Short-term hemodynamic and neuroendocrine effects of pimobendan and benazapril in dogs with myxomatous mitral valve disease and congestive heart failure

J Vet Intern Med. 2013 Nov-Dec;27(6):1452-62. doi: 10.1111/jvim.12217. Epub 2013 Oct 15.

Abstract

Background: Pimobendan and benazepril are frequently used with diuretics to treat dogs in congestive heart failure (CHF) caused by myxomatous mitral valve disease (MMVD).

Aim: To compare the short-term effects of pimobendan versus benazepril on pump function, heart size, and neuroendocrine profile in dogs with CHF caused by MMVD.

Animals: Sixteen client-owned dogs.

Material and methods: Seven-day prospective single-blinded study of dogs stabilized on furosemide monotherapy, randomized to pimobendan (0.4-0.6 mg/kg/day) or benazepril (0.25-1.0 mg/kg/day). Dogs had first-pass radionuclide angiocardiography, and heart size was measured by radiography and echocardiography. Circulating neuroendocrine hormones were measured.

Results: Baseline variables did not differ between treatment groups. Greater decreases in the pimobendan than in the benazepril group were found for heart rate (P = .001), heart rate-normalized pulmonary transit time (P = .02), left atrial size (P = .03), and systolic and diastolic left ventricular diameters (P < .001 and P = .03, respectively) and volumes (P < .001 and P = .02, respectively), whereas ejection fraction increased more (P = .02) in the pimobendan group. Of the neuroendocrine hormones, only N-terminal proatrial natriuretic peptide (NT-ProANP) differed (P = .04) between groups. Within groups, plasma aldosterone increased (P = .01), and NT-proANP (P = .01) and NT-proB-type (P = .02) natriuretic peptide decreased in the pimobendan group, and NT-proANP (P = .02) and plasma vasopressin (P = .01) decreased in the benazepril group.

Conclusions and clinical importance: Pimobendan improves short-term cardiac function more than benazepril in dogs with CHF caused by MMVD. Pimobendan treatment enables the heart to work at smaller end-systolic and diastolic dimensions while maintaining adequate forward stroke volume. Some of the treatment responses found in neuroendocrine profile might have therapeutic relevance.

Keywords: Canine; Heart rate; Heart size; Mitral regurgitation; Therapy.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldosterone / blood
  • Animals
  • Atrial Natriuretic Factor / blood
  • Benzazepines / pharmacology*
  • Benzazepines / therapeutic use
  • Cardiotonic Agents / pharmacology*
  • Cardiotonic Agents / therapeutic use
  • Diuretics / pharmacology
  • Diuretics / therapeutic use
  • Dog Diseases / drug therapy
  • Dog Diseases / physiopathology*
  • Dogs
  • Echocardiography / veterinary
  • Female
  • Furosemide / pharmacology
  • Furosemide / therapeutic use
  • Heart Failure / drug therapy
  • Heart Failure / physiopathology
  • Heart Failure / veterinary*
  • Heart Rate / physiology
  • Heart Valve Diseases / drug therapy
  • Heart Valve Diseases / physiopathology
  • Heart Valve Diseases / veterinary*
  • Male
  • Mitral Valve / drug effects
  • Mitral Valve / physiopathology*
  • Natriuretic Peptide, Brain / blood
  • Organ Size / physiology
  • Peptide Fragments / blood
  • Prospective Studies
  • Protein Precursors / blood
  • Pyridazines / pharmacology*
  • Pyridazines / therapeutic use
  • Stroke Volume / physiology
  • Vasopressins / blood

Substances

  • Benzazepines
  • Cardiotonic Agents
  • Diuretics
  • N-terminal proatrial natriuretic peptide
  • Peptide Fragments
  • Protein Precursors
  • Pyridazines
  • pro-brain natriuretic peptide (1-76)
  • Vasopressins
  • Natriuretic Peptide, Brain
  • pimobendan
  • Aldosterone
  • Furosemide
  • Atrial Natriuretic Factor
  • benazepril