Analysis of isovolumic relaxation in failing hearts by monoexponential time constants overestimates lusitropic change and load dependence: mechanisms and advantages of alternative logistic fit.

BACKGROUND Failing hearts display slow relaxation with apparent increased load sensitivity. However, inaccuracies of monoexponential analysis can contribute to these observations, and different qualitative and quantitative results might be obtained by alternative models. We tested whether pressure relaxation of failing hearts consistently deviates from a monoexponential waveform, leading to overestimations of lusitropic change and load sensitivity by monoexponential-derived time constants. METHODS AND RESULTS Fourteen dogs were studied before and after tachycardia pacing-induced heart failure. Relaxation time constants were derived by monoexponential fits (tau(E)) with zero or nonzero asymptotes and by a logistic fit (tau(L)). tau(L) assumes nonlinear relations between pressure and its first derivative, whereas tau(E) assumes a linear dependence. Load sensitivity of tau was tested by comparing beats during vena caval occlusion. tau(E) prolonged by 75% to 80% with heart failure, 3 times more than tau(L) (P<0.01). tau(E) displayed marked load sensitivity in failing hearts, shortening during preload reduction, whereas tau(L) was little changed by the same loading maneuver. Neither tau(L) nor tau(E) varied with preload in control hearts. The discrepancy between tau(E) and tau(L) results was due to nonmonoexponential decay reflected by nonlinear pressure-time derivative of pressure plots, which was enhanced with heart failure (P<0.01). This nonlinearity was reduced by beta-adrenergic stimulation, lowering preload sensitivity of tau(E) to control levels. CONCLUSIONS Isovolumic relaxation in failing hearts deviates from a monoexponential waveform, leading to overestimated relaxation delay and increased load sensitivity of monoexponential time constants. This deviation is under beta-adrenergic modulation. The logistic model improves the fit-to-real pressure decay in failing hearts, providing more stable measures of relaxation.