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followed by an inability to depolarize, leading to   then ‘meet’ in the center portion of the testing slide,
            bradycardia and/or other bradyarrhythmias    forming a concentration cell. The resulting electri-
  VetBooks.ir  (although rarely tachyarrythmias may occur).   cal potential of this junction between reference
                                                         solution and sample solution is measured (i.e. the
            Hyperkalemic animals may also be acidemic. Often
            hyperkalemia occurs concurrently with decreased
                                                         trations and types. Specifically, a volt meter is used
            renal  excretion  of  acids,  but acidemia  may  also   ‘junction cell’) and correlated to the ionic concen-
            occur when hydrogen ions translocate out of the   to determine the electrical potential and a micro-
            cells into the bloodstream in exchange for potas-  processor mathematically converts this voltage into
            sium ions shifting into the cells to improve the   the concentration of the ion in the blood sample.
            hyperkalemia (see Fig. 8.4).                 Typically, there is either an ion-specific membrane
                                                         through the test electrode so that only the electro-
                                                         lyte of interest can move into the junction cell and
            8.2  How the Monitor Works
                                                         be measured or separate ISE for each electrolyte to
            When measuring electrolytes, clinicians are limited   be measured.
            to either measuring them on a bench-top analyzer   Direct and indirect ISE techniques exist.  With
            as part of a full chemistry panel (either in-house or   direct ISE, the blood sample is presented to the
            sent out to a laboratory) or via a point-of-care   electrode and the electrolyte levels are directly
            analyzer. There are two main ways that laboratory   measured. With  indirect  ISE,  the  blood sample  is
            machines measure electrolytes – flame photometry   first diluted in a buffer by the machine before being
            (flame atomic emission spectrometry) or ion-selective   presented to the electrode; this allows for measure-
            electrodes (ISE). Flame photometry is an older   ment of the electrolyte activity versus the concen-
            technology where the sample is heated via a flame   tration  of  the  buffer  solution.  This  yields  values
            or burner until the liquid portion of the sample   most closely correlated to flame photometry which
            evaporates, leaving the ions. These ions are excited   is the historic gold standard. Most laboratories and
            when they absorb energy from the flame and, after   point-of-care instrumentation use indirect ISE.
            the  heat  is  removed,  they  return  to  their  normal   Most bedside point-of-care analyzers use a minia-
            (non-excited state) while giving off a characteristic   turized version of ion-specific electrode technology
            wavelength of radiation. This radiation signature   to determine electrolyte concentrations which may
            and its magnitude is measured by the analyzer and   be direct or indirect ISE.
            in turn is proportional to the concentration of the   Laboratory machines also use colorimetry to
            electrolyte in the blood.                    measure total calcium and phosphorus in labora-
              The downside of flame photometry is that for   tory analyzers. The complexed and ionized calcium
            electrolytes other than sodium and potassium, the   in the blood reacts with a dye such as orthocresol-
            absorption and resulting release of radiation from   phthalein to form a colored complex; this complex
            the electrolytes is too variable to be reliable and/or   is measured spectrophotometrically and the amount
            the analyzers cannot detect electrolytes at a low   (density) of the color is indicative of the volume of
            enough level to be clinically useful. In addition,   calcium.  A similar technique is used for free or
            some electrolytes can alter the flame temperature   complexed inorganic phosphorus, except a differ-
            or react with the flame or environment to make   ent dye (molybdate) is used.
            new compounds (e.g. calcium combines with oxy-
            gen from the flame to form CaO), nullifying their
            ability to be measured. Therefore, if flame atomic   8.3  Indications
            emission spectrometry is used, it is limited to deter-
            mining potassium and sodium levels.          Sodium
              The other major technology used in laboratory   When handling emergency or critical care patients,
            machines is ISE to measure electrolyte concentra-  sodium  is generally a marker of the volume  of
            tions. This technology is used for sodium, chloride,   water in the plasma relative to the amount of
            ionized calcium, and potassium.  With ISE, one   sodium ions. Monitoring sodium is most impor-
            electrode is in contact with or contains a reference   tant in animals with kidney disease (or other non-
            solution with a known concentration of an electro-  renal causes of diuresis such as hyperglycemia or
            lyte to be measured and the other electrode is in   mannitol administration), polyuria/polydipsia,
            contact with the blood sample. The two solutions   vomiting, and/or diarrhea.  Clinicians can alter


             162                                                                     E.J. Thomovsky
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