Literature DB >> 26335955

Respiratory tract exacerbations revisited: ventilation, inflammation, perfusion, and structure (VIPS) monitoring to redefine treatment.

Harm A W M Tiddens1,2, Stephen M Stick3,4, Jim M Wild5, Pierluigi Ciet1,2, Geoffrey J M Parker6,7,8, Armin Koch9, Jens Vogel-Claussen10.   

Abstract

For cystic fibrosis (CF) patients older than 6 years there are convincing data that suggest respiratory tract exacerbations (RTE) play an important role in the progressive loss of functional lung tissue. There is a poor understanding of the pathobiology of RTE and whether specific treatment of RTE reduces lung damage in the long term. In addition, there are limited tools available to measure the various components of CF lung disease and responses to therapy. Therefore, in order to better understand the impact of RTE on CF lung disease we need to develop sensitive measures to characterize RTE and responses to treatment; and improve our understanding of structure-function changes during treatment of RTE. In this paper we review our current knowledge of the impact of RTE on the progression of lung disease and identify strategies to improve our understanding of the pathobiology of RTE. By improving our knowledge regarding RTE in CF we will be better positioned to develop approaches to treatment that are individualized and that can prevent permanent structural damage. We suggest the development of a ventilation, perfusion, inflammation and structure (VIPS)-MRI suite that supplies the clinician with data on ventilation, inflammation, perfusion, and structure in one MRI session. VIPS-MRI could be an important step to better understand the factors that contribute to and limit treatment efficacy of RTE.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  lung disease; magnetic resonance imaging; pathobiology

Mesh:

Substances:

Year:  2015        PMID: 26335955     DOI: 10.1002/ppul.23266

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  5 in total

1.  Diffusion weighted imaging in cystic fibrosis disease: beyond morphological imaging.

Authors:  Pierluigi Ciet; Goffredo Serra; Eleni Rosalina Andrinopoulou; Silvia Bertolo; Mirco Ros; Carlo Catalano; Stefano Colagrande; Harm A W M Tiddens; Giovanni Morana
Journal:  Eur Radiol       Date:  2016-02-12       Impact factor: 5.315

2.  Ultrashort Echo-Time Magnetic Resonance Imaging Is a Sensitive Method for the Evaluation of Early Cystic Fibrosis Lung Disease.

Authors:  David J Roach; Yannick Crémillieux; Robert J Fleck; Alan S Brody; Suraj D Serai; Rhonda D Szczesniak; Stephanie Kerlakian; John P Clancy; Jason C Woods
Journal:  Ann Am Thorac Soc       Date:  2016-11

Review 3.  Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?

Authors:  Sarath C Ranganathan; Graham L Hall; Peter D Sly; Stephen M Stick; Tonia A Douglas
Journal:  Am J Respir Crit Care Med       Date:  2017-06-15       Impact factor: 21.405

Review 4.  Molecular Imaging of Pulmonary Inflammation and Infection.

Authors:  Chiara Giraudo; Laura Evangelista; Anna Sara Fraia; Amalia Lupi; Emilio Quaia; Diego Cecchin; Massimiliano Casali
Journal:  Int J Mol Sci       Date:  2020-01-30       Impact factor: 5.923

Review 5.  [Imaging in respiratory infections].

Authors:  Sabine Dettmer; Jens Vogel-Claussen
Journal:  Pneumologe (Berl)       Date:  2021-07-03
  5 in total

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