Abstract 4357670: Abnormal Oxygen Pulse Trajectory Differentiates Anatomic Complexity and Functional Classification in Adults with Congenital Heart Disease

M Matthew Campbell S Sangeeta Shah (VCU Pauley Heart Center, Richmond, Virginia, United States) S Sierra Rouse (VCU School of Medicine, Richmond, Virginia, United States) Óscar Reyes Y Yongdeok Shin (VCU Pauley Heart Center, Richmond, Virginia, United States) B Brad Bakken (VCU Pauley Heart Center, Richmond, Virginia, United States) A Alexa Coe (VCU School of Medicine, Richmond, Virginia, United States) J Jessica Hallam (VCU Pauley Heart Center, Richmond, Virginia, United States) M Meghana Kapa (VCU School of Medicine, Richmond, Virginia, United States) M Margaret Lefebvre (VCU School of Medicine, Richmond, Virginia, United States) P Pengyang Li (virginia commonwealth university, Richmond, Virginia, United States) H Hannah Padgett (VCU Pauley Heart Center, Richmond, Virginia, United States) I Inna Tchoukina (VCU Pauley Heart Center, Richmond, Virginia, United States) J Justin Canada (Virginia Commonwealth University, Richmond, Virginia, United States)

Abstract

Background: Cardiopulmonary exercise testing (CPET) including measures of peak oxygen consumption (V O2peak ) and peak oxygen pulse (O 2pulse ) is commonly used for adult congenital heart disease (ACHD) surveillance. However, less is known of the significance of the O 2pulse trajectory, which reflects the kinetics of stroke volume and peripheral oxygen extraction during exercise. The extent to which O 2pulse trajectory correlates with underlying anatomic complexity, New York Heart Association (NYHA) functional status, and cardiovascular function in ACHD patients remains unclear. Objectives: To assess the relationship between anatomic complexity, functional status, and cardiac function with O 2pulse trajectory in a heterogeneous ACHD population. Methods: We performed a single center retrospective analysis of ACHD patients who underwent CPET as part of their clinical evaluation. Demographics, clinical history, CPET data, and cardiac magnetic resonance imaging results were manually extracted from the medical record. Anatomic complexity was classified as simple, moderate, or great based on 2018 AHA/ACC guidelines. Functional status was determined using VO 2peak to estimate NYHA class equivalent. The O 2pulse trajectory was qualitatively defined as normal or abnormal (flat or decreasing). Data are presented as mean (SD) or number (%). Chi-square and analysis of variance was performed to compare O 2pulse trajectory groups. Results: A total of 223 ACHD patients (36 [12] years old, 55% female, 74% White race) had an evaluable O 2pulse trajectory. An abnormal O 2pulse trajectory (n=109 [49%]) was associated with increasing ACHD complexity (Figure 1; P=0.047) and NYHA classification (P=0.023). Reductions in both right and left ventricular ejection fraction were associated with abnormal O 2pulse trajectory (RVEF: [normal vs abnormal trajectory]: 55 (10)% vs. 49 (14)%, P=0.001&LVEF: 58 (8)% vs. 53 (9)%, P=0.002). Subjects with an abnormal O 2pulse trajectory demonstrated significantly greater right (but not left) ventricular end-diastolic and end-systolic indexed volumes (RVEDVI: 88 (31) mL vs. 109 (52) mL, P=0.004&RVESVI: 40 (18) mL vs. 61 (44) mL, P<0.001). Conclusions: Greater anatomic complexity, higher NYHA classification, and worsening (right > left) ventricular function are associated with an abnormal O 2pulse trajectory in a heterogenous ACHD population. The clinical utility of this additional CPET parameter, reflecting O 2pulse kinetics, requires further study.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (14)

M

Matthew Campbell

S

Sangeeta Shah

VCU Pauley Heart Center, Richmond, Virginia, United States

S

Sierra Rouse

VCU School of Medicine, Richmond, Virginia, United States

Óscar Reyes

Y

Yongdeok Shin

VCU Pauley Heart Center, Richmond, Virginia, United States

B

Brad Bakken

VCU Pauley Heart Center, Richmond, Virginia, United States

A

Alexa Coe

VCU School of Medicine, Richmond, Virginia, United States

J

Jessica Hallam

VCU Pauley Heart Center, Richmond, Virginia, United States

M

Meghana Kapa

VCU School of Medicine, Richmond, Virginia, United States

M

Margaret Lefebvre

VCU School of Medicine, Richmond, Virginia, United States

P

Pengyang Li

virginia commonwealth university, Richmond, Virginia, United States

H

Hannah Padgett

VCU Pauley Heart Center, Richmond, Virginia, United States

I

Inna Tchoukina

VCU Pauley Heart Center, Richmond, Virginia, United States

J

Justin Canada

Virginia Commonwealth University, Richmond, Virginia, United States