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1208   PART X   Joint Disorders


            effective as monotherapy in some dogs with idiopathic poly-  FELINE PERIOSTEAL PROLIFERATIVE
            arthritis and is well tolerated. Leflunomide is administered   POLYARTHRITIS
  VetBooks.ir  at an initial dose of 3 to 4 mg/kg PO q24h, and the dose is   Periosteal proliferative polyarthritis occurs most often in
                                                                 young adult male cats, but female cats can also be affected.
            adjusted to maintain a trough plasma level of 20 mg/mL.
            (See Chapter 72 for more information on immunosuppres-
                                                                 adenopathy, and edema of the skin and soft tissues overlying
            sive treatment.)                                     Clinical signs include fever, stiff gait, joint pain, lymph-
              Some therapeutic success may be expected if treatment is   the joints, particularly the carpus and hock. Synovial fluid
            initiated before joint damage is severe. In most cases,   analysis reveals a neutrophilic pleocytosis, and culture is
            however, damage to the articular cartilage is severe before   negative. Initially, the radiographic changes are mild and
            the diagnosis is made. Many dogs require additional therapy   include periarticular soft tissue swelling and mild periosteal
            with analgesics such as tramadol to control joint discomfort.   proliferation. With time, the periosteal proliferation worsens
            RA is a relentlessly progressive disorder, and even with   and periarticular osteophytes, subchondral cysts, and col-
            appropriate therapy most dogs show deterioration with time.   lapse of the joint space may be noted. A treatment trial with
            Surgical procedures can occasionally be used to improve   doxycycline to rule out infectious polyarthritis should be
            joint stability and pain. Synovectomy, arthroplasty, joint   considered prior to institution of immunosuppressive treat-
            replacement, and arthrodesis may decrease pain and improve   ment.  Treatment  with  glucocorticoids  (prednisolone  or
            function.                                            prednisone) lessens the severity of signs and may slow pro-
                                                                 gression of disease, but it is not curative. About half of treated
            EROSIVE POLYARTHRITIS                                cats have a reasonable quality of life when treated lifelong
            OF GREYHOUNDS                                        with glucocorticoids and analgesics. There may be further
            An erosive IMPA occurs in Greyhounds from 3 to 30    improvement when more potent immunosuppressive drugs
            months of age. This disorder is primarily seen in Austra-  are administered. (Table 69.3)
            lia and Great Britain. The proximal interphalangeal joints,
            carpi, hocks, elbows, and stifles are most commonly affected.   FELINE RHEUMATOID-LIKE ARTHRITIS
            Clinical  signs  include  generalized  stiffness,  joint  pain  or   Feline rheumatoid-like arthritis has an insidious onset, with
            swelling, and a single or multiple-limb lameness that may   the slow development of lameness, stiffness, and joint defor-
            be intermittent. The synovial membrane is infiltrated with   mity over weeks to months. Middle-aged and older cats are
            lymphocytes  and  plasma  cells,  and  synovial  fluid  analysis   affected, and Siamese cats may be predisposed. Systemic
            also reveals an increase in lymphocytes. There is exten-  illness and fever do not usually occur, so most affected cats
            sive necrosis of deep articular cartilage zones, with rela-  are not examined until severe joint deformities are evident
            tive sparing of the superficial surface cartilage. Mycoplasma   (Lemetayer et al., 2014). Synovial fluid analysis reveals mild
            spuman was isolated from one affected Greyhound, so it   to moderate mixed inflammation. Radiographically there are
            is important to rule out infectious causes of polyarthritis   severe subchondral central and marginal erosions, and peri-
            in affected dogs; trial therapy with antibiotics may be war-  articular swelling that initially progresses to extensive bone
            ranted. Therapy is as for refractory idiopathic immune-  destruction and gross joint deformities. Rheumatoid-like
            mediated  nonerosive  polyarthritis.  Response  to  treatment    arthritis should be suspected in cats with erosive, deforming
            is variable.                                         polyarthritis once infectious causes have been eliminated

            FELINE EROSIVE IMMUNE MEDIATED
            POLYARTHRITIS                                               TABLE 69.3
            Two  uncommon  immune  mediated  disorders  cause  joint   Drugs Used in the Treatment of Immune-Mediated
            damage and destruction in cats. One is a periosteal prolifera-  Polyarthritis in Cats
            tive polyarthritis characterized by marked periosteal new
            bone formation and the second is a deforming arthritis   Prednisolone  2 mg/kg q12h initially, then taper
            resembling RA in humans and dogs. When first described,   Cyclosporine  2.5-5.0 mg/kg PO q12h
            both of these disorders were thought to be variants of one   Leflunomide  10 mg/cat PO q24h
            disorder referred to as chronic progressive polyarthritis   Chlorambucil  2 mg/cat PO q48h
            (CPP). All of the originally reported cases were male cats, all             2
            were positive for antibodies against feline syncytium-forming   Methotrexate  2.5 mg/m  PO q48h
            virus (FeSFV), and approximately 60% were infected with   Leflunomide/Methotrexate Protocol for Rheumatoid-Like
            FeLV or FIV or both. There was speculation that CPP was   Arthritis:
            caused by chronic immune stimulation secondary to FeSFV   Leflunomide  10 mg/cat PO q24h until improvement
            infection in immunosuppressed genetically predisposed               Then 10 mg/cat PO twice weekly
            cats. FeSFV is, however, a widespread retrovirus of cats, and   Methotrexate  2.5 mg/cat PO q12h for 3 doses once
            experimental infection with FeSFV does not cause polyar-              a week until improvement
            thritis, so the association between this virus and the mani-        Then 2.5 mg/cat PO weekly
            festations of CPP is uncertain.
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