Page 220 - Clinical Small Animal Internal Medicine
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188  Section 3  Cardiovascular Disease

            Table 19.1  (Continued)
  VetBooks.ir  Drug             Indications    Dose                               Comments/Adverse Effects


             Calcium channel blockers
             Diltiazem          HCM            Cat: 7.5 mg/cat q8h                Bradycardia, hypotension
                                Atrial fibrillation  Cat: Cardizem CD 10 mg/kg q24h  Gastrointestinal signs
                                               Cat: Dilacor 30 mg/cat q12h
                                Atrial fibrillation  Dog: 0.5–1.5 mg/kg q8h
                                               Cardizem CD or Dilacor XR
                                               (sustained release) 3 mg/kg BID
             Verapamil          HCM            Cat: 1–5 mg/kg q12h                Potent negative inotrope
                                                                                  Titrate over 2–3 weeks
             Calcium Channel Blocker
             Aspirin            Antiplatelet   Dog: 1–5 mg/kg q24h                Gastrointestinal signs
                                               Cat: 20–81 mg/cat q72h
             Clopidogrel        Antiplatelet   Cat: 18.75 mg/cat q24h             Well tolerated
                                               Dog: 3–5 mg/kg q24h
             Nutritional supplements
             Taurine            Taurine deficiency  Dog: 35 mg/kg q12h            Long‐term supplementation needed
             L‐carnitine        L‐carnitine    Dog: 50 mg/kg q8h                  Unknown efficacy
                                deficiency
            ACE, angiotensin converting enzyme; BID, twice a day (bis in die); CHF, congestive heart failure; HCM, hypertrophic cardiomyopathy;
            RAAS, renin‐angiotensin‐aldosterone system; SID, once a day (semel in die).


            CHF and ACEI are considered the first‐line choice for   known renal dysfunction, benazepril is often the ACEI of
            vasodilator therapy in dogs and cats with CHF. In humans,   choice due to its nonrenal excretion, especially in feline
            angiotensin receptor blockers can be used if ACEI are not   patients. Lisinopril is absorbed in its active form and does
            tolerated (intractable cough is a common side‐effect), but   not require hepatic metabolism to be active. Lisinopril is
            relatively little is known about the use of angiotensin   excreted in the urine, and this drug could be chosen for
            receptor blockers in veterinary patients with chronic CHF.  patients with concurrent cardiac and hepatic disease.
                                                                In general, ACEI are well tolerated. The most common
            ACE Inhibitors                                    adverse events are azotemia and hypotension. In the
            ACE inhibitors are commonly used, including benazepril   authors’ experience, initiating  full dosing of an ACEI
            (0.25–0.5 mg/kg PO q12–24h in dogs and cats), enalapril   during concomitant aggressive diuretic treatment of
            (0.5 mg/kg PO S‐BID in dogs and cats), lisinopril (0.25–  acute CHF can occasionally lead to hypotension and
            0.5 mg/kg PO SID in dogs), ramipril (0.25 mg/kg PO SID   severe azotemia. ACEI do not appear essential for the
            in dogs), and imidipril (0.25–0.5 mg/kg PO SID in dogs).   successful resolution of acute CHF, and the authors usu-
            There is no obvious clinical benefit of one ACEI over the   ally initiate ACEI therapy only once patients are stable
            other and their differences lie in their absorption, metab-  with only mild or no remaining CHF (see Treatment of
            olism, and excretion. Benazepril is activated in the liver to   Acute Heart Failure later) and when hydration status and
            benazeprilat and, in dogs, is equally excreted by the bil-  blood pressure are adequate. ACEI are not particularly
            iary and renal routes while in cats, benazepril is primarily   potent arterial vasodilators and their benefits are most
            excreted by the biliary route. Enalapril is activated in the   likely due to the long‐term suppression of the RAAS.
            liver to its active metabolite, enalaprilat, and excreted by   The authors recommend checking a baseline renal and
            the kidneys. Lisinopril is absorbed in its active form and   electrolyte profile and within the first 10 days after start-
            excreted by the kidney while ramipril may have more   ing the medication. Owners should be instructed to
            effect on tissue‐specific RAAS and is partially excreted in   monitor for poor appetite, lethargy, vomiting, or changes
            the urine and feces.                              in water consumption or urine output.
             The authors typically use enalapril as the first choice   In instances where underlying renal insufficiency or
            due to long‐standing clinical experience with this agent   volume depletion is present, the authors occasionally
            as well as the convenient sizes of commercially available   start enalapril at either 0.5 mg/kg q24h or 0.25 mg/kg
            tablets in the US (2.5, 5, 10, and 20 mg). In instances of   BID for the first 3–5 days of treatment and titrating to a
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