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584   Leptospirosis


           •  Other causes of hepatic injury (e.g., bacterial   PCR assays:      •  Intravenous fluid therapy as needed to replace
            cholangiohepatitis, toxic hepatopathy, sepsis,   •  Sensitive  and  specific;  may  be  positive  in   initial deficits, guided by quantification of
  VetBooks.ir  Initial Database               •  Identifies Leptospira but not serovars  large-volume fluid administration, whereas
                                                                                   urine production. Polyuric patients may need
                                                early infection before rise in specific antibody
            idiopathic chronic hepatitis [p. 442])
                                                detected by MAT is present.
                                                                                   anuric/oliguric patients must not be fluid
           •  CBC
                                                                                   overloaded and may need dialysis.
                                                persist in urine. Because the exact timing of
            ○   White blood cells (WBCs): neutrophilia;   •  Leptospires appear in blood first and then   •  Management of kidney and liver injury and
              ± left shift, lymphopenia, monocytosis  appearance is not known, both urine and   other consequences of infection (pp. 23, 269,
            ○   Red blood cells (RBCs): mild to moderate   blood testing is recommended.  and 442)
              nonregenerative anemia          •  False-negatives are possible and are especially
            ○   Platelets: thrombocytopenia in > 50% of   likely after the start of antibiotic therapy.  Recommended Monitoring
              patients; may be severe         Point-of-care assays:              •  Renal,  hepatic,  and  electrolyte  parameter
           •  Serum biochemistry profile      •  Point-of-care and laboratory ELISA tests are   monitoring to assess response to treatment
            ○   Azotemia and hyperphosphatemia are   available.                    and to adjust therapy
              common.                         •  Formats  that  detect  IgM  (Witness  Lepto,   •  Blood pressure because systemic hypertension
            ○   Increased alanine aminotransferase (ALT),   Zoetis) and IgG (SNAP Lepto, IDEXX) are   may occur and require treatment (p. 1065)
              alkaline phosphatase (ALP), and bilirubin   available.             •  Urine  output  monitoring  is  essential  in
              are common in azotemic patients; however,   •  Assays  are  subject  to  some  of  the  same   patients with AKI (p. 23).
              isolated hepatic injury is rare.  limitations as MAT testing, with the pos-  •  Monitor for development of complications
            ○   Electrolyte  disturbances:  hyponatremia,   sibility of a false-negative early in disease   (DIC, respiratory failure) (pp. 27 and 269).
              hypochloremia, and hypokalemia occur   and false-positive related to vaccination.
              in some cases; however, dogs with oliguria   •  As  with  other  types  of  testing  for  lepto-   PROGNOSIS & OUTCOME
              or anuria develop hyperkalemia.   spirosis, these point-of-care assays must be
            ○   Metabolic acidosis (low pH on blood   interpreted in light of history, signs, and   •  Survival rates for dogs with clinical lepto-
              gas analysis, low bicarbonate concentra-  often in combination with other types of   spirosis: 70%-85%
              tion), often accompanied by increased     tests.                   •  Patients  with  AKI  may  become  oliguric
              anion gap                       Other (often unrewarding and not recommended)  or  anuric.  These  patients  benefit  from
            ○   Hypoalbuminemia  due  to  vasculitis  or   •  Dark-field   microscopy:   false-negatives   dialysis or continuous renal replacement
              severe liver dysfunction          common                             therapy  (CRRT)  and  often  do  well  after
           •  Urinalysis                      •  Organism identification in tissues section:   treatment.
            ○   Isosthenuria/hyposthenuria      invasive                         •  Patients  may  recover  clinically  but  have
            ○   Signs  of  tubular  damage:  glucosuria,   •  PCR of tissue section: invasive  persistent evidence of liver and kidney injury.
              proteinuria, granular casts     •  Urine or blood culture: fastidious organisms;   Many continue to improve over the following
            ○   Polyuria,  oliguria, and  anuria  are all   false-negatives common  months, whereas others have chronic disease
              possible.                                                            (p. 167).
           •  Thoracic radiographs: interstitial to severe    TREATMENT
            reticulonodular pattern, alveolar infiltrates                         PEARLS & CONSIDERATIONS
            with pulmonary involvement and effusion   Treatment Overview
            are possible.                     Treatment goals are to eliminate leptospires,   Comments
           •  Abdominal radiography and ultrasonography:   maintain renal perfusion and urine output,   •  Leptospirosis should be considered as a dif-
            ±  enlargement  of  liver,  spleen,  kidneys;   prevent disease progression, contain shedding   ferential in any case of AKI, fever, vasculitis,
            renomegaly, pyelectasia, increased renal   in the environment, and treat associated condi-  and/or acute or chronic liver disease in a
            cortical echogenicity, perinephric effusion,   tions (kidney injury, hepatic insufficiency, DIC,   dog.
            and a medullary rim sign (medullary band   uveitis).                 •  Due  to  zoonotic  potential,  precautions
            of increased echogenicity)                                             should be taken when handling suspected
           •  Coagulation  profile  (p.  1325):  prolonga-  Acute General Treatment  leptospirosis patients.
            tions of prothrombin time and/or partial   •  Whenever possible, doxycycline should be   •  Early identification, isolation, and treatment
            thromboplastin time with increased FDP   used as the initial antimicrobial because it   (e.g., antibiotics) are important for the
            are common.                         treats the leptospiremia and clears the carrier   patient’s recovery and to reduce the risk of
                                                state that leads to environmental shedding.   transmission.
           Advanced or Confirmatory Testing     If urine is to be submitted for PCR testing,   •  Canine leptospirosis is a reportable disease in
           Microscopic agglutination test (MAT) and PCR   collect sample before or as soon as possible   some U.S. states; contact regional authorities.
           are the most commonly used diagnostic tests.   after antimicrobial treatment is begun.  •  Hemodialysis and CRRT are widely avail-
           MAT titer should not be used to determine   ○   Doxycycline 5 mg/kg PO or IV q 12h   able  and  should  be  considered  for  AKI
           causative serovar:                     for 2 weeks                      patients.
           •  Initial titer with acute illness often negative  •  Doxycycline  concentrates  in  bile  and  is
           •  Suggestive                        excreted in the feces, and supraphysiologic   Prevention
            ○   Single  titer  ≥  1:800  in  unvaccinated   serum concentrations may occur in patients   •  At-risk  dogs  should  be  vaccinated.  Dogs
              animals                           with  liver  disease.  In  these  patients,  beta-  at risk include pets living in urban areas if
            ○   Titer ≥ 1:6400 in vaccinated animal, or   lactam antibiotics (e.g., penicillin, ampicillin)   their environment could be contaminated
              titer > 800 to a nonvaccine serovar and   can be initially used to clear the leptospi-  by wildlife or rodents.
              a concurrent titer  < 400 to a vaccine    remia. This must be followed with 2 weeks   •  Currently,  bivalent  vaccines  containing
              serovar                           of doxycycline to clear the carrier state.  icterohaemorrhagiae and  Canicola serovars
           •  Diagnostic                        ○   Ampicillin 20 mg/kg IV q 6h, with dose   and vaccines containing icterohaemorrhagiae,
            ○   Paired titers 2-4 weeks apart with fourfold   reduction for azotemic dogs, or  Canicola, grippotyphosa, and Pomona serovars
              increase from first to second titer or   ○   Penicillin sodium 25,000-40,000 U/kg IV   are available in North America. These vac-
              seroconversion from negative to positive   q 12h, with dose reduction for azotemic   cines produce serospecific immunity but may
              titer                               dogs                             offer some immunity to antigenically similar

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