Vaso-active therapy can improve 6-min walk distance in patients with pulmonary hypertension and fibrotic interstitial lung disease

Summary Background Dyspnea and functional limitation in interstitial lung diseases (ILD) are not always adequately explained by the degree of compromise in pulmonary function alone. Pulmonary hypertension (PH) is felt to be a major contributor to morbidity and mortality in these patients. It is not...

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Published in:Respiratory medicine Vol. 102; no. 7; pp. 1015 - 1020
Main Authors: Minai, Omar A, Sahoo, D, Chapman, J.T, Mehta, A.C
Format: Journal Article
Language:English
Published: Oxford Elsevier Ltd 01-07-2008
Elsevier
Elsevier Limited
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Summary:Summary Background Dyspnea and functional limitation in interstitial lung diseases (ILD) are not always adequately explained by the degree of compromise in pulmonary function alone. Pulmonary hypertension (PH) is felt to be a major contributor to morbidity and mortality in these patients. It is not clear whether treatment with newer vaso-active agents benefits patients with PH in the setting of moderate or severe ILD. Methods Medical records of patients followed at our institution between July 2001 and June 2005 were reviewed to identify patients with moderate or severe fibrotic ILD and PH. Data regarding demographics, hemodynamics, and clinical characteristics at baseline and during follow-up were collected. Results We identified 19 patients who met our inclusion criteria and in whom vaso-active therapy [epoprostenol ( N =10), bosentan ( N =9)] was initiated. Most patients [(15/19(79%)] showed an initial positive response to therapy and improved their 6-min walk distance (6MWD) by >50 m (responders) and 12/15 (80%) improved by at least 1 WHO functional class. At 1-year follow-up, 7 of 15 (47%) ‘responders’ had deteriorated significantly. None of the patients died during 1 year of follow-up. Conclusions Epoprostenol and bosentan produced short-term functional benefit in our patients with PH and moderate or severe restrictive ILD. The generalizability of these results awaits the results of larger, prospective, randomized trials in such patients.
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ISSN:0954-6111
1532-3064
DOI:10.1016/j.rmed.2008.02.002