Literature DB >> 9651666

Effect of parasympathetic blockade on the signal-averaged electrocardiogram.

E H Christiansen1, O Frøbert.   

Abstract

Low parasympathetic activity is associated with late potentials detected at a noise level of 0.4 microV in a signal-averaged electrocardiogram (SAECG) following myocardial infarction. In contrast, at a noise level of 0.2 microV, lowering parasympathetic activity influences late potential parameters in the opposite direction in healthy subjects. The aim of this study was to estimate the relationship between parasympathetic activity and the SAECG obtained at noise levels of 0.4 and 0.2 microV in healthy subjects. Two SAECG recordings in 10 healthy subjects were obtained at noise levels of 0.2 and 0.4 microV before and after parasympathetic blockade using atropine (1 mg). Signal-averaged QRS duration (SA-QRS), late potential duration (LPD) defined as duration of terminal signals below 40 microV, and root mean square voltage of the terminal 40 ms of the averaged QRS (RMS40) were measured. At a noise level of 0.2 microV SA-QRS reduced from 124 +/- 14 to 114 +/- 17 ms (P = 0.008), LPD from 37 +/- 10 to 28 +/- 14 ms (P = 0.01), and RMS40 increased from 26 +/- 22 to 41 +/- 25 microV (P = 0.006) during parasympathetic blockade compared to baseline values. At a noise level of 0.4 microV the SA-QRS (115 +/- 15 ms) and LPD (29 +/- 11 ms) were lower and the RMS40 (37 +/- 23 microV) was higher compared to the noise level 0.2 microV, and no systematic alterations of the three variables were found during parasympathetic blockade. The parasympathetic nervous system may induce a very low-amplitude late potential in the SAECG. The data suggest that parasympathetic activity and a low noise level may lead to a false late potential-positive SAECG in low arrhythmia risk subjects. Therefore, we recommend the use of a noise level of 0.4 microV or identification of high arrhythmia risk patients by late potential and low parasympathetic activity.

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Year:  1998        PMID: 9651666     DOI: 10.1007/bf02281121

Source DB:  PubMed          Journal:  Clin Auton Res        ISSN: 0959-9851            Impact factor:   4.435


  31 in total

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