Acid-Base Flashcards
Fanconi Syndrome
PCT reabsorptive defect Metabolic acidosis (proximal tubular acidosis)
Bartter Syndrome
Defect in NKCC (Autosomal Recessive)
HypoKalemia
Metabolic alkalosis
HyperCalciuria
Gitelman Syndrome
NC defect (Autosomal Recessive)
Hypokalemia, HypoMagenesemia
Metabolic alkalosis
HypoCalciuria
Liddle Syndrome
Gain of function of ENaC in CT (Autosomal Dominant) Hypertension HypoKalemia Metabolic alkalosis Low aldosterone
Syndrome of Apparent Mineralocorticoid Excess
Cortisol can bind mineralocorticoid-R Hypertension HypoKalemia Metabolic alkalosis Low aldosterone Acquired from licorice
Shifts K+ into cell (hypoKalemia)
Hypoosmolarity
Alkalosis
Beta-agonists (Na/K ATPase increase)
Insulin (Na/K ATPase increase)
Shifts K+ out of cell (hyperKalemia)
Digitalis (blocks Na/K ATPase) Hyperosmolarity Lysis (tumor lysis, crush, rhabdomyolisis) Acidosis Beta-blockers High blood sugar Succinylcholine (burns and trauma)
Respiratory Acidosis Causes
Airway obstruction Acute lung injury Chronic lung injury Opioids, sedative Weakening of respiratory muscles
Elevated anion gap metabolic acidosis causes
Methanol Uremia DKA Propylene glycol Isoniazid, iron Lactic acids Ethylene glycol Salicylates (late)
Normal anion gap metabolic acidosis causes
Hyperalimentation Addison's RTAs Diarrhea Acetazolamide Spironolactone Saline
Respiratory alkalosis causes
Hysteria Hypoxemia Salicylates (early) Tumor Pulmonary embolism
Metabolic alkalosis causes
Loop diuretics
Vomiting
Antacid use
Hyperaldosteromism
Type 1 RTA (Distal Tubule)
Normal AG, hyperchloremic metabolic acidosis
Urine pH >5.5
alpha cells can’t secrete H+ (no urine acidification), so no new HCO3- is generated leading to metabolic acidosis
Hypokalemia
Risk of calcium phosphate stones (pH)
Causes: amphotericin B, analgesics, congenitial UT obstruction
Type 2 RTA (PCT)
Normal AG, hyperchloremic metabolic acidosis
Urine pH <5.5
Defect in HCO3- reabsorption and increased excretion
Alpha-cells can acidify urine so that’s fine
HypoKalemia
Causes: Fanconi syndrome, CA inhibitors
Type 4 RTA (DCT/CD)
Normal AG, hyperchloremic metabolic acidosis
Urine pH <5.5
Caused by hypoaldosteronism which leads to decreased ammonia genesis in the PCT and less NH4+ excretion from an inability to buffer acid in the distal nephron
Alpha-cells also won’t be able to secrete H+
Causes: hypoaldosteronism from inhibition, Addison’s, diabetic hypreninism, ACEIs, ARBs, NSAIDs, heparine, cyclosporine) Also aldo. resistance (Spironolactone, obstruction, Bactrim)