Tamargo Juan, Caballero Ricardo, Delpón Eva
Department of Pharmacology, School of Medicine, Universidad Complutense, Madrid, 28040, Spain.
Discov Med. 2014 Nov;18(100):249-54.
Hyperkalemia (serum potassium >5.5 mmol/L) may result from increased potassium intake, impaired distribution between the intracellular and extracellular spaces, and/or reduced renal excretion. Renin-angiotensin-aldosterone system inhibitors (RAASIs) represent an important therapeutic strategy in patients with hypertension, heart failure, chronic kidney disease, and diabetes, but hyperkalemia is a key limitation to fully titrate RAASIs in these patients who are most likely to benefit from treatment. Thus, we need new drugs to control hyperkalemia in these patients while maintaining the use of RAASIs. We review two new polymer-based, non-systemic agents under clinical development, patiromer calcium and zirconium silicate, designed to increase potassium loss via the gastrointestinal tract for the management of hyperkalemia.
高钾血症(血清钾>5.5 mmol/L)可能由钾摄入增加、细胞内和细胞外间隙分布受损及/或肾排泄减少引起。肾素-血管紧张素-醛固酮系统抑制剂(RAASIs)是高血压、心力衰竭、慢性肾脏病和糖尿病患者的重要治疗策略,但高钾血症是充分滴定这些最可能从治疗中获益患者的RAASIs的关键限制因素。因此,我们需要新药在维持RAASIs使用的同时控制这些患者的高钾血症。我们综述了两种正在临床开发的新型聚合物基非全身性药物,即帕替罗姆钙和硅酸锆,它们旨在通过胃肠道增加钾的流失以治疗高钾血症。