Does Severity of Airflow Obstruction Correlate to Static Lung Volumes
Pulmonary Disease, Chronic Obstructive
About this trial
This is an interventional basic science trial for Pulmonary Disease, Chronic Obstructive focused on measuring airflow obstruction, plethysmography, lung volumes
Eligibility Criteria
Inclusion Criteria: A minimum of 10 patients from each group will be included; normal lung function/ no airflow obstruction (FEV1/FVC >70%), mild airflow obstruction (FEV1/FVC <70% and FEV1 >80% predicted), moderate airflow obstruction (FEV1/FVC <70% and FEV1 50-80% predicted), severe airflow obstruction (FEV1/FVC <70% and FEV1 30-50% predicted) and very severe (FEV1/FVC <70% and FEV1 >30% predicted). Al patients will be over the age of 18 with no upper age limit. No children will be included in this study. Patients must have withheld their inhalers. Exclusion Criteria: [15:10] Jessica Armstrong Contraindications to performing the test include (if occurred within last 8 weeks): Heart attack Stroke Haemoptysis Pneumothorax Surgery to the abdomen/thorax Eye surgery An individuals spirometry cannot be included if: There is a cough during the first second of the manoeuvre A leak at the mouthpiece Early termination of manoeuvre Sub optimal effort They are unable to comprehend the instructions Obstruction of the mouthpiece (tongue/teeth) Lung volume measurements cannot be included if: There is a leak around the mouthpiece The patient has a ruptured eardrum They are unable to comprehend the instructions Obstruction of the mouthpiece (tongue/teeth) The patient is on supplementary oxygen and cannot come off it (this must be discontinued for a suitable period prior to nitrogen washout) Patients who are CO2 retainers may not be able to undergo nitrogen washout The patients test results must meet the acceptability criteria of the ARTP pulmonary function testing statement (updated 2020). For spirometry this states that there must be 3 technically acceptable attempts within 150ml, however, if the the individual has an FVC <1.00L this can be 100ml. Nitrogen washout requires two technically acceptable attempts within 10% (as per trust policy), whereas, for body plethysmography three technically acceptable attempts should be obtained within 5%.
Sites / Locations
Arms of the Study
Arm 1
Other
Obtaining lung volume measurements in patients with airflow obstruction
All patients involved in this study will be attending a pulmonary function test as part of their routine patient treatment pathway, requested by their consultant. Potential participants will be sent a patient information sheet prior to their lung function test. The pulmonary function test begins routinely, with the pre-test questions. Spirometry will then be performed. If the patient's results are variable and the repeatability criteria are not met, the patient will not be asked to take part in the study, and no additional tests (not requested by the consultant routinely) will be carried out. If the patient has normal or obstructive results (FEV1/FVC <70%) the patient will sign the consent form and both lung volume tests will be conducted. They must be able to follow the instructions for both nitrogen washout and body plethysmography, and the results must also meet the acceptability and repeatability criteria.