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儿童溶血尿毒综合征中红细胞生成素的应用:一项初步随机对照试验。

Erythropoietin in children with hemolytic uremic syndrome: a pilot randomized controlled trial.

机构信息

Nephrology Unit, Hospital General de Niños Pedro de Elizalde, Montes de Oca 40, 1270, Ciudad Autónoma de Buenos Aires, Argentina.

Division of Inmunology, Hospital General de Niños Pedro de Elizalde, Hospital General de Niños Pedro de Elizalde, Montes de Oca 40, 1270, Ciudad Autónoma de Buenos Aires, Argentina.

出版信息

Pediatr Nephrol. 2022 Oct;37(10):2383-2392. doi: 10.1007/s00467-022-05474-9. Epub 2022 Feb 15.

Abstract

BACKGROUND

The efficacy of recombinant human erythropoietin (rHuEPO) in sparing red blood cell (RBC) transfusions in children with hemolytic uremic syndrome related to Shiga toxin-producing Escherichia coli (STEC-HUS) is uncertain.

METHODS

We conducted a pilot randomized controlled open trial between December 2018 and January 2021. Children were randomized to the intervention (subcutaneous rHuEPO 50 U/kg three times weekly until discharge + RBC transfusion if hemoglobin ≤ 7 g/dL and/or hemodynamic instability) or to the control arm (RBC transfusion if hemoglobin ≤ 7 g/dL and/or hemodynamic instability). Primary outcome was the number of RBC transfusions received during hospitalization. Secondary outcomes were to explore whether baseline EPO levels were adequate to the degree of anemia, to correlate selected acute phase parameters with the number of RBC transfusions, and to assess possible adverse events.

RESULTS

Twelve patients per arm were included; they were comparable at recruitment and throughout the disease course. Median number of RBC transfusions was similar between groups (1.5, p = 0.76). Most patients had baseline EPO levels adequate to the degree of anemia, which did not correlate with the number of transfusions (r = 0.19, p = 0.44). Conversely, baseline (r = 0.73, p = 0.032) and maximum lactic dehydrogenase levels (r = 0.78, p = 0.003), creatinine peak (r = 0.71, p = 0.03) and dialysis duration (r = 0.7, p = 0.04) correlated significantly with RBC requirements. No side effects were recorded.

CONCLUSION

In children with STEC-HUS, the administration of rHuEPO did not reduce the number of RBC transfusions. Larger studies addressing higher doses and similar severity of kidney failure at rHuEPO initiation (e.g. at start of dialysis) are warranted.

TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT03776851. A higher resolution version of the Graphical abstract is available as Supplementary information.

摘要

背景

重组人促红细胞生成素(rHuEPO)在治疗产志贺样毒素大肠杆菌(STEC)相关溶血尿毒症综合征(HUS)患儿中减少红细胞(RBC)输注的疗效尚不确定。

方法

我们于 2018 年 12 月至 2021 年 1 月期间开展了一项试点随机对照开放试验。患儿被随机分为干预组(皮下注射 rHuEPO,50U/kg,每周 3 次,直至出院,血红蛋白(Hb)≤7g/dL 且/或血流动力学不稳定时给予 RBC 输注)或对照组(Hb≤7g/dL 且/或血流动力学不稳定时给予 RBC 输注)。主要结局为住院期间接受的 RBC 输注次数。次要结局为探索基线 EPO 水平是否与贫血程度相匹配,以及是否将选定的急性期参数与 RBC 输注次数相关联,并评估可能的不良反应。

结果

每组纳入 12 例患儿;在招募时和疾病过程中,两组患儿具有可比性。两组的 RBC 输注中位数相似(1.5,p=0.76)。大多数患儿的基线 EPO 水平与贫血程度相匹配,且与输注次数无关(r=0.19,p=0.44)。相反,基线(r=0.73,p=0.032)和最大乳酸脱氢酶(r=0.78,p=0.003)、血肌酐峰值(r=0.71,p=0.03)和透析持续时间(r=0.7,p=0.04)与 RBC 需求显著相关。未记录到不良反应。

结论

在 STEC-HUS 患儿中,rHuEPO 的使用并未减少 RBC 输注的次数。需要开展更大规模的研究,以确定更高剂量和 rHuEPO 起始时(例如开始透析时)相似严重程度的肾衰患者的疗效。

试验注册

ClinicalTrials.gov 标识符:NCT03776851。更清晰的图文摘要版本可在补充信息中查看。

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