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- W2476670223 abstract "Supplemental oxygen for patients with idiopathic pulmonary fibrosis (IPF) who experience rest, nocturnal, or exertional desaturation can improve symptoms and quality of life. However, there is no data to show that supplemental oxygen improves survival, although it can improve exercise capacity [1, 2]. Towards the late stages of IPF, high-flow oxygen devices such as an oxymizer or high humidity high-flow nasal cannula may be needed to maintain adequate oxygen saturations and ameliorate symptoms. Oxymizers provide a reservoir of oxygen to draw from on inhalation, which increases the net oxygen concentration delivered to the patient for a given liter flow. High-flow nasal cannulas allow the clinician to control the liter flow (typically 30–50 L/min) and percentage FiO2, allowing for very high concentrations of oxygen to be delivered by a comfortable interface. Figure 8.1 shows a variety of available devices to provide higher level flow oxygen for patients with high oxygen requirements." @default.
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- W2476670223 date "2016-01-01" @default.
- W2476670223 modified "2023-09-28" @default.
- W2476670223 title "Non-pharmacologic Management of Idiopathic Pulmonary Fibrosis" @default.
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- W2476670223 doi "https://doi.org/10.1007/978-3-319-32794-5_8" @default.
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