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IN THE NAME OF GOD

This update focuses on areas pertinent to occupational pulmonary function testing, including the critical role of technicians, recommended changes in testing procedures, equipment validation, quality control, and infection control. It also covers indications for spirometry and technician training to ensure accurate results. Quality control measures, including hygiene and infection control, are discussed, along with equipment quality control.

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IN THE NAME OF GOD

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  1. IN THE NAME OF GOD SPIROMETRY UPDATE

  2. ATS 1994 Update • Areas pertinent to occupational pulmonary function testing • Critical role of technician in obtaining accurate results. • Recommended changes in testing procedure. • Equipment validation. • Quality control • Infection control and hygiene concerns

  3. Spirometric testing

  4. Lung Volumes and Capacities • Pulmonary volumes are measured • Pulmonary capacities are calculated

  5. INDICATIONS FOR SPIROMETRY

  6. Indications • Primary prevention • Pre-placement and fitness-for-duty examinations • Physical demands of a job (heavy manual labor, fire fighting); • Characteristics of respiratory use (prolonged use of negative-pressure mask under conditions of heavy physical exertion and/or heat stress - not required by OSHA); • Research and monitoring of health status in groups of workers.

  7. Indications • Secondary prevention • Medical surveillance programs – workers at risk of developing occupationally related respiratory disorders • Baseline and periodic evaluations • Mandated OSHA regulations (asbestos, cadmium, coke oven emissions or cotton dust) • Local mandated medical surveillance program • Component of workplace health promotion program

  8. Indications • Tertiary prevention • Clinical evaluation of symptomatic individuals • Restrictive • Obstructive • Combined ventilatory defects • Disability under Social Security Administration • Federal Coal Mine Health and Safety Act • Workers’ compensation setting

  9. Technician Training • From Preamble to OSHA Cotton Dust Standard, 1978: • “The key to reliable pulmonary function testing is the technician’s way of guiding the employee through a series of respiratory maneuvers; • The most important quality of a pulmonary function technician is the motivation to do the very best test on every employee;

  10. Technician Training • The technician must also be able to judge the degree of effort and cooperation of the subject; • Test results obtained by a technician who lacks these skills are not only useless, but also convey false information which could be harmful to the employee.”

  11. Quality Control • Technician needs to be aware of patient-related problems when performing FVC maneuvers • Submaximal effort • Leaks between lips and mouthpiece • Incomplete inspiration or expiration (prior to or during forced maneuvers) • Hesitation at start of the expiration

  12. Quality Control • Cough ( particularly within the first second of expiration) • Glottis closure • Obstruction of mouthpiece by the tongue • Vocalization during forced maneuver • Poor posture

  13. Problematic examples compared with well-performed maneuvers.

  14. Quality Control • Errors that inflate test results • Poor testing technique • Extra breath through nose • Slight submaximal expiratory effort • Accept/save curve with large hesitation, even when flagged by spirometer • Flow-type spirometer malfunctions during subject test • Inaccurate zeroing of sensor (performed before each expiration; or • Sensor characteristic change between expirations due to warming, deposition of mucous, or condensation of water vapor.

  15. Problematic examples compared with well-performed maneuvers.

  16. Quality Control • Error that reduce test results • Leaks in volume spirometer or breathing tubes • Reduce FVCs significantly but are not visible in spirograms until leak is very large • Checking for leaks at least daily in the calibrations check is essential

  17. Quality Control • Hygiene and Infection Control • Recommendation: • Direct contact • Potential for transmission of URI, enteric infections, and blood borne infections; • Most likely surface for contact are mouthpieces and immediate proximal surface of valves or tubing.

  18. Quality Control • Recommendation: • Indirect contact • Potential for transmission of TB, various viral infections, and possible opportunistic infections and nosocomial pneumonia; • Possible contamination of mouthpieces and proximal valves and tubing.

  19. Quality Control • Prevention • Proper hand washing and/or use of barrier device. • Use of disposable mouthpieces, nose clips, etc. • Spirometers using close circuit technique should be flushed at least five time over entire volume range. • Provide proper attention to environmental engineering control where TB or other diseases are spread by droplet nuclei might be encountered.

  20. Quality Control • Prevention • Take special precaution when testing patients with hemoptysis, open sores on oral mucosa, or bleeding gums. • Extra precautions with know transmissible infectious diseases. • Regular use of in-line filters (not mandated). • Manufacturers encouraged to design instrumentation that can be easily disassembled for disinfection.

  21. Quality Control • Equipment quality control • Volume • Must be checked at least daily with a 3-liter calibrated syringe. • Syringe accuracy • Calibration syringe must have an accuracy of at least 15 ml or at least 0.5% of full scale (15 ml for a 3-liter syringe. • Leak test • Volumetric spirometry systems must be checked daily.

  22. Quality Control • Equipment quality control • Linearity • Volume spirometers must have their calibration checked over the entire volume range quarterly (in one liter increments). • Time • Assessing mechanical recorder time scale accuracy with a stopwatch must be performed at least quarterly. • Other QA procedures • Calibration with physical standard (practice of using laboratory personnel as “known subjects”) • Adhere to ATS recommendations for computer software for spirometers.

  23. Quality Control • Equipment Quality Control

  24. Spirometry Parameters

  25. Spirometry Parameters • Forced Vital Capacity • FVC • Forced Expiratory Volume in One Second • FEV1 • Forced Expiratory Volume in One Second Expressed as a Percentage of the Forced Vital Capacity • FEV1/FVC % • Mean Forced Expiratory Flow during the Middle Half of the Forced Vital Capacity • FEF 25-75%

  26. FVC • Definition: • Defined as the maximal amount of air that can be exhaled forcefully after a maximal inspiration or the most air a person can blow out after taking the deepest possible breath.

  27. FVC - forced vital capacity • defines maximum volume of exchangeable air in lung (vital capacity) • forced expiratory breathing maneuver • requires muscular effort and some patient training • initial (healthy) FVC values approx 4 liters • slowly diminishes with normal aging • significantly reduced FVC suggests damage to lung parenchyma • restrictive lung disease (fibrosis) • loss of functional alveolar tissue (atelectasis) • FVC volume reduction trend over time (years) is key indicator • intra-subject variability factors • age • sex • height • ethnicity

  28. FVC • End of Test Criteria • The volume time curve show an obvious plateau • Plateau defined as no change in volume for at least one second. • Subject cannot or should not continue further exhalation. • The forced expiration is of reasonable duration.

  29. PEF

  30. FEV1 • Definition: • The volume of air exhaled during the first second of a forced expiratory maneuver. • normal FEV1 about 3 liters • FEV1 needs to be normalized to individual’s vital capacity (FVC)

  31. FEV1 • Steps for determination of the FEV1: • Determine Time Zero using the back extrapolation technique; • Measure over one second from Time Zero; • Draw a straight line up from the point where Time = one second and the point where the straight line intersects is the FEV1.

  32. PEF

  33. FEV1/FVC% • Definition: • The value expresses the volume of air the worker exhales in one second as a percent of the total volume of air that is exhaled. • Calculated by using largest valid FEV1 and largest FVC even if they are not from the same tracing. • Find largest valid FEV1 • Find largest valid FVC • Divide FEV1 by FVC • Multiply by 100 to obtain percentage.

  34. FEF25-75% • Definition: • The mean expiratory flow during the middle half of the FVC • More sensitive than FEV1. • Considerably more variability than FVC and FEV1. • ATS recommends only be considered after determining presence and clinical severity of impairment and should not be used to diagnosis disease in individual patients

  35. PEF - Peak Expiratory Flow rate • measures airflow limitations in large (central) airways • large airways are rate-limiting for airflow in healthy patients • large airway flow limitations important in asthma • PEF measurements recommended for asthma management • spirometry is recommended to help make the diagnosis of asthma • PEF not recommend to evaluate patients for COPD • cannot measure small airway airflow limitations • advantages of PEF tests • measurements within a minute (three short breaths) • uses simple, safe, hand-held devices that typical, costs $20 • disadvantages of PEF tests (compared to spirometry) • insensitive to obstruction of small airways (mild or early obstruction) • PEF is very dependent on patient effort (large intra-subject variability) • mechanical PEF meters are much less accurate than spirometers

  36. BTPS • Definition: • Gas (air) at: • Body Temperature (37°C) • Ambient Pressure (surrounding air pressure) • Saturated with water vapor (relative humidity = 100% as is the case in the lungs)

  37. BTPS • Spirometric test requiring conversion to BTPS • FEV1, FVC, and FEF25-75% all represent volume (volume per unit of time) – must be converted to BTPS. • FEV1/FVC% is ratio of volumes – doesnot have to be converted.

  38. Points to remember: Temperature Ambient temperatures should be recorded to within 1°C. Spirometric testing should only be done with ambient temperatures between 17° - 40°C. BTPS

  39. Reproducibility (Variability) • ATS recommends obtaining three (3) valid tracings with reproducible FVC’s and FEV1. • The two largest valid FVC’s are examined to determine there is no more than a .2 liter (200 ml) difference between them. • The two largest valid FEV1 are examined to determine there is no more than a .2 liter (200 ml) difference between them.

  40. Points to Remember • FVC • Convert answer to BTPS when needed. • FEV1 • Excessive variability and extrapolated volume must be calculated to determine if additional maneuvers are needed. • Convert to BTPS when needed. • FEV1 and FVC • Always use largest volume from an acceptable tracing to ensure maximal results.

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