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肾脏病与透析肾移植杂志 ›› 2026, Vol. 35 ›› Issue (4): 334-339.DOI: 10.3969/j.issn.1006⁃298X.2026.04.006

• 论著 • 上一篇    下一篇

达依泊汀 α 治疗维持性血液透析患者促红细胞生成素低反应性贫血的临床观察

  

  • 出版日期:2026-08-28 发布日期:2026-08-31

Darbepoetin alfa for erythropoietin hyporesponsive anemia in hemodialysis patients

  • Online:2026-08-28 Published:2026-08-31

摘要: 目的:探讨达依泊汀 α(darbepoetin alfa,DA) 治疗维持性血液透析 (maintenance hemodialysis,MHD) 患者促红细胞生成素低反应性贫血的临床疗效。 方法:回顾性分析 2024 年 3 月至 2025 年 3 月在国家肾脏疾病临床医学研究中心规律行 MHD 的促红细胞生成素低反应性贫血患者资料,由短效红细胞生成素切换为 DA 治疗,监测血红蛋白 (hemoglobin,Hb) 和铁代谢指标的变化,观察 DA 的临床疗效。 结果:20 例 MHD 患者中男性 14 例、女性 6 例,年龄 52.10±14.27 岁,中位透析龄 118.9 (27,236) 个月,基线 Hb 97.60±6.99g/L,DA 初始剂量 40μg / 周,治疗 4 周、12 周 Hb 分别升至 110.45±13.02g/L、115.25±15.08g/L, 重复测量方差分析显示治疗时间对 Hb 水平的影响具有统计学意义 [F=34.787 (1.344,25.536),P<0.001, 偏 η2=0.647]。18 例 (90%) 患者用药后 Hb 有不同程度的升高,其中 14 例 (70%) Hb 升至 110g/L 以上。治疗 12 周时有 9 例 (45%) 患者 DA 减量使用,平均 DA 治疗剂量为 33.05±7.98μg / 周。血清铁蛋白较基线有所下降 [90.5 (45.07,199.42) ng/mL vs 53.35 (21.82,192.6) ng/mL,P=0.126], 但血清铁、转铁蛋白饱和度无明显变化。用药前后收缩压、舒张压亦无明显改变,临床亦未出现死亡、心肌梗死、血栓形成等不良事件。 结论:DA 可能有助于改善 MHD 患者促红细胞生成素低反应性贫血,且短期治疗过程中安全性良好。

关键词: 达依泊汀 α, 肾性贫血, 促红细胞生成素低反应性, 血液透析

Abstract: Objective: This study aimed to evaluate the clinical efficacy of darbepoetin alfa in the treatment of erythropoietin (EPO) hyporesponsive anemia in maintenance hemodialysis (MHD) patients. Methods: A retrospective analysis was conducted on MHD patients with EPO⁃hyporesponsive anemia who were switched from short⁃acting EPO to darbepoetin alfa between March 2024 and March 2025. Changes in hemoglobin (Hb) levels and iron metabolism parameters were monitored after the switch. Results: Twenty hemodialysis patients (14 males and 6 females) were enrolled, an average age was 52.10±14.27 years and a median dialysis vintage of 118.9 (27, 236) months. Baseline Hb was 97.60±6.99 g/L, and the initial dose of darbepoetin alfa was 40 μg/week. After 4 and 12 weeks of treatment, Hb levels increased to 110.45± 13.02 g/L and 115.25± 15.08 g/L, respectively. Repeated measures ANOVA showed a statistically significant effect of treatment duration on Hb levels [F=34.787(1.344, 25.536), P<0.001, partial η2=0.647]. Among the patients, 18 (90%) showed varying degrees of increase in Hb after treatment, with 14 (70%) achieving Hb levels above 110 g/L. At 12 weeks of treatment, the dose of darbepoetin alfa was reduced in 9 patients (45%), with an average maintenance dose of 33.05± 7.98 μg/week. Serum ferritin levels decreased compared to baseline [90.5 (45.07, 199.42) ng/mL vs 53.35 (21.82, 192.6) ng/mL, P=0.126], while serum iron and transferrin saturation showed no obvious changes. There were no significant changes in systolic blood pressure and diastolic blood pressure before and after treatment, and no adverse events such as death, myocardial infarction, or thrombosis occurred clinically. Conclusion: DA may help to improve EPO hyporesponsive anemia in MHD patients, with good safety in the short-term treatment.