Association between sputum culture results and pulmonary changes in children with cystic fibrosis

Background and Objectives: Despite the significant improvement in the prognosis of cystic fibrosis (CF), it is still regarded as the most common life-shortening genetic disease in Caucasian populations. This disease is the most important cause of chronic lung disease and exocrine pancreatic insuffi...

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Main Authors: Fatemeh Khani Nozari, Mohammadreza Modaresi, Bahar Allahverdi, Roohollah Shirzadi, Mahsa Fattahi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2023-11-01
Series:Iranian Journal of Microbiology
Subjects:
Online Access:https://ijm.tums.ac.ir/index.php/ijm/article/view/4112
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author Fatemeh Khani Nozari
Mohammadreza Modaresi
Bahar Allahverdi
Roohollah Shirzadi
Mahsa Fattahi
author_facet Fatemeh Khani Nozari
Mohammadreza Modaresi
Bahar Allahverdi
Roohollah Shirzadi
Mahsa Fattahi
author_sort Fatemeh Khani Nozari
collection DOAJ
description Background and Objectives: Despite the significant improvement in the prognosis of cystic fibrosis (CF), it is still regarded as the most common life-shortening genetic disease in Caucasian populations. This disease is the most important cause of chronic lung disease and exocrine pancreatic insufficiency in infancy and childhood. The aim of our study was to assess the potential association between bacterial colonization detected by sputum cultures and pulmonary structural and functional changes in Iranian children with CF. Materials and Methods: In this cross-sectional study, 76 CF children ≥6 years old registered in the CF Foundation of Children’s Medical Center Hospital, Tehran, Iran, who underwent high resolution CT scan (HRCT), pulmonary function test, and sputum cultures within a month of each other during the study period were included. For each patient, demographic characteristics (age and sex), results of sputum cultures, forced expiratory volume in 1st second (FEV1), and chest HRCT findings based on the Bhalla scoring system were recorded in a check list. Results: Sixty seven percent of the patients had positive sputum cultures, with the most commonly isolated microorganism being Pseudomonas aeruginosa (mucoid strain). Based on categorization of Bhalla scores, none of the patients had severe pulmonary involvement. FEV1 was mainly >70%. There was a statistically significant correlation between colonization with mucoid P. aeruginosa and lower Bhalla scores in children aged 14-16 years (P=0.001). Colonization with mucoid P. aeruginosa was also significantly associated with patient's age (P=0.020) and FEV-1 (P=0.001). Conclusion: Severity of lung involvement in CF children is clearly dependent to mucoid P. aeruginosa colonization in airways and this notorious bacterium is the most prevalent one in Iranian CF children. Prompt identification and eradication by proper nebulized and systemic antibiotics can have valueless effects on patients’ quality of life and prevent lifelong destructive complications such as bronchiectasis. Timely lung CT scan wisely advised by expert CF treatment team can meticulously detect injuries and it seems to act more efficacious than -still helpful- clinical scores and pulmonary function tests.
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spelling doaj.art-90781c0fa2ea498699de4cfdaedbea0c2023-12-12T04:53:15ZengTehran University of Medical SciencesIranian Journal of Microbiology2008-32892008-44472023-11-0115610.18502/ijm.v15i6.14136Association between sputum culture results and pulmonary changes in children with cystic fibrosisFatemeh Khani Nozari0Mohammadreza Modaresi1Bahar Allahverdi2Roohollah Shirzadi3Mahsa Fattahi4Pediatric Physician, Pediatric Center of Excellence, Tehran University of Medical Science, Tehran, IranPediatric Pulmonary Disease and Sleep Medicine Research Center, Pediatric Center of Excellence, Tehran University of Medical Science, Tehran, IranPediatric Gastroenterologist, Tehran University of Medical Sciences, Children's Medical Center, The Pediatrics Center of Excellence, Research Center for Pediatric Gastroenterology and HepatologyPediatric Respiratory and Sleep Medicine Research Center, Children's Medical Center, Tehran University of Medical Sciences, Tehran, IranCenter for Research and Training in Skin Diseases and Leprosy Background and Objectives: Despite the significant improvement in the prognosis of cystic fibrosis (CF), it is still regarded as the most common life-shortening genetic disease in Caucasian populations. This disease is the most important cause of chronic lung disease and exocrine pancreatic insufficiency in infancy and childhood. The aim of our study was to assess the potential association between bacterial colonization detected by sputum cultures and pulmonary structural and functional changes in Iranian children with CF. Materials and Methods: In this cross-sectional study, 76 CF children ≥6 years old registered in the CF Foundation of Children’s Medical Center Hospital, Tehran, Iran, who underwent high resolution CT scan (HRCT), pulmonary function test, and sputum cultures within a month of each other during the study period were included. For each patient, demographic characteristics (age and sex), results of sputum cultures, forced expiratory volume in 1st second (FEV1), and chest HRCT findings based on the Bhalla scoring system were recorded in a check list. Results: Sixty seven percent of the patients had positive sputum cultures, with the most commonly isolated microorganism being Pseudomonas aeruginosa (mucoid strain). Based on categorization of Bhalla scores, none of the patients had severe pulmonary involvement. FEV1 was mainly >70%. There was a statistically significant correlation between colonization with mucoid P. aeruginosa and lower Bhalla scores in children aged 14-16 years (P=0.001). Colonization with mucoid P. aeruginosa was also significantly associated with patient's age (P=0.020) and FEV-1 (P=0.001). Conclusion: Severity of lung involvement in CF children is clearly dependent to mucoid P. aeruginosa colonization in airways and this notorious bacterium is the most prevalent one in Iranian CF children. Prompt identification and eradication by proper nebulized and systemic antibiotics can have valueless effects on patients’ quality of life and prevent lifelong destructive complications such as bronchiectasis. Timely lung CT scan wisely advised by expert CF treatment team can meticulously detect injuries and it seems to act more efficacious than -still helpful- clinical scores and pulmonary function tests. https://ijm.tums.ac.ir/index.php/ijm/article/view/4112Cystic fibrosis;Children;Bhalla score;Sputum culture;Forced expiratory volume in 1st second
spellingShingle Fatemeh Khani Nozari
Mohammadreza Modaresi
Bahar Allahverdi
Roohollah Shirzadi
Mahsa Fattahi
Association between sputum culture results and pulmonary changes in children with cystic fibrosis
Iranian Journal of Microbiology
Cystic fibrosis;
Children;
Bhalla score;
Sputum culture;
Forced expiratory volume in 1st second
title Association between sputum culture results and pulmonary changes in children with cystic fibrosis
title_full Association between sputum culture results and pulmonary changes in children with cystic fibrosis
title_fullStr Association between sputum culture results and pulmonary changes in children with cystic fibrosis
title_full_unstemmed Association between sputum culture results and pulmonary changes in children with cystic fibrosis
title_short Association between sputum culture results and pulmonary changes in children with cystic fibrosis
title_sort association between sputum culture results and pulmonary changes in children with cystic fibrosis
topic Cystic fibrosis;
Children;
Bhalla score;
Sputum culture;
Forced expiratory volume in 1st second
url https://ijm.tums.ac.ir/index.php/ijm/article/view/4112
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