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USPTO Patent Application: System to Monitor Respiration During Sedation

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Summary

The USPTO has published a patent application for a system designed to monitor patient respiration during sedation using nasal pressure and oxygen flow. The application details a method for identifying breathing patterns and delivering controlled oxygen pulses to ensure patient safety.

Published by USPTO on changeflow.com . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

This document is a USPTO patent application (US20260083926A1) for a system and method to monitor a sedated patient's respiration. The proposed system identifies end expiratory pauses, delivers precise pulses of high-flow oxygen (approx. 30 L/min for <0.5 seconds), and synthesizes a respiratory signal based on nasal pressure and oxygen flow measurements. The goal is to determine the patient's breathing pattern, rate, and frequency.

As this is a patent application, it does not impose immediate regulatory requirements or compliance deadlines on healthcare providers or medical device manufacturers. However, it signals potential future technological advancements in patient monitoring during sedation. Companies involved in developing medical devices for respiratory monitoring or sedation management should be aware of this patented technology.

Archived snapshot

Mar 26, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

System To Monitor Respiration During Sedation With Nasal Pressure And Oxygen Flow

Application US20260083926A1 Kind: A1 Mar 26, 2026

Inventors

Joseph Orr, Trey Blackwell

Abstract

This disclosure relates to systems and methods for monitoring sedated patients that are receiving supplemental oxygen flows. A method of monitoring a patient's breathing while sedated includes identifying an end expiratory pause in the patient's breathing pattern and obtaining a first respiratory signal corresponding to a nasal pressure of a patient. The method may also include delivering a pulse of high-flow oxygen during the end expiratory pause at a rate of about 30 liters-per-minute (L/min) and delivering the pulse of high-flow oxygen during the end expiratory pause for less than 0.5 seconds. The method may further include measuring a peak nasal pressure and a peak oxygen flow and synthesizing a second respiratory signal. The second respiratory signal may correspond to the peak nasal pressure and the peak oxygen flow, and may be normalized for the patient. The method may additionally include determining the patient's breathing pattern, rate, or frequency.

CPC Classifications

A61M 16/024 A61M 16/0003 A61M 16/0051 A61M 16/0672 A61M 16/202 A61M 2016/0027 A61M 2016/0033 A61M 2202/0007 A61M 2202/0216 A61M 2205/183 A61M 2205/3327 A61M 2205/3334 A61M 2205/502 A61M 2205/581 A61M 2205/583 A61M 2210/0618 A61M 2230/005 A61M 2230/42

Filing Date

2024-09-25

Application No.

18896846

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Named provisions

System To Monitor Respiration During Sedation With Nasal Pressure And Oxygen Flow

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Classification

Agency
USPTO
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260083926A1

Who this affects

Applies to
Healthcare providers Medical device makers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Patient Monitoring Medical Device Development
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Medical Devices Patient Safety

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