Page 730 - Small Animal Internal Medicine, 6th Edition
P. 730

702    PART V   Urinary Tract Disorders


            wk. Presumptive adverse effects included vomiting, hyper-  effect on systemic blood pressure and in cats may contribute
            tension, seizures, and fever. Because of its structure and   to increased urinary loss of potassium and hypokalemia by
  VetBooks.ir  lower dosage, darbepoetin alfa is thought to be less likely to   activation of the renin-angiotensin system. Diuretics (e.g.,
                                                                 furosemide, hydrochlorothiazide) generally are not used to
            result in antibody formation when used in dogs and cats.
            Canine and feline recombinant erythropoietin have been
                                                                 concern about dehydration and prerenal azotemia. The effect
            synthesized and been shown to be effective but are not com-  treat hypertension in dogs and cats with CKD because of
            mercially available.                                 of ACE inhibitors on systemic blood pressure may be modest,
              Calcitriol. In the kidney, 25–hydroxycholecalciferol is   but other potentially beneficial effects warrant their use in
            converted to the active form of vitamin D 3 , 1,25–  dogs and cats with CKD (see earlier). Dihydropyridine
            dihydroxycholecalciferol (calcitriol), by 1α–hydroxylase in   calcium channel blockers (e.g., amlodipine) are effective for
            the tubular cells. The 1α-hydroxylase is stimulated by PTH   treatment of hypertension in cats at a dosage of 0.625 to
            and hypophosphatemia and inhibited by calcitriol and   1.25 mg PO, q24h.  Amlodipine  can be used in  dogs at a
            FGF-23. The major effects of calcitriol are to increase the   dosage of 0.1 to 0.5 mg/kg PO, q12h. Gingival hyperplasia is
            intestinal absorption of calcium (and phosphate), facilitate   an uncommon and reversible adverse effect in dogs. Nondi-
            PTH–mediated bone resorption of calcium and phosphorus,   hydropyridine calcium channel blockers (e.g., verapamil,
            increase renal tubular reabsorption of calcium (and phos-  diltiazem) may decrease proteinuria and be renoprotective
            phate), and provide negative feedback control on PTH syn-  in humans but have not been evaluated for this purpose in
            thesis by the parathyroid glands; a relative lack of this effect   dogs and cats.
            plays an important role in the development of renal second-
            ary hyperparathyroidism in patients with CKD.        SUPPORTIVE CARE
              Calcitriol is helpful in the management of renal second-  Some owners can be taught to administer fluids subcutane-
            ary hyperparathyroidism because of its ability to feed back   ously to their animals at home. This is particularly conve-
            to calcitriol receptors in the parathyroid glands and decrease   nient for cats and small dogs. For example, if the owner
            PTH synthesis and secretion. If the [Ca]  × [P i ] solubility   is willing to learn the technique and the cat is coopera-
            product is more than 60 to 70, calcitriol therapy should be   tive, 60 mL of lactated Ringer’s solution can be given sub-
            avoided  because of  the risk  of  soft  tissue  mineralization.   cutaneously two or three times per day. If the owner has
            Calcitriol should only be used after hyperphosphatemia has   noticed that the cat did not absorb previously administered
            been adequately controlled by a low-phosphorus diet and   fluids, additional fluid should not be given. Also, if the
            oral phosphorus binders, if necessary. A very low dosage of   owner experiences technical difficulty administering fluids
            calcitriol (2.5–3.5 ng/kg/day) has been used in dogs and cats   subcutaneously, it is preferable for fluids to be adminis-
            with CKD to prevent or reverse renal secondary hyperpara-  tered on an outpatient basis at the veterinary clinic. The
            thyroidism. Serial serum calcium concentrations should be   additional fluid support appears to have beneficial effects
            monitored to detect hypercalcemia. Serum PTH concentra-  on the animal’s quality of life, and in one study, 47% of
            tions fall dramatically in dogs and cats with CKD treated   cats with CKD were reported to be receiving subcutane-
            with calcitriol, and survival time may be increased.  ous fluids as part of their treatment. If the owner is having
              Anabolic steroids                                  difficulty getting the animal to eat, a feeding tube should
              Many products are available but there are no long-term   be considered to ensure adequate caloric intake and facili-
            studies demonstrating the efficacy of anabolic steroids in   tate administration of medications. Most cats tolerate per-
            dogs and cats with CKD. The anabolic steroid stanozolol   cutaneously placed gastrostomy tubes well for extended
            (Winstrol-V) has equivocal effects in dogs with CKD. In cats,   periods of time, and this approach can make medical man-
            it is hepatotoxic and has been associated with increased liver   agement much easier and less stressful for the owner and
            enzyme activities, vitamin K-responsive coagulopathy, cho-  the cat.
            lestasis, and hepatic lipidosis. Anabolic steroids usually are
            not recommended for dogs and cats with CKD.          Course and Prognosis
              Blood pressure control agents                      The rate of progression of CKD varies among individual
              The presence of systemic hypertension is a risk factor for   animals, and affected dogs and cats may live months to years.
            uremic crises, more rapid progression, and mortality in dogs   The slope of the relationship of the reciprocal of the SCr (1/
            with  CKD.  In cats, it  can  be  difficult  to  decide  whether   SCr) versus time may give a rough indication of the rate of
            hypertension really is present because of the white coat   progression of CKD. Findings that warrant a poor prognosis
            effect. Dogs and cats with a systolic blood pressure of 150 to   include severe intractable anemia, inability to maintain fluid
            159 mm Hg and evidence of end-organ damage (e.g., cardio-  balance, and progressive azotemia, despite fluid therapy and
            vascular or ocular complications) are candidates for antihy-  conservative medical management.
            pertensive treatment. Those with a systolic blood pressure of
            160 to 179 mm Hg or higher are candidates for treatment,   Suggested Readings
            regardless of evidence of target organ damage.       Chalhoub S, et al. The use of darbepoetin to stimulate erythropoi-
              Most commercial diets formulated for dogs and cats with   esis in anemia of chronic kidney disease in cats: 25 cases. J Vet
            CKD are low in salt. Sodium restriction may have a limited   Intern Med. 2012;26:363.
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