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Abstract #0090

Venous Return in Chronic Obstructive Pulmonary Disease Assessed with 4D Flow MRI

Timothy W Houston1, David Dushfunian 2, Michael Markl2, Oliver Wieben1, Martin R. Prince3, Wei Shen3, James Carr2, David A. Bluemke1, Michael Backman3, Sachin Jambawalikar3, Bharath Ambale Venkatesh4, Joao Lima4, Prachi Agarwal5, John Paul Finn6, Christopher B. Cooper6, Jing Liu7, Yoo Jin Lee7, Joyce Schroeder8, Dalane W. Kitzman9, and Graham Barr3
1University of Wisconsin-Madison, Madison, WI, United States, 2Northwestern University Feinberg School of Medicine, Chicago, IL, United States, 3Columbia University, New York, NY, United States, 4Johns Hopkins University School of Medicine, Baltimore, MD, United States, 5University of Michigan School of Medicine, Ann Arbor, MI, United States, 6University of California Los Angeles, Los Angeles, CA, United States, 7University of California San Francisco, San Francisco, CA, United States, 8University of Utah School of Medicine, Salt Lake City, UT, United States, 9Wake Forest University, Winston-Salem, NC, United States

Synopsis

Keywords: Heart Failure, Blood vessels, COPD, Hemodynamics, Heart Failure, 4D Flow

Motivation: Chronic obstructive pulmonary disease (COPD) and emphysema are associated with hemodynamic changes in the pulmonary vasculature, possibly related to increased intra-thoracic pressure during expiration, altering venous return into the thorax.

Goal(s): Assess the association of respiratory dysfunction with hemodynamic parameters of venous return.

Approach: Velocity, kinetic energy, and stasis in the superior vena cava and inferior vena cava were quantified with 4D Flow MRI in 72 subjects across the COPD spectrum in an ongoing study (SPIROMICS HF).

Results: Our results show an association of impaired (reduced) venous return to the thorax with airway obstruction as assessed by spirometry.

Impact: This study demonstrates impaired venous return in subjects with COPD, which warrant further investigations into the cardiopulmonary interactions of right heart flow in COPD and its potential value as a noninvasive marker of disease progression.

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