Pharm
Patiromer
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Patiromer
, Veltassa
See Also
Sodium Zirconium Cyclosilicate
Patiromer (Veltassa)
Kayexalate
(
Sodium Polystyrene Sulfonate
)
Hyperkalemia
Hyperkalemia Management
Indications
Chronic
Hyperkalemia
Contraindications
Bowel Obstruction
Fecal Impaction
Severe
Constipation
Mechanism
Potassium
binding agent
Exchanges
Calcium
for free
Potassium
in the
Gastrointestinal Tract
Passes through the
Gastrointestinal Tract
(bound to
Potassium
) without absorption
Results in greater
Potassium
excretion in the stool, and hence lower
Serum Potassium
levels
Efficacy
Not effective or indicated in acute, life threatening
Hyperkalemia
Expected to lower
Serum Potassium
0.7 mEq/L at 4 weeks
Precautions
Delayed onset of action
Use other rapid acting measures to lower
Potassium
in life-threatening
Hyperkalemia
Electrolyte
loss
Monitor
Potassium
and
Magnesium
levels
Magnesium Supplementation
as needed
Drug Interaction
with oral medications (decreases absorption of other medications)
Avoid other oral medications for at least 3 hours before and 3 hours after Patiromer
Dosing
Start: 8.4 g once daily
Next: Increase to16.8 g once daily after at least one week if needed
Next: Increase to 25.2 g once daily (max dose) after at least one week at 16.8 g dose if needed
Adverse Effects
Electrolyte
s
Hypomagnesemia
(5-9%)
Hypokalemia
(5%)
Gastrointestinal (increased
Incidence
in elderly patients)
Transient
Constipation
(7%)
Diarrhea
(5%)
Nausea
(2%)
Abdominal Pain
(2%)
Flatulence
(2%)
Hypersensitivity
Lip edema (<1%)
References
Lovecchio (2017) Crit Dec Emerg Med 31(2): 24
Chaitman (2016) P T 41(1): 43-50+PMID:26765867 [PubMed]
Kim (2023) Am Fam Physician 107(1): 59-70 [PubMed]
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