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·药物与临床·


          罗沙司他或重组人促红素联合静脉用铁剂治疗维持性血液透析

          合并肾性贫血的疗效与安全性比较
                                                                Δ

          刘 江 ,丁文飞,文 莉(西南医科大学附属医院肾病内科,四川 泸州 646000)
                *
                                 #
          中图分类号  R969.4;R973      文献标志码  A      文章编号  1001-0408(2025)19-2422-06
          DOI  10.6039/j.issn.1001-0408.2025.19.11

          摘   要  目的  比较罗沙司他与重组人促红素(rHuEPO)分别联合静脉用铁剂治疗维持性血液透析(MHD)合并肾性贫血(RA)患
          者的疗效与安全性。方法  回顾性纳入2022年1月至2024年6月在西南医科大学附属医院接受MHD治疗且合并RA的152例患
          者的病历资料,按治疗方案分为观察组(72例)和对照组(80例)。两组患者均接受MHD 及静脉用铁剂治疗,观察组加用罗沙司
          他,对照组加用rHuEPO,疗程均为12周。比较两组患者治疗前后贫血指标、铁代谢指标、炎症因子、心功能参数、生活质量评分以
          及治疗过程中的不良反应发生情况。结果  治疗12周后,两组患者的血红蛋白、红细胞计数、红细胞压积、血清铁、转铁蛋白、总铁
          结合力、转铁蛋白饱和度、左室射血分数、E/A值、心输出量、健康调查简表评分、肾脏疾病生存质量简表评分均较治疗前显著升高
          或增多(P<0.05),铁蛋白、C 反应蛋白、白细胞介素 6、肿瘤坏死因子 α、脑钠肽、氨基末端脑钠肽前体水平均较治疗前显著降低
         (P<0.05);观察组患者上述指标水平的改善程度均显著优于对照组(P<0.05)。观察组患者不良反应总发生率显著低于对照组
         (P<0.05)。结论  罗沙司他联合静脉用铁剂治疗在改善MHD合并RA患者的贫血状况、铁代谢情况、炎症状态、心功能及生活质
          量方面均优于rHuEPO联合静脉用铁剂治疗,且前者安全性更佳。
          关键词  罗沙司他;重组人促红素;维持性血液透析;肾性贫血;终末期肾病

          Efficacy  and  safety  comparison  of  roxadustat  versus  recombinant  human  erythropoietin  combined  with
          intravenous iron for renal anemia in patients undergoing maintenance hemodialysis
          LIU Jiang,DING Wenfei,WEN Li(Dept.  of  Nephrology,  the  Affiliated  Hospital  of  Southwest  Medical
          University, Sichuan Luzhou 646000, China)

          ABSTRACT    OBJECTIVE  To  compare  the  efficacy  and  safety  of  roxadustat  versus  recombinant  human  erythropoietin
         (rHuEPO),  each  combined  with  intravenous  iron  supplementation,  in  the  treatment  of  renal  anemia (RA)  in  patients  undergoing
          maintenance  hemodialysis (MHD).  METHODS  A  retrospective  analysis  was  conducted  on  the  medical  records  of  152  patients
          diagnosed with RA and receiving MHD at the Affiliated Hospital of Southwest Medical University between January 2022 and June
          2024. According to the treatment regimen, patients were divided into observation group (n=72) and control group (n=80). Both
          groups of patients received MHD and intravenous iron therapy, with the observation group additionally receiving roxadustat and the
          control  group  receiving  rHuEPO,  both  for  a  treatment  duration  of  12  weeks.  Changes  in  anemia  indicators,  iron  metabolism
          parameters, inflammatory markers, cardiac function parameters, quality of life scores before and after therapy, and adverse events
          during treatment were compared between the two groups. RESULTS  After 12 weeks of treatment, both groups showed significant
          increase  in  hemoglobin,  red  blood  cell  count,  hematocrit,  serum  iron,  transferrin,  total  iron  binding  capacity,  transferrin
          saturation,  left  ventricular  ejection  fraction,  E/A  ratio,  cardiac  output,  36-Item  Short  Form  Health  Survey  score,  and  Kidney
          Disease  Quality  of  Life  Short  Form  score  compared  to  baseline (P<0.05).  Conversely,  the  levels  of  ferritin,  C-reactive  protein,
          interleukin-6,  tumor  necrosis  factor-α,  brain  natriuretic  peptide,  and  N-terminal  pro-B-type  natriuretic  peptide  were  significantly
          reduced (P<0.05).  The  improvements  in  the  observation  group  were  significantly  greater  than  those  in  the  control  group (P<
          0.05).  Moreover,  the  incidence  of  adverse  events  was  significantly  lower  in  the  observation  group  compared  to  the  control  group
                                                             (P<0.05).  CONCLUSIONS  Compared  to  rHuEPO  combined
              Δ 基金项目 四川省科技计划项目(No.2023NSFSC1530)              with  intravenous  iron  supplementation,  roxadustat  combined
             *第一作者 医师,硕士。研究方向:血液透析患者的相关并发症。
                                                              with  intravenous  iron  supplementation  is  more  effective  in
          E-mail:liujiangc@163.com
              # 通信作者 讲师,博士。研究方向:肾脏疾病的发病机制。                    improving  anemia,  iron  metabolism,  inflammatory  status,
          E-mail:wenlixnydfy@163.com                          cardiac  function,  and  quality  of  life  in  patients  with  RA


          · 2422 ·    China Pharmacy  2025 Vol. 36  No. 19                            中国药房  2025年第36卷第19期
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