Frontiers in Pharmacology (Jul 2024)

Effectiveness, safety, and treatment pattern of sodium zirconium cyclosilicate in Chinese patients with hyperkalemia: interim analysis from a multicenter, prospective, real-world study (Actualize Study)

  • Nan Shen,
  • Lihong Zhang,
  • Jing Yang,
  • Yongqiang Lin,
  • Xinyu Liu,
  • Xudong Cai,
  • Juan Cao,
  • Qiang Zhu,
  • Xun Luo,
  • Xin Wan,
  • Henglan Wu,
  • Jianming Ye,
  • Chunyan Shan,
  • Hua Xie,
  • Yifan Wu,
  • Yanping Cao,
  • Jianmin Wang,
  • Xiaoyong Yu,
  • Huimin Wang,
  • Jingdong He,
  • Shaojiang Tian,
  • Fenglei Wu,
  • Xinxin Jiang,
  • Lu Li,
  • Li Zuo,
  • Zhaohua Wang,
  • Changying Xing,
  • Xun Yin,
  • Jianrong Zhao,
  • Cong Ma,
  • Gang Long,
  • Qing Li,
  • Yao Hu,
  • Yifan Shi,
  • Hongli Lin

DOI
https://doi.org/10.3389/fphar.2024.1398953
Journal volume & issue
Vol. 15

Abstract

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Introduction: Sodium zirconium cyclosilicate (SZC) is a nonabsorbed cation-exchanger approved in China for the treatment of hyperkalemia [HK; serum potassium (sK+) levels >5.0 mmol/L]. This is the first real-world study aimed to assess the effectiveness, safety, and treatment patterns of SZC in Chinese patients with HK. Here we present the results of the first interim analysis.Methods: This multicenter, prospective, cohort study included patients aged ≥18 years with documented HK within 1-year before study enrollment day. These patients were followed up for 6 months from the enrollment day after initiating SZC treatment. The treatment was categorized into correction phase (FAS-P1) and maintenance phase (FAS-P2 new and ongoing users). Subgroup analysis was performed in patients on hemodialysis (FAS-H). The primary objective was evaluation of safety profile of SZC; secondary objectives included assessment of treatment patterns of SZC and its effectiveness.Results: Of 421 screened patients, 193, 354, and 162 patients were enrolled in the FAS-P1, FAS-P2, and FAS-H groups, respectively. sK+ levels were reduced significantly from 5.9 mmol/L to 5.0 mmol/L after the correction phase. For the maintenance phase, the mean sK+ levels were maintained at 5.2 mmol/L and 5.0 mmol/L in the FAS-P2 new and ongoing user, respectively, and 5.3 mmol/L in the FAS-H subgroup. A considerable proportion of patients showed normokalemia after 48 h of SZC treatment (FAS-P1:51.3%) which was maintained up to 6 months in the maintenance phase (FAS-P2:44%). SZC was well-tolerated.Conclusion: SZC was effective and safe for the treatment of HK in real-world clinical practice in China.

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