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1.
J Clin Rheumatol ; 25(7): 304-307, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-30028804

RESUMO

BACKGROUND: Patients with systemic sclerosis (SSc) undergo chest radiographs and high-resolution computed tomography (HRCT) of the thorax both for interstitial lung disease (ILD) detection and for disease progression monitoring. OBJECTIVE: The aim of this study was to assess whether lung ultrasound (LUS) is a useful screening tool for ILD in patients with SSc in comparison with HRCT. METHODS: This was a longitudinal cohort study carried out from December 2015 to April 2016. An LUS was performed to examine B-lines in 67 consecutive patients who met the 2013 American College of Rheumatology/European League Against Rheumatism classification criteria for SSc and had a previous HRCT. B-lines were quantified and classified according to the score modified from Picano. Severity and extent of lung involvement on the HRCT were determined by means of the Warrick score. RESULTS: Twenty-nine patients had both abnormal HRCT (Warrick score >7) and abnormal LUS, 2 had a mild score (6-15 B-lines), and 27 had either moderate or severe scores (≥16 B-lines). Of the 38 patients with negative HRCT, 25 presented some degree of lung involvement on the LUS. Thus, LUS has a sensitivity of 100% and a specificity of 34%. Receiver operating characteristic curve analysis showed the analytic relation between the number of B-lines and the presence of ILD on the HRCT (area under the curve, 0.80; 95% confidence interval, 0.69-0.90). CONCLUSIONS: Lung ultrasound may be a method to detect abnormal lung findings in a noninvasive manner in patients with SSc. Because of its high sensitivity, a low score almost rules out the need for an HRCT.


Assuntos
Doenças Pulmonares Intersticiais , Pulmão/diagnóstico por imagem , Escleroderma Sistêmico , Ultrassonografia/métodos , Argentina , Progressão da Doença , Feminino , Humanos , Doenças Pulmonares Intersticiais/diagnóstico , Doenças Pulmonares Intersticiais/etiologia , Doenças Pulmonares Intersticiais/fisiopatologia , Masculino , Programas de Rastreamento/métodos , Pessoa de Meia-Idade , Radiografia Torácica/métodos , Reprodutibilidade dos Testes , Testes de Função Respiratória/métodos , Escleroderma Sistêmico/complicações , Escleroderma Sistêmico/fisiopatologia , Sensibilidade e Especificidade , Tomografia Computadorizada por Raios X/métodos
2.
Rev. argent. reumatol ; 29(2): 35-41, jun. 2018.
Artigo em Espanhol | LILACS | ID: biblio-980535

RESUMO

Las vasculitis sistémicas son un grupo heterogéneo de enfermedades que se caracterizan por presentar inflamación de los vasos sanguíneos, provocando el daño de la pared vascular. Pueden afectar cualquier tipo de vaso del organismo, por lo cual el compromiso se da en varios órganos o sistemas. Estos procesos presentan una alta mortalidad que se ve reducida con el diagnóstico y tratamiento precoz. Se presenta una revisión con las pautas diagnósticas y alternativas terapéuticas


Systemic vasculitis are a heterogeneous group of diseases that are characterized by inflammation of the blood vessels, causing damage to the vascular wall. The causes or the type of vessel of the organism by which the commitment is given in various organs or systems. These processes have a high mortality that is minimized with the diagnosis and early treatment. A review is presented with the diagnostic guidelines and therapeutic alternatives


Assuntos
Vasculite , Sistema Nervoso
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