Doppler echocardiogram, oxygen saturation and submaximum capacity of exercise in patients with cystic fibrosis
- PMID: 17157083
- DOI: 10.1016/j.jcf.2006.10.009
Doppler echocardiogram, oxygen saturation and submaximum capacity of exercise in patients with cystic fibrosis
Abstract
Study objectives: To determine the relationship between pulmonary arterial systolic pressure (PASP) and submaximum capacity of exercise, using the six-minute walk test (6MWT) in patients with cystic fibrosis (CF), and to investigate the relation between echocardiographic findings and results of 6MWT, clinical scores, chest radiograph scores and lung function tests.
Design: This was a prospective cross-sectional study in patients with CF (16 years and older) with clinical stability, attending the Adult CF Program at the Hospital de Clínicas de Porto Alegre. The patients had Doppler echocardiography and performed a 6MWT. As well as pulmonary function tests and chest roentgenograms, and a clinical score was obtained for all patients.
Results: The study included 39 patients with a mean age of 23.7+/-6.3 years. There were no significant correlation between the distance walked and PASP, diameter of the right ventricle (DRV) and pulmonary acceleration time (p>0.05). We observed a significant correlation among PASP and the SpO(2) at rest (r=-0.73; p<0.001), SpO(2) at the end of the 6MWT (r= -0.45; p=0.006), clinical score (r= -0.55; p=0.001), chest radiograph score (r= -0.33; p=0.049), FEV1 (r= -0.63; p< 0.001), and FVC (r=-0.55; p=0.001). Right ventricular outflow tract flow acceleration time (Ac T) was significantly correlated only with the FEV1 (r=0.32; p=0.047). RVD was significantly correlated with SpO(2) at rest (r= -0.44; p=0.005) and clinical score (r= -0.38; p=0.017). The SpO(2) at rest was the single best predictor of PASP and this effect was independent of the relationship between other independent variables (p=0.001). The declining pulmonary function was significantly associated with PASP (p<0.001), SpO(2) at rest (p=0.001), SpO(2) at the end of the 6MWT (p=0.007) and difference between peripheral oxygen saturation at resting and at the end of the 6MWT (p=0.025).
Conclusion: The PASP was not significantly correlated with the distance walked during the 6MWT in patients with CF. The PASP was strongly correlated with oxygen status at rest. The SpO(2) at rest was the best predictor of PASP. Also, PASP was strongly correlated with Shwachman-Kulczycki score, FEV(1), and FVC in this population.
Similar articles
-
Pulmonary hypertension as estimated by Doppler echocardiography in adolescent and adult patients with cystic fibrosis and their relationship with clinical, lung function and sleep findings.Clin Respir J. 2018 Feb;12(2):754-761. doi: 10.1111/crj.12590. Epub 2016 Dec 29. Clin Respir J. 2018. PMID: 27925430
-
Glucose intolerance in patients with cystic fibrosis: sex-based differences in clinical score, pulmonary function, radiograph score, and 6-minute walk test.Respir Care. 2011 Mar;56(3):290-7. doi: 10.4187/respcare.00726. Epub 2011 Jan 21. Respir Care. 2011. PMID: 21255491
-
Submaximal exercise capacity in adolescent and adult patients with cystic fibrosis.J Bras Pneumol. 2007 May-Jun;33(3):263-9. doi: 10.1590/s1806-37132007000300006. J Bras Pneumol. 2007. PMID: 17906786 English, Portuguese.
-
Oxygen transport and utilisation during exercise in cystic fibrosis: contributors to exercise intolerance.Exp Physiol. 2020 Dec;105(12):1979-1983. doi: 10.1113/EP088106. Epub 2020 Nov 11. Exp Physiol. 2020. PMID: 33119143 Review.
-
The impact of long COVID on physical and cardiorespiratory parameters: A systematic review.PLoS One. 2025 Jun 4;20(6):e0318707. doi: 10.1371/journal.pone.0318707. eCollection 2025. PLoS One. 2025. PMID: 40465774 Free PMC article.
Cited by
-
Pulmonary hypertension survival effects and treatment options in cystic fibrosis.Curr Opin Pulm Med. 2013 Nov;19(6):652-61. doi: 10.1097/MCP.0b013e3283659e9f. Curr Opin Pulm Med. 2013. PMID: 24048083 Free PMC article. Review.
-
Determinants of 6-minute walk distance in patients with idiopathic pulmonary fibrosis undergoing lung transplant evaluation.Pulm Circ. 2016 Mar;6(1):30-6. doi: 10.1086/685022. Pulm Circ. 2016. PMID: 27076905 Free PMC article.
-
Polysomnographic differences associated with pulmonary hypertension in patients with advanced lung disease due to cystic fibrosis.Lung. 2014 Jun;192(3):413-9. doi: 10.1007/s00408-014-9573-x. Epub 2014 Mar 27. Lung. 2014. PMID: 24671311
-
Non-invasive Ventilation for Children With Chronic Lung Disease.Front Pediatr. 2020 Nov 11;8:561639. doi: 10.3389/fped.2020.561639. eCollection 2020. Front Pediatr. 2020. PMID: 33262959 Free PMC article. Review.
-
The Impact of Pulmonary Arterial Pressure on Exercise Capacity in Mild-to-Moderate Cystic Fibrosis: A Case Control Study.Pulm Med. 2012;2012:252345. doi: 10.1155/2012/252345. Epub 2012 Jul 29. Pulm Med. 2012. PMID: 22900167 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Research Materials