RP was performed with
Alice PDx (Philips-Respironics, USA)
level
III devices
9 (link) with
a flow sensor, airway pressure proximal to the mask, thoracic and abdominal
effort measured with inductive plethysmography, and finger pulse oximeter.
During titration,
single circuit continuous positive pressure
devices (Trilogy-Philips and
Bipap A40-Philips non-invasive
ventilators) were connected to obtain data on leaks (total leak), tidal volume,
and point-to-point time pressure curves through a digital communication port
(connectivity module).
Only ventilatory pressure modes and interfaces
with intentional leaks were used.
For the adaptation period, the treating team selected the most appropriate
settings and interfaces based on the usual protocol findings (morning arterial
blood gas without supplemental oxygen; at rest, seated, and awake; clinical and
ventilator software data
Encore Pro II and
Direct View-Philips) and recordings
were taken at ICU patients' bedside at night and without supplemental
O
2.
Before RP, authors do not contact the patient and did not interfere with the
ventilation protocol or ICU effectiveness monitoring (downloaded software data,
oximetry, etc.). The RP was performed during the period immediately prior to the
discharge of the hospital during the planning of the home use of the NIV, with
ambient air to facilitate the identification of respiratory events.
Borsini E., Ernst G., Blanco M., Blasco M., Bosio M., Salvado A, & Nigro C. (2017). Respiratory polygraphy monitoring of intensive care patients receiving non-invasive ventilation. Sleep Science, 10(1), 35-40.