Volume Calibration with Cardiac MRI vs Hypertonic Saline for Right Ventricular Pressure-Volume Loops with Exercise: Impact on ventricular function and ventricular-vascular coupling.

IF 6.4 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Farhan Raza, Chris G Lechuga, Oliver Wieben, Naomi C Chesler
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引用次数: 0

Abstract

Right ventricular (RV) pressure-volume (PV) loops require post-acquisition volume calibration by cardiac MRI (CMR) or hypertonic saline (HS). We defined the impact of these two volume calibration methods on rest-to-exercise ventricular contractility (end-systolic elastance: Ees), arterial afterload (Ea) and coupling (Ees/Ea). In a prospective study, 82 RV PV-loop datapoints (rest, exercise stages-every 25watts and recovery) and CMR were acquired in 19 participants. In comparison to CMR, HS-based calibration over-estimated RV end-systolic volume at rest, mean (SD) by +38 mL (48) and end-diastolic volume by +46 mL (68), resulting in underestimated RVEF by -8%. However, Ees and Ea were similar at rest (r2=0.76 and 0.71 respectively, p<0.001 for both) and Ees:Ea was identical (r2=1.00, p<0.001). Exercise metrics also remained similar: RV reserve (ΔEes) and change in coupling (ΔEes/Ea). In comparison to CMR (gold-standard), HS-based calibration under-estimates RVEF at rest, however it is a robust approach for measuring coupling and RV reserve.

用心脏磁共振成像与高渗盐水对运动时右心室压力-容积环路进行容积校准:对心室功能和心室-血管耦合的影响。
右心室(RV)压力-容积(PV)环路需要通过心脏磁共振成像(CMR)或高渗盐水(HS)进行采集后容积校准。我们确定了这两种容积校准方法对静息-运动心室收缩力(收缩末弹性:Ees)、动脉后负荷(Ea)和耦合(Ees/Ea)的影响。在一项前瞻性研究中,19 名参与者获得了 82 个 RV PV 环数据点(静息、运动阶段--每 25 瓦特和恢复期)和 CMR。与 CMR 相比,基于 HS 的校准高估了静息时 RV 收缩末期容积,平均(SD)+38 mL(48),舒张末期容积+46 mL(68),导致 RVEF 被低估了 -8%。然而,Ees 和 Ea 在静息时相似(r2 分别为 0.76 和 0.71,p2=1.00,p2=0.71)。
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来源期刊
CiteScore
10.10
自引率
6.70%
发文量
1667
审稿时长
69 days
期刊介绍: The Journal of Heart and Lung Transplantation, the official publication of the International Society for Heart and Lung Transplantation, brings readers essential scholarly and timely information in the field of cardio-pulmonary transplantation, mechanical and biological support of the failing heart, advanced lung disease (including pulmonary vascular disease) and cell replacement therapy. Importantly, the journal also serves as a medium of communication of pre-clinical sciences in all these rapidly expanding areas.
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