicillin ,Bacteremia ,Poster Abstracts ,Linezolid ,Medicine ,Vancomycin ,Daptomycin ,business ,medicine.drug - Abstract
Background E. faecalis (Efc) isolates are usually susceptible to ampicillin (AMP). AMP-based regimens are the standard of care for enterococcal infections, although other antibiotics are often used as definitive treatment. We thus compared outcomes of patients with cancer and Efc bacteremia treated with AMP-containing (ACR) and non-AMP-containing antibiotic regimens (NACR). Methods A multicenter, prospective, observational cohort study conducted at MD Anderson Cancer Center, Henry Ford Hospital, and Memorial Hermann Health System. Eligible patients were ≥ 18 years old, diagnosed with cancer, and had at least one Efc bloodstream isolate collected from 12/2015 to 12/2018. Patients with polymicrobial infections were excluded. Patients were divided into two groups: i) ACR and ii) NACR. ACR included patients who received AMP at any time during treatment; other antimicrobials were permitted. NACR patients did not receive AMP at any time. The primary outcome compared desirability of outcome ranking (DOOR) between ACR and NACR at day 14. The DOOR consisted of six hierarchical levels: 1 - death; 2 - inpatient without microbiological cure (MC) and with acute kidney injury (AKI); 3 - inpatient without MC and without AKI; 4 - inpatient admitted with MC and with AKI; 5 - inpatient with MC and without AKI; 6 - alive and discharged. Comparison of DOORs between ACR and NACR was performed using inverse probability of treatment weighted (IPTW) ordered logistic regression. Results Seventy-one patients were included (ACR, n = 35; NACR, n = 36). No difference was seen in DOORs at day 14 between ACR and NACR (odds ratio [OR] 1.14, 95% Confidence Interval [CI] 0.45 – 2.92, p=0.78). No difference was observed for all-cause mortality at day 14 (OR 0.6, 95% CI 0.09 – 3.77, p=0.58) or day 30 (OR 0.42, 95% CI 0.09 – 1.94, p=0.27). Patients treated with ACR received a lower median duration of other antibiotics at any point during treatment compared to NACR: daptomycin (2 v 4 days) vancomycin (2 v 4 days), and linezolid (1 v 2 days). Conclusion Patients with cancer and Efc bloodstream infections had similar outcomes when treated with ACR and NACR. ACR were associated with less use of broad-spectrum antimicrobials. Future research should focus on the ecologic impact of use of NACR. Disclosures Marcus Zervos, MD, Melinta Therapeutics (Grant/Research Support) Cesar A. Arias, MD, MSc, PhD, FIDSA, Entasis Therapeutics (Scientific Research Study Investigator)MeMed (Scientific Research Study Investigator)Merck (Grant/Research Support)
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- 2020
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28. Vancomycin-Resistant Enterococci
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Ana C. Bardossy, Katherine Reyes, and Marcus J. Zervos
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0301 basic medicine ,Microbiology (medical) ,medicine.medical_specialty ,business.industry ,Transmission (medicine) ,media_common.quotation_subject ,030106 microbiology ,Outbreak ,Vancomycin-Resistant Enterococci ,biochemical phenomena, metabolism, and nutrition ,030501 epidemiology ,bacterial infections and mycoses ,03 medical and health sciences ,Infectious Diseases ,Hygiene ,Health care ,Epidemiology ,medicine ,Antimicrobial stewardship ,Infection control ,0305 other medical science ,business ,Intensive care medicine ,media_common - Abstract
Vancomycin-resistant enterococci (VRE) infections have acquired prominence as a leading cause of health care-associated infections. Understanding VRE epidemiology, transmission modes in health care settings, risk factors for colonization, and infection is essential to prevention and control of VRE infections. Infection control strategies are pivotal in management of VRE infections and should be based on patient characteristics, hospital needs, and available resources. Hand hygiene is basic to decrease acquisition of VRE. The effectiveness of surveillance and contact precautions is variable and controversial in endemic settings, but important during VRE outbreak investigations and control. Environmental cleaning, chlorhexidine bathing, and antimicrobial stewardship are vital in VRE prevention and control.
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- 2016
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29. Nosocomial Outbreak of a Novel Extended-Spectrum β-Lactamase Salmonella enterica Serotype Isangi Among Surgical Patients
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Mary B. Perri, Katherine Reyes, Robert J. Tibbetts, Yuan Xin, George J Alangaden, Jennifer J Pietsch, Marcus J. Zervos, Patricia Starr, Linoj Samuel, Geehan Suleyman, Dora Vager, and Eman Chami
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Adult ,Male ,0301 basic medicine ,Microbiology (medical) ,Serotype ,Michigan ,medicine.medical_specialty ,Salmonella ,Epidemiology ,030106 microbiology ,Serogroup ,Disease cluster ,medicine.disease_cause ,beta-Lactamases ,Disease Outbreaks ,Microbiology ,Young Adult ,03 medical and health sciences ,Postoperative Complications ,0302 clinical medicine ,Internal medicine ,medicine ,Pulsed-field gel electrophoresis ,Humans ,Infection control ,030212 general & internal medicine ,Aged ,Aged, 80 and over ,Cross Infection ,biology ,business.industry ,Outbreak ,Middle Aged ,medicine.disease ,biology.organism_classification ,Epidemiologic Studies ,Infectious Diseases ,Salmonella enterica ,Bacteremia ,Salmonella Infections ,Female ,business - Abstract
OBJECTIVENosocomial outbreaks caused by Salmonella are rare. We describe the investigation and control of a cluster of novel extended-spectrum β-lactamase (ESBL) Salmonella enterica serotype Isangi in a hospital in southeastern Michigan.METHODSAn epidemiologic investigation, including case-control study, assessment of infection control practices and environmental cultures, was performed to identify modes of transmission. Healthcare workers (HCWs) exposed to case patients were screened. Strain relatedness was determined using pulsed-field gel electrophoresis (PFGE); ESBL confirmation was conducted using real-time PCR. Control measures were implemented to prevent further transmission.RESULTSBetween September 2 and October 22, 2015, 19 surgical patients, including 10 organ transplant recipients and 1 HCW, had positive S. Isangi cultures. Of these case patients and HCW, 13 had gastroenteritis, 2 had bacteremia, 1 had surgical-site infection, and 4 were asymptomatic. Pulsed-field gel electrophoresis (PFGE) showed 89.5% similarity among the isolates in these cases. Isolates with resistant-phenotypes possessed plasmid-mediated CTX-M15 ESBL. A total of 19 case patients were compared with 57 control participants. Case patients had significantly higher odds of exposure to an intraoperative transesophageal (TEE) probe (adjusted odds ratio 9.0; 95% confidence interval, 1.12–72.60; P=.02). Possible cross-transmission occurred in the HCW and 2 patients. Cultures of TEE probes and the environment were negative. The outbreak ended after removal of TEE probes, modification of reprocessing procedures, implementation of strict infection control practices, and enhanced environmental cleaning.CONCLUSIONSWe report the first nosocomial ESBL S. Isangi outbreak in the United States. Multiple control measures were necessary to interrupt transmission of this gastrointestinal pathogen. Exposure to possibly contaminated TEE probes was associated with transmission. Periodic monitoring of reprocessing procedures of TEE probes may be required to ensure optimal disinfection.Infect Control Hosp Epidemiol 2016;37:954–961
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- 2016
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30. Evaluation of contact precautions for methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus
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Marcus J. Zervos, Katherine Reyes, George Alangaden, Jennifer J. Pietsch, Muhammad Yasser Alsafadi, Laura Johnson, Ana C. Bardossy, Patricia Starr, Eman Chami, and Daniela Moreno
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Methicillin-Resistant Staphylococcus aureus ,medicine.medical_specialty ,Epidemiology ,Bacteremia ,030501 epidemiology ,medicine.disease_cause ,Staphylococcal infections ,Vancomycin-Resistant Enterococci ,Microbiology ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,Humans ,Infection control ,Vancomycin-resistant Enterococcus ,030212 general & internal medicine ,Retrospective Studies ,Cross Infection ,Infection Control ,biology ,business.industry ,Health Policy ,Public Health, Environmental and Occupational Health ,Pneumonia, Ventilator-Associated ,Staphylococcal Infections ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,medicine.disease ,biology.organism_classification ,Methicillin-resistant Staphylococcus aureus ,Discontinuation ,Infectious Diseases ,Enterococcus ,Staphylococcus aureus ,Population Surveillance ,0305 other medical science ,business - Abstract
Background There are limited controlled data demonstrating contact precautions (CPs) prevent methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) infections in endemic settings. We evaluated changes in hospital-acquired MRSA and VRE infections after discontinuing CPs for these organisms. Methods This is a retrospective study done at an 800-bed teaching hospital in urban Detroit. CPs for MRSA and VRE were discontinued hospital-wide in 2013. Data on MRSA and VRE catheter-associated urinary tract infections (CAUTIs), ventilator-associated pneumonia (VAP), central line–associated bloodstream infections (CLABSIs), surgical site infections (SSIs), and hospital-acquired MRSA bacteremia (HA-MRSAB) rates were compared before and after CPs discontinuation. Results There were 36,907 and 40,439 patients hospitalized during the two 12-month periods: CPs and no CPs. Infection rates in the CPs and no-CPs periods were as follows: (1) MRSA infections: VAP, 0.13 versus 0.11 ( P = .84); CLABSI, 0.11 versus 0.19 ( P = .45); SSI, 0 versus 0.14 ( P = .50); and CAUTI, 0.025 versus 0.033 ( P = .84); (2) VRE infections: CAUTI, 0.27 versus 0.13 ( P = .19) and CLABSI, 0.29 versus 0.3 ( P = .94); and (3) HA-MRSAB rates: 0.14 versus 0.11 ( P = .55), respectively. Conclusions Discontinuation of CPs did not adversely impact endemic MRSA and VRE infection rates.
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- 2017
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31. Multidrug-resistant Organisms in Hospitals: What Is on Patient Hands and in Their Rooms?
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Vineet Chopra, Mary Beth Perri, Kristen Gibson, Sanjay Saint, Lona Mody, Julia Mantey, Keith S Kaye, Sarah Altamimi, Hugo Sax, Katherine Reyes, Marco Cassone, Laraine Washer, Jie Cao, Marcus J. Zervos, University of Zurich, and Mody, Lona
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Microbiology (medical) ,Adult ,Male ,medicine.medical_specialty ,media_common.quotation_subject ,610 Medicine & health ,030501 epidemiology ,medicine.disease_cause ,2726 Microbiology (medical) ,new acquisition ,10234 Clinic for Infectious Diseases ,03 medical and health sciences ,contamination ,0302 clinical medicine ,Paired samples ,Hygiene ,Internal medicine ,Drug Resistance, Multiple, Bacterial ,acute care hospitals ,medicine ,Humans ,In patient ,030212 general & internal medicine ,Typing ,Prospective Studies ,Articles and Commentaries ,Equipment and Supplies, Hospital ,multidrug-resistant organisms ,media_common ,Aged ,Cross Infection ,Bacteria ,Transmission (medicine) ,business.industry ,2725 Infectious Diseases ,Bacterial Infections ,Middle Aged ,colonization ,Hand ,Methicillin-resistant Staphylococcus aureus ,Hospitals ,Multiple drug resistance ,Infectious Diseases ,Staphylococcus aureus ,Printing, Three-Dimensional ,Female ,0305 other medical science ,business - Abstract
Background The impact of healthcare personnel hand contamination in multidrug-resistant organism (MDRO) transmission is important and well studied; however, the role of patient hand contamination needs to be characterized further. Methods Patients from 2 hospitals in southeast Michigan were recruited within 24 hours of arrival to their room and followed prospectively using microbial surveillance of nares, dominant hand, and 6 high-touch environmental surfaces. Sampling was performed on admission, days 3 and 7, and weekly until discharge. Paired samples of methicillin-resistant Staphylococcus aureus (MRSA) isolated from the patients’ hand and room surfaces were evaluated for relatedness using pulsed-field gel electrophoresis and staphylococcal cassette chromosome mec, and Panton-Valentine leukocidin typing. Results A total of 399 patients (mean age, 60.8 years; 49% male) were enrolled and followed for 710 visits. Fourteen percent (n = 56/399) of patients were colonized with an MDRO at baseline; 10% (40/399) had an MDRO on their hands. Twenty-nine percent of rooms harbored an MDRO. Six percent (14/225 patients with at least 2 visits) newly acquired an MDRO on their hands during their stay. New MDRO acquisition in patients occurred at a rate of 24.6/1000 patient-days, and in rooms at a rate of 58.6/1000 patient-days. Typing demonstrated a high correlation between MRSA on patient hands and room surfaces. Conclusions Our data suggest that patient hand contamination with MDROs is common and correlates with contamination on high-touch room surfaces. Patient hand hygiene protocols should be considered to reduce transmission of pathogens and healthcare-associated infections., In a prospective study of 399 hospital patients, we show that multidrug-resistant organisms (MDROs) on patient hands are common on admission and correlate with room contamination. New MDRO acquisition is frequent, suggesting a need to develop patient hand hygiene protocols in hospitals.
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- 2018
32. Culturing practices and the care of the urinary catheter in reducing NHSN-defined catheter-associated urinary tract infections: The tale of two teaching hospitals
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Katherine Reyes, Marcus J. Zervos, Karen Jones, Ana C. Bardossy, Susan Szpunar, Mohamad G. Fakih, Takiah Williams, and George Alangaden
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Microbiology (medical) ,Adult ,medicine.medical_specialty ,Epidemiology ,Urinary system ,MEDLINE ,Urinary catheter care ,Urine ,030501 epidemiology ,03 medical and health sciences ,Antimicrobial Stewardship ,0302 clinical medicine ,Intensive care ,medicine ,Humans ,030212 general & internal medicine ,Hospitals, Teaching ,Urinary catheter ,Cross Infection ,Infection Control ,business.industry ,Catheter ,Intensive Care Units ,Infectious Diseases ,Multicenter study ,Catheter-Related Infections ,Emergency medicine ,Urinary Tract Infections ,0305 other medical science ,business - Abstract
We compared interventions to improve urinary catheter care and urine culturing in adult intensive care units of 2 teaching hospitals. Compared to hospital A, hospital B had lower catheter utilization, more compliance with appropriate indications and maintenance, but higher urine culture use and more positive urine cultures per 1,000 patient days.
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- 2018
33. Impact and Limitations of the 2015 National Health and Safety Network Case Definition on Catheter-Associated Urinary Tract Infection Rates
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George Alangaden, Rachna Jayaprakash, Marcus J. Zervos, Patricia Starr, Katherine Reyes, Ana C. Bardossy, Anjali C. Alangaden, and Odaliz Abreu-Lanfranco
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Microbiology (medical) ,Michigan ,medicine.medical_specialty ,Epidemiology ,Urinary system ,030501 epidemiology ,03 medical and health sciences ,0302 clinical medicine ,Intensive care ,Humans ,Medicine ,030212 general & internal medicine ,Intensive care medicine ,Retrospective Studies ,Catheter-associated urinary tract infection ,National health ,Cross Infection ,business.industry ,Guideline adherence ,Retrospective cohort study ,Intensive Care Units ,Infectious Diseases ,Catheter-Related Infections ,Urinary Tract Infections ,Guideline Adherence ,0305 other medical science ,business - Abstract
Application of the new 2015 NHSN definition of catheter-associated urinary tract infection (CAUTI) in intensive care units reduced CAUTI rates by ~50%, primarily due to exclusion of candiduria. This significant reduction in CAUTI rates resulting from the changes in the definition must be considered when evaluating effectiveness of CAUTI prevention programs.Infect Control Hosp Epidemiol2017;38:239–241
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- 2016
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34. 2191. Hepatitis A Outbreak in Southeast Michigan: No Longer a Third World Disease
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Amit T Vahia, Katherine Reyes, Marcus J. Zervos, Sarah Altamimi, and Helina Misikir
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business.industry ,Third world ,Office visits ,Outbreak ,Hepatitis A ,Disease ,medicine.disease ,Vaccination ,Transplantation ,Abstracts ,Infectious Diseases ,B. Poster Abstracts ,Oncology ,Hospital admission ,Medicine ,business ,Demography - Abstract
Background Hepatitis A (Hep A) is a self-limiting diarrheal illness occurring in underdeveloped countries. August 2016 marked the onset of an outbreak in Southeast Michigan. Our study characterizes the presentation and clinical course of Hep A patients that presented to our healthcare system. Methods This study included all Hep A positive cases that presented to Henry Ford Health System from August 2016 to December 2017. Electronic medical records were reviewed for demographics, sexual history, travel history, food exposure, illicit drug use, signs, symptoms and outcomes. Data were also collected on healthcare units of presentation, screening, and care including emergency department, clinic, inpatient hospitalization, or transfer from another facility. Outcomes included hospitalization, consultations with hepatology and transplant, re-admission, and death. Results A total of 166 cases were reviewed; Figure 1 displays the cases per month. The average age was 51 years and 54% were male. The most common symptoms were abdominal pain (47%) and nausea (42.8). Underlying conditions included illicit drug use (23%), alcohol abuse (22%), and diabetes (18.6%). Three percent of cases traveled outside of the state within 2 weeks prior to diagnosis. Twenty-three percent had history of illicit drug use and 4.2% were food handlers. Table 1 displays the healthcare unit where Hep A serology was ordered. One hundred Twenty-two (73.5%) cases were hospitalized, 44 (26.5%) required ICU admission and seven (4.2%) were readmitted within 30 days. Ninety-two cases (55%) required hepatology evaluation, 25 were evaluated for transplantation and one (0.6%) received a liver transplant. Eighteen (10.8%) patients died, two of which were never hospitalized). Figure 1. Number of cases per month and year. Table 1. Healthcare Unit Where Hep A Serology Was Ordered Admission 114 (68.6%) Office visit 31 (18.7) Lab encounter 13 (7.8) ED 8 (4.8) Total 166 Conclusion High clinical suspicion is crucial during an outbreak. Most of our cases were diagnosed with Hep A during inpatient admission after presenting with abdominal pain and nausea. In an outbreak setting, consider testing for immunity from history of previous exposure or vaccination. High hospital admission, morbidity and mortality were seen. Disclosures All authors: No reported disclosures.
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- 2018
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35. 622. The Accessory Genome in Enterococcal Bacteremia: Results from the Vancomycin-Resistant Enterococcal Bacteremia Outcomes Study (VENOUS)
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Shelby Simar, Blake Hanson, German Contreras, Katherine Reyes, Pranoti V Sahasrabhojane, Helina Misikir, Catherine Liu, Yohei Doi, Fernanda Barberis, Lilian Abbo, An Q Dinh, Maria Spencer, Marcus Zervos, Samuel L Aitken, David van Duin, Samuel A Shelburne, Truc T Tran, Jose M Munita, Cesar A Arias, and Maria de los Angeles Spencer
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biology ,business.industry ,biochemical phenomena, metabolism, and nutrition ,biology.organism_classification ,medicine.disease_cause ,Microbiology ,Accessory genome ,Enterococcal bacteremia ,Abstracts ,Infectious Diseases ,Oncology ,Enterococcus ,Vancomycin resistant ,Poster Abstracts ,medicine ,Vancomycin ,Vancomycin-resistant Enterococcus ,business ,medicine.drug - Abstract
Background Vancomycin-resistant enterococci (VRE) are a major cause of nosocomial bloodstream infections. Enterococci exhibit remarkable genomic plasticity and can recombine through the acquisition of genetic material via mobile genetic elements (MGEs), including resistance genes. The accessory genome plays a major role in the evolution of enterococci within the human host. Thus, dissecting the entire genome (pan-genome) is of paramount importance to characterize the population structure of enterococci causing disease. Methods VENOUS is an ongoing prospective, observational study of adults with enterococcal bacteremia. From September 2016 to March 2018, E. faecalis (Efs) and E. faecium (Efm) were collected in 14 hospitals of a single hospital system and a major cancer center in Houston, TX, and a general hospital in Detroit, MI. Short- and long-read genomic sequencing were performed with Illumina MiSeq and Oxford Nanopore Technologies GridION X5, respectively. A proprietary bioinformatics pipeline was utilized for genome assembly and further analyses. Results 156 Efs and 98 Efm isolates from single patients were analyzed. The average proportion of core genes in each genome was 64.6% (53.0–74.1) and 49.1% (45.2–51.0) for Efs and Efm, respectively. The vanA gene cluster was identified in 5.1% (8/157) of Efs and 57.1% (56/98) of Efm. The plasmid-encoded aac(6′)-Ie-aph(2″)-Ia gene conferring high-level resistance to aminoglycosides was found in 37.6% (59/157) Efs, seven of which also possessed vanA. Long-read sequencing of vanA-harboring plasmids from a subset of VRE revealed that the vanA cluster was carried in plasmids ranging from 31.7 to 132.3 kb. Although the vanA operon was fairly conserved, insertions of MGE were identified in the intergenic regions of vanS/vanH and vanX/vanY. Furthermore, a variety of MGE insertions mediated integration of the vanA operon, including IS1216 and IS256 (figure). Conclusion Accessory genes, including AMR genes, comprise a significant proportion of the enterococcal pan-genome, indicating major genetic plasticity within these organisms. Acquired resistance genes seem to have a high degree of recombination and play a substantial role in the expansion of the genomic repertoire in clinical isolates. Disclosures Samuel L. Aitken, PharmD, Melinta Therapeutics: Grant/Research Support, Research Grant; Merck, Sharpe, and Dohme: Advisory Board; Shionogi: Advisory Board.
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- 2019
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36. Enterococcal Infections in Adults
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Katherine Reyes, Marcus J. Zervos, and Jisha John
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0301 basic medicine ,biology ,medicine.drug_class ,business.industry ,030106 microbiology ,Antibiotics ,biochemical phenomena, metabolism, and nutrition ,biology.organism_classification ,medicine.disease ,Enterococcus faecalis ,Microbiology ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Antibiotic resistance ,Enterococcus ,chemistry ,Bacteremia ,Linezolid ,medicine ,030212 general & internal medicine ,Daptomycin ,business ,Enterococcus faecium ,medicine.drug - Abstract
Enterococci (once called group D streptococci) were first described as human pathogens in 1899, historically thought to be endogenously acquired pathogens from human intestinal flora. Enterococcus faecalis is the most common pathogen, while Enterococcus faecium has become prevalent in hospital-acquired infections. Enterococci have resurfaced with reports of changes in epidemiology, treatment failures, and increasing complexity in antimicrobial resistance patterns. Enterococci have a variety of intrinsic antibiotic resistances and have shown the ability to acquire new resistance genes and mutations. Vancomycin resistance in enterococci is predominantly a healthcare-associated phenomenon. Urinary tract infections and bacteremia are the most common infections caused by enterococci, while endocarditis is the most serious. Enterococci are also commonly found in intra-abdominal, pelvic, and soft tissue infections, often part of a mixed flora. Less common infections are meningitis, osteomyelitis, and septic arthritis. Immunosuppression, long-term colonization, the ability to disseminate widely between patients, and the capacity to form biofilms have made enterococci major pathogens in hospitals, prompting enhanced efforts to identify optimal infection control measures and best therapeutic approaches to improve outcomes.
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- 2017
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37. Vancomycin-Resistant Enterococci: Epidemiology, Infection Prevention, and Control
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Katherine, Reyes, Ana Cecilia, Bardossy, and Marcus, Zervos
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Cross Infection ,Infection Control ,Humans ,Hand Hygiene ,Gram-Positive Bacterial Infections ,Vancomycin-Resistant Enterococci - Abstract
Vancomycin-resistant enterococci (VRE) infections have acquired prominence as a leading cause of health care-associated infections. Understanding VRE epidemiology, transmission modes in health care settings, risk factors for colonization, and infection is essential to prevention and control of VRE infections. Infection control strategies are pivotal in management of VRE infections and should be based on patient characteristics, hospital needs, and available resources. Hand hygiene is basic to decrease acquisition of VRE. The effectiveness of surveillance and contact precautions is variable and controversial in endemic settings, but important during VRE outbreak investigations and control. Environmental cleaning, chlorhexidine bathing, and antimicrobial stewardship are vital in VRE prevention and control.
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- 2016
38. Influenza Vaccine Effectiveness Against Antigenically Drifted Influenza Higher Than Expected in Hospitalized Adults: 2014-2015
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Caroline Cheng, Brendan Flannery, Suzanne E. Ohmit, Katherine Reyes, Emily T. Martin, Joshua G. Petrie, Ryan E. Malosh, Jill M. Ferdinands, Adam S. Lauring, Arnold S. Monto, and Lois Lamerato
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0301 basic medicine ,Microbiology (medical) ,Adult ,Male ,medicine.medical_specialty ,Adolescent ,Influenza vaccine ,030106 microbiology ,Comorbidity ,medicine.disease_cause ,History, 21st Century ,Antigenic drift ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Ambulatory care ,Risk Factors ,Internal medicine ,Influenza, Human ,Influenza A virus ,medicine ,Humans ,030212 general & internal medicine ,Aged ,Aged, 80 and over ,business.industry ,Length of Stay ,Middle Aged ,Antigenic Variation ,Confidence interval ,Vaccination ,Hospitalization ,Infectious Diseases ,Specimen collection ,Influenza Vaccines ,Case-Control Studies ,Immunology ,Human mortality from H5N1 ,Female ,business - Abstract
BACKGROUND The 2014-2015 influenza season was severe, with circulating influenza A (H3N2) viruses that were antigenically drifted from the vaccine virus. Reported vaccine effectiveness (VE) estimates from ambulatory care settings were markedly decreased. METHODS Adults, hospitalized at 2 hospitals in southeast Michigan for acute respiratory illnesses, defined by admission diagnoses, of ≤10 days duration were prospectively enrolled. Throat and nasal swab specimens were collected, combined, and tested for influenza by real-time reverse transcription polymerase chain reaction. VE was estimated by comparing the vaccination status of those testing positive for influenza with those testing negative in logistic regression models adjusted for age, sex, hospital, calendar time, time from illness onset to specimen collection, frailty score, and Charlson comorbidity index (CCI). RESULTS Among 624 patients included in the analysis, 421 (68%) were vaccinated, 337 (54%) were female, 220 (35%) were age ≥65 years, and 92% had CCI > 0, indicating ≥1 comorbid conditions. Ninety-eight (16%) patients tested positive for influenza A (H3N2); among 60 (61%) A (H3N2) viruses tested by pyrosequencing, 53 (88%) belonged to the drifted 3C.2a genetic group. Adjusted VE was 43% (95% confidence interval [CI], 4-67) against influenza A (H3N2); 40% (95% CI, -13 to 68) for those
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- 2016
39. 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
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Samuel A. Shelburne, Pranoti Sahasrabhojane, Marcus J. Zervos, Jose M. Munita, Samuel L. Aitken, Cesar A. Arias, German A. Contreras, Katherine Reyes, Helina Misikir, and Heather Garza
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Enterococcal bacteremia ,Abstracts ,medicine.medical_specialty ,Infectious Diseases ,B. Poster Abstracts ,Oncology ,business.industry ,Internal medicine ,medicine ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,business ,Cohort study - Abstract
Background Enterococci often cause hospital-associated bloodstream infections in critically ill and immunocompromised patients. Prospective studies to assess the clinical impact of enterococcal bacteremia (EB) are lacking. We conducted a prospective study to investigate the clinical and microbiological factors associated with mortality in EB. Methods Adults with EB were prospectively followed in three US tertiary hospitals from September 2016 to March 2018. Individuals with EB for whom follow-up blood culture data within 7 days of index culture were available were included. Microbiologic failure (MF) was defined as clearance of bacteremia ≥4 days after the first blood culture. The main outcome was hospital mortality. Results A total of 282 patients were included with 69 (24%) infected with vancomycin-resistant enterococci (VRE). The majority of patients were male (60%) with a median age of 63 years. Median length of hospitalization for VRE patients was longer (25 d) than non-VRE (13 days, P < 0.001). E. faecium corresponded to 77% of VRE isolates, whereas E. faecalis comprised 72% of non-VRE. The average time to first blood culture was 16 days for VRE vs. 4 days for non-VRE (P < 0.001). Patients with VRE were more likely to have hematological malignancy or bone marrow transplant (P < 0.003), whereas patients infected non-VRE were more likely to have solid tumors (P = 0.02). The most common antibiotic used was daptomycin as monotherapy for both VRE and non-VRE with a median dose of 8 mg/kg for both groups. Overall mortality was 25% (43% vs. 20% in VRE vs. non-VRE patients, respectively; P < 0.0001). Factors significantly associated with mortality in univariate analyses included ICU admission, prolonged hospitalization, hematological malignancy, use of immunosuppressive therapy, hemodialysis, neutropenia (3, infection with VRE and MF. ICU admission (RR 3.3; 95% CI 1.7–7.5, neutropenia (RR 4.1; 95% CI 1.3–12.9), Pitt bacteremia score >3 (RR 6.8; 95% CI 2.6–18.0), MF (RR 4.7; 95% CI 2.2–10.3) and infection with VRE (RR 4.1; 95% CI 1.1–16.6) remained significantly associated with mortality in multivariate analyses. Conclusion The presence of VRE in EB and MF are associated with increased mortality. EB represent a major burden of disease in hospital settings. Disclosures C. Arias, Merck & Co., Inc.: Grant Investigator, Research support. MeMed: Grant Investigator, Research support. Allergan: Grant Investigator, Research support.
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- 2018
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40. Clinical and economic outcomes in patients with community‐acquired Staphylococcus aureus pneumonia
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Nadia Z. Haque, Charu Taneja, Sophia Zilber, James Spalding, Smita Kothari, Marcus J. Zervos, Paola Osaki Kyan, Andrew F. Shorr, Gerry Oster, Katherine Reyes, and Carol Moore
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Adult ,Male ,Staphylococcus aureus ,Pediatrics ,medicine.medical_specialty ,Adolescent ,Leadership and Management ,medicine.medical_treatment ,Assessment and Diagnosis ,law.invention ,Young Adult ,Pharmacotherapy ,law ,Outcome Assessment, Health Care ,Pneumonia, Staphylococcal ,Humans ,Medicine ,Hospitals, Teaching ,Care Planning ,Aged ,Retrospective Studies ,Medical Audit ,business.industry ,Health Policy ,Bacterial pneumonia ,Retrospective cohort study ,General Medicine ,Middle Aged ,medicine.disease ,Intensive care unit ,United States ,Hospital medicine ,Community-Acquired Infections ,Pneumonia ,Regimen ,Female ,Fundamentals and skills ,Hemodialysis ,business - Abstract
BACKGROUND: While the clinical and economic consequences of S. aureus pneumonia in healthcare settings have been well documented, much less is known about community-acquired S. aureus pneumonia (CAP). METHODS: We retrospectively identified all patients admitted to a large US urban teaching hospital between January 2005 and May 2008 with pneumonia and positive blood or respiratory cultures for S. aureus within 48 hours of admission. Patients with suspected healthcare-associated pneumonia (HCAP) were excluded from the study sample, using established criteria (eg, recent hospitalization, admission from nursing home, hemodialysis). Patients were designated as having methicillin-resistant (MRSA) or methicillin-susceptible (MSSA) CAP based on initial S. aureus isolates. Initial therapy was designated “appropriate” vs. “inappropriate” based on expected susceptibility of the organism to the regimen received. RESULTS: We identified a total of 128 CAP patients with S. aureus isolates; mean (standard deviation [SD]) age was 60 (17) years. A total of 55 patients (43%) had initial cultures positive for MRSA. Patients with MRSA CAP were more likely to receive inappropriate initial therapy (24 [44%] vs. 13 [18%] for MSSA; P = 0.002). Approximately 25% of all patients underwent surgery for pneumonia, 69% received mechanical ventilation, 79% were admitted to intensive care unit (ICU), and 24% died in hospital. Mean (SD) length of stay was 17.0 (15.7) days, and total hospital charges averaged $127,922 ($154,605) per patient; there were no significant differences between patients with MRSA vs. MSSA CAP. CONCLUSION: Outcomes are poor, hospital stays are long, and costs of care are high in patients with S. aureus CAP, and do not differ between those with MRSA vs. MSSA. Journal of Hospital Medicine 2010. © 2010 Society of Hospital Medicine.
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- 2010
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41. Epidemiology of Community-Acquired and Health Care-Associated Staphylococcus aureus Pneumonia
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Marcus J. Zervos, Paola Osaki Kyan, Gerry Oster, Sophia Zilber, Andrew F. Shorr, Smita Kothari, Katherine Reyes, Carol Moore, Charu Taneja, James Spalding, and Nadia Z. Haque
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Microbiology (medical) ,Pneumonia ,medicine.medical_specialty ,Infectious Diseases ,Staphylococcus aureus ,business.industry ,Internal medicine ,Epidemiology ,medicine ,medicine.disease ,medicine.disease_cause ,business ,Health care associated - Published
- 2010
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42. Risk Factors for Quinolone-Resistant Escherichia coli Urinary Tract Infection
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Katherine Reyes, Gustavo Adolfo Vasquez, Eduardo M. Luna, Marcus J. Zervos, and Hugo R. Siu
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Microbiology (medical) ,Infectious Diseases ,medicine.drug_class ,Escherichia coli urinary tract infection ,business.industry ,Urinary system ,medicine ,medicine.disease_cause ,Quinolone ,business ,Escherichia coli ,Microbiology - Abstract
Background:Escherichia coli is the leading cause of urinary tract infections (UTI). Current Infectious Diseases Society of America (IDSA) guidelines recommend the use of fluoroquinolones when resistance to trimethoprim-sulfamethoxazole is greater than 10% to 20%. Identification of risk factors for f
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- 2009
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43. Comparative evaluation of epidemiology and outcomes of methicillin-resistant Staphylococcus aureus (MRSA) USA300 infections causing community- and healthcare-associated infections
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Mary Beth Perri, Susan M. Donabedian, Nadia Z. Haque, Marcus J. Zervos, Carol Moore, Ameet Hingwe, Katherine Reyes, Susan L. Davis, and Dora Vager
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Adult ,Male ,Methicillin-Resistant Staphylococcus aureus ,Microbiology (medical) ,medicine.medical_specialty ,Genotype ,medicine.disease_cause ,Coronary artery disease ,Risk Factors ,Internal medicine ,Epidemiology ,medicine ,Humans ,Pharmacology (medical) ,Intensive care medicine ,Retrospective Studies ,Cross Infection ,business.industry ,Osteomyelitis ,Retrospective cohort study ,General Medicine ,Middle Aged ,Staphylococcal Infections ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,medicine.disease ,Methicillin-resistant Staphylococcus aureus ,Anti-Bacterial Agents ,Bacterial Typing Techniques ,Community-Acquired Infections ,Pneumonia ,Treatment Outcome ,Infectious Diseases ,Staphylococcus aureus ,Female ,business ,Kidney disease - Abstract
Methicillin-resistant Staphylococcus aureus (MRSA) USA300 clone is commonly found in the community and is being increasingly reported in the healthcare setting. A retrospective analysis was conducted to compare the epidemiology and outcomes between community-associated (CA) and healthcare-associated (HA) USA300 MRSA infections. The study enrolled 160 subjects with USA300 MRSA infections (47.5% CA-MRSA and 52.5% HA-MRSA). Failure in the HA group was higher (38.1%) compared with the CA group (23.7%) (P = 0.05). Predictors of failure included male gender, age, presence of any co-morbidity, coronary artery disease, chronic kidney disease, history of MRSA, previous admission, fluoroquinolone exposure, HA infection and osteomyelitis (P ≤ 0.05). Independent predictors of failure were osteomyelitis, history of MRSA, male gender and pneumonia. Recurrent disease was found in 32.6% of cases. Overall, USA300 MRSA most commonly causes infection of the skin and skin structure, however, 20% of subjects can experience more invasive disease with infection of the bloodstream, lung or bone. Failure rates are higher in subjects with healthcare risk factors or if the infection was acquired in the hospital, with these subjects experiencing more invasive infections such as bacteraemia, pneumonia or osteomyelitis.
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- 2009
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44. Resources for Infection Prevention and Control on the World Wide Web
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Katherine Reyes, Laura E. Johnson, and Marcus J. Zervos
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Microbiology (medical) ,Infection Control ,Internet ,medicine.medical_specialty ,business.industry ,Occupational safety and health ,World Wide Web ,Long-term care ,Infectious Diseases ,Nursing ,Communicable Disease Control ,Epidemiology ,Health care ,Health Resources ,Humans ,Medicine ,Infection control ,The Internet ,Professional association ,business ,Health policy - Abstract
This review summarizes infection prevention resources on the Internet. Web sites are presented in 8 categories: guidelines, policies, and regulatory bodies; health care-associated infection and multidrug-resistant organisms; surveillance, reporting, and initiatives; antibiotic use; employee health; long-term care facilities; facility and environmental infection control; and professional societies, educational opportunities, and listserves. For example, links to the National Surgical Quality Improvement Program and National Healthcare Safety Network reports are provided among resources for infection surveillance, reporting, and initiatives. A link to guidelines for infection prevention in health care workers is listed with other information regarding employee health. The Web address for the Society for Healthcare Epidemiology of America guidelines for infection control in long-term care facilities is listed with resources for long-term care facilities. Guidelines for construction and environmental services are summarized with other information regarding facility and environmental infection control. This review summarizes the most useful and up-to-date infection prevention resources on the Internet and will simplify the search for pertinent information.
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- 2009
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45. Gram-negative endocarditis
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Katherine Reyes and Milagros P. Reyes
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Multiple drug resistance ,medicine.medical_specialty ,Infectious Diseases ,business.industry ,medicine.medical_treatment ,Epidemiology ,medicine ,Endocarditis ,Intensive care medicine ,business ,medicine.disease ,Antimicrobial ,Central venous catheter - Abstract
Aerobic gram-negative bacilli are rare causes of endocarditis. The epidemiology and risk factors for developing gram-negative endocarditis are evolving. New pathogens, some of which are multidrug resistant, are emerging. The role of nosocomial infections, particularly central venous catheter infections, is increasing. Medical and surgical outcomes appear to be improving with more effective antimicrobial therapy and aggressive surgical management.
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- 2008
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46. Global initiative for meticillin-resistant Staphylococcus aureus pneumonia (GLIMP): an international, observational cohort study
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Stefano Aliberti, Luis F Reyes, Paola Faverio, Giovanni Sotgiu, Simone Dore, Alejandro H Rodriguez, Nilam J Soni, Marcos I Restrepo, Patricia Karina Aruj, Silvia Attorri, Enrique Barimboim, Juan Pablo Caeiro, María I Garzón, Victor Hugo Cambursano, Adrian Ceccato, Julio Chertcoff, Florencia Lascar, Fernando Di Tulio, Ariel Cordon Díaz, Lautaro de Vedia, Maria Cristina Ganaha, Sandra Lambert, Gustavo Lopardo, Carlos M Luna, Alessio Gerardo Malberti, Nora Morcillo, Silvina Tartara, Claudia Pensotti, Betiana Pereyra, Pablo Gustavo Scapellato, Juan Pablo Stagnaro, Sonali Shah, Felix Lötsch, Florian Thalhammer, Jean Louis Vincent, Kurt Anseeuw, Camille A Francois, Eva Van Braeckel, Marcel Zannou Djimon, Jules Bashi, Roger Dodo, Simone Aranha Nouér, Peter Chipev, Milena Encheva, Darina Miteva, Diana Petkova, Adamou Dodo Balkissou, Eric Walter Pefura Yone, Bertrand Hugo Mbatchou Ngahane, Ning Shen, Jin-fu Xu, Carlos Andres Bustamante Rico, Ricardo Buitrago, Fernando Jose Pereira Paternina, Jean-Marie Kayembe Ntumba, Vesna Vladic Carevic, Marko Jakopovic, Mateja Jankovic, Zinka Matkovic, Ivan Mitrecic, Marie-Laure Bouchy Jacobsson, Anette Bro Christensen, Uffe Christian Heitmann Bødtger, Christian Niels Meyer, Andreas Vestergaard Jensen, Gertrud Baunbæk-knudsen, Pelle Trier Petersen, Stine Andersen, Ibrahim El-Said Abd El-Wahhab, Nesreen Elsayed Morsy, Hanaa Shafiek, Eman Sobh, Kedir Abdella Abdulsemed, Fabrice Bertrand, Christian Brun-Buisson, Etienne de Montmollin, Muriel Fartoukh, Jonathan Messika, Pierre Tattevin, Abdo Khoury, Bernard Ebruke, Michael Dreher, Martin Kolditz, Matthias Meisinger, Mathias W Pletz, Stefan Hagel, Jan Rupp, Tom Schaberg, Marc Spielmanns, Petra Creutz, Norton Suttorp, Beatrice Siaw-Lartey, Katerina Dimakou, Dimosthenis Papapetrou, Evdoxia Tsigou, Dimitrios Ampazis, Evangelos Kaimakamis, Mohit Bhatia, Raja Dhar, George D'Souza, Rajiv Garg, Parvaiz A Koul, P A Mahesh, B S Jayaraj, Kiran Vishnu Narayan, Hirennappa B Udnur, Shashi Bhaskara Krishnamurthy, Surya Kant, Rajesh Swarnakar, Sneha Limaye, Sundeep Salvi, Keihan Golshani, Vera M Keatings, Ignacio Martin-Loeches, Yasmin Maor, Jacob Strahilevitz, Salvatore Battaglia, Maria Carrabba, Piero Ceriana, Marco Confalonieri, Antonella d'Arminio Monforte, Bruno Del Prato, Marino De Rosa, Riccardo Fantini, Giuseppe Fiorentino, Maria Antonia Gammino, Francesco Menzella, Giuseppe Milani, Stefano Nava, Gerardo Palmiero, Roberta Petrino, Barbra Gabrielli, Paolo Rossi, Claudio Sorino, Gundi Steinhilber, Alessandro Zanforlin, Fabio Franzetti, Manuela Carugati, Manuela Morosi, Elisa Monge, Mauro Carone, Vincenzo Patella, Simone Scarlata, Andrea Comel, Kiyoyasu Kurahashi, Zeina Aoun Bacha, Daniel Barajas Ugalde, Omar Ceballos Zuñiga, José F Villegas, Milic Medenica, E M W van de Garde, Deebya Raj Mihsra, Poojan Shrestha, Elliott Ridgeon, Babatunde Ishola Awokola, Ogonna N O Nwankwo, Adefuye Bolanle Olufunlola, Segaolu Olumide, Kingsley N Ukwaja, Muhammad Irfan, Lukasz Minarowski, Skoczynski Szymon, Felipe Froes, Pedro Leuschner, Mariana Meireles, Cláudia Ferrão, João Neves, Sofia B Ravara, Victoria Brocovschii, Chesov Ion, Doina Rusu, Cristina Toma, Daniela Chirita, Carmen Mihaela Dorobat, Alexei Birkun, Anna Kaluzhenina, Abdullah Almotairi, Zakeya Abdulbaqi Ali Bukhary, Jameela Edathodu, Amal Fathy, Abdullah Mushira Abdulaziz Enani, Nazik Eltayeb Mohamed, Jawed Ulhadi Memon, Abdelhaleem Bella, Nada Bogdanovic, Branislava Milenkovic, Dragica Pesut, Luis Borderìas, Noel Manuel Bordon Garcia, Hugo Cabello Alarcón, Catia Cilloniz, Antoni Torres, Vicens Diaz-Brito, Xavier Casas, Alicia Encabo González, Maria Luisa Fernández-Almira, Miguel Gallego, Inmaculada Gaspar-GarcÍa, Juan González del Castillo, Patricia Javaloyes Victoria, Elena Laserna Martínez, Rosa Malo de Molina, Pedro J Marcos, Rosario Menéndez, Ana Pando-Sandoval, Cristina Prat Aymerich, Alicia Lacoma de la Torre, Ignasi García-Olivé, Jordi Rello, Silvia Moyano, Francisco Sanz, Oriol Sibila, Ana Rodrigo-Troyano, Jordi Solé-Violán, Ane Uranga, Job FM van Boven, Ester Vendrell Torra, Jordi Almirall Pujol, Charles Feldman, Ho Kee Yum, Arnauld Attannon Fiogbe, Ferdaous Yangui, Semra Bilaceroglu, Levent Dalar, Ufuk Yilmaz, Artemii Bogomolov, Naheed Elahi, Devesh J Dhasmana, Andrew Feneley, Rhiannon Ions, Julie Skeemer, Gerrit Woltmann, Carole Hancock, Adam T Hill, Banu Rudran, Silvia Ruiz-Buitrago, Marion Campbell, Paul Whitaker, Alexander Youzguin, Anika Singanayagam, Karen S Allen, Veronica Brito, Jessica Dietz, Claire E Dysart, Susan M Kellie, Ricardo A Franco-Sadud, Garnet Meier, Mina Gaga, Thomas L Holland, Stephen P Bergin, Fayez Kheir, Mark Landmeier, Manuel Lois, Girish B Nair, Hemali Patel, Katherine Reyes, William Rodriguez-Cintron, Shigeki Saito, Julio Noda, Cecilia I Hinojosa, Stephanie M Levine, Luis F Angel, Antonio Anzueto, K Scott Whitlow, John Hipskind, Kunal Sukhija, Vicken Totten, Richard G Wunderink, Ray D Shah, Kondwelani John Mateyo, Lorena Noriega, Ezequiel Alvarado, Mohamed Aman, Lucía Labra, Aliberti, S., Reyes, L. F., Faverio, P., Sotgiu, G., Dore, S., Rodriguez, A. H., Soni, N. J., Restrepo, M. I., Aruj, P. K., Attorri, S., Barimboim, E., Caeiro, J. P., Garzon, M. I., Cambursano, Vh., Ceccato, A., Chertcoff, J., Lascar, F., Di Tulio, F., Cordon Diaz, A., de Vedia, L., Ganaha, M. C., Lambert, S., Lopardo, G., Luna, C. M., Malberti, A. G., Morcillo, N., Tartara, S., Pensotti, C., Pereyra, B., Scapellato, P. G., Stagnaro, J. P., Shah, S., Lotsch, F., Thalhammer, F., Vincent, J. L., Anseeuw, K., Francois, C. A., Van Braeckel, E., Djimon, M. Z., Bashi, J., Dodo, R., Aranha Nouer, S., Chipev, P., Encheva, M., Miteva, D., Petkova, D., Balkissou, A. D., Pefura Yone, E. W., Mbatchou Ngahane, B. H., Shen, N., Xu, J. F., Bustamante Rico, C. A., Buitrago, R., Pereira Paternina, F. J., Kayembe Ntumba, J. M., Vladic Carevic, V., Jakopovic, M., Jankovic, M., Matkovic, Z., Mitrecic, I., Bouchy Jacobsson, M. L., Bro Christensen, A., Heitmann Bodtger, U. C., Meyer, C. N., Vestergaard Jensen, A., Baunbaek-Knudsen, G., Trier Petersen, P., Andersen, S., El-Said Abd El-Wahhab, I., Elsayed Morsy, N., Shafiek, H., Sobh, E., Abdulsemed, K. A., Bertrand, F., Brun-Buisson, C., de Montmollin, E., Fartoukh, M., Messika, J., Tattevin, P., Khoury, A., Ebruke, B., Dreher, M., Kolditz, M., Meisinger, M., Pletz, M. W., Hagel, S., Rupp, J., Schaberg, T., Spielmanns, M., Creutz, P., Suttorp, N., Siaw-Lartey, B., Dimakou, K., Papapetrou, D., Tsigou, E., Ampazis, D., Kaimakamis, E., Bhatia, M., Dhar, R., D'Souza, G., Garg, R., Koul, P. A., Mahesh, P. A., Jayaraj, B. S., Narayan, K. V., Udnur, H. B., Krishnamurthy, S. B., Kant, S., Swarnakar, R., Limaye, S., Salvi, S., Golshani, K., Keatings, V. M., Martin-Loeches, I., Maor, Y., Strahilevitz, J., Battaglia, S., Carrabba, M., Ceriana, P., Confalonieri, M., d'Arminio Monforte, A., Del Prato, B., De Rosa, M., Fantini, R., Fiorentino, G., Gammino, M. A., Menzella, F., Milani, G., Nava, S., Palmiero, G., Petrino, R., Gabrielli, B., Rossi, P., Sorino, C., Steinhilber, G., Zanforlin, A., Franzetti, F., Carugati, M., Morosi, M., Monge, E., Carone, M., Patella, V., Scarlata, S., Comel, A., Kurahashi, K., Aoun Bacha, Z., Barajas Ugalde, D., Ceballos Zuniga, O., Villegas, J. F., Medenica, M., van de Garde, Emw., Raj Mihsra, D., Shrestha, P., Ridgeon, E., Ishola Awokola, B., Nwankwo, Ono., Olufunlola, A. B., Olumide, S., Ukwaja, K. N., Irfan, M., Minarowski, L., Szymon, S., Froes, F., Leuschner, P., Meireles, M., Ferrao, C., Neves, J., Ravara, S. B., Brocovschii, V., Ion, C., Rusu, D., Toma, C., Chirita, D., Dorobat, C. M., Birkun, A., Kaluzhenina, A., Almotairi, A., Bukhary, Zaa., Edathodu, J., Fathy, A., Mushira Abdulaziz Enani, A., Eltayeb Mohamed, N., Ulhadi Memon, J., Bella, A., Bogdanovic, N., Milenkovic, B., Pesut, D., Borderias, L., Bordon Garcia, N. M., Cabello Alarcon, H., Cilloniz, C., Torres, A., Diaz-Brito, V., Casas, X., Encabo Gonzalez, A., Fernandez-Almira, M. L., Gallego, M., Gaspar-GarcIa, I., Gonzalez Del Castillo, J., Javaloyes Victoria, P., Laserna Martinez, E., Malo de Molina, R., Marcos, P. J., Menendez, R., Pando-Sandoval, A., Prat Aymerich, C., Lacoma de la Torre, A., Garcia-Olive, I., Rello, J., Moyano, S., Sanz, F., Sibila, O., Rodrigo-Troyano, A., Sole-Violan, J., Uranga, A., van Boven, J. F., Vendrell Torra, E., Pujol, J. A., Feldman, C., Kee Yum, H., Fiogbe, A. A., Yangui, F., Bilaceroglu, S., Dalar, L., Yilmaz, U., Bogomolov, A., Elahi, N., Dhasmana, D. J., Feneley, A., Ions, R., Skeemer, J., Woltmann, G., Hancock, C., Hill, A. T., Rudran, B., Ruiz-Buitrago, S., Campbell, M., Whitaker, P., Youzguin, A., Singanayagam, A., Allen, K. S., Brito, V., Dietz, J., Dysart, C. E., Kellie, S. M., Franco-Sadud, R. A., Meier, G., Gaga, M., Holland, T. L., Bergin, S. P., Kheir, F., Landmeier, M., Lois, M., Nair, G. B., Patel, H., Reyes, K., Rodriguez-Cintron, W., Saito, S., Noda, J., Hinojosa, C. I., Levine, S. M., Angel, L. F., Anzueto, A., Whitlow, K. S., Hipskind, J., Sukhija, K., Totten, V., Wunderink, R. G., Shah, R. D., Mateyo, K. J., Noriega, L., Alvarado, E., Aman, M., Labra, L., Aliberti S., Reyes L.F., Faverio P., Sotgiu G., Dore S., Rodriguez A.H., Soni N.J., Restrepo M.I., Aruj P.K., Attorri S., Barimboim E., Caeiro J.P., Garzon M.I., Cambursano VH., Ceccato A., Chertcoff J., Lascar F., Di Tulio F., Cordon Diaz A., de Vedia L., Ganaha M.C., Lambert S., Lopardo G., Luna C.M., Malberti A.G., Morcillo N., Tartara S., Pensotti C., Pereyra B., Scapellato P.G., Stagnaro J.P., Shah S., Lotsch F., Thalhammer F., Vincent J.L., Anseeuw K., Francois C.A., Van Braeckel E., Djimon M.Z., Bashi J., Dodo R., Aranha Nouer S., Chipev P., Encheva M., Miteva D., Petkova D., Balkissou A.D., Pefura Yone E.W., Mbatchou Ngahane B.H., Shen N., Xu J.F., Bustamante Rico C.A., Buitrago R., Pereira Paternina F.J., Kayembe Ntumba J.M., Vladic Carevic V., Jakopovic M., Jankovic M., Matkovic Z., Mitrecic I., Bouchy Jacobsson M.L., Bro Christensen A., Heitmann Bodtger U.C., Meyer C.N., Vestergaard Jensen A., Baunbaek-Knudsen G., Trier Petersen P., Andersen S., El-Said Abd El-Wahhab I., Elsayed Morsy N., Shafiek H., Sobh E., Abdulsemed K.A., Bertrand F., Brun-Buisson C., de Montmollin E., Fartoukh M., Messika J., Tattevin P., Khoury A., Ebruke B., Dreher M., Kolditz M., Meisinger M., Pletz M.W., Hagel S., Rupp J., Schaberg T., Spielmanns M., Creutz P., Suttorp N., Siaw-Lartey B., Dimakou K., Papapetrou D., Tsigou E., Ampazis D., Kaimakamis E., Bhatia M., Dhar R., D'Souza G., Garg R., Koul P.A., Mahesh P.A., Jayaraj B.S., Narayan K.V., Udnur H.B., Krishnamurthy S.B., Kant S., Swarnakar R., Limaye S., Salvi S., Golshani K., Keatings V.M., Martin-Loeches I., Maor Y., Strahilevitz J., Battaglia S., Carrabba M., Ceriana P., Confalonieri M., d'Arminio Monforte A., Del Prato B., De Rosa M., Fantini R., Fiorentino G., Gammino M.A., Menzella F., Milani G., Nava S., Palmiero G., Petrino R., Gabrielli B., Rossi P., Sorino C., Steinhilber G., Zanforlin A., Franzetti F., Carugati M., Morosi M., Monge E., Carone M., Patella V., Scarlata S., Comel A., Kurahashi K., Aoun Bacha Z., Barajas Ugalde D., Ceballos Zuniga O., Villegas J.F., Medenica M., van de Garde EMW., Raj Mihsra D., Shrestha P., Ridgeon E., Ishola Awokola B., Nwankwo ONO., Olufunlola A.B., Olumide S., Ukwaja K.N., Irfan M., Minarowski L., Szymon S., Froes F., Leuschner P., Meireles M., Ferrao C., Neves J., Ravara S.B., Brocovschii V., Ion C., Rusu D., Toma C., Chirita D., Dorobat C.M., Birkun A., Kaluzhenina A., Almotairi A., Bukhary ZAA., Edathodu J., Fathy A., Mushira Abdulaziz Enani A., Eltayeb Mohamed N., Ulhadi Memon J., Bella A., Bogdanovic N., Milenkovic B., Pesut D., Borderias L., Bordon Garcia N.M., Cabello Alarcon H., Cilloniz C., Torres A., Diaz-Brito V., Casas X., Encabo Gonzalez A., Fernandez-Almira M.L., Gallego M., Gaspar-GarcIa I., Gonzalez Del Castillo J., Javaloyes Victoria P., Laserna Martinez E., Malo de Molina R., Marcos P.J., Menendez R., Pando-Sandoval A., Prat Aymerich C., Lacoma de la Torre A., Garcia-Olive I., Rello J., Moyano S., Sanz F., Sibila O., Rodrigo-Troyano A., Sole-Violan J., Uranga A., van Boven J.F., Vendrell Torra E., Pujol J.A., Feldman C., Kee Yum H., Fiogbe A.A., Yangui F., Bilaceroglu S., Dalar L., Yilmaz U., Bogomolov A., Elahi N., Dhasmana D.J., Feneley A., Ions R., Skeemer J., Woltmann G., Hancock C., Hill A.T., Rudran B., Ruiz-Buitrago S., Campbell M., Whitaker P., Youzguin A., Singanayagam A., Allen K.S., Brito V., Dietz J., Dysart C.E., Kellie S.M., Franco-Sadud R.A., Meier G., Gaga M., Holland T.L., Bergin S.P., Kheir F., Landmeier M., Lois M., Nair G.B., Patel H., Reyes K., Rodriguez-Cintron W., Saito S., Noda J., Hinojosa C.I., Levine S.M., Angel L.F., Anzueto A., Whitlow K.S., Hipskind J., Sukhija K., Totten V., Wunderink R.G., Shah R.D., Mateyo K.J., Noriega L., Alvarado E., Aman M., Labra L., Aliberti, S, Reyes, L, Faverio, P, Sotgiu, G, Dore, S, Rodriguez, A, Soni, N, and Restrepo, M
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Male ,antibiotic resistance ,Prevalence ,MRSA ,medicine.disease_cause ,pneumonia ,staphylococcus aureus ,Global Health ,Cohort Studies ,0302 clinical medicine ,Community-acquired pneumonia ,Risk Factors ,Retrospective Studie ,Community-Acquired Infection ,030212 general & internal medicine ,education.field_of_study ,Cross Infection ,Respiratory tract infections ,Methicillin-Resistant Staphylococcus aureu ,Staphylococcal Infections ,Hospitals ,Community-Acquired Infections ,Infectious Diseases ,Infectious diseases ,Female ,Human ,Methicillin-Resistant Staphylococcus aureus ,medicine.medical_specialty ,Population ,Admission ,staphylococcus aureu ,Settore MED/10 - Malattie Dell'Apparato Respiratorio ,03 medical and health sciences ,Hospital ,Internal medicine ,medicine ,Humans ,Risk factor ,education ,Intensive care medicine ,Staphylococcal Infection ,Retrospective Studies ,Aged ,business.industry ,Risk Factor ,Odds ratio ,Pneumonia ,medicine.disease ,Methicillin-resistant Staphylococcus aureus ,030228 respiratory system ,Methicillin Resistance ,Cohort Studie ,business - Abstract
BACKGROUND: Antibiotic resistance is a major global health problem and pathogens such as meticillin-resistant Staphylococcus aureus (MRSA) have become of particular concern in the management of lower respiratory tract infections. However, few data are available on the worldwide prevalence and risk factors for MRSA pneumonia. We aimed to determine the point prevalence of MRSA pneumonia and identify specific MRSA risk factors in community-dwelling patients hospitalised with pneumonia.METHODS: We did an international, multicentre study of community-dwelling, adult patients admitted to hospital with pneumonia who had microbiological tests taken within 24 h of presentation. We recruited investigators from 222 hospitals in 54 countries to gather point-prevalence data for all patients admitted with these characteristics during 4 days randomly selected during the months of March, April, May, and June in 2015. We assessed prevalence of MRSA pneumonia and associated risk factors through logistic regression analysis.FINDINGS: 3702 patients hospitalised with pneumonia were enrolled, with 3193 patients receiving microbiological tests within 24 h of admission, forming the patient population. 1173 (37%) had at least one pathogen isolated (culture-positive population). The overall prevalence of confirmed MRSA pneumonia was 3·0% (n=95), with differing prevalence between continents and countries. Three risk factors were independently associated with MRSA pneumonia: previous MRSA infection or colonisation (odds ratio 6·21, 95% CI 3·25-11·85), recurrent skin infections (2·87, 1·10-7·45), and severe pneumonia disease (2·39, 1·55-3·68).INTERPRETATION: This multicountry study shows low prevalence of MRSA pneumonia and specific MRSA risk factors among community-dwelling patients hospitalised with pneumonia.FUNDING: None.
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- 2016
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47. Risk factors associated with vancomycin-resistant enterococcus (VRE) and methicillin-resistant Staphylococcus aureus (MRSA) co-infection
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Ana C. Bardossy, Marcus J. Zervos, Daniela Moreno, Katherine Reyes, Helina Misikir, Mary Beth Perri, Khulood Rizvi, Geehan Suleyman, and Pam Hartman
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business.industry ,medicine ,Vancomycin-resistant Enterococcus ,General Medicine ,medicine.disease_cause ,business ,Methicillin-resistant Staphylococcus aureus ,Co infection ,Microbiology - Published
- 2016
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48. High vancomycin serum trough is not associated with reduction of mortality in methicillin-resistant Staphylococcus aureus bloodstream infections
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Tooba Rehman, Meredith Mahan, Pedro Ayau Aguilar, Katherine Reyes, Ana C. Bardossy, Mary Beth Perri, Khulood Rizvi, Guillermo Sánchez Rosenberg, Marcus J. Zervos, Daniela Moreno, Pamela Hartman, Ayesha Niazy, Vanthida Huang, Geehan Suleyman, and Tyler Prentiss
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business.industry ,Trough (geology) ,Medicine ,Vancomycin ,General Medicine ,business ,medicine.disease_cause ,Methicillin-resistant Staphylococcus aureus ,Microbiology ,medicine.drug - Published
- 2016
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49. Influence of Minimum Inhibitory Concentration in Clinical Outcomes of Enterococcus faecium Bacteremia Treated With Daptomycin: Is it Time to Change the Breakpoint?
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Mini Kamboj, Samuel A. Shelburne, Jose M. Munita, Cesar A. Arias, Lina P Carvajal, Katherine Reyes, Eric G. Pamer, Marcus J. Zervos, Diana Panesso, Truc T. Tran, Javier A. Adachi, Rodrigo Hasbun, Jinnethe Reyes, Jessica D. Lewis, Costi D. Sifri, Sandra Rincon, Bhavarth S. Shukla, Panesso, Diana [0000-0002-4049-9702], Rincon Núñez, Sandra [0000-0002-8482-4554], and Carvajal Ortiz, Lina Paola [0000-0001-8301-8836]
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0301 basic medicine ,Microbiology (medical) ,Male ,medicine.medical_specialty ,Desnutrición ,E. faecium ,medicine.drug_class ,030106 microbiology ,Antibiotics ,Enterococcus faecium ,Bacteremia ,Drug resistance ,Microbial Sensitivity Tests ,Microbiology ,03 medical and health sciences ,Minimum inhibitory concentration ,0302 clinical medicine ,Daptomycin ,Internal medicine ,Drug Resistance, Bacterial ,medicine ,polycyclic compounds ,Humans ,Blood culture ,030212 general & internal medicine ,MIC ,Articles and Commentaries ,Gram-Positive Bacterial Infections ,Retrospective Studies ,medicine.diagnostic_test ,biology ,business.industry ,Retrospective cohort study ,biochemical phenomena, metabolism, and nutrition ,Middle Aged ,medicine.disease ,biology.organism_classification ,bacterial infections and mycoses ,Anti-Bacterial Agents ,carbohydrates (lipids) ,Infectious Diseases ,Antibacterianos ,lipids (amino acids, peptides, and proteins) ,Female ,business ,medicine.drug - Abstract
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.
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- 2015
50. Comparative Effectiveness of Vancomycin Versus Daptomycin for MRSA Bacteremia With Vancomycin MIC1 mg/L: A Multicenter Evaluation
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Thomas P. Lodise, Marcus J. Zervos, Katherine Reyes, James A. McKinnell, Karri A. Bauer, Romic Eskandarian, Kimberly D Leuthner, Darren L. Culshaw, Joyce Bensman, Annie Wong-Beringer, Saira B. Chaudhry, Winter J. Smith, Kenneth C. Lamp, Robert Adamson, Pamela A. Moise, Michael Virata, and Debra A. Goff
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0301 basic medicine ,Male ,Methicillin-Resistant Staphylococcus aureus ,medicine.medical_specialty ,030106 microbiology ,Bacteremia ,Microbial Sensitivity Tests ,medicine.disease_cause ,law.invention ,03 medical and health sciences ,Daptomycin ,Interquartile range ,law ,Recurrence ,Vancomycin ,Internal medicine ,Medicine ,Humans ,Pharmacology (medical) ,Treatment Failure ,Propensity Score ,Aged ,Retrospective Studies ,Pharmacology ,business.industry ,Retrospective cohort study ,biochemical phenomena, metabolism, and nutrition ,Acute Kidney Injury ,Middle Aged ,Staphylococcal Infections ,bacterial infections and mycoses ,medicine.disease ,Methicillin-resistant Staphylococcus aureus ,Intensive care unit ,Anti-Bacterial Agents ,Intensive Care Units ,Treatment Outcome ,Anesthesia ,Multivariate Analysis ,Trough level ,Regression Analysis ,Female ,Neoplasm Recurrence, Local ,business ,medicine.drug - Abstract
Purpose Clinical studies comparing vancomycin with alternative therapy for methicillin-resistant Staphylococcus aureus (MRSA) bacteremia are limited. The objective of this study was to compare outcomes of early daptomycin versus vancomycin treatment for MRSA bacteremia with high vancomycin MICs in a geographically diverse multicenter evaluation. Methods This nationwide, retrospective, multicenter (N = 11), matched, cohort study compared outcomes of early daptomycin with vancomycin for MRSA bloodstream infection (BSI) with vancomycin MICs 1.5 to 2 µg/mL. Matching variables, based on propensity regression analysis, included age, intensive care unit (ICU), and type of BSI. Outcomes were as follows: (1) composite failure (60-day all-cause mortality, 7-day clinical or microbiologic failure, 30-day BSI relapse, or end-of-treatment failure (EOT; discontinue/change daptomycin or vancomycin because of treatment failure or adverse event]); (2) nephrotoxicity; and (2) day 4 BSI clearance. Findings A total of 170 patients were included. The median (interquartile range) age was 60 years (50–74); the median (range) Acute Physiology and Chronic Health Evaluation II score was 15 (10–18); 31% were in an ICU; and 92% had an infectious disease consultation. BSI types included endocarditis/endovascular (39%), extravascular (55%), and central catheter (6%). The median daptomycin dose was 6 mg/kg, and the vancomycin trough level was 17 mg/L. Overall composite failure was 35% (59 of 170): 15% due to 60-day all-cause mortality, 14% for lack of clinical or microbiologic response by 7 days, and 17% due to failure at end of therapy (discontinue/change because of treatment failure or adverse event). Predictors of composite failure according to multivariate analysis were age >60 years (odds ratio, 3.7; P P = 0.03). Notable differences between treatment groups were seen with: (1) end of therapy failure rates (11% vs 24% for daptomycin vs vancomycin; P = 0.025); (2) acute kidney injury rates (9% vs 23% for daptomycin vs vancomycin; P = 0.043); and (3) day 4 bacteremia clearance rates for immunocompromised patients (n = 26) (94% vs 56% for daptomycin vs vancomycin; P = 0.035). Implications Results from this multicenter study provide, for the first time, a geographically diverse evaluation of daptomycin versus vancomycin for patients with vancomycin-susceptible MRSA bacteremia with vancomycin MIC values >1 µg/mL. Although the overall composite failure rates did not differ between the vancomycin and daptomycin groups when intensively matched according to risks for failure, the rates of acute kidney injury were significantly lower in the daptomycin group. These findings suggest that daptomycin is a useful therapy for clinicians treating patients who have MRSA bacteremia. Prospective, randomized trials should be conducted to better assess the potential significance of elevated vancomycin MIC.
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- 2015
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