Sánchez-Escuredo A, Batista F, Cases A, Torregrosa J-V
Nephrology and Renal Transplant Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Nephrology and Renal Transplant Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Transplant Proc. 2015 Jan-Feb;47(1):73-5. doi: 10.1016/j.transproceed.2014.12.006.
Anemia after kidney transplantation (KT) has a negative impact on graft and patient survival. Anemia management includes iron supplements and erythropoiesis-stimulating agents (ESAs). Most ESAs require short frequency of administration and conversion to ESAs with longer half-life are complex.
This study was performed to assess the efficacy of continuous erythropoietin receptor activator (CERA) in hemoglobin (Hb) maintenance after conversion from shorter-acting ESAs with a simple conversion scheme in kidney transplant recipients.
This is an open-label, prospective, single-arm, single-center, 12-month follow-up study including 77 anemic KT patients with stable renal function. Baseline and monthly measurements of Hb, iron, and creatinine were performed. The conversion scheme from darbepoetin alfa or epoetin was as follows: <30 μg or 5000 IU/week was switched to 75 μg/mo; between 30-50 or 5000-8000 was switched to 100 μg/mo; >50 μg or 8000 IU was changed to 150 μg/month of CERA. Dose adjustments were performed to maintain Hb levels between 10 g/dL and 12 g/dL.
The mean age was 57 ± 19 years. The mean time of conversion after KT was 61 ± 49 months. Before conversion, 62.9% of patients were administered epoetin and 37.1% with darbepoetin alfa. Baseline Hb is noted at 10.6 ± 1.3 g/dL. Thirteen percent of patients started receiving CERA at doses of 50 μg/mo, 66% at 75 μg/mo, 13% at 100 μg/mo, and 8% at 150 μg/mo. During the first month, 21% required dose adjustment (6% were increased, 15% were decreased). The final Hb was 11.2 ± 0.8 g/dL. Iron and creatinine levels remained stable during the follow-up examination.
We propose a simple scheme of conversion from short-acting ESAs to a once-monthly dose of CERA that provides sustained Hb levels within the recommended target with small dose adjustments and low CERA doses.
肾移植(KT)后贫血对移植物和患者存活有负面影响。贫血管理包括补充铁剂和促红细胞生成素(ESA)。大多数ESA需要短给药频率,且转换为半衰期更长的ESA很复杂。
本研究旨在评估在肾移植受者中,通过简单转换方案从短效ESA转换为持续促红细胞生成素受体激活剂(CERA)后,其在维持血红蛋白(Hb)水平方面的疗效。
这是一项开放标签、前瞻性、单臂、单中心、为期12个月的随访研究,纳入77例肾功能稳定的贫血KT患者。对Hb、铁和肌酐进行基线及每月测量。从阿法依泊汀或依泊汀转换的方案如下:<30μg或5000IU/周转换为75μg/月;30 - 50μg或5000 - 8000IU转换为100μg/月;>50μg或8000IU转换为每月150μg的CERA。进行剂量调整以维持Hb水平在10g/dL至12g/dL之间。
平均年龄为57±19岁。KT后平均转换时间为61±49个月。转换前,62.9%的患者使用依泊汀,37.1%的患者使用阿法依泊汀。基线Hb为10.6±1.3g/dL。分别有13%的患者开始接受50μg/月剂量的CERA,66%接受75μg/月,13%接受100μg/月,8%接受150μg/月。在第一个月期间,21%的患者需要调整剂量(6%增加,15%减少)。最终Hb为11.2±0.8g/dL。随访检查期间铁和肌酐水平保持稳定。
我们提出了一个从短效ESA转换为每月一次剂量CERA的简单方案,该方案通过小剂量调整和低CERA剂量,在推荐目标范围内提供持续的Hb水平。