5 results on '"Martínez Martínez Adela Leyre"'
Search Results
2. Association between multifocality and one-year post-surgery response to treatment in papillary thyroid cancer
- Author
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Iglesias Hernández Natalia Covadonga, Martínez Martínez Adela Leyre, Mendiolea Andoni Monzón, Pascual Ignacio Merlo, Alday Amelia Oleaga, Calles Romero Laura Araceli, and Fano Miguel Paja
- Subjects
Oncology ,medicine.medical_specialty ,business.industry ,Internal medicine ,medicine ,Post surgery ,medicine.disease ,business ,Response to treatment ,Papillary thyroid cancer - Published
- 2020
3. ¿Hay vida después de teduglutida?
- Author
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Martínez Martínez,Adela Leyre, Calles Romero,Laura Araceli, Etxeberria Martín,Eider, Monasterio Jiménez,Oihana, Zabalegui Eguinoa,Alba, Paja Fano,Miguel, Monzón Mediolea,Andoni, Cadenas González,Aida, Cabriada Nuno,José Luis, and Iglesias Hernández,Natalia Covadonga
- Subjects
Teduglutida ,Soporte parenteral ,Fallo intestinal ,Síndrome de intestino corto - Abstract
Resumen El fallo intestinal (FI) se define como una reducción de la función intestinal por debajo del mínimo necesario para la absorción de nutrientes y que precisa suplementación intravenosa para mantener la salud y/o el crecimiento. La causa más frecuente es el síndrome de intestino corto (SIC). Aproximadamente el 50 % de los pacientes con SIC presenta FI y requiere soporte parenteral. La teduglutida es un análogo del péptido-2 similar al glucagón (GLP-2) humano aprobado para el tratamiento de pacientes con SIC. Los resultados de ensayos clínicos han probado su eficacia: se reducen el volumen y los días de administración de nutrición parenteral y fluidoterapia. Pocas publicaciones evalúan los efectos sobre la función intestinal a largo plazo en pacientes respondedores tras la suspensión de teduglutida. Se describe un paciente con SIC tipo I (yeyunostomía terminal) debido a múltiples intervenciones quirúrgicas por enfermedad de Crohn, que recibió tratamiento con liraglutida un año y teduglutida secuencial durante 21 meses. Con el primero, se objetivó una reducción en la necesidad de aporte y débito por yeyunostomía. El análogo del GLP-2 consiguió una mayor reducción del desequilibrio hídrico que permitió suspender la sueroterapia nocturna, con ganancia ponderal y mantenimiento de parámetros nutricionales, situación mantenida dos años después de su suspensión.
- Published
- 2020
4. [Is there life after teduglutide?]
- Author
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Martínez Martínez AL, Calles Romero LA, Etxeberría Martín E, Monasterio Jiménez O, Zabalegui Eguinoa A, Paja Fano M, Monzón Mendiolea A, Cadenas González A, Cabriada Nuno JL, and Iglesias Hernández NC
- Subjects
- Crohn Disease therapy, Fluid Therapy, Humans, Jejunostomy, Liraglutide therapeutic use, Male, Middle Aged, Parenteral Nutrition, Product Recalls and Withdrawals, Gastrointestinal Agents adverse effects, Gastrointestinal Agents therapeutic use, Intestinal Diseases drug therapy, Peptides adverse effects, Peptides therapeutic use, Short Bowel Syndrome drug therapy
- Abstract
Introduction: Intestinal failure (IF) is defined as a reduction in intestinal function below the minimum necessary for the absorption of nutrients, requiring intravenous supplementation to maintain health and/or growth. The most common cause is short bowel syndrome (SBS). Approximately 50% of patients with SBS have IF and require parenteral support. Teduglutide is a human glucagon-like peptide-2 analogue (GLP-2) approved for the treatment of patients with SBS. Clinical trial results have proven its efficacy by reducing volume and days of administration of parenteral nutrition and fluid therapy. Few publications evaluate the effects on long-term bowel function in respondent patients after teduglutide suspension. A patient with type I SBS (terminal jejunostomy) due to multiple surgeries for Crohn's disease, who was treated with liraglutide for one year and sequential teduglutide for 21 months, is described. With the former, a reduction in the need for contribution and debit by jejunostomy was observed. The GLP-2 analogue achieved a greater reduction in the hydric disbalance that allowed the suspension of the nocturnal suerotherapy, with weight gain and maintenance of nutritional parameters; situation maintained two years after its suspension.
- Published
- 2020
- Full Text
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5. Diagnostic and treatment delay in primary hyperparathyroidism. A pending issue.
- Author
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Paja-Fano M, Martínez-Martínez AL, and Monzón-Mendiolea A
- Subjects
- Female, Humans, Hypercalcemia complications, Hyperparathyroidism, Primary etiology, Male, Middle Aged, Retrospective Studies, Delayed Diagnosis, Hyperparathyroidism, Primary diagnosis, Hyperparathyroidism, Primary therapy, Time-to-Treatment
- Abstract
Introduction: Primary hyperparathyroidism (PHPT) remains underdiagnosed among patients with hypercalcemia, potentially causing increased morbidity., Objective: To identify in surgically operated patients the presence of overlooked hypercalcemia and patients with criteria for surgery (CFS) for PHPT at least one year prior to referral to Endocrinology, and to determine whether this diagnostic delay leads to increased morbidity., Methods: An observational study was carried out in 116 consecutive patients. We evaluated electronic medical records registered at least 12 months prior to referral and divided them in four groups: hypercalcemia with CFS (group 1), hypercalcemia without CFS (group 2), normocalcemia (group 3), and cases without previous biochemical evaluation (group 4)., Results: A total of 84 patients (72.4%) had a previous measurement of serum calcium at a time interval of ≥ 12 months. Sixty-six (56.9%) had hypercalcemia and 43 of them (37%) had ≥ 1 CFS, with an average delay of 57 months in receiving proper evaluation. Almost half of the calcemia measurements in group 1 had been made in the emergency room. Patients from group 1 were younger, and had a greater frequency of nephrolithiasis and renal impairment than patients in group 4. The serum calcium values at referral were similar in both groups and higher than the values found in patients from the other two groups., Discussion: In patients with PHPT and CFS, referral to an endocrinologist is made with an average delay of almost 5 years. The identified causes of this delay, which conditions more kidney disease, are unrecognized hypercalcemia and/or unawareness of the surgical criteria, while calcium elevations promote referral. Interventions are needed to avoid this delay in the diagnosis and resolution of PHPT., (Copyright © 2020 SEEN y SED. Publicado por Elsevier España, S.L.U. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
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