Abstract
Pulmonary hypertension (PH) is associated with decreased survival in patients with pulmonary fibrosis and combined pulmonary fibrosis and emphysema. Main pulmonary artery (PA) diameter and PA diameter/ascending aortic diameter (PA/AA) ratio, as measured on CT, have recently emerged as specific markers for PH. Our single-center retrospective study found that PA/AA ratio > 1 is associated with decreased survival in individuals with pulmonary fibrosis, with or without emphysema. Our study also describes markers of cardiac remodeling, and the echocardiographic diagnosis of PH in this patient population.
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Funding
No funding was received for conducting this study. This work was performed using resources and facilities of the Providence VA Medical Center. SR was supported by Grants from the NIH (1P20GM103652-01 and 5R01HL130230). Statistical support was provided through Advance Clinical and Translational Research (Advance-CTR) U54GM115677.
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FZ, MJ, SR conceptualized and designed this project, FZ and JM were responsible for data gathering, MKA performed radiological measurements, YW and DF performed statistical analysis. All authors contributed to drafting the manuscript.
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The authors declare that they have no conflict of interest.
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This study was performed after approval of the Providence VAMC Institutional Review Board.
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Zeba, F., Yanning, W., Melek, J. et al. Prognostic Significance of Pulmonary Artery to Aorta Ratio and Other CT Markers in Pulmonary Fibrosis With and Without Emphysema. Lung 199, 677–680 (2021). https://doi.org/10.1007/s00408-021-00490-2
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DOI: https://doi.org/10.1007/s00408-021-00490-2