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879.e2  Renal Tubular Acidosis




            Renal Tubular Acidosis                                                                 Client Education
                                                                                                         Sheet
  VetBooks.ir                                 Etiology and Pathophysiology       Initial Database

            BASIC INFORMATION
                                              Causes:                            •  CBC: typically unremarkable
           Definition                         •  Inherited:  dogs,  Fanconi  syndrome  or   •  Serum  biochemistry  profile:  hypokalemia,
                                                                        +
                                                                     +
           Renal tubular acidosis (RTA) is an uncommon   congenital defect of the H /K -ATPase     hyperchloremia, normal anion gap, decreased
           group of renal tubular disorders that result   pump                     total CO 2
           in hyperchloremic metabolic acidosis with a   •  Acquired               ○   Hyperkalemia and hyponatremia may
           normal glomerular filtration rate.   ○   Any substance that can cause renal   be seen with aldosterone deficiency or
           •  The tubular defect may result in decreased   tubular  toxicity;  toxins  (e.g.,  heavy   resistance (type IV RTA).
                               −
            tubular resorption of HCO 3  (proximal RTA)   metals,  ethylene  glycol,  4-pentenoate,   •  Blood gas analysis: hyperchloremic metabolic
            or defective acid secretion (distal RTA).  maleic  acid),  drugs  (e.g.,  gentamicin,   acidosis is expected.
           •  Proximal  RTA  may  be  recognized  along   cephalosporins,  outdated  tetracycline,   •  Urinalysis: proximal RTA = pH < 6; distal
            with proximal tubular resorption defects of   cisplatin,  salicylate,  streptozotocin,   RTA = pH > 6. Glucosuria is common in
            glucose, phosphate, sodium, potassium, uric   zonisamide),  some  jerky  treats;  copper   proximal RTA only.
            acid,  and  amino  acids  as  part  of  Fanconi   storage  disease  (dogs);  neoplasia  (mul-  •  Urine culture: urinary tract infection with
            syndrome.                             tiple  myeloma);  hypoparathyroidism   urease-producing bacteria must be ruled out.
                                                  with  concurrent  hypovitaminosis  D;   •  Abdominal radiographs or ultrasound: rule
           Synonyms                               Escherichia coli  pyelonephritis  (cats);   out nephrolithiasis or urolithiasis (distal RTA
           •  Classic or type I: distal RTA       leptospirosis  (dogs);  hepatic  lipidosis   only).
           •  Type II: proximal RTA               (cats); immune-mediated disease (dogs);
           •  Type  III:  combination  of  types  I  and  II;   ischemia-induced  acute  kidney  injury;   Advanced or Confirmatory Testing
            extremely rare                        hypoaldosteronism or aldosterone resis-  •  Glomerular filtration rate: normal. Measure-
           •  Type IV: hypoaldosteronism or aldosterone   tance (e.g., spironolactone)  ment not routinely required
            resistance causing distal RTA; hyperkalemic   Mechanisms:            •  If aldosterone deficiency is suspected, diag-
            RTA                               •  Proximal RTA:                     nostic evaluation for hypoadrenocorticism
                                                ○   Dysfunction  of  the  proximal  tubule,   should be initiated (p. 512).
           Epidemiology                           leading to decreased bicarbonate resorption  •  Differentiation of proximal and distal RTA
           SPECIES, AGE, SEX                    ○   Distal tubular bicarbonate resorption   (important for therapeutic management):
           RTA  is  rare  in  dogs  and  cats.  Age  of  onset   mechanisms are intact.  ○   Urinary fractional excretion of HCO 3 −
                                                                                                         −
           depends on cause (inherited, 3-4 years of age;   ○   Acidosis is less severe than in distal RTA   ■   Failure to conserve HCO 3  (fractional
           acquired, any age).                    because the distal tubule is able to partially   excretion  >5%) in an animal with
                                                  compensate.                          hyperchloremic metabolic acidosis indi-
           GENETICS, BREED PREDISPOSITION     •  Distal RTA                            cates proximal RTA, but some animals
           Dogs:  basenjis,  border  terriers,  Norwegian   ○   Impaired hydrogen ion secretion in the   have reduced fractional excretion due
           elkhounds,  schnauzers,  Shetland  sheepdogs   collecting ducts             to reduced plasma concentration of
                                                                                           −
           (Fanconi syndrome)                   ○   Urinary acid secretion is decreased, little   HCO 3 . In these circumstances, alkali
                                                  change in bicarbonate resorption     is administered to normalize plasma
           RISK FACTORS                         ○   Nephrocalcinosis,  urolithiasis  (typically   HCO 3 , and then fractional excretion
                                                                                           −
           See Etiology and Pathophysiology.      calcium phosphate), bone demineraliza-  is measured:
                                                  tion, and potassium wasting are possible   ❏   Normal (<5%) with distal RTA
           ASSOCIATED DISORDERS                   features.                            ❏   Markedly increased (>15%) with
           •  Nephrolithiasis/urolithiasis (distal RTA)                                  proximal RTA
           •  Bone demineralization (distal RTA)   DIAGNOSIS                       ○   Ammonium chloride tolerance test:
           •  Hypokalemic myopathy                                                   administer  110-200 mg/kg ammonium
           •  Chronic kidney disease (CKD)    Diagnostic Overview                    chloride PO. Monitor urine pH before
                                              RTA  should  be  considered  in  animals  with   and q 1h for 6 hours after administration.
           Clinical Presentation              hyperchloremic metabolic acidosis recognized   ■   In  healthy  dogs  and  cats,  urine  pH
           HISTORY, CHIEF COMPLAINT           on serum biochemical and blood gas analysis.   should decrease to a minimum of 5.0
           Some or all may be present:        Specific findings on diagnostic tests differ   and  5.5,  respectively,  4  hours  after
           •  Polyuria/polydipsia             depending on the form of RTA (distal, proxi-  ammonium chloride administration.
           •  Anorexia                        mal, hyperkalemic).                    ■   Failure to acidify urine is consistent
           •  Lethargy                                                                 with distal RTA.
           •  Weakness                        Differential Diagnosis                 ■   Caution should be exercised when
           •  Signs consistent with urolithiasis (distal RTA)  •  Hyperchloremic  metabolic  acidosis:  diar-  considering this test because it worsens
           •  Animals with proximal RTA often lack any   rhea,  Fanconi  syndrome,  posthypocapnic   acidemia.
            signs of illness.                   metabolic  acidosis,  dilutional  acidosis,
                                                hypoadrenocorticism, medications (carbonic    TREATMENT
           PHYSICAL EXAM FINDINGS               anhydrase inhibitors, spironolactone, ammo-
           •  ± Renomegaly                      nium chloride)                   Treatment Overview
           •  ± Dehydration                   •  Alkaline urine: urinary tract infection with   Treatment  goals  are  resolution  of  acidemia,
                                                                                                              −
           •  ± Poor haircoat                   urease-producing  bacteria  (e.g.,  Proteus,   maintenance  of  total  CO 2  or  HCO 3   >
           •  ± Muscular weakness               Staphylococcus, Klebsiella spp), postprandial,   12 mEq/L, and correction of hypokalemia if
           •  ± Weight loss                     dietary                          present.
           •  ± Respiratory muscle impairment

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