Exercise testing for children with cystic fibrosis: A systematic review
Ray Lei Lang1, Kellie Stockton2, Christine Wilson2
1School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, Australia.
Pediatric Pulmonology
|May 27, 2020
Summary
This review assesses exercise tests for children with cystic fibrosis (CF), finding the cardiopulmonary exercise test (CPET), 6-minute walk test (6MWT), and modified shuttle test (MST) offer fair to good psychometric properties.
Area of Science:
- Pediatric Pulmonology
- Exercise Physiology
- Rehabilitation Science
Background:
- Exercise testing is crucial for assessing exercise capacity in pediatric cystic fibrosis (CF) patients.
- A systematic review of psychometric properties of available exercise tests for this population was lacking.
Purpose of the Study:
- To systematically review the psychometric properties of exercise tests used in children aged 8-18 with CF.
- To provide guidance for selecting appropriate exercise tests for this population.
Main Methods:
- A systematic literature search was conducted across multiple databases (PubMed, Web of Science, etc.) for studies published after 1950.
- Included studies reported original psychometric data for exercise capacity measures in children with CF (ages 8-18).
- The COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN) checklist was used to evaluate psychometric evidence.
Main Results:
- 1025 papers were identified, with 46 included, covering 15 different exercise tests.
- Tests included incremental cardiopulmonary exercise test (CPET) via cycle or treadmill, 6-minute walk test (6MWT), modified shuttle test (MST), and others.
- The CPET, 6MWT, and MST demonstrated fair to good psychometric properties, though each has unique clinical benefits and drawbacks.
Conclusions:
- A wide range of exercise tests exist for pediatric CF patients, with variable psychometric quality.
- The CPET, 6MWT, and MST are recommended due to their relatively robust psychometric evidence.
- A Selection Guide was developed to aid clinicians and researchers in choosing the most suitable exercise test based on specific needs.
Keywords:
cardiopulmonary exercise testingchildren exercise stress testingphysiotherapy in cystic fibrosisMore Related Videos
Related Concept Videos
Cystic Fibrosis: Management
368
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
Sinus disease and chronic...
368
Exercise Stress Test
871
Introduction
Exercise stress testing, commonly known as a treadmill test, is a noninvasive procedure used to evaluate cardiovascular function and diagnose heart conditions.
Definition
An exercise stress test measures the heart's response to exertion using a treadmill or stationary bicycle. Chest electrodes record the heart's electrical activity through an ECG, and blood pressure is monitored regularly.
Purposes
Exercise stress testing, commonly known as a treadmill test, is a noninvasive procedure used to evaluate cardiovascular function and diagnose heart conditions.
Definition
An exercise stress test measures the heart's response to exertion using a treadmill or stationary bicycle. Chest electrodes record the heart's electrical activity through an ECG, and blood pressure is monitored regularly.
Purposes
871
Chronic Obstructive Pulmonary Disease-IV: Assessement and Diagnostic Studies
3.0K
Assessing and diagnosing Chronic Obstructive Pulmonary Disease (COPD) involves a detailed approach that includes a comprehensive review of medical history, physical examination, and a variety of diagnostic tests. This thorough evaluation is essential to ensure an accurate diagnosis and guide effective management strategies.
Medical History
Medical History
3.0K
Pulmonary Function Tests
628
Pulmonary Function Tests (PFTs)
Pulmonary Function Tests are crucial diagnostic tools for assessing respiratory function, particularly in patients with chronic respiratory disorders. They comprehensively evaluate lung volumes, ventilatory function, breathing mechanics, diffusion, and gas exchange. These tests help diagnose pulmonary diseases and play a significant role in monitoring disease progression, evaluating disability, and assessing response to therapy.
PFTs involve using a spirometer, a...
Pulmonary Function Tests are crucial diagnostic tools for assessing respiratory function, particularly in patients with chronic respiratory disorders. They comprehensively evaluate lung volumes, ventilatory function, breathing mechanics, diffusion, and gas exchange. These tests help diagnose pulmonary diseases and play a significant role in monitoring disease progression, evaluating disability, and assessing response to therapy.
PFTs involve using a spirometer, a...
628
Cystic Fibrosis: Pathogenesis
638
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
638


