Renal Tubular Acidosis
The term renal tubular acidosis (RTA) describes a group of disorders whose individual features reflect the site and mechanism of failure in tubular hydrogen ion transport (Fig. 34-3). Type I, or classic distal RTA, represents an inability of the collecting duct to maintain a gradient of free hydrogen ion between the blood and the urine. This failure to maintain a hydrogen ion gradient may be due to increased backleak of hydrogen ion from the tubular lumen to blood or to a failure in the hydrogen secretory mechanism. Type I RTA is expressed as an inability to lower urine pH (the free hydrogen ion concentration) in the face of an acid challenge. Type II, or proximal RTA, involves an impairment in the rate of hydrogen ion secretion and therefore bicarbonate reabsorption in the proximal tubule. Proximal RTA is expressed as bicarbonaturia that persists until the serum bicarbonate concentration and the filtered load of bicarbonate fall to levels that match the reduced proximal tubular absorptive capacity. Finally, Type IV RTA designates a defect in mineralocor-ticoid-dependent hydrogen ion secretion in the distal nephron. Type IV RTA usually accompanies some form of renal interstitial disease (as in lead or diabetic nephropathies) and results either from diminished aldosterone secretion or from a failure of collecting duct response to aldosterone.
Distal RTA may occur sporadically as an isolated disorder or may be secondary to a systemic disease or toxin. Prominent causes of distal RTA include primary and secondary hypergammaglobulinemias, nephrocalcinosis, amyloidosis, sickle cell disease, and amphotericin B administration.
Children often present with lethargy, anorexia, stunted growth, and bone disease. Adults have similar symptoms, often with bone pain or pathological fractures, and a high incidence of renal stones. The origin of these symptoms appears to be bone buffering of hydrogen ion over an extended period. This leads to bone calcium loss and hypercalciuria in the presence of an alkaline urine. Disordered calcium metabolism is expressed as rickets in children and osteomalacia’, nephrocalcinosis, and nephrolithasis in adults. The distinguishing laboratory features include hyperchloremic metabolic acidosis with hypokalemia and a urinary pH that is consistently above pH 6.0 to 6.5.
An inability to lower urine pH below 5.3 in the face of spontaneous acidosis or an acid load (given as oral NH4C1] is diagnostic. Administration of a single dose of the loop diuretic furosemide also aids in the diagnosis of distal RTA. Normal individuals and those with Type I, gradient-limited RTA increase urinary acid secretion concomitant to the increased delivery of Na+ to the distal nephron.
Treatment of distal RTA is accomplished by oral alkali replacement, either as sodium bicarbonate or as Shohl’s solution, at the rate of 1 to 3 mEq/kg/day. The 60 to 70 mEq of bicarbonate required to treat Type I RTA correspond to the normal contribution of the distal nephron to H+ excretion. Correction of acidosis by this means leads to cessation of hypercalciuria and renal stone formation and correction of hypokalemia, but normal growth and bone development in children require administration of several hundred milhequivalents of bicarbonate daily.
Proximal RTA occurs rarely as an isolated lesion and is most often seen as a part of the Fanconi syndrome. Proximal RTA is a self-limiting process m that normal acidification of urine, measured both as a maximum reduction in urine pH and as a normal excretion of ammonia and titratable acid, is seen when the serum bicarbonate level reaches a reduced, steady-state value. This value is usually 14 to 18 mEq/L and represents the maximal resorptive capacity of the proximal tubule in the disorder. At this moderate level of extracellular buffer reduction, daily H+ excretion is complete and long-term buffer deficits do not develop as in distal RTA.
Clinical signs and symptoms are few in proximal RTA and relate to growth retardation. Hyperchloremic metabolic acidosis is evident in all: cases. Hypokalemia, the result of increased deliv-” ery of sodium bicarbonate to the distal nephron,*, is prominent. Hypercalciuria, nephrocalcinosis4 and nephrolithiasis are absent. The urine pH can’ reach values of 4.5 to 5.0 as long as the serurrr bicarbonate level is below the proximal tubular! resorptive threshold. The diagnosis is confirmed” by the infusion of bicarbonate and observation of an increase in urine pH and bicarbonaturia at subnormal levels of serum bicarbonate. The treatment of proximal RTA with alkali replacement is virtually impossible because any elevation of the serum bicarbonate above the absorptive capacity of the proximal tubule results in quantitative urinary excretion of the added bicarbonate. Modest salt depletion, thereby increasing general proximal tubular absorption, will aid in raising the serum bicarbonate concentration.
Type IV RTA results from a diminished mineralocorticoid effect in the distal nephron and is expressed as a decrease in the secretory rates of potassium and hydrogen. There are two forms of the disorder. Aldosterone levels may be reduced, either from primary adrenal disease, in which case renin levels are elevated, or from renal interstitial disease, in which case renin levels are grossly reduced. Alternatively, adequate levels of aldosterone may be present but the distal nephron is unresponsive to its effect. This type of the disorder may be caused either by disease of the distal nephron; by the aldosterone-blocking diuretic, spironolactone; or by the potassium-sparing diuretics, triamterene and amiloride.
Since both potassium and hydrogen secretion are blunted, hyperkalemia accompanies the hy-perchloremic metabolic acidosis of Type IV RTA. This is in contrast to the hypokalemia seen in Types I and II. A mild degree of renal insufficiency is present in many of these patients. They often demonstrate relative salt wasting, that is, an inability to reduce urinary sodium excretion during salt restriction. Hyperkalemia decreases the renal generation and excretion of the major urinary buffer, ammonium. Therefore, patients with Type IV RTA have a decrease in total acid excretion, although the urine pH may be appropriately acidic. Basal and stimulated renin plus aldosterone levels should be measured in these patients.
Mineralocorticoid replacement, as fludrocortisone, is effective therapy in patients with an absolute reduction in aldosterone. Because increased sodium delivery to the distal nephron augments potassium and hydrogen secretion even in the absence of aldosterone, a high-salt diet plus a loop diuretic (furosemide) will increase both potassium and hydrogen excretion in all these patients. Reduction of the serum potassium alone increases urinary ammonium excretion and net urinary acid excretion and restores the hydrogen balance in some of these patients.
- PRINCIPLES OF CARDIOPULMONARY RESUSCITATION
- MYOCARDIAL DISEASE - MYOCARDITIS
- BROliCHIECTASIS
- CIRCULATORY PHYSIOLOGY
- Outcome and Prognosis
- Amyloidosis
- CARDIOMYOPATHY
- Urinalysis, Renal ‘Tubular Function, and Urine Flow Rate
- Hepatic Encephalopathy
- BILIRUBIN METABOLISM
- LABORATORY TESTS OF LIVER FUNCTION AND DISEASE
- PULMOIIARY FUNCTION EVALUATION
- PERFUSION
- ELECTRICAL CONDUCTION SYSTEM
- Incidence
- TREATMENT OF MALABSORPTION
- EMPHYSEMA
- Tocainide
- HEMODIALYSIS AND HEMOPERFUSION IN THE TREATMENT OF DRUG OVERDOSES
- Hypertrophic Cardiomyopathy
- Upper GI Bleeding
- Alterations in Drug Doses in Patients with Renal Failure
- PERICARDIAL EFFUSIOH
- Procainamide
- SMOKING CESSATION
- Urinary Tract Obstruction
- Indirect
- Portal Hypertension
- PERIPHERAL VENOUS DISEASE
- Nephrosclerosis
- Nephrogenic Diabetes Insipidus (NDI)
- CHEST WALL DISEASE
- DISORDERS ASSOCIATED WITH MALABSORPTION
- Etiology and Pathogenesis
- CONSTRICTIVE PERICARDITIS