Page 585 - Fluid, Electrolyte, and Acid-Base Disorders in Small Animal Practice
P. 585

572        FLUID THERAPY


            are  prohibitively  expensive  unless  high  caseload  allows   oxygenation  in  many  clinical  shock  syndromes. 24,63,68
            nearly  constant  usage,  whereas  portable  blood  gas   However, there are other clinical syndromes that can lead
            analyzers can easily pay for themselves in just a few years.   to hyperlactatemia, including diabetic ketoacidosis, neo­
            One  disadvantage  of  blood  gas  analysis  (arterial  or   plasia, drugs and toxins, hepatic insufficiency, gastroin­
            venous)  is  that  the  results  obtained  represent  a  single   testinal  disease,  or  metabolic  disorders.  Normal
            moment in time, although the status of the patient may   reference  intervals  vary  with  the  equipment  used,  but
            change minute by minute. The partial pressure of oxygen   changes  in  lactate  concentration  in  combination  with
            reflects the amount of oxygen dissolved in plasma and the   other clinical indicators of shock are useful for monitor­
            saturation of hemoglobin with oxygen can be determined   ing effectiveness of therapy. Lactate concentration should
            from the oxyhemoglobin dissociation curve.           decrease over time if successful cardiovascular resuscita­
               Arterial  blood  gas  analysis  provides  information   tion  from  shock  has  occurred.  Occasionally,  lactate
            regarding gas exchange in the lung and arterial acid-base   concentration will increase transiently after initiation of
            balance.  Arterial  blood  samples  are  most  commonly   therapy because improved perfusion results in a “wash­
            collected from the femoral or dorsal pedal artery into a   out”  of  waste  products  that  did  not  previously  enter
            preheparinized  syringe.  The  partial  pressure  of  oxygen   the systemic circulation. Lactate measurement has been
            in arterial blood (PaO 2 ) represents the adequacy of gas   shown to be an effective predictor of gastric necrosis in
            exchange in the lung.                                dogs with GDV and thus serves as a useful predictor of
               A “mixed venous” blood gas sample must be obtained   prognosis and survival. 24
            from the pulmonary artery, which requires placement of a
            specialized  catheter.  The  partial  pressure  of  oxygen  in   ADDITIONAL THERAPIES
            mixed venous blood (PvO 2 ) is a reflection of perfusion
            of  tissues  on  a  global  basis.  Normal  PvO 2  values  range   Various forms of shock can all lead to hypotension despite
            from 35 to 45 mm Hg. Values less than 30 mm Hg indi­  intravascular volume resuscitation, therefore necessitating
            cate poor perfusion and oxygen delivery to the peripheral   the  use  of  vasopressor  and/or  inotrope  therapy
            tissues. If a thermodilution catheter is not placed in the   (Table 23-7). Since both cardiac output and systemic vas­
            pulmonary artery to collect blood for PvO 2  determina­  cular resistance affect oxygen delivery to the tissues, ther­
            tion, a jugular catheter placed to monitor CVP can be   apy for hypotensive patients includes maximizing cardiac
            used to collect a venous blood sample that may approxi­  function with fluid therapy and inotropic drugs and/or
            mate a true mixed venous sample.                     modifying  vascular  tone  with  vasopressor  agents.  The
               Acid-base analysis from a blood gas sample is reviewed   most  commonly  used  vasopressors  are  exogenous
            in Chapter 9.                                        catecholamines (epinephrine, norepinephrine, dopamine,
                                                                 and phenylephrine). Vasopressin, a nonadrenergic vaso­
            PULSE OXIMETRY                                       pressor  agent,  has  also  been  used  for  the  treatment  of
            Pulse  oximetry  measures  the  saturation  of hemoglobin   catecholamine-refractory vasodilatory shock.
            with oxygen (SaO 2 ) and can be monitored continuously   Different sympathomimetics cause various changes in
            and noninvasively. The PaO 2  provides information about   the  cardiovascular  system,  depending  on  the  specific
            oxygen dissolved in plasma, whereas SaO 2  provides infor­  receptor stimulation caused by the drug. 133  Convention­
            mation concerning the oxygenation of red blood cells. To   ally,  adrenergic  receptor location  and  function  involves
            be  of  value,  pulse  oximetry  requires  pulsatile  flow  of   the a 1 -and  b 2 -receptors located on the vascular smooth
            blood to the extremities (interdigital web, digit) where   muscle cells that lead to vasoconstriction and vasodilata­
            it is measured. Many patients with shock have decreased   tion, respectively, while b 1 -receptors in the myocardium
            blood flow, especially to the extremities, which limits the   primarily modulate inotropic and chronotropic activity.
            effectiveness of pulse oximetry. The device may also be   In  addition,  there  are  dopaminergic-1  receptors  in  the
            applied to the tongue for accurate readings, but this tech­  renal,  coronary,  and  mesenteric  microvasculature  that
            nique is difficult in the conscious patient. Other common   mediate vasodilatation and dopaminergic-2 receptors in
            areas for probe placement are the ear, axilla, vulva, and   the  synaptic  nerve  terminals  that  inhibit  the  release  of
            prepuce. A rectal probe may be of value in the conscious,   norepinephrine.
            recumbent patient.                                     Dopamine has various potential actions on adrenergic
                                                                 and dopaminergic receptors. 133   Primarily dopaminergic
            LACTATE                                              effects  are  seen  at  low  intravenous  doses  (1  to
            The clinical use of lactate measurement has gained popu­  5 mg/kg/min),  mainly  b-adrenergic  effects  are  seen  at
            larity and acceptance in veterinary practice over the past   moderate  doses  (5  to  10 mg/kg/min),  mixed  a- and
            10 years due to the accessibility and reasonable cost of   b-adrenergic  effects  are  present  at  high  doses  (10  to
            portable lactate analyzers. An elevated blood lactate con­  15 mg/kg/min),  and  primarily  a-adrenergic  effects  are
            centration is frequently a marker of anaerobic metabolism   seen at very high doses (15 to 20 mg/kg/min). The actual
            and  has  been  correlated  with  inadequate  tissue   dose  response  relationship  is  unpredictable  in  a  given
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