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veterinary patients develop hypertension secondary to   angiotensin  II  production. Common  ACEi  include
            another disease process (see Table 2.2). Therefore, if a   both enalapril and benazepril, while the most studied
  VetBooks.ir  patient is assessed as hypertensive, further evaluation   ARB in veterinary medicine is currently telmisartan.
                                                         Aldosterone blockage (e.g. spironolactone) can have
            to deduce the underlying condition should be pursued
            and, if warranted, appropriate therapy for that condi-
                                                         The effect is typically mild and this class of drugs is
            tion should be implemented. The classification of the   antihypertensive effects by reducing blood volume.
            degree of hypertension is based on the risk of TOD   infrequently used in the treatment of hypertension.
            and is outlined in Table 2.3.                 One effect of angiotensin II is efferent arteriole
              Dogs and cats measuring in the range of pre-  constriction in the kidney glomerulus; therefore,
            hypertension are not usually treated with antihy-  angiotensin II blockade via ACEi or ARB induces
            pertensive medications. However, monitoring the   efferent arteriolar dilation. This can have the effect
            patient’s blood pressure more frequently (e.g. every   of  decreasing  glomerular  filtration  rate (GFR).
            6 months) may be warranted to ensure the animal   Therefore, care should be taken before starting
            does not develop true hypertension.          either of these medications in dehydrated patients
              If the patient is diagnosed with hypertension or   which may already have a decreased GFR.
            severe hypertension, anti-hypertensive therapy is   Whenever ACEi or ARB are prescribed, renal val-
            indicated. Efforts should be directed at diagnosing   ues should be monitored.
            and  treating  any  underlying  disease  while  anti-  In addition, blockade of the RAAS, and specifi-
            hypertensive therapy is initiated. The goal for anti-  cally the aldosterone regulation of sodium and
            hypertensive therapy in most cases is a gradual   potassium,  can lead  to hyperkalemia;  electrolytes
            reduction in blood pressure over the course of   must be periodically monitored in patients receiv-
            several days with repeated blood pressure evalua-  ing ACEi or ARB, and require repeated monitoring
            tion performed 7–10 days later. This slower adjust-  as the drug dose is increased.  Although hypona-
            ment is preferable because autoregulatory vascular   tremia is a theoretical concern, the degree of aldos-
            function within the target organs, especially within   terone blockade is usually insufficient to cause
            the brain and kidneys, may have become relatively   drastic changes in sodium; water movement with
            well-adapted to chronic hypertension. When that   sodium typically maintains normal sodium levels.
            has occurred, sudden normalization or decrease in   In cases of severe hypertension, multimodal ther-
            blood pressure may potentially lead to hypoperfu-  apy is likely indicated and is achieved through a
            sion within those organs. Therefore, treatment is   combination of RAAS inhibition and calcium chan-
            initially started at the lower end of the dose range   nel blockade. Calcium channel blockers (CCB) func-
            with a gradual increase in dose or frequency as   tion by preventing calcium entry into excitable cells.
            indicated by the patient’s clinical response.  As calcium is critical to smooth muscle contraction,
              Occasionally dogs suffer from a disease process   CCB cause smooth muscle dilation; this mechanism
            that mandates specific therapy for hypertension (e.g.   leads to a decrease in SVR and (presuming the car-
            aldosterone secreting tumor requiring aldosterone   diac output stays constant) a decrease in blood pres-
            blockade). However, in most cases, dogs are initially   sure (Fig. 2.3). Dogs should not receive CCB
            treated with drugs which inhibit RAAS (see Fig. 2.4).   treatment as their lone treatment for hypertension as
            Angiotensin converting enzyme inhibitors (ACEi)    CCB have the effect of afferent arteriole dilation
            are currently most widely used in veterinary medi-  within the kidney glomerulus.  This can blunt the
            cine, but alternative options include angiotensin   protective effects of autoregulation in the kidney and
            receptor blockers (ARB)  and aldosterone receptor   subject the glomerulus to a greater degree of hyper-
            blockers. Both  ACEi and  ARB serve to block    tension and potential damage. In some cases, CCB


            Table 2.3.  Categories of hypertension in dogs and cats.
                                Pre-hypertensive (low    Hypertensive (moderate    Severely hypertensive
                                    risk of TOD)         risk of TOD)        (high risk of TOD)
             Systolic blood pressure   140–159            160–179               ≥180
              (mmHg)
            TOD, target organ damage.


             38                                                                           D.S. Foy
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