Already a subscriber? 
MADCAD.com Free Trial
Sign up for a 3 day free trial to explore the MADCAD.com interface, PLUS access the
2009 International Building Code to see how it all works.
If you like to setup a quick demo, let us know at support@madcad.com
or +1 800.798.9296 and we will be happy to schedule a webinar for you.
Security check
Please login to your personal account to use this feature.
Please login to your authorized staff account to use this feature.
Are you sure you want to empty the cart?
IEEE Standard for Health Informatics -- Device Interoperability -- Part 10429: Personal Health Device Communication -- Device Specialization - Spirometry (Published), 2022
- IEEE Std 11073‐10429™‐2022 Front cover
- Important Notices and Disclaimers Concerning IEEE Standards Documents
- Participants
- Introduction
- Contents
- 1. Overview [Go to Page]
- 1.1 Scope
- 1.2 Purpose
- 1.3 Word usage
- 1.4 Context
- 2. Normative references
- 3. Definitions, acronyms, and abbreviations [Go to Page]
- 3.1 Definitions
- 3.2 Acronyms and abbreviations
- 4. Introduction to ISO/IEEE 11073 personal health devices [Go to Page]
- 4.1 General
- 4.2 Introduction to IEEE 11073-20601 modeling constructs [Go to Page]
- 4.2.1 General
- 4.2.2 Domain information model
- 4.2.3 Service model
- 4.2.4 Communication model
- 4.2.5 Implementing the models
- 4.3 Compliance with other standards
- 5. Spirometry device concepts and modalities [Go to Page]
- 5.1 General
- 5.2 Spirometry tests
- 5.3 Home spirometry measures [Go to Page]
- 5.3.1 Forced expiratory volume in 1 s (FEV1)
- 5.3.2 Peak expiratory flow (PEF)
- 5.4 Common spirometry measures [Go to Page]
- 5.4.1 Forced vital capacity
- 5.4.2 Slow vital capacity (SVC)
- 5.4.3 Forced expiratory volume in six seconds (FEV6)
- 5.5 Spirometry measures used for children [Go to Page]
- 5.5.1 Forced expiratory volume in 0.5 s (FEV0.5)
- 5.5.2 Forced expiratory volume in 0.75 s (FEV0.75).
- 5.6 Spirometry measures normalized to FVC, SVC, and FEV6 [Go to Page]
- 5.6.1 Ratio of forced expiratory volume in 1 s/FVC (FEV1/FVC)
- 5.6.2 Ratio of forced expiratory volume in 1 s/SVC (FEV1/SVC)
- 5.6.3 Ratio of Forced Expiratory Volumes in 1 s and 6 s (FEV1/FEV6)
- 5.6.4 Ratio of forced expiratory volume in 0.5 s/FVC (FEV0.5/FVC)
- 5.6.5 Ratio of forced expiratory volume in 0.75 s/FVC (FEV0.75/FVC)
- 5.7 Spirometry measures related to forced expiratory flow [Go to Page]
- 5.7.1 Forced expiratory flow at 25 % of FVC (FEF25)
- 5.7.2 Forced expiratory flow at 50 % of FVC (FEF50)
- 5.7.3 Forced expiratory flow at 75 % of FVC (FEF75)
- 5.7.4 Forced expiratory flow between 25 % and 75 % of FVC (FEF25–75)
- 5.8 Spirometry measures related to forced inspiration [Go to Page]
- 5.8.1 Forced inspiratory vital capacity (FIVC)
- 5.8.2 Forced inspiratory volume in 1 s (FIV1)
- 5.8.3 Forced inspiratory flow at 25 % of FIVC (FIF25)
- 5.8.4 Forced inspiratory flow at 50 % of FIVC (FIF50)
- 5.8.5 Forced inspiratory flow at 75 % of FIVC (FIF75)
- 5.8.6 Peak inspiratory flow (PIF)
- 5.9 Spirometry measures related to volume during unforced breathing [Go to Page]
- 5.9.1 Tidal volume (TV)
- 5.9.2 Inspiratory capacity measured from tidal volume (IC)
- 5.9.3 Expiratory reserve volume (ERV)
- 5.9.4 Inspiratory reserve volume (IRV)
- 5.9.5 Inspiratory vital capacity measured from maximal exhalation (IVC)
- 5.10 Spirometry measures related to BTPS correction, calibration verification/check, and technical factors [Go to Page]
- 5.10.1 Body temperature-pressure-saturated (BTPS) correction factor
- 5.10.2 Ambient air pressure
- 5.10.3 Ambient room temperature
- 5.10.4 Patient-immediate ambient relative humidity
- 5.10.5 Date/Time of last calibration verification/check session
- 5.10.6 Last calibration verification/check session, number of calibration verifications
- 5.10.7 Last calibration verification/check session, volumes measured
- 5.10.8 Last calibration verification/check session, number of failed calibration verifications
- 5.10.9 History of calibration verification/check sessions
- 5.10.10 Testing position
- 5.10.11 Nose clips
- 5.10.12 Bronchodilator
- 5.11 Spirometry measures related to test quality assessment [Go to Page]
- 5.11.1 Forced expiratory time (FET)
- 5.11.2 Back-extrapolated volume (BEV, EVOL, Vext)
- 5.11.3 Achievement of end of forced expiration (EOFE)
- 5.11.4 FIVC-FVC
- 5.11.5 Point at which expiratory flow ceases
- 5.11.6 Individual FVC maneuver acceptability
- 5.11.7 Number of acceptable FVC maneuvers
- 5.11.8 Between-maneuver FVC reproducibility
- 5.11.9 Between-maneuver FEV1 reproducibility
- 5.11.10 FVC quality grade
- 5.11.11 FEV1 quality grade
- 5.12 Spirometry waveform measures [Go to Page]
- 5.12.1 Volume-time waveform (VT)
- 5.12.2 Flow-time waveform (FT)
- 5.13 Interpretive spirometry measures [Go to Page]
- 5.13.1 Reference equations [Go to Page]
- 5.13.1.1 Assigned sex at birth
- 5.13.1.2 Gender Identity
- 5.13.1.3 Age
- 5.13.1.4 Height
- 5.13.1.5 Weight
- 5.13.1.6 Body mass index
- 5.13.1.7 GLI-2012 racial/ethnic group
- 5.13.1.8 NHANES-III racial/ethnic group
- 5.13.2 LLN FEV1
- 5.13.3 LLN FVC
- 5.13.4 LLN FEV6
- 5.13.5 LLN SVC
- 5.13.6 LLN FEV0.5
- 5.13.7 LLN FEV0.75
- 5.13.8 LLN FEV1/FVC
- 5.13.9 LLN FEV1/FEV6
- 5.13.10 LLN FEV1/SVC
- 5.13.11 Z-score FEV1
- 5.13.12 Z-score FVC
- 5.13.13 Z-score FEV6
- 5.13.14 Z-score SVC
- 5.13.15 Z-score FEV0.5
- 5.13.16 Z-score FEV0.75
- 5.13.17 Z-score FEV1/FVC
- 5.13.18 Z-score FEV1/FEV6
- 5.13.19 Z-Score FEV1/SVC
- 5.13.20 Percent predicted FEV1
- 5.13.21 Percent predicted FVC
- 5.13.22 Percent predicted FEV6
- 5.13.23 Percent predicted SVC
- 5.13.24 Percent predicted FEV0.5
- 5.13.25 Percent predicted FEV0.75
- 5.14 Graphical representation of some spirometry measures [Go to Page]
- 5.14.1 Spirometry volumes
- 5.14.2 Spirometry volume-time curve
- 5.14.3 Prediction equations and Z-score
- 5.14.4 Back extrapolated volume (BEV)
- 6. Spirometer domain information model [Go to Page]
- 6.1 Overview
- 6.2 Class extensions
- 6.3 Object instance hierarchy
- 6.4 Types of configuration [Go to Page]
- 6.4.1 General
- 6.4.2 Standard configuration
- 6.4.3 Extended configuration
- 6.4.4 Spirometry sessions [Go to Page]
- 6.4.4.1 Observation-Id and Observation-Ref-List attributes
- 6.4.4.2 Measurement references
- 6.4.4.3 Measurement time stamping
- 6.4.4.4 Measurement quality analyses
- 6.4.4.5 Spirometry agent workflows and measurement delivery
- 6.4.4.6 Spirometry measurements
- 6.4.4.7 Behavior on incomplete sessions
- 7. Spirometer service model [Go to Page]
- 7.1 General
- 7.2 Object access services
- 7.3 Object access event report services
- 8. Spirometer communication model [Go to Page]
- 8.1 Overview
- 8.2 Communications characteristics
- 8.3 Association procedure [Go to Page]
- 8.3.1 General
- 8.3.2 Agent procedure—association request
- 9. Operating procedure [Go to Page]
- 9.1 General
- 9.2 GET Spirometer MDS attributes
- 9.3 Measurement data transmission
- 9.4 Time synchronization
- 10. Test associations
- 11. Conformance [Go to Page]
- 11.1 Applicability
- 11.2 Conformance specification
- 11.3 Levels of conformance [Go to Page]
- 11.3.1 General
- 11.3.2 Conformance level 1: Base conformance
- 11.3.3 Conformance level 2: Extended nomenclature (ASN.1 and/or ISO/IEEE Std 11073-10101)
- 11.4 Implementation conformance statements [Go to Page]
- 11.4.1 General format
- 11.4.2 General implementation conformance statement
- 11.4.3 DIM MOC implementation conformance statement
- 11.4.4 MOC attribute ICS
- 11.4.5 MOC notification implementation conformance statement
- 11.4.6 MOC nomenclature conformance statement
- Annex A (informative) Bibliography
- Annex B (normative) Any additional ASN.1 definitions [Go to Page]
- B.1 Observation-Id data type
- B.2 Observation-Ref-List data type
- Annex C (normative) Systematic names for nomenclature [Go to Page]
- C.1 Nomenclature, data dictionary, and codes for spirometry [Go to Page]
- C.1.1 Introduction
- C.1.2 Base concepts
- C.1.3 First set of differentiating criteria [Go to Page]
- C.1.3.1 Semantic link "type:"
- C.1.3.2 Semantic link "has direction:"
- C.1.3.3 Semantic link "of form"
- C.1.4 Second set of differentiating criteria [Go to Page]
- C.1.4.1 Semantic link "concerns:"
- C.1.5 Third set of differentiating criteria [Go to Page]
- C.1.5.1 Semantic link "procedure used:"
- C.1.6 Code table
- Annex D (normative) Allocation of identifiers
- Annex E (informative) Message sequence examples
- Annex F (informative) Protocol data unit examples [Go to Page]
- F.1 General
- F.2 Association information exchange [Go to Page]
- F.2.1 General
- F.2.2 Extended configuration [Go to Page]
- F.2.2.1 General
- F.2.2.2 Association request
- F.2.2.3 Association response
- F.2.3 Previously known extended configuration [Go to Page]
- F.2.3.1 General
- F.2.3.2 Association request
- F.2.3.3 Association response
- F.3 Configuration information exchange [Go to Page]
- F.3.1 General
- F.3.2 Extended configuration [Go to Page]
- F.3.2.1 General
- F.3.2.2 Remote operation invoke event report configuration
- F.3.2.3 Remote operation response event report configuration
- F.3.3 Known configuration
- F.4 GET MDS attributes service [Go to Page]
- F.4.1.1 General
- F.4.1.2 Get all medical device system attributes request
- F.4.1.3 Get response with all MDS attributes
- F.5 Data reporting [Go to Page]
- F.5.1 Session Start
- F.5.2 Response to confirmed measurement data transmission
- F.5.3 Settings
- F.5.4 Examining the Time Stamps
- F.5.5 Maneuver Subsession Start
- F.5.6 The RTSA Transmissions
- F.5.7 Maneuver Summary Measurements
- F.5.8 Maneuver Subsession Stop
- F.5.9 Second Maneuver Subsession
- F.5.10 Session Summary Measurements and Session Stop Indicator
- F.6 Disassociation [Go to Page]
- F.6.1 Association release request
- F.6.2 Association release response [Go to Page]
