Literature DB >> 28087053

Six-Minute Walk Test Results Predict Risk of Hospitalization for Youths with Cystic Fibrosis: A 5-Year Follow-Up Study.

Márcio V F Donadio1, João P Heinzmann-Filho2, Fernanda M Vendrusculo2, Patrícia X H Frasson3, Paulo J C Marostica4.   

Abstract

OBJECTIVE: To evaluate the association of 6-minute walk test (6MWT) and other variables (anthropometry, chronic Pseudomonas aeroginosa colonization, pulmonary function, and respiratory muscle strength) with the risk of hospitalization for pulmonary exacerbation in children and adolescents with cystic fibrosis (CF). STUDY
DESIGN: Cohort study that included patients with CF aged 6-18 years. All participants underwent spirometry, manovacuometry, and 6MWT during the 5-year follow-up. Anthropometric and clinical data were collected and the time to first hospitalization, total days of hospitalization, and antibiotic use during follow-up was recorded.
RESULTS: A total of 26 patients with CF, mean age 10.2 ± 2.8 years, were included. The group had mild impairment of lung function with a significant decline in forced expiratory volume in 1 second (P = .019) over the 5 years. Respiratory muscle strength and 6MWT proved to be preserved, although maximum inspiratory pressure increased (P < .001) and maximum expiratory pressure and 6-minute walk distance (6MWD) remained stable. There were inverse associations of 6MWD in meters (r = -0.813, P < .001) and z score (r = -0.417, P = .015) with total days of hospitalization. Moreover, there was a reduction in the risk of a first hospitalization (Cox HR 0.32; P = .037) in patients with a greater 6MWD.
CONCLUSIONS: We found an association between the 6MWT and the risk of hospitalization in children and adolescents with CF. Furthermore, functional capacity apparently does not follow the expected decline in pulmonary function over time, whereas inspiratory muscle strength increases with disease progression.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  disease progression; prognosis; respiratory function tests

Mesh:

Year:  2017        PMID: 28087053     DOI: 10.1016/j.jpeds.2016.11.071

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  4 in total

1.  FACTORS ASSOCIATED TO QUALITY OF LIFE IN CHILDREN AND ADOLESCENTS WITH CYSTIC FIBROSIS.

Authors:  Nelbe Nesi Santana; Célia Regina Moutinho de Miranda Chaves; Christine Pereira Gonçalves; Saint Clair Dos Santos Gomes Junior
Journal:  Rev Paul Pediatr       Date:  2020-06-19

2.  REPRODUCIBILITY OF PHYSIOLOGICAL VARIABLES OF THE SIX-MINUTE WALK TEST IN HEALTHY STUDENTS.

Authors:  Patrícia Morgana Rentz Keil; Janaína Cristina Scalco; Renata Maba Gonçalves Wamosy; Camila Isabel Santos Schivinski
Journal:  Rev Paul Pediatr       Date:  2020-08-28

3.  EFFECTS OF PHYSICAL EXERCISE DURING HOSPITALIZATION IN CHILDREN AND ADOLESCENTS WITH CANCER: A SYSTEMATIC REVIEW.

Authors:  Scárlat da Silva Santos; Luciane Dalcanale Moussalle; João Paulo Heinzmann-Filho
Journal:  Rev Paul Pediatr       Date:  2020-10-05

4.  Functional respiratory imaging in relation to classical outcome measures in cystic fibrosis: a cross-sectional study.

Authors:  Eline Lauwers; Annemiek Snoeckx; Kris Ides; Kim Van Hoorenbeeck; Maarten Lanclus; Wilfried De Backer; Jan De Backer; Stijn Verhulst
Journal:  BMC Pulm Med       Date:  2021-08-04       Impact factor: 3.317

  4 in total

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