Page 700 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
P. 700

Respir atory system: 3.3 Medical conditions of the upper respir atory tr act          675



  VetBooks.ir  A viruses, and which cross react with equine influ-  qPCR testing can be used to confirm the end of
                                                         virus shedding if required.
          enza A viruses, are used at some competitions for
                                                           Equine influenza is controlled principally by
          rapid initial diagnosis. Serology carried out using a
          haemagglutination inhibition assay is the standard   vaccination. A variety of vaccines are available
          diagnostic test, but single radial haemolysis (SRH)   including inactivated (whole killed virus) and sub-
          is more useful for monitoring response to vacci-  unit canary pox recombinant vaccines. These are
          nation and in epidemiological studies. SRH titres   all delivered by intramuscular injection. In North
          provide a measure of protective immunity such that   America, an intranasal modified live virus vaccine
          horses with titres >150 mm  generally show clinical   is also available. Current OIE recommendations
                                 2
          and virological protection against challenge with   are that vaccines should contain strains represen-
          homologous virus and horses with titres >85 mm   tative of American Florida Clade 1 and Clade 2
                                                      2
          and <150 mm  showing clinical protection.      sublineages of virus, although vaccines containing
                      2
                                                         genetically ‘out of date’ strains can provide effec-
          Management                                     tive protection against currently circulating strains.
          Influenza is usually a self-limiting disease provided   Vaccination against equine influenza is required
          clinical cases are properly managed. Affected horses   by many organisations and has been mandatory in
          should be rested for 3 weeks and, if stabled, kept   racing and equestrian sports since the 1980s. The
          in a dust-free environment with good air hygiene.   primary vaccination course consists of two injec-
          Continued training and poor air hygiene delay   tions given 21–92 days apart, with a third dose given
          recovery, predispose to secondary infection and may   150–215 days later. Annual boosters are given there-
          cause chronic post-viral fatigue syndromes. Broad-  after. Horses may not race until 8 days after any vac-
          spectrum antimicrobials are often administered, but   cination. Although British Horseracing Authority
          unnecessary antimicrobial use should be avoided,   (UK) rules specify that booster doses be given every
          unless bacterial super-infection has been diagnosed.   12 months, there is evidence that to provide opti-
          Non-steroidal anti-inflammatory drugs (NSAIDs)   mum immunity in young horses in training, an addi-
          may be used to control pyrexia if required. Other   tional 6-month, rather than 12-month booster after
          treatments may be employed (e.g. clenbuterol [to   the  third  vaccination  of  the  primary  course  may
          improve ciliary clearance] and mucolytics) but are   be required before adopting the routine of annual
          not usually required. Antiviral influenza A drugs are   boosters. FEI regulations require 6-monthly boost-
          effective in horses in reducing severity and duration   ers for all competition horses. An immunity gap
          of disease, but selection of resistant virus strains is a   may also occur in young Thoroughbreds between
          concern and their use should therefore be restricted   V2 and V3 of the primary course, due to decrease of
          to humans.                                     SRH antibody titres below those required to induce
            Strict infection control including suspension of   clinical protection. In the face of an epizootic,
          movement on and off infected premises should be   immunity can be maximised by giving the third
          employed to prevent spread of infection to adja-  vaccination of the primary course 2–3 months after
          cent yards. Within the affected yard, barrier pre-  the second vaccination and subsequent boosters at
          cautions should be established to try to prevent   6-monthly intervals, taking into account that this is
          spread. The virus is easily inactivated by many   off-label use of vaccines. Mares may be vaccinated
          disinfectants, including 1% bleach, 70% ethanol,   8–4 weeks before foaling to provide optimum lev-
          iodine-based disinfectants, quaternary ammo-   els of colostral antibody. Foals born to vaccinated
          nium disinfectants, peroxygen disinfectants and   mares should not be vaccinated for equine influenza
          phenolics. Infected horses typically shed the virus   before 4 months of age.
          for 6–7 days, and it is advisable to maintain iso-
          lation until there are no more clinical signs and  Prognosis
          body  temperature  is  normal  for at  least  5  days.   The prognosis for full recovery is good.
   695   696   697   698   699   700   701   702   703   704   705