University of California-Davis, Veterinary Medical Center San Diego, San Diego, CA, USA
Doença Valvular Degenerativa: Diagnóstico e Tratamento
Chronic degenerative valvular disease is the most common cardiovascular disease in small animals, and is also known as endocardiosis or myxomatous valve degeneration.
It is seen more commonly in older small-breed dogs, and males appear to be predisposed and develop more severe disease.
Anatomy
Mitral valve (dog) - large anterior leaflet, smaller posterior leaflet and small commissural cusps between the two leaflets. Both leaflets are semicircular and are attached to the mitral valve annulus (fibrous ring) and to the papillary muscles (through chordae tendineae).
Tricuspid valve - two primary leaflets and multiple commissural cusps. The mural leaflet is significantly larger than the septal leaflet.
Aortic valve - three semi-lunar cusps.
Pathology
Mitral valve lesions are the most common, but the tricuspid valve and rarely the aortic valve can also be affected.
Gross inspection reveals thickened and redundant valve leaflets. The free margins of the leaflets are the most commonly affected areas, which have nodules and are opaque.
Mitral valve prolapse - a portion of the body of the leaflet protrudes into the left atrium.
Structures involved: leaflets and chordae tendineae
Lesions:
Redundancy of the leaflets
Lengthening of the chordae tendineae
Thickened and/or fenestrated leaflets
Histopathology
The atrioventricular valves have four layers:
Atrialis (endocardial)
Spongiosa (collagen, fibroblasts, elastic fibers, and mucopolysaccharides)
Fibrosa (collagen bundles)
Ventricularis (endocardial)
In myxomatous AV degeneration the spongiosa increases in size and the fibrosa degenerates. A significant increase in extracellular matrix is observed and fibroblasts proliferate forming nodules.
Etiology
Likely hereditary. Evidence suggests that degenerative valvular disease is inherited as a polygenic threshold trait in Cavalier King Charles spaniels.
Pathophysiology
Valvular regurgitation → increased atrial volume → atrial dilatation
Eccentric hypertrophy → annular dilation → worsening regurgitation
Increased atrial pressure → congestive heart failure
Severe regurgitation → decreased forward flow
-Decreased forward flow → renin-angiotensin-aldosterone system (RAAS) stimulation
Pulmonary hypertension can develop secondary to chronic pulmonary venous hypertension.
Myocardial failure usually occurs in the latter stages of the disease and is more commonly identified in large-breed dogs.
Atrial tears/rupture can cause cardiac tamponade secondary to acute hemopericardium.
History/Clinical Signs
Coughing, labored breathing, syncope, distended abdomen
Physical Exam
Mucous membrane color and CRT, jugular veins, thoracic auscultation and peripheral pulses.
Common PE findings:
Heart murmur, increased intensity of the first heart sound, systolic click, third heart sound, arrhythmias, tachypnea/tachycardia, crackles and wheezes, distended jugular veins, brisk femoral pulses.
Diagnostic Tests
Thoracic radiographs, ECG, echocardiogram, blood pressure, laboratory tests.
Laboratory tests
B-type natriuretic factor/peptide (BNP) and cardiac troponin-I (TnI)
Real-time 3D echocardiography
Real time three-dimensional echocardiography is a new ultrasound modality that provides comprehensive views of cardiac valves. This technique potentially provides a more accurate echocardiographic means of evaluating cardiac chamber volumes and a more precise postoperative tool.
Asymptomatic Disease
ACE inhibitors
Pimobendan?
β-blockers?
Heart Failure
Congestive heart failure is the end result of severe heart disease
Clinical syndrome of congestion and edema
Poor peripheral perfusion +/- systemic hypotension
Acute Treatment
Oxygen, diuretics, vasodilators and positive inotropes
Loop diuretics
Potent diuretics
Block Na+/K+/2Cl- co-transport
Increase K+, Mg++, and Ca++ excretion
Intermittent IV boluses or continuous rate infusion (CRI)
IV boluses: furosemide 2–4 mg/kg q4–8 h
Vasodilators
Sodium nitroprusside
Produces nitric oxide in vascular smooth muscle
Intravenous
Peripheral vasodilation: arteriolar and venodilator
Hydralazine
0.5–3 mg/kg PO BID
Alters Ca++ metabolism
Acts on vascular smooth muscle (arterioles)
Increases aortic compliance and decreases peripheral vascular resistance and BP
Nitroglycerine
Relaxes vascular smooth muscle
Veins
Dose-dependent effect on arterioles
Decrease myocardial oxygen demand
Improve coronary artery circulation
Metabolites vasodilator activity
Positive inotropes
Dobutamine
Synthetic catecholamine
Beta 1 agonist; some beta 2 and alpha 1 effects
Increases contractility
Mild chronotropic, arrhythmogenic, and vasodilatory effects
Chronic Treatment
Diuretics
Loop diuretics
Thick ascending loop of Henle
Furosemide: 2–4 mg/kg PO BID–TID (dogs); 1–4 mg/kg PO BID–TID (cats)
Torsemide (0.2–0.4 mg/kg PO BID)
Thiazides
Hydrochlorothiazide (1–4 mg/kg EOD–BID)
Na+/Cl- channel in the distal convoluted tubule
K+ sparing diuretics/aldosterone blockers
Spironolactone: 1–4 mg/kg PO BID–TID
Distal tubule
Inhibits aldosterone
Decreases myocardial fibrosis?
Restore baroreceptor function CHF
Vasodilators
ACE inhibitors
Enalapril: 0.5 mg/kg PO BID
Benazepril: 0.5 mg/kg PO SID–BID)
Decrease efferent arteriole pressure and the glomerular filtration rate (GFR)
Calcium channel blockers
Amlodipine: 0.1–0.5 mg/kg PO SID
Inhibits calcium flux across cell membranes (vascular smooth muscle > cardiac)
Depresses automaticity and conduction velocity (cardiac muscle)
Phosphodiesterase-5 inhibitors
Sildenafil: 1 mg/kg PO TID
Tadalafil: 1 mg/kg PO SID–BID
Prevent enzymatic hydrolysis of cGMP
Smooth muscle relaxation
Positive Inotropes
Pimobendan:
0.2–0.3 mg/kg PO BID–TID
Inodilator
Phosphodiesterase-3 inhibitor
Ca++ sensitizer
Quest study: improves median survival time and quality of life
Digitalis glycosides (Digoxin)
Inhibit Na+/K+ ATPase
Positive inotrope
Decreased AVN conduction
Caution with renal disease
Toxicity - GI signs, arrhythmias
Recent clinical trials concerning the use of ACE inhibitors, β-blockers, spironolactone, and pimobendan in asymptomatic disease and heart failure will be reviewed.
QUEST - Pimobendan vs. benazepril trial in patients with congestive heart failure secondary to degenerative mitral valve disease.
VETPROOF (follow-up) - Enalapril trial in asymptomatic patients with degenerative mitral valve disease.
Benazepril study - University of Alfort - Benazepril trial in asymptomatic patients with degenerative mitral valve disease.
Spironolactone studies - spironolactone reduces the risk of cardiac death and is safe to use in dogs in congestive heart failure secondary to degenerative valve disease.
EPIC study - multicenter study evaluating the use of pimobendan in asymptomatic patients with degenerative mitral valve disease.
References
1. Kittleson MD, Kienle R. Small Animal Cardiovascular Medicine. St. Louis, MO: Mosby; 1998.
2. Plumbs Veterinary Drugs, online edition.
3. Lefebvre HP, Ollivier E, et al. Safety of spironolactone in dogs with chronic heart failure because of degenerative valvular disease: a population-based, longitudinal study. J Vet Intern Med. 2013;27(5):1083–91.
4. Bernay F, Bland JM, et al. Efficacy of spironolactone on survival in dogs with naturally occurring mitral regurgitation caused by myxomatous mitral valve disease. J Vet Intern Med. 2010;24(2):331–41.
5. Häggström J, Boswood A, et al. Longitudinal analysis of quality of life, clinical, radiographic, echocardiographic, and laboratory variables in dogs with myxomatous mitral valve disease receiving pimobendan or benazepril: the QUEST study. J Vet Intern Med. 2013;27(6):1441–51.
6. Atkins CE, Keene BW, et al. Results of the veterinary enalapril trial to prove reduction in onset of heart failure in dogs chronically treated with enalapril alone for compensated, naturally occurring mitral valve insufficiency. J Am Vet Med Assoc. 2007;231(7):1061–9.
7. Pouchelon JL, Chetboul V, et al. Effect of benazepril on survival and cardiac events in dogs with asymptomatic mitral valve disease: a retrospective study of 141 cases. J Vet Intern Med. 2008;22(4):905–14.