13th International Congress
THE "NEW FRONTIERS"
OF ARRHYTHMIAS 1998

January 24-31, 1998
Marilleva, Trento, Italy

RT-237

Dual chamber pacing with optimized AV delay in congestive heart failure patients: 6th month results of a randomized study

S. Mangiameli, D. Castelli, G. Doria, P. Lo Giudice, G. Chiaranda and ISSC Group.
Divisione di Cardiologia, Ospedale Garibaldi, Catania, Italy

Introduction

Dual chamber pacing has been found to improve symptoms and NYHA Class in patients with dilated cardiomyo-pathy and congestive heart failure1-3. Subsequently these results were partially confirmed4 or completely contradicted5,6, probably because the results were derived from observational studies with small, heterogeneous patient populations. In addition, it is unknown whether all subjects with left ventricular systolic dysfunction respond to dual-chamber pacing or whether the beneficial effect is limited to a select subgroup of patients. The hemodynamic mechanisms of this "electrical" therapy may be resumed in three main physiopathologic statements:
1) the reduction of mitral regurgitation. Sequential pacing with short AV interval leads to an activated atrium during the expulsive stage of the left ventricle, thus determining the reduction of the ventriculoatrial gradient, the diastolic mitral regurgitation and the early mitral valve closure1,7;
2) a better utilization of the Frank-Starling mechanism obtained by restoring the atrioventricular synchronization8;
3) a better sequence of the activation-relaxation induced by sequential pacing compared with that realized by the normal conduction pathways3,4,9. This mechanism may reduce the apical activation delay, that it's very pronounced in dilated hearts, and, consequently, the wall stress.
From these previous statements it appears evident that only a small, select group of patients may benefit from DDD pacing with shortened AV delay.

Key Words

Pacing - congestive heart failure
dual chamber pacing, optimized-programmed AV interval, dilated cardiomyopathy, Italian Study on Stimulation in Cardiomyopathy/ISSC trial, left ventricular filling, OA

 

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