Page 469 - Small Animal Internal Medicine, 6th Edition
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CHAPTER 28   General Therapeutic Principles   441


            management  of  gastroparesis  (in  which  it  is  usually  more   the dog is unknown but suggested to be 10-40 mg/kg SC
            effective than metoclopramide) and small intestinal ileus. It   q12-24h.
  VetBooks.ir  has rarely been reported to be beneficial in dogs with mega-  used in dogs with colonic inflammation. This drug is gener-
                                                                   Salicylazosulfapyridine (sulfasalazine [Azulfidine]) is
            esophagus (perhaps because the dogs had gastroesophageal
            reflux). Cisapride is no longer available from human phar-
                                                                 It is a combination of sulfapyridine and 5-aminosalicylic acid.
            macies but is generally available from veterinary pharmacies.   ally not beneficial in animals with small intestinal problems.
            It is typically available only as an oral preparation, but can   Colonic  bacteria split the  molecule, and 5-aminosalicylic
            be formulated for parenteral use. It has few significant   acid (probably the active moiety) is subsequently “depos-
            adverse effects, although intoxication with large doses may   ited” on diseased colonic mucosa. Dogs generally receive
            cause diarrhea, muscular tremors, ataxia, fever, aggression,   50 to 60 mg/kg divided into three doses daily, but not to
            and other central nervous system signs. It should not be used   exceed 3 g daily. Sulfasalazine given orally may be effective at
            concurrently with drugs that are hepatic P450 inhibitors or   lower-than-expected doses if used in combination with glu-
            that inhibit P-glycoprotein. Erythromycin stimulates motilin   cocorticoids. Anecdotally, 15 to 20 mg/kg/day, sometimes
            receptors and enhances gastric motility at doses less than   divided into twice-daily doses, is often tolerated by cats,
            required for antibacterial activity (i.e., 0.5-1 mg/kg). It may   but they must be closely observed for salicylate intoxication
            also increase intestinal motility. Nizatidine and ranitidine are   (i.e., lethargy, anorexia, vomiting, hyperthermia, tachypnea).
            H 2  receptor antagonists that have some gastric prokinetic   Some cats that vomit or become hyporexic may tolerate the
            effects at  routinely  administered  doses.  Bethanechol  (Ure-  medication if it is given in enteric-coated tablets. Many dogs
            choline) is an acetylcholine analog that stimulates intestinal   with colitis respond to therapy in 3 to 5 days. However, the
            motility and secretion. It produces strong contractions that   drug may have to be given for 2 weeks before one decides
            can cause pain or injure the animal; hence, it is infrequently   that it is ineffective. If signs of colitis resolve, the dose should
            used except for increasing urinary bladder contractions.   be gradually reduced. If the patient cannot be weaned off the
            Obstruction of an outflow area can be a contraindication to   drug entirely, the lowest effective dose should be used and
            the use of prokinetic drugs because vigorous contractions   the animal monitored regularly for drug-induced adverse
            against such a lesion may cause pain or perforation. Obstruc-  effects (especially those resulting from the sulfa moiety). Sul-
            tion of the urinary outflow tract is also a contraindication to   fasalazine may cause transient or permanent keratoconjunc-
            the use of bethanechol.                              tivitis sicca. Other possible complications include cutaneous
              Pyridostigmine (Mestinon) inhibits acetylcholinesterase   vasculitis, arthritis, bone marrow suppression, diarrhea, and
            and is used to treat myasthenia gravis. It is preferred over   any other problem reported with sulfa drugs or NSAIDs.
            physostigmine and neostigmine. It is used for the treatment   Olsalazine and mesalamine contain or are metabolized to
            of acquired megaesophagus due to localized myasthenia. It   5-aminosalicylic acid but do not have the sulfa, which is
            must be used cautiously because overdose may cause toxic-  responsible for most of sulfasalazine’s adverse effects. In
            ity accompanied by signs of parasympathetic overload (e.g.,   people they are as effective as sulfasalazine but safer. Olsala-
            vomiting, miosis, diarrhea).                         zine and mesalamine have been used effectively in dogs.
                                                                 They are given in a dose generally about half that of sulfasala-
                                                                 zine. Keratoconjunctivitis sicca has also developed in dogs
            ANTIINFLAMMATORY AND                                 receiving mesalamine.
            ANTISECRETORY DRUGS                                    Glucocorticoids are potentially indicated in animals with
                                                                 chronic alimentary tract inflammation (e.g., moderate to
            Intestinal antiinflammatory or antisecretory drugs (or both)   marked inflammatory bowel diseases) that is unresponsive
            are indicated for lessening fluid losses due to diarrhea or for   to well-designed elimination diets and/or antimicrobial
            controlling intestinal inflammation that is unresponsive to   therapy. Prednisolone is preferred over prednisone. Rela-
            dietary or antibacterial therapy.                    tively high doses (i.e., prednisolone, 2.2 mg/kg/day PO) are
              Bismuth subsalicylate (Pepto-Bismol, Kaopectate)  is   often used initially, and the dose is tapered to find the lowest
            effective in many dogs with acute enteritis (see Table 28.6),   effective dose. Dexamethasone is sometimes effective when
            probably because of the antiprostaglandin activity of the   prednisolone is not, but dexamethasone is much more
            salicylate moiety. Its main disadvantages are that the salicy-  ulcerogenic than prednisolone. If oral administration is a
            late is absorbed (warranting cautious use in cats or dogs   problem in a cat, long-lasting steroid injections (e.g., methyl-
            receiving nephrotoxic drugs), it turns stools black (mimick-  prednisolone acetate) may be tried. Methylprednisolone
            ing melena), and it must be administered orally (many   appears to be a more effective antiinflammatory than pred-
            animals dislike its taste). Bismuth is bactericidal for certain   nisolone, requiring only 80% of the dose used when admin-
            organisms (e.g., Helicobacter spp.).                 istering prednisolone. Budesonide (Entocort) is a steroid
              Octreotide (Sandostatin) is a synthetic analog of soma-  that is largely eliminated from the body by first-pass metabo-
            tostatin that inhibits alimentary tract motility and secretion   lism in the liver, thus diminishing (but not totally eliminat-
            of gastrointestinal hormones and fluids. It has had limited   ing) systemic steroid side effects. It is primarily indicated in
            use in dogs and cats but might be helpful in selected animals   patients who are  known  to  respond  to  prednisolone  but
            with intractable diarrhea or lymphangiectasia. The dose in   cannot tolerate that steroid’s side effects.
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