US2023213368A1PendingUtilityA1

Portable spirometer

Assignee: HEALTHUP SPOLKA AKCYJNAPriority: Oct 20, 2016Filed: Dec 29, 2022Published: Jul 6, 2023
Est. expiryOct 20, 2036(~10.2 yrs left)· nominal 20-yr term from priority
G01F 1/6845A61B 5/0205A61B 5/087G01F 1/44G01F 1/68A61B 5/0002A61B 5/02438A61B 5/14552A61B 2560/0214A61B 2560/0252A61B 2560/0257A61B 2562/0271A61B 2562/028A61B 2562/029
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Claims

Abstract

The invention relates to a spirometer (1) comprising a MEMS-based thermal fluid flow sensor (13, 13.1, 13.2) for generating a signal in response to a fluid flow generated during inhalation or exhalation; and a microcontroller (14) for calculating the fluid flow from the signal generated by the flow sensor (13, 13.1, 13.2). The spirometer (1) may be connected to other devices, such as a smartphone or a personal computer or any other computing unit which is adapted to collect, store, analyse, exchange and/or display data. The invention further describes the use of the spirometer (1) in measuring a user's lung performance and/or monitoring it over time. Furthermore, the spirometer (1) may be provided in a system together with an air quality measurement device for determining the air quality at a location of interest; and a computing unit for collecting, analysing and correlating the user's lung performance data obtained from the spirometer (1) with the air quality data, and optionally geolocalisation data of said location.

Claims

exact text as granted — not AI-modified
1 . A portable electronic spirometer ( 1 ) comprising:
 (a) a tubular mouthpiece ( 2 ) with
 a proximal opening ( 3 ) for insertion into the mouth of a user, 
 a distal opening ( 4 ), 
 a main fluid channel ( 5 ) extending between the proximal opening ( 3 ) and the distal opening ( 4 ), 
 a first lateral opening ( 6 ), 
 a second lateral opening ( 7 ) positioned at a longitudinal distance to the first lateral opening ( 6 ), and 
 a flow restrictor ( 8 ) positioned in the main fluid channel ( 5 ) between the first and the second lateral opening ( 6  and  7 ); and 
   (b) a main body ( 9 ) with
 a first fluid opening ( 10 ) connectible with the first lateral opening ( 6 ) of the mouthpiece ( 2 ), 
 a second fluid opening ( 11 ) connectible with the second lateral opening ( 7 ) of the mouthpiece ( 2 ), 
 a bypass fluid channel ( 12 ) extending between the first and the second fluid opening ( 10  and  11 ), 
 a MEMS-based thermal fluid flow sensor ( 13 ) positioned at the bypass fluid channel ( 12 ) for generating a signal in response to the fluid flow in the bypass fluid channel ( 12 ), and 
 a microcontroller ( 14 ) connected with the fluid flow sensor ( 13 ) for calculating the fluid flow from the signal generated by the flow sensor ( 13 ). 
   
     
     
         2 - 15 . (canceled) 
     
     
         16 . A method for measuring a health parameter of a human subject selected from:
 (c) a forced vital capacity,   (d) a forced expiratory volume,   (e) a peak expiratory flow,   (f) a forced expiratory flow (FEF),   (g) a maximum voluntary ventilation (MVV),   (h) a mean expiratory flow,   (i) a slow vital capacity (SVC),   (j) a functional residual capacity (FRC),   (k) an expiratory reserve volume (ERV),   (l) a maximum speed of expiration,   (m) a forced inspiratory volume (FIV),   (n) a forced inspiratory vital capacity (FIVC),   (o) a peak inspiratory flow (PIF),   
       or any combination of these, the method comprising a step of the human subject performing a breathing manoeuvre through the spirometer ( 1 ) of  claim 1 . 
     
     
         17 . A system comprising:
 the portable electronic spirometer ( 1 ) of  claim 1 , and   a first air quality measurement device comprising communication means adapted for data exchange with the portable electronic spirometer ( 1 ) and/or with a separate computing unit, and equipped with one or more air quality sensors, preferably selected from the group consisting of humidity sensors, temperature sensors, atmospheric pressure sensors, MOS-type gas sensors (metal-oxide-semiconductor), airborne-particles sensors, pollen sensors, ozone (O 3 ) sensors, nitrogen dioxide (NO 2 ) sensors, sulfur dioxide (SO 2 ) sensors and carbon monoxide (CO) sensors, for determining determine the air quality at the location of the first air quality measurement device, and optionally   a separate computing unit adapted to collect and analyse at least the data obtained from the spirometer ( 1 ) of  claim 1  and from the first air quality measurement device.   
     
     
         18 - 23 . (canceled) 
     
     
         24 . A method for measuring one or more health parameters of a human subject selected from
 a) a forced vital capacity (FVC),   b) a forced expiratory volume (FEV),   c) a peak expiratory flow (PEF),   d) a forced expiratory flow (FEF),   e) a maximum voluntary ventilation (MVV),   f) a mean expiratory flow,   g) a slow vital capacity (SVC),   h) a functional residual capacity (FRC),   i) an expiratory reserve volume (ERV),   j) a maximum speed of expiration,   k) a forced inspiratory volume (FIV),   l) a forced inspiratory vital capacity (FIVC),   m) a peak inspiratory flow (PIF),   or any combination of these, the method comprising a step of the human subject performing a breathing manoeuvre through the spirometer ( 1 ) of  claim 1 ;   wherein the one or more health parameters are correlated with air quality data, and optionally geolocalisation data, derived from the system of  claim 1 .

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