Use of epoetin alfa in very preterm infants with birthweight below 1500 gram

A. L. Karpova, A. V. Mostovoy, L.A. Anikeeva, A.P. Khoteeva, S.V. Semenova, L. N. Karpov, S.V. Martirosyan, A. Zaplatnikov
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Abstract

Purpose of the research was to evaluate the effect of the administration of epoetin alfa (Eralfon®️) after 8 days of life in very preterm infants with birthweight below 1500 gram and gestational age below 310/7 weeks on the anemia of prematurity, on hemoglobin levels in blood at the age of six months and on retinopathy of prematurity. Materials and methods used: a retrospective study of 105 very preterm infants was conducted at the two perinatal centers, L.A. Vorokhobov Moscow City Clinical Hospital No. 67 of the Moscow Department of Healthcare (Moscow, Russia) and Yaroslavl Oblast Regional Perinatal Center (Yaroslavl, Russia), who were divided into two groups, G1 (56) who did not receive epoetin alpha (EA) at 1 to 2 months of life (the so-called “no EA Group”) and were nursed at the Yaroslavl Oblast Regional Perinatal Center; and G2 (49) who received EA at 1 to 2 months of life (the “EA Group”) and were nursed at the L.A. Vorokhobov Moscow City Clinical Hospital No. 67 of the Moscow Department of Healthcare. In the “EA Group,” there was late (after the 8th day of life) EA administration at a dose of 200 units/kg at once subcutaneously 3 times per week for 6 weeks. Results: hemoglobin levels in peripheral blood on the first day of life had no statistically significant differences. The level of hemoglobin in peripheral blood at the age of 6 months was statistically significantly higher in preterm infants who had received EA at 1 to 2 months of life. The development of the anemia of prematurity was statistically significantly less frequently recorded in the “EA Group:” 40 out of 49 (82.0%) vs. 54 out of 56 (96.0%), p=0.022. Erythrocyte transfusion in the “no EA Group” was performed in 38 out of 56 (67.8%), 25 out of 49 (51.0%) in the “EA group,” p=0.079, OR 0.49 [0.22, 1.08], RR 0.71 [0.47, 1.06]. Children who were in need of high-frequency oscillatory ventilation (HFOV) have not only had statistically significantly more frequent need for erythrocyte transfusion but also statistically significantly more often developed BPD and retinopathy of prematurity at the stage that requires surgical intervention. Conclusion: late EA administration in preterm infants with birthweight below 1500 gram reduces the risk of the development of the anemia of prematurity, increases the level of hemoglobin in peripheral blood at the age of six months old and does not increase the risk for development of retinopathy of prematurity.
在出生体重低于 1500 克的早产儿中使用环氧乙烷α
研究目的是评估对出生体重低于 1500 克、胎龄低于 310/7 周的极早产儿在出生 8 天后服用epoetin alfa (Eralfon®️)对早产儿贫血、6 个月时血液中血红蛋白水平和早产儿视网膜病变的影响。使用的材料和方法:在两家围产中心(L.A. Vorokhobov Moscow City Clinical Hospital No.这些婴儿被分为两组,G1(56 名)在出生后 1 至 2 个月未接受α-环氧乙烷(EA)治疗(即所谓的 "无 EA 组"),在雅罗斯拉夫尔州地区围产中心接受护理;G2(49 名)在出生后 1 至 2 个月接受 EA 治疗(即所谓的 "EA 组"),在 L. A. Vorokhobov 莫斯科市临床医院(俄罗斯莫斯科)和雅罗斯拉夫尔州地区围产中心(俄罗斯雅罗斯拉夫尔)接受护理。A. Vorokhobov 莫斯科市第 67 临床医院进行护理。在 "EA 组",后期(出生第 8 天后)给予 EA,剂量为 200 单位/公斤,每周 3 次皮下注射,持续 6 周。结果:出生第一天外周血中的血红蛋白水平在统计学上没有显著差异。在出生 1 至 2 个月时接受过 EA 治疗的早产儿,6 个月时外周血中的血红蛋白水平在统计学上明显更高。从统计学角度看,"EA 组 "出现早产儿贫血的频率明显较低:49 例中有 40 例(82.0%),而 56 例中有 54 例(96.0%),P=0.022。无 EA 组 "56 例中有 38 例(67.8%)进行了红细胞输注,"EA 组 "49 例中有 25 例(51.0%)进行了红细胞输注,P=0.079,OR 0.49 [0.22, 1.08],RR 0.71 [0.47, 1.06]。需要高频振荡通气(HFOV)的患儿不仅需要输红细胞的次数明显增多,而且在需要手术干预的阶段出现 BPD 和早产儿视网膜病变的次数也明显增多。结论:对出生体重低于 1500 克的早产儿晚用 EA 可降低早产儿贫血的发病风险,提高 6 个月大时外周血中的血红蛋白水平,并且不会增加早产儿视网膜病变的发病风险。
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