Page 714 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
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Respir atory system: 3.4 Medical conditions of the lower respir atory tr act          689



  VetBooks.ir  (PCR) assays based on detecting the VapA gene pro-  idea that not all foals require treatment. Increasing
                                                         numbers of resistant isolates have been identified
          vide increased sensitivity over culture but should be
          interpreted in light of clinical signs and imaging, as
                                                         recommendations have shifted away from treating
          they may yield positive results in foals without clini-  with the advent of antimicrobial use. Consequently,
          cal disease. Similarly, serology and faecal culture are   every foal with mild thoracic ultrasound changes but
          unreliable because seroconversion and GI tract colo-  with no clinical signs. Instead, it is recommended
          nisation in the absence of disease are common.  that foals with minor changes be monitored more
                                                         frequently, but only be treated if disease becomes
          Management                                     clinical.
          The intracellular persistence of R. equi makes anti-  Practical measures to reduce exposure to R. equi
          microbial treatment difficult. Treatment with mac-  include maintaining young foals (<4 weeks old)
          rolide antimicrobials, which are concentrated in   on clean grass paddocks and avoiding dusty, over-
          macrophages and thus target the site  of bacterial   crowded dirt paddocks with little grass. This reduces
          persistence, is recommended in combination with   the environmental burden and hence the risk of
          rifampin. The historical treatment is long-term   infection of the foal in its first weeks of life. To limit
          (1–2 months) oral combination therapy with eryth-  propagation of the disease at the farm level, affected
          romycin (estolate 25 mg/kg p/o q6 h, phosphate   foals may be removed from pasture, since they
          37.5  mg/kg p/o q12 h) and rifampin (5–10 mg/kg   shed high numbers of bacteria in faeces. In high-
          p/o q12–24 h). A newer alternative to erythromycin   risk  facilities,  hyperimmune  equine  plasma  can  be
          is azithromycin, which allows reduced-frequency   administered to newborn foals at birth and again at
          dosing (10 mg/kg p/o q24 h for 5 days, then q48 h)   3–4 weeks of age to reduce the risk of respiratory
          and possibly reduced side-effects. Clarithromycin   infection early in life.
          (7.5 mg/kg p/o q12 h) in combination with rifampin
          is also widely used and has been shown to have supe-  Prognosis
          rior clinical efficacy when compared with treatment   The prognosis is poor for foals with severe pulmo-
          with erythromycin and rifampin. Combination    nary disease, even if treated aggressively. For foals
          therapy is always recommended to reduce chances   with less severe disease the prognosis is moderate
          of resistant isolate development. Treatment can be   to good. Foals that recover do progress into train-
          expensive and adverse reactions, including fatal   ing and have an effective athletic life. Racing per-
          clostridial diarrhoea or hyperthermia, may occur.   formance in Thoroughbreds does not seem to be
          Hyperthermia, most common with use of erythro-  affected. The prognosis for foals with extrapulmo-
          mycin, occurs because foals lose the ability to sweat   nary abscesses is generally poor.
          properly; care should be taken to provide adequate
          shade or fans during periods of increased environ-  BACTERIAL PNEUMONIA
          mental temperature and humidity. Foals with severe
          pulmonary signs  may require hospitalisation, oxy-  Definition/overview
          gen therapy, inhalation and systemic therapy with   Bacterial pneumonia is characterised by inflamma-
          bronchodilators and fluid therapy.             tion of the lungs that occurs because of bacterial
            Close  surveillance  of  foals  for  signs  of  respira-  colonisation of the pulmonary parenchyma. Most
          tory disease, including regular haematology screens   cases are secondary to viral respiratory infection,
          to identify foals with raised total white blood cells   although primary bacterial infections can occur.
          (WBCs), neutrophilia and raised fibrinogen, allows
          early identification of affected foals. On enzootically  Aetiology/pathophysiology
          infected farms, serial monitoring of thoracic ultra-  Common pathogens isolated from bacterial pneu-
          sounds can also help detect foals in the early stages   monia in adult horses include  Streptococcus zooepi-
          of the disease. However, many foals with ultraso-  demicus,  beta-haemolytic  Streptococcus  spp.  and
          nographic changes will clear the infection without   gram-negative organisms such as  Pasteurella  spp.,
          developing clinical signs of disease, supporting the   Escherichia coli, Klebsiella spp., Enterobacter spp. and
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