Page 983 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
P. 983

958                                        CHAPTER 7



  VetBooks.ir  Samples should be submitted as soon as cantharidin  RENAL PHARMACOLOGY
           toxicosis is suspected because cantharidin is elimi-
                                                          The reader should refer to the specific disease in the
           nated within 3–4 days.
                                                          text for drug use, drug selection, dose and route of
           Management                                     administration.
           Treatment is supportive. The source of toxin must
           be removed. Potentially exposed animals should be  Beta-lactam antibiotics
           treated orally with mineral oil (4–6 litres via naso-  Penicillins are often used in the urinary tract because
           gastric tube) or activated charcoal (1–3 g/kg via   they possess a number of beneficial properties. They
           nasogastric tube). Mineral oil acts as a mild laxative   are bactericidal, have a wide margin of safety and a
           and absorbs lipid-soluble cantharidin, which aids in   relatively low incidence of adverse effects, and many
           the elimination of cantharidin from the intestine.   achieve very high levels in urine because of renal
           Mineral oil and activated charcoal should not be   excretion. Microorganisms that are reported to be
           administered concurrently.                     resistant in vitro are often, in fact, sensitive in vivo
             Intravenous balanced electrolyte solution admin-  because of the high drug concentrations that may
           istration (120–180 ml/kg/day) should be com-   be achieved in urine, particularly alkaline urine.
           menced.  Administration of diuretics (furosemide   Acidification of the urine may affect the pharmaco-
           1  mg/kg i/v or i/m q6 h) has been recommended   kinetic variables of penicillin. Intravenous adminis-
           to increase cantharidin excretion after the patient   tration of ampicillin, however, can be combined with
           is rehydrated. Supplementation of i/v fluids with   urinary acidifiers.
           calcium borogluconate may be required and is ide-  Cephalosporins have the same mechanism of
           ally based on repeated evaluation of serum ionised   action as penicillins and also achieve very high con-
           calcium level.  Magnesium  supplementation  is less   centrations in urine. In general, cephalosporins have
           commonly required but can be achieved by admin-  a broader spectrum with enhanced gram-negative
           istration of magnesium sulphate (0.2–1.0 g/kg dis-  activity compared with penicillins. Both penicillins
           solved in 4 litres of warm water q12 h).       and cephalosporins are effective against most anaer-
             Analgesics are usually required and should be   obes. Penicillins and cephalosporins rarely cause
           administrated sparingly. NSAIDs should be avoided   renal tubular damage and renal disease.
           if possible or given at reduced doses (flunixin meglu-
           mine ≤0.5 mg/kg i/v q12 h; ketoprofen ≤1.1 mg/  Sulphonamides
           kg i/v or i/m q24 h) and only after hypovolaemia is   Sulphonamides are typically used in combination
           corrected with i/v fluid therapy. Alpha-2 agonists   with trimethoprim, which provides broad-spectrum
           and opioids are good alternatives for short-term   bactericidal activity. They are eliminated by a com-
           analgesia.                                     bination of renal excretion and metabolism in the
             Prophylactic treatment with appropriate antibiot-  liver. The trimethoprim/sulphadiazine combination
           ics to prevent the development of secondary cystitis   is more suitable for treatment of urinary tract infec-
           has been recommended but may not be necessary in   tion than trimethoprim/sulphamethoxazole; sulpha-
           most cases. If antimicrobials are used, nephrotoxic   methoxazole is largely metabolised before urinary
           drugs should be avoided.                       excretion. Alkaline urine improves the solubility
                                                          of sulphonamides after they undergo acetylisation.
           Prognosis                                      They should not be given in combination with urine
           The prognosis is variable and depends on the amount   acidifiers. Crystalluria, haematuria and obstruction
           of cantharidin that was ingested and the time from   of renal tubules, although rare, have been reported
           the onset of signs to the start of appropriate treat-  after administration of sulphonamides. Acidic urine
           ment. Laminitis has occasionally been associated   and dehydration may predispose to the development
           with cantharidin toxicosis.                    of the above problems.
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