Acid/Base disorders Flashcards
What are ABG’s used for
monitoring oxygenation, ventilation, acid base balance
quantifying level of carboxyhemoglobin and methhemoglobin
How do you draw an ABG
from artery (MC radial)
mix with anticoag (heparin)
put on ice
take to the lab ASAP, results w/in 5-15 min
What are the ABG’s
pH 7.35-7.45 pO2: 80-100 O2 sat: >95 pCO2: 35-45 HCO3: 22-26
pO2 is used to determine
how well a patient is oxygenated (better than an O2 sat), NOT for determining acid-base conditions
What is our body’s normal physiology
body maintains homeostasis with strict control of hydrogen ions
buffer systems keep pH in normal range
acidosis/alkalosis are disorders
acidemia and alkalemia are pH of blood
What are respiratory and metabolic problems
Resp acidosis: pCO2 >45
Resp alkalosis: pCO2 <35
Met acidosis: HCO3 <22
Met alkalosis: HCO3 >26
Acid base disorders indicate
underlying disease process- so Tx underlying disease!
You can have up to 3 AB d/o- we have to figure out the primary one and treat it
(but you can only have ONE respiratory AB d/o)
What is the compensatory process
body will compensate for an AB d/o with the opposite
Respiratory compensation for metabolic d/o= fast
metabolic compensation for resp d/o= days-weeks
What causes metabolic acidosis
high anion gap: MUDPILES (methanol, uremia, DKA, propylene glycol, iron, lactate, ethanol, salicylate/starvation)
non-high anion gap: diarrhea (you lose more bicarb), RTA, Acetazolamide, spironalactone, Hyperchloremia
How do you treat metabolic acidosis
Sodium bicarb (band aid)
allow for respiratory compensation (hyperventilation, low CO2)
treat underlying cause
What is renal tubular acidosis
defects in H+ secretion and urinary acidification
Metabolic acidosis + NORMAL anion gap
What are the 2 types of renal tubular acidosis
Type 1: failure to excrete H+
Type 2: failure to reabsorb filtered HCO3
Explain Type 1 RTA (distal)
AI disease and hypercalciuria (or genetic) cause H+ to not be excreted
Tx: correct metabolic acidosis (sodium bicarb), give potassium citrate if persistent hypokalemia
Explain Type 2 RTA (proximal)
Defect in proximal bicarb reabsorption, or other defects in proximal tubule that inhibit reabsorption of phosphate, glucose, uric acid, and amino acids
-Fanconi syndrome: generalized proximal tubular dysfunction caused by multiple myeloma or acetazolamide
How do you treat Type 2 RTA
correct academia
Vitamin D and phosphate
+/- thiazide