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Optiflow tm

Manufactured by Fisher & Paykel Healthcare
Sourced in New Zealand

The Optiflow TM is a respiratory care device manufactured by Fisher & Paykel Healthcare. It is designed to provide high-flow nasal oxygen therapy to patients. The device delivers a precise blend of heated and humidified oxygen through a nasal cannula, providing respiratory support.

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Lab products found in correlation

3 protocols using optiflow tm

1

Technetium-99m DTPA Aerosol Delivery

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Diethylenetriaminepentaacetic acid labeled with 1 millicurie (37 MBq) of Technetium-99m (DTPA-Tc99m) in 0.9% saline to a total volume of 1 mL was administered via vibrating mesh nebulizer (VMN: Aerogen Solo, Aerogen Ltd., Galway, Ireland) placed at the inlet of a passover humidifier filled with sterile water and attached to a corrugated heated wire tubing and medium-sized adult nasal cannula (OptiflowTM; Fisher&Paykel Healthcare, Auckland, New Zealand) (Figure 2).
Oxygen was dispensed from a calibrated back pressure compensated flowmeter at 10, 30, and 50 L/min. Gas passed through the nebulizer connector, carrying aerosol into the inlet of the humidifier filled with water. For heated humidity, the water in the humidifier and circuit were heated to 34–36 °C. For unheated conditions, water in the humidifier was room temperature (20–22 °C) and the circuit was unheated.
After device setup and temperature stabilization, subjects were seated and nasal cannula prongs were placed in the nostrils. An orofacial mask with filter (Vital Signs, San Diego, California, USA) was placed over the cannula and lightly sealed to the face. Subjects were instructed to breathe normally and allotted 2 min to acclimate to the setup prior to dosing. The 1 mL dose was placed in the nebulizer reservoir and administered to completion.
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2

High-Flow Nasal Cannula Weaning Criteria

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Adult patients who were treated with HFNC in the ICU were included in this study. The Optiflow TM system with an O2 / air blender and a heated humidifier at 40°C (MR850, Fisher & Paykel Healthcare, Auckland, New Zealand) was used. On the one hand, patients were liberated from HFNC when the HFNC setting was weaned to 30 L / min flow at FIO2 of 0.21-0.30. On the other hand, patients were eligible when oxygen saturation was ≥ 90% with respiratory rate < 40 / min. Exclusion criteria
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3

High-Flow Oxygen Delivery and Room Ventilation Study

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The study was carried out in single-occupancy rooms. Clinical researchers performed sampling and patient care to limit the number of room entries and maintain typical room traffic. Otherwise standard care was provided.
Four experimental conditions were created by delivering oxygen through HFNC (Optiflow TM and AIRVO TM , Fisher & Paykel Healthcare Ltd, Auckland, New Zealand) or simple oxygen mask (OM) (Soundway Ò , Ningbo Shengyurui Medical Appliances Co. Ltd, Ningbo, China) with room ventilation of six or 12 air changes per hour (ACH). Samples were obtained in all four conditions with each patient in a crossover design. The order in which the oxygen delivery devices were applied was randomized using a computer-generated randomization sequence concealed in sealed envelopes. For HFNC, 60 L/min gas flow was applied. Inspiratory fraction of oxygen (FiO 2 ) for HFNC and the oxygen flow for OM were adjusted to maintain oxygen saturation !92%. There was a washout period at 12 ACH between testing the two devices. Six ACH and 12 ACH were chosen based on common Intensive Care Unit and Airborne Infection Isolation room standards [3] .
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