Spirometry was conducted using a Micro Medical Spiro USB Spirometer and analysed with Spida 5 software (Cardinal Health, UK). Spirometry was completed in accordance with the American Thoracic Society and European Respiratory Society guidelines38. Each participant completed a minimum of three successful manoeuvres with at least 1–2 min rest between each manoeuvre while wearing a nose clip. The manoeuvres were rejected if: participants prematurely stopped exhalation, coughed during the first second of exhalation, lips were not fully sealed around the mouthpiece and/or the effort appeared submaximal. The test session was concluded when the largest two FEV1 and the largest two FVC were each within 0.15 L of each other in at least 3 manoeuvres38. If these criteria were not met, a maximum of eight manoeuvres were repeated until the criteria were met. Parameters assessed included: FEV1, FVC, FEV1/FVC ratio, Peak Expiratory Flow (PEF), and predicted values. The coefficient of variation (CV) for FEV1, FVC and PEF was 2.09%, 2.25% and 2.80%, respectively.
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