D Peckham, A Watson, K Pollard, C Etherington, S.P Conway 

Slides:



Advertisements
Similar presentations
2015 Alzheimer's disease facts and figures Alzheimer's & Dementia: The Journal of the Alzheimer's Association Volume 11, Issue 3, Pages (March.
Advertisements

How surgeons can find information online? Martin Hewitt International Journal of Surgery Volume 5, Issue 6, Pages (December 2007) DOI: /j.ijsu
Long-term non-invasive ventilation in cystic fibrosis — Experience over two decades William G. Flight, Jonathan Shaw, Susan Johnson, A. Kevin Webb, Andrew.
Use of the insulin pump in treat cystic fibrosis related diabetes Dana S. Hardin, Julie Rice, Mark Rice, Randall Rosenblatt Journal of Cystic Fibrosis.
Volume 46, Issue 3, Pages (March 2007)
ARFI and transient elastography for characterization of cystic fibrosis related liver disease: First longitudinal follow-up data in adult patients  Thomas.
Cheryl Cameron, Mark W. Lodes, William M. Gershan 
Effects of ivacaftor on severely ill patients with cystic fibrosis carrying a G551D mutation  Helge Hebestreit, Annette Sauer-Heilborn, Rainald Fischer,
The prevalence of “risky behaviour” in adults with cystic fibrosis
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation  Kris De Boeck, Anne Munck, Seth Walker, Albert Faro,
P. Whitaker, N. Shaw, J. Gooi, C. Etherington, S. Conway, D. Peckham 
The immediate effect of musculoskeletal physiotherapy techniques and massage on pain and ease of breathing in adults with cystic fibrosis  Annemarie Lee,
Development, validation, and implementation of a questionnaire assessing disease knowledge and understanding in adult cystic fibrosis patients  Karen.
William G. Flight, Jonathan Shaw, Susan Johnson, A
ARFI and transient elastography for characterization of cystic fibrosis related liver disease: First longitudinal follow-up data in adult patients  Thomas.
How does heart rate recovery after sub-maximal exercise correlate with maximal exercise testing in children with CF?  Sarah P. Cohen, David M. Orenstein 
H. Grasemann, E. Tullis, F. Ratjen  Journal of Cystic Fibrosis 
Megan R. Nelson, Craig R. Adamski, Audrey Tluczek 
Measures of body habitus are associated with lung function in adults with cystic fibrosis: A population-based study  Doug L. Forrester, Alan J. Knox,
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation  Kris De Boeck, Anne Munck, Seth Walker, Albert Faro,
Ludger Dorlöchter, Malin Carlsson, Edda J. Olafsdottir, Ola D
Laura Viviani, Baroukh M. Assael, Eitan Kerem 
Cirrhosis and other liver disease in cystic fibrosis
John Widger, Sarath Ranganathan, Philip J. Robinson 
The ease of breathing test tracks clinical changes in cystic fibrosis
Controlled clinical trials in cystic fibrosis — are we doing better?
Feasibility of using pedometers to measure daily step counts in cystic fibrosis and an assessment of its responsiveness to changes in health state  Bradley.
Anju Anand, Elizabeth Tullis, Anne Stephenson, Preyanka Abhyankar 
Claire J. Tipping, Rebecca L. Scholes, Narelle S. Cox 
The predictive potential of the sweat chloride test in cystic fibrosis patients with the G551D mutation  Verena I. Seliger, David Rodman, Fredrick Van.
Hypertonic saline and recombinant human DNase: a randomised cross-over pilot study in patients with cystic fibrosis  Manfred Ballmann, Horst von der Hardt 
A.H. Gifford  Journal of Cystic Fibrosis 
Treatment of resistant distal intestinal obstruction syndrome with a modified antegrade continence enema procedure  I.J. Clifton, A.M. Morton, N.S. Ambrose,
Economic effects of an eradication protocol for first appearance of Pseudomonas aeruginosa in cystic fibrosis patients: 1995 vs. 2009  Yolanda P. Lillquist,
Cystic fibrosis related diabetes in an extremely young patient
Predicting hypoxia in cystic fibrosis patients during exposure to high altitudes  Wolfgang Kamin, Birthe Fleck, Dirk-Mathias Rose, Oliver Thews, Wolfgang.
Antonia V. Bennett, Donald L. Patrick, James F. Lymp, Todd C
Molecular analysis of changes in Pseudomonas aeruginosa load during treatment of a pulmonary exacerbation in cystic fibrosis  D.W. Reid, R. Latham, I.L.
Correlation of sweat chloride and percent predicted FEV1 in cystic fibrosis patients treated with ivacaftor  Meredith C. Fidler, Jack Beusmans, Paul Panorchan,
Different opinions of physicians on the importance of measures to prevent acquisition of Pseudomonas aeruginosa from the environment  Gratiana Steinkamp,
Depression and anxiety in adolescents and adults with cystic fibrosis in the UK: A cross- sectional study  Alistair J.A. Duff, Janice Abbott, Carolyn Cowperthwaite,
Ultrasound and magnetic resonance imaging assessment of joint disease in symptomatic patients with cystic fibrosis arthropathy  G. Fitch, K. Williams,
Anastasios Lekkas, Khin M. Gyi, Margaret E. Hodson 
Narelle S. Cox, Jennifer Follett, Karen O. McKay 
Novel concepts in evaluating antimicrobial therapy for bacterial lung infections in patients with cystic fibrosis  Geraint B. Rogers, Lucas R. Hoffman,
Effect of ivacaftor in patients with advanced cystic fibrosis and a G551D-CFTR mutation: Safety and efficacy in an expanded access program in the United.
Nutritional decline in cystic fibrosis related diabetes: The effect of intensive nutritional intervention  H. White, K. Pollard, C. Etherington, I. Clifton,
Trends in pathogens colonising the respiratory tract of adult patients with cystic fibrosis, 1985–2005  F.A. Millar, N.J. Simmonds, M.E. Hodson  Journal.
F. Vermeulen, P. Lebecque, K. De Boeck, T. Leal 
Lung clearance index during hospital admission in school-age children with cystic fibrosis  Liam Welsh, Christopher Nesci, Haily Tran, Marisol Tomai,
H. White, A.M. Morton, S.P. Conway, D.G. Peckham 
J.E. Spahr, R.B. Love, M. Francois, K. Radford, K.C. Meyer 
Reviewer Acknowledgment
Bigna M. Keller, Carmen Casaulta Aebischer, Richard Kraemer, Martin H
Serum-surfactant SP-D correlates inversely to lung function in cystic fibrosis  Hanne Vebert Olesen, Uffe Holmskov, Peter Oluf Schiøtz, Grith Lykke Sørensen 
D.F. Waterhouse, A.M. McLaughlin, C.G. Gallagher 
Effect of nebulized colistin sulphate and colistin sulphomethate on lung function in patients with cystic fibrosis: a pilot study  E.M. Westerman, P.P.H.
Experience using centralized spirometry in the phase 2 randomized, placebo-controlled, double-blind trial of denufosol in patients with mild to moderate.
The role of respiratory viruses in adult patients with cystic fibrosis receiving intravenous antibiotics for a pulmonary exacerbation  C. Etherington,
‘Peeling paint’ dermatitis as a presenting sign of cystic fibrosis
Beta-lactam allergy in adults with cystic fibrosis
Predictors of non-referral of patients with cystic fibrosisfor lung transplant evaluation in the United States  Kathleen J. Ramos, Bradley S. Quon, Kevin.
Cheryl Cameron, Mark W. Lodes, William M. Gershan 
Lutz Goldbeck, Sven Zerrer, Tim G. Schmitz  Journal of Cystic Fibrosis 
Khin M. Gyi, Margaret E. Hodson, Magdi Y. Yacoub 
David Adeboyeku, Sandra Scott, Margaret E. Hodson 
A safe protocol for rapid desensitization in patients with cystic fibrosis and antibiotic hypersensitivity  Henry J. Legere, Ross I. Palis, Tito Rodriguez.
Population pharmacokinetics of tobramycin administered thrice daily and once daily in children and adults with cystic fibrosis  D.J. Touw, A.J. Knox,
Cystic fibrosis and pregnancy in the modern era: A case control study
H. White, A.M. Morton, D.G. Peckham, S.P. Conway 
Presentation transcript:

Predictors of desaturation during formal hypoxic challenge in adult patients with cystic fibrosis  D Peckham, A Watson, K Pollard, C Etherington, S.P Conway  Journal of Cystic Fibrosis  Volume 1, Issue 4, Pages 281-286 (December 2002) DOI: 10.1016/S1569-1993(02)00100-5

Fig. 1 This figure demonstrates the distribution of FEV1 according to the various subgroups of the PaO2 taken at the end of a formal pre-flight hypoxic challenge. Journal of Cystic Fibrosis 2002 1, 281-286DOI: (10.1016/S1569-1993(02)00100-5)

Fig. 2 Comparison between baseline PaO2 and level of hypoxia following in flight assessment. Journal of Cystic Fibrosis 2002 1, 281-286DOI: (10.1016/S1569-1993(02)00100-5)

Fig. 3 This figure demonstrates the distribution of the N score according to the various subgroups of the PaO2 (kPa) taken at the end of a formal pre-flight hypoxic challenge. Journal of Cystic Fibrosis 2002 1, 281-286DOI: (10.1016/S1569-1993(02)00100-5)