Lung Diseases Interstitial
Mostrando 1-12 de 52 artigos, teses e dissertações.
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1. Barreras de acceso en la atención de las enfermedades pulmonares intersticiales en Colombia
Abstract There is a growing amount of information regarding the management of interstitial lung diseases in the world. However, barriers in access to health systems affect adherence to treatment standards for these patients. This article aims to explore the perspectives of pulmonologists about the barriers in the diagnosis and treatment of patients with inte
Saude soc.. Publicado em: 09/12/2019
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2. 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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3. Imaging in idiopathic pulmonary fibrosis: diagnosis and mimics
Idiopathic pulmonary fibrosis is a chronic disease of unknown etiology that usually has a progressive course and is commonly associated with a poor prognosis. The main symptoms of idiopathic pulmonary fibrosis, including progressive dyspnea and dry cough, are often nonspecific. Chest high-resolution computed tomography is the primary modality used in the ini
Clinics. Publicado em: 04/02/2019
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4. Clinical and pathological aspects of idiopathic pulmonary fibrosis in cats
RESUMO: As enfermidades pulmonares intersticiais são um grupo de doenças difusas do parênquima pulmonar, nas quais a fibrose pulmonar está incluída. O objetivo deste trabalho é caracterizar os achados clínicos e patológicos da fibrose pulmonar idiopática em três gatas, e avaliar possíveis agentes etiológicos através dos exames bacteriológicos,
Pesq. Vet. Bras.. Publicado em: 2019-02
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5. Dermatomyositis: analysis of 109 patients surveyed at the Hospital das Clínicas (HCFMUSP), São Paulo, Brazil
BACKGROUND: Dermatomyositis affects striated muscles, skin and other organs. OBJECTIVE: To characterize the disease from January 1992 to December 2002, assessing its classification, cutaneous and systemic manifestations, and also laboratory results, therapeutic and prognostic findings compared to those in the literature. METHODS: Data were obtained from
An. Bras. Dermatol.. Publicado em: 2014-09
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6. Immunohistochemical detection of virus through its nuclear cytopathic effect in idiopathic interstitial pneumonia other than acute exacerbation
Idiopathic interstitial pneumonias include complex diseases that have a strong interaction between genetic makeup and environmental factors. However, in many cases, no infectious agent can be demonstrated, and these clinical diseases rapidly progress to death. Theoretically, idiopathic interstitial pneumonias could be caused by the Epstein-Barr virus, cytome
Braz J Med Biol Res. Publicado em: 18/11/2013
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7. Fatores preditores da qualidade de vida relacionada à saúde física e mental em pacientes com doença pulmonar intersticial : uma análise multifatorial / Predictors of physical and mental health-related quality of life in patients with interstitial lung disease : a multifactorial analysis
Objetivo: Avaliar fatores preditores da qualidade de vida relacionada à saúde (QVRS) em pacientes com doença pulmonar intersticial (DPI). Métodos: Estudo transversal com 63 pacientes, submetidos a provas de função pulmonar e teste de caminhada de seis minutos. Foram aplicados os seguintes instrumentos: Medical Outcomes Study 36-item Short-form Survey (
Publicado em: 2011
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8. Desaturation - distance ratio: a new concept for a functional assessment of interstitial lung diseases
INTRODUCTION: The functional evaluation has become increasingly important in the understanding and management of patients with interstitial lung diseases. The cardiopulmonary exercise test and the six-minute walk test (6MWT), through their isolated variables, have been used to do this evaluation, with some limitations. OBJECTIVES: We proposed a new composite
Clinics. Publicado em: 2010
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9. Fibrose pulmonar idiopática simultânea a enfisema em pacientes tabagistas = Idiopathic pulmonary fibrosis and enphysema in smokers / Idiopathic pulmonary fibrosis and emphysema in smokers
Objetivo: Descrever os achados clínicos e funcionais de pacientes com enfisema em lobos superiores e fibrose pulmonar idiopática (FPI) em lobos inferiores, recentemente descrita na literatura. Métodos: Um grupo de 11 pacientes com a presença simultânea de enfisema e FPI foi identificado retrospectivamente. Todos os pacientes realizaram tomografia comput
Publicado em: 2010
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10. Hemorragia alveolar fatal: estudo histológico detalhado de necropsias / Fatal alveolar hemorrhage: detailed histological analysis of necropsies
Alveolar haemorrhage is a syndrome presented by many diseases each one with its particular physiopathologic mechanism resulting in pulmonary bleeding. The detailed histological analysis of these patients can help understanding this syndrome. In this study we reviewed and described histological findings of lung slides and medical records from patients whose c
Publicado em: 2009
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11. Evaluation of the mechanics of the respiratory system using PV curves in patients with idiopathic pulmonary fibrosis / Avaliação da mecânica do sistema respiratório através da obtenção de curva PV em pacientes com pneumonia intersticial idiopática
The objective of this study was to evaluate small airways compromise in Idiopathic Pulmonary Fibrosis (IPF) using pressure-volume (PV) curves of the respiratory system. We collected PV curves from twelve patients before lung biopsy, which confirmed IPF in seven patients and Hipersensitivity Pneumonia in five. All curves were fitted with a sigmoid model, V =
Publicado em: 2008
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12. Tomographic evaluation of the small airways in the interstitial lung diseases / Avaliação tomográfica do acometimento das pequenas vias aéreas nas doenças intersticiais do pulmão
The pathogenesis of idiophatic pulmonary fibrosis (IPF), the most common form of idiopathic interstitial pneumonias, is not completely understood. It is related to a type I pneumocyte injury with loss of basement membrane integrity and failure of normal re-epithelialization and re-endothelialization leading to fibroblast proliferation and extra cellular matr
Publicado em: 2007