Lung Fibrosis
Mostrando 1-12 de 716 artigos, teses e dissertações.
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1. Brazilian initial experience with lung transplantation due to irreversible lung fibrosis post-COVID-19 in a national reference center: a cohort study
ABSTRACT BACKGROUND: Lung transplantation (LTx) has been discussed as an option for treating irreversible lung fibrosis post-coronavirus disease 2019 (COVID-19), in selected cases. OBJECTIVES: To report on the initial experience and management of end-stage lung disease due to COVID-19 at a national center reference in Brazil. DESIGN AND SETTING: Cohort
Sao Paulo Medical Journal. Publicado em: 2022
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2. Approach and anesthetic management for kidney transplantation in a patient with bilateral lung transplantation: case report
Abstract Lung transplantation is the last resort for end-stage lung disease treatment. Due to increased survival, lung recipients present an increased likelihood to be submitted to anesthesia and surgery. This case report describes a 23-year-old female patient with history of lung transplantation for cystic fibrosis, with multiple complications, and chronic
Brazilian Journal of Anesthesiology. Publicado em: 2022
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3. Upper Airway Findings and Markers of Lung Disease Progression in Patients with Cystic Fibrosis
Abstract Introduction Cystic fibrosis (CF) is a genetic disease that limits the quality of life mainly due to respiratory symptoms. The relationship between findings of the upper airways and CF lung disease is not yet completely understood. Objective The aim of the present study is to describe the most frequent nasal findings and pathogens in patients with
Int. Arch. Otorhinolaryngol.. Publicado em: 2020-12
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4. Complete Atrioventricular Block and Cardiopulmonary Involvement in Rapidly Progressive Systemic Sclerosis
Abstract The heart and lung are target organs in systemic sclerosis (SSc) and similar symptoms (dyspnea and cough) may make the differential diagnosis between the two lesions difficult. In addition, complete atrioventricular block (CAVB) is a rare complication of this disease. This case report is about a patient with SSc and pulmonary fibrosis who was admitt
Int. J. Cardiovasc. Sci.. Publicado em: 2020-05
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5. Association between lung function, thoracoabdominal mobility and posture in cystic fibrosis: pilot study
Resumo Introdução: A deterioração da função pulmonar é a principal causa de mortalidade na fibrose cística (FC), portanto é fundamental estudar diferentes fatores que se relacionam com esta variável. Objetivo: Verificar em indivíduos FC, a associação da função pulmonar com a mobilidade toracoabdominal e a postura. Método: Estudo piloto tra
Fisioter. mov.. Publicado em: 13/01/2020
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6. Lung ultrasound assessment of response to antibiotic therapy in cystic fibrosis exacerbations: a study of two cases
J. bras. pneumol.. Publicado em: 25/11/2019
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7. Adesão de adolescentes com fibrose cística a terapia de reposição enzimática: fatores associados
Resumo O objetivo deste artigo é avaliar a prevalência e os fatores associados à adesão a terapia de reposição enzimática em adolescentes com Fibrose cística. Estudo transversal, descritivo e observacional. Foram coletados dados sociodemográficos e clínicos. Os instrumentos utilizados para avaliar adesão foram: questionário de Morisky-Green e a d
Ciênc. saúde coletiva. Publicado em: 25/11/2019
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8. High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening
OBJECTIVE: High-resolution computed tomography (HRCT) allows the early detection of pathological changes in the lung structure, and reproducible scoring systems can be used to quantify chest computed tomography (CT) findings in patients with cystic fibrosis (CF). The aim of the study was to describe early HRCT findings according to a validated scoring syste
Clinics. Publicado em: 21/10/2019
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9. Complete Atrioventricular Block and Cardiopulmonary Involvement in Rapidly Progressive Systemic Sclerosis
Abstract The heart and lung are target organs in systemic sclerosis (SSc) and similar symptoms (dyspnea and cough) may make the differential diagnosis between the two lesions difficult. In addition, complete atrioventricular block (CAVB) is a rare complication of this disease. This case report is about a patient with SSc and pulmonary fibrosis who was admitt
Int. J. Cardiovasc. Sci.. Publicado em: 19/08/2019
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10. Maternal and Perinatal Outcomes in Pregnant Women with Cystic Fibrosis
Resumo Objetivo Avaliar os desfechos maternos e perinatais de gestações em mulheres portadoras de fibrose cística (FC) e disfunção pulmonar grave. Métodos Série de casos visando a avaliação dos desfechos maternos e perinatais em gestações únicas de mulheres com diagnóstico de FC. Foram incluídos todos os casos de gestações únicas de paci
Rev. Bras. Ginecol. Obstet.. Publicado em: 19/06/2019
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11. Familial pulmonary fibrosis: a heterogeneous spectrum of presentations
RESUMO Objetivo: Descrever as características clínicas, funcionais e radiológicas de um grupo de casos índice diagnosticados com fibrose pulmonar familiar (FPF) no Brasil. Métodos: Trinta e cinco pacientes com FPF (18 mulheres; 51,4%), com mediana de idade de 66,0 anos (variação: 35,5-89,3 anos), responderam a um questionário padronizado e foram su
J. bras. pneumol.. Publicado em: 10/06/2019
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12. Melatonin effects on pulmonary tissue in the experimental model of Hepatopulmonary Syndrome
RESUMO Objetivo: Avaliar as alterações pulmonares de animais com Síndrome Hepatopulmonar (SHP), submetidos à ligadura de ducto biliar (LDB), bem como o efeito antioxidante da Melatonina (MEL). Métodos: Dezesseis ratos machos da espécie Wistar, divididos em quatro grupos: Sham, Grupo LDB, Grupo Sham + MEL e LDB + MEL. Foram avaliadas a histologia pulm
J. bras. pneumol.. Publicado em: 30/05/2019