Results 171 to 180 of about 212,426 (301)

Vasopressin use across shock states: international insights from an international ESICM-endorsed survey: the PRESS Survey. [PDF]

Crit Care
Jozwiak M, Cousin VL, De Backer D, Malbrain MLNG, Monnet X, Messina A, Chew MS, Cardiovascular Dynamics section of the European Society of Intensive Care Medicine.   +7 more
europepmc   +1 more source

Septic shock—an update [PDF]

The Indian Journal of Pediatrics, 1982
openaire   +3 more sources

Anti‐ADAMTS13 Antibodies Trajectory is Associated With ADAMTS13 Recovery in Immune‐Mediated TTP

American Journal of Hematology, EarlyView.
Anti‐ADAMTS13 IgG antibodies titer trajectory from baseline to day 7–14 post‐TPE as a reliable approach to identify iTTP patients at risk of late response to the triplet therapy regimen. ABSTRACT Current triplet regimens associating therapeutic plasma exchange (TPE), immunosuppression with corticosteroids and rituximab, and caplacizumab have ...
Marie Robert, Arthur Mageau, Ygal Benhamou, François Provôt, Jehane Fadlallah, Lionel Galicier, Elie Azoulay, Hafid Ait‐Oufella, Tomas Urbina, Pascale Poullin, Alain Wynckel, Coralie Poulain, Nihal Martis, Pierre Perez, Virginie Rieu, Yahsou Delmas, Jean‐Michel Halimi, Christelle Barbet, Amélie Seguin, Valérie Chatelet, Jean‐François Augusto, Mathieu Legendre, Olivier Moranne, Carole Philipponnet, Bérengère Cador, Raïda Bouzid, Bérangère S. Joly, Agnès Veyradier, Paul Coppo, on behalf of the French Reference Center for Thrombotic Microangiopathies   +29 more
wiley   +1 more source

Evaluation of Stress Dose Hydrocortisone Tapers in Septic Shock. [PDF]

Hosp Pharm
Gilchrist HE, Roginski M, Esteves A.
europepmc   +1 more source

Cold Agglutinin Syndrome Secondary to Mycoplasma pneumoniae Infection in Adults: Results From a Large French Observational Study (MyCOLD Study)

American Journal of Hematology, EarlyView.
Summary of the main results of the MYCOLD studies. ABSTRACT Mycoplasma pneumoniae (MP), primarily a respiratory pathogen, can cause extra‐pulmonary manifestations including cold agglutinin syndrome (CAS). We conducted a national, multicenter, observational, ambispective study to describe the characteristics, risk factors, and outcomes of MP‐associated ...
Kevin Chevalier, Matthieu Holub, Romain Palich, Karine Blanckaert, Laurent Gilardin, Louis Terriou, Bérangère Arnould, Solal Bellaiche, Samuel Deshayes, Julie Mérindol, Simon Rolland, Simon Valentin, Rishma Amarsy, Sylvain Audia, Virginie Baltes, Amaury Barret, Pierre‐Louis Cariou, Jessy Cattelan, Hortense Chassepot, Dorothée Chopin, Mélissa Clément, Marine Coeffier, Thibault Comont, Soline De Monteynard, Charles Declerck, Pauline Durand, Mikael Ebbo, Gaël Galli, Amélie Godot, Sarra Hamrouni, Charlotte Kaeuffer, Jean‐Emmanuel Kahn, Ludovic Lassel, Sophie Leautez, Anne‐Lise Lecapitaine, Gwenael Le Moal, David Luque Paz, Martin Martinot, Natacha Mrozek, Valentine Pagis, Thomas Perpoint, Valéry Salle, Jean‐François Viallard, Clément Viguier, Matthieu Mahevas, Bertrand Godeau, Etienne Crickx, Marc Michel   +47 more
wiley   +1 more source

Tocilizumab in improving the hemodynamics of septic children with vasoplegia shock. [PDF]

Crit Care
Lee EP, Lin JJ, Chen SH, Wu HP.
europepmc   +1 more source

Prenatal Brain Abnormalities in Sodium‐Dependent Multivitamin Transporter Deficiency

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT In treatable neurometabolic disorders, early diagnosis and prompt initiation of treatment are key to improved survival and outcomes. Biallelic variants in SLC5A6 cause sodium‐dependent multivitamin transporter deficiency (OMIM # 618973), which is treatable with high‐dose pantothenic acid, biotin, and alpha lipoic acid.
Eri Ogawa, Kenjiro Kosaki, Toshiki Takenouchi   +2 more
wiley   +1 more source

Vascular hyporesponsiveness to norepinephrine is a major but not exclusive determinant of mortality in septic shock. [PDF]

Ann Intensive Care
Goury A, Djerada Z, Teboul JL, Hamzaoui O.   +3 more
europepmc   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Expression of inflammatory factors and distribution of pathogens in patients with septic shock and their correlation with prognosis: a cross-sectional study. [PDF]

Rev Inst Med Trop Sao Paulo
Chen J, Tan M, Xiang T.
europepmc   +1 more source