Longitudinal monitoring of disease progression in children with mild CF using hyperpolarised gas MRI and LCI

Laurie Smith (Sheffield, United Kingdom), Laurie Smith, Ina Aldag, Paul Hughes, Felix Horn, Helen Marshall, Graham Norquay, Guilhem Collier, David Hughes, Chris Taylor, Alex Horsley, Jim Wild

Source: International Congress 2016 – The best is yet to come in terms of lung function
Session: The best is yet to come in terms of lung function
Session type: Oral Presentation
Number: 284
Disease area: Paediatric lung diseases

Congress or journal article abstractSlide presentation

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
Laurie Smith (Sheffield, United Kingdom), Laurie Smith, Ina Aldag, Paul Hughes, Felix Horn, Helen Marshall, Graham Norquay, Guilhem Collier, David Hughes, Chris Taylor, Alex Horsley, Jim Wild. Longitudinal monitoring of disease progression in children with mild CF using hyperpolarised gas MRI and LCI. Eur Respir J 2016; 48: Suppl. 60, 284

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Comparison of phase III slope analysis from MBW with hyperpolarised gas MRI in children with mild CF
Source: International Congress 2016 – The future of lung function is beginning now
Year: 2016

Oxygen-enhanced MR (OE-MR): Correlation to CT Brody score in cystic fibrosis patients
Source: International Congress 2016 – Cystic fibrosis: monitoring and management
Year: 2016



Detection of early-stage lung disease in cystic fibrosis; comparing the sensitivity of 3He and 1H MRI, CT and LCI
Source: International Congress 2014 – Cystic fibrosis: assessment and treatment
Year: 2014


HRCT in the evaluation of functional decay in IPF
Source: International Congress 2016 – IPF: from pathogenesis to treatment I
Year: 2016

Lung functions and imaging characteristics of the patients with combined pulmonary fibrosis and emphysema
Source: International Congress 2015 – IPF: clinical aspects
Year: 2015

Differences in regional pulmonary function between children with cystic fibrosis and healthy children determined by electrical impedance tomography
Source: Annual Congress 2013 –Cystic fibrosis: physiotherapy, exercise and lung function in adults and children
Year: 2013

MBW and MRI as sensitive markers of stable CF lung disease and at exacerbation in children and adolescents
Source: International Congress 2015 – Cystic fibrosis: assessment and treatment
Year: 2015


Longitudinal assessment of Lung Clearance Index as a marker of disease progression in a cohort of children with cystic fibrosis and normal spirometry
Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology
Year: 2020




Does the lung clearance index track with disease progression in early childhood?
Source: International Congress 2015 – Cystic fibrosis: physiology, biomarkers, microbiology and miscellaneous
Year: 2015


LATE-BREAKING ABSTRACT: Early following up of gas trapping with computed tomography during normal breathing in infant with Cystic Fibrosis
Source: International Congress 2015 – Cystic fibrosis: microbiology, immunology and assessment
Year: 2015

Single-breath washout and association with structural lung changes in children with cystic fibrosis
Source: International Congress 2016 – Advanced lung function testing in childhood respiratory and sleep disease
Year: 2016


Lung clearance Index changes over time among patients with cystic fibrosis
Source: International Congress 2015 – New findings in paediatric respiratory physiology
Year: 2015


Disease progression in IPF assessed using pulmonary function tests and functional respiratory imaging (FRI) – A pilot study
Source: International Congress 2014 – COPD and PAH related imaging
Year: 2014


Longitudinal monitoring of lung microstructure with HP gas diffusion-weighted MRI in mild cystic fibrosis children
Source: International Congress 2017 – Cystic fibrosis: monitoring and biomarkers
Year: 2017



Exercise testing and multiple breath washout as markers of lung disease among patients with cystic fibrosis
Source: International Congress 2015 – Cystic fibrosis: physiology, biomarkers, microbiology and miscellaneous
Year: 2015

Imaging cystic fibrosis lung disease with MRI
Source: Eur Respir Monogr 2015; 70: 188-206
Year: 2015


Ability of lung clearance index to track changes in a routine clinical CF setting
Source: International Congress 2015 – Paediatric respiratory physiology
Year: 2015

A new gold standard for assessing CT in early CF lung disease?
Source: International Congress 2014 – Cystic fibrosis: assessment and treatment
Year: 2014

Feasibility of unsedated lung MRI in preschoolers with Cystic fibrosis – a comparison to lung function.
Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology
Year: 2020




Annual change of LCI among patients with cystic fibrosis
Source: International Congress 2016 – Cystic fibrosis: monitoring and management
Year: 2016