Page 1504 - Small Animal Internal Medicine, 6th Edition
P. 1504

1476   PART XIV   Infectious Diseases


            lymph nodes of dogs with chronic monocytotropic ehrlichi-  blood sample for testing and place it in an EDTA tube before
            osis than other causes of lymphadenopathy (Mylonakis et al.,   treatment. In one recent study tissues (lymph nodes, spleen,
  VetBooks.ir  2011b). Polyarthritis due to E. canis was not detected in one   liver, bone marrow, and blood) from naturally infected dogs
                                                                 were assayed by PCR. Blood and lymph nodes were the most
            experimental study (Theodorou et al., 2015). If nondegen-
            erate neutrophils are detected in synovial fluid from dogs
                                                                 mately 30% of the samples (Gal et al., 2007). In one study,
            with polyarthritis, E. ewingii and A. phagocytophilum may be   likely to be positive but were falsely negative in approxi-
            the more likely causes. Bone marrow aspirates in dogs with   PCR performed on blood and splenic aspirates were equiva-
            chronic ehrlichiosis typically reveal myeloid, erythroid, and   lent for making the diagnosis of  E. canis infection (Faria
            megakaryocytic hypoplasia in association with lymphoid   et al., 2010). Repeated testing with serology and PCR assays
            and plasma cell hyperplasia. However, myelofibrosis was   may be required to accurately determine the infection status
            not detected in one study of 10 affected dogs (Mylonakis   of some individual dogs (Kidd et al., 2017) and is recom-
            et al., 2010). Morulae from  E. canis are rarely detected in   mended in general for most vector borne diseases (Maggi
            the cytoplasm of mononuclear cells. Ehrlichiosis generally   et al., 2014).
            causes mononuclear pleocytosis and increased protein con-
            centrations in cerebrospinal fluid. Antiplatelet antibodies,   Treatment
            antinuclear antibodies, antierythrocyte antibodies (by direct   Supportive  care  should  be  provided  as  indicated.  Several
            Coombs test), and rheumatoid factors are detected in some   different tetracycline, doxycycline, chloramphenicol, and
            dogs with ehrlichiosis, leading to an inappropriate diagnosis   imidocarb diproprionate protocols have been used. The
            of primary immune-mediated disease (Smith et al., 2004).  ACVIM Infectious Disease Study Group currently recom-
              No pathognomonic  radiographic signs  appear  in dogs   mends doxycycline (10 mg/kg PO q24h for at least 28 days).
            with ehrlichiosis. The polyarthritis is nonerosive, and dogs   Doxycycline administered at 5 mg/kg, PO, q12h has also
            with respiratory signs most commonly have increased pul-  been studied and can be effective. In one study of experimen-
            monary interstitial markings, but alveolar patterns can occur.  tally infected dogs, ticks still could acquire  E. canis from
              Identification of morulae in cells documents  Ehrlichia   feeding on dogs previously treated with doxycycline for 14
            infection, but it is uncommon with monocytotropic strains.   days (Schaefer et al., 2007). In an experimental study, mino-
            Examination of buffy coat smears or blood smears made   cycline at 10 mg/kg, PO, twice daily for 28 days had similar
            from blood collected from an ear margin vessel may increase   results to doxycycline at 10 mg/kg, PO, once daily for 28 days
            the chances of finding morulae. Some Ehrlichia spp. can be   (Jenkins et al., 2018). Whether  E. canis infection persists
            grown on cultured cells, but the procedure is low yield and   appears to vary in part on the basis of when treatment is
            expensive and so is not clinically useful.           initiated. For example, experimentally infected dogs treated
              Most commercial laboratories (using IFAs) and point-  during the acute or subclinical phases became PCR-negative
            of-care diagnostic tests use reagents that detect antibodies   as clinical parameters improved, but dogs treated during the
            against E. canis in serum. These tests are generally used as   chronic phase were intermittently PCR-positive after treat-
            the first screening procedures in dogs suspected to have   ment (McClure et al., 2010).
            ehrlichiosis. If serum antibodies against E. canis are detected   Clinical signs and thrombocytopenia should rapidly
            in a dog with clinical findings consistent with ehrlichio-  resolve. If clinical abnormalities are not resolving within
            sis, a presumptive diagnosis of canine ehrlichiosis infection   7 days, other differential diagnoses should be consid-
            should be made and appropriate treatment begun. However,   ered. Results of studies that used imidocarb diproprionate
            detection of antibodies alone is not diagnostic of ehrlichio-  (5-7 mg/kg intramuscular (IM) or SC repeated in 14 days)
            sis because many dogs are subclinically infected. In addi-  to treat canine ehrlichiosis have been variable. Some patients
            tion, negative test results do not totally exclude ehrlichiosis   develop pain at the injection site, salivation, oculonasal dis-
            from the list of differential diagnoses because clinical disease   charge, diarrhea, tremors, and dyspnea after administration
            can be detected before seroconversion and not all Ehrlichia   of this drug. Quinolones are not effective for the treatment
            spp. induce antibodies that are consistently detected in all   of E. canis infections in dogs.
            E. canis assays. If not stated by the company, veterinarians   Positive antibody titers have been detected for up to 31
            should contact specific test providers to determine whether   months after therapy in some naturally infected dogs. Dogs
            the assay to be used detected antibodies against E. canis, E.   with low (<1:1024) antibody titers generally revert to nega-
            chaffeensis, and E. ewingii.                         tive by 1 year after therapy. Dogs with antibody titers greater
              PCR assays are now available commercially and can be   than 1:1024 often maintain positive antibody titers after
            used to detect organism-specific DNA in peripheral blood.   therapy. Whether these dogs are persistent carriers of the
            It can be performed on joint fluid, aqueous humor, cerebro-  organism is undetermined. On the basis of these findings
            spinal fluid, and tissues.  Blood PCR assay  results can  be   antibody titers are considered to be ineffective for monitor-
            positive before seroconversion in some experimentally inoc-  ing response to therapy. Monitoring resolution of thrombo-
            ulated dogs and positive results document infection, whereas   cytopenia and hyperglobulinemia as markers of therapeutic
            positive serologic tests only document exposure (Moroff    elimination of the organism may be more effective.
            et al.,  2014).  Because  antibiotic  treatment  rapidly  induces   Results of studies have been variable on whether ehrlichial
            negative blood PCR results, the clinician should draw the   infections are cleared by treatment and repeated infections
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