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利用动态治疗方案来理解红细胞生成刺激剂低反应性。

Using dynamic treatment regimes to understand erythropoietin-stimulating agent hyporesponsiveness.

机构信息

Division of Nephrology, Seattle Children's Hospital, Seattle, WA, USA.

Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, USA.

出版信息

Pediatr Nephrol. 2018 Aug;33(8):1411-1417. doi: 10.1007/s00467-018-3948-9. Epub 2018 Apr 4.

Abstract

BACKGROUND

Erythropoietin-stimulating agent hyporesponsiveness (ESAH) is associated with increased cardiovascular mortality in patients with end-stage renal disease (ESRD) on hemodialysis. Dynamic treatment regimes (DTR), a clinical decision support (CDS) tool that guides the prescription of specific therapies in response to variations in patient states, have been used to guide treatment for chronic illnesses that require frequent monitoring and therapy changes. Our objective is to explore the role of utilizing a DTR to reduce ESAH in pediatric hemodialysis patients.

METHODS

Retrospective analysis of ESRD patients on hemodialysis who received ESAs. Dosing was adjusted using a locally developed protocol designed to target a hemoglobin between 10 and 12 g/dl. Analyzing this protocol as a DTR, we assessed adherence to the protocol over time measuring how the hyporesponse index (ESA dose/hemoglobin value) changed due to varying levels of adherence.

RESULTS

Eighteen patients met study criteria. Median hemoglobin was 11.4 g/dl (range 6.1-15.4), and median weekly ESA dose (darbepoetin-equivalent) was 0.4 mcg/kg/dose (range 0-2.1). Full adherence to the DTR was identified in 266 (71%) of the 4-week periods, with a median average adherence score of 0.80 (range 0.63-0.91). As adherence to the DTR improved, ESAH decreased. During the last 12 weeks, 13 out of 18 patients had lower average ESA/hemoglobin ratio than the first 12 weeks.

CONCLUSIONS

A DTR appears to be well-suited to the treatment of anemia in ESRD and reduces ESAH. Our work shows the potential of DTRs to drive the development and evaluation of clinical practice guidelines.

摘要

背景

促红细胞生成素刺激剂低反应性(ESAH)与血液透析的终末期肾病(ESRD)患者心血管死亡率增加有关。动态治疗方案(DTR)是一种临床决策支持(CDS)工具,用于指导特定治疗方法的处方,以响应患者状态的变化,已用于指导需要频繁监测和治疗改变的慢性疾病的治疗。我们的目标是探讨利用 DTR 减少儿科血液透析患者 ESAH 的作用。

方法

对接受 ESA 的血液透析 ESRD 患者进行回顾性分析。剂量调整使用本地开发的方案进行,旨在将血红蛋白目标设定在 10-12g/dl 之间。将该方案分析为 DTR,我们评估了随着时间的推移对方案的依从性,通过测量由于依从性的不同导致的低反应指数(ESA 剂量/血红蛋白值)的变化来评估。

结果

18 名患者符合研究标准。中位血红蛋白为 11.4g/dl(范围 6.1-15.4),中位每周 ESA 剂量(达贝泊汀等效物)为 0.4mcg/kg/剂量(范围 0-2.1)。在 4 周的时间里,有 266 个(71%)周期完全符合 DTR,中位平均依从性评分为 0.80(范围 0.63-0.91)。随着 DTR 的依从性提高,ESAH 降低。在最后 12 周,18 名患者中有 13 名的平均 ESA/血红蛋白比值低于前 12 周。

结论

DTR 似乎非常适合 ESRD 贫血的治疗,并降低了 ESAH。我们的工作表明 DTR 有潜力推动临床实践指南的制定和评估。

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Dynamic Treatment Regimes.
Annu Rev Stat Appl. 2014;1:447-464. doi: 10.1146/annurev-statistics-022513-115553.
3
Dynamic treatment regimes: technical challenges and applications.
Electron J Stat. 2014;8(1):1225-1272. doi: 10.1214/14-ejs920.
4
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Pediatr Nephrol. 2014 Oct;29(10):2021-8. doi: 10.1007/s00467-014-2820-9. Epub 2014 May 3.
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6
Management of anemia in children receiving chronic peritoneal dialysis.
J Am Soc Nephrol. 2013 Mar;24(4):665-76. doi: 10.1681/ASN.2012050433. Epub 2013 Mar 7.
7
Secondary analysis of the CHOIR trial epoetin-alpha dose and achieved hemoglobin outcomes.
Kidney Int. 2008 Sep;74(6):791-8. doi: 10.1038/ki.2008.295. Epub 2008 Jul 2.
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Mechanism of increased mortality risk with erythropoietin treatment to higher hemoglobin targets.
Clin J Am Soc Nephrol. 2007 Nov;2(6):1274-82. doi: 10.2215/CJN.02380607. Epub 2007 Oct 17.

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