Page 768 - Small Animal Internal Medicine, 6th Edition
P. 768

PART SIX                          Endocrine Disorders
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                   PART VI   Endocrine Disorders
                                              Richard W. Nelson and Ann-Marie Della Maggiore


  VetBooks.ir             CHAPTER                               46






                                    Disorders of the


                             Hypothalamus and


                                     Pituitary Gland









            POLYURIA AND POLYDIPSIA                              and usually have a psychogenic or behavioral basis for the
                                                                 compulsive water consumption (see the discussion of psy-
            Water consumption and urine production are controlled by   chogenic PD, p. 7). A complete discussion of the diagnostic
            complex interactions between plasma osmolality, fluid   approach to PU-PD is presented in Chapter 38. An index
            volume in the vascular compartment, the thirst center, the   of suspicion for most of the endocrinopathies that cause
            kidney, the pituitary gland, and the hypothalamus. Dysfunc-  PU-PD can be raised after a review of the history, physical
            tion in any of these areas results in the clinical signs of   examination findings, and results of a complete blood count
            polyuria (PU) and polydipsia (PD). In dogs normal water   (CBC), serum biochemistry panel, serum thyroxine (T 4 )
            intake  is  usually  less  than  80 mL/kg  of  body  weight/24 h.   concentration (cat), urinalysis, and urine culture. Specific
            Water intake between 80 and 100 mL/kg/24 h is suggestive   tests may be necessary to confirm the diagnosis (Table 46.1).
            of PD but may be normal in some dogs. Water intake greater   See the appropriate chapters in this section for a more com-
            than 100 mL/kg/24 h confirms PD. Similar values are used   plete discussion of the diagnosis and treatment of each of
            for cats, although most cats drink considerably less than   these endocrinopathies.
            these amounts. Normal urine output ranges between 20 and   Occasionally, physical examination findings and initial
            45 mL/kg/24 h (1-2 mL/kg/h). PU in the dog and cat has   blood and urine test results are normal in dogs and cats with
            been defined as urine production greater than 50 mL/  PU  and  PD.  Differential  diagnoses  in  these  dogs  and  cats
            kg/24 h, although it is possible for urine production to be   include diabetes insipidus, psychogenic PD, hyperadreno-
            abnormal within the limits of these normal values in indi-  corticism, mild renal insufficiency without azotemia, mild
            vidual dogs and cats.                                hepatic insufficiency (most notably with portosystemic
              A  variety  of  metabolic  disturbances  can  cause  PU-PD.   shunts), and the early stages of hypoadrenocorticism. Hyper-
            Primary polyuric disorders can be classified on the basis of   adrenocorticism, hypoadrenocorticism, renal insufficiency,
            the  underlying  pathophysiology  into  primary  pituitary   and hepatic insufficiency should be ruled out before diag-
            (central) and nephrogenic diabetes insipidus (NDI), second-  nostic tests for diabetes insipidus or psychogenic PD are
            ary NDI, osmotic diuresis-induced PU, and interference   performed. Diagnostic tests to consider include evaluation
            with the hypothalamic-pituitary secretion of arginine vaso-  of the range of urine specific gravities obtained from several
            pressin (AVP). The most common form of diabetes insipidus   urine samples (discussed in the next paragraph), tests for
            is acquired secondary NDI. This form includes a variety of   hyperadrenocorticism (e.g., urine cortisol/creatinine ratio,
            renal and metabolic disorders in which the renal tubules lose   low-dose dexamethasone suppression test), hypoadrenocor-
            the ability to respond adequately to AVP. Most of these   ticism (e.g., baseline serum cortisol concentration), liver
            acquired forms are potentially reversible after elimination of   function tests (e.g., measurement of preprandial and post-
            the underlying illness.                              prandial bile acid concentrations), determination of the
              Secondary NDI results from interference with the normal   urine protein/creatinine (P:C) ratio, and abdominal ultraso-
            interaction of AVP and renal tubular AVP receptors, prob-  nography. Ideally, all realistic causes of secondary acquired
            lems with the generation of intracellular cyclic adenosine   NDI should be ruled out before tests for primary pituitary
            monophosphate (cAMP), problems with renal tubular cell   and NDI and psychogenic PD are performed.
            function, or loss of the renal medullary interstitial concen-  Critical evaluation of urine specific gravity measured
            tration gradient. Primary polydipsic disorders occur in dogs   from several urine samples obtained by the client at different

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