Chen J Y
Department of Pediatrics, Chung Shan Medical and Dental College Hospital, Taichung, Taiwan, ROC.
J Formos Med Assoc. 1996 Nov;95(11):839-44.
Blood cultures were performed on 141 newborn infants who had clinical features or laboratory data indicative of sepsis between January 1993 and April 1995. Clinical features included respiratory deterioration, poor activity, abdominal distension and apnea. Abnormal laboratory data included leukocytosis, leukopenia, elevated C-reactive protein values or increased immature neutrophil counts. The 141 neonates with suspected bacterial infections received antibiotic therapy and were randomly divided into two groups. One group received a single dose of 500 mg/kg of intravenous immunoglobulin (IVIG), while the other group received placebo (0.9% sodium chloride). Patients with negative blood cultures were excluded from this study. A total of 56 neonates with positive blood cultures were enrolled in this study. The IVIG-treated group and placebo-treated group consisted of 10 premature and 18 term neonates, respectively. Another 10 healthy premature and healthy 18 term neonates were selected as the control group. Serum IgG values increased significantly 1 and 2 weeks after administration of IVIG in the IVIG-treated group. However, there was no significant difference in the duration of treatment and mortality between the IVIG-treated and placebo-treated groups. Our preliminary observations suggest that administration of 500 mg/kg IVIG to neonates with sepsis had no effect on reducing mortality. In addition, it shortened neither the duration of antibiotic therapy nor hospitalization. No adverse reactions to the IVIG infusions were noted during the study.
1993年1月至1995年4月期间,对141例有临床特征或实验室数据提示败血症的新生儿进行了血培养。临床特征包括呼吸恶化、活动减少、腹胀和呼吸暂停。异常实验室数据包括白细胞增多、白细胞减少、C反应蛋白值升高或未成熟中性粒细胞计数增加。这141例疑似细菌感染的新生儿接受了抗生素治疗,并被随机分为两组。一组接受单次静脉注射500mg/kg免疫球蛋白(IVIG),另一组接受安慰剂(0.9%氯化钠)。血培养阴性的患者被排除在本研究之外。本研究共纳入56例血培养阳性的新生儿。IVIG治疗组和安慰剂治疗组分别由10例早产儿和18例足月儿组成。另外选取10例健康早产儿和18例健康足月儿作为对照组。IVIG治疗组在给予IVIG后1周和2周血清IgG值显著升高。然而,IVIG治疗组和安慰剂治疗组在治疗持续时间和死亡率方面没有显著差异。我们的初步观察表明,给败血症新生儿静脉注射500mg/kg IVIG对降低死亡率没有效果。此外,它既没有缩短抗生素治疗的持续时间,也没有缩短住院时间。在研究期间未观察到IVIG输注的不良反应。