Literature DB >> 1721217

RR variability and baroreflex sensitivity in patients with ventricular tachycardia associated with normal heart and patients with ischemic heart disease.

J S Gill1, T Farrell, A Baszko, D E Ward, A J Camm.   

Abstract

Recent studies have suggested that disordered autonomic function, particularly the loss of protective vagal reflexes are associated with an increased incidence of arrhythmic deaths following myocardial infarction (MI). Heart rate variability (HRV) and baroreflex sensitivity (BRS) are measures of myocardial autonomic function and predict arrhythmic deaths post-MI. Patients with ventricular tachycardia associated with a "normal heart" frequently have exercise-induced arrhythmia suggesting that the autonomic nervous system is important in the genesis of this form of ventricular tachycardia (VT). This study examines HRV and BRS in patients with VT associated with a "normal heart" and compares these values to patients post-MI with and without evidence of arrhythmia. Twenty patients with VT associated with a "normal heart," 16 patients with MI but without arrhythmia on follow-up, and 11 patients with MI and VT on follow-up were studied. HRV was measured from 24-hour Holter recordings and BRS was measured from plots of change in systolic blood pressure versus change in heart rate following an intravenous injection of 0.4-0.6 mg phenylephrine. HRV was significantly higher in the patients with VT associated with a normal heart (34.2 +/- 10.8 msec) compared to the patients post-MI, without (23.7 +/- 6.7 msec) and with (14.8 +/- 3.8 msec) arrhythmia (F = 9.2, P less than 0.001) and these differences were unaffected by adjustment for age.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1721217     DOI: 10.1111/j.1540-8159.1991.tb02808.x

Source DB:  PubMed          Journal:  Pacing Clin Electrophysiol        ISSN: 0147-8389            Impact factor:   1.976


  1 in total

1.  Heart rate variability is altered following spinal cord injury.

Authors:  D C Bunten; A L Warner; S R Brunnemann; J L Segal
Journal:  Clin Auton Res       Date:  1998-12       Impact factor: 4.435

  1 in total

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