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Your search keyword '"Del Orbe Barreto, Rafael Andrés"' showing total 11 results
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11 results on '"Del Orbe Barreto, Rafael Andrés"'

1. ADAMTS13 recovery in acute thrombotic thrombocytopenic purpura after caplacizumab therapy

Author

Abio Calvete, Mariola, Albert, Albert, Alberto López García, Alberto, Alegre, Adrian, Alkorta Eizagirre, Aitziber, Alonso Escobar, María Nieves, Alonso Madrigal, Cristina, Amunarriz, Cristina, Antelo Caamaño, María Luisa, Arbona Castaño, Cristina, Ballester Ruiz, Maria Carmen, Ballina Martín, Belén, Berberana Fernández de Murias, Margarita, Berrueco Moreno, Ruben, Bueno, Jose Luis, Calderón López, María Teresa, Chica Gullón, Esther, Cid Vidal, Joan, Contreras Barbeta, Enric, Cuéllar Pérez-Ávila, Clara, de la Rubia Comos, Javier, Del Orbe Barreto, Rafael Andres, Del Río Garma, Julio, Díaz Valdés, José R., Diaz-Ricart, Maribel, Diez Gallarreta, Zuriñe, Dueñas Hernando, Virginia, Eguia, Blanca, Escoda, Lourdes, Fernández Docampo, Marta, Fernandez Fuertes, Fernando, Fernández Muñoz, Hermogenes, Fernández Sánchez de Mora, Maria Carmen, Fernandez Zarzoso, Miguel, Fidalgo, Teresa, Flores Ballester, Elena, Fonte Feal, Cristina, Galvez, Francisco Javier, Garcia Arroba Peinado, Jose, García Candel, Faustino, Garcia Erce, Jose Antonio, García Gala, José María, Gimeno, JJ, Gómez, Delia, Gómez Seguí, Inés, Gomez Vazquez, Maria Jesus, Gonzalez, Carlos, González Fernández, Fernando Ataulfo, Gonzalez Porras, Jose Ramon, Gonzalez Rodriguez, Victoria Paz, Goterris Viciedo, Rosa, Guerra Domínguez, Luisa, Guillén García, Helga, Hernandez, Adoracion, Hernández Castellet, José Carlos, Hernandez Mohedo, Francisca, Hernandez Vazquez, Laura, Hidalgo Soto, Marta, Hong Tam, Azueg Hang, Kerguelen Fuentes, Ana Lilia, Leal Bento, Marta, Lopes, Raquel, López, Olga, López Chuliá, Francisca, Maria Jose Busto, Maria Jose, Martín Hernández, María Paz, Martinez Estefano, Elvira, Martinez Nieto, Jorge, Martinez Redondo, Consuelo, Martinez Revuelta, Eva, Medina Marrero, Laura, Mingot Castellano, María Eva, Morales Sanz, María Dolores, Moreno, Gemma, Moreno Beltrán, Mª Esperanza, Moreno Chulilla, Jose Antonio, Nistal Gil, Sara, Oliva Hernandez, Ana Yurena, Pascual, Teresa, Pascual Izquierdo, Crisina, Paumard Rodríguez, Elena, Pecos, Patricia, Peña Marcos, Francisco, Pereira Coelho, Daniela Sofia, Pérez Segura, Gloria Maria, Perez-Lopez, Olga, Prieto Pareja, Elena, Ramiro, Laia, Richart López, Luis Alberto, Rodriguez Dominguez, Maria Jesus, Rodriguez Nuñez, Antonio, Ruiz Sainz, María Elena, Saez Serrano, Isabel, Salinas Argente, Ramón, Sanchez, Maria Elena, Sanchez Anton, Piva, Sánchez Fernández, Mª Soledad, Sebastian, Elena, Simona, Gabriela, Solanich Moreno, Xabier, Soledad Casado, Soledad, Tallón, Jose David, Turcu, Violeta, Valledor Méndez, Manuel, Vidan Y Estevez, Julia, Viejo Llorente, Aurora, Bienert, Álvaro, Serrano, Alfons, Llorente, Laura, Campuzano, Verónica, Tallón, Inmaculada, Pons, Verónica, Linares, Mónica, Valles, Ana, Martínez Francés, Antonio, Freiria, Carmen, González Arias, Elena, Araujo, Enmanuel, Marco de Lucas, Fernando, López, Juan Antonio, Uribe Barrientos, Marisol, Calviño, Michael, Gómez Calafat, Montse, Marco Vera, Pascual, Fariña, Sabela, Zalba, Saioa, Monsalvo, Silvia, Escamilla, Virginia, Mingot-Castellano, María-Eva, García-Candel, Faustino, Martínez-Nieto, Jorge, García-Arroba, José, de la Rubia-Comos, Javier, Gómez-Seguí, Inés, Paciello-Coronel, María-Liz, Valcárcel-Ferreiras, David, Jiménez, Moraima, Cid, Joan, Lozano, Miquel, García-Gala, José-María, Angós-Vazquez, Sonia, Vara-Pampliega, Miriam, Guerra-Domínguez, Luisa, Ávila-Idrobo, Laura-Francisca, Oliva-Hernandez, Ana, Zalba-Marcos, Saioa, Tallón-Ruiz, Inmaculada, Ortega-Sánchez, Sandra, Goterris-Viciedo, Rosa, Moreno-Jiménez, Gemma, Domínguez-Acosta, Lourdes, Araiz-Ramírez, María, Hernández-Mateos, Luis, Flores-Ballesteros, Elena, del Río-Garma, Julio, and Pascual-Izquierdo, Cristina

Published
2024
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3. Validation of the Artificial Intelligence Prognostic Scoring System for Myelodysplastic Syndromes in chronic myelomonocytic leukaemia: A novel approach for improved risk stratification

Author

Mosquera Orgueira, Adrian, primary, Perez Encinas, Manuel Mateo, additional, Diaz Varela, Nicolas, additional, Wang, Yu‐Hung, additional, Mora, Elvira, additional, Diaz‐Beya, Marina, additional, Montoro, Maria Julia, additional, Pomares Marin, Helena, additional, Ramos Ortega, Fernando, additional, Tormo, Mar, additional, Jerez, Andres, additional, Nomdedeu, Josep, additional, de Miguel Sanchez, Carlos, additional, Arenillas, Leonor, additional, Carcel, Paula, additional, Cedena Romero, Maria Teresa, additional, Xicoy Cirici, Blanca, additional, Rivero Arango, Eugenia, additional, Del Orbe Barreto, Rafael Andrés, additional, Benlloch, Luis, additional, Lin, Chien‐Chin, additional, Tien, Hwei‐Fang, additional, Pérez Míguez, Carlos, additional, Crucitti, Davide, additional, Díez Campelo, María, additional, and Valcárcel, David, additional

Published
2024
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4. IMPLEMENTACIÓN DE LA PCR DIGITAL PARA EL DIAGNÓSTICO PRENATAL NO INVASIVO DE LA ENFERMEDAD DE CÉLULAS FALCIFORMES. ESTUDIO PILOTO.

Author

Benito, Sara Ferrer, Álvarez, Miguel Gómez, Torrejón Martínez, María Josefa, Rubio, Montserrat López, del Orbe Barreto, Rafael Andrés, Juanis, Jaime Arbeteta, Muruzabal Siges, María Josefa, Salido Fiérrez, Eduardo José, Mateo, Aránzazu García, Recasens, Valle, Nieto, Jorge Martínez, Martínez, Ana Villegas, González Fernández, Fernando Ataúlfo, Ortega Montero, Ana Belén, Moreno, Laura García, León, Soraya Ramiro, Gradilla, Paloma Ropero, and Cuesta, Celina Benavente

Published
2024
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5. Supervised Machine Learning Improves Risk Stratification in Newly Diagnosed Myelodysplastic Syndromes: An Analysis of the Spanish Group of Myelodysplastic Syndromes

Author

Mosquera Orgueira, Adrian, Perez Encinas, Manuel, Diaz Varela, Nicolas A, Mora, Elvira, Díaz-Beyá, Marina, Montoro, María Julia, Pomares, Helena, Ramos, Fernando, Tormo, Mar, Jerez, Andres, Nomdedeu, Josep F, De Miguel Sanchez, Carlos, Leonor, Arenillas, Cárcel, Paula, Cedena Romero, Maria Teresa, Xicoy, Blanca, Rivero, Eugenia, del Orbe Barreto, Rafael Andres, Diez-Campelo, Maria, Benlloch, Luis E., Crucitti, Davide, and Valcárcel, David

Published
2022
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6. Clinical management of the acute complications of sickle cell anemia: 11 years of experience in a tertiary hospital

Author

Pediatría, Pediatria, Reparaz Goñi, Patricia, Serrano Pejenaute, Idoya, Adán Pedroso, Rosa, Astigarraga Aguirre, María Iciar, De Pedro Olabarri, Jimena, Echebarria Barona, Aizpea Beatriz, García Ariza, Miguel, López Almaraz, Ricardo, Del Orbe Barreto, Rafael Andrés, Vara Pampliega, Miriam, González Urdiales, Paula, Pediatría, Pediatria, Reparaz Goñi, Patricia, Serrano Pejenaute, Idoya, Adán Pedroso, Rosa, Astigarraga Aguirre, María Iciar, De Pedro Olabarri, Jimena, Echebarria Barona, Aizpea Beatriz, García Ariza, Miguel, López Almaraz, Ricardo, Del Orbe Barreto, Rafael Andrés, Vara Pampliega, Miriam, and González Urdiales, Paula

Abstract

Sickle cell disease is an emerging anemia in Europe leading to high morbidity with severe acute complications requiring hospital admission and chronic consequences. The management of these patients is complex and needs interdisciplinary care. The objective is to analyze clinical characteristics and management of patients with sickle cell disease admitted for acute complications. Methods: Retrospective descriptive study of admissions for acute complications of patients with sickle cell disease under 16 years of age in a tertiary hospital between 2010 and 2020. Clinical, laboratory and radiological data were reviewed. Results: We included 71 admissions corresponding to 25 patients, 40% diagnosed by neonatal screening. Admissions increased during this period. The most frequent diagnoses were vaso-occlusive crisis (35.2%), febrile syndrome (33.8%) and acute chest syndrome (32.3%). Nine patients required critical care at PICU. Positive microbiological results were confirmed in 20 cases, bacterial in 60%. Antibiotic therapy was administered in 86% of cases and the vacci-nation schedule of asplenia was adequately fulfilled by 89%. Opioid analgesia was required in 28%. Chronic therapy with hydroxyurea prior to admission was used in 41%. Conclusions: Acute complications requiring hospital admission are frequent in patients with sickle cell disease, being vaso-occlusive crisis and febrile syndrome the most common. These patients need a high use of antibiotics and opioid analgesia. Prior diagnosis facilitates the recog-nition of life-threatening complications such as acute chest syndrome and splenic sequestration. Despite the prophylactic and therapeutic measures currently provided to these patients, many patients suffer acute complications that require hospital management.

Published
2022

7. Clinical management of the acute complications of sickle cell anemia: 11 years of experience in a tertiary hospital

Author

Reparaz Goñi, Patricia, Serrano Pejenaute, Idoya, Adán Pedroso, Rosa, Astigarraga Aguirre, María Iciar, De Pedro Olabarri, Jimena, Echebarria Barona, Aizpea Beatriz, García Ariza, Miguel, López Almaraz, Ricardo, Del Orbe Barreto, Rafael Andrés, Vara Pampliega, Miriam, and González Urdiales, Paula

Subjects
fever, anemia sickle cell/complications, pediatrics, acute chest syndrome, neonatal screening
Abstract

Sickle cell disease is an emerging anemia in Europe leading to high morbidity with severe acute complications requiring hospital admission and chronic consequences. The management of these patients is complex and needs interdisciplinary care. The objective is to analyze clinical characteristics and management of patients with sickle cell disease admitted for acute complications. Methods: Retrospective descriptive study of admissions for acute complications of patients with sickle cell disease under 16 years of age in a tertiary hospital between 2010 and 2020. Clinical, laboratory and radiological data were reviewed. Results: We included 71 admissions corresponding to 25 patients, 40% diagnosed by neonatal screening. Admissions increased during this period. The most frequent diagnoses were vaso-occlusive crisis (35.2%), febrile syndrome (33.8%) and acute chest syndrome (32.3%). Nine patients required critical care at PICU. Positive microbiological results were confirmed in 20 cases, bacterial in 60%. Antibiotic therapy was administered in 86% of cases and the vacci-nation schedule of asplenia was adequately fulfilled by 89%. Opioid analgesia was required in 28%. Chronic therapy with hydroxyurea prior to admission was used in 41%. Conclusions: Acute complications requiring hospital admission are frequent in patients with sickle cell disease, being vaso-occlusive crisis and febrile syndrome the most common. These patients need a high use of antibiotics and opioid analgesia. Prior diagnosis facilitates the recog-nition of life-threatening complications such as acute chest syndrome and splenic sequestration. Despite the prophylactic and therapeutic measures currently provided to these patients, many patients suffer acute complications that require hospital management.

Published
2022

8. Germinal Predisposition in Myelodysplastic Syndromes in Young Adults without a Preexisting Disorder or Organ Dysfunction: Identification of Deleterious Variants in Microsatellite Instability Genes

Author

Chen-Liang, Tzu Hua, Hurtado López, Ana M, Zurdo, María, Such, Esperanza, Teruel-Montoya, Raul, Palomo, Laura, Jimenez, María-José, del Orbe Barreto, Rafael Andres, Navarro, Blanca, López Cadenas, Félix, Salido, Eduardo José, Benet, Carmen, Muiña, Begoña, de Oña, Raquel, de Haro, Nuria, Ramos, Fernando, Arnan Sangerman, Montserrat, Hernandez, Francisca Maria, Ortuño, Francisco José, Senent, Leonor, Vicente, Ana, Díez-Campelo, María, Hermosin, Maria Lourdes, Bernal Del Castillo, Teresa, Tormo, Mar, Arrizabalaga, Beatriz, Xicoy, Blanca, Cervera, José, Sole, Francesc, Sanz, Guillermo F., and Jerez, Andres

Published
2019
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9. Paradoxical Findings in Patients with Paroxysmal Nocturnal Hemoglobinuria Treated with C5 Inhibitors: Suboptimal Disease Control Perceived As Satisfactory

Author

Gaya, Anna, Fuertes, Luis Fernando Fernández, Ballesteros Andrés, Mónica, De La Iglesia Íñigo, Silvia, Del Orbe Barreto, Rafael Andrés, Fernández Fuertes, Fernando, Gonzalez, Ana Pilar, Jarque, Isidro, Lavilla, Esperanza, Nuñez Vasquez, Ramiro, Salido, Eduardo José, Vahí, Maria, and Vallejo, Carlos

Abstract

Introduction: The introduction of C5 inhibitors (C5i) for the treatment of patients with paroxysmal nocturnal hemoglobinuria (PNH) has resulted in lower morbidity and mortality rates. However up to 86% of patients still experience anemia and fatigue in 63% of them which may impact their quality of life (QoL). The SATURNO study aimed to assess PNH patient and physician satisfaction with C5i treatment, along with the impact of the disease and clinical outcomes.

Published
2023
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10. Towards an External Quality Assessment for Next Generation Sequencing in the Diagnosis of Rare Inherited Anaemias

Author

Roy, Noemi, Proven, Melanie, Roberts, Irene, Tamary, Hannah, Swinkels, Dorine W., Patricia, Aguilar-Martinez, Bianchi, Paola, Colombatti, Raffaella, Russo, Roberta, Clark, Barnaby, Sanchez, Mayka, DEL Orbe Barreto, Rafael Andres, Fermo, Elisa, Viprakasit, Vip, Korchuenjit, Jiraporn, Magalhães Maia, Tabita, Smith, Frances, Manu, Maria del Mar, Da Costa, Lydie, Marzollo, Antonio, Hozdelarastrollo, Anabelen, Arrizabalaga, Beatriz, Barbara, Delasalle, and Iolascon, Achille

Published
2018
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11. Germline and Acquired Genetic Variants in Myelodysplastic Syndromes in Young Adults without a Preexisting Disorder or Organ Dysfunction

Author

Chen-Liang, Tzu Hua, Hurtado López, Ana M, Palomo, Laura, Bernal Del Castillo, Teresa, Tormo, Mar, Hermosin, Maria Lourdes, Jimenez, María-José, Blanca, Navarro, Such, Esperanza, DEL Orbe Barreto, Rafael Andres, de Haro, Nuria, López Cadenas, Félix, Muiña, Begoña, de Oña, Raquel, Benet, Carmen, Salido, Eduardo José, Teruel-Montoya, Raul, Ramos, Fernando, Senent, Leonor, Díez-Campelo, Maria, Arrizabalaga, Beatriz, Xicoy, Blanca, Ortuño, Francisco José, Solé, Francesc, Sanz, Guillermo, and Jerez, Andres

Published
2018
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