Haque K N, Remo C, Bahakim H
Department of Paediatrics, College of Medicine, Riyadh, Saudi Arabia.
Clin Exp Immunol. 1995 Aug;101(2):328-33. doi: 10.1111/j.1365-2249.1995.tb08359.x.
In a prospective double-blind study, standard intravenous immunoglobulin (IVIG) was compared with an IgM-enriched IVIG in the treatment of neonatal sepsis. The two treatment groups were also compared with matched controls. One hundred and thirty babies (65 in each group) ranging from 0 to 24 days old, 480 to 4200 g in weight and born between 24 and 42 weeks of gestation who had, or were suspected of having, sepsis were given either standard IVIG or IgM-enriched IVIG (250 mg/kg per day) for 4 days in addition to supportive and antibiotic therapy. A further 65 babies who received similar supportive, antibiotic and fluids but not IVIG were used as matched controls. Mortality from infection in 'culture proven sepsis' was 3/44 (6.8%) in the IgM-enriched IVIG group, 6/42 (14.2%) in the standard IVIG group, and 11/43 (25.5%) in the control group (P = 0.017, IgM versus control, P = 0.19 standard IVIG versus control). There was no statistical difference in the outcome between the two immunoglobulin therapy groups (P = 0.25). The study indicates that IVIG improves outcome in neonatal sepsis when used as an adjunct to supportive and antibiotic therapy, but larger studies are required to confirm this.
在一项前瞻性双盲研究中,将标准静脉注射免疫球蛋白(IVIG)与富含IgM的IVIG用于治疗新生儿败血症进行了比较。两个治疗组还与配对对照组进行了比较。130名年龄在0至24天、体重480至4200克、孕周在24至42周之间且患有或疑似患有败血症的婴儿,除了接受支持治疗和抗生素治疗外,还接受了标准IVIG或富含IgM的IVIG(每天250毫克/千克)治疗,为期4天。另有65名接受了类似支持治疗、抗生素治疗和补液但未接受IVIG的婴儿作为配对对照组。在“经培养证实的败血症”中,富含IgM的IVIG组的感染死亡率为3/44(6.8%),标准IVIG组为6/42(14.2%),对照组为11/43(25.5%)(P = 0.017,IgM组与对照组相比,P = 0.19,标准IVIG组与对照组相比)。两个免疫球蛋白治疗组之间的结果无统计学差异(P = 0.25)。该研究表明,IVIG作为支持治疗和抗生素治疗的辅助手段用于新生儿败血症时可改善预后,但需要更大规模的研究来证实这一点。