Why the study?
Does patiromer effectively reduce serum potassium and maintain a favorable safety profile in patients with hyperkalemia?
Does patiromer effectively reduce serum potassium and maintain a favorable safety profile in patients with hyperkalemia?
Patiromer is an effective and generally well-tolerated potassium binder that may facilitate the optimal dosing of RAAS inhibitors in patients with heart failure and CKD.
Patiromer shows acceptable short-term tolerability in CKD/HF; leaves open long-term safety questions in broader real-world use.
INTRODUCTION: Hyperkalemia (HK) occurs often among patients with chronic kidney disease (CKD) and heart failure (HF) and those treated with renin-angiotensin-aldosterone system inhibitors (RAASI). Even small deviations from normal potassium levels carry increased risk of mortality. Patiromer is approved for treatment of HK and has been shown in clinical trials to reduce serum potassium among patients with HK and comorbid conditions. Areas covered: We review pooled data from two clinical trials of patiromer in patients with CKD and HK, safety of patiromer in special populations, drug-drug interaction (DDI) studies, and other studies in healthy volunteers. Expert opinion: Potassium must be maintained within a narrow range to avoid increased risk of mortality. Patients with CKD and HF and those receiving RAASI require careful monitoring of potassium levels. Patiromer effectively reduces serum potassium, and gastrointestinal adverse events (AEs) are the most common patiromer-associated AEs. Effective management of HK with patiromer may allow use of RAASI at optimal doses as recommended by treatment guidelines. Future research should examine the potential for potassium binders, including patiromer, to extend use of RAASI in appropriate patient populations.
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Pitt et al. (2018) studied this question.
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