Abstract

HomeRadiologyVol. 260, No. 3 PreviousNext Reviews and CommentaryEditorialCT Detection of Pulmonary Hypertension in Interstitial Lung Disease: The Glass Is Half FullAthol Wells Athol Wells Author AffiliationsFrom the Interstitial Lung Disease Unit, Royal Brompton Hospital, Sydney Street, London SW3 6NP, England.Address correspondence to the author (e-mail: [email protected]).Athol Wells Published Online:Sep 1 2011https://doi.org/10.1148/radiol.11111251MoreSectionsFull textPDF ToolsImage ViewerAdd to favoritesCiteTrack CitationsPermissionsReprints ShareShare onFacebookTwitterLinked In AbstractThin-section CT is not a consistently reliable surrogate for right-sided heart catheterization in interstitial lung disease, but this conclusion does not in any way detract from other possible applications of thin-section CT in this field.References1 Hansell DM. Small airways diseases: detection and insights with computed tomography. Eur Respir J 2001;17(6):1294–1313. Crossref, Medline, Google Scholar2 Corte TJ, Wort SJ, Gatzoulis MA, Macdonald P, Hansell DM, Wells AU. Pulmonary vascular resistance predicts early mortality in patients with diffuse fibrotic lung disease and suspected pulmonary hypertension. Thorax 2009;64(10):883–888. Crossref, Medline, Google Scholar3 Zisman DA, Karlamangla AS, Ross DJet al.. High-resolution chest CT findings do not predict the presence of pulmonary hypertension in advanced idiopathic pulmonary fibrosis. Chest 2007;132(3):773–779. Crossref, Medline, Google Scholar4 Devaraj A, Wells AU, Meister MG, Corte TJ, Hansell DM. The effect of diffuse pulmonary fibrosis on the reliability of CT signs of pulmonary hypertension. Radiology 2008;249(3):1042–1049. Link, Google Scholar5 Baughman RP, Engel PJ, Meyer CA, Barrett AB, Lower EE. Pulmonary hypertension in sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 2006;23(2):108–116. Medline, Google Scholar6 Maher TM, Wells AU. 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Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative. AJR Am J Roentgenol 2003;181(1):51–55. Crossref, Medline, Google Scholar11 Devaraj A, Wells AU, Meister MG, Loebinger MR, Wilson R, Hansell DM. Pulmonary hypertension in patients with bronchiectasis: prognostic significance of CT signs. AJR Am J Roentgenol 2011;196(6):1300–1304. Crossref, Medline, Google Scholar12 Devaraj A, Wells AU, Meister MG, Corte TJ, Wort SJ, Hansell DM. Detection of pulmonary hypertension with multidetector CT and echocardiography alone and in combination. Radiology 2010;254(2):609–616. Link, Google Scholar13 Raghu G, Collard HR, Egan JJet al.. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis—evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 2011;183(6):788–824. Crossref, Medline, Google ScholarArticle HistoryReceived June 16, 2011; accepted June 16; final version accepted June 20.Published online: Sept 2011Published in print: Sept 2011 FiguresReferencesRelatedDetailsCited ByA Possible Anatomic Explanation for Inaccuracies in the Derivation of Pulmonary Artery Pressure, with Thin-Section CT, in Interstitial Lung FibrosisEric N. C. 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