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促红细胞生成素对透析患者疲劳影响的系统评价

Systematic review of the impact of erythropoiesis-stimulating agents on fatigue in dialysis patients.

作者信息

Johansen Kirsten L, Finkelstein Fredric O, Revicki Dennis A, Evans Christopher, Wan Shaowei, Gitlin Matthew, Agodoa Irene L

机构信息

Nephrology Section, San Francisco VA Medical Center, San Francisco, CA, USA.

出版信息

Nephrol Dial Transplant. 2012 Jun;27(6):2418-25. doi: 10.1093/ndt/gfr697. Epub 2011 Dec 20.

Abstract

BACKGROUND

One of the cardinal symptoms of anemia in chronic kidney disease (CKD) patients is fatigue. Recently, results from Trial to Reduce Cardiovascular Events with Aranesp Therapy (TREAT) raised questions about the role of erythropoiesis-stimulating agents (ESAs) in improving fatigue and the appropriate hemoglobin (Hb) target in anemic patients with CKD. These discussions should be considered with all available evidence to determine the level of benefits and risks associated with ESA therapy on fatigue among both early-stage CKD patients and end-stage renal disease patients on dialysis.

METHODS

The study was a systematic review of the literature on fatigue in adults on maintenance dialysis therapy. The requirement for inclusion in the review was the measurement of fatigue before and after ESA treatment. Outcomes that were assessed were fatigue as measured by the Kidney Disease Questionnaire, the 36-item Short-Form general health survey, the Nottingham Health Profile, the Profile of Mood States or the Functional Assessment of Chronic Illness Therapy-Fatigue scale. Several different measures of fatigue were used in the studies.

RESULTS

Fifteen articles met the criteria for inclusion, including 10 distinct studies and one extension study. There was one placebo-controlled randomized clinical trial (RCT) and one extension, five single-arm, three high versus low, one intravenous versus subcutaneous and one switch from epoetin alfa to darbepoetin alfa. The only placebo-controlled RCT found a 22-26% improvement in fatigue. Single-arm cohort studies demonstrated a reduction in fatigue after a substantial increase in Hb. Studies with a baseline Hb <10 g/dL and partial correction to a minimum Hb ≥ 10 g/dL showed an average improvement in fatigue of 34.6%. Studies with a baseline Hb ≥ 11 g/dL and full correction to a minimum Hb ≥ 12 g/dL showed an average improvement in fatigue of 5.5%, while studies with no change in Hb (either placebo or control group) showed a decline of 0.7% in fatigue outcomes.

CONCLUSION

Partial correction of anemia with ESA results in improvement of fatigue among patients on dialysis, most strikingly in those patients with baseline Hb levels <10 g/dL.

摘要

背景

慢性肾脏病(CKD)患者贫血的主要症状之一是疲劳。最近,促红细胞生成素刺激剂(ESA)治疗降低心血管事件试验(TREAT)的结果引发了关于ESA在改善疲劳方面的作用以及CKD贫血患者合适的血红蛋白(Hb)目标的问题。应结合所有现有证据来考虑这些讨论,以确定ESA治疗对早期CKD患者和接受透析的终末期肾病患者疲劳相关的获益和风险水平。

方法

该研究是对维持性透析治疗的成人疲劳相关文献的系统评价。纳入该评价的要求是测量ESA治疗前后的疲劳情况。评估的结局是通过肾脏病问卷、36项简短通用健康调查、诺丁汉健康概况、情绪状态量表或慢性病治疗功能评估 - 疲劳量表测量的疲劳。研究中使用了几种不同的疲劳测量方法。

结果

15篇文章符合纳入标准,包括10项不同的研究和1项扩展研究。有1项安慰剂对照随机临床试验(RCT)和1项扩展研究、5项单臂研究、3项高剂量与低剂量对比研究、1项静脉注射与皮下注射对比研究以及1项从阿法依泊汀转换为达贝泊汀的研究。唯一的安慰剂对照RCT发现疲劳改善了22% - 26%。单臂队列研究表明,Hb大幅升高后疲劳减轻。基线Hb <10 g/dL且部分纠正至最低Hb≥10 g/dL的研究显示疲劳平均改善34.6%。基线Hb≥11 g/dL且完全纠正至最低Hb≥12 g/dL的研究显示疲劳平均改善5.5%,而Hb无变化(安慰剂或对照组)的研究显示疲劳结局下降了0.7%。

结论

使用ESA部分纠正贫血可改善透析患者的疲劳,在基线Hb水平<10 g/dL的患者中最为显著。

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