Sympathomimetic infusion and cardiac repolarization: the normative effects of epinephrine and isoproterenol in healthy subjects.

Effects of Epinephrine and Isoproterenol on QT Interval.Introduction: Catecholamines are known to affect cardiac repolarization, and provocation with either isoproterenol or epinephrine has been proposed as a tool for uncovering latent repolarization abnormalities. This study systematically compares...

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Publicado en:Journal of Cardiovascular Electrophysiology Vol. 17; no. 9; pp. 983 - 990
Autores principales: Magnano AR, Talathoti N, Hallur R, Bloomfield DM, Garan H
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Sep2006
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Sep2006
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        atl: Sympathomimetic infusion and cardiac repolarization: the normative effects of epinephrine and isoproterenol in healthy subjects.
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        au:
          Magnano AR
          Talathoti N
          Hallur R
          Bloomfield DM
          Garan H
        affil: Division of Cardiology/Clinical Cardiac Electrophysiology, Columbia University College of Physicians and Surgeons, 161 Fort Washington Avenue HIP 5-551, New York, NY 10032. arm6@columbia.edu.
      sug:
        subj:
          Autonomic Nervous System
          Epinephrine Therapeutic Use
          Isoproterenol Therapeutic Use
          Electrophysiology
          Funding Source
          Long QT Syndrome
          Human
      ab: Effects of Epinephrine and Isoproterenol on QT Interval.Introduction: Catecholamines are known to affect cardiac repolarization, and provocation with either isoproterenol or epinephrine has been proposed as a tool for uncovering latent repolarization abnormalities. This study systematically compares the effects of isoproterenol and epinephrine infusions on QT interval (QT), T waves and U waves in normal subjects.Methods and Results: Twenty-four normal subjects (29 +/- 8 years) were evaluated during graded infusions of up to 0.30 microg/kg/minute epinephrine and 5.0 microg/minute isoproterenol. Heart rates at peak doses were 81 +/- 13 bpm at 0.28 +/- 0.04 microg/kg/minute epinephrine and 104 +/- 5 bpm at 2.4microg/minute isoproterenol. The longest absolute QT increase was 4 +/- 5 msec above baseline during isoproterenol (P < 0.001) and 12 +/- 23 msec during epinephrine (P = 0.07), while the longest corrected QT interval (QTc) increase was 67 +/- 28 msec (P < 0.0001) and 79 +/- 40 msec (P < 0.0001) above baseline during isoproterenol and epinephrine, respectively (P = 0.12 for difference). There was a 2-fold increase in U-wave amplitude during each intervention (P < 0.001). The specificity of paradoxical QT prolongation (>/=30 msec at 0.05 microg/kg/minute or >/=35 msec at 0.10 microg/kg/minute epinephrine) and an increase in QTc >/=600 msec at any dose epinephrine were 100%. However, the specificity of other proposed criteria that utilized QTc measurement (>/=30 msec at 0.10 microg/kg/minute or >/=65 msec at any dose) was poor whether all leads or only lead II were assessed.Conclusion: Both epinephrine and isoproterenol are associated with QTc prolongation and amplification of the U wave in normal subjects. The specificity of proposed criteria for epinephrine provocation in diagnosis of the long-QT syndrome is variable; however, paradoxical QT prolongation at low-dose epinephrine or a QTc >/=600 msec is highly specific.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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