RTA Flashcards

1
Q

What is Renal tubular Acidosis?

A

Group of hyperchloraemic metabolic acidoses

  • Secondary to abnormality in urine acidification
  • Impaired acid excretion
  • Impaired bicarb reabsorption
  • GFR preserved

Electrolytes show ↓HCO3 , ↑Cl , N Anion Gap

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2
Q

What is the equation for Anion Gap?

A

Cations – Anions = Anion Gap

(Na+ + K+) – (Cl- + HCO3-) = 10-20 mmol/L

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3
Q

What are classifications of Renal Tubular Acidosis?

A
  • Type 1: Distal RTA : Inadequate H+ secretion (↓K)
  • Type 2: Proximal RTA : Inadequate HCO3 reabsorption (↓K)
  • Type 4: Distal RTA with ↑K. Mineralocorticoid deficiency
  • Type 3: Rare (mixture of type 1 & 2) people die before birth though
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4
Q

What is the role of kidney in H+ homeostasis?

A

PROXIMAL TUBULE

  • Reabsorption of HCO3 (80%)
  • Reabsorption of glucose, amino acids, organic anions, phosphate

DISTAL TUBULE

  • Regeneration of remaining HCO3 (20%)
  • Secretion of H+
  • NH4+ generation from glutamine
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5
Q

What are features of Type 1 (Distal RTA)?

A
  • Failure to lower urine pH (<5.5)
  • Impaired NH4+ excretion
  • Intact HCO3 reabsorption
  • Nephrocalcinosis, urolithiasis
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6
Q

What are features of Type 2 (Proximal RTA)?

A
  • Impaired HCO3 reabsorption
  • Isolated/generalised defect e.g as part of Fanconi’s Syndrome
  • Bicarbonaturia (low threshold for bicarb reabsorption)
  • Intact H+ secretion in distal cells
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7
Q

What are features of Type 3/mixed RTA?

A
  • Initially used to describe transient & severe form of distal RTA in infants
  • Currently used to describe a rare autosomal recessive syndrome resulting from carbonic anhydrase II deficiency
  • Features of both proximal and distal RTA
  • In addition to RTA, patients suffer osteoporosis, cerebral calcification & mental retardation
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8
Q

What are features of incomplete distal RTA?

A
  • Persistently high urine pH (even after an acute acid load)
  • Hypocitraturia
  • Normal HCO3 (no metabolic acidosis) as able to maintain net H+ excretion
  • Hypercalciuria + hypocitraturia = nephrolithiasis
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9
Q

What are features of Type 4 RTA (Hypoaldosteronism)?

A

Aldosterone deficiency or tubular resistance to action of aldosterone

Features

  • Hyperkalaemia (impaired K secretion)
  • Mild acidosis (impaired H+ secretion)
  • Impaired secretion of NH4+
  • Appropriately low urine pH (≤5.3 in presence of acidosis)
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10
Q

How is RTA diagnosed?

A
  • Hyperchloraemic metabolic acidosis not explained by bicarbonate losses from the intestinal tract should raise the suspicion of RTA
  • Plasma potassium (low in RTA 1 & 2, high in RTA 4)
  • Presence of other features of Fanconi syndrome suggest type 2 RTA.
  • Amount of bicarb required to correct acidosis can help distinguish between type 1 and type 2 RTA (type 2 requires much more bicarb)
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11
Q

What are some dynamic function tests for RTA?

A
  • Early morning/first pass urine after overnight fast pH <5.5
  • Urinary acidification test NH4Cl 100mg/kg body weight. Measure urine pH every hour for 8h
  • NH4Cl can be unpleasant & is not used in patients with liver disease - Calcium chloride 1mmol/kg body weight
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12
Q

What will results for dynamic function tests for RTA?

A
  • Normal: Urine pH will fall below 5.5 at least once
  • Distal RTA (type 1) - urine pH fails to fall below 5.5 & often stays above 6.5
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13
Q

What is Fractional Excretion of HCO3?

A

Can be used to confirm Dx RTA type 2 (proximal)

([UHCO3/PHCO3] / [Ucreat/Pcreat]) x 100%

  • Proximal RTA: >10-15%
  • Distal RTA: <10%
  • (but can only use if plasma HCO3 is >20mmol/L)
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14
Q

How can NH4 excretion be measured?

A

NH4 excretion can be measured but is estimated by calc anion gap

  • UAG = Na + K – Cl
  • In the presence of acidosis a negative UAG indicates pRTA and positive UAG indicates dRTA (type 1 or 4)

Osmolal gap

  • UOG = Osmo – 2Na – 2K – urea – glu
  • This also estimates NH4 excretion
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15
Q

How is Renal Tubular Acidosis managed?

A
  • Type 1: Administer bicarb 1-2mmol/kg/day
  • Type 2: Bicarb 5-15 mmol/kg/day (+K)
  • Type 4: Fludrocortisone 0.1-0.2 mg/bds for mineralocorticoid deficiency OR diuretic therapy + low K diet if mineralocorticoid resistant
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16
Q

What is TTKG (Trans-Tubular K [Potassium] Gradient) calculation?

A
  • Indicates level of aldosterone
  • Normal TTKG ~ 8-9
  • In hyperkalaemia TTKG should be >10
  • If hyperkalaemic & TTKG <7 = possible mineralocorticoid deficiency
  • If hypokalaemic TTKG should be <3