Page 720 - Fluid, Electrolyte, and Acid-Base Disorders in Small Animal Practice
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Hemodialysis and Extracorporeal Blood Purification  707


            severely azotemic animals to prevent manifestations of  COMPLICATIONS OF
            dialysis disequilibrium syndrome.                   HEMODIALYSIS
              Application of extracorporeal therapies should not be
            limited to single modalities but should be sequenced and  The clinical and procedural complications associated with
            combined to best match the clinical course and kinetics of  hemodialysis in humans and animals have been
            the toxicant. Continuous versus intermittent therapies  reviewed. 34,59,78,147  The most serious complications
            should not be considered mutually exclusive but rather  include those associated with the interaction of the
            complimentary. There is little justification not to include  patient with the dialysis machinery, vascular access, hemo-
            a dialytic device with a hemoperfusion cartridge when  dynamic stability, and solute disequilibrium. Hemodialy-
            contemplating hemoperfusion. For many toxins, hemo-  sis is a technically complex therapy applied to patients
            dialysis has the potential to improve toxin clearance in  with profound physiologic and metabolic derangements.
            concert  with  hemoperfusion  despite  theoretical  Therapeutic complications can be anticipated from both
            predictions to the contrary (Figure 29-12). Dose, blood  the technical aspects of the process, the dynamic
            concentration, changes in protein binding of the toxin,  oscillations of solute and fluid homeostasis, exposure to
            concurrent drugs/toxins, acid-base status, membrane  nonbiologic materials, and sources of contamination
            type, and other variables may influence the diffusive  and toxicities associated with procedural and medical
            potential of a toxin under different clinical conditions.  therapies. Often it is difficult to distinguish whether
            The presence of the hemodialyzer in the extracorporeal  adverse events are caused by the severity of the uremia,
            circuit provides the potential for better thermal regula-  the intensity of its treatment, or the consequences of
            tion and opportunity to correct coexisting fluid volume,  the intervention. The frequency and severity of
            electrolyte, acid-base, or uremic complications. Place-  complications related to homeostatic excursions early
            ment of the hemodialyzer after the hemoperfusion    in dialysis diminish as the patient adapts to the
            cartridge also helps to prevent depletion of calcium and  procedures and the uremia is controlled, but they often
            glucose  by  charcoal  sorbents  and  isolates  the  are replaced by more subtle homeostatic imbalances
            hemoperfusion cartridge from the ultrafiltration control  imposed chronically.
            system that may promote excessive fluid removal and    The number and relative frequency but not the types
            hemoconcentration in the dialyzer should pressure   of complications encountered in veterinary dialysis have
            increase in the sorbent bed.                        changed over the past 25 years. In early years, dialysis dis-
              Hemoperfusion with activated charcoal is generally  equilibrium and hemorrhage related to anticoagulation
            safe but poses potential disadvantages or complications  were the most common causes of fatal complications.
            not generally experienced with hemodialysis. One of  Now, fatal dialysis-related complications are rarely
            the principal concerns is the innate hemocompatibility  encountered. Even in severely uremic patients, dialysis
            of the adsorbent. Hemoperfusion with activated charcoal  disequilibrium  is  averted  by  tailoring  dialysis
            (as well as other sorbent materials) can cause thrombocy-  prescriptions to each patient and by use of precautionary
            topenia and leukopenia because platelets and leukocytes  measures including slow, less intensive prescriptions, pro-
            become adhered to the sorbent or entrapped in fibrin  phylactic mannitol administration, and sodium profiling
            films or clots formed on the charcoal. Platelets are  to minimize osmotic shifts in high-risk patients.
            destroyed also by surface irregularities of the charcoal  Symptomatic hypotension remains a persistent threat
            bed. These effects are not unique to activated charcoal  because of the increasing willingness to dialyze smaller
            and are potential complications of polymer-based    patients and those with critical comorbidities. Blood pres-
            sorbents. Thrombocytopenia can be especially problem-  sure should be monitored at 15- to 30-minute intervals
            atic if daily treatments are required that preclude ade-  throughout the dialysis session to remain proactive and
            quate regeneration of platelets between treatments. If  attentive to this concern. The susceptibility to hypoten-
            hemoperfusion is not combined with hemodialysis, the  sive events is influenced by body size, hydration status,
            patient may experience significant cooling because of  the severity of the uremia, the presence of concurrent car-
            the duration the extracorporeal blood is exposed to room  diac disease or co-morbid conditions (e.g., hemorrhage,
            temperature. The sorbent bed also may become saturated  anemia, sepsis, pancreatitis), and current medications
            at unpredictable times during the treatment resulting in  (e.g., antihypertensives, diuretics). For cats and small
            incomplete removal of the toxin. Saturation of the sor-  dogs, the volume of the extracorporeal circuit may exceed
            bent is easily demonstrated by measuring the extraction  25% to 30% of the intravascular volume and cause
            ratio [(A tox –V tox )/A tox ] across the device or its whole  hypovolemia as the circuit is filled. The rapid removal
            blood clearance [Q b   extraction ratio], where A tox and  of plasma solutes in the early stages of a dialysis treatment
            V tox are the concentrations of the solute or toxin at the  decreases intravascular volume and opposes refilling of
            inlet and outlet of the hemoperfusion cartridge, respec-  fluid from the extravascular space. Excessive or rapid
            tively, and Q b is the blood flow rate.             ultrafiltration that exceeds vascular refilling is the most
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