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Bipap a40

Manufactured by Philips
Sourced in United States

The BiPAP A40 is a non-invasive ventilation device designed to provide respiratory support. It delivers positive airway pressure to assist with breathing. The device is intended for use in a medical or home setting, as prescribed by a healthcare professional.

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6 protocols using bipap a40

1

Titration of BiPAP Ventilation during DISE

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The BiPAP A40 (Philips Respironics, Murrysville, PA, USA) in PAP mode was used for titration. PAP titration was performed immediately after DISE with the patient in supine position. An overpressure ventilation mask (Respironics PerforMax Full-face mask, Philips Respironics, Murrysville, PA, USA) of appropriate size was applied to the patient’s face. A special connecting valve (Philips Respironics, Murrysville, PA, USA) was inserted between the mask and the device hose, through which a flexible endoscope was inserted into the nose and nasopharynx. The mask was subsequently fixed with straps.
Sleep endoscopy was then performed under overpressure ventilation. The start of the examination was at a pressure of 6 hPa. Gradually, the PAP was elevated (always after at least 30 s) in the range of 6, 8, 10, 12, 14, and 18 hPa. At each pressure tested, an evaluation was performed by two physicians independently. The efficiency of overpressure ventilation was assessed visually, and at the same time the values of blood oxygen saturation measured on a finger of the upper limb were monitored.
The Kezirian VOTE classification was used for evaluation at each PAP tested to observe the effect of increasing pressure on the obstruction of the monitored localities.
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2

Chronic NIV Initiation for Patients

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Patients randomised to in-hospital initiation were initiated on chronic NIV according to the regular procedures on our pulmonary ward. We used a bilevel positive airway pressure (BiPAP)-set ventilator (BiPAP A40 and BiPAP A30, Philips Respironics, Murrysville, Pennsylvania, USA) and adjusted the settings to achieve normocapnia during the night or at least a reduction in nocturnal mean PtCO2of 20% compared with the first night of spontaneous breathing.29 (link) The initiation period was finished and the patient was discharged home once he or she could sleep at least 6 consecutive hours with the ventilator and the gas exchange goals were achieved. When necessary, our specialised nurse joined the patients at home to instal the ventilator.
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3

Remote Initiation of Chronic NIV

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Patients randomised to home initiation were initiated on chronic NIV completely at their home, using telemedicine. Ventilator data were retrieved via a GPRS system clicked on the back of the ventilator (BiPAP A40 and BiPAP A30, Philips Respironics), which sent data to an online platform (Encore Anywhere, Philips Respironics). Changes in ventilator settings could be made remotely. Also, PtCO2 was measured (SenTec DM, Software V-STATS V.4.0, SenTec AG, Therwil, Switzerland) and these data were retrieved remotely via a high-end ambulatory remote monitoring device (Dyna-vision, Techmedic International, Broek op Langedijk, the Netherlands). The specialised nurse visited the patient at day 1 to instal the equipment, explain all procedures, and to practice with NIV, and the last day to return the telemedicine/measurement devices and finish the initiation period. For a detailed explanation of the home initiation, see online repository.
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4

Polysomnography Titration for Home NIV

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RP was performed with Alice PDx (Philips-Respironics, USA) level
III
devices9 (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
O2.
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.
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5

PAP Titration During Sleep Endoscopy

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Titration was performed using the BiPAP A40 (Philips Respironics, Florida, USA) in PAP mode. PAP titration was performed immediately after DISE. An appropriately sized overpressure ventilation mask (Respironics PerforMax Full-face mask; Philips Respironics, Florida, USA) was applied to the patient’s face. A special connecting valve (Philips Respironics, Florida, USA) was inserted between the mask and the device hose, through which a flexible endoscope was inserted into the nasopharynx and upper airways (Figure 1).
Sleep endoscopy was then performed under overpressure ventilation. The examination started at a pressure of 6.0 hPa. The pressure on the PAP was gradually elevated (in the range of 6.0, 8.0, 10.0, 12.0, 14.0, and 18.0 hPa (Figure 2). The efficiency of treatment was visually assessed, with simultaneous monitoring of the blood oxygen saturation. At each tested PAP pressure, the VOTE classification was used for evaluation [12 (link)].
We compared the findings among the examined patients. Notably, we observed which areas of the upper airways responded better to PAP treatment and in which areas PAP had worse effects.
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6

Noninvasive Ventilation for Patient Support

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noninvasive ventilator (BiPAP A40, Philips Respironics, Amsterdam, Netherlands) was applied for ventilation treatment and Bi-level positive pressure noninvasive ventilation mode was adopted. The oxygen concentration and respiratory rate were 5 to 10 L and 15 to 20/min, inspiratory and expiratory pressure were set as 8 cmH2O and 4 cmH2O respectively. During the treatment period, oxygen flow, inspiratory and expiratory volume were adjusted according to the patient’s specific conditions and tolerance, and these parameters were modulated once every 5 to 10 minutes and 2 to 4 cmH2O each time.
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