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532   Immunodeficiency Syndromes, Dog


            ○   Chronic myelogenous leukemia    •  Genetic  tests  are  available  for  some   Chronic Treatment
            ○   Pelger-Huët anomaly: hyposegmentation   congenital immunodeficiency syndromes   •  Humoral immunodeficiency
  VetBooks.ir  persistent degenerative left shift without    TREATMENT           •  Cell-mediated immunodeficiency
                                                                                   ○   Supportive therapy tailored to treating
              of nuclei in granulocytes and monocytes;
                                                  (e.g., TNS, CLAD).
                                                                                     recurrent microbial infections
              toxic change or any signs of illness
              (incidental finding)
            ○   Other infectious disease that can cause   Treatment Overview       ○   Supportive care with frequent monitoring
                                                                                     for opportunistic infections; proceed with
              a neutrophilic leukocytosis with  a left     Substantial variation in severity may exist for a   aggressive treatment when warranted
              shift                           given immunodeficiency syndrome. Therefore,   ○   Dwarf Weimaraners respond to thymosin
                                              treatment intensity, treatment success, and   fraction 5 therapy (1 mg/kg SQ q 24h
           Initial Database                   prognosis  are  individually  variable.  Some   for 7 days).
           Appropriate diagnostic testing based on clinical   individuals require minimal treatment (inter-  •  Combined (B-cell and T-cell) immunodefi-
           presentation:                      mittent antimicrobial treatment during clinical   ciency
           •  Minimal database: CBC, serum biochemistry   exacerbation), whereas in others, euthanasia is   ○   Bone marrow transplantation
            profile, urinalysis with culture and sensitivity,   the most humane option. Control opportunistic   •  Phagocytic immunodeficiency
            fecal exam, thoracic radiographs can reflect   infections with antimicrobials and supportive   ○   Bone marrow transplantation
            concurrent infection (e.g., evidence of bacte-  care; hospitalize when necessary.
            rial pneumonia)                                                      Nutrition/Diet
           •  Other tests directed toward site of infection   Acute General Treatment  •  Caloric  requirements  of  the  critically  ill
            (e.g., airway lavage if pneumonia, biopsy of   Supportive care to treat opportunistic infections:  patient may be less than those of a healthy
            skin lesion)                      •  Antibiotics are used for confirmed bacterial   animal.
           •  Humoral (B-cell) immunodeficiency disorder:   infections. Empirical antibiotics may be used   ○   Resting energy requirement (RER): RER
            no specific change                  initially, pending culture and sensitivity results.   = 70 × body weight (kg) 0.75
           •  Cell-mediated  (T-cell)  immunodeficiency   Antibiotic selection is based on suspected   ○   RER approximation: 30 × body weight
            disorder: normal/decreased lymphocyte count  bacterial population of involved site.  (kg) + 70
           •  Combined (B-cell and T-cell) immunodefi-  ○   Skin: gram-positive bacteria most common;   •  If anorexia persists after infection treated,
            ciency disorder: normal/decreased lymphocyte     consider cephalosporins (cephalexin     feeding tubes may be required.
            count (average, 1000 cells/mcL); possibly low   22 mg/kg PO q 8-12h) or penicillins
            total protein due to low globulin levels; agam-  (amoxicillin 22 mg/kg PO q 8h)  Drug Interactions
            maglobulinemia (protein electrophoresis)  ○   Oral cavity and respiratory tract  •  When  using  chloramphenicol,  consider
           •  Functional  phagocytic  immunodeficiency   ■   Gram-positive cocci: consider cepha-  human risks (myelosuppression, aplastic
            disorder:  persistent  leukocytosis  with   losporins 22 mg/kg PO, IV q 8h  or   anemia; wear gloves).
            regenerative  left  shift;  neutrophil  count    trimethoprim-sulfadiazine 15-30 mg/  •  When  using  aminoglycosides,  ensure  that
            > 200,000 cells/mcL                    kg SQ, IM, IV q 12h (lower end of   patient is well hydrated and has adequate
           •  CLAD:  marked  leukocytosis;  leukocytes   dosage range for larger dogs)  renal function.
            cannot escape the vasculature         ■   Gram-negative  rods:  trimethoprim-  •  Fluoroquinolones  can  affect  cartilage  in
           •  Cyclic neutropenia: neutrophil count within   sulfadiazine 15-30 mg/kg SQ, IM, IV   growing puppies.
            or below reference range               q 12h (lower end of dosage range for
           •  Trapped neutrophil syndrome: neutropenia  larger dogs) or enrofloxacin 5-10 mg/  Possible Complications
                                                   kg IV q 24h or gentamicin 8 mg/kg   •  Sepsis
           Advanced or Confirmatory Testing        IV, IM, SQ q 24h              •  Recurring and resistant infections
           If congenital immunodeficiency is suspected,   ■   Bordetella infection: doxycycline 5 mg/
           consult with small animal internal medicine spe-  kg IV, PO q 12h or chloramphenicol     Recommended Monitoring
           cialist or veterinary immunologist. Functional   50 mg/kg IV, SQ, PO q 8h; enrofloxa-  Monitoring of appetite, activity, temperature,
           testing may require immediate assay.    cin 5-10 mg/kg slow IV, IM, PO q 24 h  and CBCs can aid in the early detection of
           •  Specific tests are tailored to the suspected   ■   Mixed populations: consider fluoroqui-  infection.
            immunodeficiency.                      nolones (enrofloxacin 5-10 mg/kg PO
           •  CLAD: biopsy of lesion shows bacteria ±   or slow IV q 24h) or beta-lactamase–   PROGNOSIS & OUTCOME
            necrosis but no neutrophil infiltration.  resistant  penicillins  (amoxicillin-
           •  Humoral immunodeficiency: serum protein   clavulanate 10-20 mg/kg PO q 12h)   •  Humoral immunodeficiency: fair to good
            electrophoresis to evaluate immunoglobulin   or macrolides (azithromycin 5-10 mg/  •  Cell-mediated immunodeficiency: poor
            concentrations, quantitation of serum immu-  kg PO q 24h × 1-5 days)  •  Combined (B-cell and T-cell) immunode-
            noglobulin, and serum C3 for C3 deficiency  •  Due to possibility of opportunistic fungal, viral,   ficiency: poor. Affected animals usually die
           •  Cell-mediated immunodeficiency: lympho-  and protozoal infections, empirical antibiotic   between 2 and 4 months of age from systemic
            cyte transformation (blastogenesis) evaluates   therapy may be inadequate or may select for   bacterial or viral infections.
            the ability of the T cell to proliferate after   resistant strains of bacteria; diagnostic samples   •  Phagocytic immunodeficiency: poor
            stimulation; measurement of growth hormone     for culture should be obtained before treat-
            or insulin-like growth factor 1 if dwarfism   ment, and judicious antibiotic use is warranted.   PEARLS & CONSIDERATIONS
            is suspected (available only in research   •  Nebulization  and  coupage  for  bacterial
            laboratories)                       pneumonia (p. 795)               Comments
           •  Cyclic neutropenia: bone marrow aspirate/  •  Disinfection  of  cutaneous  wounds  with   The diseases listed here are rare but are often
            biopsy                              diluted (0.05%) chlorhexidine solution  severe, and several have a poor/guarded prognosis.
           •  Functional phagocytic immunodeficiency  ○   With standard 4% chlorhexidine solution,
            ○   Bactericidal assays: measure the ability of   dilute 1 part chlorhexidine  to 80 parts   Prevention
              neutrophils to phagocytize or kill bacteria,   water to obtain a 0.05% concentration.  •  If molecular testing is possible, use genetic
              or to generate reactive oxygen species  ○   The same concentration may be used as an   screening for predisposed animals.
            ○   Polymerase chain reaction (PCR): to iden-  ear wash for otitis and as an oral antiseptic   •  If congenital immunodeficiency is identified,
              tify affected, normal, or carrier animals  rinse for stomatitis.     avoid breeding related animals.

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