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极低出生体重新生儿静脉注射免疫球蛋白制剂的处置情况。

Disposition of an immunoglobulin intravenous preparation in very low birth weight neonates.

作者信息

Noya F J, Rench M A, Garcia-Prats J A, Jones T M, Baker C J

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030.

出版信息

J Pediatr. 1988 Feb;112(2):278-83. doi: 10.1016/s0022-3476(88)80070-2.

Abstract

To assess the disposition, tolerance, and toxicity of an intravenous preparation of immunoglobulin (IGIV) in very low birth weight (VLBW) neonates, we administered single doses of 500 or 750 mg/kg to 20 neonates with birth weights between 750 and 1500 g during the first week of life. The infusion of this product was well tolerated. Modest changes in hemoglobin, hematocrit, and total hemolytic complement occurred as expected. Hepatic toxic effects were not detected. Mean peak IgG concentrations were 1564 and 1316 mg/dL for the high-dose and low-dose groups, respectively. Mean IgG concentrations were very similar for both groups on postinfusion days 1, 4, 7, 14, 21, and 28. IgG concentrations remained above 300 mg/dL in seven of 10 infants in each group by day 21, and in six of the high-dose group and seven of the low-dose group by day 28. Mean elimination half-lives were 22.6 and 22.8 days in the high-dose and low-dose groups, respectively. These data provide a basis for assessment of potential efficacy of IGIV in the prevention of late-onset infection in VLBW neonates.

摘要

为评估静脉注射免疫球蛋白(IGIV)制剂在极低出生体重(VLBW)新生儿中的处置、耐受性和毒性,我们在出生后第一周给20例出生体重在750至1500克之间的新生儿单次注射500或750毫克/千克。该产品的输注耐受性良好。血红蛋白、血细胞比容和总溶血补体出现了预期的适度变化。未检测到肝毒性作用。高剂量组和低剂量组的平均IgG峰值浓度分别为1564和1316毫克/分升。两组在输注后第1、4、7、14、21和28天的平均IgG浓度非常相似。到第21天,每组10名婴儿中有7名的IgG浓度保持在300毫克/分升以上,到第28天,高剂量组有6名、低剂量组有7名婴儿的IgG浓度保持在300毫克/分升以上。高剂量组和低剂量组的平均消除半衰期分别为22.6天和22.8天。这些数据为评估IGIV预防VLBW新生儿晚发性感染的潜在疗效提供了依据。

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