An evaluation strategy for potential QTc prolongation with chronic azithromycin therapy in cystic fibrosis  Patrick John Lenehan, Craig M. Schramm, Melanie.

Slides:



Advertisements
Similar presentations
J.H.K. Hull, W. Tucker, A.G. Hatrick, R.K. Knight, T.B.L. Ho 
Advertisements

Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
Effects of ivacaftor on severely ill patients with cystic fibrosis carrying a G551D mutation  Helge Hebestreit, Annette Sauer-Heilborn, Rainald Fischer,
Cystic fibrosis-related bone disease in children: Examination of peripheral quantitative computed tomography (pQCT) data  Denise S.K. Brookes, Julie N.
Zhumin Zhang, Suzanne M. Shoff, HuiChuan J. Lai 
Platelet proinflammatory activity in clinically stable patients with CF starts in early childhood  Alexander Sturm, Helge Hebestreit, Corinne Koenig,
Zachary M. Sellers, Lori McGlocklin, Andrea Brasch 
Dynamics of serum procalcitonin in patients after major neurosurgery
Towards an individualized protocol for workload increments in cardiopulmonary exercise testing in children and adolescents with cystic fibrosis  H.J.
HbA1c as a screening tool for cystic fibrosis related diabetes
R. Roberts, L. Speight, J. Lee, L. George, R. I. Ketchell, D. Lau, J
How does heart rate recovery after sub-maximal exercise correlate with maximal exercise testing in children with CF?  Sarah P. Cohen, David M. Orenstein 
J.H.K. Hull, W. Tucker, A.G. Hatrick, R.K. Knight, T.B.L. Ho 
Single high-dose oral vitamin D3 (stoss) therapy — A solution to vitamin D deficiency in children with cystic fibrosis?  Darren Shepherd, Yvonne Belessis,
Megan R. Nelson, Craig R. Adamski, Audrey Tluczek 
Urinary incontinence in 9���16��year olds with cystic fibrosis compared to other respiratory conditions and a normal group  W.J. Browne, C.J. Wood, M.
Statistical limitations of percent ideal body weight as measure for nutritional failure in patients with cystic fibrosis  T.O. Hirche, H. Hirche, S. Jungblut,
A longitudinal analysis of chronic MRSA and Pseudomonas aeruginosa co-infection in cystic fibrosis: A single-center study  Maret L. Maliniak, Arlene A.
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
Delayed publication of clinical trials in cystic fibrosis
Increased serum concentration of G-CSF in cystic fibrosis patients with chronic Pseudomonas aeruginosa pneumonia  P.Ø. Jensen, C. Moser, A. Kharazmi,
Adherence to nebulised therapies in adolescents with cystic fibrosis is best on week- days during school term-time  Rosemary Ball, Kevin W. Southern, Pamela.
Long-term azitromycin treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection; an observational cohort study  Christine Rønne.
Anju Anand, Elizabeth Tullis, Anne Stephenson, Preyanka Abhyankar 
D. Stevens, P.J. Oades, N. Armstrong, C.A. Williams 
Claire J. Tipping, Rebecca L. Scholes, Narelle S. Cox 
Cystic fibrosis mortality trend in Italy from 1970 to 2011
Influence of digital clubbing on oxygen saturation measurements by pulse-oximetry in cystic fibrosis patients  Filip Van Ginderdeuren, Karlien Van Cauwelaert,
Evaluation of salt supplementation in CF infants
A treatment evaluator tool to monitor the real-world effectiveness of inhaled aztreonam lysine in cystic fibrosis  Barry J Plant, Damian G Downey, Joe.
Gerd Döring, Patrick Flume, Harry Heijerman, J. Stuart Elborn 
Vitamin A and lung function in CF
Exercise-induced hypoxemia and cardiac arrhythmia in cystic fibrosis
A.H. Gifford  Journal of Cystic Fibrosis 
Economic effects of an eradication protocol for first appearance of Pseudomonas aeruginosa in cystic fibrosis patients: 1995 vs. 2009  Yolanda P. Lillquist,
Tregony Simoneau, Gregory S. Sawicki, Carly E. Milliren, Henry A
M. Al-Aloul, M. Jackson, G. Bell, M. Ledson, M. Walshaw 
Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India  Shivaram S. Shastri, Madhulika Kabra, Sushil.
Maximal daily dose of pancreatic enzyme replacement therapy in infants with cystic fibrosis: A reconsideration  Drucy Borowitz, Daniel Gelfond, Karen.
Saliva cyclic GMP increases during anaesthesia
Novel concepts in evaluating antimicrobial therapy for bacterial lung infections in patients with cystic fibrosis  Geraint B. Rogers, Lucas R. Hoffman,
Australian epidemic strain pseudomonas (AES-1) declines further in a cohort segregated cystic fibrosis clinic  Amanda L. Griffiths, Danielle F. Wurzel,
Gender differences in treatment adherence among youth with cystic fibrosis: Development of a new questionnaire  Joän M. Patterson, Melanie Wall, Jerica.
Higher risk of hospitalization among females with cystic fibrosis
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 
A new method of sweat testing: the CF Quantum®sweat test
Ruth H. Keogh, Sanja Stanojevic  Journal of Cystic Fibrosis 
V. Thompson, N. Mayer-Hamblett, M. Kloster, D. Bilton, P.A. Flume 
Determining presence of lung disease in young children with cystic fibrosis: Lung clearance index, oxygen saturation and cough frequency  E.M. Bakker,
Diabetes mellitus and survival in cystic fibrosis patients after lung transplantation  Markus Hofer, Christoph Schmid, Christian Benden, Rudolf Speich,
Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
J.E. Spahr, R.B. Love, M. Francois, K. Radford, K.C. Meyer 
The impact of switching to the new global lung function initiative equations on spirometry results in the UK CF Registry  Sanja Stanojevic, Janet Stocks,
Serum-surfactant SP-D correlates inversely to lung function in cystic fibrosis  Hanne Vebert Olesen, Uffe Holmskov, Peter Oluf Schiøtz, Grith Lykke Sørensen 
Neuromuscular monitoring in intensive care patients: milliamperage requirements for supramaximal stimulation†  N.J.N. Harper, R. Greer, D. Conway  British.
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
Exercise-induced hypoxemia and cardiac arrhythmia in cystic fibrosis
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 
Elisabeth P. Dellon, Margaret W. Leigh, James R. Yankaskas, Terry L
Changing thresholds and incidence of antibiotic treatment of cystic fibrosis pulmonary exacerbations, 1995–2005  Donald R. VanDevanter, Eric P. Elkin,
Improved early diagnosis of Pseudomonas aeruginosa by real-time PCR to prevent chronic colonisation in a paediatric cystic fibrosis population  Elaine.
Absence of a gender gap in survival
Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience  C.R.
Presentation transcript:

An evaluation strategy for potential QTc prolongation with chronic azithromycin therapy in cystic fibrosis  Patrick John Lenehan, Craig M. Schramm, Melanie Sue Collins  Journal of Cystic Fibrosis  Volume 15, Issue 2, Pages 192-195 (March 2016) DOI: 10.1016/j.jcf.2015.11.012 Copyright © 2015 European Cystic Fibrosis Society. Terms and Conditions

Fig. 1 Correlation between QTc intervals obtained before (QTc pre) and after (QTc post) starting chronic azithromycin (AZI) therapy. (A) QTc post values were directly related to QTc pre values (R2=0.25), with mean±S.E.M. slope 0.43±0.15 (p=0.0075) and intercept 236±61ms (p=0.0007) compared to the line of identity (dashed line). (B) Bland Altman plot of the difference between paired post and pre QTc values versus the average of the paired pre and post values. Note the absence of any fixed (i.e., vertical displacement) or proportional (i.e., slope) difference of azithromycin on the QTc interval. Journal of Cystic Fibrosis 2016 15, 192-195DOI: (10.1016/j.jcf.2015.11.012) Copyright © 2015 European Cystic Fibrosis Society. Terms and Conditions

Fig. 2 Influence of age on change in QTc with azithromycin therapy. (A) The ΔQTc was greater in patients >12years of age (n=11) compared to patients <12years of age (n=16). p=0.046 by Mann–Whitney U test. (B) ΔQTc increased significantly in adolescent male patients (n=7; *p=0.047 vs. 0 by Wilcoxon Signed Rank testing), as compared to child male (n=11), adolescent female (n=4), and child female patients (n=5). Box plots depict median values (central lines), interquartile ranges (shaded boxes), 10th and 90th percentiles (bars), and outlying points. p=0.043 by Kruskal–Wallis test. Journal of Cystic Fibrosis 2016 15, 192-195DOI: (10.1016/j.jcf.2015.11.012) Copyright © 2015 European Cystic Fibrosis Society. Terms and Conditions