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极低出生体重儿预防性静脉注射免疫球蛋白治疗的应用

The use of prophylactic intravenous immunoglobulin therapy in very low birthweight infants.

作者信息

Chou Y H, Yau K I

机构信息

Division of Neonatology, Chang Gung Children's Hospital, Taipei, Taiwan, R.O.C.

出版信息

Changgeng Yi Xue Za Zhi. 1998 Dec;21(4):371-6.

PMID:10074720
Abstract

BACKGROUND

Nosocomial infections are a major cause of death in premature infants, especially in very low birthweight (VLBW) infants. The VLBW infants have low serum immunoglobulin G levels, which may have an effect on infections in early infancy. Thus, prophylactic administration of intravenous immunoglobulin (IVIG) is proposed to maintain higher immunoglobulin G and reduce the rate of hospital-acquired infection.

MATERIALS AND METHODS

A study for the effects of prophylactic IVIG therapy in VLBW infants was performed. A total of 61 VLBW infants were enrolled, and divided into the IVIG group (n = 31) and the control group (n = 30). The dose for each infant was 750-1000 mg/kg for those whose birthweight was less than 1000 g, and 500-750 mg/kg for infants whose birthweight was between 1001 and 1500 g. The control group received saline infusion. The infusions were given every 2 weeks until the infant weighed 1800 g, or was discharged.

RESULTS

The results showed: there were no major differences in the perinatal and neonatal characteristics between the two groups, consistently higher IgG levels were found in the IVIG group, and the age of first documented sepsis was earlier in the control group.

CONCLUSION

In this study, the prophylactic IVIG therapy may give substantially higher IgG levels, which may last for 2 months. However, a prophylactic effect for hospital-acquired infections was not observed.

摘要

背景

医院感染是早产儿死亡的主要原因,尤其是极低出生体重(VLBW)婴儿。极低出生体重婴儿血清免疫球蛋白G水平较低,这可能会影响婴儿早期的感染情况。因此,有人提出预防性静脉注射免疫球蛋白(IVIG)以维持较高的免疫球蛋白G水平并降低医院获得性感染的发生率。

材料与方法

进行了一项关于预防性IVIG治疗对极低出生体重婴儿影响的研究。共纳入61例极低出生体重婴儿,分为IVIG组(n = 31)和对照组(n = 30)。出生体重小于1000 g的婴儿,每例的剂量为750 - 1000 mg/kg;出生体重在1001至1500 g之间的婴儿,剂量为500 - 750 mg/kg。对照组接受生理盐水输注。每2周输注一次,直至婴儿体重达到1800 g或出院。

结果

结果显示:两组围产期和新生儿特征无显著差异,IVIG组的IgG水平始终较高,且对照组首次记录到败血症的年龄更早。

结论

在本研究中,预防性IVIG治疗可能使IgG水平大幅升高,且可能持续2个月。然而,未观察到对医院获得性感染的预防作用。

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The use of prophylactic intravenous immunoglobulin therapy in very low birthweight infants.极低出生体重儿预防性静脉注射免疫球蛋白治疗的应用
Changgeng Yi Xue Za Zhi. 1998 Dec;21(4):371-6.
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A controlled trial of intravenous immune globulin to reduce nosocomial infections in very-low-birth-weight infants. National Institute of Child Health and Human Development Neonatal Research Network.静脉注射免疫球蛋白降低极低出生体重儿医院感染的对照试验。美国国立儿童健康与人类发展研究所新生儿研究网络。
N Engl J Med. 1994 Apr 21;330(16):1107-13. doi: 10.1056/NEJM199404213301602.
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Preterm infants with low immunoglobulin G levels have increased risk of neonatal sepsis but do not benefit from prophylactic immunoglobulin G.免疫球蛋白G水平低的早产儿发生新生儿败血症的风险增加,但预防性使用免疫球蛋白G并无益处。
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Am J Perinatol. 1995 Sep;12(5):306-9. doi: 10.1055/s-2007-994481.
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Multicenter study to assess safety and efficacy of INH-A21, a donor-selected human staphylococcal immunoglobulin, for prevention of nosocomial infections in very low birth weight infants.一项多中心研究,旨在评估供体选择的人葡萄球菌免疫球蛋白INH - A21预防极低出生体重儿医院感染的安全性和有效性。
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Prophylactic intravenous administration of immune globulin in preterm infants: effect on serum immunoglobulin concentrations during the first year of life.早产儿预防性静脉注射免疫球蛋白:对生命第一年血清免疫球蛋白浓度的影响。
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Intravenous immunoglobulin for sepsis prevention in preterm infants.静脉注射免疫球蛋白用于预防早产儿败血症
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Immunoglobulin serum levels in very low birth weight infants treated with different intravenous preparations.接受不同静脉制剂治疗的极低出生体重儿的免疫球蛋白血清水平
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Intravenous immune globulin for the prevention of nosocomial infection in low-birth-weight neonates. The Multicenter Group for the Study of Immune Globulin in Neonates.静脉注射免疫球蛋白预防低体重新生儿医院感染。新生儿免疫球蛋白研究多中心小组。
N Engl J Med. 1992 Jul 23;327(4):213-9. doi: 10.1056/NEJM199207233270401.

引用本文的文献

1
Intravenous immunoglobulin for preventing infection in preterm and/or low birth weight infants.静脉注射免疫球蛋白预防早产和/或低出生体重儿感染
Cochrane Database Syst Rev. 2020 Jan 29;1(1):CD000361. doi: 10.1002/14651858.CD000361.pub4.