The goal of this clinical trial is to evaluate whether telemonitoring, added to the usual process of adaptation to home mechanical ventilation (HMV), achieves a more efficient correction of hypoventilation (reduction of hypercapnia).
Chronic hypercapnic respiratory failure with indication for home mechanical ventilation.
Patients who require ventilation with spontaneous-timed mode.
Signing of informed consent.
Patient already treated with mechanical ventilation or home CPAP.
Patient requiring mechanical ventilation as life support.
Pregnancy.
Cognitive impairment that makes it impossible to understand the informed consent for the study.
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead sponsor
Societat Catalana de Pneumologia (SOCAP)
Collaborator
Sociedad Española de Neumología y Cirugía Torácica
Collaborator