Forced Spirometry and Related Tests
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New Spirometry Interpretation Algorithm Primary Care Respiratory Alliance of Canada Approach
Critical Appraisal New spirometry interpretation algorithm Primary Care Respiratory Alliance of Canada approach Anthony D. D’Urzo MD MSc CCFP FCFP Itamar Tamari MD CCFP FCFP Jacques Bouchard MD Reuven Jhirad MD CCFP FCFP Pieter Jugovic MD MSc CCFP Clinical question Is there a need for a new spirometry interpretation algorithm that contains decision-making criteria consistent with current guidelines on asthma1 and chronic obstructive pulmonary disease (COPD)2 diagnosis? Using spirometry to distinguish between COPD and asthma Office spirometry provides valuable information about the relationship between flow and volume in relation to lung function and can be useful for diagnosing common conditions such as asthma and COPD.1,2 Mechanical abnor- malities of the respiratory system can be classified as either obstructive (flow-related) or restrictive (volume-related) ventilatory defects; obstructive defects are much more common in clinical practice. The relationship between flow and volume is described well by BOTTOM LINE • An algorithm commonly promoted in the ratio of the forced expiratory volume in 1 second (FEV1) to the forced vital capacity (FVC). These measurements can be easily obtained with a primary care is limited by its focus on using simple office spirometer during a forced expiratory maneuver. The ratio changes in forced expiratory volume in 1 second (FEV ) to distinguish asthma from of FEV1 to FVC can be useful to identify obstructive, restrictive, and com- 1 bined (obstructive-restrictive) defects, but it is important to recognize that chronic obstructive pulmonary disease total lung capacity, a more sophisticated measurement (and not the FVC), (COPD). The new algorithm consolidates is the best measurement to confirm a diagnosis of pulmonary restriction.3 current spirometric concepts that are consistent with both asthma and COPD Traditionally an FEV1-FVC ratio below 0.70 has been used to define a pure obstructive defect if the FVC is within normal limits. -
Pulse Oximetry Is Essential in Home Management of Elderly COVID-19 Patients Md
55 Bangladesh J Otorhinolaryngol 2020; 26(1): 55-67 Case Report Pulse Oximetry is Essential in Home Management of Elderly COVID-19 Patients Md. Abdullah Al Harun1, Mohammad Murad Hossain2, Mohammad Anwarul Bari3, Nazmul Ahsan Siddiqi Rubel4, Mohammad Enamul Karim5, Nadia Siddiquee6, Mohammad Delwar Hossain7, Farhana Sultana8, Ahmmad Taous9, AKM Monwarul Islam10, Salma Khatun11, AHM Afzalul Haque12, Mohammad Mahbub-Ul Haque13, KM Mamun Murshed14, Syed Atiqullah15, Abu Mohammad Ekramul Hoque16, Mohammad Abdullah17 Abstract Background: Coronavirus disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Corona Virus-2 (SARS-CoV-2) is in Pandemic form and has affected people of 215 countries. It produces symptoms like fever, cough, shortness of breath, sore throat, headache, loss of taste, smell or appetite and many other rare symptoms. But the most important symptom is shortness of breath due to hypoxia. In a normal individual oxygen saturation (SpO2) is at least 95% and patient feels shortness of breath when SpO2 falls below 90% with some exception. SARS-CoV-2, a newly emergent coronavirus has the peculiarity to produce silent hypoxia, meaning SpO2< 90% or less like 80%, 70%, 60% without shortness of breath. Silent hypoxia can be diagnosed by monitoring SpO2 with pulse oximeter. For management of COVID-19, early symptoms like fever & cough, SpO2 should be monitored by pulse oximeter, followed by immediate correction of hypoxia by O2 supplementation and prophylactic oral or injectable anticoagulant to prevent thromboembolism and thus death rate can be reduced. Case summary: A 72-year-old man presented with the complaints of fever and headache followed by cough, fatigue, anorexia, loss of taste and appetite in next few days but no shortness of breath. -
Standardisation of Spirometry
Eur Respir J 2005; 26: 319–338 DOI: 10.1183/09031936.05.00034805 CopyrightßERS Journals Ltd 2005 SERIES ‘‘ATS/ERS TASK FORCE: STANDARDISATION OF LUNG FUNCTION TESTING’’ Edited by V. Brusasco, R. Crapo and G. Viegi Number 2 in this Series Standardisation of spirometry M.R. Miller, J. Hankinson, V. Brusasco, F. Burgos, R. Casaburi, A. Coates, R. Crapo, P. Enright, C.P.M. van der Grinten, P. Gustafsson, R. Jensen, D.C. Johnson, N. MacIntyre, R. McKay, D. Navajas, O.F. Pedersen, R. Pellegrino, G. Viegi and J. Wanger CONTENTS AFFILIATIONS Background ............................................................... 320 For affiliations, please see Acknowledgements section FEV1 and FVC manoeuvre .................................................... 321 Definitions . 321 CORRESPONDENCE Equipment . 321 V. Brusasco Requirements . 321 Internal Medicine University of Genoa Display . 321 V.le Benedetto XV, 6 Validation . 322 I-16132 Genova Quality control . 322 Italy Quality control for volume-measuring devices . 322 Fax: 39 103537690 E-mail: [email protected] Quality control for flow-measuring devices . 323 Test procedure . 323 Received: Within-manoeuvre evaluation . 324 March 23 2005 Start of test criteria. 324 Accepted after revision: April 05 2005 End of test criteria . 324 Additional criteria . 324 Summary of acceptable blow criteria . 325 Between-manoeuvre evaluation . 325 Manoeuvre repeatability . 325 Maximum number of manoeuvres . 326 Test result selection . 326 Other derived indices . 326 FEVt .................................................................. 326 Standardisation of FEV1 for expired volume, FEV1/FVC and FEV1/VC.................... 326 FEF25–75% .............................................................. 326 PEF.................................................................. 326 Maximal expiratory flow–volume loops . 326 Definitions. 326 Equipment . 327 Test procedure . 327 Within- and between-manoeuvre evaluation . 327 Flow–volume loop examples. 327 Reversibility testing . 327 Method . -
Spirometry (Adult) Guideline
Document Number # QH-GDL-386:2012 Spirometry (Adult) Respiratory Science Custodian/Review Officer: 1. Purpose Chief Allied Health Officer This guideline provides recommendations regarding best practice to support high quality spirometry practice Version no: 1.0 throughout Queensland Health facilities. Applicable To: 2. Scope All Health Practitioners performing adult This guideline provides information for all health spirometry practitioners who perform adult spirometry as part of their clinical duties. Approval Date: 26/11/2012 This guideline provides the minimum requirements for obtaining acceptable and repeatable pre- and post- Effective Date: 26/11/2012 bronchodilator (reversibility) spirometric data using both volume and flow-measuring devices. Next Review Date: 26/11/2013 3. Related documents Authority: This guideline is primarily based on the following Chair – State-wide Clinical Measurements Network documents taken from the series “ATS/ERS Task Force: Standardisation of Lung Function Testing” Approving Officer General considerations for lung function testing 1 Chief Allied Health Officer (2005). Standardisation of spirometry (2005). 2 References from alternate sources of information have Supersedes: Nil been identified in this document. Key Words: spirometry, spiro, respiratory, Policy and Standard/s: measure, spirogram, spirometric, bronchodilator, flow-volume loop, peak Informed Decision-making in Healthcare (QH-POL- flow 346:2011) 3 Accreditation References: Procedures, Guidelines, Protocols EQuIP and other criteria and standards Australian Guidelines for the prevention and control of infection in healthcare (CD33:2010) 4 2005 American Thoracic Society and European Respiratory Society (ATS/ERS) guidelines 1, 2 Version No.: 1.0; Effective From: 26 November 2012 Page 1 of 31 Printed copies are uncontrolled Queensland Health: Spriometry (Adult) Queensland Health Paediatric Spirometry Guideline Forms and templates Nil 4. -
Pulmonary Function Test (PFT)
Pulmonary Function Test (PFT) St. James Mercy Hospital Respiratory Therapy, 1st Floor 411 Canisteo St. Hornell, NY 14843 607-324- 8159 To schedule an appointment: 607-324-2879 To fax to scheduling: 607-324-8221 What is pulmonary function testing and why is it done? Pulmonary function tests (also called PFTs or lung function tests) help determine how well your lungs are functioning. The results of these tests tell your physician how much air your lungs can hold, how quickly you can move air into and out of your lungs, and how well your lungs are able to use oxygen and get rid of carbon dioxide. The tests help your physician determine if you have a lung disease, help provide a measure of how significant your lung disease is, and can show how well the treatment for your lung disease is working. How is a pulmonary function test done? Pulmonary function testing is usually done by a specially trained respiratory therapist or technician. For most pulmonary function tests, you will be asked to wear a nose clip to make sure that no air passes through your nose during the test. You will be asked to breathe into a mouthpiece that is connected to a machine called a spirometer. The technician may encourage you to breathe deeply during parts of the test to get the best results. Following all of the technician's instructions will help provide the most accurate results. How do I prepare for my test? You should not eat a heavy meal just before this test. You should not smoke for six hours before the test. -
Effect of Inspiratory Flow Rate on Bronchomotor Tone in Normal and Asthmatic Subjects
Thorax: first published as 10.1136/thx.39.2.86 on 1 February 1984. Downloaded from Thorax 1984;39:86-92 Effect of inspiratory flow rate on bronchomotor tone in normal and asthmatic subjects W HIDA, M ARAI, C SHINDOH, Y-N LIU, H SASAKI, T TAKISHIMA From the First Department ofInternal Medicine, Tohoku University School of Medicine, Sendai, Japan ABSTRACT The effect of the inspiratory flow rate during deep inspiration on the regulation of bronchomotor tone was studied in nine normal and 22 asthmatic subjects. Changes in bronchial tone were assessed by respiratory resistance measured by an oscillation method. In normal subjects with bronchoconstriction induced by methacholine a rapid deep inspiration reduced respiratory resistance more than a slow deep inspiration. Asthmatic subjects with spontaneous airway narrowing showed an increase in respiratory resistance after deep inspiration that was greater after rapid than after slow deep inspiration. On the other hand, in asthmatics with methacholine induced bronchoconstriction, bronchodilatation occurred after deep inspiration and this was also greater after rapid than after slow deep inspiration. Lignocaine inhalation attenuated both bronchoconstriction and bronchodilatation induced by both slow and rapid deep inspiration. These results suggest that the effects of deep inspiration are mediated at least in part via receptors in the airways. It is suggested that in asthmatic patients with spontaneous broncho- constriction irritant receptor activity will be increased in proportion to the speed of inspiration. After methacholine induced bronchoconstriction stretch receptor activity is likely to behave in a similar fashion, leading to an opposite effect. http://thorax.bmj.com/ A deep inspiration has been reported to produce a carbachol induced bronchoconstriction, and they transient decrease in airway calibre in some asthma- suggested that this might have been due to greater tic subjects.' 2 In contrast, in the presence of phar- stimulation of stretch receptors at higher flows. -
Global Strategy for Asthma Management and Prevention, 2019. Available From
DISTRIBUTE OR COPY NOT DO MATERIAL- COPYRIGHTED ASTHMA MANAGEMENT AND PREVENTION GLOBAL STRATEGY FOR Updated 2019 9 Global Strategy for Asthma Management and Prevention (2019 update) DISTRIBUTE OR COPY NOT DO The reader acknowledges that this reportMATERIAL- is intended as an evidence-based asthma management strategy, for the use of health professionals and policy-makers. It is based, to the best of our knowledge, on current best evidence and medical knowledge and practice at the date of publication. When assessing and treating patients, health professionals are strongly advised to use their own professional judgment, and to take into account local or national regulations and guidelines. GINA cannot be held liable or responsible for inappropriate healthcare associated with the use of this document, including any use which is not in accordance with applicable local or national regulations or COPYRIGHTEDguidelines. This document should be cited as: Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention, 2019. Available from: www.ginasthma.org 1 Table of contents Tables and figures ............................................................................................................................................................... 5 Preface ................................................................................................................................................................................. 7 Members of GINA committees (2018) ................................................................................................................................ -
Effect of Chronic Bronchitis on Changes in Pulmonary Function Caused by Irradiation Ofthe Lungs
Thorax: first published as 10.1136/thx.20.4.303 on 1 July 1965. Downloaded from Thorax (1965), 20, 303. Effect of chronic bronchitis on changes in pulmonary function caused by irradiation of the lungs B. I. HOFFBRAND,1 P. M. S. GILLAM,' AND P. J. D. HEAF' From the Chest Department, University College Hospital, London In a previous paper (Gillam, Heaf, Hoffbrand, and Group 3: A history of chronic cough with Hilton, 1964) it was shown that, contrary to wide- sputum and recurrent chest infections or breath- spread opinion, the presence of co-existing chronic lessness or both. This group will be referred to as bronchitis does not interfere with the treatment of the severe bronchitic group. A subgroup 3a was bronchial carcinoma by radiotherapy. Patients derived from group 3 and consisted of those with severe chronic bronchitis can be given the patients in group 3 with a forced expiratory same dose of irradiation as those with mild volume in one second (F.E.V.j.0) of 1,250 ml. or bronchitis or with previously normal lungs. less. Group 3a thus consisted largely of those Survival after radiotherapy for bronchial carci- patients with the severest bronchitis of all. noma is not shortened by co-existing chronic Group 1 was similar to groups 2 and 3 in bronchitis. The incidence of exacerbations of respect of age, sex, previous lung resections, and bronchitis both during and after radiotherapy is radiotherapy received. Group 1, however, con- no more than might be expected in such a group tained a higher proportion of patients with more extensive and more anaplastic tumours. -
Hypoxaemia in Wheezy Infants After Bronchodilator Treatment
Arch Dis Child: first published as 10.1136/adc.62.10.997 on 1 October 1987. Downloaded from Archives of Disease in Childhood, 1987, 62, 997-1000 Hypoxaemia in wheezy infants after bronchodilator treatment A PRENDIVILLE, A ROSE, D L MAXWELL, AND M SILVERMAN Department of Paediatrics and Neonatal Medicine, and Division of Respiratory Medicine, Royal Postgraduate Medical School, London SUMMARY The response of the bronchi to nebulised salbutamol was measured in five recurrently wheezy infants. Changes in oxygenation (measured by pulse oximeter and transcutaneous P02 electrodes) and carbon dioxide (measured by transcutaneous PCO2 electrode) were recorded at the same time. Neither nebulised saline nor salbutamol caused any changes in the measurements of airway function. A significant drop in mean oxygen saturation of 2% and of transcutaneous oxygen tension of 1*3 kPa occurred after nebulised salbutamol. No significant change occurred in measurements of transcutaneous carbon dioxide tension, nor was there any significant change in any of these measurements after 2-5 ml of nebulised saline had been given as a control. These results suggest that nebulised salbutamol may cause significant hypoxaemia, in wheezy infants probably by inducing ventilation/perfusion disturbance. copyright. Nebulised selective P2-adrenoceptor agonists are All were wheezy at the time of testing. The still used in the treatment of wheezing in infants in reproducibility of the response to salbutamol was spite of the evidence that they may be ineffective. 1-3 assessed two weeks later in four of the infants. The Recently they have been shown to cause deteriora- fifth infant did not have a repeat study because he tion in peripheral airways function in this age developed severe bronchoconstriction after the group.4 Because the techniques used for measur- initial treatment with salbutamol. -
Human Respiratory Tract
Thorax: first published as 10.1136/thx.36.1.52 on 1 January 1981. Downloaded from Thorax, 1981, 36, 52-55 Deposition of pressurised aerosols in the human respiratory tract STEPHEN P NEWMAN, DEMETRI PAVIA, FOLKE MOREN, NOIRIN F SHEAHAN, AND STEWART W CLARKE From the Departments of Medical Physics and Thoracic Medicine, The Royal Free Hospital, London, and A B Draco, Lund, Sweden ABSTRACT Although the use of pressurised aerosol inhalers is widespread, little is known about the actual deposition of the aerosol in the respiratory tract, since this has previously been diffi- cult to measure. We have incorporated Teflon particles (mean diameter 2 Itm) with aerodynamic properties similar to those of bronchodilator drug crystals into pressurised aerosol canisters. Controlled inhalations by eight patients with obstructive airways disease showed that on average 8-8% of the dose was deposited in the lungs (3 0% in the alveoli and 5'8% on the conducting airways) and 80% in the mouth. These figures are in good agreement with previous indirect estimates of deposition based on metabolic studies. The remainder of the dose was either expired (1 0%) or deposited in the aerosol actuator (9P8%). This method should have wide application for measurement of deposition patterns under various conditions and for assessment of thera- peutic effects. Since the identification of specific 62 receptors in centages of the dose deposited on the conducting http://thorax.bmj.com/ the human respiratory tract,' selective sympatho- airways and in the alveoli are unknown. In this mimetic bronchodilator aerosols have been in paper we present the first direct measurement of common use for the treatment of asthma. -
COPD Diagnosis Related to Different Guidelines and Spirometry Techniques Lennart Nathell1,2, Madelene Nathell1, Per Malmberg3 and Kjell Larsson*4
Respiratory Research BioMed Central Review Open Access COPD diagnosis related to different guidelines and spirometry techniques Lennart Nathell1,2, Madelene Nathell1, Per Malmberg3 and Kjell Larsson*4 Address: 1Personal Injury Prevention Section, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden , 2Medical advisor, Deparment of Medical Affairs, Boehringer Ingelheim, Stockholm, 3National Institute for Working Life, Stockholm, Sweden and 4National Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden Email: Lennart Nathell - [email protected]; Madelene Nathell - [email protected]; Per Malmberg - [email protected]; Kjell Larsson* - [email protected] * Corresponding author Published: 4 December 2007 Received: 26 March 2007 Accepted: 4 December 2007 Respiratory Research 2007, 8:89 doi:10.1186/1465-9921-8-89 This article is available from: http://respiratory-research.com/content/8/1/89 © 2007 Nathell et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract The aim was to compare the diagnosis of COPD among smokers according to different international guidelines and to compare the outcome when using slow (SVC) and forced vital capacity (FVC). In order to find current smokers a questionnaire was sent to persons who had been on sick leave for more than two weeks. Those who smoked more than 8 cigarettes per day were invited to perform a spirometry. Totally 3,887 spirometries were performed. In this sample 10.2% fulfilled the NICE COPD-criteria, 14.0% the GOLD COPD-criteria and 21.7% the ERS COPD criteria. -
Drugs Used in Asthma and COPD
Drugs used in Asthma and COPD Objective : 1. Different types of drugs used for treatment of asthma 2. Differentiate between treatment and prophylactic therapy for asthma 3. Recognize the different types of bronchodilators regarding pharmacokinetics, pharmacodynamics, uses and side effects. 4. Identify the different anti-inflammatory drugs for asthma in respect to kinetics, dynamics, uses and side effects. § Addi-onal Notes § Important § Explanaon –Extra- For any correc-on, sugges-on or any useful informaon do not hesitate to contact us: [email protected] Bronchial Asthma It is a chronic inflammatory disorder of bronchial airways that result in airway obstruction in response to external stimuli (as pollen grains, cold air and tobacco smoke). • Asthma produces recurrent episodic attack of : Acute bronchoconstriction, Shortness of breath, Chest tightness, Wheezing, Rapid respiration, Cough. Symptoms • Symptoms can happen each time the airways are irritated by inhaled irritants or allergens. • Infection, Stress, Exercise (cold air), Pets, Seasonal changes, Emotional conditions, Some drugs as aspirin, β- blockers. Causes • Airway hyper-reactivity: abnormal sensitivity of the airways to any external stimuli. • Inflammation:↑ edema, swelling +↑ Thick mucus production. Characters • Bronchospasm (constriction of the bronchial smooth muscles). of airways Irritant receptors in upper airways. We want to enhance the Afferent nerves sympathetic or (sensory) inhibit the C-fiber receptors in lower airways. parasympathetic in this case. Airways Innervations Parasympathetic supply M3 receptors in smooth muscles and glands: Bronchoconstriction and Increase mucus secretion. Efferent nerves (motor nerves) No sympathetic supply but β2 receptors in smooth Afferent nerves (sensory) are stimulated by: muscles and glands: Bronchodilatation, Decrease mucus - Exogenous chemicals or irritants secretion.