Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Year range
1.
São Paulo; s.n; 2011. [137] p. tab, graf.
Thesis in Portuguese | LILACS | ID: lil-609441

ABSTRACT

Introdução: a variabilidade clínica da fibrose cística (FC) levou ao desenvolvimento de diferentes sistemas de escores de avaliação de sua gravidade. Como nem sempre é possível fazer a monitorizarão do paciente com exames radiológicos, tomográficos, funcionais e clínicos simultaneamente, o entendimento das correlações entre esses métodos é um ponto importante para que a equipe multiprofissional dos centros de FC selecione o método mais adequado na sua rotina de atendimento. Objetivo: avaliar a gravidade das alterações clínicas, estruturais e funcionais de uma população de pacientes com fibrose cística por meio de escores clínicos, radiológicos, tomográficos e testes funcionais e analisar as correlações, por pareamento entre os escores de Shwachman-Kulczychi (E-SK), Brasfield (E. Brasfield), Bhalla (E. Bhalla), espirometria e teste de caminhada de seis minutos (TC6M). Métodos: Estudo transversal prospectivo em pacientes com idade entre 3-21 anos. Foram realizados no mesmo dia: espirometria, TC6M, radiografia de tórax (RX), tomografia computadorizada (TC) de tórax e avaliação do estadio clínico. Utilizou-se a regressão linear (coeficiente de correlação de Spearman) para a análise das correlações entre os exames. Foi construída uma Curva ROC para avaliar o melhor ponto de corte para o valor de escore de Brasfield que indicaria a presença de bronquiectasias na TC. Resultados: 43 pacientes foram avaliados, 19F/24M, 10,5 ± 4,7 anos, com mediana de E. Bhalla, E. Brasfield e E-SK de 10, 17 e 70, respectivamente. Os valores médios (% previsto) de capacidade vital forçada (CVF), volume expiratório forçado no primeiro segundo (VEF1) e fluxo expiratório forçado entre 25 e 75 % da capacidade vital (FEF25-75%) foram, respectivamente, 70,4 ± 26, 59,2 ± 26, 47,4 ± 35,8. Houve correlações significativas entre quase todos os parâmetros estudados. Apenas não houve correlação estatisticamente significativa entre escore do teste de caminhada de seis minutos (Z-TC6M) e...


Introduction: The clinical variability of cystic fibrosis (CF) led to the development of different scoring systems to evaluate its severity. As it is not always possible to simultaneously assess CF patient with radiography, tomography, functional tests and clinical status, understanding the correlations between these methods is important for the multidisciplinary team of CF centers to select the most suitable method in their routine attendance. Objective: To assess the severity of the clinical, structural and functional characteristics of a population of CF patients by means of clinical scores, chest radiography (CXR), chest tomography (CT) and pulmonary functional tests and to analyze the correlations between Shwachman-Kulczychi score (SK), Brasfield score (Brasfield), Bhalla score (Bhalla), spirometry and six minute walk test (6-MWT). Method: A cross-sectional and prospective study including patients aged 3-21 years-old. Spirometry, 6-MWT, CRX, CT and evaluation of clinical status were performed on the same day. Linear regression (Spearman correlation coefficient) was performed to analyze the correlations between the tests. A ROC curve was constructed to assess the best value for the Brasfield score that would indicate the presence of bronchiectasis on CT. Results: A total of 43 patients were evaluated, 19F/24M, 10.5 ± 4.7 years, with median Bhalla, Brasfield and SK scores of 10, 17 and 70, respectively. Mean values (% predicted) forced vital capacity (FVC), forced expiratory volume in one second (FEV1) and forced expiratory flow between 25 and 75% of vital capacity (FEF25-75%) were respectively 70.4 ± 26, 26 ± 59.2, 47.4 ± 35.8. There were significant correlations among almost all parameters studied. Only there was no statistically significant correlation between Z-6MWT and air trapping + mosaic perfusion (r = -0.35), FEV1 70% and SK (r = -0.04), FEV1 70% and Bhalla (r = -0.32), FEV1 70% and Brasfield (r = 0.14), FEV1 70% and Z-6MWT (r = 0.14). ROC curve...


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Adolescent , Adult , Cystic Fibrosis , Radiography, Thoracic , Respiratory Function Tests , Spirometry
2.
Clinics ; Clinics;66(6): 979-983, 2011. graf, tab
Article in English | LILACS | ID: lil-594365

ABSTRACT

INTRODUCTION: The Shwachman-Kulczycki score was the first scoring system used in cystic fibrosis to assess disease severity. Despite its subjectivity, it is still widely used. OBJECTIVE: To study correlations among forced expiratory volume in one second (FEV1), chest radiography, chest computed tomography, 6-minute walk test, and Shwachman-Kulczycki score in patients with cystic fibrosis and to test whether the Shwachman-Kulczycki score is still useful in monitoring the severity of the disease. METHODS: A cross-sectional prospective study was performed to analyze the correlations (Spearman). Patients with clinically stable cystic fibrosis, aged 3-21 years, were included. RESULTS: 43 patients, 19F/24M, mean age 10.5 + 4.7 years, with a median Shwachman-Kulczycki score of 70 were studied. The median Brasfield and Bhalla scores were 17 and 10, respectively. The mean Z score for the 6-minute walk test was -1.1 + 1.106 and the mean FEV1 was 59 + 26 (as percentage of predicted values). The following significant correlations versus the Shwachman-Kulczycki score were found: FEV1 (r = 0.76), 6-minute walk test (r = 0.71), chest radiography (r = 0.71) and chest computed tomography (r = -0.78). When patients were divided according to FEV1, a statistically significantly correlation with the Shwachman-Kulczycki score was found only in patients with FEV1 <70 percent (r = 0.67). CONCLUSIONS: The Shwachman-Kulczycki score remains an useful tool for monitoring the severity of cystic fibrosis, adequately reflecting the functional impairment and chest radiography and tomography changes, especially in patients with greater impairment of lung function. When assessing patients with mild lung disease its limitations should be considered and its usefulness in such patients should be evaluated in larger populations.


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Male , Young Adult , Cystic Fibrosis/physiopathology , Lung/physiopathology , Severity of Illness Index , Cross-Sectional Studies , Cystic Fibrosis , Forced Expiratory Volume , Linear Models , Prospective Studies , Respiratory Function Tests , Walking/physiology
SELECTION OF CITATIONS
SEARCH DETAIL