中国血液净化 ›› 2024, Vol. 23 ›› Issue (06): 441-444.doi: 10.3969/j.issn.1671-4091.2024.06.009

• 临床研究 • 上一篇    下一篇

达依泊汀α治疗血液透析贫血对血红蛋白变异情况的观察

熊 健    季冬云   刘平平   陈 雷   

  1. 230031 合肥,1合肥金楠肾病专科医院血液净化中心
  • 收稿日期:2024-01-30 修回日期:2024-02-26 出版日期:2024-06-12 发布日期:2024-06-12
  • 通讯作者: 陈雷 E-mail:chen19912008@163.com

The observation of hemoglobin variation in anemic hemodialysis patients treated with darbepoetin alfa

XIONG Jian, JI Dong-yun, LIU Ping-ping, CHEN Lei   

  1. Blood Purification Center, Hefei Jin’nan Kidney Disease Specialized Hospital, Hefei 230031, China
  • Received:2024-01-30 Revised:2024-02-26 Online:2024-06-12 Published:2024-06-12
  • Contact: 230031 合肥,1合肥金楠肾病专科医院血液净化中心 E-mail:chen19912008@163.com

摘要: 目的 探讨达依泊汀α用于治疗血液透析贫血的疗效以及对血红蛋白变异幅度的影响。方法 选取合肥金楠肾病专科医院2022年8月—2023年9月的维持性血液透析患者38人,随机分为2组。观察组给予达依泊汀α治疗,对照组给予短效红细胞生成素治疗。研究分为治疗矫正期和治疗维持期,每月定期检测血红蛋白、生化及第0、第5个月的铁代谢情况等指标。比较2组治疗前后血红蛋白水平,分析血红蛋白水平变化趋势,并统计不良事件。 结果 观察组(n=17)和对照组(n=19)患者治疗前血红蛋白比较差异无统计学意义(t=0.174,P=0.863),治疗结束后2组血红蛋白水平差异无统计学意义(t=0.809,P=0.425)。2组不良事件发生率差异无统计学意义(心力衰竭事件、内瘘闭塞均P=1.000)。治疗矫正期观察组的血红蛋白上升更明显且更稳定(F=3.624,P=0.034)。 结论 达依泊汀α具有和短效红细胞生成素相当的安全性和治疗效果,并且能够维持血红蛋白水平的稳定增长,降低血红蛋白的变异幅度。

关键词: 达依泊汀α, 贫血, 血红蛋白, 红细胞生成素

Abstract: Objective  To investigate the efficacy of darbepoetin alfa for the treatment of anemia and its effect on hemoglobin variation in hemodialysis patients.  Methods  A total of 38 stable hemodialysis patients treated in Hefei Jin'nan Kidney Disease Specialized Hospital from August 2022 to September 2023 were selected and randomly divided into two groups, observation group (n=19; 2 dropped out) received darbepoetin alfa treatment, and control group (n=19) received conventional short-acting erythropoiesis stimulating agent treatment. The study consisted of a correction phase and a maintenance phase, with assays of hemoglobin and biochemical indicators monthly, and iron metabolism indicators at 0 and 5th months. Independent samples t-test was used to compare hemoglobin levels before and after treatment between the two groups. Paired t-test was used for before-after self-control comparisons in each group. Repeated measures analysis was performed to examine the trend of hemoglobin change in both groups over time. Chi-square test was used for adverse event analysis.  Results  There was no significant difference in pretreatment hemoglobin level between the two groups (t=0.174, P=0.863). Post-treatment hemoglobin level also had no significant difference (t=0.809, P=0.425). No significant differences in adverse events (heart failure events, P=1.000; fistula occlusion,          P=1.000) were found between the two groups. During the correction phase, the observation group showed a more pronounced and stable hemoglobin increase (F=3.624, P=0.034).  Conclusion  Darbepoetin alfa has the safety and efficacy comparable to those of short-acting erythropoiesis stimulating agents, and can maintain hemoglobin at a stable increase level with less variability.

Key words: Darbepoetin alfa, Anemia, Hemoglobin, Erythropoiesis stimulating agent

中图分类号: