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19  Management of Heart Failure  197

                 Nitroprusside is a potent mixed vasodilator capable of   to rapidly acting short‐term effects in acute CHF. The
  VetBooks.ir  both venous and arterial vasodilation. It acts by releasing   rate‐limiting factors affecting ACEI use include azotemia
                                                                  and systemic arterial hypotension. The authors occa-
               nitric oxide, which induces vascular smooth muscle
               relaxation. Nitroprusside is metabolized very rapidly and
                                                                  lized  with diuretics, positive inotropes, and  other
               is administered via CRI (1–10 μg/kg/min in dogs). Its   sionally delay initiation of ACEI until acute CHF is stabi-
               rate‐limiting factor is systemic arterial hypotension, and   vasodilators, and are especially cautious in patients
               blood pressure monitoring is highly recommended dur-  already suffering from systemic hypotension or in those
               ing use. Typically, the dosage is adjusted to achieve a sys-  that required very high doses of diuretics to alleviate
               tolic arterial blood pressure no lower than 90 mmHg.   congestion and are significantly dehydrated. In these
               The short half‐life of nitroprusside allows clinicians to   cases, ACEI administration might be delayed until the
               effectively make changes in infusion rates in response to   patient’s hydration status and renal bloodwork are
               blood pressure. Nitroprusside, while highly effective, is   reevaluated. They are then prescribed as part of the
               only occasionally used due to its need for CRI and sensi-  chronic CHF therapy with close monitoring of renal
               tivity to light that requires the administration set to be   bloodwork and systemic blood pressure.
               covered in light‐protective wrapping. Similar to dopa-
               mine or dobutamine, nitroprusside infusions are given   Additional Therapies for Acute CHF
               short term, typically not longer than 48 hours. At very
               high doses or for extended periods of administration,   Oxygen supplementation is provided in cases of res-
               accumulation of nitroprusside metabolites such as   piratory compromise and hypoxemia. Inspired O 2  con-
               cyanogen can result in toxicity. Nitroprusside is rarely   centration is typically increased to 40% through the use
               used in cats. At the time of writing, supply shortages of   of oxygen cages or, in the case of large dogs, nasal insuf-
               nitroprusside have severely curtailed its use and alterna-  flation. Manual removal of pleural, pericardial, or
               tive nitric oxide donors such as IV nitroglycerin (1–10 μg/  abdominal fluid should be performed if these effusions
               kg/min) have been used.                            are a cause of respiratory compromise. In patients that
                                                                  are extremely anxious, mild sedation with morphine
                                                                  (0.1–1.0 mg/kg SC/IM in dogs), acepromazine (0.1–
               ACE Inhibitors
                                                                  0.2 mg/kg SC/IM in dogs) or butorphanol (0.1–0.3 mg/
               ACE inhibitors form a cornerstone of therapy of chronic   kg IM/IV in dogs or cats) can be considered. Care must
               CHF. Their utility in acute life‐threatening CHF is less   be taken to avoid oversedation as further compromise
               evident. Compared to hydralazine or nitroprusside, the   of respiratory function can result. Bronchodilators
               arterial dilating effects of ACEI are modest. ACEI’s abil-  such as aminophylline or theophylline or cough sup-
               ity to decrease AT II and aldosterone production appears   pressants such as hydrocodone are rarely needed in
               more beneficial over longer periods of time as opposed   cases of acute CHF.


                 Further Reading


               Atkins C, Bonagura J, Ettinger S, et al. Guidelines for the   Haggstrom J, Boswood A, O’Grady M, et al. Effect of
                 diagnosis and treatment of canine chronic valvular heart   pimobendan or benazepril hydrochloride on survival
                 disease. J Vet Intern Med 2009; 23: 1142–50.       times in dogs with congestive heart failure caused by
               Boswood A, Haggstrom J, Gordon SG, et al. Effect of   naturally occurring myxomatous mitral valve disease:
                 pimobendan in dogs with preclinical myxomatous mitral   the QUEST study. J Vet Intern Med 2008; 22: 1124–35.
                 valve disease and cardiomegaly: the EPIC study – a   Luis Fuentes V. Treatment of congestive heart failure. In:
                 randomized clinical trial. J Vet Intern Med 2016; 30:   Luis Fuentes V, Johnson LR, Dennis S, eds. BSAVA
                 1765–79.                                           Manual of Canine and Feline Cardiorespiratory
               Ferasin L, Defrancesco T. Management of acute heart   Medicine. Gloucester, UK: British Small Animal
                 failure in cats. J Vet Cardiol 2015; 17(Suppl 1): S173–89.  Veterinary Association, 2010, pp. 153–9.
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