To evaluate a novel advanced physiological monitoring system to improve nocturnal non-invasive ventilation (NIV) in Neuromuscular disease (NMD), Chest wall disease (CWD), Chronic Obstructive Pulmonary Disease (COPD) and Obesity Hypoventilation Syndrome (OHS) patients. By enhancing sleep comfort, adherence to ventilation will increase which, in turn, will improve ventilatory failure, quality of life and reduce length of admission during initiation of therapy. We aim to incorporate this technology into routine clinical practice.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
58
Ventilation parameters will be manipulated and titrated according to physiological measurements including signal from parasternal EMG and patient- ventilator asynchrony.
Guy's and St. Thomas' NHS Trust
London, United Kingdom
Royal Brompton Hospital
London, United Kingdom
Adherence with ventilation
Data on patient reported compliance and ventilator recorded compliance will be collected.
Time frame: 3 months
health related quality of life
SRI, RAND-36, visual analogue scores, St. George's respiratory questionnaire
Time frame: 3 month
length of hospital stay for initiation of home mechanical ventilation
Time frame: 3 months
gas exchange
overnight oximetry, overnight capnography,arterial oxygenation, arterial carbon dioxide
Time frame: 3 months
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