Acid-Base Abnormalities Flashcards
Normal pH range?
7.35-7.45
Metabolic acidosis + Resp compensation is (normal anion gap)
HARD-ASS
Hyperalimentation
Addison’s disease
Renal tubular Necrosis
Diarrhoea (may also give hypokalaemia)
Acetazolamide
Sprionolactone
Saline infusion
Anion gap equation
AG= [K+] + [Na+] - [Cl-] - [HCO3-]
Normal range: 10-18 mmol/L
Metabolic acidosis with Resp Comp (Elevated anion gap)
Lactate: shock, sepsis, hypoxia
Ketones: diabetic ketoacidosis, alcohol
Urate: renal failure
Acid poisoning: salicylates, methanol
Resp acidosis
COPD
Decompensation in life threatening asthma/ pulmonary oedema
Neuromuscular disease
Obesity hypoventilation syndrome
Drugs: benzodiazepines/ opioid overdose
Respiratory alkalosis
anxiety leading to hyperventilation
pulmonary embolism
salicylate poisoning*
CNS disorders: stroke, subarachnoid haemorrhage, encephalitis
altitude
pregnancy
*salicylate overdose leads to a mixed respiratory alkalosis and metabolic acidosis. Early stimulation of the respiratory centre leads to a respiratory alkalosis whilst later the direct acid effects of salicylates (combined with acute renal failure) may lead to an acidosis
Metabolic alkalosis
Metabolic alkalosis
Metabolic alkalosis may be caused by a loss of hydrogen ions or a gain of bicarbonate. It is due mainly to problems of the kidney or gastrointestinal tract
Causes
vomiting / aspiration
(e.g. peptic ulcer leading to pyloric stenos, nasogastric suction)
vomiting may also lead to hypokalaemia
diuretics
hypokalaemia
primary hyperaldosteronism
Cushing’s syndrome
Bartter’s syndrome
Bartter’s syndrome
Bartter syndrome is an autosomal recessive disorder of salt reabsorption resulting in extracellular fluid volume depletion with low/normal blood pressure. Thickening of ascending loop of Henle.
SX: periodic paralysis, lethargy, salt cravings, polydipsia and polyuria, nocturnal urination, stunted growth, vomiting
Dx: usually excess amniotic fluid (polyhydramnios) 24-30 wks gestation,
Tx: Na, Cl and K supplementation +- spironolactone
Renal tubular acidosis
-Type 1 RTA (distal)
inability to generate acid urine (secrete H+) in distal tubule
causes hypokalaemia
causes include idiopathic, rheumatoid arthritis, SLE, Sjogren’s,
Complications inc. renal stones+ nephrocalcinosis
-Type 2 RTA (proximal)
decreased HCO3- reabsorption in proximal tubule
causes hypokalaemia
complications include osteomalacia
causes include idiopathic, as part of Fanconi syndrome, Wilson’s disease
Type 3 (mixed) Type 4 (hyperkalaemia)
DKA management
0.9% sodium chloride and a fixed-rate insulin infusion at 0.1 units/kg/hr.
Diabetic ketoacidosis: once blood glucose is < 14 mmol/l an infusion of 10% dextrose should be started at 125 mls/hr in addition to the saline regime
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