Prognostic value of cardiopulmonary exercise testing in patients with systemic sclerosis.

Cardiopulmonary exercise Prognosis Pulmonary function Pulmonary hypertension Systemic sclerosis

Journal

BMC pulmonary medicine
ISSN: 1471-2466
Titre abrégé: BMC Pulm Med
Pays: England
ID NLM: 100968563

Informations de publication

Date de publication:
29 Nov 2019
Historique:
received: 13 04 2019
accepted: 20 11 2019
entrez: 1 12 2019
pubmed: 1 12 2019
medline: 8 5 2020
Statut: epublish

Résumé

Systemic sclerosis (SSc) is a severe rheumatic disease of the interstitial tissue, in which heart and lung involvement can lead to disease-specific mortality. Our study tests the hypothesis that in addition to established prognostic factors, cardiopulmonary exercise testing (CPET) parameters, particularly peak oxygen uptake (peakVO We retrospectively assessed 210 patients (80.9% female) in 6 centres over 10 years with pulmonary testing and CPET. Survival was analysed with Cox regression analysis (adjusted for age and gender) by age, comorbidity (Charlson-Index), body weight, body-mass index, extensive interstitial lung disease, pulmonary artery pressure (measured by echocardiography and invasively), and haemodynamic, pulmonary and CPET parameters. Five- and ten-year survival of SSc patients was 93.8 and 86.9%, respectively. There was no difference in survival between patients with diffuse (dcSSc) and limited cutaneous manifestation (lcSSc; p = 0.3). Pulmonary and CPET parameters were significantly impaired. Prognosis was worst for patients with pulmonary hypertension (p = 0.007), 6-min walking distance < 413 m (p = 0.003), peakVO

Sections du résumé

BACKGROUND BACKGROUND
Systemic sclerosis (SSc) is a severe rheumatic disease of the interstitial tissue, in which heart and lung involvement can lead to disease-specific mortality. Our study tests the hypothesis that in addition to established prognostic factors, cardiopulmonary exercise testing (CPET) parameters, particularly peak oxygen uptake (peakVO
SUBJECTS AND METHODS METHODS
We retrospectively assessed 210 patients (80.9% female) in 6 centres over 10 years with pulmonary testing and CPET. Survival was analysed with Cox regression analysis (adjusted for age and gender) by age, comorbidity (Charlson-Index), body weight, body-mass index, extensive interstitial lung disease, pulmonary artery pressure (measured by echocardiography and invasively), and haemodynamic, pulmonary and CPET parameters.
RESULTS RESULTS
Five- and ten-year survival of SSc patients was 93.8 and 86.9%, respectively. There was no difference in survival between patients with diffuse (dcSSc) and limited cutaneous manifestation (lcSSc; p = 0.3). Pulmonary and CPET parameters were significantly impaired. Prognosis was worst for patients with pulmonary hypertension (p = 0.007), 6-min walking distance < 413 m (p = 0.003), peakVO

Identifiants

pubmed: 31783745
doi: 10.1186/s12890-019-1003-7
pii: 10.1186/s12890-019-1003-7
pmc: PMC6884803
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

230

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Auteurs

Ralf Ewert (R)

Department of Internal Medicine, University Greifswald, Greifswald, Germany.

Till Ittermann (T)

Institute for Community Medicine, University Greifswald, Greifswald, Germany.

Dirk Habedank (D)

Department of Cardiology, DRK Kliniken Berlin, Berlin, Germany. d.habedank@drk-kliniken-berlin.de.

Matthias Held (M)

Missio Clinic, Würzburg, Germany.

Tobias J Lange (TJ)

Department of Internal Medicine II, University Medical Center Regensburg, Regensburg, Germany.

Michael Halank (M)

Department of Internal Medicine I, University Hospital of TU Dresden, Dresden, Germany.

Jörg Winkler (J)

PSL Pulmonary Study Center, Leipzig, Germany.

Sven Gläser (S)

Department of Internal Medicine, Vivantes Kliniken Berlin, Spandau, Germany.

Horst Olschewski (H)

Department of Internal Medicine, Medical University of Graz, Division of Pulmonology, Graz, Austria.
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.

Gabor Kovacs (G)

Department of Internal Medicine, Medical University of Graz, Division of Pulmonology, Graz, Austria.
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.

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