Relationship between functional and X-ray alterations in patients with cystic fibrosis
Autor(a) principal: | |
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Data de Publicação: | 2003 |
Outros Autores: | , , , , |
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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Jornal de Pneumologia |
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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 |
_version_ |
1754847947752734720 |