Skip to main content
. 2023 Apr 5;24:89. doi: 10.1186/s12882-023-03145-x

Table 2.

Comparison of potassium exchange resins for the treatment of hyperkalemia

Drug name Sodium polystyrene sulfonate (SPS) Patiromer Sodium zirconium cyclosilicate (SZC)
Trade name Kayexalate®, Kionex® Veltessa® Lokelma®
FDA approval 1958 (prior to drug regulation laws) 2015 2018
Onset of action 2–24 h 2 h 1 h
Mode of action The sulfonate molecule exists as sulfonic acid in its ionic state and allows for interaction with a Na+ counterion. In this method, Na+ is exchanged for K+ within the gastrointestinal tract Utilizes the high colonic K+ concentration and exchanges its Ca2+ counterion for it. The attached fluorine atom at the alpha-carbon position of patiromer causes electron-withdrawing effects and generates a lower pKa compared to colonic pH. This allows the resin to exist in an ionized state and bind K+ effectively Selectively binds to K+ throughout the length of the gastrointestinal tract. SZC mimics physiological K+ ion channels by utilizing a thermodynamically favorable binding pocket unique to the size of K+
Degree of K+ lowering 1.04 mEq/La 0.6 mEq/Lb 0.4 mEq/Lc
Location of efficacy Large intestine Distal colon Small intestine and large intestine
Toxicity Na+ loading/fluid overload, hypomagnesemia, hypocalcemia, colonic necrosis Hypomagnesemia Edema
Side effects Nausea, vomiting, diarrhea, constipation, abdominal pain Mild-severe constipation, abdominal pain Constipation, abdominal pain
Exchange ion Na+ Ca2+ H+, Na+
Selectivity Non-specific, K+, Ca2+, Mg2+ Specific, K+ (low specificity, Mg2+) Highly specific, K+ and ammonium
Resin size  ~ 11–124 µm  ~ 100 µm  > 3 µm (non-absorbed)
Molecular composition Polymer resin consisting of sulfonate and attached vinylbenzene (styrene) R group Polymer resin with attached carboxylic acid and fluorine atom at alpha carbon position Three-dimensional, seven-member ring lattice made up of alternating zirconium and silicate atoms with adjoining oxygen atoms

a1.04 mEq/L mean decrease of serum K+ compared to placebo treatment; SPS was given at a dosage of 30 g/day for 7 days [18]

b0.6 mEq/L decrease of serum K+ 2 h post-treatment with a single dosage of 25.2 g [19]

c0.4 mEq/L decrease of serum K+ at 2 h post-treatment with dosage of 10 g 3 times daily; clinically significant decrease of K+ observed at 1 h [21]