Agarwal Anil, Silver Marcia R, Walczyk Michael, Liu Wei, Audhya Paul
The Ohio State University Medical Center, Columbus, OH 43210, USA.
J Am Med Dir Assoc. 2007 Feb;8(2):83-90. doi: 10.1016/j.jamda.2006.07.007. Epub 2006 Sep 29.
To evaluate the efficacy of once-monthly darbepoetin alfa in maintaining hemoglobin (Hb) levels between 10 and 12 g/dL in older subjects receiving darbepoetin alfa every 2 weeks.
A secondary analysis of a 29-week multicenter, open-label, single-arm study with an initial 2-week screening/baseline period, followed by a 20-week once-monthly darbepoetin alfa dose titration period and an 8-week evaluation period.
Twenty treatment centers in the United States.
Subjects with CKD who were not receiving dialysis and whose hemoglobin levels were > or =10 g/dL with darbepoetin alfa every 2 weeks.
Darbepoetin alfa administered once monthly and titrated to maintain Hb level between 10 and 12 g/dL, inclusive.
The proportion of subjects maintaining a mean Hb concentration of 10 to 12 g/dL, inclusive, while receiving once-monthly darbepoetin alfa during the evaluation period (weeks 21 to 29); the mean change in Hb levels and darbepoetin alfa doses between baseline and the evaluation period; and the treatment relationship, frequency, severity, and outcomes of all adverse events. Analyses were stratified by age (<65, > or =65, and > or =75 years).
Seventy-nine percent of subjects aged > or =65 years and 80% of subjects aged > or =75 years maintained their Hb levels within the specified target range, compared with 80% of subjects aged <65 years who maintained their Hb levels within the specified target range. Hemoglobin levels and darbepoetin alfa doses did not change significantly from baseline to the evaluation period. Darbepoetin alfa administered once monthly was well tolerated in all age groups.
Darbepoetin alfa administered once monthly effectively maintained target Hb levels in older subjects with CKD (not receiving dialysis) who were maintained previously with an every 2 weeks darbepoetin alfa regimen.
评估每月一次的达贝泊汀α在使每2周接受一次达贝泊汀α治疗的老年受试者血红蛋白(Hb)水平维持在10至12 g/dL之间的疗效。
一项为期29周的多中心、开放标签、单臂研究的二次分析,初始为期2周的筛查/基线期,随后是为期20周的每月一次达贝泊汀α剂量滴定期和为期8周的评估期。
美国的20个治疗中心。
未接受透析且每2周使用达贝泊汀α时血红蛋白水平≥10 g/dL的慢性肾脏病患者。
每月一次给予达贝泊汀α并进行滴定,以将Hb水平维持在10至12 g/dL(含)之间。
在评估期(第21至29周)接受每月一次达贝泊汀α治疗期间,将平均Hb浓度维持在10至12 g/dL(含)的受试者比例;基线期和评估期之间Hb水平和达贝泊汀α剂量的平均变化;以及所有不良事件的治疗相关性、频率、严重程度和结局。分析按年龄(<65岁、≥65岁和≥75岁)分层。
≥65岁的受试者中有79%,≥75岁的受试者中有80%将其Hb水平维持在指定目标范围内,而<65岁的受试者中有80%将其Hb水平维持在指定目标范围内。从基线期到评估期,Hb水平和达贝泊汀α剂量无显著变化。所有年龄组对每月一次给予的达贝泊汀α耐受性良好。
对于先前每2周接受一次达贝泊汀α治疗方案维持治疗的老年慢性肾脏病(未接受透析)患者,每月一次给予达贝泊汀α可有效维持目标Hb水平。