Skip to main content
 

Main menu

  • Home
  • Content
    • Current Issue
    • Editor's Commentary
    • Coming Next Month
    • Archives
    • Most-Read Papers of 2021
  • Authors
    • Author Guidelines
    • Submit a Manuscript
  • Reviewers
    • Reviewer Information
    • Create Reviewer Account
    • Reviewer Guidelines: Original Research
    • Reviewer Guidelines: Reviews
    • Appreciation of Reviewers
  • CRCE
    • Through the Journal
    • JournalCasts
    • AARC University
    • PowerPoint Template
  • Open Forum
    • 2022 Call for Abstracts
    • 2021 Abstracts
    • Previous Open Forums
  • Podcast
    • English
    • Español
    • Portugûes
    • 国语
  • Videos
    • Video Abstracts
    • Author Interviews
    • Highlighted Articles
    • The Journal

User menu

  • Subscribe
  • My alerts
  • Log in

Search

  • Advanced search
American Association for Respiratory Care
  • Subscribe
  • My alerts
  • Log in
American Association for Respiratory Care

Advanced Search

  • Home
  • Content
    • Current Issue
    • Editor's Commentary
    • Coming Next Month
    • Archives
    • Most-Read Papers of 2021
  • Authors
    • Author Guidelines
    • Submit a Manuscript
  • Reviewers
    • Reviewer Information
    • Create Reviewer Account
    • Reviewer Guidelines: Original Research
    • Reviewer Guidelines: Reviews
    • Appreciation of Reviewers
  • CRCE
    • Through the Journal
    • JournalCasts
    • AARC University
    • PowerPoint Template
  • Open Forum
    • 2022 Call for Abstracts
    • 2021 Abstracts
    • Previous Open Forums
  • Podcast
    • English
    • Español
    • Portugûes
    • 国语
  • Videos
    • Video Abstracts
    • Author Interviews
    • Highlighted Articles
    • The Journal
  • Twitter
  • Facebook
  • YouTube
Research ArticleOriginal Research

The Value of Measuring Inspiratory Capacity in Subjects With Cystic Fibrosis

Daphna Vilozni, Adi Dagan, Moran Lavie, Ifat Sarouk, Bat-El Bar-Aluma, Moshe Ashkenazi, Sarina Levy Mendelovich, Yael Betzalel and Ori Efrati
Respiratory Care August 2018, 63 (8) 981-987; DOI: https://doi.org/10.4187/respcare.05920
Daphna Vilozni
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: [email protected]
Adi Dagan
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Moran Lavie
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Ifat Sarouk
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Bat-El Bar-Aluma
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Moshe Ashkenazi
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Sarina Levy Mendelovich
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Yael Betzalel
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Ori Efrati
Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Israel.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • References
  • Info & Metrics
  • PDF
Loading

References

  1. 1.↵
    1. Kreda SM,
    2. Davis CW,
    3. Rose MC
    . CFTR, mucins, and mucus obstruction in cystic fibrosis. Cold Spring Harb Perspect Med 2012;2(9):a009589.
    OpenUrlAbstract/FREE Full Text
  2. 2.↵
    1. Puchelle E,
    2. Bajolet O,
    3. Abély M
    . Airway mucus in cystic fibrosis. Paediatr Respir Rev 2002;3(2):115–119.
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Horsley A,
    2. Siddiqui S
    . Putting lung function and physiology into perspective: cystic fibrosis in adults. Respirology 2015;20(1):33–45.
    OpenUrlPubMed
  4. 4.↵
    1. Kerem E,
    2. Viviani L,
    3. Zolin A,
    4. MacNeill S,
    5. Hatziagorou E,
    6. Ellemunter H,
    7. et al
    . ECFS Patient Registry Steering Group. Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS patient registry. Eur Respir J 2014;43(1):125–33.
    OpenUrlAbstract/FREE Full Text
  5. 5.↵
    1. Kerem E,
    2. Reisman J,
    3. Corey M,
    4. Canny GJ,
    5. Levison H
    . Prediction of mortality in patients with cystic fibrosis. N Engl J Med 1992;326(18):1187–1191.
    OpenUrlCrossRefPubMedWeb of Science
  6. 6.↵
    1. Vilozni D,
    2. Lavie M,
    3. Ofek M,
    4. Sarouk I,
    5. Bar-Aluma BE,
    6. Dagan A,
    7. et al
    . Consequences of expiratory flow limitation at rest in subjects with cystic fibrosis. Ann Am Thorac Soc 2016;13(6):825–832.
    OpenUrl
  7. 7.↵
    1. Casanova C,
    2. Cote C,
    3. de Torres JP,
    4. Aguirre-Jaime A,
    5. Marin JM,
    6. Pinto-Plata V,
    7. Celli BR
    . Inspiratory-to-total lung capacity ratio predicts mortality in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2005;171(6):591–597.
    OpenUrlCrossRefPubMedWeb of Science
  8. 8.
    1. Tantucci C,
    2. Duguet A,
    3. Similowski T,
    4. Zelter M,
    5. Derenne JP,
    6. Milic-Emili J
    . Effect of salbutamol on dynamic hyperinflation in chronic obstructive pulmonary disease patients. Eur Respir J 1998;12(4):799–804.
    OpenUrlAbstract
  9. 9.
    1. O'Donnell DE
    . Breathlessness in patients with chronic airflow limitation. Mechanisms and management. Chest 1994;106(3):904–912.
    OpenUrlCrossRefPubMedWeb of Science
  10. 10.↵
    1. Diaz O,
    2. Villafranca C,
    3. Ghezzo H,
    4. Borzone G,
    5. Leiva A,
    6. Milic-Emil J,
    7. Lisboa C
    . Role of inspiratory capacity on exercise tolerance in COPD patients with and without expiratory flow limitation at rest. Eur Respir J 2000;16(2):269–275.
    OpenUrlAbstract/FREE Full Text
  11. 11.↵
    1. Reddy RM,
    2. Guntupalli KK
    . Review of ventilatory techniques to optimize mechanical ventilation in acute exacerbation of chronic obstructive pulmonary disease Int J Chron Obstruct Pulmon Dis 2007;2(4):441–452.
    OpenUrlPubMed
  12. 12.↵
    1. Calverley PMA
    . Dynamic hyperinflation: is it worth measuring. Proc Am Thoracic Soc 2006;3(3):239–244.
    OpenUrl
  13. 13.↵
    1. Boni E,
    2. Corda L,
    3. Franchini D,
    4. Chiroli P,
    5. Damiani GP,
    6. Pini L,
    7. et al
    . Volume effect and exertional dyspnoea after bronchodilator in patients with COPD with and without expiratory flow limitation at rest. Thorax 2002;57(6):528–532.
    OpenUrlAbstract/FREE Full Text
  14. 14.↵
    1. Vilozni D,
    2. Lavie M,
    3. Ofek M,
    4. Sarouk I,
    5. Efrati O
    . Cough characteristics and FVC maneuver in cystic fibrosis. Respir Care 2014;59(12):1912–1917.
    OpenUrlAbstract/FREE Full Text
  15. 15.↵
    1. Miller MR,
    2. Hankinson J,
    3. Brusasco V,
    4. Burgos F,
    5. Casaburi R,
    6. Coates A,
    7. et al
    . ATS/ERS Task Force. Standardization of spirometry. Eur Respir J 2005;26(2):319–338.
    OpenUrlAbstract/FREE Full Text
  16. 16.↵
    1. Quanjer PH,
    2. Stanojevic S,
    3. Cole TJ,
    4. Baur X,
    5. Hall GL,
    6. Culver BH,
    7. et al
    . ERS Global Lung Function Initiative. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations. Eur Respir J 2012;40(6):1324–1343.
    OpenUrlAbstract/FREE Full Text
  17. 17.↵
    1. Cole TJ,
    2. Stanojevic S,
    3. Stocks J,
    4. Coates AL,
    5. Hankinson JL,
    6. Wade AM
    . Age- and size-related reference ranges: a case study of spirometry through childhood and adulthood. Statist Med 2009;28(5):880–898.
    OpenUrlCrossRef
  18. 18.↵
    1. Wanger J,
    2. Clausen JL,
    3. Coates A,
    4. Pedersen OF,
    5. Brusasco V,
    6. Burgos F,
    7. et al
    . Standardization of the measurement of lung volumes. Eur Respir J 2005;26(3):511–522.
    OpenUrlAbstract/FREE Full Text
  19. 19.↵
    1. Polgar G,
    2. Promadhat V
    . Pulmonary function testing in children: techniques and standards. Philadelphia, W. B. Saunders, 1971.
  20. 20.↵
    1. Quanjer PH,
    2. Tammeling GJ,
    3. Cotes JE,
    4. Pedersen OF,
    5. Peslin R,
    6. Yernault JC
    . Lung volumes and forced ventilatory flows. Report Working Party Standardization of Lung Function Tests, European Community for Steel and Coal. Official Statement of the European Respiratory Society. Eur Respir J 1993;6(Suppl 16):5–40.
    OpenUrlFREE Full Text
  21. 21.↵
    1. Ries AL,
    2. Sosa G,
    3. Prewitt L,
    4. Friedman PJ,
    5. Harwood IR
    . Restricted pulmonary function in cystic fibrosis. Chest 1988;94(3):575–579.
    OpenUrlCrossRefPubMedWeb of Science
  22. 22.
    1. Holland AE,
    2. Denehy L,
    3. Wilson JW
    . Does expiratory flow limitation predict chronic dyspnoea in adults with cystic fibrosis? Eur Respir J 2006;28(1):96–101.
    OpenUrlAbstract/FREE Full Text
  23. 23.↵
    1. Rosenthal M
    . Annual assessment spirometry, plethysmography, and gas transfer in cystic fibrosis: do they predict death or transplantation. Pediatr Pulmonol 2008;43(10):945–952.
    OpenUrlCrossRefPubMedWeb of Science
  24. 24.↵
    1. Davis SD,
    2. Fordham LA,
    3. Brody AS,
    4. Noah TL,
    5. Retsch-Bogart GZ,
    6. Qaqish BF,
    7. et al
    . Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis. Am J Respir Crit Care Med 2007;175(9):943–950.
    OpenUrlCrossRefPubMedWeb of Science
  25. 25.↵
    1. Ratjen F,
    2. Döring G
    . Cystic fibrosis. Lancet 2003;361(9358):681–689.
    OpenUrlCrossRefPubMedWeb of Science
  26. 26.↵
    1. Diwakar A,
    2. Adam RJ,
    3. Michalski AS,
    4. Tamegnon MM,
    5. Fischer AJ,
    6. Launspach JL,
    7. et al
    . Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis. Laryngoscope 2015;125(10):2398–2404.
    OpenUrlCrossRefPubMed
  27. 27.↵
    1. Harris RS,
    2. Hess DR,
    3. Venegas JG
    . An objective analysis of the pressure–volume curve in the acute respiratory distress syndrome. Am J Respir Crit Care Med 2000;161(2 part 1):432–439.
    OpenUrlCrossRefPubMedWeb of Science
  28. 28.↵
    1. Brochard L
    . What is a pressure–volume curve? Crit Care 2006;10(4):156.
    OpenUrlPubMed
  29. 29.↵
    1. Vilozni D,
    2. Lavie M,
    3. Ofek M,
    4. Sarouk I,
    5. Bar-Aluma BE,
    6. Dagan A,
    7. et al
    . Consequences of expiratory flow limitation at rest in subjects with cystic fibrosis. Ann Am Thorac Soc 2016;13(6):825–832.
    OpenUrl
  30. 30.↵
    1. O'Donnell DE
    . Ventilatory limitations in chronic obstructive pulmonary disease. Med Sci Sports Exerc 2001;33(Suppl 7):S647–S655.
    OpenUrlCrossRefPubMedWeb of Science
  31. 31.↵
    1. Hirche TO,
    2. Knoop C,
    3. Hebestreit H,
    4. Shimmin D,
    5. Solé A,
    6. Elborn JS,
    7. et al
    . Practical guidelines: lung transplantation in patients with cystic fibrosis. Pulm Med 2014;2014:621342.
    OpenUrlPubMed
PreviousNext
Back to top

In this issue

Respiratory Care: 63 (8)
Respiratory Care
Vol. 63, Issue 8
1 Aug 2018
  • Table of Contents
  • Table of Contents (PDF)
  • Cover (PDF)
  • Index by author

 

Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on American Association for Respiratory Care.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
The Value of Measuring Inspiratory Capacity in Subjects With Cystic Fibrosis
(Your Name) has sent you a message from American Association for Respiratory Care
(Your Name) thought you would like to see the American Association for Respiratory Care web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
The Value of Measuring Inspiratory Capacity in Subjects With Cystic Fibrosis
Daphna Vilozni, Adi Dagan, Moran Lavie, Ifat Sarouk, Bat-El Bar-Aluma, Moshe Ashkenazi, Sarina Levy Mendelovich, Yael Betzalel, Ori Efrati
Respiratory Care Aug 2018, 63 (8) 981-987; DOI: 10.4187/respcare.05920

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero

Share
The Value of Measuring Inspiratory Capacity in Subjects With Cystic Fibrosis
Daphna Vilozni, Adi Dagan, Moran Lavie, Ifat Sarouk, Bat-El Bar-Aluma, Moshe Ashkenazi, Sarina Levy Mendelovich, Yael Betzalel, Ori Efrati
Respiratory Care Aug 2018, 63 (8) 981-987; DOI: 10.4187/respcare.05920
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Results
    • Discussion
    • Conclusions
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • References
  • PDF

Related Articles

Cited By...

Keywords

  • spirometry
  • cystic fibrosis
  • lung function
  • lung volumes
  • FEV1
  • trapped air

Info For

  • Subscribers
  • Institutions
  • Advertisers

About Us

  • About the Journal
  • Editorial Board
  • Reprints/Permissions

AARC

  • Membership
  • Meetings
  • Clinical Practice Guidelines

More

  • Contact Us
  • RSS
American Association for Respiratory Care

Print ISSN: 0020-1324        Online ISSN: 1943-3654

© Daedalus Enterprises, Inc.

Powered by HighWire