Abstract:BackgroundPortable oxygen concentrators (POCs) typically include pulse flow (PF) modes to conserve oxygen. The primary aims of this study were to develop a predictive in vitro model for inhaled oxygen delivery using a set of realistic airway replicas, and to compare PF for a commercial POC with steady flow (SF) from a compressed oxygen cylinder.MethodsExperiments were carried out using a stationary compressed oxygen cylinder, a POC, and 15 adult nasal airway replicas based on airway geometries derived from med… Show more
“…In Chen et al, 10 testing was limited to a single POC evaluated at 2 integer pulse settings, one high (6) and one low (2). It was found that intersubject variability among 15 airway geometries had only a small (Ͻ5% coefficient of variation) impact on volume-averaged F IO 2 values.…”
Section: Selection Of a Representative Airway Replicamentioning
confidence: 99%
“…It was found that intersubject variability among 15 airway geometries had only a small (Ͻ5% coefficient of variation) impact on volume-averaged F IO 2 values. 10 Therefore, it was deemed reasonable to use only a single representative replica for comparative testing in the present work. A single replica was selected on the criterion that the volume-averaged F IO 2 value obtained by using this replica (for either continuous flow oxygen or pulse flow) was closest to the average value obtained across the set of 15 replicas.…”
Section: Selection Of a Representative Airway Replicamentioning
confidence: 99%
“…The challenge of establishing equivalence between continuous flow oxygen and nominal pulse flow device settings on different devices is well known 5,9 and provides motivation for the development of physiologically representative in vitro testing methods. Chen et al 10 recently outlined a methodology to compare pulse flow oxygen delivery from a commercially available POC with continuous flow oxygen delivery from a stationary cylinder by using a set of 15 realistic airway replicas. Use of these replicas, together with a lung simulator in in vitro experiments allowed for precise control of simulated breathing parameters in anatomically representative models of the upper airways and made it possible to account for potential intersubject variability due to variance in airway geometries as well as allowing modes of failure to be assessed when a POC failed to detect an inspiratory effort.…”
Section: Introductionmentioning
confidence: 99%
“…By measuring the real-time oxygen concentration at the airway replica outlet (representative of the trachea) during inspiration, a volume-averaged F IO 2 was obtained that represented the fraction of oxygen contained in a given inhaled tidal volume (V T ). 10 In other words, these volumeaveraged F IO 2 values represent the ratios between the total volume of inhaled oxygen (including both supplemental oxygen and oxygen in the entrained air) and the inhaled V T , and provide a common basis for comparison between pulse flow and continuous flow oxygen. 10 In building on this recent work, the present study had 2 primary objectives.…”
Section: Introductionmentioning
confidence: 99%
“…10 In other words, these volumeaveraged F IO 2 values represent the ratios between the total volume of inhaled oxygen (including both supplemental oxygen and oxygen in the entrained air) and the inhaled V T , and provide a common basis for comparison between pulse flow and continuous flow oxygen. 10 In building on this recent work, the present study had 2 primary objectives. The first was to compare the performance of several POCs against each other and against continuous flow oxygen by using volume-averaged F IO 2 at the trachea as a measure of oxygen delivery.…”
BACKGROUND: Portable oxygen concentrators (POCs) deliver oxygen in intermittent pulses. The challenge of establishing equivalence between continuous flow oxygen and nominal pulse flow settings on different POCs is well known. In vitro bench measurements and in silico mathematical modeling were used to compare the performance of 4 POCs versus continuous flow oxygen by predicting the F IO 2 at the trachea and entering the acini. METHODS: Each of the 4 POCs was connected to a 3-dimensional printed replica of a human adult nasal airway via nasal cannula. A test lung simulated 3 breathing patterns representative of a patient with COPD at rest, during exercise, and while asleep. POCs were tested for each breathing pattern at all integer pulse flow settings. Volume-averaged F IO 2 was calculated by analyzing oxygen concentrations and inhalation flow over time. In vitro oxygen waveforms were then combined with a single-path mathematical model of the lungs to assess oxygen transport through the conducting airways. In vitro experiments and mathematical modeling were repeated for continuous flow oxygen. RESULTS: Continuous flow oxygen consistently delivered more (>2% absolute) oxygen in terms of volume-averaged F IO 2 for all nominally equivalent pulse flow settings of >2. Differences were also observed when comparing performances between different POCs, particularly at high device settings (5 and 6). Simulations showed that efficiency of delivery to the acinar region of the lungs was higher in pulse flow than in continuous flow oxygen but that continuous flow oxygen generally delivered a higher absolute volume of oxygen. Differences in absolute oxygen delivery per breath between continuous flow oxygen and pulse flow were smaller for acinar delivery than for tracheal delivery. CONCLUSIONS: Significant differences in POC performance based on volume-averaged F IO 2 were found between pulse flow and continuous flow oxygen, and among pulse flow modes in different POCs. Although pulse flow was a more efficient mode of delivery than continuous flow oxygen, continuous flow oxygen delivered a greater absolute volume of oxygen per breath. Key words: long-term oxygen therapy (LTOT); ambulatory oxygen; portable oxygen concentrator (POC); lung simulator; nasal cannula; chronic obstructive pulmonary disease; oxygen therapy; lung model; trumpet model; pulse. [Respir Care 2019;64(2):117-129.
“…In Chen et al, 10 testing was limited to a single POC evaluated at 2 integer pulse settings, one high (6) and one low (2). It was found that intersubject variability among 15 airway geometries had only a small (Ͻ5% coefficient of variation) impact on volume-averaged F IO 2 values.…”
Section: Selection Of a Representative Airway Replicamentioning
confidence: 99%
“…It was found that intersubject variability among 15 airway geometries had only a small (Ͻ5% coefficient of variation) impact on volume-averaged F IO 2 values. 10 Therefore, it was deemed reasonable to use only a single representative replica for comparative testing in the present work. A single replica was selected on the criterion that the volume-averaged F IO 2 value obtained by using this replica (for either continuous flow oxygen or pulse flow) was closest to the average value obtained across the set of 15 replicas.…”
Section: Selection Of a Representative Airway Replicamentioning
confidence: 99%
“…The challenge of establishing equivalence between continuous flow oxygen and nominal pulse flow device settings on different devices is well known 5,9 and provides motivation for the development of physiologically representative in vitro testing methods. Chen et al 10 recently outlined a methodology to compare pulse flow oxygen delivery from a commercially available POC with continuous flow oxygen delivery from a stationary cylinder by using a set of 15 realistic airway replicas. Use of these replicas, together with a lung simulator in in vitro experiments allowed for precise control of simulated breathing parameters in anatomically representative models of the upper airways and made it possible to account for potential intersubject variability due to variance in airway geometries as well as allowing modes of failure to be assessed when a POC failed to detect an inspiratory effort.…”
Section: Introductionmentioning
confidence: 99%
“…By measuring the real-time oxygen concentration at the airway replica outlet (representative of the trachea) during inspiration, a volume-averaged F IO 2 was obtained that represented the fraction of oxygen contained in a given inhaled tidal volume (V T ). 10 In other words, these volumeaveraged F IO 2 values represent the ratios between the total volume of inhaled oxygen (including both supplemental oxygen and oxygen in the entrained air) and the inhaled V T , and provide a common basis for comparison between pulse flow and continuous flow oxygen. 10 In building on this recent work, the present study had 2 primary objectives.…”
Section: Introductionmentioning
confidence: 99%
“…10 In other words, these volumeaveraged F IO 2 values represent the ratios between the total volume of inhaled oxygen (including both supplemental oxygen and oxygen in the entrained air) and the inhaled V T , and provide a common basis for comparison between pulse flow and continuous flow oxygen. 10 In building on this recent work, the present study had 2 primary objectives. The first was to compare the performance of several POCs against each other and against continuous flow oxygen by using volume-averaged F IO 2 at the trachea as a measure of oxygen delivery.…”
BACKGROUND: Portable oxygen concentrators (POCs) deliver oxygen in intermittent pulses. The challenge of establishing equivalence between continuous flow oxygen and nominal pulse flow settings on different POCs is well known. In vitro bench measurements and in silico mathematical modeling were used to compare the performance of 4 POCs versus continuous flow oxygen by predicting the F IO 2 at the trachea and entering the acini. METHODS: Each of the 4 POCs was connected to a 3-dimensional printed replica of a human adult nasal airway via nasal cannula. A test lung simulated 3 breathing patterns representative of a patient with COPD at rest, during exercise, and while asleep. POCs were tested for each breathing pattern at all integer pulse flow settings. Volume-averaged F IO 2 was calculated by analyzing oxygen concentrations and inhalation flow over time. In vitro oxygen waveforms were then combined with a single-path mathematical model of the lungs to assess oxygen transport through the conducting airways. In vitro experiments and mathematical modeling were repeated for continuous flow oxygen. RESULTS: Continuous flow oxygen consistently delivered more (>2% absolute) oxygen in terms of volume-averaged F IO 2 for all nominally equivalent pulse flow settings of >2. Differences were also observed when comparing performances between different POCs, particularly at high device settings (5 and 6). Simulations showed that efficiency of delivery to the acinar region of the lungs was higher in pulse flow than in continuous flow oxygen but that continuous flow oxygen generally delivered a higher absolute volume of oxygen. Differences in absolute oxygen delivery per breath between continuous flow oxygen and pulse flow were smaller for acinar delivery than for tracheal delivery. CONCLUSIONS: Significant differences in POC performance based on volume-averaged F IO 2 were found between pulse flow and continuous flow oxygen, and among pulse flow modes in different POCs. Although pulse flow was a more efficient mode of delivery than continuous flow oxygen, continuous flow oxygen delivered a greater absolute volume of oxygen per breath. Key words: long-term oxygen therapy (LTOT); ambulatory oxygen; portable oxygen concentrator (POC); lung simulator; nasal cannula; chronic obstructive pulmonary disease; oxygen therapy; lung model; trumpet model; pulse. [Respir Care 2019;64(2):117-129.
The present work examines regional deposition within the nose for nasal sprays over a large and wide ranging parameter space by using numerical simulation. A set of 7 realistic adult nasal airway geometries was defined based on computed tomography images. Deposition in 6 regions of each nasal airway geometry (the vestibule, valve, anterior turbinate, posterior turbinate, olfactory, and nasopharynx) was determined for varying particle diameter, spray cone angle, spray release direction, particle injection speed, and particle injection location. Penetration of nasal spray particles through the airway geometries represented unintended lung exposure. Penetration was found to be relatively insensitive to injection velocity, but highly sensitive to particle size. Penetration remained at or above 30% for particles exceeding 10 μm in diameter for several airway geometries studied. Deposition in the turbinates, viewed as desirable for both local and systemic nasal drug delivery, was on average maximized for particles ranging from ~20 to 30 μm in diameter, and for low to zero injection velocity. Similar values of particle diameter and injection velocity were found to maximize deposition in the olfactory region, a potential target for nose-to-brain drug delivery. However, olfactory deposition was highly variable between airway geometries, with maximum olfactory deposition ranging over 2 orders of magnitude between geometries. This variability is an obstacle to overcome if consistent dosing between subjects is to be achieved for nose-to-brain drug delivery.
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