Degenerative mitral valve disease (DMVD) and dilated cardiomyopathy are the most common types of acquired heart disease in dogs. Although innovative therapies such as surgical repair of the mitral valve and gene therapy are emerging, medical treatment remains the mainstay for most dogs in the preclinical phase as well as dogs with congestive heart failure (CHF).<\/p>\n
This article reviews drugs commonly used for the management of these common diseases: pimobendan, diuretics, renin-angiotensin-aldosterone system inhibitors, and aldosterone antagonists.<\/p>\n
Take-Home Points<\/strong><\/p>\n Although innovative therapies for common acquired heart diseases in dogs are emerging, medical treatment with diuretics, pimobendan, renin-angiotensin-aldosterone system (RAAS) inhibitors, and aldosterone antagonists remains the mainstay for most dogs with congestive heart failure (CHF)<\/a>. <\/span><\/p>\n This first of 2 articles reviews drugs commonly used for the management of preclinical and clinical degenerative mitral valve disease (DMVD)<\/a> and dilated cardiomyopathy (DCM)<\/a> in dogs (<\/span>TABLE 1<\/b><\/span>). It includes insight regarding when to perform dose escalation, key clinical data available, monitoring plans, and side effects associated with these common therapies. TABLE<\/b><\/span><\/span>\u00a02<\/b><\/span> <\/b>summarizes the staging of heart disease and CHF according to the American College of Veterinary Internal Medicine consensus guidelines.<\/span><\/p>\n Approval status:<\/b> Pimobendan<\/a> is approved for management of CHF in dogs with DCM or DMVD and marketed as Vetmedin for this indication. It is also marketed as Vetmedin-CA1 for the indication of delaying CHF onset in dogs with preclinical DMVD (stage B2), for which it has been conditionally approved by the U.S. Food and Drug Administration (FDA) based on a study that showed clinical benefit in this population but was not designed to meet all FDA requirements for approval.3<\/sup> A pivotal study is currently in progress (EPOCHAL, <\/span>dogheartstudy.com<\/span><\/a>) that is designed to fulfill FDA requirements for approval of pimobendan for preclinical DMVD.<\/span><\/p>\n Manufacturer:<\/b> Boehringer Ingelheim Animal Health (<\/span>bi-animalhealth.com<\/span><\/a>)<\/span><\/p>\n Mechanism of action: <\/b>Pimobendan is an inodilator, meaning it has both positive inotropic and vasodilatory effects. Increased sensitization of the cardiomyocyte to calcium leads to increased\u00a0contractility (inotropy), and inhibition of phosphodiesterase 3 and 5 enzymes leads to smooth muscle relaxation.4<\/sup> Both increased contractility and afterload reduction increase stroke volume and cardiac output.4<\/sup><\/span><\/p>\n Cardiac indications:<\/b> Pimobendan is indicated for preclinical (stage B2) and clinical (stage C and D) DMVD and DCM patients.3,5-7<\/sup> <\/span><\/p>\n Administration:<\/b> The starting dosage is 0.25 to 0.3 mg\/kg PO q12h, with higher doses and dose frequency in patients with refractory CHF. In the authors\u2019 experience, most dogs tolerate dosage increases, and the added inodilation could minimize the amount of diuretic needed to control signs of fluid retention. Pimobendan can be suspended with water immediately before administration. Some formulations have variable bioavailability and stability; therefore, consultation with a veterinary pharmacist is recommended if compounding is desired.\u00a0<\/span><\/p>\n Key clinical data:<\/b> The EPIC trial showed that pimobendan delays the onset of CHF by approximately 15 months in dogs with preclinical DMVD compared to placebo.3<\/sup> The QUEST study showed that pimobendan was superior to benazepril in dogs with CHF secondary to DMVD.5<\/sup> The PROTECT study showed that pimobendan delays the onset of CHF and\/or sudden cardiac death by approximately 9\u00a0months in Doberman pinschers with preclinical DCM.7<\/sup> An earlier study demonstrated a survival benefit of pimobendan in Doberman pinschers with DCM and CHF.6<\/sup><\/span><\/p>\n Monitoring\/side effects:<\/b> No biochemical monitoring is necessary in patients treated solely with pimobendan. Vomiting, diarrhea, anorexia, and lethargy occur rarely. <\/span><\/p>\n Approval status:<\/b> Furosemide is approved for the treatment of CHF in dogs.<\/span><\/p>\n Manufacturer: <\/b>Various<\/span><\/p>\n Mechanism of action:<\/b> Furosemide is a loop diuretic that binds to the sodium-potassium-chloride cotransporter in the kidney at the thick ascending limb of the loop of Henle. This inhibits electrolyte resorption, subsequently causing loss of sodium, potassium, chloride, and water in the urine. Magnesium and calcium are also lost into the renal tubule. The loss of sodium and water in the urine (diuresis) results in decongestion due to removal of excess fluid from the intracellular and intravascular spaces, driven by Starling\u2019s forces. Furosemide also causes pulmonary vasodilation and increased renal blood flow through prostaglandin synthesis, which is most evident when administered intravenously.<\/span><\/p>\n Cardiac indications:<\/b> Furosemide is used to relieve fluid accumulation associated with CHF, regardless of underlying etiology. Furosemide is contraindicated when pericardial effusion is the cause of right-sided CHF because it reduces preload. Furosemide is not indicated in preclinical disease.\u00a0<\/span><\/p>\n Administration:<\/b> Pharmacokinetic differences related to administration route are important considerations for dosing frequency. Diuresis occurs for 1 hour after intravenous, 2 to 3 hours after intramuscular, 4 hours after subcutaneous, and 6 hours after oral administration. <\/span><\/p>\n Acute CHF:<\/b> Intravenous or intramuscular furosemide is commonly administered as a bolus of 2 mg\/kg in dogs. This dose can be repeated at 1- to 2-hour intervals until the respiratory rate decreases, at which time the dose and\/or frequency are reduced. Alternatively, furosemide can be administered as a constant-rate infusion starting at 0.6 mg\/kg\/h, which allows for downward dosage adjustments based on respiratory rates; the authors rarely use an infusion for longer than 6 to 8 hours. The infusion line should be covered to prevent light degradation. Regardless of method used, the cumulative intravenous furosemide dose for acute CHF should be tracked to avoid excessive doses. In the authors\u2019 practice, most patients require a cumulative intravenous furosemide dose <10\u00a0mg\/kg to treat acute pulmonary edema.<\/p>\n Chronic CHF:<\/b> A typical starting dosage for orally administered furosemide in dogs is 1 to 2 mg\/kg q12h. The dosage can be increased to address recurrent CHF by increasing the amount given or the frequency; however, if the total daily dose exceeds 6 to 8 mg\/kg\/d, transition to torsemide should be considered. Furosemide\u2019s variable bioavailability (10% to 90%) might account for poor diuretic responsiveness, especially in dogs with gastrointestinal disease or right-sided CHF. In humans, concurrent food administration reduces bioavailability by 30%, and nonsteroidal anti-inflammatory drugs decrease the efficacy of loop diuretics because they compete for secretion into the renal tubule.8,9<\/sup><\/p>\n Key clinical data:<\/b> Furosemide is generally accepted as lifesaving treatment in dogs with dyspnea from acute CHF, but no clinical trial data are available to demonstrate a survival benefit. Multiple studies in healthy and diseased dogs provide pharmacokinetic and pharmacodynamic data to guide dosing.10,11<\/sup><\/span><\/p>\n Monitoring:<\/b> Body weight, hydration status, and select serum biochemical parameters (i.e., blood urea nitrogen, creatinine, sodium, potassium, chloride, bicarbonate) should be monitored in patients receiving furosemide 1\u00a0to 2 weeks after drug initiation or dosage change and at regular intervals thereafter.\u00a0<\/span><\/p>\n Side effects: <\/b>Diuresis and natriuresis cause polyuria with reactive polydipsia. If diuresis is excessive, it reduces intravascular volume and induces electrolyte loss with signs such as lethargy, weakness, loss of appetite, and vomiting. High furosemide doses can cause hypochloremic metabolic alkalosis in addition to azotemia. Furosemide stimulates the RAAS indirectly via volume depletion and directly by impairing salt sensing in the kidney. Chronic furosemide administration reduces its own efficacy (tolerance), likely due to RAAS activation and upregulation of sodium-retentive mechanisms distal to the loop of Henle. Loop diuretics should be used at the lowest effective dosages and with adjunctive therapies to minimize the risk of adverse effects.<\/span><\/p>\n Approval status:<\/b> Enalapril is approved to treat CHF in dogs; however, the brand Enacard is no longer available. The combination of benazepril and spironolactone (Cardalis) is FDA approved for the treatment of CHF in dogs.\u00a0<\/span><\/p>\n Manufacturer:<\/b> Various. Cardalis is manufactured by Ceva Animal Health (<\/span>cardalis.com<\/span><\/a>).<\/span><\/p>\n Mechanism of action:<\/b> Angiotensin-converting enzyme inhibitors (ACEIs) reduce the formation of angiotensin\u00a0II (Ang II) by inhibiting angiotensin-converting enzyme, thereby lessening the vasoconstrictive, sodium-retentive, aldosterone-<\/span>stimulating, and inflammatory actions of Ang II. ACEIs also reduce the metabolism of angiotensin 1\u20137 and bradykinin, both of which promote vasodilation and <\/span>natriuresis.12<\/sup> They have minimal antihypertensive effects. While benazepril is eliminated through hepatic and renal mechanisms, enalapril is entirely renally excreted.\u00a0<\/span><\/p>\n Cardiac indications: <\/b>ACEIs are indicated for the treatment of stable CHF in dogs. They are not usually administered in the acute CHF setting. Because aldosterone is not adequately suppressed in 30% to <\/span>40% of dogs receiving ACEIs (aldosterone breakthrough),<\/span> concurrent spironolactone is recommended. Strong evidence for benefit of ACEI therapy in preclinical DMVD is lacking, although some experts prescribe ACEIs in dogs with stage B2 DMVD.1<\/sup><\/span><\/p>\n Administration: <\/b>ACEIs are administered at 0.25 to 0.5\u00a0mg\/kg PO q12h to q24h, with doses and frequency varying between agents. One study suggests that twice daily dosing optimizes cardioprotective benefits.13<\/sup> Reductions in enalapril dose or dose frequency should be considered for dogs with renal disease.<\/span><\/p>\n Key clinical data:<\/b> Early clinical studies demonstrated reductions in mortality and morbidity in dogs with CHF treated with ACEIs.14-16<\/sup> More recently, a prospective study did not find additional benefit of ACEIs over pimobendan and diuretic therapy17<\/sup>; however, dogs in this study were not receiving spironolactone and were on low ACEI doses and high furosemide doses. The importance of comprehensive RAAS suppression in dogs with CHF was evidenced by the BESST trial, which showed superior outcomes for dogs treated with benazepril and spironolactone compared to benazepril alone.18<\/sup> The BESST was the basis for the FDA approval of Cardalis; however, this study did not include pimobendan.18<\/sup><\/span><\/p>\n Monitoring:<\/b> Select serum biochemical variables (i.e., blood urea nitrogen, creatinine, sodium, potassium, chloride) should be evaluated before treatment, 1 to 2\u00a0weeks after initiation of therapy, and periodically thereafter or as dictated clinically. ACEIs can cause hyperkalemia<\/a>, although this occurs infrequently, especially with concurrent diuretic use. A small rise in serum creatinine (typically <0.3 mg\/dL) is expected after ACEI initiation due to reduction of Ang II, resulting in efferent arteriolar vasodilation. Increases greater than 0.3 mg\/dL warrant consideration of diuretic or ACEI dose adjustments. Although the antihypertensive effect of ACEIs is minimal, blood pressure monitoring should ideally be performed at each recheck.<\/span><\/p>\n\n
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<\/a><\/p>\nPimobendan<\/h2>\n
(Vetmedin, Vetmedin-CA1)<\/h3>\n
Furosemide<\/h2>\n
Angiotensin-Converting Enzyme Inhibitors<\/h2>\n
(Enalapril, Benazepril, Ramipril, Captopril, Lisinopril)<\/h3>\n