Performance comparison of ventricular and arterial dP/dtmax for assessing left ventricular systolic function during different experimental loading and contractile conditions.
No Thumbnail Available
Identifiers
Date
2018-11-29
Authors
Monge Garcia, Manuel Ignacio
Jian, Zhongping
Settels, Jos J
Hunley, Charles
Cecconi, Maurizio
Hatib, Feras
Pinsky, Michael R
Advisors
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
Maximal left ventricular (LV) pressure rise (LV dP/dtmax), a classical marker of LV systolic function, requires LV catheterization, thus surrogate arterial pressure waveform measures have been proposed. We compared LV and arterial (femoral and radial) dP/dtmax to the slope of the LV end-systolic pressure-volume relationship (Ees), a load-independent measure of LV contractility, to determine the interactions between dP/dtmax and Ees as loading and LV contractility varied. We measured LV pressure-volume data using a conductance catheter and femoral and radial arterial pressures using a fluid-filled catheter in 10 anesthetized pigs. Ees was calculated as the slope of the end-systolic pressure-volume relationship during a transient inferior vena cava occlusion. Afterload was assessed by the effective arterial elastance. The experimental protocol consisted of sequentially changing afterload (phenylephrine/nitroprusside), preload (bleeding/fluid bolus), and contractility (esmolol/dobutamine). A linear-mixed analysis was used to assess the contribution of cardiac (Ees, end-diastolic volume, effective arterial elastance, heart rate, preload-dependency) and arterial factors (total vascular resistance and arterial compliance) to LV and arterial dP/dtmax. Both LV and arterial dP/dtmax allowed the tracking of Ees changes, especially during afterload and contractility changes, although arterial dP/dtmax was lower compared to LV dP/dtmax (bias 732 ± 539 mmHg⋅s- 1 for femoral dP/dtmax, and 625 ± 501 mmHg⋅s- 1 for radial dP/dtmax). Changes in cardiac contractility (Ees) were the main determinant of LV and arterial dP/dtmax changes. Although arterial dP/dtmax is a complex function of central and peripheral arterial factors, radial and particularly femoral dP/dtmax allowed reasonably good tracking of LV contractility changes as loading and inotropic conditions varied.
Description
MeSH Terms
Adrenergic beta-1 Receptor Antagonists
Animals
Cardiotonic Agents
Catheterization, Central Venous
Myocardial Contraction
Nitroprusside
Phenylephrine
Propanolamines
Swine
Vasodilator Agents
Ventricular Function, Left
Weights and Measures
Animals
Cardiotonic Agents
Catheterization, Central Venous
Myocardial Contraction
Nitroprusside
Phenylephrine
Propanolamines
Swine
Vasodilator Agents
Ventricular Function, Left
Weights and Measures
DeCS Terms
CIE Terms
Keywords
Arterial pressure, Contractility, Left ventricular function, dP/dtmax