Page 228 - Small Animal Internal Medicine, 6th Edition
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200    PART I   Cardiovascular System Disorders


              Coughing or (less often) dyspnea after treatment can be   as levamisole or stibophen as adulticides is not recom-
            related to the HWD itself (pneumonitis), inflammatory reac-  mended. Levamisole does not consistently kill adult HWs,
  VetBooks.ir  tion in the lungs and pulmonary vasculature secondary to   although it is somewhat effective against male worms and
                                                                 may sterilize adult female worms.
            worm  die-off,  or  dead  worm  fragments  causing  PTE. In
                                                                   The use of a flexible alligator forceps with fluoroscopic or
            general, these reactions are steroid responsive and can be
            mitigated by administration of antiinflammatory prednisone   transesophageal echocardiographic guidance has been advo-
            course concurrently with melarsomine. Most clinical signs   cated as a way to reduce the worm burden in accessible seg-
            noted in dogs treated with melarsomine have been behav-  ments of the main or branch pulmonary arteries before
            ioral (e.g., tremors, lethargy, unsteadiness and ataxia, rest-  adulticide  therapy, even in dogs without caval syndrome.
            lessness); respiratory (e.g., panting, shallow breathing,   Removing as many worms as feasible reduces the risk for
            labored respirations, crackles); or injection-site related (e.g.,   postadulticide PTE in heavily infected dogs. However, this
            edema, redness, tenderness, vocalization, increased aspartate   procedure is not routinely performed due to requirements
            aminotransferase and creatine kinase activities). Injection   for imaging equipment and technical expertise, the need for
            site reactions are generally mild to moderate and resolve   sedation or anesthesia, and the potential for worm breakage
            within 4 (to 12) weeks. Occasionally these reactions are   with exacerbated pulmonary reaction.
            severe. The manufacturer reports that firm nodules might
            persist indefinitely at the sites. General signs of lethargy,   POSTADULTICIDE PULMONARY
            depression, and anorexia occur in about 15% or fewer dogs;   THROMBOEMBOLIC COMPLICATIONS
            other adverse effects, including fever, vomiting, and diar-  Pulmonary arterial disease worsens from 5 to 30 days after
            rhea, occur occasionally. Adverse effects generally are mild   adulticide therapy and can be especially severe in previously
            at recommended doses. Hepatic and renal changes have not   symptomatic dogs. Dead and dying worms promote throm-
            proved clinically relevant in animals receiving recommended   bosis and pulmonary artery obstruction, with exacerbation
            doses of melarsomine. Overall, melarsomine causes less sys-  of platelet adhesion, myointimal proliferation, villous hyper-
            temic toxicity than its predecessor, thiacetarsamide. Never-  trophy, granulomatous arteritis, perivascular edema, and
            theless, melarsomine has a low margin of safety. Overdose   hemorrhage. Severe ventilation-perfusion mismatch may
            may cause collapse, severe salivation, vomiting, respiratory   result  from  pulmonary  hypoperfusion,  hypoxic  vasocon-
            distress resulting from pulmonary inflammation and edema,   striction and bronchoconstriction, pulmonary inflamma-
            stupor, and death.                                   tion, and fluid accumulation. PTE is most likely to occur 7
              Strict exercise restriction should be enforced for 4 to 6   to 10 days after adulticide therapy but can occur up to 4
            weeks after each dose of adulticide therapy to reduce the   weeks later. As expected, the caudal and accessory lung lobes
            effects of adult worm death and PTE. The rest period for   are most commonly and severely affected. Pulmonary blood
            working dogs should probably be longer because increased   flow obstruction and increased vascular resistance further
            pulmonary  blood  flow  in  response  to  exercise  exacerbates   strain  the  RV  and  increase  oxygen  demand.  Poor  cardiac
            pulmonary capillary bed damage and subsequent fibrosis.  output and hypotension can result.
              HW Ag testing (with concurrent microfilaria testing) is   Depression, fever, tachycardia, tachypnea or dyspnea, and
            recommended 6 months after the final adulticide injection;   cough are common clinical signs. Hemoptysis, right-sided
            results should be negative with successful treatment. Many   CHF, collapse, or death can also occur. Interstitial and alveo-
            dogs are HW Ag-negative by 3 to 4 months after adulticide   lar pulmonary inflammation and fluid accumulation cause
            therapy. Persistent antigenemia 6 months after three-dose   pulmonary crackles on auscultation. Focal lung consolida-
            melarsomine protocol may occur due to latent worm die-off,   tion can cause areas of muffled lung sounds. Thoracic radio-
            persistence of a small number of live worms postadulticide,   graphs show patchy alveolar infiltrates with air bronchograms,
            or reinfection if monthly preventative was not given consis-  especially near the caudal lobar arteries. Thrombocytopenia
            tently. The Ag test should be repeated again 6 months later.   or neutrophilia with a left shift may be seen on CBC.
            A positive Ag test 12 months posttreatment despite adher-  Treatment of PTE (whether it occurs before or after adul-
            ence to a monthly preventative schedule suggests persistent   ticide  therapy)  includes  strict  rest  (i.e.,  cage  confinement)
            infection. Because the three-dose melarsomine protocol kills   and glucocorticoid therapy to reduce pulmonary inflamma-
            98% of worms, some dogs will remain Ag positive after treat-  tion (e.g., prednisone, 0.5 mg/kg PO q12h for a week, then
            ment due to presence of a small number of residual worms.   decreasing to 0.5 mg/kg q24h for a week, then decreasing
            The decision to repeat adulticide therapy is guided by the   again to 0.5 mg/kg q48h for 1 to 2 additional weeks). Supple-
            patient’s overall health, performance expectations, and age.   mental oxygen therapy is recommended to reduce hypoxia-
            Complete worm kill is probably not necessary; even if a few   mediated pulmonary vasoconstriction, and sildenafil
            adult  HWs survive, pulmonary arterial disease improves   (1-3 mg/kg PO q8-12h) is indicated to decrease pulmonary
            considerably after adulticide therapy.               vascular resistance. Antiplatelet therapy (clopidogrel or
              Thiacetarsamide is an older arsenical agent that previ-  aspirin), as well as anticoagulant therapy (unfractionated
            ously was the only adulticide available. It had no advantages   heparin or low-molecular-weight heparin), may be consid-
            and greater toxicity potential compared with melarsomine   ered for severe cases of thromboembolism. A bronchodilator
            and is no longer used. Likewise, the use of other drugs such   (e.g., oral theophylline, 10 mg/kg q12h); judicious fluid
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