Literature DB >> 33683561

The correlation between 6-min walk test and respiratory parameters in children with cystic fibrosis.

Zahra Roshanzamir1, Rohola Shirzadi2, Mohammadreza Modaresi1.   

Abstract

BACKGROUND: The 6-min walk test (6MWT) is a sub-maximal exercise test and has been widely used for evaluating of exercise capacity of patients with cystic fibrosis (CF) in recent years. Few studies have examined the relationship between 6MWT and parameters used to assess the severity of the disease in children with CF. In this study, we have examined this relationship to find out if 6MWT can be a marker of the severity of cystic fibrosis.
METHODS: A cross-sectional study was done to analyze the correlations among spirometry parameters, body mass index (BMI), chest tomography (CT), and 6MWT. CF patients, aged 7-14 years, were involved.
RESULTS: Seventy-six patients, 32F/44M, mean age 10.49 ± 3.18 years, were studied. The mean distance in 6MWT was 447 ± 84.1. The following correlations versus distance were found: FEV1 (r = 0.255, p = 0.026), FVC(r = 0.285, p = 0.013), FEF25-75% (r = 0.546, p < 0.001), BMI (r = 0.163, p = 0.160), and CT (r = 0.075, p = 0.520).The following correlations versus O2 saturation (SpO2) decline were found: FEV1 (r = -0.393, p < 0.001), FVC (r = -0.431, p < 0.001), FEF25-75% (r = -0.296, p = 0.010), BMI (r = 0.042, p = 0.721), and CT (r = -0.196, p = 0.090). There was a significant correlation between 6MWT (distance and SpO2 decline) and pulmonary function test. There was no significant correlation between BMI, chest CT, and 6MWT.
CONCLUSIONS: 6MWT can be applied beside spirometry and chest CT for CF patients follow up.
© 2021. Royal Academy of Medicine in Ireland.

Entities:  

Keywords:  Chest tomography; Cystic fibrosis; Six-minute walk test; Spirometry

Mesh:

Year:  2021        PMID: 33683561     DOI: 10.1007/s11845-021-02564-9

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  1 in total

Review 1.  Multi-modality monitoring of cystic fibrosis lung disease: the role of chest computed tomography.

Authors:  Harm A W M Tiddens; Stephen M Stick; Stephanie Davis
Journal:  Paediatr Respir Rev       Date:  2013-07-02       Impact factor: 2.726

  1 in total
  1 in total

1.  Health-Related Quality of Life Assessment: An Inexpensive Tool for Cystic Fibrosis Care.

Authors:  Sneha Varkki
Journal:  Indian J Pediatr       Date:  2021-12-22       Impact factor: 1.967

  1 in total

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