Relationship between functional and X-ray alterations in patients with cystic fibrosis

Detalhes bibliográficos
Autor(a) principal: Fernandes,Andréia Kist
Data de Publicação: 2003
Outros Autores: Mallmann,Felipe, John,Ângela Beatriz, Faccin,Carlo Sasso, Dalcin,Paulo de Tarso Roth, Barreto,Sérgio Saldanha Menna
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal de Pneumologia
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-35862003000400006
Resumo: BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction, resulting in air trapping in the lungs. OBJECTIVE: To assess the associations between airflow limitation, pulmonary volume and X-ray findings in patients with cystic fibrosis. METHOD: A cross-sectional retrospective study. Review of spirometric, plethysmographic, and chest X-ray findings of outpatients (age ³ 16 years). The airflow findings were classified as within normal limits or as airflow obstruction: mild, moderate or severe obstructive alteration. RESULTS: A total of 23 patients (15 male and eight female; mean age, 21 ± 5.9 years) were studied. Six of them were within normal limits, four had a mild, five had a moderate, and eight had a severe obstructive alteration. There was an association between airflow limitation and the increase of residual volume (p = 0.006) and also with the Brasfield score (p = 0.001), but not with the total lung capacity (p = 0.33). There was a correlation between residual volume and Brasfield score (r = 0,73, p = 0,002), but not with the total pulmonary capacity. Moreover, according to X-ray criteria, the air trapping was correlated only with the residual volume (p = 0.006). CONCLUSION: In patients with cystic fibrosis (age ³ 16 years), the progressive airflow limitation is accompanied by an increase in residual volume, while the total pulmonary capacity remains normal or tends to decrease. The X-ray score was associated with airflow limitation and residual volume, but not with total lung capacity.
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spelling Relationship between functional and X-ray alterations in patients with cystic fibrosisCystic fibrosisPulmonary diseaseLung volume measurementsRadiography/thoracicBACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction, resulting in air trapping in the lungs. OBJECTIVE: To assess the associations between airflow limitation, pulmonary volume and X-ray findings in patients with cystic fibrosis. METHOD: A cross-sectional retrospective study. Review of spirometric, plethysmographic, and chest X-ray findings of outpatients (age ³ 16 years). The airflow findings were classified as within normal limits or as airflow obstruction: mild, moderate or severe obstructive alteration. RESULTS: A total of 23 patients (15 male and eight female; mean age, 21 ± 5.9 years) were studied. Six of them were within normal limits, four had a mild, five had a moderate, and eight had a severe obstructive alteration. There was an association between airflow limitation and the increase of residual volume (p = 0.006) and also with the Brasfield score (p = 0.001), but not with the total lung capacity (p = 0.33). There was a correlation between residual volume and Brasfield score (r = 0,73, p = 0,002), but not with the total pulmonary capacity. Moreover, according to X-ray criteria, the air trapping was correlated only with the residual volume (p = 0.006). CONCLUSION: In patients with cystic fibrosis (age ³ 16 years), the progressive airflow limitation is accompanied by an increase in residual volume, while the total pulmonary capacity remains normal or tends to decrease. The X-ray score was associated with airflow limitation and residual volume, but not with total lung capacity.Sociedade Brasileira de Pneumologia e Tisiologia2003-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-35862003000400006Jornal de Pneumologia v.29 n.4 2003reponame:Jornal de Pneumologiainstname:Sociedade Brasileira de Pneumologia e Tisiologia da Universidade de São Paulo (SBPT-USP)instacron:USP10.1590/S0102-35862003000400006info:eu-repo/semantics/openAccessFernandes,Andréia KistMallmann,FelipeJohn,Ângela BeatrizFaccin,Carlo SassoDalcin,Paulo de Tarso RothBarreto,Sérgio Saldanha Mennaeng2003-12-02T00:00:00Zoai:scielo:S0102-35862003000400006Revistahttps://www.scielo.br/j/jpneu/gridPUBhttp://www.scielo.br/oai/scielo-oai.phpjpneumo@terra.com.br0102-35861678-4642opendoar:2003-12-02T00:00Jornal de Pneumologia - Sociedade Brasileira de Pneumologia e Tisiologia da Universidade de São Paulo (SBPT-USP)false
dc.title.none.fl_str_mv Relationship between functional and X-ray alterations in patients with cystic fibrosis
title Relationship between functional and X-ray alterations in patients with cystic fibrosis
spellingShingle Relationship between functional and X-ray alterations in patients with cystic fibrosis
Fernandes,Andréia Kist
Cystic fibrosis
Pulmonary disease
Lung volume measurements
Radiography/thoracic
title_short Relationship between functional and X-ray alterations in patients with cystic fibrosis
title_full Relationship between functional and X-ray alterations in patients with cystic fibrosis
title_fullStr Relationship between functional and X-ray alterations in patients with cystic fibrosis
title_full_unstemmed Relationship between functional and X-ray alterations in patients with cystic fibrosis
title_sort Relationship between functional and X-ray alterations in patients with cystic fibrosis
author Fernandes,Andréia Kist
author_facet Fernandes,Andréia Kist
Mallmann,Felipe
John,Ângela Beatriz
Faccin,Carlo Sasso
Dalcin,Paulo de Tarso Roth
Barreto,Sérgio Saldanha Menna
author_role author
author2 Mallmann,Felipe
John,Ângela Beatriz
Faccin,Carlo Sasso
Dalcin,Paulo de Tarso Roth
Barreto,Sérgio Saldanha Menna
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Fernandes,Andréia Kist
Mallmann,Felipe
John,Ângela Beatriz
Faccin,Carlo Sasso
Dalcin,Paulo de Tarso Roth
Barreto,Sérgio Saldanha Menna
dc.subject.por.fl_str_mv Cystic fibrosis
Pulmonary disease
Lung volume measurements
Radiography/thoracic
topic Cystic fibrosis
Pulmonary disease
Lung volume measurements
Radiography/thoracic
description BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction, resulting in air trapping in the lungs. OBJECTIVE: To assess the associations between airflow limitation, pulmonary volume and X-ray findings in patients with cystic fibrosis. METHOD: A cross-sectional retrospective study. Review of spirometric, plethysmographic, and chest X-ray findings of outpatients (age ³ 16 years). The airflow findings were classified as within normal limits or as airflow obstruction: mild, moderate or severe obstructive alteration. RESULTS: A total of 23 patients (15 male and eight female; mean age, 21 ± 5.9 years) were studied. Six of them were within normal limits, four had a mild, five had a moderate, and eight had a severe obstructive alteration. There was an association between airflow limitation and the increase of residual volume (p = 0.006) and also with the Brasfield score (p = 0.001), but not with the total lung capacity (p = 0.33). There was a correlation between residual volume and Brasfield score (r = 0,73, p = 0,002), but not with the total pulmonary capacity. Moreover, according to X-ray criteria, the air trapping was correlated only with the residual volume (p = 0.006). CONCLUSION: In patients with cystic fibrosis (age ³ 16 years), the progressive airflow limitation is accompanied by an increase in residual volume, while the total pulmonary capacity remains normal or tends to decrease. The X-ray score was associated with airflow limitation and residual volume, but not with total lung capacity.
publishDate 2003
dc.date.none.fl_str_mv 2003-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-35862003000400006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-35862003000400006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0102-35862003000400006
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Pneumologia e Tisiologia
publisher.none.fl_str_mv Sociedade Brasileira de Pneumologia e Tisiologia
dc.source.none.fl_str_mv Jornal de Pneumologia v.29 n.4 2003
reponame:Jornal de Pneumologia
instname:Sociedade Brasileira de Pneumologia e Tisiologia da Universidade de São Paulo (SBPT-USP)
instacron:USP
instname_str Sociedade Brasileira de Pneumologia e Tisiologia da Universidade de São Paulo (SBPT-USP)
instacron_str USP
institution USP
reponame_str Jornal de Pneumologia
collection Jornal de Pneumologia
repository.name.fl_str_mv Jornal de Pneumologia - Sociedade Brasileira de Pneumologia e Tisiologia da Universidade de São Paulo (SBPT-USP)
repository.mail.fl_str_mv jpneumo@terra.com.br
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