Your browser doesn't support javascript.
loading
Utility and validity of dynamic chest radiography in cystic fibrosis (dynamic CF): an observational, non-controlled, non-randomised, single-centre, prospective study.
FitzMaurice, Thomas Simon; McNamara, Paul Stephen; Nazareth, Dilip; McCann, Caroline; Bedi, Ram; Shaw, Matthew; Walshaw, Martin.
Affiliation
  • FitzMaurice TS; Adult CF Unit, Liverpool Heart and Chest Hospital NHS Trust, Liverpool, UK thomas.fitzmaurice@lhch.nhs.uk.
  • McNamara PS; Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
  • Nazareth D; Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
  • McCann C; Institute in the Park, Alder Hey Children's Hospital, Liverpool, UK.
  • Bedi R; Adult CF Unit, Liverpool Heart and Chest Hospital NHS Trust, Liverpool, UK.
  • Shaw M; Institute of Infection and Global Health, University of Liverpool, Liverpool, UK.
  • Walshaw M; Department of Radiology, Liverpool Heart and Chest Hospital NHS Trust, Liverpool, UK.
BMJ Open Respir Res ; 7(1)2020 03.
Article in En | MEDLINE | ID: mdl-32217535
ABSTRACT

INTRODUCTION:

Dynamic chest radiography (DCR) uses novel, low-dose radiographic technology to capture images of the thoracic cavity while in motion. Pulmonary function testing is important in cystic fibrosis (CF). The tolerability, rapid acquisition and lower radiation and cost compared with CT imaging may make DCR a useful adjunct to current standards of care. METHODS AND

ANALYSIS:

This is an observational, non-controlled, non-randomised, single-centre, prospective study. This study is conducted at the Liverpool Heart and Chest Hospital (LHCH) adult CF unit. Participants are adults with CF. This study reviews DCR taken during routine CF Annual Review (n=150), validates DCR-derived lung volumes against whole body plethysmography (n=20) and examines DCR at the start and end of pulmonary exacerbations of CF (n=20). The primary objectives of this study are to examine if DCR provides lung function information that correlates with PFT, and lung volumes that correlate whole body plethysmography. ETHICS AND DISSEMINATION This study has received the following approvals HRA REC (11 December 2019) and LHCH R&I (11 October 2019). Results are made available to people with CF, the funders and other researchers. Processed, anonymised data are available from the research team on request. TRIAL REGISTRATION NUMBER ISRCTN 64994816.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Radiography, Thoracic / Cystic Fibrosis / Lung Type of study: Clinical_trials / Observational_studies Limits: Humans Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Radiography, Thoracic / Cystic Fibrosis / Lung Type of study: Clinical_trials / Observational_studies Limits: Humans Language: En Year: 2020 Type: Article