HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Acute hemodynamic effects of piroximone (MDL 19,205) in patients with moderate congestive heart failure: comparison with sodium nitroprusside.

Abstract
Piroximone (MDL 19,205), a new imidazolone derivative, was given intravenously to 14 patients with congestive heart failure (NYHA class II-III), while under constant daily doses of digitalis and diuretics. In the first 3 patients, we determined the dose safely eliciting a favorable hemodynamic response. The subsequent 11 patients received 1 mg/kg of piroximone intravenously, and the hemodynamic effects were compared with those of sodium nitroprusside (SN) at a dose-lowering mean blood pressure by 10-20 mm Hg. Piroximone increased heart rate (13.2 +/- 2.0 beats/min, mean +/- SEM) and lowered mean arterial pressure (9 +/- 2.3 mm Hg). Both agents reduced similarly wedge pressure (6.5 +/- 2.9 and 9 +/- 2.9 mm Hg, respectively, for SN and piroximone) and total peripheral resistance. Cardiac index was increased less by SN (15%) than piroximone (48%) (p less than 0.001), and stroke work index significantly enhanced only by piroximone (p less than 0.001). The changes in loading conditions induced by the two agents being similar, it is likely that piroximone not only acts by peripheral vasodilation, but also possesses positive inotropic properties. Myocardial oxygen demand, assessed indirectly by tension-time index, was not affected by piroximone. Thus, piroximone appears to combine well-balanced vasodilator and inotropic properties which make this new agent potentially very useful for the management of congestive heart failure.
AuthorsR Arbogast, C M Brandt, J L Fincker, P J Schechter
JournalJournal of cardiovascular pharmacology (J Cardiovasc Pharmacol) 1986 Jan-Feb Vol. 8 Issue 1 Pg. 82-9 ISSN: 0160-2446 [Print] United States
PMID2419699 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Ferricyanides
  • Imidazoles
  • Nitroprusside
  • piroximone
Topics
  • Adult
  • Aged
  • Blood Pressure (drug effects)
  • Cardiac Output (drug effects)
  • Drug Evaluation
  • Drug Tolerance
  • Female
  • Ferricyanides (pharmacology)
  • Heart Failure (drug therapy, physiopathology)
  • Heart Rate (drug effects)
  • Hemodynamics (drug effects)
  • Humans
  • Imidazoles (administration & dosage, adverse effects, pharmacology)
  • Male
  • Middle Aged
  • Myocardial Contraction (drug effects)
  • Nitroprusside (pharmacology)
  • Vasodilation (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: