Journalartikel
Autorenliste: Reichenberger, F.; Voswinckel, R.; Schulz, R.; Mensch, O.; Ghofrani, H. A.; Olschewski, H.; Seeger, W.
Jahr der Veröffentlichung: 2009
Seiten: 1713-1718
Zeitschrift: Respiratory Medicine
Bandnummer: 103
Heftnummer: 11
ISSN: 0954-6111
eISSN: 1532-3064
Open Access Status: Bronze
DOI Link: https://doi.org/10.1016/j.rmed.2009.05.004
Verlag: Elsevier
Background: Pulmonary arterial hypertension is a serious complication in scleroderma and early diagnosis is warranted. Patients and methods: 33 Scleroderma patients (mean age 54 [SD 11] years) with normal systolic pulmonary artery pressure (sPAP), right and left ventricular parameters at rest were enrolled in this study. They were investigated by echocardiography during physical. exercise and hypoxia. A hypertensive pulmonary vascular reaction was diagnosed when sPAP inappropriately increased during exercise compared to individual. exercise tolerance, or if sPAP was >40 mm Hg during hypoxia exposure, respectively. Results: In 17 patients there was a normal increase of sPAP at exercise of 34 [8] mm Hg (mean VO2 max 70 [17]% predicted), and 29 [5] mm Hg during hypoxia. Sixteen patients developed a hypertensive pulmonary vascular response with a sPAP of 47 [9] mm Hg during exercise (VO2-max 64 [15]% pred.), and 54 [7] mm Hg mm Hg during hypoxia, respectively. The sPAP/VO2 max ratio was higher in patients with a hypertensive response (0.76 [0.17] vs. 0.49 [0.12] p < 0.0001). There was no difference in scleroderma subtype, duration of disease, gender or age between groups. During a 3-year follow up one patient with a hypertensive response developed manifest pulmonary arterial hypertension. Conclusion: Non-invasive assessment of pulmonary circulation during physical, exercise and/or hypoxia enables screening for pulmonary vascular dysfunction in scleroderma. (C) 2009 Elsevier Ltd. All rights reserved.
Abstract:
Zitierstile
Harvard-Zitierstil: Reichenberger, F., Voswinckel, R., Schulz, R., Mensch, O., Ghofrani, H., Olschewski, H., et al. (2009) Noninvasive detection of early pulmonary vascular dysfunction in scleroderma, Respiratory Medicine, 103(11), pp. 1713-1718. https://doi.org/10.1016/j.rmed.2009.05.004
APA-Zitierstil: Reichenberger, F., Voswinckel, R., Schulz, R., Mensch, O., Ghofrani, H., Olschewski, H., & Seeger, W. (2009). Noninvasive detection of early pulmonary vascular dysfunction in scleroderma. Respiratory Medicine. 103(11), 1713-1718. https://doi.org/10.1016/j.rmed.2009.05.004
Schlagwörter
ARTERIAL-HYPERTENSION; DOPPLER-ECHOCARDIOGRAPHY; ECHOCARDIOGRAPHY; Pulmonary hypertension; SCLERODERMA; SYSTEMIC-SCLEROSIS