Cargando…

Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department

Sickle cell disease (SCD ORPHA232; OMIM 603903) is a rare hereditary red cell disorder, which global distribution is changed in the last decade due to immigration-fluxes from endemic areas to Western-countries. One of the main clinical manifestations of SCD are the acute painful vaso-occlusive crisi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Forni, Gian Luca, Finco, Gabriele, Graziadei, Giovanna, Balocco, Manuela, Rigano, Paolo, Perrotta, Silverio, Olivieri, Oliviero, Cappellini, Maria Domenica, De Franceschi, Lucia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230640/ https://www.ncbi.nlm.nih.gov/pubmed/24957117 http://dx.doi.org/10.1186/1750-1172-9-91

Ejemplares similares

Current challenges in the management of patients with sickle cell disease – A report of the Italian experience
por: Russo, Giovanna, et al.
Publicado: (2019)

Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from three decades of follow-up in a high-income setting
por: Pinto, Valeria Maria, et al.
Publicado: (2022)

Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm
por: Baronciani, Donatella, et al.
Publicado: (2021)

COVID 19 and Hemoglobinopathies: Update of the Italian Experience
por: Motta, Irene, et al.
Publicado: (2020)

Development of Algorithm for Clinical Management of Sickle Cell Bone Disease: Evidence for a Role of Vertebral Fractures in Patient Follow-up
por: De Franceschi, Lucia, et al.
Publicado: (2020)

Management of the Sickle Cell Trait: An Opinion by Expert Panel Members
por: Pinto, Valeria Maria, et al.
Publicado: (2023)

New Therapeutic Options for the Treatment of Sickle Cell Disease
por: Matte, Alessandro, et al.
Publicado: (2019)

Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective
por: Bou-Fakhredin, Rayan, et al.
Publicado: (2022)

P1449: SAFETY PROFILE OF KETOROLAC CONTINUOUS INFUSION IN SICKLE CELL RELATED ACUTE VASO-OCCLUSIVE CRISIS
por: Maria Pinto, Valeria, et al.
Publicado: (2023)

Redox Balance in β-Thalassemia and Sickle Cell Disease: A Love and Hate Relationship
por: Bou-Fakhredin, Rayan, et al.
Publicado: (2022)

Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemia
por: Derchi, Giorgio, et al.
Publicado: (2022)

Sickle cell maculopathy: Identification of systemic risk factors, and microstructural analysis of individual retinal layers of the macula
por: Dell’Arti, Laura, et al.
Publicado: (2018)

P129: NARRATING SICKLE CELL DISEASE: THE EXPERIENCES OF PATIENTS AND CARGIVERS
por: De Franceschi, L, et al.
Publicado: (2022)

Iron overload-related heart failure in a patient with transfusion-dependent myelodysplastic syndrome reversed by intensive combined chelation therapy
por: Pinto, Valeria, et al.
Publicado: (2015)

Real-World Evidence on Disease Burden and Economic Impact of Sickle Cell Disease in Italy
por: De Franceschi, Lucia, et al.
Publicado: (2022)

Changes in the quality of life of people with thalassemia major between 2001 and 2009
por: Gollo, Giorgia, et al.
Publicado: (2013)

A relative ADAMTS13 deficiency supports the presence of a secondary microangiopathy in COVID 19
por: Martinelli, Nicola, et al.
Publicado: (2020)

Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
por: Ferraresi, Marta, et al.
Publicado: (2023)

Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhood
por: Colombatti, Raffaella, et al.
Publicado: (2013)

Glucose-6-phosphate dehydrogenase deficiency associated hemolysis in COVID-19 patients treated with hydroxychloroquine/chloroquine: New case reports coming out
por: De Franceschi, Lucia, et al.
Publicado: (2020)

Acute hemolysis by hydroxycloroquine was observed in G6PD-deficient patient with severe COVD-19 related lung injury
por: De Franceschi, Lucia, et al.
Publicado: (2020)

Pathophisiology of Sickle Cell Disease and New Drugs for the Treatment
por: De Franceschi, Lucia
Publicado: (2009)

Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy
por: Graziadei, Giovanna, et al.
Publicado: (2022)

Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study
por: Cappellini, Maria Domenica, et al.
Publicado: (2019)

Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene
por: Punzo, Francesca, et al.
Publicado: (2011)

Hepcidin Levels and Their Determinants in Different Types of Myelodysplastic Syndromes
por: Santini, Valeria, et al.
Publicado: (2011)

First and Second Level Haemoglobinopathies Diagnosis: Best Practices of the Italian Society of Thalassemia and Haemoglobinopathies (SITE)
por: Mandrile, Giorgia, et al.
Publicado: (2022)

Thalassaemia is paradoxically associated with a reduced risk of in‐hospital complications and mortality in COVID‐19: Data from an international registry
por: El‐Battrawy, Ibrahim, et al.
Publicado: (2022)

Accelerating the Development of Heat Tolerant Tomato Hybrids through a Multi-Traits Evaluation of Parental Lines Combining Phenotypic and Genotypic Analysis
por: Olivieri, Fabrizio, et al.
Publicado: (2021)

Ultraviolet A phototest positivity is associated with higher free erythrocyte protoporphyrin IX concentration and lower transferrin saturation values in erythropoietic protoporphyria
por: Genovese, Giovanni, et al.
Publicado: (2021)

Phenotypic and Molecular Selection of a Superior Solanum pennellii Introgression Sub-Line Suitable for Improving Quality Traits of Cultivated Tomatoes
por: Calafiore, Roberta, et al.
Publicado: (2019)

Genomic Dissection of a Wild Region in a Superior Solanum pennellii Introgression Sub-Line with High Ascorbic Acid Accumulation in Tomato Fruit
por: Aliberti, Antonietta, et al.
Publicado: (2020)

Influenza Vaccination in Asplenia: Improving Quality of Care in Time of Coronavirus
por: Di Maio, Nicoletta, et al.
Publicado: (2020)

Access Rate to the Emergency Department for Venous Thromboembolism in Relationship with Coarse and Fine Particulate Matter Air Pollution
por: Martinelli, Nicola, et al.
Publicado: (2012)

Incidence of cancer and related deaths in hemoglobinopathies: A follow‐up of 4631 patients between 1970 and 2021
por: Origa, Raffaella, et al.
Publicado: (2022)

Exjade® (deferasirox, ICL670) in the treatment of chronic iron overload associated with blood transfusion
por: Cappellini, Maria Domenica
Publicado: (2007)

Advances in hemoglobin disorders
por: Cappellini, Maria Domenica
Publicado: (2018)

EHA Research Roadmap on Hemoglobinopathies and Thalassemia: An Update
por: Iolascon, Achille, et al.
Publicado: (2019)

Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
por: Russo, Roberta, et al.
Publicado: (2010)

Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta Thalassemia
por: Di Maggio, Rosario, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_04dfkudfgb3bb282tm9ss6buls