The measurement of hypopharyngeal FIO2, is a simple and rapid method for evaluating oxygen delivery systems in clinical practice. Hypopharyngeal FIO2 measurements were compared to other established methods of inspired gas measurement, namely, tracheal gas sampling and exhaled gas analysis. Hypopharyngeal sampling and exhaled gas analysis. Hypopharyngeal sampling compared favourably with these methods. Furthermore, arterial blood gas samples from patients receiving oxygen by aerosol mask correlated with the hypopharyngeal measurements but not with the delivery system's settings. In normal, healthy subjects, the authors studied variables known to influence FIO2. Using nasal prongs as well as an aerosol mask system, the authors studied the interaction of the wall flow rates, the concentration (Venturi) settings (in the case of the aerosol mask), and the subject's respiratory rate. Under these controlled conditions of tidal breathing, the hypopharyngeal FIO2 was directly related to the total flow of gas from the delivery system and the concentration of the Venturi setting but inversely related to the respiratory rate. Hypopharyngeal gas sampling offers a simple method for evaluating and correcting a patient's inspired oxygen concentration.
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http://dx.doi.org/10.1097/00003246-198007000-00010 | DOI Listing |
Head Neck
November 2020
Section of Cardiac Surgery, Department of Surgery, University of Chicago, Chicago, Illinois, USA.
Background: Patients requiring intensive upper airway reconstruction are anatomically restricted in terms of the respiratory support they can receive. While intraoperative extracorporeal membrane oxygenation (ECMO) has been effectively utilized, little has been shown regarding the utility of ECMO for long-term support in these patients.
Methods: We demonstrate how a patient with tongue and hypopharyngeal squamous cell carcinoma that necessitated upper airway reconstruction was supported with veno-venous (VV) ECMO due to postoperative respiratory failure and an inability to maintain a stable airway.
Pediatr Pulmonol
October 2019
Department of Neonatology, Division of Pediatrics, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Background: Low flow nasal cannula (LFNC) are frequently used in preterm infants. However, the delivered inspired oxygen concentration and airway pressures are not well established.
Objective: To determine the fraction of inspired oxygen (FiO ) and hypopharyngeal pressures generated by LFNC at different gas flows, gas mixture concentrations and infant's weight.
Anaesth Intensive Care
November 2011
Critical Care Complex, Middlemore Hospital, Auckland, New Zealand.
In this study, we evaluated the performance of a humidified nasal high-flow system (Optiflow, Fisher and Paykel Healthcare) by measuring delivered FiO, and airway pressures. Oxygraphy, capnography and measurement of airway pressures were performed through a hypopharyngeal catheter in healthy volunteers receiving Optiflow humidified nasal high flow therapy at rest and with exercise. The study was conducted in a non-clinical experimental setting.
View Article and Find Full Text PDFRespir Care
September 2001
Division of Critical Care Medicine, Department of Pediatrics, University of Miami School of Medicine/Jackson Memorial Hospital, Miami, Florida 33101-6960, USA.
Objective: Measure the fraction of inspired oxygen (F(IO(2))) in infants receiving supplemental oxygen via nasal cannula and identify clinical variables that affect F(IO(2)).
Methods: Hypopharyngeal gas samples were obtained from 20 infants receiving oxygen via nasal cannula at flows between 0 and 4 L/min. F(IO(2)) was calculated using the alveolar gas equation and measurements of partial pressure of oxygen in the samples and the barometric pressure.
Sleep
November 1998
Medical Service, John F. Dingell Veterans Affairs Medical Center, Detroit, Mich 48202, USA.
The purpose of this study was to determine whether episodic hypoxic exposure would elicit long term facilitation (LTF) of ventilation (V(I)) in sleeping humans. Twenty subjects gave written informed consent. Of these, six subjects were unable to maintain stable stage 2 sleep or deeper for a majority of the experiment and their data were excluded from the analysis.
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