Characteristic | Sodium polystyrene sulfonate23 | Sodium zirconium cyclosilicate25 | Patiromer24,29 |
---|---|---|---|
Mechanism | Nonabsorbed cation-exchange resin | Inorganic cation exchanger with a crystalline structure that entraps K+ | Nonabsorbed cation-exchanger polymer that binds K+ |
Site | Colon | Entire GI tract | Colon |
Exchange ion for potassium | Sodium | Sodium | Calcium |
Onset of action | Hours to days | 1 hour | 4 to 7 hours |
Enablement of RAAS inhibitors | Not on label or shown | Not on label About 70% of patients in phase 2 and 3 studies were receiving RAAS inhibitors at baseline | On label 99.4% of patients in phase 2 and 3 studies were receiving RAAS inhibitors at baseline |
Adverse events | GI stenosis, intestinal ischemia, ischemic colitis, rectal hemorrhage, GI necrosis, intestinal perforation with fatal outcomes, hypomagnesemia, hypokalemia, hypocalcemia | Mild-to-moderate GI effects, edema, hypokalemia (0%–11%, dose-dependent effect) | Mild-to-moderate GI effects, hypomagnesemia, hypokalemia (3%–5.6%) |
Recommended dose | Oral: 15 g, 1–4 times daily Rectal: 30–50 g, 1–2 times daily | 10 g 3 times daily for up to 48 hours, then 5–10 g once a day. No more than 10 g once a day for maintenance therapy | 8.4 g once a day. Dose can be titrated at ≥ 1-wk intervals in 8.4 g increments to a maximum of 25.2 g once a day |
Daily list price and funding | Generic | $12.50 (5 g), $25 (10 g); negative CADTH recommendation* | $13 (flat); positive CADTH recommendation* |
Note: CADTH = Canadian Agency for Drugs and Technologies in Health, GI = gastrointestinal, K+ = potassium, RAAS = renin–angiotensin–aldosterone system.
↵* CADTH is a government agency that undertakes an evaluation of the clinical and cost-effectiveness evidence on a drug, and provides recommendations on reimbursement. A positive recommendation means that CADTH supports reimbursement. A negative recommendation means that it does not support reimbursement. The recommendations are nonbinding.