Idiopathic Pulmonary Fibrosis, Obstructive Sleep Apnea, Sleep Disturbance, Sleep Hypoventilation
Conditions
Brief summary
Home sleep studies - which allow the measurement of breathing while the person sleeps - will be performed on patients with fibrotic interstitial lung disease attending two of the UK's largest respiratory medicine services.The study will investigate at how symptoms, and breathing and exercise tests differ between these two groups after 12 months of study.
Detailed description
The interstitial lung diseases are a group of diseases in which patients develop uncontrolled scarring (called fibrosis) within the lung. This causes failure of the lung and patients become progressively more breathless over time. The commonest of these diseases is idiopathic pulmonary fibrosis and this is a devastating condition with a survival of 3-5 years. Many people with fibrotic interstitial lung diseases have disrupted sleep as well as low oxygen levels at night or obstructive sleep apnoea (OSA - pauses in breathing at night time due to obstruction of the upper airway). Patients with low oxygen levels at night have a worse quality of life, with fatigue during the day and survive for less long. 102 patients from specialist clinics at Guy's and St Thomas' and the Royal Brompton and Harefield NHS Foundation Trusts will be recruited. This research is funded by a grant from the British Lung Foundation. The investigators aim to compare patients with and without low oxygen levels at night by observing how their disease and quality of life changes over a year. Patients will be asked to complete a two-night home sleep study which will involve wearing a probe over the finger connected to a sensor on the wrist. Patients will also be provided with a home spirometer to measure their breathing at home daily during the study. Lung function testing (which is part of normal clinical practice), a six-minute walk test and quality of life questionnaires will be performed at the beginning of the study. These investigations will be repeated at six and twelve months and this will tell us how night time oxygen levels affect the progression of the disease, quality of life, exercise tolerance, hospitalisation frequency and survival of these patients.
Interventions
None listed
Sponsors
Royal Brompton & Harefield NHS Foundation Trust
Guy's and St Thomas' NHS Foundation Trust
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
20 Years to 90 Years
Inclusion criteria
* MDT diagnosis of fibrotic interstitial lung disease including but not limited to idiopathic pulmonary fibrosis (IPF), non-specific interstitial pneumonitis (NSIP), chronic hypersensitivity pneumonitis (CHP), fibrotic organising pneumonia and unclassifiable fibrotic lung disease. * Competent to provide written consent in English
Exclusion criteria
* Presence of an underlying connective tissue disease * Daytime/resting hypoxaemia with pO2 \<8.0 * Other indication for oxygen therapy * 3% ODI \>15 events/hour studied or established on CPAP * Predominant emphysema on CT * Inability to provide informed consent or complete health-related quality of life questionnaires in English * Current participation in a research project which might alter lung function or sleep study results
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Quality of life measured by King's Brief Interstitial Lung Disease Questionnaire (K-BILD) | 0 months,12 months | Change in K-BILD score from baseline at 12 months in patients with nocturnal hypoxaemia vs those without (defined as time spent with SpO2\<90% of \> 10% total sleep time) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Diffusion capacity of the lung for carbon monoxide (DLCO) | 12 months | Change in DLCO from baseline at 6 and 12 months in patients with nocturnal hypoxaemia vs those without |
| Pittsburgh Sleep Quality Index (PSQI) | 0 months, 6 months, 12 months | PSQI score at baseline, and change at 6 and 12 months in patients with nocturnal hypoxaemia vs those without |
| Insomnia Severity Index (ISI) | 0 months, 6 months, 12 months | ISI score at baseline, and change at 6 and 12 months in patients with nocturnal hypoxaemia vs those without |
| Forced vital capacity (FVC) | 12 months | Annualised decline in FVC in patients with nocturnal hypoxaemia vs those without |
| Exacerbation frequency and hospitalisation | 12 months | Exacerbation frequency and hospitalisation |
| Mortality | 12 months | Mortality |
| Six-minute walk test (6MWT) | 0 months 6 months, 12 months | Total distance (in metres) and minimum oxygen saturation during 6MWT at baseline, 6 and 12 months |
Countries
United Kingdom
Outcome results
None listed