Page 157 - Small Animal Internal Medicine, 6th Edition
P. 157

CHAPTER 6   Acquired Valvular and Endocardial Disease   129


            making the diagnosis is unclear. The presence of pulmonary   may help support respiratory muscle function. Bronchodila-
            lobar venous distension suggests that CHF is imminent,   tors can potentially increase the risk for tachyarrhythmias,
  VetBooks.ir  however this is not always seen. When it is unclear if respira-  though. In dogs with moderate- to large-volume pleural effu-
                                                                 sion, thoracocentesis should be done as expeditiously as pos-
            tory signs are caused by heart failure or a noncardiac cause,
            an initial furosemide trial (e.g., 1-2 mg/kg PO q8-12h) for 2
                                                                 to impede respiration also should be drained. Close moni-
            to 3 days can be helpful. Plasma NT-proBNP measurement   sible to improve pulmonary function; ascites severe enough
            also can be useful. Some clinicians add an ACEI during the   toring for the patient’s response to therapy and any adverse
            therapeutic trial for suspected CHF. Cardiogenic pulmonary   effects (e.g., hypotension, azotemia, electrolyte abnormali-
            edema usually responds rapidly, so if CHF was the cause, the   ties, arrhythmias, drug toxicity, and so on) is important for
            owner should see rapid improvement in RR and effort as well   optimizing care (see Chapter 3, p. 65 for additional informa-
            as reduced (cardiogenic) cough. In these cases, triple therapy   tion). Mild to moderate azotemia is common after aggressive
            is instituted along with recommendation for moderate   diuretic therapy. Slow oral “self-rehydration” is effective for
            dietary salt restriction. Depending on the individual case, it   most patients. Because it can exacerbate congestive signs,
            may be possible to reduce the dose of furosemide somewhat,   parenteral fluid therapy is avoided whenever possible (see
            using RRR monitoring as a guide. On the other hand, cough-  Chapter 3, p. 65, section of monitoring and follow-up after
            ing or other respiratory signs that persist despite furosemide   acute CHF treatment).
            trial makes a diagnosis of CHF unlikely. Nevertheless, confu-
            sion is still possible in some cases because a cough from   TRANSITION TO HOME CARE
            airway irritation may resolve spontaneously, or furosemide   After the patient is stabilized, medications are adjusted over
            may have a mild antiinflammatory or antitussive effect.  the next several days to weeks to determine the best regimen
                                                                 for long-term treatment. Furosemide is titrated to the lowest
            MODERATE TO SEVERE SIGNS OF CHF                      dose and longest interval that controls signs of congestion.
            Fulminant pulmonary edema with shortness of breath at rest   RRR monitoring over time helps guide this (see p. 74). An
            is a true emergency. Aggressive therapy, but with gentle han-  ACEI is recommended for chronic therapy if another vaso-
            dling, is crucial in these fragile patients. Cage rest, supple-  dilator was used initially. The ACEI can be dosed once daily
            mental oxygen, high-dose (e.g., 2-4 mg/kg q1-4h initially)   to start as the patient is weaned off the other (arteriolar)
            parenteral furosemide, and vasodilator therapy are indicated   vasodilator over a couple days. The ACEI can be increased
            (see  Box 3.1,  p. 62). Intravenous (IV) nitroprusside or   to q12h dosing over the next several days to a week. Client
            hydralazine (PO or IV) can be used for acute therapy for   education about the purpose and potential adverse effects
            rapid arteriolar vasodilating effect. BP must be closely moni-  of prescribed medications, RRR monitoring, diet, activity
            tored. A low dose is used in animals already receiving an   restrictions, follow-up schedule, and other recommenda-
            ACEI. Amlodipine is another alternative, although onset of   tions is important.
            action is slower. Amlodipine can significantly decrease LA
            pressure and MR regurgitant jet severity compared to ACEI,   MONITORING HEART FAILURE THERAPY
            however up to four days are needed for full effect. Topical   Continued monitoring  is important, especially for renal
            nitroglycerin can be used in combination with an arteriolar   function, serum electrolyte concentrations, BP, and recur-
            dilator in an attempt to reduce pulmonary venous pressure   rent congestive signs. Intermittent arrhythmias can trigger
            by direct venodilation. Pimobendan dosing is begun (or con-  decompensated congestive failure, as well as episodes of
            tinued) as soon as possible.                         transient  weakness  or  syncope.  Cough-induced  syncope,
              Heart  rate  and  rhythm  should  be  monitored. For  the   atrial rupture, or other causes of reduced cardiac output also
            control of supraventricular tachyarrhythmias, diltiazem or a   can occur. Despite periodic recurrence of CHF signs, with
            β-blocker (see Table 4.2, p. 90) can be used instead of or in   proper management many dogs with CMVD enjoy a good
            addition  to  digoxin.  Although  several days  are needed  to   quality of life for several months to years after signs of failure
            achieve therapeutic digoxin serum concentration with oral   first appear. Dogs with recently diagnosed or decompensated
            maintenance doses, IV digoxin is not recommended. Therapy   CHF should be rechecked more frequently (every few days
            for ventricular tachyarrhythmias is warranted in occasional   to every week or so) until their condition is stable; those with
            cases. For dogs with CMVD that require BP support or when   chronic heart failure that is well controlled can be reevalu-
            myocardial function is poor, other more potent inotropic   ated less often but usually at least three to four times per year.
            agents (e.g., dobutamine or dopamine) can be given IV (see
            Box 3.1, p. 62).
              Mild sedation is used to reduce anxiety (e.g., butorphanol;   COMMON COMPLICATIONS
            see Box 3.1, p. 62). Patient handling should be minimized,
            and radiographs and other diagnostic procedures postponed   END-STAGE/REFRACTORY (STAGE D)
            until the respiratory status is more stable. A bronchodilator   HEART FAILURE
            (e.g., theophylline, aminophylline) sometimes is used when   Recurrent acute CHF should be treated in-hospital as
            bronchospasm induced by severe pulmonary edema is sus-  described previously (see Box 3.1, p. 62). Pleural and abdom-
            pected; although the efficacy of this is unclear, these agents   inal effusions are drained as needed to maintain patient
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