4.3 Article

The tolerability and safety profile of patiromer: a novel polymer-based potassium binder for the treatment of hyperkalemia

期刊

EXPERT OPINION ON DRUG SAFETY
卷 17, 期 5, 页码 525-535

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14740338.2018.1462335

关键词

Chronic kidney disease; congestive heart failure; diabetes mellitus; hyperkalemia; patiromer; potassium; renin-angiotensin-aldosterone system

资金

  1. Relypsa, Inc., a Vifor Pharma Group Company
  2. Relypsa, Inc.

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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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