Page 822 - Problem-Based Feline Medicine
P. 822

814  PART 10  CAT WITH SIGNS OF NEUROLOGICAL DISEASE


            – Lead poisoning induces gastrointestinal (anorexia,  cats are rare. Hypoglycemia is typically associated
               vomiting, diarrhea, constipation), renal (polyuria,  with insulin overdose in a diabetic patient, hypocal-
               polydipsia) and neurological (depression, central  cemia is mainly seen after bilateral thyroidectomy,
               blindness, hyperexcitability, running fits, seizures,  and hepatoencephalopathy causes episodic signs,
               vocalization, ataxia, head pressing, opisthotonos,  which rarely occur in intoxications.
               paraparesis) signs. Megaesophagus with regurgita-
                                                        Inflammatory conditions (e.g. encephalitides,
               tion and pharyngeal/laryngeal paresis has been
                                                        polyneuropathies) need to be ruled out. Usually his-
               observed with chronic lead poisoning in cats.
                                                        tory and physical examination findings differentiate
            – Bromethalin acute toxicity causes tremors,
                                                        these from intoxications.
               hyperexcitability, hyperesthesia, depression,
               fever, anisocoria, positional nystagmus, extensor
               rigidity, opisthotonos and seizures (running fits  Treatment
               and generalized). Death may sometimes be
                                                        With dermal exposure it is important to bath the cat
               delayed up to 2–3 weeks in cats. Chronic intox-
                                                        with soap or detergent to remove the toxin from the hair
               ication with lower dosages causes occasional
                                                        and skin. Intoxication with anti-flea and -tick sprays,
               vomiting, ascending paresis and ataxia with pro-
                                                        dips, and aerosols containing insecticides such as
               prioceptive deficits, depressed spinal reflexes
                                                        pyrethrins, carbamates, organophosphates often occurs
               (patellar and withdrawal), tremors, depression
                                                        via dermal exposure.
               and lateral recumbency. Recovery is possible
               after exposure is discontinued.          When ingestion has occurred within the previous
            – Penitrem mycotoxins.                      2 hours, emesis may be indicated or contraindicated,
                                                        according to the specific toxin and formulation that was
                                                        ingested. Emesis may be induced with hydrogen perox-
          Diagnosis
                                                        ide 3% (2 ml/kg PO) or apomorphine (0.03–0.04 mg IV
          Diagnosis is based on a history of exposure to a toxin  or 0.04–0.08 mg/kg IM).  Gastric lavage performed
          capable of producing the observed signs within the doc-  under general anesthesia may be beneficial if emesis is
          umented time for exposure.                    not effective. Enemas also may be useful.  Activated
                                                        charcoal (0.1–1.0 mg/kg q 8–12 h) preferably adminis-
          Toxicologic analysis may be diagnostic when per-
                                                        tered with a cathartic such as magnesium sulfate (250
          formed on the following:
                                                        mg/kg) or 70% sorbitol (3 ml/kg) is also indicated to
          ● Tissues (e.g. liver, kidney, fat, brain) for organochlo-
                                                        reduce gastrointestinal absorption.
            rines, organophosphates, strychnine, lead, etc.
          ● Vomitus and stomach content (for bromethalin,  Atropine sulfate (0.02–0.04 mg/kg IM or SC) will
            strychnine, methaldehyde).                  decrease salivation and muscarinic signs associated
          ● Urine (for strychnine).                     with organophosphate and other poisoning, but because
          ● Blood for lead concentration and acethyl-   of the risk of fatal bronchospasm it is only recom-
            cholinesterase activity (organophosphate poisoning).  mended if marked bradycardia is present.

          Toxicity as a cause of seizures can be excluded when  Pralidoxime chloride (2-PAM, Protopam chloride) is
          (a) there are no other diffuse neurological signs preced-  useful to reactivate cholinesterase (10–15 mg/kg IM or
          ing the seizure onset (e.g. tremors, hyperexcitability), (b)  SC q 8–12 h) and control nicotinic signs of organophos-
          when partial seizures occur, (c) when isolated seizures  phate poisoning. It is most effective if exposure was
          are interspersed with periods of normalcy, or (d) when  within the previous 24–48 hours, if exposure was by the
          focal neurological signs or deficits are present.  dermal route and if a slowly eliminated compound was
                                                        involved (e.g. fenthion, chlorpyrifos).
          Differential diagnosis                        Diphenhydramine also has antinicotinic activity.
          Metabolic disturbances that are severe enough to  Chelation therapy (e.g. calcium EDTA and/or penicil-
          cause obvious neurological signs including seizures in  lamine) is indicated for lead poisoning.
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