Forced oscillation technique in patient with scleroderma, idiopathic pulmonary fibrosis (IPF) and connective tissue diseases

E. Bucchioni, V. Fasano, M. Mastrangelo, R. Bossi, L. Allegra (Milan, Italy)

Source: Annual Congress 2002 - Airway obstruction measurement (FOT - NEP) sleep and lung sound analysis
Session: Airway obstruction measurement (FOT - NEP) sleep and lung sound analysis
Session type: Poster Discussion
Number: 313
Disease area: Interstitial lung diseases

Congress or journal article abstract

Abstract

The forced oscillation techique (FOT) is a non invasive method to measure mechanical impedance of respiratory system. Aim of our study was to evaluate resistance (R5-R20) and reactance (X5-X20) in patients with scleroderma, idiopathic pulmonary fibrosis (IPF) and connective tissue diseases.
We studied 8 patients with connective tissue diseases: systemic lupus erythematosus (SLE) and Rheumatiod arthritis, group A ( mean age 59±]14 yr; 1 male), 16 patients with diagnosis of scleroderma, group B (mean age 57±]11yr; 1 male) and 10 patients with IPF, group C (mean age 62±]11yr; 7 males). Total resipiratory resistance and reactance at 5 Hz and 20 Hz (frequency of impulse generated by the oscillator) were performed by means of the FOT. We measured FVC, FEV1, R5, R20, X5 and X20. We observed in group C a statistical decrease of R5, R20, X20 and a statistical increase in X5 compared to group A; a statistical decrease in R20, X20 and increase in X5 compared to group B. However no significant differences were found between group A and B (table). We conclude that FOT tecnique, as the spirometric test, is a sensitive method to follow up severe interstitial lung disesase.

GroupsFVC%FEV1%R5%R20%X5%X20%
C56±]1261±]1391±]2071±]19882±]69929±]88
B85±]1086±]21110±]34101±]29341±]256324±]240
p<0.02<0.02ns<0.02<0.05<0.05


GroupsFVC%FEV1%R5%R20%X5%X20%
C56±]1261±]1391±]2071±]19882±]69929±]88
A92±]1180±]8132±]33114±]22218±]421129±]87
p<0.02<0.02<0.02<0.01<0.05<0.05




Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
E. Bucchioni, V. Fasano, M. Mastrangelo, R. Bossi, L. Allegra (Milan, Italy). Forced oscillation technique in patient with scleroderma, idiopathic pulmonary fibrosis (IPF) and connective tissue diseases. Eur Respir J 2002; 20: Suppl. 38, 313

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:
Genomic comparison of fibrotic rheumatoid arthritis-associated ILD and idiopathic pulmonary fibrosis
Source: International Congress 2015 – Connective tissue disorders
Year: 2015

Etablishing rhesus model of pulmonary fibrosis (PF) for the new drug evaluation
Source: International Congress 2015 – IPF: from bench to bedside
Year: 2015

ILD-India registry: Idiopathic pulmonary fibrosis (IPF) and connective tissue disease (CTD) associated interstitial lung disease (CTD-ILD)
Source: International Congress 2016 – Clinical aspects of ILD
Year: 2016


The ratio AGE/RAGE is increased in idiopathic pulmonary fibrosis
Source: International Congress 2015 – Connective tissue disorders
Year: 2015


Significance of histopathologic features suggesting connective tissue disease in idiopathic pulmonary fibrosis
Source: International Congress 2015 – Connective tissue disorders
Year: 2015

Clinical features of usual interstitial pneumonia-correlation between idiopathic pulmonary fibrosis and connective tissue disease associated with usual interstitial pneumonia
Source: International Congress 2016 – Connective tissue disorders
Year: 2016

Significance of connective tissue disease features in idiopathic interstitial pneumonia
Source: Eur Respir J 2012; 39: 661-668
Year: 2012



Interstitial lung disease
Source: Eur Respir Rev 2013; 22: 26-32
Year: 2013



Combined pulmonary emphysema and fibrosis in connective tissue disease
Source: Annual Congress 2009 - Idiopathic pulmonary fibrosis: concepts and mechanisms
Year: 2009

Relevance of the expert ILD clinical-radiological evaluation of referred cases to the MDT
Source: International Congress 2016 – Clinical aspects of ILD
Year: 2016


Occult connective tissue diseases mimicking idiopathic interstitial pneumonias
Source: Eur Respir J 2008; 31: 11-20
Year: 2008



Lysyl oxidases in idiopathic pulmonary fibrosis: A key participant in collagen I matrix remodelling
Source: International Congress 2015 – Airway remodelling: recent developments
Year: 2015

The impact of definition of ILD on WHO group Classification of PH in scleroderma
Source: Annual Congress 2013 –Pulmonary circulation: clinical pulmonary hypertension I
Year: 2013

Clinical efficacy of pirfenidone in patients with severe fibrosing interstitial pneumonia
Source: International Congress 2015 – Treatment of IPF
Year: 2015


Analysis of inflammatory networks in interstitial lung disease in patients with rheumatoid arthritis
Source: International Congress 2016 – Connective tissue disorders
Year: 2016

Serum surfactant protein D (SP-D) and annual decline of diffusion capacity are prognostic factors for combined pulmonary fibrosis with emphysema (CPFE) in idiopathic pulmonary fibrosis (IPF)
Source: Annual Congress 2013 –Clinical respiratory physiology in different diseases
Year: 2013


Pulmonary hypertension in interstitial lung disease
Source: Eur Respir J 2008; 31: 1357-1367
Year: 2008



Pulmonary function involvement in scleroderma
Source: Annual Congress 2013 –Diffuse parenchymal lung disease II
Year: 2013

A multicentre evaluation of inter-multidisciplinary team agreement for diagnosis in diffuse lung disease
Source: International Congress 2016 – Epidemiological and clinical data regarding the modern management of chronic lung diseases
Year: 2016

Index of histological activity in idiopathic pulmonary fibrosis (IPF) and chronic interstitial lung diseases (CHILD)
Source: Eur Respir J 2004; 24: Suppl. 48, 533s
Year: 2004