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26  Canine Myocardial Disease  261

               in addition to delay in disease progression and prolon-  sinus rhythm may be physiologically ideal, rate control is
  VetBooks.ir  gation of survival. Strategies include intravascular vol-  much more feasible. Evidence suggests that the combina-
                                                                  tion of diltiazem with digoxin is more efficacious for rate
               ume reduction to resolve pulmonary edema or decrease
               cavitary effusions, improvement in hemodynamic
                                                                  <125 bpm on Holter recording is ideal, and given higher
                 performance through decreased systemic vascular   control than either drug alone. A target mean HR
               resistance  and improved contractility, neurohumoral   HR in hospital, target mean HR on in‐hospital ECG
               modulation, arrhythmia management, and nutritional   should be <140–150 bpm. Alternative therapy choices
               management.                                        include a beta‐blocker or sotalol, though beta‐blockers
                 The mainstay of treatment of edema and effusions   should not be initiated in the setting of acute or poorly
               remains diuretics, with furosemide the most commonly   managed heart failure.
               used agent. It may be administered orally or intrave-  Cardiac cachexia is identified commonly in DCM CHF
               nously depending on the severity of CHF and whether   patients and nutritional support is an important part of
               the patient is being treated as an inpatient or outpatient.   therapy. Due to anorexia, increased energy require-
               Following edema resolution, the dose may be lowered to   ments, and production of inflammatory cytokines, lean
               the effective dose that maintains the patient free of   muscle mass is lost in the chronic heart failure patient.
                 respiratory signs and edema. Given its relatively short   Management involves providing adequate calories and
               duration of action, dosing more than twice daily may be   protein, and there is evidence that supplementation with
               more effective. Substantive pleural effusion or ascites   omega‐3 fatty acids is beneficial. While diets restricted
               should be relieved with thoraco‐ and abdominocentesis,   in sodium are commonly advocated, the effects on qual-
               respectively.                                      ity of life or survival have not been assessed in dogs.
                 Angiotensin converting enzyme inhibitor is indicated
               for RAAS blockade and vasodilatory effects, particularly   Overt DCM – Severe Life‐Threatening CHF
               in the setting of furosemide use which heightens RAAS   Parenteral means of decreasing intravascular volume,
               stimulation. The results of veterinary clinical trials using   increasing contractility, decreasing vascular resistance,
               enalapril and benazepril report improved quality of life,   and treating arrhythmias may be necessary in cases of
               and although the improvements in survival did not reach   severe CHF. Administration of oxygen by nasal prongs,
               statistical significance for DCM dogs, there is clear   cannula or cage is indicated in the case of hypoxia.
                 evidence of mortality reduction in human patients and   Administration of intravenous (IV) furosemide by bolus
               ACEI use is considered standard therapy in dogs with   or constant rate infusion (CRI) is the single most impor-
               DCM and CHF.                                       tant and effective strategy to initiate promptly. Multiple
                 Three placebo‐controlled trials have found signifi-  boluses may be administered 30–60 minutes apart until
               cantly longer time to treatment failure or longer survival   the respiratory rate drops 50% from initial presentation
               time in DCM dogs treated with pimobendan in addition   or effort improves. If there is inadequate response after
               to diuretics and ACEI, so pimobendan is considered part   three doses, CRI should be initiated. Alternatively, one
               of standard therapy for CHF due to DCM.            bolus followed immediately by CRI is preferred if the
                 The  aldosterone  antagonist  spironolactone  signifi-  patient has preexisting azotemia or is particularly severe.
               cantly reduces morbidity and mortality in humans with   Careful monitoring of volume status, renal function, and
               CHF and LV systolic dysfunction. While similar evidence   electrolytes is required. Thoracocentesis is indicated if
               is lacking in dogs with DCM, a study in Dobermans with   substantive pleural effusion is contributing to dyspnea.
               CHF suggested a reduced risk of AF with spironolactone   If rapid AF is present, initiation of IV diltiazem is indi-
               therapy. Spironolactone is often used in the patient that   cated to reduce HR below 140–150 bpm. In cases of VA
               is  still  symptomatic  despite use of  triple  therapy  with   in the setting of CHF, treatment may be warranted if VT
               furosemide, ACEI, and pimobendan, whereas some,    is present, signs of weakness or collapse are present, or
               including the author, advocate using it initially as part of   the patient is a breed with a high incidence of SD such as
               standard therapy. Spironolactone is licensed for use in   Dobermans and boxers. IV lidocaine is typically the first
               dogs with CHF in Europe.                           treatment of choice.
                 Management of the overt DCM patient with VA        In the absence of arrhythmias, IV furosemide may be
               includes optimal management of congestion and hemo-  enough to stabilize some patients whereas others will
               dynamics to reduce sympathetic nervous system stimu-  require the addition of a parenteral positive inotrope +/−
               lation and improve perfusion. Specific AA therapy may   vasodilator. Dobutamine CRI is the IV positive inotrope
               also be indicated. Patients with VA may be managed as   of choice for treatment of severe edema and hypoten-
               outlined above for the preclinical stage. DCM patients   sion. Side‐effects include nausea/vomiting and exacerba-
               with AF and in‐hospital HR >150 bpm are candidates for   tion of VA, in which case the dose should be decreased.
               rate control with AA therapy. While cardioversion to   It is important to note that if AF is present, IV diltiazem
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