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Safety and efficacy of flestolol, a new ultrashort-acting beta-adrenergic blocking agent, for supraventricular tachyarrhythmias.

Abstract
Flestolol, a new ultrashort-acting (half-life 6.9 minutes) beta-blocking drug, was administered by intravenous infusion to 18 patients with new-onset atrial fibrillation or flutter and rapid ventricular response (120 beats/min or more for at least 30 minutes). Drug dose of flestolol was progressively increased until at least 1 of 3 endpoints was achieved: at least a 20% reduction in heart rate from baseline, heart rate 100 beats/min or less, or conversion to normal sinus rhythm. Flestolol was then administered as a maintenance infusion up to 24 hours. When flestolol was discontinued, patients were monitored for 1 additional hour. The mean ventricular response at baseline of 133 +/- 12 beats/min decreased to 103 +/- 20 beats/min at the end of flestolol titration (p less than 0.0001). Fourteen patients (78%) achieved defined endpoints. All 14 patients who continued to receive maintenance infusion had a sustained response. When flestolol was discontinued, ventricular response increased 33 +/- 23% within 60 minutes. The only adverse effect seen was hypotension in 2 patients. Flestolol is effective in slowing ventricular response in new-onset atrial fibrillation and flutter, maintains a therapeutic effect during continuous infusion and rapidly loses therapeutic effect when discontinued.
AuthorsJ S Steinberg, R J Katz, J C Somberg, D Keefe, A R Laddu, J Burge
JournalThe American journal of cardiology (Am J Cardiol) Vol. 58 Issue 10 Pg. 1005-8 (Nov 01 1986) ISSN: 0002-9149 [Print] United States
PMID2877563 (Publication Type: Clinical Trial, Comparative Study, Journal Article)
Chemical References
  • Adrenergic beta-Antagonists
  • Fluorobenzenes
  • Propanolamines
  • flestolol
  • esmolol
Topics
  • Adrenergic beta-Antagonists (therapeutic use, toxicity)
  • Adult
  • Aged
  • Atrial Fibrillation (drug therapy)
  • Atrial Flutter (drug therapy)
  • Blood Pressure (drug effects)
  • Clinical Trials as Topic
  • Female
  • Fluorobenzenes
  • Half-Life
  • Humans
  • Hypotension (chemically induced)
  • Male
  • Middle Aged
  • Myocardial Contraction (drug effects)
  • Propanolamines (therapeutic use, toxicity)
  • Time Factors

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