Page 996 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
P. 996

Cardiovascular system                                    971



  VetBooks.ir  agitated saline solution, allows for the evaluation of   in humans, and skeletal muscular damage is  com-
            Contrast echocardiography, injecting a dye or
                                                         mon. The myocardial isoenzymes are also present
          the direction of flow across shunts and across valves.
          This is less commonly performed now, as colour-flow   in skeletal muscle, and therefore, any skeletal muscle
                                                         damage may confound the detection of myocardial
          imaging is available on many ultrasound machines.   injury because of the skeletal origin of isoenzyme
          In a fractious animal, sedation may be required to   elevations. In the absence of skeletal muscle injury,
          allow for safe examination. It is important to recog-  CK and LDH isoenzyme elevation may be sugges-
          nise, however, that functional assessment will not be   tive of myocardial injury.
          possible. Alpha-2 agonists have been shown to dra-  More recently, troponin protein assays have been
          matically reduce systolic function.            developed to assess myocardial disease in humans.
            Advanced imaging modalities including tissue   Cardiac troponin T (cTnT) and I (cTnI) subunits are
          Doppler imaging and speckle tracking, where myo-  distinct from those of skeletal origin. Specific assays
          cardial function may be closely interrogated may be   have been developed and have been evaluated in the
          of value in select cases (e.g. suspected toxic cardio-  horse. cTnI has been considered more sensitive and
          myopathy) This is limited to referral centres.  specific to myocardial tissue than earlier assays for
                                                         troponin T because of the relatively higher concen-
          Laboratory evaluation                          tration in cardiac muscle when compared with skel-
          of cardiac disease                             etal muscle. New (3rd-generation) cTnT assays are
          Routine serum biochemistry and haematology may   considered to be of similar diagnostic sensitivity as
          be beneficial. A murmur detected in a dehydrated or   cTnI assays. Troponin assays should be performed
          anaemic animal may relate to the underlying cause   when   myocardial disease or  myocardial damage is
          of the haematological abnormality rather than to     suspected. High conservation across species means
          cardiac disease. Electrolyte disturbances may be the   that tests designed for human use should be capable
          cause of arrhythmias. Haematological and biochem-  of detecting troponin proteins in equine samples.
          ical  evidence  of  inflammation,  such  as  increased   There are many different cTnI tests, each targeting
          white blood cell count, fibrinogen or globulins, may   a separate portion of the cTnI protein. As much as a
          raise suspicion of bacterial endocarditis as a cause for   100-fold variation in the reported value is possible.
          a sudden-onset cardiac murmur. Laboratory assays   It is essential, therefore, that the tests are compared
          may be of value for assessing the systemic effects of   only with themselves and normal values established
          heart failure (e.g. azotaemia due to poor renal perfu-  for each test.
          sion). Arterial blood gas analysis may aid reaching a
          diagnosis (e.g. low values [<40 mmHg] in congenital  Cardiac catheterisation
          shunting).                                     Cardiac catheterisation may provide additional
            Most antiarrhythmic medications have  nar-   information regarding the direction of flow across a
          row therapeutic ranges, therefore serial analysis   shunt and the cardiovascular effects of an abnormal
          of serum levels of these medications is needed   finding. This technique has declined in popularity
          to optimise therapy. For example, blood levels   with the increased availability of ultrasonography
          of quinidine should be assessed repeatedly dur-  and is limited to referral centres, where personnel
          ing administration; this is to minimise the risks   familiar with the procedure and specialised equip-
          associated  with  quinidine  toxicity  in  addition  to   ment are available. Interventional procedures (such
          determining whether therapeutic levels have been   as coil placement in patent ductus arteriosus [PDA]
          attained.                                      or transvenous pacemaker placement) involving car-
            Elevations  in  serum  creatine  kinase  (CK)  and   diac catheterisation are uncommon in the horse.
          lactate dehydrogenase (LDH) levels are often asso-  Angiography is infrequently used in horses. More
          ciated with muscular damage. In humans, CK and   often, it is used to evaluate limb perfusion, particu-
          LDH isoenzymes specific to myocardial tissue have   larly distal limb perfusion, rather than as part of a
          been used to assess myocardial injury. In horses,   cardiac examination. Echocardiography has replaced
          myocardial disease is significantly less common than   angiography in many cases.
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