Abstract Introduction: Nasal polyposis is often found in patients with cystic fibrosis. Objective: To assess the incidence of nasal polyposis, the response to medical treatment, recurrence and the need for surgical intervention in children and adolescents with cystic fibrosis during a three-year follow...
Corticoesteroides/uso terapéutico,
Brasil/epidemiología,
Fibrosis Quística/complicaciones,
Fibrosis Quística/epidemiología,
Estudios de Seguimiento,
Incidencia,
Cavidad Nasal/diagnóstico por imagen,
Cavidad Nasal/patología,
Pólipos Nasales/complicaciones,
Pólipos Nasales/tratamiento farmacológico,
Pólipos Nasales/epidemiología,
Pólipos Nasales/patología,
Cirugía Endoscópica por Orificios Naturales/métodos,
Estudios Prospectivos,
Recurrencia,
Índice de Severidad de la Enfermedad,
Factores de Tiempo,
Resultado del Tratamiento
Abstract Objective: Interleukin 8 protein promotes inflammatory responses, even in airways. The presence of interleukin 8 gene variants causes altered inflammatory responses and possibly varied responses to inhaled bronchodilators. Thus, this study analyzed the interleukin 8 variants (rs4073, rs2227306,...
Broncodilatadores/uso terapéutico,
Estudios Transversales,
Fibrosis Quística/tratamiento farmacológico,
Fibrosis Quística/genética,
Regulador de Conductancia de Transmembrana de Fibrosis Quística/genética,
Genotipo,
Interleucina-8/efectos de los fármacos,
Interleucina-8/genética,
Mutación,
Reacción en Cadena de la Polimerasa,
Polimorfismo de Longitud del Fragmento de Restricción,
Índice de Severidad de la Enfermedad,
Espirometría
ABSTRACT CONTEXT AND OBJECTIVE: The prevalence of a variety of potentially pathogenic microorganisms in cystic fibrosis patients, such as methicillin-resistant Staphylococcus aureus (MRSA), has increased over the past decade. Given the increasing prevalence of MRSA and the few data available in the lite...
Chest physiotherapy is an essential component of cystic fibrosis treatment. Its aim is to delay lung deterioration and preserve physical function, improving quality of life and long-term results. It is possible to proceed early, even when the child is asymptomatic.The therapist must be a competent profes...
RESUMEN Objetivos. Caracterizar a nivel molecular las bacterias patógenas de las vías respiratorias de pacientes peruanos con fibrosis quística (FQ). Materiales y métodos. Se caracterizaron las comunidades bacterianas cultivables a partir de muestras de esputo de pacientes pediátricos y adultos ...
Bacterias/genética,
Bacterias/aislamiento & purificación,
Fibrosis Quística/microbiología,
Sistema Respiratorio/microbiología,
Infecciones del Sistema Respiratorio/microbiología,
Fibrosis Quística/complicaciones,
Perú,
Proteoma,
ARN Bacteriano/análisis,
ARN Ribosómico 16S/análisis,
Infecciones del Sistema Respiratorio/complicaciones,
Esputo/microbiología
ABSTRACT Objective: To determine the prevalence of malnutrition in patients attending an adult cystic fibrosis (CF) program and to investigate the associations of malnutrition with the clinical characteristics of those patients. Methods: This was a cross-sectional study involving patients with clinic...
Índice de Masa Corporal,
Estudios Transversales,
Fibrosis Quística/complicaciones,
Desnutrición/diagnóstico,
Desnutrición/epidemiología,
Desnutrición/etiología,
Programas Nacionales de Salud,
Estado Nutricional,
Valor Predictivo de las Pruebas,
Prevalencia,
Pruebas de Función Respiratoria,
Sensibilidad y Especificidad,
Espirometría
RESUMO Objetivo: Avaliar os resultados dos exames utilizados para identificar a sensibilização IgE-mediada ao Aspergillus fumigatus em pacientes com fibrose cística. Métodos: Estudo transversal descritivo com amostra de conveniência de 86 pacientes com fibrose cística, acompanhados em Serviço ...
Abstract Introduction: High-frequency audiometry may contribute to the early detection of hearing loss caused by ototoxic medications. Many ototoxic drugs are widely used in the treatment of patients with cystic fibrosis. Early detection of hearing loss should allow known harmful drugs to be identified ...
Athanazio, Rodrigo Abensur;
Silva Filho, Luiz Vicente Ribeiro Ferreira da;
Vergara, Alberto Andrade;
Ribeiro, Antônio Fernando;
Riedi, Carlos Antônio;
Procianoy, Elenara da Fonseca Andrade;
Adde, Fabíola Villac;
Reis, Francisco José Caldeira;
Ribeiro, José Dirceu;
Torres, Lídia Alice;
Fuccio, Marcelo Bicalho de;
Epifanio, Matias;
Firmida, Mônica de Cássia;
Damaceno, Neiva;
Ludwig-Neto, Norberto;
Maróstica, Paulo José Cauduro;
Rached, Samia Zahi;
Melo, Suzana Fonseca de Oliveira.
ABSTRACT Cystic fibrosis (CF) is an autosomal recessive genetic disorder characterized by dysfunction of the CFTR gene. It is a multisystem disease that most often affects White individuals. In recent decades, various advances in the diagnosis and treatment of CF have drastically changed the scenario, re...
Abstract In Brazil the knowledge about methicillin-resistant Staphylococcus aureus infection in cystic fibrosis patients is scarce. This study aimed to determine the incidence of respiratory tract colonization and the identification rates after a standardized treatment. A retrospective cohort was perform...
Antibacterianos/uso terapéutico,
Brasil,
Fibrosis Quística/microbiología,
Estudios de Seguimiento,
Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos,
Staphylococcus aureus Resistente a Meticilina/aislamiento & purificación,
Pruebas de Sensibilidad Microbiana,
Estudios Retrospectivos,
Infecciones Estafilocócicas/tratamiento farmacológico,
Infecciones Estafilocócicas/microbiología,
Factores de Tiempo,
Resultado del Tratamiento
