Novel approaches to management of hyperkalaemia in kidney transplantation

被引:13
|
作者
Rizk, John [1 ]
Quan, David [2 ]
Gabardi, Steven [3 ,4 ]
Rizk, Youssef [5 ]
Kalantar-Zadeh, Kamyar [6 ,7 ]
机构
[1] Arizona State Univ, Edson Coll, Phoenix, AZ 85281 USA
[2] Univ Calif San Francisco, UCSF Med Ctr, San Francisco, CA USA
[3] Brigham & Womens Hosp, Dept Transplant Surg, Boston, MA USA
[4] Harvard Med Sch, Dept Med, Boston, MA USA
[5] Amer Univ, Dept Family Med, Beirut Med Ctr, Beirut, Lebanon
[6] Univ Calif Irvine, Div Nephrol, Hypertens & Kidney Transplantat, Sch Med, Orange, CA USA
[7] Univ Calif Los Angeles, Dept Epidemiol, Ucla Fielding Sch Publ Hlth, Los Angeles, CA USA
来源
关键词
hyperkalaemia; kidney transplantation; management; potassium;
D O I
10.1097/MNH.0000000000000657
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Medications used frequently after kidney transplantation, including calcineurin inhibitors, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, beta blockers and antimicrobials, are considered the leading culprit for posttransplant hyperkalaemia in recipients with a well functioning allograft. Other risk factors include comorbidities such as diabetes, hypertension and heart failure; and consumption of a potassium-enriched diet. We review the mechanisms for hyperkalaemia following kidney transplantation that are addressed using nonpharmacological and pharmacological interventions. We also discuss emerging therapeutic approaches for the management of recurrent hyperkalaemia in solid organ transplantation, including newer potassium binding therapies. Recent findings Patiromer and sodium zirconium cyclosilicate are emerging potassium binders approved for the treatment of hyperkalaemia. Patiromer is a polymer that exchanges potassium for calcium ions. In contrast, sodium zirconium cyclosilicate is a nonpolymer compound that exchanges potassium for sodium and hydrogen ions. Both agents are efficacious in the treatment of chronic or recurrent hyperkalaemia and may result in fewer gastrointestinal side effects than older potassium binders such as sodium polystyrene sulfonate and calcium polystyrene sulfonate. Large-scale clinical studies have not been performed in kidney transplant patients. Patiromer may increase serum concentrations of tacrolimus, but not cyclosporine. Sodium zirconium cyclosilicate does not appear to compromise tacrolimus pharmacokinetics, although it may have a higher sodium burden. Patiromer and sodium zirconium cyclosilicate may be well tolerated options to treat asymptomatic hyperkalaemia and have the potential to ease potassium dietary restrictions in kidney transplant patients by maintaining a plant-dominant, heart-healthy diet. Their efficacy, better tolerability and comparable cost with respect to previously available potassium binders make them an attractive therapeutic option in chronic hyperkalaemia following kidney transplantation.
引用
收藏
页码:27 / 37
页数:11
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