Suppr超能文献

每月注射一次的阿法达贝泊汀可维持稳定透析患者的血红蛋白水平。

Darbepoetin alfa administered once monthly maintains haemoglobin levels in stable dialysis patients.

作者信息

Jadoul Michel, Vanrenterghem Yves, Foret Michel, Walker Rowan, Gray Stephen J

机构信息

Department of Nephrology, Cliniques Saint Luc, Université Catholique de Louvain, Brussels, Belgium.

出版信息

Nephrol Dial Transplant. 2004 Apr;19(4):898-903. doi: 10.1093/ndt/gfh021.

Abstract

BACKGROUND

Darbepoetin alfa, a glycoprotein that stimulates erythropoiesis by the same mechanism as endogenous erythropoietin, has a 3-fold longer terminal half-life than recombinant human erythropoietin, allowing for an extended dosing interval. Darbepoetin alfa is currently recommended for once-weekly and once every 2 weeks administration in patients with chronic renal failure (CRF). The objective of this study was to explore once-monthly administration in this patient population.

METHODS

Clinically stable dialysis patients (mean haemoglobin concentration, 10.0-13.0 g/dl) receiving stable darbepoetin alfa therapy administered once every 2 weeks in a long-term treatment study were converted to darbepoetin alfa once every 3 weeks for 20 weeks and then, if haemoglobin concentrations were successfully maintained between 10.0 and 13.0 g/dl, were converted to darbepoetin alfa once every 4 weeks for 20 weeks. The darbepoetin alfa dose was titrated to maintain haemoglobin within a target range (-1.0 to +1.5 g/dl of baseline haemoglobin, and between 10.0 and 13.0 g/dl). Success with the extended dosing interval was defined as maintenance of mean haemoglobin >/=10.0 g/dl during a 4-week evaluation at the end of the dosing period.

RESULTS

Of the 54 patients who entered the study, 38 patients were converted to darbepoetin alfa administered once every 4 weeks. Of these, 36 patients were considered evaluable and 30 (83%) of those evaluable patients successfully maintained the target haemoglobin. For successful patients the mean (SD) haemoglobin during evaluation was 11.16 (0.60) g/dl, and the mean change in haemoglobin from baseline to evaluation was -0.26 g/dl (95% CI: -0.51, -0.01). The median change from baseline in average weekly darbepoetin alfa dose was 1.61 microg (95% CI: 0.00, 4.75). Adverse events were consistent with those expected for this patient population.

CONCLUSIONS

Darbepoetin alfa, administered once monthly, maintained haemoglobin effectively and safely in most dialysis patients stabilized previously on once every 2 weeks dosing. Once-monthly dosing may optimize anaemia management for patients with CRF and for health care providers.

摘要

背景

达比加群酯是一种糖蛋白,通过与内源性促红细胞生成素相同的机制刺激红细胞生成,其终末半衰期比重组人促红细胞生成素长3倍,从而允许延长给药间隔。目前推荐对慢性肾衰竭(CRF)患者每周给药一次或每2周给药一次达比加群酯。本研究的目的是探讨在该患者群体中每月给药一次的情况。

方法

在一项长期治疗研究中,接受每2周一次稳定剂量达比加群酯治疗且临床稳定的透析患者(平均血红蛋白浓度为10.0 - 13.0 g/dl),先转换为每3周一次达比加群酯治疗20周,然后,如果血红蛋白浓度成功维持在10.0至13.0 g/dl之间,则转换为每4周一次达比加群酯治疗20周。达比加群酯剂量进行滴定以将血红蛋白维持在目标范围内(基线血红蛋白值±1.0至±1.5 g/dl,且在10.0至13.0 g/dl之间)。延长给药间隔的成功定义为在给药期结束时的4周评估期间平均血红蛋白维持≥10.0 g/dl。

结果

进入研究的54例患者中,38例患者转换为每4周一次达比加群酯给药。其中,36例患者被认为可评估,这些可评估患者中有30例(83%)成功维持了目标血红蛋白水平。对于成功的患者,评估期间的平均(标准差)血红蛋白为11.16(0.60)g/dl,从基线到评估时血红蛋白的平均变化为 - 0.26 g/dl(95%可信区间: - 0.51, - 0.01)。达比加群酯平均每周剂量从基线的中位数变化为1.61μg(95%可信区间:0.00,4.75)。不良事件与该患者群体预期的一致。

结论

对于先前每2周给药一次已稳定的大多数透析患者,每月给药一次达比加群酯可有效且安全地维持血红蛋白水平。每月给药一次可能会优化CRF患者及医疗服务提供者的贫血管理。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验