Resting and exercise cardiorespiratory function in survivors of congenital diaphragmatic hernia
Autor: | Desmond Bohn, Ian Adatia, Donna L. Wilkes, Jane Schneiderman-Walker, Allan L. Coates, Daniel Trachsel, Hiran Selvadurai |
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Rok vydání: | 2006 |
Předmět: |
Pulmonary and Respiratory Medicine
Male medicine.medical_specialty Adolescent Diaphragmatic breathing Physical exercise Pulmonary function testing Cardiovascular Physiological Phenomena Cohort Studies Oxygen Consumption Heart Rate Internal medicine Forced Expiratory Volume medicine Humans Diaphragmatic hernia Body Weights and Measures Exertion Survivors Cardiac Output Child Hernia Diaphragmatic Exercise Tolerance business.industry Pulmonary Gas Exchange Congenital diaphragmatic hernia Cardiorespiratory fitness Stroke Volume medicine.disease Pulmonary hypertension Respiratory Function Tests Residual Volume Cross-Sectional Studies Pediatrics Perinatology and Child Health Physical therapy Cardiology Exercise Test Respiratory Physiological Phenomena Female business Hernias Diaphragmatic Congenital Lung Volume Measurements |
Zdroj: | Pediatric pulmonology. 41(6) |
ISSN: | 8755-6863 |
Popis: | Our objective was to study exercise capacity and cardiorespiratory response to exertion in survivors of congenital diaphragmatic hernia (CDH). This was a cross-sectional cohort study of 23 CDH survivors, aged 10-16 years, and 23 gender- and age-matched controls. Exercise testing was performed on a cycle ergometer, with cardiac output measurements made using exponential CO2 rebreathing. Pretest cardiorespiratory assessment was done by echocardiography and pulmonary function testing. Statistical analysis was performed using Student's t-test, regression analysis, and longitudinal model computing with spatial covariance structure. No echocardiographic evidence for pulmonary hypertension was found at rest (right ventricular systolic pressures, 27 +/- 6 mmHg). Mean pulmonary artery diameter on the side of the CDH was significantly smaller than contralaterally, but was within normal range (z-score, 0 +/- 1.1 vs. 1.2 +/- 1.6, P < 0.01). Exercise capacity was mildly reduced in CDH compared to controls and predictive data (maximum workload, 77% +/- 12% vs. 91% +/- 16% of predicted, P < 0.01). Cardiorespiratory response to exertion was not significantly different between groups. In conclusion, most adolescent CDH survivors have nearly normal exercise capacity and cardiorespiratory response to exertion. This study may prove useful in comparisons with future cohorts comprising more severely affected individuals now surviving due to improved neonatal care. |
Databáze: | OpenAIRE |
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