ELECTROLYTES (Na & K)
ELECTROLYTES (Na & K)
ELECTROLYTES (Na & K)
Determination of Osmolality:
Specimen: Serume, Urine
Principle: Increase Osmolality = Decrease freezing point and Vapor pressure
Osmometer: Operate by freezing point depression using standardized using sodium chloride
reference solutions.
(Note: Increase pure water loss = increase ECF osmolality)
OSMOLAL GAP = Measured Osmolality - Calculated Osmolality
Normal Moderately Elevated Markedly elevated Hypoosmolality
Dehydration Ketoacidosis Poisoning with: Hyponatremia
Hyperglycemia w/o Renal Acidosis -Ethanol
ketoacidosis Lactic Acidosis -Methanol
Hypernatremia -Isopropanol
Azotemia -Ehtylene glycol
Diabetes insipidus -Diethyl ether
-Paraldehyde
-Trichloroethane
-Salicylate
FUNCTIONS OF ELECTROLYTES:
-Maintenance of Osmotic pressure and hydrations/volume regulation: Na, K, Cl
-Buffering functions/Acid-base Balance: HCO3, K, Cl
-Cofactors/Activators in enzyme reactions: Ca, Mg, Zinc
-Normal neuromuscular excitability: Ca, K, Mg
-Redox reaction/Electron transport: Iron
-Myocardial rhythm and contractility: K, Mg, Ca
-Regulation of ATPase ion pumps: Mg
-Blood coagulation: Ca, Mg
-Production of ATP from glucose: Mg, Phosphate
ANION GAP
-difference between the sum of the concentrations of the principal/unmeasured cations
and of the principal/unmeasured anions
-Represents the unmeasured net negative charge on plasma proteins
-Useful in: Detecting errors in analysis
(From HENRY’s)
*HAGMA (High Anion Gap Metabolic Acidosis): MUDPILES
(Methanol, Uremia, Diabetic Ketoacidosis, Propylene glycol, Iron, Lactic Acidosis, Ethylene glycol,
Salicylates)
*NAGMA (Normal Anion Gap Metabolic Acidosis: Diarrhea, RTA, Addison’s dse
*LAP (Low Anion Gap): Hypoalbuminemia, Hypercalcemia, Elevated Myeloma proteins
SODIUM
-most adversely affected by improper type of water used
-MOST ABUNDAT CATION IN THE ECF/CHIEF BASE OF THE BLOOD
-Main function are water pull
-Osmotic activity of ECF
-Blood volume regulation
-Neuromuscular Excitability
-Levels are regulated by:
-ADH (Water retention) = Dilutional Hyponatremia
- Aldosterone = Increasedd Na reabsorption
- Atrial natriuretic factor = decreases Na reabsorption in the DCT
-Normal value
-Kidney: Renal threshold for Na = 110-130 mmol/L
-Serum/ Plasma: 135-145 mmol/L
-24 hr urine: 40-220 mmol/dL
-CSF: 136-150 mmol/L
Pseudohyponatremia:
-for every 100 mg/dL increase in glucose, serum sodium decreases by 1.6 mmol/L
Laboratory Determination:
1. Flame Emission Photometry
2. Ion-Selective Electrode - Glass Electrode for Na
3. Colorimetric Method: Albanese-Lein Method)
- Sodium + zinc Uranyl Acetate = Sodium Uranyl Acetate precipitate
- Sodium Uranyl Acetate precipitate + water = yellow solution
POTASSIUM
-MAJOR INTRACELLULAR CATION
-Concentraion:
- CELL: Inside (20x greater) > Outside
- 90% free or exchangeable; 10% bound to RBC, bone and brain tissues
-KIDNEY - primary that controls extracellular K
-Proximal tubule: Compelety reabsorbs of filtered K
-Distal tubule and Collecting ducts: principal regulation of K excretion
-Secreted in the gastric juice and reabsorbed by the small intestines
-Functions:
-Neuromuscular excitabilty
-Contraction of the heart
-ICF volume and H+ concentration
-Influenced by pH: for every 0.1 unit pH decrease, there is 0.4 increase of K
Pseudohyperkalemia:
-Due to: Specimen hemolysis, delayed separation of seerum, EDTA contamination,
fist clenching with torniquet use, prolonged torniquet application, thrombocytosis,
Leukemia, IV fluid contamination.
Pseudohypokalemia:
- Due to: Leukocytosis (>11.0)
Sample Consideration:
- Plasma K+ is lower than serum by 0.1-0.7 mmol/L
Laboratory determinations:
1. Colorimetric Method - K+ is determined in a specifically prepared mixture of sodium
tetraphenylboron producing colloidal suspension whose turbidity is proportional to the K+
concentration in the sample
a) Lockhead and Purcell
2. FES (Color: Violet)
3. ISE
a) Glass that is permeable selectively to sodiium
b) Membrane impregnated with Valinomycin (has changed activity just the
right size to admit K and exclude others)
4. AAS