重组人促红细胞生成素治疗HIV感染患者贫血的趋势。

The Open AIDS Journal Pub Date : 2011-01-01 Epub Date: 2011-12-29 DOI:10.2174/1874613601105010113
Patrick S Sullivan, Debra L Hanson, James T Richardson, John T Brooks
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引用次数: 3

摘要

背景:红细胞生成素(EPO)对血红蛋白(Hb)终点>11 g/dL治疗贫血可能增加严重不良心血管事件的风险。方法:我们使用1996-2003年来自青少年HIV疾病谱项目(ASD)和1996-2006年来自HIV门诊研究(HOPS)的医疗记录数据来描述轻度、中度或重度贫血HIV感染患者的EPO处方模式。我们计算了处方促生成素和治疗Hb>12 g/dL的比例,并测试了随时间的趋势。我们计算了第一次EPO处方时血红蛋白的中位数,并使用线性回归描述了时间变化。结果:在37,395例ASD患者和7,005例HOPS患者中,中度贫血患者EPO处方随时间增加;对于重度贫血患者,EPO处方仅在ASD患者中增加。在ASD患者中,EPO处方的Hb随着时间的推移而下降(中位数=8.5 g/dL),但在HOPS患者中没有下降(中位数为9.5 g/dL)。epo治疗后Hb>12 g/dL的ASD患者比例为18.3%,且稳定;HOPS患者比例为56.7%,且随时间增加(p = 0.03)。结论:到2006年,EPO处方在中度或重度贫血患者中逐年增加。许多接受EPO治疗的患者治疗后Hb>12 g/dL。根据2011年FDA的建议,需要改变以前的处方做法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Trends in the Treatment of Anemia Using Recombinant Human Erythropoietin in Patients with HIV Infection.

Trends in the Treatment of Anemia Using Recombinant Human Erythropoietin in Patients with HIV Infection.

Trends in the Treatment of Anemia Using Recombinant Human Erythropoietin in Patients with HIV Infection.

Trends in the Treatment of Anemia Using Recombinant Human Erythropoietin in Patients with HIV Infection.

Background: Treating anemia with erythropoietin (EPO) to hemoglobin (Hb) endpoints >11 g/dL may increase risk of serious adverse cardiovascular events.

Methods: We used medical records data (1996-2003 from the Adolescent Spectrum of HIV Disease Project [ASD] and 1996-2006 from the HIV Outpatient Study [HOPS]) to describe EPO prescription patterns for mildly, moderately, or severely anemic HIV-infected patients. We calculated proportions prescribed EPO and treated to Hb>12 g/dL, and tested for trends over time. We calculated median hemoglobin at first EPO prescription, and described temporal changes using linear regression.

Results: Among 37,395 patients in ASD and 7,005 patients in HOPS, EPO prescription increased over time for moderately anemic patients; for patients with severe anemia, EPO prescription increased only among ASD patients. Hb at EPO prescription decreased over time in ASD patients (median=8.5 g/dL), but not in HOPS patients (median 9.5 g/dL). Percentage of EPO-treated patients with post-treatment Hb>12 g/dL was 18.3% in ASD and stable, and was 56.7% in HOPS and increased over time (p = 0.03).

Conclusions: Through 2006, EPO prescription increased over time for patients with moderate or severe anemia. Many patients treated with EPO had post-treatment Hb>12 g/dL. Based on 2011 FDA recommendations, changes in previous prescription practices will be needed.

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