Results 11 to 20 of about 316 (117)

Multiple organ dysfunction after trauma [PDF]

BJS (British Journal of Surgery), Volume 107, Issue 4, Page 402-412, March 2020., 2020
As trauma practice advances, postinjury multiple organ dysfunction syndrome (MODS) is changing. The aim of this study was to characterize contemporary MODS in trauma critical care. Three patterns of MODS were identified, all present on admission, with distinct clinical associations. SOFA, Sequential Organ Failure Assessment. Present from admission with
E. Cole, S. Gillespie, P. Vulliamy, K. Brohi, on behalf of the Organ Dysfunction in Trauma (ORDIT) study collaborators, H. Akkad, K. Apostolidou, R. Ardley, C. Aylwin, C. Bassford, S. Bonner, A. Brooks, T. Cairns, M. Cecconi, F. Clark, G. Dempsey, E. Denison Davies, R. Docking, J. Eddlestone, D. Ellis, J. Evans, M. Galea, M. Healy, D. Horner, R. Howarth, J. Jansen, J. Jones, C. Kaye, J. Keep, D. Kerslake, J. Kilic, M. Leong, V. Martinson, B. McIldowie, S. Michael, J. Millo, M. Morgan, R. O'Leary, J. Oram, L. Ortiz‐Ruiz De Gordoa, K. Porter, S. Raby, J. Service, D. Shaw, J. D. Smith, N. Smith, M. Stotz, E. Thomas, M. Thomas, A. Vincent, G. Ward, I. Welters   +51 more
wiley   +2 more sources

PACIENTE PEDIÁTRICO COM SÍNDROME DE EVANS E SARS-COV-2 [PDF]

Hematology, Transfusion and Cell Therapy, 2020
I.C.N. Alencar, T.B. Sampaio, A. Angel, J.A.P. Braga   +3 more
doaj   +2 more sources

UEG Week 2025 Poster Presentations [PDF]

United European Gastroenterol J
United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley   +2 more sources

Síndrome de Evans - presentación atípica de un linfoma raro

Galicia Clínica, 2022
Evans Syndrome is a rare autoimmune condition characterized by two or more cytopenias, usually autoimmune haemolytic anaemia and immune thrombocytopenic purpura. It can be primary/idiopathic or secondary to other diseases.
Catarina Teles Neto, Marta Valentim, Filipa Pedro, Pedro Luís, Ana Gameiro, Luís Siopa   +5 more
doaj   +1 more source

Síndrome de Evans y embarazo en la adolescencia: reporte de un caso y revisión de la literatura

Revista Colombiana de Obstetricia y Ginecología, 2016
Objetivo: presentar el caso de una gestante adolescente con síndrome de Evans, y hacer una revisión de la literatura respecto a su tratamiento y pronóstico durante el embarazo.
David Andrés Viveros Carreño, Arturo José Parada Baños   +1 more
doaj   +1 more source

Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa

Special Care in Dentistry, Volume 40, Issue S1, Page 3-81, November 2020., 2020
ABSTRACT Background Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral features. Aims To provide (a) a complete review of the oral manifestations in those living with each type of inherited EB, (b) the current best practices for managing oral health care of people living with EB, (c) the current ...
Susanne Krämer, James Lucas, Francisca Gamboa, Miguel Peñarrocha Diago, David Peñarrocha Oltra, Marcelo Guzmán‐Letelier, Sanchit Paul, Gustavo Molina, Lorena Sepúlveda, Ignacio Araya, Rubén Soto, Carolina Arriagada, Anne W Lucky, Jemima E Mellerio, Roger Cornwall, Fatimah Alsayer, Reinhard Schilke, Mark Adam Antal, Fernanda Castrillón, Camila Paredes, Maria Concepción Serrano, Victoria Clark   +21 more
wiley   +1 more source

Síndrome de Evans en lactantes

Boletín Médico del Hospital Infantil de México, 2017
Introducción: El síndrome de Evans se caracteriza por la disminución de, al menos, dos líneas celulares en ausencia de otros diagnósticos. Anteriormente, se definía como el desarrollo simultáneo o secuencial de trombocitopenia inmune primaria y anemia ...
Olivia Alejandra Flores-Montes, Martha Cecilia Escobar-Orduño, Mónica Lozano-Garcidueñas, Jaime Guadalupe Valle-Leal   +3 more
doaj   +1 more source

Infección invasiva por Listeria monocytogenes en un paciente con síndrome de Evans.

Ciencia & Salud, 2020
Listeria monocytogenes es una bacteria intracelular facultativa que tiene predilección por causar infecciones del sistema nervioso central en humanos.
Erick José Méndez Ramírez, Jeinny Maroto Fernández   +1 more
doaj   +1 more source

Abstract

, 2022
Research and Practice in Thrombosis and Haemostasis, Volume 6, Issue S1, October 2022.
wiley   +1 more source

AVALIAÇÃO DAS INDICAÇÕES DE PLASMAFÉRESE EM PACIENTES DE HOSPITAL DE HEMATOLOGIA E HEMOTERAPIA DE PERNAMBUCO

Hematology, Transfusion and Cell Therapy, 2023
Objetivos: Caracterizar as indicações de Plasmaférese Terapêutica (PT) em pacientes de hospital de hematologia e hemoterapia de Pernambuco conforme classificação da American Society for Apheresys (ASFA).
LFE Costa, AN Machado, LMS Sitcovsky
doaj   +1 more source