Primary objectives: evaluate the efficacy of noninvasive ventilation (NIV) treatment versus continuous positive airway pressure (CPAP) and life style modification treatment in Obesity Hypoventilation Syndrome (OHS), with PCO2 (first phase) and days of hospitalization (second phase) analyzed as a primary variables and percentage of dropouts for medical reasons and mortality as operative variables. As secondary variables: Measure functional and clinical improvement during sleep and wakefulness, quality of life, echocardiography and the incidence and blood pressure and evolution of cardiovascular events. Objectives secondaries:role of apneogenic sleep events on molecular inflammation, endothelial damage and the genesis of diurnal hypercapnia. Methods:prospective, randomized controlled trial. Patients with OHS will be divided initially into two groups based on their apnea-hypopnea index (AHI) score, \>=30 and \< 30, using conventional polysomnography. The AHI \>=30 group will be randomized to CPAP, NIV or life style modification treatments. The AHI \<=30 groups will be randomized to NIV or life style modification treatments. Treatment efficacy at the medium- and long-term will be analyzed by comparing groups. The role of apneic events and leptin in the genesis of daytime alveolar hypoventilation will be analyzed by comparing the daytime PCO2/AHI coefficient between responders and non-responders to CPAP treatment, and the evolution of leptin levels in the four branches of the study. The role of apneic events in metabolic and biochemical alterations and endothelial dysfunction will be analyzed by comparing basal and post-treatment levels of related substances between groups, with and without significant AHI.
The AHI \>=30 group will be analyzed to CPAP, NIV or life style modification treatments for two mouths.Once an evaluation is done during this period, the life style modification treatment will be randomized with the NIV/CPAP treatment for a continuation of three years.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
440
life style modification, noninvasive ventilation, CPAP
Hospital San Pedro de Alcántara. Servicio Extremeño de Salud
Cáceres, Spain
Days of hospitalization
Days of hospitalization
Time frame: at least three years
PaCO2
PaCO2
Time frame: at the end of first two months
Number of Dropouts for Medical reasons and mortality
Number of Dropouts for Medical reasons and mortality
Time frame: at least three years
quality of life
quality of life
Time frame: two months and three years
respiratory function
respiratory function
Time frame: two months and three years
polysomnographic parameters
polysomnographic parameters
Time frame: two months
molecular inflammation and endothelial dysfunction
molecular inflammation and endothelial dysfunction
Time frame: two months and three years
echocardiographic parameters
echocardiographic parameters
Time frame: two months and three years
Blood pressure and new cardiovascular events
Blood pressure and new cardiovascular events
Time frame: three years
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